• The COVID-19 Vaccine Antigen Is ANTHRAX
    Dr. Ariyana Love
    By Dr. Ariyana Love

    Covid-19 vaccines use self-replicating, programmable nanotechnology and synthetic, modified RNA (modRNA) otherwise known as Spike Protein.

    We are told that a vaccine antigen is used in the Covid-19 technology to “evoke an immune response” but what if the Covid-19 vaccine antigen is ANTHRAX?

    “…hardly any natural pathogens are really well suited to being biowarfare agents from a military point of view. Such a bioweapon must fulfill a variety of demands: it needs to be produced in large amounts, it must act fast, it must be environmentally robust, and the disease must be treatable… only a minority of natural pathogens are suitable for military purposes. “Anthrax is of course the first choice because the causative agent, B. anthracis, fulfills nearly all of these specifications.”

    Anthrax was developed by Russia in 1950. According to the NIH, the USSR’s ‘invisible anthrax’ was created by introducing an “alien gene” into the highly deadly Bacillus Anthracis bacteria. This means that Cross-Species-Genomics capability was acquired by governments before 1950. A lethal bacterium and an alien gene were genetically altered and blended together to produce the deadly bioweapon known as Anthrax. Russia’s Anthrax could be treated with antibiotics even several days after exposure, and thus it met the requirements under the Biological Weapons Convention.

    A bioweapon of choice, Anthony Fauci decided to increase Anthrax lethality and the NIH began genetic attenuation before 2006. Through GAIN-and-LOSS-of-Function the NIH produced a more drastic and deadly Anthrax that’s resistant to antibiotics and more.

    According to a University of Minnesota publication, the United States D.O.D smuggled shipments of live B anthracis spores from the Army’s Dugway Proving Ground in Utah, to other labs in the United States and abroad (Source: USA Today). The U.S. Army sent shipments of live samples of Anthrax to 86 labs outside the U.S. over a period of 10 years (Source: The Daily Beast).

    Transfers of samples of live B anthracis and the H5N1 influenza bioweapon were sent from CDC labs to other labs. CDC correspondence released under the Freedom of Information Act shows that labs studying bioterror pathogens “have failed over and over to comply with important safety and security regulations.”

    The D.O.D. tried to cover for the CDC, claiming “system failure” was to blame for the lab leaks, but we already know that the D.O.D spearheaded this “Covid-19 vaccine” roll-out.


    Please see: Aerosolized inoculation of Anthrax – Aerosolized Intratracheal Inoculation of Recombinant Protective Antigen (rPA) Vaccine Provides


    In 2007, Anthony Fauci created the H7N9 bioweapon, otherwise known as the “influenza vaccine.” The NIH, CCP and the Israeli state collaborated through GAIN-and-LOSS-of-Function to produce the H7N9 “flu vaccine” and the new and improved “Aerosolized Anthrax Vaccine”.

    Ofir Israeli from the Israel Institute of Biological Research, sequenced the Bacillus anthracis V770-NP1-R Strain in 2014, creating a synthetic chemical bioweapon. The Israeli state oversaw the animal trials for the Anthrax “vaccine” and told us it was safe and effective. Meanwhile, the Israeli company called Sanofi Pasteur developed the first H7N9 “vaccine” and trialed it for the NIH in 2014. Also in 2014, the NIH developed the H7N9 “influenza vaccine” to be droplet transmissible.

    Simultaneously, in 2014 China achieved a 99% transmissibility of the H7N9 “flu vaccine”. China also trialed the first aerosolized intratracheal Anthrax “vaccine” on mice. The study revealed severe side effects.


    PLEASE SEE: NIH Using DEAD CORPSES To Make “Virus”; Gain Of Function Weaponized Dead Corpses


    The Israeli state, NIH and China turned their new and improved Anthrax bioweapon into an attenuated antigen to be used in vaccines under the guise of “evoking an immune response” and “vaccine immunity.” The nations have been intentionally poisoned with biowarfare.

    In March 2022, the Russian military discovered that the Covid-19 bioweapons are being developed in U.S. biolabs in Ukraine. This includes the plague, Ebola, Filoviruses’, Anthrax and more. Anthrax causes hemorrhaging. So does Ebola and Marburg.

    Ebola is used in the J&J and Sinovax jabs, while Filovirus is used in Moderna. Ebola and Marburg are both Anthrax. H7N9 is used in all “flu vaccines” while Anthrax is being used as a “vaccine adjuvant” in all Covid-19 jabs and swabs.

    Through Loss-Of-Function, genetic deletions were performed inside the B. anthracis bacteria to improve replication of the bacteria in vivo. This ensured hospital protocols would not work to stop the Anthrax from replicating inside the human body after inoculation due to it being antibiotic resistant.

    The B. anthracis bacteria was also genetically modified to survive in insect hosts so as not to sporulate before it’s injected into the human host by a Bill Gates GMO mosquito which is part of DARPA’s weaponized insect project called The Sentinels.

    Incidentally, the CDC owns the Anthrax isolate patent that was funded by the U.S. Government. This is treason. The CDC also says that a bioterrorist attack would most likely be Anthrax.

    Please see: Malaria Parasites In “Vaccines” Target Placenta, Kill Babies In Utero

    SPIKE PROTEIN IS AEROSOLIZED ANTHRAX

    There are 232 B. anthracis genomes that are currently available in the GenBank database. There’s an Anthrax “vaccine” for cattle and two strains are licensed for use in humans. There exist two patents for an “Aerosolized Anthrax Vaccine.”

    The first Anthrax “vaccine” patent for humans is partly owned by the U.S. Government. The second is a “Recombinant Anthrax Vaccine”.

    “The spores of the toxigenic, nonencapsulated B. anthracis STI-1 strain and the cell-free PA-based “vaccines” consisting of aluminum hydroxide-adsorbed supernatant material from cultures of the toxigenic, nonencapsulated B. anthracis strain V770-NPI-R or alum-precipitated culture filtrate from the Sterne strain. Each of these Anthrax toxins are being used for “cellular entry in humans“. The LF is a metalloprotease recently shown to cleave the amino termini of the mitogen-activated protein kinase kinases 1 and 2, which results in their inactivation.”

    The above quote from the Recombinant Anthrax Vaccine patent reveals that the poisonous Anthrax “antigen” is being used to genetically modify the genome of humans (cellular entry into humans). By cleaving to the amino termini, protein kinases 1 and 2 are inactivated. This is accomplished by genetic deletions.

    The molecular basis of Anthrax “vaccines” includes “spores and DNA plasmids” that are entering human cells.

    The following quote about the Anthrax “protective antigen” is particularly revealing:

    “PA (protective antigen) is the common receptor binding domain of the toxins and can interact with the two different effector domains, EF and LF, to mediate their entry into target cells (14).”

    Anthrax is being used to “regulate gene expression by binding to DNA sequences and modulating transcriptional activity through their effector domains”.

    Pharma has essentially found a way to encode any synthetic proteins into the human genome from any species they want, including bacteria. The “Aerosolized Anthrax Antigen” is being encoded into target cells to make those cells produce the chemical drug called Anthrax. This is how the Anthrax “vaccine” is aerosolized. Once a person is inoculated with the Covid-19 bioweapon through subcutaneous injection or nasopharyngeal delivery with contaminated PCR swabs, the weapon system will begin genetic deletions and encoding the genome of target cells with the Anthrax spike protein. A person begins producing the toxic spike protein and shedding Anthrax into the air, exposing everyone to Inhalation Anthrax. It’s a weapon system that is intentionally aerosolized.

    This study admits that the Anthrax spores from B. anthracis STI-1 strain and B. anthracis strain V770-NPI-R used in the “aerosolized Anthrax vaccines” are toxigenic. The Sterne strain which is used to inoculate our food supply (animals) is also genotoxic.

    This NIH study explains how a “replicon” of the Bacillus anthracis bacteria was cloned into an Escherichia coli (E. coli) “vector” using cross-species-genomics. These two bacteria were synthetically fused together to enhance lethality.

    ALHYDROGEL

    According to the “aerosolized Anthrax vaccine” patents, the so-called “vaccine adjuvant” used is a DARPA weapon system called Alhydrogel.

    Hydrogel technology was developed over many years during a collaboration between DARPA and Profusa, a private biotech company specializing in the development of tissue-integrated biosensors. In 2018, DARPA published a video revealing their intention to use this biosensing technology for both military and public health.

    In the Alhydrogel invention, Anthrax was fused together into a nanogel called Alhydrogel, consisting of fibrous nanoparticles (Nanofibers) that are “antigen specific to CD4+ T cells”.

    In layman’s terms, the nanorobots are intentionally programmed to target and alter the genome of CD4-T cells, inducing cell death. This essential part of our immune system (T-cells) stop foreign invaders from entering our cells. Destroying our T-cells enables the government’s operating system to take root in the body and quicken death.

    Alhydrogel is infused with 750 μg of aluminum, making it magnetic. Nanofibers are used for self-assembly and electrospinning, for tissue engineering and delivery of drugs and chemicals into the brain. Being magnetic and nanotech based, the Alhydrogel can replicate everywhere in the body and wire a new neural network.

    Astonishingly, Alhydrogel is already the most widely used vaccine adjuvant! There are many Alhydrogel patents that contain toxic cocktails that will overwhelm anyone’s immune system.

    This Alhydrogel patent demonstrates it’s use of the B anthracis bacteria, E. coli, N. gonorrhoeae, Chlamydia, Staphylococcus, TB and more. It also contains the H5N1 influenza bioweapon, RNA, DNA synthesis and Polysorbate 80 for Blood Brain Barrier (BBB) permeability. This begs the question, where do venereal diseases come from?

    This Nature article reveals that 2% Alhydrogel is used in all Covid-19 “vaccines”. Previously, aluminum salts were the only adjuvants licensed for vaccine use in humans in the U.S. In recent decades, nanoparticle adjuvants in hydrated gels were introduced. The article continues by saying that the “influenza vaccine” was the first to use Alhydrogel.

    “Aluminum salt-based adjuvants such as alhydrogel have been a mainstay of vaccines for decades” boasts Christopher B. Fox and colleagues at the Infectious Disease Research Institute in Seattle, USA.

    Both nanoparticles and Anthrax have been used in vaccines for decades already, without the Informed Consent of the public.

    Alhydrogel was improved and transformed into the Nanoalum adjuvant.

    Here, we introduce a top-down manufacturing process—high-pressure microfluidization—to generate aluminum oxyhydroxide nanoparticles, hereupon referred to as nanoalum, using the clinically approved Alhydrogel adjuvant as the precursor.

    Alhydrogel is also carried in the lipid coating of nanoparticles.

    The “Aerosolized Anthrax Vaccines” also contain SEQ ID NO: 1 which is owned by the Pirbright Institute (Bill & Melinda Gates). SEQ ID NO: 1 contains the world’s most deadly genetically modified parasites.


    Please see: MEGA BOMBS! GMO Parasites Are The mRNA Vector!


    ANTHRAX SYMPTOMS AND TREATMENT

    Anthrax has been deployed on the population by three methods; injection, inhalation and skin penetration. The mortality rate for Anthrax varies depending on the method of exposure. It’s approximately 20% fatality for cutaneous Anthrax and 25–75% for Gastrointestinal Anthrax. Inhalation Anthrax is by far the worst with a fatality rate that is 80% or higher. Inhalation Anthrax is what we’re all being exposed to from the Covid-19 jabs and contaminated PCR swabs.

    Antibiotics constitute the mainstay of treatment against Anthrax, despite the fact that they won’t work to stop its replication due to the NIH, China and Israel’s GAIN-and-LOSS-of-Function enhancements (antibiotic resistance).

    Pharmaceutical experimental genotoxic drugs such as Oblitoxaximab and Raxibacumab are being touted as Anthrax treatments but these are monoclonal antibodies. We know from the monoclonal antibody patents that they’re also the “mRNA vaccine” weapon system. Anytime you inject recombinant proteins or modRNA into humans, it’s extremely toxic and will be rejected by our immune system 100% of the time.


    Please read: Monoclonal Antibodies Is mRNA Gene Knockdown Tech, Encoding HIV – Patent Review


    Pharma wants us to believe that the only known effective “prevention” against Anthrax is the Anthrax “vaccine”. However, the Anthrax “vaccine” inoculation given to U.S. military troops was a horrific disaster. U.S. Army statistics that were never published, show the Anthrax “vaccine” induces turbo cancers.

    The toxicological harms of Anthrax are many. It causes severe heart issues. Could this be a contributing factor to Myocarditis and Pericarditis?

    Anthrax also coagulates the blood.

    “Pathophysiological changes associated with anthrax lethal toxin included loss of plasma proteins, decreased platelet count, slower clotting times, fibrin deposits in tissue sections, and gross and histopathological evidence of hemorrhage. These findings suggest that blood vessel leakage and hemorrhage lead to disseminating intravascular coagulation and/or circulatory shock as an underlying pathophysiological mechanism.”

    Read more here and here.

    Anthrax induces hemorrhaging. So this explains all the excessive bleeding people have experienced over the last 4 years, following Covid-19 inoculation and from aerosolized exposure, otherwise known as the “shedding” phenomenon. This is a result of Inhalation Anthrax.

    It becomes clear that the newly dubbed “White Lung Syndrome” and the Chinese ‘pneumonia’ outbreak is none other than Inhalation Anthrax. Mycoplasma pneumonia is on the rise, and it’s listed on Pfizer’s internal documentation as a known Adverse Effect of the Covid-19 inoculation.


    This study reveals that Mycoplasma Pneumonia is aerosolized. WHO also confirms this phenomenon is Mycoplasma Pneumonia.

    All naturally occurring bacterium have cell walls. Mycoplasmas are spherical to filamentous cells with no cell walls. It’s genetically manipulated in a laboratory by GAIN-of-Function for the purpose of enhancing replication inside the human body, making it more lethal.

    Mice “treated” with anthrax lethal toxin (LT) exhibit hemorrhage and liver damage. Monocyte procoagulant responses to anthrax peptidoglycan are reinforced by proinflammatory cytokine signaling and histological lesions in the spleen.

    Anthrax has already been tested on the public. According to the NIH, Anthrax spores were intentionally released into “some environments” in NYC during 9/11. According to the NIH, the FBI launched an investigation called “Amerithrax”. It was “one of the largest and most complex (investigation) in the history of law enforcement”, according to the FBI.

    Heroine users in Europe have been tested with Injection Anthrax.

    Our skies are sprayed with smart dust and chemicals daily. Our governments have launched an all-out war against their constituents. We are being poisoned in a myriad of ways, so please keep this in mind:

    “Anthrax is easy to produce in large quantities, highly lethal, relatively easy to develop as a weapon, easily spread over a large area, easily stored and dangerous for a long time. Given appropriate weather and wind conditions, 50 kilograms of aerosolised anthrax spores released from an aircraft along a 2 kilometer line could create a lethal cloud of anthrax spores that would extend beyond 20 kilometers downwind. The aerosol cloud would be colorless, odorless and invisible following its release. Given the small size of the spores, people indoors would receive the same amount of exposure as on the street. There are currently no atmospheric warning systems to detect an aerosol cloud of anthrax spores. The first sign of a bioterrorist attack would most likely be patients presenting with symptoms of inhalation anthrax. A 1970 analysis by World Health Organization concluded that the release of aerosolized anthrax upwind to a population of 5,000,000 could lead to an estimated 250,000 casualties, of whom as many as 100,000 could be expected to die. A later analysis, by the Office of Technology Assessment of the U.S. Congress estimated that 130,000 to 3 million deaths could occur following the release of 100 kilograms of aerosolized anthrax over Washington D.C., making such an attack as lethal as a hydrogen bomb.”

    TREATMENT

    If you have been inoculated with Covid-19 or PCR swabbed, and you are suffering from heart pain, unusual bleeding, skin rashes and abrasions, it could be Injection Anthrax. If you are “unvaccinated” and hemorrhaging from being around “vaccinated”, then you may have been exposed to Inhalation Anthrax.

    Many doctors, including myself, have documented persistent bleeding rectally, violent bleeding vaginally, nasally and in the eyes. Since October 4th, I have received many reports of a red eye syndrome where the entire eye is blood-red. This makes sense because eye tissue is more sensitive. If you have been exposed to Inhalation Anthrax, you may feel hot and severely flushed, and you may break out in big, red splotches on your skin, followed by a completely red eye in the morning.

    Although they don’t get much attention, “anti-toxins have long been considered an essential ‘adjunctive’ therapy, and remain so”, according to the NIH. Anti-toxins are the natural medicines that detox poisons. In other words, you need an effective natural medicine detox protocol.

    I have been successfully detoxing people from the Covid-19 bioweapons for three years. Since I began treating people presenting with Anthrax poisoning with strong antibacterials, my clients are experiencing quicker detox results. If you would like to schedule a consultation with me, please do so through my online booking system.

    Please follow me on Telegram @drloveariyana and X @drloveariyana.

    If you would like to donate to my research, please do so here.


    UPDATE: My Anthrax article is now fully edited and published on Substack. Please review and SHARE.

    The Covid-19 Vaccine Antigen Is ANTHRAX

    Read more:
    https://open.substack.com/pub/drloveariyana/p/the-covid-19-vaccine-antigen-is-anthrax?r=2juwfo&utm_campaign=post&utm_medium=web&showWelcomeOnShare=true


    https://donshafi911.blogspot.com/2024/02/the-covid-19-vaccine-antigen-is-anthrax.html
    The COVID-19 Vaccine Antigen Is ANTHRAX Dr. Ariyana Love By Dr. Ariyana Love Covid-19 vaccines use self-replicating, programmable nanotechnology and synthetic, modified RNA (modRNA) otherwise known as Spike Protein. We are told that a vaccine antigen is used in the Covid-19 technology to “evoke an immune response” but what if the Covid-19 vaccine antigen is ANTHRAX? “…hardly any natural pathogens are really well suited to being biowarfare agents from a military point of view. Such a bioweapon must fulfill a variety of demands: it needs to be produced in large amounts, it must act fast, it must be environmentally robust, and the disease must be treatable… only a minority of natural pathogens are suitable for military purposes. “Anthrax is of course the first choice because the causative agent, B. anthracis, fulfills nearly all of these specifications.” Anthrax was developed by Russia in 1950. According to the NIH, the USSR’s ‘invisible anthrax’ was created by introducing an “alien gene” into the highly deadly Bacillus Anthracis bacteria. This means that Cross-Species-Genomics capability was acquired by governments before 1950. A lethal bacterium and an alien gene were genetically altered and blended together to produce the deadly bioweapon known as Anthrax. Russia’s Anthrax could be treated with antibiotics even several days after exposure, and thus it met the requirements under the Biological Weapons Convention. A bioweapon of choice, Anthony Fauci decided to increase Anthrax lethality and the NIH began genetic attenuation before 2006. Through GAIN-and-LOSS-of-Function the NIH produced a more drastic and deadly Anthrax that’s resistant to antibiotics and more. According to a University of Minnesota publication, the United States D.O.D smuggled shipments of live B anthracis spores from the Army’s Dugway Proving Ground in Utah, to other labs in the United States and abroad (Source: USA Today). The U.S. Army sent shipments of live samples of Anthrax to 86 labs outside the U.S. over a period of 10 years (Source: The Daily Beast). Transfers of samples of live B anthracis and the H5N1 influenza bioweapon were sent from CDC labs to other labs. CDC correspondence released under the Freedom of Information Act shows that labs studying bioterror pathogens “have failed over and over to comply with important safety and security regulations.” The D.O.D. tried to cover for the CDC, claiming “system failure” was to blame for the lab leaks, but we already know that the D.O.D spearheaded this “Covid-19 vaccine” roll-out. Please see: Aerosolized inoculation of Anthrax – Aerosolized Intratracheal Inoculation of Recombinant Protective Antigen (rPA) Vaccine Provides In 2007, Anthony Fauci created the H7N9 bioweapon, otherwise known as the “influenza vaccine.” The NIH, CCP and the Israeli state collaborated through GAIN-and-LOSS-of-Function to produce the H7N9 “flu vaccine” and the new and improved “Aerosolized Anthrax Vaccine”. Ofir Israeli from the Israel Institute of Biological Research, sequenced the Bacillus anthracis V770-NP1-R Strain in 2014, creating a synthetic chemical bioweapon. The Israeli state oversaw the animal trials for the Anthrax “vaccine” and told us it was safe and effective. Meanwhile, the Israeli company called Sanofi Pasteur developed the first H7N9 “vaccine” and trialed it for the NIH in 2014. Also in 2014, the NIH developed the H7N9 “influenza vaccine” to be droplet transmissible. Simultaneously, in 2014 China achieved a 99% transmissibility of the H7N9 “flu vaccine”. China also trialed the first aerosolized intratracheal Anthrax “vaccine” on mice. The study revealed severe side effects. PLEASE SEE: NIH Using DEAD CORPSES To Make “Virus”; Gain Of Function Weaponized Dead Corpses The Israeli state, NIH and China turned their new and improved Anthrax bioweapon into an attenuated antigen to be used in vaccines under the guise of “evoking an immune response” and “vaccine immunity.” The nations have been intentionally poisoned with biowarfare. In March 2022, the Russian military discovered that the Covid-19 bioweapons are being developed in U.S. biolabs in Ukraine. This includes the plague, Ebola, Filoviruses’, Anthrax and more. Anthrax causes hemorrhaging. So does Ebola and Marburg. Ebola is used in the J&J and Sinovax jabs, while Filovirus is used in Moderna. Ebola and Marburg are both Anthrax. H7N9 is used in all “flu vaccines” while Anthrax is being used as a “vaccine adjuvant” in all Covid-19 jabs and swabs. Through Loss-Of-Function, genetic deletions were performed inside the B. anthracis bacteria to improve replication of the bacteria in vivo. This ensured hospital protocols would not work to stop the Anthrax from replicating inside the human body after inoculation due to it being antibiotic resistant. The B. anthracis bacteria was also genetically modified to survive in insect hosts so as not to sporulate before it’s injected into the human host by a Bill Gates GMO mosquito which is part of DARPA’s weaponized insect project called The Sentinels. Incidentally, the CDC owns the Anthrax isolate patent that was funded by the U.S. Government. This is treason. The CDC also says that a bioterrorist attack would most likely be Anthrax. Please see: Malaria Parasites In “Vaccines” Target Placenta, Kill Babies In Utero SPIKE PROTEIN IS AEROSOLIZED ANTHRAX There are 232 B. anthracis genomes that are currently available in the GenBank database. There’s an Anthrax “vaccine” for cattle and two strains are licensed for use in humans. There exist two patents for an “Aerosolized Anthrax Vaccine.” The first Anthrax “vaccine” patent for humans is partly owned by the U.S. Government. The second is a “Recombinant Anthrax Vaccine”. “The spores of the toxigenic, nonencapsulated B. anthracis STI-1 strain and the cell-free PA-based “vaccines” consisting of aluminum hydroxide-adsorbed supernatant material from cultures of the toxigenic, nonencapsulated B. anthracis strain V770-NPI-R or alum-precipitated culture filtrate from the Sterne strain. Each of these Anthrax toxins are being used for “cellular entry in humans“. The LF is a metalloprotease recently shown to cleave the amino termini of the mitogen-activated protein kinase kinases 1 and 2, which results in their inactivation.” The above quote from the Recombinant Anthrax Vaccine patent reveals that the poisonous Anthrax “antigen” is being used to genetically modify the genome of humans (cellular entry into humans). By cleaving to the amino termini, protein kinases 1 and 2 are inactivated. This is accomplished by genetic deletions. The molecular basis of Anthrax “vaccines” includes “spores and DNA plasmids” that are entering human cells. The following quote about the Anthrax “protective antigen” is particularly revealing: “PA (protective antigen) is the common receptor binding domain of the toxins and can interact with the two different effector domains, EF and LF, to mediate their entry into target cells (14).” Anthrax is being used to “regulate gene expression by binding to DNA sequences and modulating transcriptional activity through their effector domains”. Pharma has essentially found a way to encode any synthetic proteins into the human genome from any species they want, including bacteria. The “Aerosolized Anthrax Antigen” is being encoded into target cells to make those cells produce the chemical drug called Anthrax. This is how the Anthrax “vaccine” is aerosolized. Once a person is inoculated with the Covid-19 bioweapon through subcutaneous injection or nasopharyngeal delivery with contaminated PCR swabs, the weapon system will begin genetic deletions and encoding the genome of target cells with the Anthrax spike protein. A person begins producing the toxic spike protein and shedding Anthrax into the air, exposing everyone to Inhalation Anthrax. It’s a weapon system that is intentionally aerosolized. This study admits that the Anthrax spores from B. anthracis STI-1 strain and B. anthracis strain V770-NPI-R used in the “aerosolized Anthrax vaccines” are toxigenic. The Sterne strain which is used to inoculate our food supply (animals) is also genotoxic. This NIH study explains how a “replicon” of the Bacillus anthracis bacteria was cloned into an Escherichia coli (E. coli) “vector” using cross-species-genomics. These two bacteria were synthetically fused together to enhance lethality. ALHYDROGEL According to the “aerosolized Anthrax vaccine” patents, the so-called “vaccine adjuvant” used is a DARPA weapon system called Alhydrogel. Hydrogel technology was developed over many years during a collaboration between DARPA and Profusa, a private biotech company specializing in the development of tissue-integrated biosensors. In 2018, DARPA published a video revealing their intention to use this biosensing technology for both military and public health. In the Alhydrogel invention, Anthrax was fused together into a nanogel called Alhydrogel, consisting of fibrous nanoparticles (Nanofibers) that are “antigen specific to CD4+ T cells”. In layman’s terms, the nanorobots are intentionally programmed to target and alter the genome of CD4-T cells, inducing cell death. This essential part of our immune system (T-cells) stop foreign invaders from entering our cells. Destroying our T-cells enables the government’s operating system to take root in the body and quicken death. Alhydrogel is infused with 750 μg of aluminum, making it magnetic. Nanofibers are used for self-assembly and electrospinning, for tissue engineering and delivery of drugs and chemicals into the brain. Being magnetic and nanotech based, the Alhydrogel can replicate everywhere in the body and wire a new neural network. Astonishingly, Alhydrogel is already the most widely used vaccine adjuvant! There are many Alhydrogel patents that contain toxic cocktails that will overwhelm anyone’s immune system. This Alhydrogel patent demonstrates it’s use of the B anthracis bacteria, E. coli, N. gonorrhoeae, Chlamydia, Staphylococcus, TB and more. It also contains the H5N1 influenza bioweapon, RNA, DNA synthesis and Polysorbate 80 for Blood Brain Barrier (BBB) permeability. This begs the question, where do venereal diseases come from? This Nature article reveals that 2% Alhydrogel is used in all Covid-19 “vaccines”. Previously, aluminum salts were the only adjuvants licensed for vaccine use in humans in the U.S. In recent decades, nanoparticle adjuvants in hydrated gels were introduced. The article continues by saying that the “influenza vaccine” was the first to use Alhydrogel. “Aluminum salt-based adjuvants such as alhydrogel have been a mainstay of vaccines for decades” boasts Christopher B. Fox and colleagues at the Infectious Disease Research Institute in Seattle, USA. Both nanoparticles and Anthrax have been used in vaccines for decades already, without the Informed Consent of the public. Alhydrogel was improved and transformed into the Nanoalum adjuvant. Here, we introduce a top-down manufacturing process—high-pressure microfluidization—to generate aluminum oxyhydroxide nanoparticles, hereupon referred to as nanoalum, using the clinically approved Alhydrogel adjuvant as the precursor. Alhydrogel is also carried in the lipid coating of nanoparticles. The “Aerosolized Anthrax Vaccines” also contain SEQ ID NO: 1 which is owned by the Pirbright Institute (Bill & Melinda Gates). SEQ ID NO: 1 contains the world’s most deadly genetically modified parasites. Please see: MEGA BOMBS! GMO Parasites Are The mRNA Vector! ANTHRAX SYMPTOMS AND TREATMENT Anthrax has been deployed on the population by three methods; injection, inhalation and skin penetration. The mortality rate for Anthrax varies depending on the method of exposure. It’s approximately 20% fatality for cutaneous Anthrax and 25–75% for Gastrointestinal Anthrax. Inhalation Anthrax is by far the worst with a fatality rate that is 80% or higher. Inhalation Anthrax is what we’re all being exposed to from the Covid-19 jabs and contaminated PCR swabs. Antibiotics constitute the mainstay of treatment against Anthrax, despite the fact that they won’t work to stop its replication due to the NIH, China and Israel’s GAIN-and-LOSS-of-Function enhancements (antibiotic resistance). Pharmaceutical experimental genotoxic drugs such as Oblitoxaximab and Raxibacumab are being touted as Anthrax treatments but these are monoclonal antibodies. We know from the monoclonal antibody patents that they’re also the “mRNA vaccine” weapon system. Anytime you inject recombinant proteins or modRNA into humans, it’s extremely toxic and will be rejected by our immune system 100% of the time. Please read: Monoclonal Antibodies Is mRNA Gene Knockdown Tech, Encoding HIV – Patent Review Pharma wants us to believe that the only known effective “prevention” against Anthrax is the Anthrax “vaccine”. However, the Anthrax “vaccine” inoculation given to U.S. military troops was a horrific disaster. U.S. Army statistics that were never published, show the Anthrax “vaccine” induces turbo cancers. The toxicological harms of Anthrax are many. It causes severe heart issues. Could this be a contributing factor to Myocarditis and Pericarditis? Anthrax also coagulates the blood. “Pathophysiological changes associated with anthrax lethal toxin included loss of plasma proteins, decreased platelet count, slower clotting times, fibrin deposits in tissue sections, and gross and histopathological evidence of hemorrhage. These findings suggest that blood vessel leakage and hemorrhage lead to disseminating intravascular coagulation and/or circulatory shock as an underlying pathophysiological mechanism.” Read more here and here. Anthrax induces hemorrhaging. So this explains all the excessive bleeding people have experienced over the last 4 years, following Covid-19 inoculation and from aerosolized exposure, otherwise known as the “shedding” phenomenon. This is a result of Inhalation Anthrax. It becomes clear that the newly dubbed “White Lung Syndrome” and the Chinese ‘pneumonia’ outbreak is none other than Inhalation Anthrax. Mycoplasma pneumonia is on the rise, and it’s listed on Pfizer’s internal documentation as a known Adverse Effect of the Covid-19 inoculation. This study reveals that Mycoplasma Pneumonia is aerosolized. WHO also confirms this phenomenon is Mycoplasma Pneumonia. All naturally occurring bacterium have cell walls. Mycoplasmas are spherical to filamentous cells with no cell walls. It’s genetically manipulated in a laboratory by GAIN-of-Function for the purpose of enhancing replication inside the human body, making it more lethal. Mice “treated” with anthrax lethal toxin (LT) exhibit hemorrhage and liver damage. Monocyte procoagulant responses to anthrax peptidoglycan are reinforced by proinflammatory cytokine signaling and histological lesions in the spleen. Anthrax has already been tested on the public. According to the NIH, Anthrax spores were intentionally released into “some environments” in NYC during 9/11. According to the NIH, the FBI launched an investigation called “Amerithrax”. It was “one of the largest and most complex (investigation) in the history of law enforcement”, according to the FBI. Heroine users in Europe have been tested with Injection Anthrax. Our skies are sprayed with smart dust and chemicals daily. Our governments have launched an all-out war against their constituents. We are being poisoned in a myriad of ways, so please keep this in mind: “Anthrax is easy to produce in large quantities, highly lethal, relatively easy to develop as a weapon, easily spread over a large area, easily stored and dangerous for a long time. Given appropriate weather and wind conditions, 50 kilograms of aerosolised anthrax spores released from an aircraft along a 2 kilometer line could create a lethal cloud of anthrax spores that would extend beyond 20 kilometers downwind. The aerosol cloud would be colorless, odorless and invisible following its release. Given the small size of the spores, people indoors would receive the same amount of exposure as on the street. There are currently no atmospheric warning systems to detect an aerosol cloud of anthrax spores. The first sign of a bioterrorist attack would most likely be patients presenting with symptoms of inhalation anthrax. A 1970 analysis by World Health Organization concluded that the release of aerosolized anthrax upwind to a population of 5,000,000 could lead to an estimated 250,000 casualties, of whom as many as 100,000 could be expected to die. A later analysis, by the Office of Technology Assessment of the U.S. Congress estimated that 130,000 to 3 million deaths could occur following the release of 100 kilograms of aerosolized anthrax over Washington D.C., making such an attack as lethal as a hydrogen bomb.” TREATMENT If you have been inoculated with Covid-19 or PCR swabbed, and you are suffering from heart pain, unusual bleeding, skin rashes and abrasions, it could be Injection Anthrax. If you are “unvaccinated” and hemorrhaging from being around “vaccinated”, then you may have been exposed to Inhalation Anthrax. Many doctors, including myself, have documented persistent bleeding rectally, violent bleeding vaginally, nasally and in the eyes. Since October 4th, I have received many reports of a red eye syndrome where the entire eye is blood-red. This makes sense because eye tissue is more sensitive. If you have been exposed to Inhalation Anthrax, you may feel hot and severely flushed, and you may break out in big, red splotches on your skin, followed by a completely red eye in the morning. Although they don’t get much attention, “anti-toxins have long been considered an essential ‘adjunctive’ therapy, and remain so”, according to the NIH. Anti-toxins are the natural medicines that detox poisons. In other words, you need an effective natural medicine detox protocol. I have been successfully detoxing people from the Covid-19 bioweapons for three years. Since I began treating people presenting with Anthrax poisoning with strong antibacterials, my clients are experiencing quicker detox results. If you would like to schedule a consultation with me, please do so through my online booking system. Please follow me on Telegram @drloveariyana and X @drloveariyana. If you would like to donate to my research, please do so here. UPDATE: My Anthrax article is now fully edited and published on Substack. Please review and SHARE. The Covid-19 Vaccine Antigen Is ANTHRAX Read more: https://open.substack.com/pub/drloveariyana/p/the-covid-19-vaccine-antigen-is-anthrax?r=2juwfo&utm_campaign=post&utm_medium=web&showWelcomeOnShare=true https://donshafi911.blogspot.com/2024/02/the-covid-19-vaccine-antigen-is-anthrax.html
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  • https://gutzy.asia/2024/02/06/minister-shanmugam-reprimands-lmws-coi-proposal-on-death-of-late-sgt-uvaraja/
    https://gutzy.asia/2024/02/06/minister-shanmugam-reprimands-lmws-coi-proposal-on-death-of-late-sgt-uvaraja/
    GUTZY.ASIA
    Minister Shanmugam reprimands LMW’s COI proposal on death of late Sgt. Uvaraja
    Minister K Shanmugam rebuked NCMP Leong Mun Wai's inquiry regarding the absence of a COI for Uvaraja Gopal, a police officer who committed suicide amid workplace bullying allegations, citing the low morale among UK police resulting from similar investigations.
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  • The Truth About HPV Vaccination, Part 2: Studies Link the Vaccines to Neurological, Autoimmune Disorders
    Researchers who looked closely into the Gardasil HPV vaccine concluded the risks from the vaccine seem to significantly outweigh the as-yet-unproven long-term benefits.

    The Epoch Times

    Miss a day, miss a lot. Subscribe to The Defender's Top News of the Day. It's free.

    By Dr. Yuhong Dong

    Editor’s Note: This second installment in a multi-part series about the human papillomavirus, or HPV, vaccine examines studies that link the vaccines to increased risk of serious neurological and autoimmune disorders. Read Part 1 here.

    Summary of key facts

    A Danish review of 79,102 female and 16,568 male subjects, found human papillomavirus (HPV) vaccines had significantly increased rates of serious nervous system disorders. Postural orthostatic tachycardia syndrome (POTS) and complex regional pain syndrome were judged “definitely associated” with the HPV vaccine.
    A large Danish and Swedish study including nearly 300,000 girls found a significant association between the HPV vaccine and increased rates of Bechet’s syndrome (rate ratio 3.37), Raynaud’s disease (1.67) and type 1 diabetes (1.29).
    A large study including 3 million Danish and Swedish women aged 18 to 44, identified seven adverse events with statistically significant increased risks following HPV vaccination: Hashimoto’s thyroiditis, celiac disease, lupus erythematosus, pemphigus vulgaris, Addison’s disease, Raynaud’s disease and encephalitis, myelitis, or encephalomyelitis.
    A 2017 French study of over 2.2 million young girls found evidence of a 3.78-fold increased risk of Guillain-Barré syndrome (GBS). A 2011 U.S. study found nearly a two-and-a-half to 10 times greater risk of acquiring GBS within six weeks post-Gardasil vaccination.
    While the underlying mechanisms causing these autoimmune reactions are not yet fully understood, some researchers speculate that the sizable overlap in protein sequences between the HPV and the human genome may cause the immune system to attack itself. Others are concerned that the adjuvants (such as aluminum) used to attract the attention of the immune system may be causing harm.
    Neurological and autoimmune disorders

    Danish review found increased nervous system disorder

    In 2020, a group of Danish scientists conducted a systematic review of the overall benefits and harms of HPV vaccines.

    Twenty-four eligible randomized controlled clinical studies were obtained, with a total of 95,670 participants, mostly women, and 49 months mean weighted follow-up.

    Almost all controls were given an active comparator vaccine (typically a hepatitis vaccine with a comparable aluminum-based adjuvant).

    Given that the adjuvant is highly immunogenic by design (it is meant to grab the attention of the immune system), this trial design makes it difficult to detect an excess risk with the HPV vaccines.

    Without true controls (such as a saline placebo), the real risks of HPV vaccination cannot be accurately assessed.

    In the vaccine group, 367 cancers were detected, compared to 490 in the comparator group.

    Younger participants (15 to 29) seemed to benefit more from the vaccine concerning preventing moderate HPV-related intraepithelial neoplasia compared to older participants (ages 21 to 72). Younger participants also had fewer fatal harms.

    Even though the studies were flawed in their design, at four years post-vaccination, those who had received the HPV vaccines had significantly increased rates of serious nervous system disorders: 49%, as well as general harms totaling 7%.

    The serious harms that were judged “definitely associated” with HPV vaccines were postural orthostatic tachycardia syndrome and complex regional pain syndrome. POTS had a nearly twofold increase in the vaccinated group.

    By July 2017, only two-thirds of the results from HPV vaccine trials had been published, and only about half the results had been posted, due to manuscript length limitations, reporting bias and confounding journal articles offering a limited view of trial outcomes.

    This Danish systematic review compiled data from all the HPV trials to offer a summary of the evidence thus far.

    Nevertheless, the investigators acknowledged that despite three years of work, the limitations of their analysis remained. These included reporting bias, incomplete reporting, data fragmentation and limited trial follow-up.

    These investigators similarly note that the trials were powered to assess the benefits of HPV vaccination, not rare harms. The degree to which benefits outweigh risks is therefore unknown.

    They concluded that future research should carefully evaluate the harms following Gardasil 9 compared to Gardasil because the former contains more than double the virus proteins and aluminum-containing adjuvant than the same dose of Gardasil.

    RFK Jr. and Brian Hooker Vax-Unvax
    RFK Jr. and Brian Hooker’s New Book: “Vax-Unvax”

    Order Now

    Large studies reveal autoimmune events

    In 2009, the HPV4 vaccine was integrated into the Danish childhood vaccination program. Since then, two large cohort studies on the HPV4 vaccine adverse events have been carried out using the hospital-based healthcare registries of Denmark and Sweden.

    The first study in Denmark and Sweden included 296,826 girls aged 10 to 17 who received a total of 696,420 HPV4 vaccine doses.

    The scientists evaluated rate ratios for autoimmune events and found no significant association for 20 out of 23 events.

    They found a significant association between the HPV4 vaccine and Bechet’s syndrome (rate ratio 3.37), Raynaud’s disease (1.67) and type 1 diabetes (1.29).

    But after further review, they concluded that there was insufficient evidence for a causal association, because of the weakness of the signal and the lack of an underlying mechanism to explain biological plausibility.

    In a second large cohort study, the same team expanded their research to more than 3 million Danish and Swedish adult women aged 18 to 44.

    The authors identified seven adverse events with statistically significant increased risks following HPV4 vaccination: Hashimoto’s thyroiditis, celiac disease, lupus erythematosus, pemphigus vulgaris, Addison’s disease, Raynaud’s disease and encephalitis, myelitis or encephalomyelitis.

    After sensitivity analyses, the association between HPV4 vaccination and celiac disease was the most robust finding.

    Celiac disease is a condition where a person’s immune system attacks the body’s own gut after eating gluten.

    As the graph below shows, the scientists used two risk periods after HPV4 vaccination: the first 180 days and after.

    1 time since first dose HPV4 vaccine coeliac cases
    Time since the first dose of the HPV4 vaccine for vaccinated coeliac cases in a cohort of Danish and Swedish women. Credit: Journal of Internal Medicine
    The authors noted that the observed 56% increased risk of celiac disease “was strong, and the increase was strikingly similar in both risk periods after vaccination.”

    Celiac disease is underdiagnosed in Denmark.

    So one possible explanation is that vaccination visits allow a chance for this and other conditions to be diagnosed and explored.

    This explanation suggests that the association between the HPV vaccine and autoimmune disorders may be coincidental.

    However, given the lack of any real control groups in these studies, as well as the growing body of scientific literature from countries around the world showing problems with the HPV vaccine, dismissing these safety signals as coincidence seems short-sighted.

    Large French study and U.S. VAERS study identify risks of Guillain-Barré Syndrome

    The concern about autoimmune disease adverse events has contributed to low HPV vaccination uptake in France.

    A 2017 study of over 2.2 million young girls in France found troubling evidence of a link with Guillain-Barré syndrome. GBS is a condition that arises when our own antibodies attack the nerves.

    The incidence of GBS was found to be 1.4 per 100,000 person-years among the vaccinated girls compared to 0.4 per 100,000 among the unvaccinated, resulting in an increased risk of GBS of more than 200%.

    The association appeared to be “particularly marked in the first months following vaccination.”

    This finding is corroborated by the pattern of adverse reactions reported worldwide. Data from a large number of case reports document similar serious adverse events associated with Gardasil administration, with nervous system disorders of autoimmune origin being the most frequently reported.

    A 2011 U.S. study found that the estimated weekly reporting rate of post-Gardasil GBS within the first six weeks (6.6 per 10,000,000) was higher than in the general population, and higher than post-Menactra and post-influenza vaccinations.

    In particular, there was nearly a two-and-a-half to 10 times greater risk of acquiring GBS within six weeks after vaccination, compared to the general population.

    Additionally, the study found Gardasil vaccination was associated with approximately eight-and-a-half times more emergency department visits, 12.5 times more hospitalizations, 10 times more life-threatening events and 26.5 times more disability than the Menactra vaccination.

    Plausible mechanisms of harm

    Despite the conflicting data in the scientific literature to date, it is clear that the HPV vaccines can cause autoimmune disorders in susceptible people. But how?

    Autoimmunity has been reported as a complication of natural infection as well as virus vaccination. This phenomenon has been observed with many viruses, including the Epstein-Barr virus, COVID-19 and HPV.

    According to a 2019 study, the HPV vaccine contains epitopes — portions of the virus proteins — that overlap with the human proteins.

    This means that if we develop antibodies to those viruses, we may also generate autoantibodies to our own cells, which is the root cause of autoimmune dysfunction.

    The study showed that most of the immunoreactive HPV L1 epi­topes are overlapping peptides present in human proteins.

    The authors explained that this “unexpected enormous size of the peptide overlap between the HPV epitopes and human proteins” is relevant, and may be why a wide variety of autoimmune diseases have been reported post-HPV vaccination, including ovarian failure, systemic lupus erythematosus, breast cancer and sudden death, among others.

    Why some people develop these conditions and others do not is unclear.

    The authors suggest that vaccines should target the few peptides that do not overlap with human proteins, but which do overlap with the other HPVs.

    Despite this overlap and the potential for causing autoimmune disease, medical doctors usually ignore or dismiss the connection. We are told that these diseases are rare.

    The human body has something called immune tolerance. This protects a person’s immune system against attacking itself. Therefore, HPV infection is also “immune tolerated,” which means it lays dormant for some time until it becomes cancerous.

    HPV vaccination was actually designed with this immune tolerance in mind.

    Given the human body’s built-in defenses against autoimmune conditions, vaccinology requires an immunogenic catalyst to get the body’s attention. This is the job of an adjuvant.

    An adjuvant is an ingredient used in a vaccine that the body recognizes as foreign. It is added to vaccines so that the body will mount a stronger immune response.

    The idea is that in attacking the adjuvant, the body will also recognize other vaccine ingredients (in this case, purified HPV proteins).

    In addition, the antigen dose is much higher than in natural infections and the capsids in the vaccine are directly exposed to systemic immune responses as opposed to the virus staying relatively hidden within the natural barrier of the skin following infection.

    The vaccine was well-designed to trigger an immune response, but this advantage may come at a cost: Generating antibodies to HPV proteins through vaccination could, theoretically, set the stage for an autoimmune attack.

    Link between HPV-vaccine-associated nervous system dysfunction and autoimmunity

    A December 2022 Danish and German study was designed to elucidate a possible mechanism of harm.

    The lead author, Dr. Jesper Mehlsen, a specialist in treating autoimmune conditions, noted that the HPV major capsid L1s antigen resembles human autonomic nerve receptors, including G-protein coupled receptors (GPCR).

    According to the researchers, in the past several years, case series of suspected vaccination side effects have pointed to three disease entities: POTS, myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) and complex regional pain syndrome. These syndromes may be associated with neuroendocrine GPCR antibodies.

    From 2011 to 2018, researchers saw 845 patients (839 females, six males) with suspected side effects following the HPV4 vaccine. The control group included vaccinated people without side effects.

    Moderate to severe fatigue was recorded in 83.3% of the patients but in none of the controls.

    A high prevalence of symptoms, such as dizziness (91%), heart palpitations (71%), nausea (80%) and hyperactive bladder suggested that the patients were experiencing some kind of autonomic dysfunction.

    Autonomic dysfunction occurs when the part of the nervous system that controls well-being and balance does not function properly.

    2 most frequent symptoms hpv vaccine
    Most frequent symptoms reported by 612 patients in Denmark. Credit: Journal of Autoimmunity
    Twenty-four percent higher antinuclear antibodies (ANA, a common type of autoantibodies) were found in patients, suggesting possible autoimmunity.

    3 antinuclear antibodies HPV vaccines
    A larger proportion of the symptomatic patients were found with a common type of autoantibodies compared to healthy controls. Credit: Journal of Autoimmunity
    Antibodies against the adrenergic ß-2-receptor and muscarinic M-2 receptors were also found significantly higher in patients.

    Many of the symptoms, including immune activation and autonomic dysregulation, could be mediated or aggravated by dysregulated autoantibodies against adrenergic receptors and impaired peripheral adrenergic function.

    The authors suggested that girls and women with probable side effects of HPV vaccination have symptoms and biological markers compatible with an autoimmune disease closely resembling that seen in ME/CFS.

    Interestingly, people who already had HPV infections at some point appeared to be at greater risk for adverse events following vaccination.

    The authors noted that “prior disease may precondition some individuals for vaccine-related adverse events.”

    They also noted that some of the adverse events resembled long-COVID symptoms.

    Universal HPV vaccination called into question

    Academic researcher at the University of British Columbia, Lucija Tomljenovic, and neuroscientist Christopher Shaw, who have closely looked into Gardasil, have argued that the risks from the vaccine seem to significantly outweigh the as-yet-unproven long-term benefits.

    In a 2012 comment published in the American Journal of Public Health, they took issue with “incomplete and inaccurate” data and poorly designed trials.

    Vaccination is unjustified if the vaccine carries any substantial risk, as healthy teenagers face little to no risk of dying from cervical cancer.

    Risk-benefit analyses must be conducted to ascertain the overall balance of benefits and harms on both individual and societal levels.

    Reprinted with permission from The Epoch Times. Dr. Yuhong Dong, a medical doctor who also holds a doctorate in infectious diseases in China, is the chief scientific officer and co-founder of a Swiss biotech company and former senior medical scientific expert for antiviral drug development at Novartis Pharma in Switzerland.

    If you or your child suffered harm after receiving the Gardasil HPV vaccine, you may have a legal claim. Please visit Wisner Baum for a free case evaluation. Click here to watch a Gardasil litigation update interview with Wisner Baum Senior Partner Bijan Esfandiari.

    The views and opinions expressed in this article are those of the authors and do not necessarily reflect the views of Children's Health Defense.

    https://childrenshealthdefense.org/defender/truth-hpv-vaccine-part-2-et/

    https://donshafi911.blogspot.com/2024/01/the-truth-about-hpv-vaccination-part-2.html
    The Truth About HPV Vaccination, Part 2: Studies Link the Vaccines to Neurological, Autoimmune Disorders Researchers who looked closely into the Gardasil HPV vaccine concluded the risks from the vaccine seem to significantly outweigh the as-yet-unproven long-term benefits. The Epoch Times Miss a day, miss a lot. Subscribe to The Defender's Top News of the Day. It's free. By Dr. Yuhong Dong Editor’s Note: This second installment in a multi-part series about the human papillomavirus, or HPV, vaccine examines studies that link the vaccines to increased risk of serious neurological and autoimmune disorders. Read Part 1 here. Summary of key facts A Danish review of 79,102 female and 16,568 male subjects, found human papillomavirus (HPV) vaccines had significantly increased rates of serious nervous system disorders. Postural orthostatic tachycardia syndrome (POTS) and complex regional pain syndrome were judged “definitely associated” with the HPV vaccine. A large Danish and Swedish study including nearly 300,000 girls found a significant association between the HPV vaccine and increased rates of Bechet’s syndrome (rate ratio 3.37), Raynaud’s disease (1.67) and type 1 diabetes (1.29). A large study including 3 million Danish and Swedish women aged 18 to 44, identified seven adverse events with statistically significant increased risks following HPV vaccination: Hashimoto’s thyroiditis, celiac disease, lupus erythematosus, pemphigus vulgaris, Addison’s disease, Raynaud’s disease and encephalitis, myelitis, or encephalomyelitis. A 2017 French study of over 2.2 million young girls found evidence of a 3.78-fold increased risk of Guillain-Barré syndrome (GBS). A 2011 U.S. study found nearly a two-and-a-half to 10 times greater risk of acquiring GBS within six weeks post-Gardasil vaccination. While the underlying mechanisms causing these autoimmune reactions are not yet fully understood, some researchers speculate that the sizable overlap in protein sequences between the HPV and the human genome may cause the immune system to attack itself. Others are concerned that the adjuvants (such as aluminum) used to attract the attention of the immune system may be causing harm. Neurological and autoimmune disorders Danish review found increased nervous system disorder In 2020, a group of Danish scientists conducted a systematic review of the overall benefits and harms of HPV vaccines. Twenty-four eligible randomized controlled clinical studies were obtained, with a total of 95,670 participants, mostly women, and 49 months mean weighted follow-up. Almost all controls were given an active comparator vaccine (typically a hepatitis vaccine with a comparable aluminum-based adjuvant). Given that the adjuvant is highly immunogenic by design (it is meant to grab the attention of the immune system), this trial design makes it difficult to detect an excess risk with the HPV vaccines. Without true controls (such as a saline placebo), the real risks of HPV vaccination cannot be accurately assessed. In the vaccine group, 367 cancers were detected, compared to 490 in the comparator group. Younger participants (15 to 29) seemed to benefit more from the vaccine concerning preventing moderate HPV-related intraepithelial neoplasia compared to older participants (ages 21 to 72). Younger participants also had fewer fatal harms. Even though the studies were flawed in their design, at four years post-vaccination, those who had received the HPV vaccines had significantly increased rates of serious nervous system disorders: 49%, as well as general harms totaling 7%. The serious harms that were judged “definitely associated” with HPV vaccines were postural orthostatic tachycardia syndrome and complex regional pain syndrome. POTS had a nearly twofold increase in the vaccinated group. By July 2017, only two-thirds of the results from HPV vaccine trials had been published, and only about half the results had been posted, due to manuscript length limitations, reporting bias and confounding journal articles offering a limited view of trial outcomes. This Danish systematic review compiled data from all the HPV trials to offer a summary of the evidence thus far. Nevertheless, the investigators acknowledged that despite three years of work, the limitations of their analysis remained. These included reporting bias, incomplete reporting, data fragmentation and limited trial follow-up. These investigators similarly note that the trials were powered to assess the benefits of HPV vaccination, not rare harms. The degree to which benefits outweigh risks is therefore unknown. They concluded that future research should carefully evaluate the harms following Gardasil 9 compared to Gardasil because the former contains more than double the virus proteins and aluminum-containing adjuvant than the same dose of Gardasil. RFK Jr. and Brian Hooker Vax-Unvax RFK Jr. and Brian Hooker’s New Book: “Vax-Unvax” Order Now Large studies reveal autoimmune events In 2009, the HPV4 vaccine was integrated into the Danish childhood vaccination program. Since then, two large cohort studies on the HPV4 vaccine adverse events have been carried out using the hospital-based healthcare registries of Denmark and Sweden. The first study in Denmark and Sweden included 296,826 girls aged 10 to 17 who received a total of 696,420 HPV4 vaccine doses. The scientists evaluated rate ratios for autoimmune events and found no significant association for 20 out of 23 events. They found a significant association between the HPV4 vaccine and Bechet’s syndrome (rate ratio 3.37), Raynaud’s disease (1.67) and type 1 diabetes (1.29). But after further review, they concluded that there was insufficient evidence for a causal association, because of the weakness of the signal and the lack of an underlying mechanism to explain biological plausibility. In a second large cohort study, the same team expanded their research to more than 3 million Danish and Swedish adult women aged 18 to 44. The authors identified seven adverse events with statistically significant increased risks following HPV4 vaccination: Hashimoto’s thyroiditis, celiac disease, lupus erythematosus, pemphigus vulgaris, Addison’s disease, Raynaud’s disease and encephalitis, myelitis or encephalomyelitis. After sensitivity analyses, the association between HPV4 vaccination and celiac disease was the most robust finding. Celiac disease is a condition where a person’s immune system attacks the body’s own gut after eating gluten. As the graph below shows, the scientists used two risk periods after HPV4 vaccination: the first 180 days and after. 1 time since first dose HPV4 vaccine coeliac cases Time since the first dose of the HPV4 vaccine for vaccinated coeliac cases in a cohort of Danish and Swedish women. Credit: Journal of Internal Medicine The authors noted that the observed 56% increased risk of celiac disease “was strong, and the increase was strikingly similar in both risk periods after vaccination.” Celiac disease is underdiagnosed in Denmark. So one possible explanation is that vaccination visits allow a chance for this and other conditions to be diagnosed and explored. This explanation suggests that the association between the HPV vaccine and autoimmune disorders may be coincidental. However, given the lack of any real control groups in these studies, as well as the growing body of scientific literature from countries around the world showing problems with the HPV vaccine, dismissing these safety signals as coincidence seems short-sighted. Large French study and U.S. VAERS study identify risks of Guillain-Barré Syndrome The concern about autoimmune disease adverse events has contributed to low HPV vaccination uptake in France. A 2017 study of over 2.2 million young girls in France found troubling evidence of a link with Guillain-Barré syndrome. GBS is a condition that arises when our own antibodies attack the nerves. The incidence of GBS was found to be 1.4 per 100,000 person-years among the vaccinated girls compared to 0.4 per 100,000 among the unvaccinated, resulting in an increased risk of GBS of more than 200%. The association appeared to be “particularly marked in the first months following vaccination.” This finding is corroborated by the pattern of adverse reactions reported worldwide. Data from a large number of case reports document similar serious adverse events associated with Gardasil administration, with nervous system disorders of autoimmune origin being the most frequently reported. A 2011 U.S. study found that the estimated weekly reporting rate of post-Gardasil GBS within the first six weeks (6.6 per 10,000,000) was higher than in the general population, and higher than post-Menactra and post-influenza vaccinations. In particular, there was nearly a two-and-a-half to 10 times greater risk of acquiring GBS within six weeks after vaccination, compared to the general population. Additionally, the study found Gardasil vaccination was associated with approximately eight-and-a-half times more emergency department visits, 12.5 times more hospitalizations, 10 times more life-threatening events and 26.5 times more disability than the Menactra vaccination. Plausible mechanisms of harm Despite the conflicting data in the scientific literature to date, it is clear that the HPV vaccines can cause autoimmune disorders in susceptible people. But how? Autoimmunity has been reported as a complication of natural infection as well as virus vaccination. This phenomenon has been observed with many viruses, including the Epstein-Barr virus, COVID-19 and HPV. According to a 2019 study, the HPV vaccine contains epitopes — portions of the virus proteins — that overlap with the human proteins. This means that if we develop antibodies to those viruses, we may also generate autoantibodies to our own cells, which is the root cause of autoimmune dysfunction. The study showed that most of the immunoreactive HPV L1 epi­topes are overlapping peptides present in human proteins. The authors explained that this “unexpected enormous size of the peptide overlap between the HPV epitopes and human proteins” is relevant, and may be why a wide variety of autoimmune diseases have been reported post-HPV vaccination, including ovarian failure, systemic lupus erythematosus, breast cancer and sudden death, among others. Why some people develop these conditions and others do not is unclear. The authors suggest that vaccines should target the few peptides that do not overlap with human proteins, but which do overlap with the other HPVs. Despite this overlap and the potential for causing autoimmune disease, medical doctors usually ignore or dismiss the connection. We are told that these diseases are rare. The human body has something called immune tolerance. This protects a person’s immune system against attacking itself. Therefore, HPV infection is also “immune tolerated,” which means it lays dormant for some time until it becomes cancerous. HPV vaccination was actually designed with this immune tolerance in mind. Given the human body’s built-in defenses against autoimmune conditions, vaccinology requires an immunogenic catalyst to get the body’s attention. This is the job of an adjuvant. An adjuvant is an ingredient used in a vaccine that the body recognizes as foreign. It is added to vaccines so that the body will mount a stronger immune response. The idea is that in attacking the adjuvant, the body will also recognize other vaccine ingredients (in this case, purified HPV proteins). In addition, the antigen dose is much higher than in natural infections and the capsids in the vaccine are directly exposed to systemic immune responses as opposed to the virus staying relatively hidden within the natural barrier of the skin following infection. The vaccine was well-designed to trigger an immune response, but this advantage may come at a cost: Generating antibodies to HPV proteins through vaccination could, theoretically, set the stage for an autoimmune attack. Link between HPV-vaccine-associated nervous system dysfunction and autoimmunity A December 2022 Danish and German study was designed to elucidate a possible mechanism of harm. The lead author, Dr. Jesper Mehlsen, a specialist in treating autoimmune conditions, noted that the HPV major capsid L1s antigen resembles human autonomic nerve receptors, including G-protein coupled receptors (GPCR). According to the researchers, in the past several years, case series of suspected vaccination side effects have pointed to three disease entities: POTS, myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) and complex regional pain syndrome. These syndromes may be associated with neuroendocrine GPCR antibodies. From 2011 to 2018, researchers saw 845 patients (839 females, six males) with suspected side effects following the HPV4 vaccine. The control group included vaccinated people without side effects. Moderate to severe fatigue was recorded in 83.3% of the patients but in none of the controls. A high prevalence of symptoms, such as dizziness (91%), heart palpitations (71%), nausea (80%) and hyperactive bladder suggested that the patients were experiencing some kind of autonomic dysfunction. Autonomic dysfunction occurs when the part of the nervous system that controls well-being and balance does not function properly. 2 most frequent symptoms hpv vaccine Most frequent symptoms reported by 612 patients in Denmark. Credit: Journal of Autoimmunity Twenty-four percent higher antinuclear antibodies (ANA, a common type of autoantibodies) were found in patients, suggesting possible autoimmunity. 3 antinuclear antibodies HPV vaccines A larger proportion of the symptomatic patients were found with a common type of autoantibodies compared to healthy controls. Credit: Journal of Autoimmunity Antibodies against the adrenergic ß-2-receptor and muscarinic M-2 receptors were also found significantly higher in patients. Many of the symptoms, including immune activation and autonomic dysregulation, could be mediated or aggravated by dysregulated autoantibodies against adrenergic receptors and impaired peripheral adrenergic function. The authors suggested that girls and women with probable side effects of HPV vaccination have symptoms and biological markers compatible with an autoimmune disease closely resembling that seen in ME/CFS. Interestingly, people who already had HPV infections at some point appeared to be at greater risk for adverse events following vaccination. The authors noted that “prior disease may precondition some individuals for vaccine-related adverse events.” They also noted that some of the adverse events resembled long-COVID symptoms. Universal HPV vaccination called into question Academic researcher at the University of British Columbia, Lucija Tomljenovic, and neuroscientist Christopher Shaw, who have closely looked into Gardasil, have argued that the risks from the vaccine seem to significantly outweigh the as-yet-unproven long-term benefits. In a 2012 comment published in the American Journal of Public Health, they took issue with “incomplete and inaccurate” data and poorly designed trials. Vaccination is unjustified if the vaccine carries any substantial risk, as healthy teenagers face little to no risk of dying from cervical cancer. Risk-benefit analyses must be conducted to ascertain the overall balance of benefits and harms on both individual and societal levels. Reprinted with permission from The Epoch Times. Dr. Yuhong Dong, a medical doctor who also holds a doctorate in infectious diseases in China, is the chief scientific officer and co-founder of a Swiss biotech company and former senior medical scientific expert for antiviral drug development at Novartis Pharma in Switzerland. If you or your child suffered harm after receiving the Gardasil HPV vaccine, you may have a legal claim. Please visit Wisner Baum for a free case evaluation. Click here to watch a Gardasil litigation update interview with Wisner Baum Senior Partner Bijan Esfandiari. The views and opinions expressed in this article are those of the authors and do not necessarily reflect the views of Children's Health Defense. https://childrenshealthdefense.org/defender/truth-hpv-vaccine-part-2-et/ https://donshafi911.blogspot.com/2024/01/the-truth-about-hpv-vaccination-part-2.html
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    The Truth About HPV Vaccination, Part 2: Studies Link the Vaccines to Neurological, Autoimmune Disorders
    Researchers who looked closely into the Gardasil HPV vaccine concluded the risks from the vaccine seem to significantly outweigh the as-yet-unproven long-term benefits.
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  • Scientists Call for Global Moratorium on mRNA Vaccines, Immediate Removal From Childhood Schedule
    A review paper published last week in the journal Cureus is the first peer-reviewed paper to call for a global moratorium on the COVID-19 mRNA vaccines. The authors say that reanalyzed data from the vaccine makers’ trials and high rates of serious post-injection injuries indicate the mRNA gene therapy vaccines should not have been authorized for use.

    Brenda Baletti, Ph.D.
    global moratorium mrna covid vaccine feature
    Miss a day, miss a lot. Subscribe to The Defender's Top News of the Day. It's free.

    Governments should endorse a global moratorium on mRNA vaccines until all questions about their safety have been thoroughly investigated, according to the authors of a new, peer-reviewed article on the COVID-19 vaccine trials and the global vaccination campaign published last week in Cureus, Journal of Medical Science.

    Cureus is a web-based peer-reviewed open-access general medical journal using prepublication peer review.

    The authors surveyed published research on the pharmaceutical companies’ vaccine trials and related adverse events. They also called for the COVID-19 vaccines to be removed immediately from the childhood immunization schedule.

    After the first reports from vaccine trials claimed they were 95% effective in preventing COVID-19, serious problems with method, execution and reporting in the trials became public, which the paper reviewed in detail.

    Evidence also shows the products never underwent adequate safety and toxicological testing, and since the vaccine rollout, researchers have identified a significant number of adverse events (AEs) and serious adverse events (SAEs).

    Authors M. Nathaniel Mead, Stephanie Seneff, Ph.D., Russ Wolfinger, Ph.D., Jessica Rose, Ph.D., Kris Denhaerynck, Ph.D., Steve Kirsch and Dr. Peter McCullough detailed the vaccines’ potential serious harms to humans, vaccine control and processing issues, the mechanisms behind AEs, the immunological reasons for vaccine inefficacy and the mortality data from the registrational trials.

    They concluded, “Federal agency approval of the COVID-19 mRNA injectable products on a blanket-coverage population-wide basis had no support from an honest assessment of all relevant registrational data and commensurate consideration of risks versus benefits.”

    They also called for the vaccines to be immediately removed from the childhood immunization schedule and for the suspension of the boosters.

    “It is unethical and unconscionable to administer an experimental vaccine to a child who has a near-zero risk of dying from COVID-19 (IFR, 0.0003%) but a well-established 2.2% risk of permanent heart damage based on the best prospective data available,” they wrote.

    Finally, the authors called for a full investigation into misconduct by the pharmaceutical companies and the regulatory agencies.

    It is the first peer-reviewed study to call for a moratorium on the COVID-19 mRNA products, Rose told The Defender.

    “Once a proper assessment of the safety and efficacy claims was made herein — upon which the emergency use authorization (EUA)’s and ultimate final authorizations were granted — it was found that the COVID-19 injectable products were neither safe nor effective,” she added.

    According to McCollough, “mRNA should never have been authorized for human use.”

    Lead author Mead told The Defender, “Our view is that any risk-benefit analysis must consider how much the presumed benefit in terms of reduced COVID-19 related mortality is offset by the potential increase in vaccine-induced mortality.”

    Here are six takeaways from the review:

    1. The COVID-19 ‘vaccines’ are reclassified gene therapies that were rushed through the regulatory process in a historically unprecedented manner

    Before the seven-month authorization process for the mRNA vaccines, no vaccine had ever gone to market without undergoing testing of at least four years, with typical timelines averaging 10 years.

    To speed the process, the companies skipped preclinical studies of potential toxicity from multiple doses and cut the typical 6-12 month observation period for identifying longer-term adverse effects and the established 10-15-year period for monitoring for long-term effects such as cancer and autoimmune disorders, the authors wrote.

    The trials prioritized documenting effective symptom reduction over SAE and mortality. This was particularly concerning, the authors argued, because mRNA products are gene therapy products reclassified as vaccines and then given EUA for the first time ever for use against a viral disease.

    However, the gene therapies’ components have not been thoroughly evaluated for safety for use as vaccines.

    There is an uninvestigated and major concern that the mRNA could transform body cells into viral protein factories — with no off-switch — that produce the spike protein for a prolonged period causing chronic systemic inflammation and immune dysfunction.

    The spike protein in the vaccine, the authors said, is associated with more severe immunopathology and other AEs than the spike protein in the virus itself.

    The authors suggested that massive government investment in mRNA technology, including hundreds of millions before the pandemic and tens of billions once it began, meant, “U.S. federal agencies were strongly biased toward successful outcomes for the registrational trials.”

    The financial incentives along with political pressures to deliver a rapid solution likely influenced a series of flawed decisions that compromised the integrity of the trials and downplayed serious scientific concerns about risks with the technology, they added.

    RFK Jr. and Brian Hooker Vax-Unvax
    RFK Jr. and Brian Hooker’s New Book: “Vax-Unvax”

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    2. Steps were taken in trials to overestimate vaccine efficacy

    Because the trials were designed to assess whether the mRNA vaccine reduced symptoms, they did not measure whether the vaccines prevented severe disease and death. Yet the vaccine makers repeatedly claimed that they do.

    “No large randomized double-blind placebo-controlled trials have ever demonstrated reductions in SARS-CoV-2 transmission, hospitalization, or death,” the authors wrote.

    Additionally, the number of people who contracted clinical COVID-19 in both the placebo and intervention groups was “too small to draw meaningful, pragmatic, or broad-sweeping conclusions with regard to COVID-19 morbidity and mortality.”

    Pfizer’s 95 % efficacy claims were based on 162 of 22,000 placebo recipients contracting PCR-confirmed COVID-19 compared to eight of 22,000 in the vaccine group. None of the placebo recipients died from COVID-19. In the Moderna trials, only one placebo death was attributed to COVID-19.

    There was also a much larger percentage of “suspected COVID-19 cases” in both groups, with participants showing COVID-19 symptoms but a negative PCR test. When factoring in those cases, measures of vaccine efficacy drop to about 19%.

    The trial subject pool was comprised of largely young and healthy individuals, excluding key groups — children, pregnant women, elderly and immunocompromised people — which can also obscure the vaccine’s actual efficacy and safety.

    Findings from reanalyses of data from the Pfizer trials can be interpreted as showing the vaccines made “no significant difference” in reducing all-cause mortality in the vaccinated versus unvaccinated groups at 20 weeks into the trial, the authors wrote.

    Even the six-month post-marketing data Pfizer presented to the U.S. Food and Drug Administration (FDA) showed no reduction in all-cause mortality from the vaccine.

    The authors reanalyzed that data, adjusting the analysis of deaths to better account for the fact that when Pfizer unblinded the study people from the placebo group took the vaccine, and found the vaccine group had a higher mortality rate (0.105%) than the unvaccinated group (0.0799%), which they said was a conservative estimate.

    One of the most glaring issues with the registrational trials, they noted, was that they exclusively focused on measuring risk reduction — the ratio of COVID-19 symptom rates in the vaccine group versus the placebo group — rather than measuring absolute risk reduction, which is the likelihood someone will show COVID-19 symptoms relative to people in the population at large.

    According to FDA guidelines, accounting for both approaches is crucial to avoid the misguided use of pharmaceutical products — but the data were omitted, leading to an overestimation of an intervention’s clinical utility.

    While both vaccines touted an approximately 95% risk reduction figure as their efficacy figure, the absolute risk reductions for Pfizer and Moderna’s vaccines were 0.7% and 1.1% respectively.

    “A substantial number of individuals would need to be injected in order to prevent a single mild-to-moderate case of COVID-19,” the authors wrote.

    As an example, using a conservative estimate that 119 people would need to be vaccinated to prevent infection, and assuming that COVID-19 had a 0.23% infection fatality rate, they wrote that approximately 52,000 vaccinations would be necessary to prevent a single COVID-19-related death.

    However, “Given trial misconduct and data integrity problems … the true benefit is likely to be much lower,” they wrote.

    And, they added, one would need to assess that benefit along with harms, which they estimate to be 27 deaths per 100,000 doses of Pfizer. That means, using the most conservative estimates, “for every life saved, there were 14 times more deaths caused by the modified mRNA injections.”

    They also noted that post-rollout evidence confirmed the efficacy claims were overstated. For example, two large cohort Cleveland clinic studies showed the vaccine could not confer protection against COVID-19 — instead, in those trials, more vaccinated people were more likely to contract COVID-19.

    One study showed the risk of “breakthrough” infection was significantly higher among people who were boosted and that more vaccinations resulted in a greater risk of COVID-19.

    A second study showed adults who were not “up-to-date” with their shots had a 23% lower incidence of COVID-19 than their “up-to-date” colleagues.

    3. The trials underestimated the adverse events, including death, despite evidence in the data.

    Harms were also underreported and underestimated for a number of reasons, according to the authors, a practice that tends to be common in randomized industry-sponsored vaccine trials in general and “exceptionally evident” here.

    First, because Pfizer unblinded the trial within just a few weeks of the emergency use authorization and allowed people in the placebo group to take the vaccine, there was not sufficient time to identify late-occurring harms because there was no longer a control group.

    “Was this necessary, given that none of the deaths in the Pfizer trial were attributed to COVID-19 as the primary cause, and given the very low IFR [infection fatality rate] for a relatively healthy population?” they asked.

    Also, trial coordinators were “haphazard” in their approach to monitoring AEs. They prioritized documenting events thought to be related to COVID-19 rather than to the vaccines for the first seven days and only recorded “unsolicited” AEs for 30-60 days. After that period, even very SAEs, like death, were not recorded. Even for the AEs recorded in the first seven days, they only solicited data from 20% of the population.

    None of the trial data was independently verified. “Such secrecy may have enabled the industry to more easily present an inflated and distorted estimate of the genetic injections’ benefits, along with a gross underestimation of potential harms,” they wrote.

    Subsequent analysis by Michels et al. revealed that deaths and other SAEs — like life-threatening conditions, inpatient hospitalization or extension of hospitalization, persistent or significant disability/incapacity, a congenital anomaly, or a medically significant event — did occur after the cutoff period and before the FDA advisory meeting where emergency authorization was recommended.

    During the first 33 weeks of the Pfizer trials, 38 subjects died, according to Pfizer’s own data, although independent research by Michels et al. estimated that that number is only approximately 17% of the actual projected number due to missing data.

    And after that, the rate of deaths continued to increase. Michaels et al. found Pfizer failed to report a substantial increase in the number of deaths due to cardiovascular events. They also found a consistent pattern of reporting delays on the date of the death on subjects’ case reports.

    Overall, the review authors reported that there were “twice as many cardiac deaths proportionately among vaccinated compared to unvaccinated subjects in the Pfizer trials.”

    In their discussion, the authors wrote “Based on the extended Pfizer trial findings, our person-years estimate yielded a 31% increase in overall mortality among vaccine recipients, a clear trend in the wrong direction.”

    This raises serious red flags about how the registrational trials were conducted, Mead said. “Assessments of the safety profile of the COVID-19 modified mRNA injections warrant an objective precautionary perspective, any substantial upward trend in all cause mortality within the intervention arm of the trial population reflects badly on the intervention.”

    4. Numbers of SAEs in the trials and post-rollout reporting are well-documented, despite claims to the contrary.

    Both Pfizer and Moderna found about 125 SAEs per 100,000 vaccine recipients, or one SAE for every 800 vaccines. However, because the trials excluded more vulnerable people, the authors note, even higher proportions of SAEs would be expected in the general population.

    The Fraiman et al. reanalysis of the Pfizer trial data found a significant 36% higher risk of SAEs, which included deaths and many life-threatening conditions in the vaccinated participants.

    Official SAEs for other vaccines average around only 1-2 per million. Fraiman et alestimated 1,250 SEAs per million vaccines, exceeding that benchmark by “at least 600-fold.”

    After the vaccine rollout, analyses of two large drug safety reporting systems in the U.S. and Europe identified signals for myocardial infarction, pulmonary embolism, cardio-respiratory arrest, cerebral infarction, and cerebral hemorrhage associated with both mRNA vaccines, along with ischemic stroke.

    And millions of AEs have been reported to those systems.

    Another study by Skidmore et al. estimated the total number of fatalities from the vaccines in 2021 alone was 289,789. Autopsy studies have also provided additional evidence of serious harms, including evidence that most COVID-19 mRNA vaccine-related deaths resulted from injury to the cardiovascular system.

    In multiple autopsy studies, German pathologist Aren Burkhardt documented the presence of vaccine-mRNA-produced spike proteins in blood vessel walls and brain tissues. This research helps to explain documented vaccine-induced toxicities affecting the nervous, immune, reproductive and other systems.

    The Pfizer data also showed an overwhelming number of adverse effects. According to a confidential document released in August 2022, Pfizer had documented approximately 1.6 million AEs affecting nearly every organ system, and one-third of them were classified as serious.

    In Pfizer’s trial, Michels and colleagues found a nearly 4-fold increase (OR 3.7, 95%CI 1.02-13.2, p = 0.03) in serious cardiac events (e.g., heart attack, acute coronary syndrome) in the vaccine group. Neither the original trial report nor Pfizer’s Summary Clinical Safety report acknowledged or commented on this safety signal.

    “The serious adverse events are all well documented,” Mead said. “Yet it’s surprising to see so many in the medical field continue to ignore or dismiss outright the latter half of the equation when considering all cause mortality trends.”

    5. The failure to appropriately test for safety and toxicity poses serious problems.

    Researchers have raised concerns that the mRNA technology is inherently unstable and difficult to store, which leads to batch variability and contamination linked to different rates of AEs.

    Recent findings by McKernan et al. that found Pfizers’ mRNA vaccines are contaminated with plasmid DNA that shouldn’t be present — and wasn’t present in the vaccines used in the trials – raising serious safety issues.

    That’s because “Process 1,” used in the trials to generate the vaccines involved in vitro transcription of synthetic DNA — essentially a “clean” process. However, that process isn’t viable for mass production, so the manufacturers used “Process 2,” which involves using E. coli bacteria to replicate the plasmids.

    Removing plasmids E coli. can result in residual plasmids in the vaccines and the effects of their presence is unknown.

    McKernan’s work also revealed the presence of DNA from simian virus 40 (SV40), an oncogenic DNA virus originally isolated in 1960 from contaminated polio vaccines, induces lymphomas, brain tumors, and other malignancies in laboratory animals, raising other safety concerns.

    Researchers from Cambridge published a paper in Nature in December 2023, where they found an inherent defect in the modified RNA instructions for the spike protein in COVID-19 immunizations that causes the machinery that translates the gene to the spike protein to “slip” about 10% of the time

    This process creates “frameshifts” that cause cells to produce “off-target” proteins in addition to the spike. These proteins, which developers either failed to look for or did not report to regulators, cause undesirable immune responses whose long-term effects are unknown.

    6. There are many different possible biological mechanisms that cause AEs and vaccine ineffectiveness.

    The review points readers to a series of papers that explain a number of different theories to explain the high number of AEs from the COVID-19 mRNA vaccines.

    “The mechanisms of molecular mimicry, antigen cross-reactivity, pathogenic priming, viral reactivation, immune exhaustion, and other factors related to immune dysfunction all reinforce the biological plausibility for vaccine-induced pathogenesis of malignant and autoimmune diseases,” they wrote. And these mechanisms of immune activation are distinct from the body’s response to a viral infection.

    They also note the toxic effects of the primary adjuvant, PEG, and of the spike protein itself.

    They close their analysis of the vaccines with a complex explanation for the different immunological basis for protection provided by the vaccines versus natural immunity through infection. They explain the mechanisms for vaccine failure and problems generated by the ability for the mRNA vaccines to perpetuate the emergence of new variants.

    https://childrenshealthdefense.org/defender/scientists-global-moratorium-mrna-vaccines-removal-childhood-schedule/


    https://donshafi911.blogspot.com/2024/01/scientists-call-for-global-moratorium.html
    Scientists Call for Global Moratorium on mRNA Vaccines, Immediate Removal From Childhood Schedule A review paper published last week in the journal Cureus is the first peer-reviewed paper to call for a global moratorium on the COVID-19 mRNA vaccines. The authors say that reanalyzed data from the vaccine makers’ trials and high rates of serious post-injection injuries indicate the mRNA gene therapy vaccines should not have been authorized for use. Brenda Baletti, Ph.D. global moratorium mrna covid vaccine feature Miss a day, miss a lot. Subscribe to The Defender's Top News of the Day. It's free. Governments should endorse a global moratorium on mRNA vaccines until all questions about their safety have been thoroughly investigated, according to the authors of a new, peer-reviewed article on the COVID-19 vaccine trials and the global vaccination campaign published last week in Cureus, Journal of Medical Science. Cureus is a web-based peer-reviewed open-access general medical journal using prepublication peer review. The authors surveyed published research on the pharmaceutical companies’ vaccine trials and related adverse events. They also called for the COVID-19 vaccines to be removed immediately from the childhood immunization schedule. After the first reports from vaccine trials claimed they were 95% effective in preventing COVID-19, serious problems with method, execution and reporting in the trials became public, which the paper reviewed in detail. Evidence also shows the products never underwent adequate safety and toxicological testing, and since the vaccine rollout, researchers have identified a significant number of adverse events (AEs) and serious adverse events (SAEs). Authors M. Nathaniel Mead, Stephanie Seneff, Ph.D., Russ Wolfinger, Ph.D., Jessica Rose, Ph.D., Kris Denhaerynck, Ph.D., Steve Kirsch and Dr. Peter McCullough detailed the vaccines’ potential serious harms to humans, vaccine control and processing issues, the mechanisms behind AEs, the immunological reasons for vaccine inefficacy and the mortality data from the registrational trials. They concluded, “Federal agency approval of the COVID-19 mRNA injectable products on a blanket-coverage population-wide basis had no support from an honest assessment of all relevant registrational data and commensurate consideration of risks versus benefits.” They also called for the vaccines to be immediately removed from the childhood immunization schedule and for the suspension of the boosters. “It is unethical and unconscionable to administer an experimental vaccine to a child who has a near-zero risk of dying from COVID-19 (IFR, 0.0003%) but a well-established 2.2% risk of permanent heart damage based on the best prospective data available,” they wrote. Finally, the authors called for a full investigation into misconduct by the pharmaceutical companies and the regulatory agencies. It is the first peer-reviewed study to call for a moratorium on the COVID-19 mRNA products, Rose told The Defender. “Once a proper assessment of the safety and efficacy claims was made herein — upon which the emergency use authorization (EUA)’s and ultimate final authorizations were granted — it was found that the COVID-19 injectable products were neither safe nor effective,” she added. According to McCollough, “mRNA should never have been authorized for human use.” Lead author Mead told The Defender, “Our view is that any risk-benefit analysis must consider how much the presumed benefit in terms of reduced COVID-19 related mortality is offset by the potential increase in vaccine-induced mortality.” Here are six takeaways from the review: 1. The COVID-19 ‘vaccines’ are reclassified gene therapies that were rushed through the regulatory process in a historically unprecedented manner Before the seven-month authorization process for the mRNA vaccines, no vaccine had ever gone to market without undergoing testing of at least four years, with typical timelines averaging 10 years. To speed the process, the companies skipped preclinical studies of potential toxicity from multiple doses and cut the typical 6-12 month observation period for identifying longer-term adverse effects and the established 10-15-year period for monitoring for long-term effects such as cancer and autoimmune disorders, the authors wrote. The trials prioritized documenting effective symptom reduction over SAE and mortality. This was particularly concerning, the authors argued, because mRNA products are gene therapy products reclassified as vaccines and then given EUA for the first time ever for use against a viral disease. However, the gene therapies’ components have not been thoroughly evaluated for safety for use as vaccines. There is an uninvestigated and major concern that the mRNA could transform body cells into viral protein factories — with no off-switch — that produce the spike protein for a prolonged period causing chronic systemic inflammation and immune dysfunction. The spike protein in the vaccine, the authors said, is associated with more severe immunopathology and other AEs than the spike protein in the virus itself. The authors suggested that massive government investment in mRNA technology, including hundreds of millions before the pandemic and tens of billions once it began, meant, “U.S. federal agencies were strongly biased toward successful outcomes for the registrational trials.” The financial incentives along with political pressures to deliver a rapid solution likely influenced a series of flawed decisions that compromised the integrity of the trials and downplayed serious scientific concerns about risks with the technology, they added. RFK Jr. and Brian Hooker Vax-Unvax RFK Jr. and Brian Hooker’s New Book: “Vax-Unvax” Order Now 2. Steps were taken in trials to overestimate vaccine efficacy Because the trials were designed to assess whether the mRNA vaccine reduced symptoms, they did not measure whether the vaccines prevented severe disease and death. Yet the vaccine makers repeatedly claimed that they do. “No large randomized double-blind placebo-controlled trials have ever demonstrated reductions in SARS-CoV-2 transmission, hospitalization, or death,” the authors wrote. Additionally, the number of people who contracted clinical COVID-19 in both the placebo and intervention groups was “too small to draw meaningful, pragmatic, or broad-sweeping conclusions with regard to COVID-19 morbidity and mortality.” Pfizer’s 95 % efficacy claims were based on 162 of 22,000 placebo recipients contracting PCR-confirmed COVID-19 compared to eight of 22,000 in the vaccine group. None of the placebo recipients died from COVID-19. In the Moderna trials, only one placebo death was attributed to COVID-19. There was also a much larger percentage of “suspected COVID-19 cases” in both groups, with participants showing COVID-19 symptoms but a negative PCR test. When factoring in those cases, measures of vaccine efficacy drop to about 19%. The trial subject pool was comprised of largely young and healthy individuals, excluding key groups — children, pregnant women, elderly and immunocompromised people — which can also obscure the vaccine’s actual efficacy and safety. Findings from reanalyses of data from the Pfizer trials can be interpreted as showing the vaccines made “no significant difference” in reducing all-cause mortality in the vaccinated versus unvaccinated groups at 20 weeks into the trial, the authors wrote. Even the six-month post-marketing data Pfizer presented to the U.S. Food and Drug Administration (FDA) showed no reduction in all-cause mortality from the vaccine. The authors reanalyzed that data, adjusting the analysis of deaths to better account for the fact that when Pfizer unblinded the study people from the placebo group took the vaccine, and found the vaccine group had a higher mortality rate (0.105%) than the unvaccinated group (0.0799%), which they said was a conservative estimate. One of the most glaring issues with the registrational trials, they noted, was that they exclusively focused on measuring risk reduction — the ratio of COVID-19 symptom rates in the vaccine group versus the placebo group — rather than measuring absolute risk reduction, which is the likelihood someone will show COVID-19 symptoms relative to people in the population at large. According to FDA guidelines, accounting for both approaches is crucial to avoid the misguided use of pharmaceutical products — but the data were omitted, leading to an overestimation of an intervention’s clinical utility. While both vaccines touted an approximately 95% risk reduction figure as their efficacy figure, the absolute risk reductions for Pfizer and Moderna’s vaccines were 0.7% and 1.1% respectively. “A substantial number of individuals would need to be injected in order to prevent a single mild-to-moderate case of COVID-19,” the authors wrote. As an example, using a conservative estimate that 119 people would need to be vaccinated to prevent infection, and assuming that COVID-19 had a 0.23% infection fatality rate, they wrote that approximately 52,000 vaccinations would be necessary to prevent a single COVID-19-related death. However, “Given trial misconduct and data integrity problems … the true benefit is likely to be much lower,” they wrote. And, they added, one would need to assess that benefit along with harms, which they estimate to be 27 deaths per 100,000 doses of Pfizer. That means, using the most conservative estimates, “for every life saved, there were 14 times more deaths caused by the modified mRNA injections.” They also noted that post-rollout evidence confirmed the efficacy claims were overstated. For example, two large cohort Cleveland clinic studies showed the vaccine could not confer protection against COVID-19 — instead, in those trials, more vaccinated people were more likely to contract COVID-19. One study showed the risk of “breakthrough” infection was significantly higher among people who were boosted and that more vaccinations resulted in a greater risk of COVID-19. A second study showed adults who were not “up-to-date” with their shots had a 23% lower incidence of COVID-19 than their “up-to-date” colleagues. 3. The trials underestimated the adverse events, including death, despite evidence in the data. Harms were also underreported and underestimated for a number of reasons, according to the authors, a practice that tends to be common in randomized industry-sponsored vaccine trials in general and “exceptionally evident” here. First, because Pfizer unblinded the trial within just a few weeks of the emergency use authorization and allowed people in the placebo group to take the vaccine, there was not sufficient time to identify late-occurring harms because there was no longer a control group. “Was this necessary, given that none of the deaths in the Pfizer trial were attributed to COVID-19 as the primary cause, and given the very low IFR [infection fatality rate] for a relatively healthy population?” they asked. Also, trial coordinators were “haphazard” in their approach to monitoring AEs. They prioritized documenting events thought to be related to COVID-19 rather than to the vaccines for the first seven days and only recorded “unsolicited” AEs for 30-60 days. After that period, even very SAEs, like death, were not recorded. Even for the AEs recorded in the first seven days, they only solicited data from 20% of the population. None of the trial data was independently verified. “Such secrecy may have enabled the industry to more easily present an inflated and distorted estimate of the genetic injections’ benefits, along with a gross underestimation of potential harms,” they wrote. Subsequent analysis by Michels et al. revealed that deaths and other SAEs — like life-threatening conditions, inpatient hospitalization or extension of hospitalization, persistent or significant disability/incapacity, a congenital anomaly, or a medically significant event — did occur after the cutoff period and before the FDA advisory meeting where emergency authorization was recommended. During the first 33 weeks of the Pfizer trials, 38 subjects died, according to Pfizer’s own data, although independent research by Michels et al. estimated that that number is only approximately 17% of the actual projected number due to missing data. And after that, the rate of deaths continued to increase. Michaels et al. found Pfizer failed to report a substantial increase in the number of deaths due to cardiovascular events. They also found a consistent pattern of reporting delays on the date of the death on subjects’ case reports. Overall, the review authors reported that there were “twice as many cardiac deaths proportionately among vaccinated compared to unvaccinated subjects in the Pfizer trials.” In their discussion, the authors wrote “Based on the extended Pfizer trial findings, our person-years estimate yielded a 31% increase in overall mortality among vaccine recipients, a clear trend in the wrong direction.” This raises serious red flags about how the registrational trials were conducted, Mead said. “Assessments of the safety profile of the COVID-19 modified mRNA injections warrant an objective precautionary perspective, any substantial upward trend in all cause mortality within the intervention arm of the trial population reflects badly on the intervention.” 4. Numbers of SAEs in the trials and post-rollout reporting are well-documented, despite claims to the contrary. Both Pfizer and Moderna found about 125 SAEs per 100,000 vaccine recipients, or one SAE for every 800 vaccines. However, because the trials excluded more vulnerable people, the authors note, even higher proportions of SAEs would be expected in the general population. The Fraiman et al. reanalysis of the Pfizer trial data found a significant 36% higher risk of SAEs, which included deaths and many life-threatening conditions in the vaccinated participants. Official SAEs for other vaccines average around only 1-2 per million. Fraiman et alestimated 1,250 SEAs per million vaccines, exceeding that benchmark by “at least 600-fold.” After the vaccine rollout, analyses of two large drug safety reporting systems in the U.S. and Europe identified signals for myocardial infarction, pulmonary embolism, cardio-respiratory arrest, cerebral infarction, and cerebral hemorrhage associated with both mRNA vaccines, along with ischemic stroke. And millions of AEs have been reported to those systems. Another study by Skidmore et al. estimated the total number of fatalities from the vaccines in 2021 alone was 289,789. Autopsy studies have also provided additional evidence of serious harms, including evidence that most COVID-19 mRNA vaccine-related deaths resulted from injury to the cardiovascular system. In multiple autopsy studies, German pathologist Aren Burkhardt documented the presence of vaccine-mRNA-produced spike proteins in blood vessel walls and brain tissues. This research helps to explain documented vaccine-induced toxicities affecting the nervous, immune, reproductive and other systems. The Pfizer data also showed an overwhelming number of adverse effects. According to a confidential document released in August 2022, Pfizer had documented approximately 1.6 million AEs affecting nearly every organ system, and one-third of them were classified as serious. In Pfizer’s trial, Michels and colleagues found a nearly 4-fold increase (OR 3.7, 95%CI 1.02-13.2, p = 0.03) in serious cardiac events (e.g., heart attack, acute coronary syndrome) in the vaccine group. Neither the original trial report nor Pfizer’s Summary Clinical Safety report acknowledged or commented on this safety signal. “The serious adverse events are all well documented,” Mead said. “Yet it’s surprising to see so many in the medical field continue to ignore or dismiss outright the latter half of the equation when considering all cause mortality trends.” 5. The failure to appropriately test for safety and toxicity poses serious problems. Researchers have raised concerns that the mRNA technology is inherently unstable and difficult to store, which leads to batch variability and contamination linked to different rates of AEs. Recent findings by McKernan et al. that found Pfizers’ mRNA vaccines are contaminated with plasmid DNA that shouldn’t be present — and wasn’t present in the vaccines used in the trials – raising serious safety issues. That’s because “Process 1,” used in the trials to generate the vaccines involved in vitro transcription of synthetic DNA — essentially a “clean” process. However, that process isn’t viable for mass production, so the manufacturers used “Process 2,” which involves using E. coli bacteria to replicate the plasmids. Removing plasmids E coli. can result in residual plasmids in the vaccines and the effects of their presence is unknown. McKernan’s work also revealed the presence of DNA from simian virus 40 (SV40), an oncogenic DNA virus originally isolated in 1960 from contaminated polio vaccines, induces lymphomas, brain tumors, and other malignancies in laboratory animals, raising other safety concerns. Researchers from Cambridge published a paper in Nature in December 2023, where they found an inherent defect in the modified RNA instructions for the spike protein in COVID-19 immunizations that causes the machinery that translates the gene to the spike protein to “slip” about 10% of the time This process creates “frameshifts” that cause cells to produce “off-target” proteins in addition to the spike. These proteins, which developers either failed to look for or did not report to regulators, cause undesirable immune responses whose long-term effects are unknown. 6. There are many different possible biological mechanisms that cause AEs and vaccine ineffectiveness. The review points readers to a series of papers that explain a number of different theories to explain the high number of AEs from the COVID-19 mRNA vaccines. “The mechanisms of molecular mimicry, antigen cross-reactivity, pathogenic priming, viral reactivation, immune exhaustion, and other factors related to immune dysfunction all reinforce the biological plausibility for vaccine-induced pathogenesis of malignant and autoimmune diseases,” they wrote. And these mechanisms of immune activation are distinct from the body’s response to a viral infection. They also note the toxic effects of the primary adjuvant, PEG, and of the spike protein itself. They close their analysis of the vaccines with a complex explanation for the different immunological basis for protection provided by the vaccines versus natural immunity through infection. They explain the mechanisms for vaccine failure and problems generated by the ability for the mRNA vaccines to perpetuate the emergence of new variants. https://childrenshealthdefense.org/defender/scientists-global-moratorium-mrna-vaccines-removal-childhood-schedule/ https://donshafi911.blogspot.com/2024/01/scientists-call-for-global-moratorium.html
    CHILDRENSHEALTHDEFENSE.ORG
    Scientists Call for Global Moratorium on mRNA Vaccines, Immediate Removal From Childhood Schedule
    A review paper published last week in the journal Cureus is the first peer-reviewed paper to call for a global moratorium on the COVID-19 mRNA vaccines. The authors say that reanalyzed data from the vaccine makers’ trials and high rates of serious post-injection injuries indicate the mRNA gene therapy vaccines should not have been authorized for use.
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  • Health benefits of the Sun: Vitamin D can reduce the risk of cancer by as much as 67%
    Rhoda WilsonDecember 28, 2023
    Vitamin D is involved in the biology of all cells in your body, including your immune cells. A large number of studies have shown raising your vitamin D level can significantly reduce your risk of cancer.

    Most recently, researchers found vitamin D and calcium supplementation lowered participants’ overall cancer risk by 30%.

    Having a serum vitamin D level of at least 40 ng/ml reduces your risk for cancer by 67% compared to having a level of 20 ng/ml or less; most cancers occur in people with a vitamin D level between 10 and 40 ng/ml.

    Higher Vitamin D Levels Lower Cancer Risk

    By Dr. Joseph Mercola

    This article was originally published on 10 April 2017.

    Thousands of studies have been done on the health effects of vitamin D, and research shows it is involved in the biology of all cells and tissues in your body, including your immune cells. Your cells actually need the active form of vitamin D to gain access to the genetic blueprints stored inside.

    This is one of the reasons why vitamin D has the ability to impact such a wide variety of health problems – from foetal development to cancer. Unfortunately, despite being easy and inexpensive to address, vitamin D deficiency is an epidemic around the world.

    It’s been estimated that as many as 90% of pregnant mothers and newborns in the sunny Mediterranean region are even deficient in vitamin D,1 thanks to chronic Sun avoidance. A simple mathematical error may also deter many Americans and Canadians from optimising their vitamin D.

    The Institute of Medicine (“IOM”) recommends a mere 600 IUs of vitamin D per day for adults. As pointed out in a 2014 paper,2 the IOM underestimates the need by a factor of 10 due to a mathematical error, which has never been corrected.

    Grassroots Health has created a petition for the IOM and Health Canada to re-evaluate its vitamin D guidelines and correct this mathematical error.3 You can help further this important cause by signing the petition on ipetitions.com.

    More recent research 4 suggests it would require 9,600 IUs of vitamin D per day to get a majority (97.5%) of the population to reach 40 nanograms per millilitre (ng/ml). The American Medical Association uses of 20 ng/ml as sufficient, but research shows 40 ng/mL should be the cutoff point for sufficiency in order to prevent a wide range of diseases, including cancer.

    Research Again Concludes Vitamin D Lowers Cancer Risk

    A large number of studies have shown raising your vitamin D level can significantly reduce your risk of cancer.

    Most recently, a randomised clinical trial 5 by researchers at Creighton University, funded by the National Institutes of Health (“NIH”), found vitamin D and calcium supplementation lowered participants’ overall cancer risk by 30%.6,7,8

    The study, which included more than 2,300 postmenopausal women from Nebraska who were followed for four years, looked at the effects of vitamin D supplementation on all types of cancer.

    Participants were randomly assigned to receive either 2,000 IUs of vitamin D3 in combination with 1,500 mg of calcium, or a placebo for the duration of the study. Blood testing revealed that 25-hydroxyvitamin D (25(OH)D) levels were significantly lower in those who did develop cancer.

    Joan Lappe, Ph.D., professor of nursing and associate dean of research at Creighton University’s College of Nursing, and lead author of the study, said:

    The study provides evidence that higher concentrations of 25(OH)D in the blood, in the context of vitamin D3 and calcium supplementation, decrease risk of cancer … While people can make their own vitamin D3 when they are in the Sun near mid-day, sunscreen blocks most vitamin D production.

    Also, due to more time spent indoors, many individuals lack adequate levels of vitamin D compounds in their blood. The results of this study lend credence to a call for more attention to the importance of vitamin D in human health and specifically in preventing cancer.

    Vitamin D Status Is Strongly Correlated with Cancer Risk

    Previous research has shown that once you reach a serum vitamin D level of 40 ng/ml, your risk for cancer diminishes by 67%, compared to having a level of 20 ng/ml or less.9,10,11,12,13,14,15

    Most cancers, they found, occurred in people with a vitamin D blood level between 10 and 40 ng/ml. The optimal level for cancer protection was identified as being between 40 and 60 ng/ml. Another study 16 published in 2015 found women with vitamin D concentrations of at least 30 ng/ml had a 55% lower risk of colorectal cancer than those who had a blood level below 18 ng/ml.

    Even earlier research, 17 published in 2005, showed women with vitamin D levels above 60 ng/ml had an 83% lower risk of breast cancer than those with levels below 20 ng/ml! The Health and Medicine Division of the National Academies of Sciences, Engineering and Medicine (formerly IOM) has also reported an association between vitamin D and overall mortality risk from all causes, including cancer.18,19

    Vitamin D also increases your chances of surviving cancer if you do get it,20,21 and this includes melanoma. 22

    Access Sun Exposure as Much as Possible and Get Your Vitamin D Level Checked

    The UVB in sunlight is what triggers your body to produce vitamin D. I firmly believe getting regular, sensible Sun exposure is the ideal way to not only optimise your vitamin D level but maximise your health as well because sunlight also has many other important health functions. I’ll review some of these in another section below.

    Regular Sun exposure provides over 1,500 different wavelengths, and we’re just now rediscovering the value of many of these other wavelengths besides UVA and UVB. For example, we now know that red and infrared light helps your body form structured water, which is important for cellular function.

    Many do not appreciate that red, near, mid and far-infrared have many important biological functions. One of them is to improve mitochondrial function, especially the 660 nm and 830 nm wavelengths, as cytochrome C oxidase in mitochondria uses these wavelengths to produce ATP more efficiently.

    Vitamin D3 supplements are a poor second resort, but if you’re unable to get sufficient Sun exposure, then it’s better than nothing. As demonstrated in the featured study – which specifically looked at the effects of supplementation – they do have some benefits.

    Also, while not addressed in this study, I strongly recommend taking your vitamin D3 with vitamin K2 and magnesium as well, since all three work in tandem. A primary consideration when it comes to vitamin D is to get your level checked, ideally twice a year, in the middle of the summer and winter, when your level is at its highest and lowest.

    What you’re aiming for is a level between 40 and 60 ng/ml year-round. Grassroots Health offers vitamin D testing at a great value through its D*Action study.

    Read more: Harness the Power of the Sun for Health (Infographic)

    How to Minimise Your Risk of Skin Cancer from Sun Exposure

    Many avoid Sun exposure for fear of melanoma, an aggressive and potentially lethal form of skin cancer. However, it’s important to realise that melanoma occurs among those with minimal Sun exposure as well.

    An important risk factor for melanoma is overexposure to UV radiation. Baking in the Sun for hours on end on a weekend here and there is not a wise choice.

    To minimise your skin cancer risk, you want to avoid sunburn at all costs. If you’re going to the beach, bring long-sleeved cover-ups and a wide-brimmed hat, and cover up as soon as your skin starts to turn pink.

    Following are some general guidelines for sensible Sun exposure. If you pay close attention to these, you can determine, within reason, safe exposure durations.

    Know your skin type based on the Fitzpatrick skin type classification system. The lighter your skin, the less exposure to UV light is necessary. The downside is that lighter skin is also the most vulnerable to damage from overexposure.
    For very fair-skinned people and those with photodermatitis, any Sun exposure may be unwanted and they should carefully measure vitamin D levels while ensuring they have an adequate intake of vitamin D, vitamin K2, magnesium and calcium.
    For most people, safe UV exposure is possible by knowing your skin type and the current strength of the Sun’s rays. There are several apps and devices to help you optimise the benefits of Sun exposure while mitigating the risks. Also, be extremely careful if you have not been in the Sun for some time. Your first exposures of the year are the most sensitive, so be especially careful to limit your initial time in the Sun.
    Vitamin D Influences Your Health in Many Ways

    The benefits of vitamin D are not restricted to cancer prevention. In fact, the list of health benefits of vitamin D is exceedingly long. As noted earlier, researchers have now realised that vitamin D affects virtually every cell and tissue in your body, so it might be easier to list what it will not affect, rather than what it will impact.

    Compelling evidence suggests that optimising your vitamin D can reduce your risk of death from any cause, 23 making it a foundational component of optimal health. Mega doses of vitamin D have also been shown to decrease the length of time critical care patients must remain hospitalised.24 Those who received 250,000 IUs for five days were released after an average of 25 days, compared to the average of 36 days for those receiving a placebo.

    Patients who received 500,000 IUs of vitamin D for five days were released after an average of just 18 days, effectively cutting their hospital stay in half. The health care savings in this instance alone are tremendous. When you add in all possible diseases and ailments vitamin D can prevent and/or ameliorate, the savings could potentially tally into the trillions each year.

    Certainly, for the average person, optimising your vitamin D level is one of the least expensive preventive care strategies at your disposal. If you suffer from any of the following ailments and still haven’t checked your vitamin D level, now may be the time to go ahead and do so, as research 25 into vitamin D has found it can help prevent and/or address:

    Osteoporosis, osteomalacia (bone softening) and hip fractures Type 1 and type 2 diabetes
    Cancer, including cancers of the breast, colon, prostate, ovaries, oesophagus and lymphatic system. Adding vitamin D to the conventional treatment for pancreatic cancer may also boost the effectiveness of the treatment 26 Hypertension (high blood pressure), cardiovascular disease and heart attacks – (According to vitamin D researcher Dr. Michael Holick, deficiency can raise your risk of heart attack by 50%. What’s worse, if you have a heart attack while vitamin D deficient, your risk of dying is nearly guaranteed)
    Obstructive sleep apnoea – In one study, 98% of patients with sleep apnoea had vitamin D deficiency, and the more severe the sleep apnoea, the more severe the deficiency27 Multiple sclerosis28 (“MS”) – Research shows MS patients with higher levels of vitamin D tend to experience fewer disabling symptoms
    Rheumatoid arthritis Reduced immune function
    Autoimmune diseases, including psoriasis Infections, including influenza
    Depression, 29 Seasonal Affective Disorder and psychiatric conditions such as schizophrenia Neurological disorders, including autism, dementia and Alzheimer’s 30
    Health Benefits of Sun Exposure Beyond Vitamin D

    There’s overwhelming evidence to suggest the human body evolved to obtain health benefits from, and to thrive in, sunlight. As previously noted in The Daily Mail:31

    Even taking the skin cancer risk fully into account, [scientists] say that getting a good dose of sunshine is statistically going to make us live longer, healthier and happier lives.

    One significant mechanism by which sunlight helps optimise your health is by triggering the release of nitric oxide (“NO”) when sunlight strikes your skin. 32 NO is a powerful blood pressure-lowering compound that helps protect your cardiovascular system, cutting your risk for both heart attacks and stroke.

    According to one 2013 study, 33 for every single skin cancer death, 60 to 100 people die from stroke or heart disease related to hypertension. So, your risk of dying from heart disease or stroke is on average 80 times greater than your risk of dying from skin cancer.

    Importantly, while higher vitamin D levels correlate with lower rates of cardiovascular disease, oral vitamin D supplements do not appear to benefit blood pressure, and the fact that supplements do not increase NO may be the reason for this. According to researcher Dr. Richard Weller:

    We suspect that the benefits to heart health of sunlight will outweigh the risk of skin cancer. The work we have done provides a mechanism that might account for this, and also explains why dietary vitamin D supplements alone will not be able to compensate for lack of sunlight.

    To get a thorough understanding of how UV light affects your cardiovascular function, read Weller’s paper, ‘Sunlight Has Cardiovascular Benefits Independently of Vitamin D’. 34 Research also shows that UV light:

    Helps treat and prevent the spread of diseases like tuberculosis. 35
    Helps anchor your circadian rhythm, helping you sleep better.
    Helps kill and prevent the spread of antibiotic-resistant bacteria. UV light at 254 nanometres acts as a potent bactericidal, killing drug-resistant strains of S. aureus and E. faecalis in as little as 5 seconds. 36
    Reduces your risk of myopia (short-sightedness). As reported by The Daily Mail: 37 “[R]esearchers believe that the neurotransmitter dopamine is responsible. It is known to inhibit the excessive eyeball growth that causes myopia. Sunshine causes the retina to release more dopamine.”
    Helps treat seasonal affective disorder and major depression. 38 Schizophrenia has also been linked to maternal lack of Sun exposure during pregnancy. 39
    Boosts men’s libido by increasing testosterone. Research reveals men’s testosterone levels rise and fall with the seasons. Researchers have also linked low vitamin D with an increased risk for erectile dysfunction. 40
    Helps maintain vitamin D status in elderly people at a lower cost than that of using oral vitamin D supplementation. 41 Not only could UV lamps help improve nursing home patients’ physical health, but they could also help relieve symptoms of depression.
    Lowers all-cause mortality. In one study,42,43 women who avoided Sun exposure had double the all-cause mortality rate of those who got regular Sun exposure. Another 54-month-long study, 44 involving more than 422,800 healthy adults, found that those who were most deficient in vitamin D had an 88% increased mortality risk.
    Embrace Sensible Sun Exposure as a Health-Promoting Habit

    Safe exposure to sunshine is possible by understanding your skin type, the UV strength at the time of exposure, and your duration of exposure. My advice has been clear: Always avoid sunburn. Once your skin develops the slightest tint of pink, cover up with clothing to avoid further exposure.

    The most important part of the equation is to pay close attention to your vitamin D level. Ideally, get your vitamin D tested during the peak of summer and at the end of winter to help guide your UV exposure and vitamin D supplementation. The evidence is overwhelming: You really do need sensible Sun exposure for optimal health.

    Since few foods contain any significant amount of vitamin D, and your body certainly was not designed to get its vitamin D from supplements, which are a modern invention, the only rational conclusion is that Sun exposure is the ideal way to raise your vitamin D level.

    Research has shown just how beautifully your body has been designed to use the Sun’s UV rays to promote health. It even has built-in “fail-safes” and self-regulatory processes to ensure you cannot produce too much vitamin D from Sun exposure. Plus, the vitamin D produced by UVB rays actually helps counteract the skin damage caused by UVA. It’s an intricate dance that simply cannot be fully duplicated with a supplement.

    Sources and References

    1 Ther Adv Musculoskelet Dis v.8(4); 2016 Aug
    2 Nutrients 2014; 6(10): 4472-4475
    3 ipetitions.com
    4 Anticancer Research 2011 Feb;31(2):607-11
    5 JAMA 2017;317(12):1234-1243
    6 Lab Manager March 30, 2017
    7 Newswise March 28, 2017
    8 Time March 28, 2017
    9 PLOS ONE 2016; 11 (4): e0152441
    10 PR Web April 6, 2016
    11 UC San Diego Health April 6, 2016
    12 Science World Report April 13, 2016
    13 Oncology Nurse Advisor April 22, 2016
    14 Tech Times April 11, 2016
    15 Chrisbeatcancer.com, Vitamin D
    16 Cancer Prev Res (Phila). 2015 Aug;8(8):675-82
    17 European Journal of Cancer 2005 May;41(8):1164-9
    18 Institute of Medicine, Committee to Review Dietary Reference Intakes for Vitamin D and Calcium, Dietary Reference Intakes for Calcium and Vitamin D
    19, 44 J Clin Endocrinol Metab 2013;98:2160-2167
    20 Anticancer Research February 2011: 31(2); 607-611
    21 UC San Diego Health System Press Release March 6, 2014
    22 Cancer Therapy Advisor March 23, 2016
    23 New York Times November 24, 2014
    24 Medical Press May 27, 2015
    25 Harvard T.H. Chan. Vitamin D
    26 Salk. FAQ on Pancreatic Cancer and Vitamin D
    27 Bel Marra Health May 3, 2016
    28 Mayo Clinic. Vitamin D and MS: Is There Any Connection?
    29 J Nutr Health Aging 1999;3(1): 5-7
    30 Int J Mol Sci. 2022 Dec 21;24(1):87. Vitamin D in Neurological Diseases
    31, 37 Daily Mail May 2, 2016
    32 Medical News Today May 8, 2013
    33 BBC News May 7, 2013
    34 Sunlight Institute January 18, 2016
    35 Science Daily March 17, 2009
    36 Ostomy Wound Management 1998 Oct;44(10):50-6
    38 Journal of Clinical Psychiatry 1991 May; 52(5): 213-6
    39 BBC News July 20, 2001
    40 New Hope Network May 2, 2016
    41 Photodermatol Photoimmunol Photomed 2001 Aug;17(4):168-71
    42 Journal of Internal Medicine 2014 Jul;276(1):77-86
    43 Business Insider May 7, 2014
    About the Author

    Dr. Joseph Mercola is the founder and owner of Mercola.com, a Board-Certified Family Medicine Osteopathic Physician, a Fellow of the American College of Nutrition and a New York Times bestselling author. He publishes multiple articles a day covering a wide range of topics on his website Mercola.com.




    Why do you think the satanic oligarchs, who want us sick, weak and gone, are blocking our sun from healing us?

    Health benefits of the Sun: Vitamin D can reduce the risk of cancer by as much as 67%

    Vitamin D is involved in the biology of all cells in your body, including your immune cells. A large number of studies have shown raising your vitamin D level can significantly reduce your risk of cancer...

    https://expose-news.com/2023/12/28/health-benefits-of-the-sun

    T.me/AgentsOfTruth
    T.me/AgentsOfTruthChat
    Health benefits of the Sun: Vitamin D can reduce the risk of cancer by as much as 67% Rhoda WilsonDecember 28, 2023 Vitamin D is involved in the biology of all cells in your body, including your immune cells. A large number of studies have shown raising your vitamin D level can significantly reduce your risk of cancer. Most recently, researchers found vitamin D and calcium supplementation lowered participants’ overall cancer risk by 30%. Having a serum vitamin D level of at least 40 ng/ml reduces your risk for cancer by 67% compared to having a level of 20 ng/ml or less; most cancers occur in people with a vitamin D level between 10 and 40 ng/ml. Higher Vitamin D Levels Lower Cancer Risk By Dr. Joseph Mercola This article was originally published on 10 April 2017. Thousands of studies have been done on the health effects of vitamin D, and research shows it is involved in the biology of all cells and tissues in your body, including your immune cells. Your cells actually need the active form of vitamin D to gain access to the genetic blueprints stored inside. This is one of the reasons why vitamin D has the ability to impact such a wide variety of health problems – from foetal development to cancer. Unfortunately, despite being easy and inexpensive to address, vitamin D deficiency is an epidemic around the world. It’s been estimated that as many as 90% of pregnant mothers and newborns in the sunny Mediterranean region are even deficient in vitamin D,1 thanks to chronic Sun avoidance. A simple mathematical error may also deter many Americans and Canadians from optimising their vitamin D. The Institute of Medicine (“IOM”) recommends a mere 600 IUs of vitamin D per day for adults. As pointed out in a 2014 paper,2 the IOM underestimates the need by a factor of 10 due to a mathematical error, which has never been corrected. Grassroots Health has created a petition for the IOM and Health Canada to re-evaluate its vitamin D guidelines and correct this mathematical error.3 You can help further this important cause by signing the petition on ipetitions.com. More recent research 4 suggests it would require 9,600 IUs of vitamin D per day to get a majority (97.5%) of the population to reach 40 nanograms per millilitre (ng/ml). The American Medical Association uses of 20 ng/ml as sufficient, but research shows 40 ng/mL should be the cutoff point for sufficiency in order to prevent a wide range of diseases, including cancer. Research Again Concludes Vitamin D Lowers Cancer Risk A large number of studies have shown raising your vitamin D level can significantly reduce your risk of cancer. Most recently, a randomised clinical trial 5 by researchers at Creighton University, funded by the National Institutes of Health (“NIH”), found vitamin D and calcium supplementation lowered participants’ overall cancer risk by 30%.6,7,8 The study, which included more than 2,300 postmenopausal women from Nebraska who were followed for four years, looked at the effects of vitamin D supplementation on all types of cancer. Participants were randomly assigned to receive either 2,000 IUs of vitamin D3 in combination with 1,500 mg of calcium, or a placebo for the duration of the study. Blood testing revealed that 25-hydroxyvitamin D (25(OH)D) levels were significantly lower in those who did develop cancer. Joan Lappe, Ph.D., professor of nursing and associate dean of research at Creighton University’s College of Nursing, and lead author of the study, said: The study provides evidence that higher concentrations of 25(OH)D in the blood, in the context of vitamin D3 and calcium supplementation, decrease risk of cancer … While people can make their own vitamin D3 when they are in the Sun near mid-day, sunscreen blocks most vitamin D production. Also, due to more time spent indoors, many individuals lack adequate levels of vitamin D compounds in their blood. The results of this study lend credence to a call for more attention to the importance of vitamin D in human health and specifically in preventing cancer. Vitamin D Status Is Strongly Correlated with Cancer Risk Previous research has shown that once you reach a serum vitamin D level of 40 ng/ml, your risk for cancer diminishes by 67%, compared to having a level of 20 ng/ml or less.9,10,11,12,13,14,15 Most cancers, they found, occurred in people with a vitamin D blood level between 10 and 40 ng/ml. The optimal level for cancer protection was identified as being between 40 and 60 ng/ml. Another study 16 published in 2015 found women with vitamin D concentrations of at least 30 ng/ml had a 55% lower risk of colorectal cancer than those who had a blood level below 18 ng/ml. Even earlier research, 17 published in 2005, showed women with vitamin D levels above 60 ng/ml had an 83% lower risk of breast cancer than those with levels below 20 ng/ml! The Health and Medicine Division of the National Academies of Sciences, Engineering and Medicine (formerly IOM) has also reported an association between vitamin D and overall mortality risk from all causes, including cancer.18,19 Vitamin D also increases your chances of surviving cancer if you do get it,20,21 and this includes melanoma. 22 Access Sun Exposure as Much as Possible and Get Your Vitamin D Level Checked The UVB in sunlight is what triggers your body to produce vitamin D. I firmly believe getting regular, sensible Sun exposure is the ideal way to not only optimise your vitamin D level but maximise your health as well because sunlight also has many other important health functions. I’ll review some of these in another section below. Regular Sun exposure provides over 1,500 different wavelengths, and we’re just now rediscovering the value of many of these other wavelengths besides UVA and UVB. For example, we now know that red and infrared light helps your body form structured water, which is important for cellular function. Many do not appreciate that red, near, mid and far-infrared have many important biological functions. One of them is to improve mitochondrial function, especially the 660 nm and 830 nm wavelengths, as cytochrome C oxidase in mitochondria uses these wavelengths to produce ATP more efficiently. Vitamin D3 supplements are a poor second resort, but if you’re unable to get sufficient Sun exposure, then it’s better than nothing. As demonstrated in the featured study – which specifically looked at the effects of supplementation – they do have some benefits. Also, while not addressed in this study, I strongly recommend taking your vitamin D3 with vitamin K2 and magnesium as well, since all three work in tandem. A primary consideration when it comes to vitamin D is to get your level checked, ideally twice a year, in the middle of the summer and winter, when your level is at its highest and lowest. What you’re aiming for is a level between 40 and 60 ng/ml year-round. Grassroots Health offers vitamin D testing at a great value through its D*Action study. Read more: Harness the Power of the Sun for Health (Infographic) How to Minimise Your Risk of Skin Cancer from Sun Exposure Many avoid Sun exposure for fear of melanoma, an aggressive and potentially lethal form of skin cancer. However, it’s important to realise that melanoma occurs among those with minimal Sun exposure as well. An important risk factor for melanoma is overexposure to UV radiation. Baking in the Sun for hours on end on a weekend here and there is not a wise choice. To minimise your skin cancer risk, you want to avoid sunburn at all costs. If you’re going to the beach, bring long-sleeved cover-ups and a wide-brimmed hat, and cover up as soon as your skin starts to turn pink. Following are some general guidelines for sensible Sun exposure. If you pay close attention to these, you can determine, within reason, safe exposure durations. Know your skin type based on the Fitzpatrick skin type classification system. The lighter your skin, the less exposure to UV light is necessary. The downside is that lighter skin is also the most vulnerable to damage from overexposure. For very fair-skinned people and those with photodermatitis, any Sun exposure may be unwanted and they should carefully measure vitamin D levels while ensuring they have an adequate intake of vitamin D, vitamin K2, magnesium and calcium. For most people, safe UV exposure is possible by knowing your skin type and the current strength of the Sun’s rays. There are several apps and devices to help you optimise the benefits of Sun exposure while mitigating the risks. Also, be extremely careful if you have not been in the Sun for some time. Your first exposures of the year are the most sensitive, so be especially careful to limit your initial time in the Sun. Vitamin D Influences Your Health in Many Ways The benefits of vitamin D are not restricted to cancer prevention. In fact, the list of health benefits of vitamin D is exceedingly long. As noted earlier, researchers have now realised that vitamin D affects virtually every cell and tissue in your body, so it might be easier to list what it will not affect, rather than what it will impact. Compelling evidence suggests that optimising your vitamin D can reduce your risk of death from any cause, 23 making it a foundational component of optimal health. Mega doses of vitamin D have also been shown to decrease the length of time critical care patients must remain hospitalised.24 Those who received 250,000 IUs for five days were released after an average of 25 days, compared to the average of 36 days for those receiving a placebo. Patients who received 500,000 IUs of vitamin D for five days were released after an average of just 18 days, effectively cutting their hospital stay in half. The health care savings in this instance alone are tremendous. When you add in all possible diseases and ailments vitamin D can prevent and/or ameliorate, the savings could potentially tally into the trillions each year. Certainly, for the average person, optimising your vitamin D level is one of the least expensive preventive care strategies at your disposal. If you suffer from any of the following ailments and still haven’t checked your vitamin D level, now may be the time to go ahead and do so, as research 25 into vitamin D has found it can help prevent and/or address: Osteoporosis, osteomalacia (bone softening) and hip fractures Type 1 and type 2 diabetes Cancer, including cancers of the breast, colon, prostate, ovaries, oesophagus and lymphatic system. Adding vitamin D to the conventional treatment for pancreatic cancer may also boost the effectiveness of the treatment 26 Hypertension (high blood pressure), cardiovascular disease and heart attacks – (According to vitamin D researcher Dr. Michael Holick, deficiency can raise your risk of heart attack by 50%. What’s worse, if you have a heart attack while vitamin D deficient, your risk of dying is nearly guaranteed) Obstructive sleep apnoea – In one study, 98% of patients with sleep apnoea had vitamin D deficiency, and the more severe the sleep apnoea, the more severe the deficiency27 Multiple sclerosis28 (“MS”) – Research shows MS patients with higher levels of vitamin D tend to experience fewer disabling symptoms Rheumatoid arthritis Reduced immune function Autoimmune diseases, including psoriasis Infections, including influenza Depression, 29 Seasonal Affective Disorder and psychiatric conditions such as schizophrenia Neurological disorders, including autism, dementia and Alzheimer’s 30 Health Benefits of Sun Exposure Beyond Vitamin D There’s overwhelming evidence to suggest the human body evolved to obtain health benefits from, and to thrive in, sunlight. As previously noted in The Daily Mail:31 Even taking the skin cancer risk fully into account, [scientists] say that getting a good dose of sunshine is statistically going to make us live longer, healthier and happier lives. One significant mechanism by which sunlight helps optimise your health is by triggering the release of nitric oxide (“NO”) when sunlight strikes your skin. 32 NO is a powerful blood pressure-lowering compound that helps protect your cardiovascular system, cutting your risk for both heart attacks and stroke. According to one 2013 study, 33 for every single skin cancer death, 60 to 100 people die from stroke or heart disease related to hypertension. So, your risk of dying from heart disease or stroke is on average 80 times greater than your risk of dying from skin cancer. Importantly, while higher vitamin D levels correlate with lower rates of cardiovascular disease, oral vitamin D supplements do not appear to benefit blood pressure, and the fact that supplements do not increase NO may be the reason for this. According to researcher Dr. Richard Weller: We suspect that the benefits to heart health of sunlight will outweigh the risk of skin cancer. The work we have done provides a mechanism that might account for this, and also explains why dietary vitamin D supplements alone will not be able to compensate for lack of sunlight. To get a thorough understanding of how UV light affects your cardiovascular function, read Weller’s paper, ‘Sunlight Has Cardiovascular Benefits Independently of Vitamin D’. 34 Research also shows that UV light: Helps treat and prevent the spread of diseases like tuberculosis. 35 Helps anchor your circadian rhythm, helping you sleep better. Helps kill and prevent the spread of antibiotic-resistant bacteria. UV light at 254 nanometres acts as a potent bactericidal, killing drug-resistant strains of S. aureus and E. faecalis in as little as 5 seconds. 36 Reduces your risk of myopia (short-sightedness). As reported by The Daily Mail: 37 “[R]esearchers believe that the neurotransmitter dopamine is responsible. It is known to inhibit the excessive eyeball growth that causes myopia. Sunshine causes the retina to release more dopamine.” Helps treat seasonal affective disorder and major depression. 38 Schizophrenia has also been linked to maternal lack of Sun exposure during pregnancy. 39 Boosts men’s libido by increasing testosterone. Research reveals men’s testosterone levels rise and fall with the seasons. Researchers have also linked low vitamin D with an increased risk for erectile dysfunction. 40 Helps maintain vitamin D status in elderly people at a lower cost than that of using oral vitamin D supplementation. 41 Not only could UV lamps help improve nursing home patients’ physical health, but they could also help relieve symptoms of depression. Lowers all-cause mortality. In one study,42,43 women who avoided Sun exposure had double the all-cause mortality rate of those who got regular Sun exposure. Another 54-month-long study, 44 involving more than 422,800 healthy adults, found that those who were most deficient in vitamin D had an 88% increased mortality risk. Embrace Sensible Sun Exposure as a Health-Promoting Habit Safe exposure to sunshine is possible by understanding your skin type, the UV strength at the time of exposure, and your duration of exposure. My advice has been clear: Always avoid sunburn. Once your skin develops the slightest tint of pink, cover up with clothing to avoid further exposure. The most important part of the equation is to pay close attention to your vitamin D level. Ideally, get your vitamin D tested during the peak of summer and at the end of winter to help guide your UV exposure and vitamin D supplementation. The evidence is overwhelming: You really do need sensible Sun exposure for optimal health. Since few foods contain any significant amount of vitamin D, and your body certainly was not designed to get its vitamin D from supplements, which are a modern invention, the only rational conclusion is that Sun exposure is the ideal way to raise your vitamin D level. Research has shown just how beautifully your body has been designed to use the Sun’s UV rays to promote health. It even has built-in “fail-safes” and self-regulatory processes to ensure you cannot produce too much vitamin D from Sun exposure. Plus, the vitamin D produced by UVB rays actually helps counteract the skin damage caused by UVA. It’s an intricate dance that simply cannot be fully duplicated with a supplement. Sources and References 1 Ther Adv Musculoskelet Dis v.8(4); 2016 Aug 2 Nutrients 2014; 6(10): 4472-4475 3 ipetitions.com 4 Anticancer Research 2011 Feb;31(2):607-11 5 JAMA 2017;317(12):1234-1243 6 Lab Manager March 30, 2017 7 Newswise March 28, 2017 8 Time March 28, 2017 9 PLOS ONE 2016; 11 (4): e0152441 10 PR Web April 6, 2016 11 UC San Diego Health April 6, 2016 12 Science World Report April 13, 2016 13 Oncology Nurse Advisor April 22, 2016 14 Tech Times April 11, 2016 15 Chrisbeatcancer.com, Vitamin D 16 Cancer Prev Res (Phila). 2015 Aug;8(8):675-82 17 European Journal of Cancer 2005 May;41(8):1164-9 18 Institute of Medicine, Committee to Review Dietary Reference Intakes for Vitamin D and Calcium, Dietary Reference Intakes for Calcium and Vitamin D 19, 44 J Clin Endocrinol Metab 2013;98:2160-2167 20 Anticancer Research February 2011: 31(2); 607-611 21 UC San Diego Health System Press Release March 6, 2014 22 Cancer Therapy Advisor March 23, 2016 23 New York Times November 24, 2014 24 Medical Press May 27, 2015 25 Harvard T.H. Chan. Vitamin D 26 Salk. FAQ on Pancreatic Cancer and Vitamin D 27 Bel Marra Health May 3, 2016 28 Mayo Clinic. Vitamin D and MS: Is There Any Connection? 29 J Nutr Health Aging 1999;3(1): 5-7 30 Int J Mol Sci. 2022 Dec 21;24(1):87. Vitamin D in Neurological Diseases 31, 37 Daily Mail May 2, 2016 32 Medical News Today May 8, 2013 33 BBC News May 7, 2013 34 Sunlight Institute January 18, 2016 35 Science Daily March 17, 2009 36 Ostomy Wound Management 1998 Oct;44(10):50-6 38 Journal of Clinical Psychiatry 1991 May; 52(5): 213-6 39 BBC News July 20, 2001 40 New Hope Network May 2, 2016 41 Photodermatol Photoimmunol Photomed 2001 Aug;17(4):168-71 42 Journal of Internal Medicine 2014 Jul;276(1):77-86 43 Business Insider May 7, 2014 About the Author Dr. Joseph Mercola is the founder and owner of Mercola.com, a Board-Certified Family Medicine Osteopathic Physician, a Fellow of the American College of Nutrition and a New York Times bestselling author. He publishes multiple articles a day covering a wide range of topics on his website Mercola.com. Why do you think the satanic oligarchs, who want us sick, weak and gone, are blocking our sun from healing us? Health benefits of the Sun: Vitamin D can reduce the risk of cancer by as much as 67% Vitamin D is involved in the biology of all cells in your body, including your immune cells. A large number of studies have shown raising your vitamin D level can significantly reduce your risk of cancer... https://expose-news.com/2023/12/28/health-benefits-of-the-sun T.me/AgentsOfTruth T.me/AgentsOfTruthChat
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    Health benefits of the Sun: Vitamin D can reduce the risk of cancer by as much as 67%
    Vitamin D is involved in the biology of all cells in your body, including your immune cells. A large number of studies have shown raising your vitamin D level can significantly reduce your risk of …
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  • The Cyber Threat Intelligence League
    Claudio RestaJanuary 18, 2024

    VT Condemns the ETHNIC CLEANSING OF PALESTINIANS by USA/Israel

    $ 280 BILLION US TAXPAYER DOLLARS INVESTED since 1948 in US/Israeli Ethnic Cleansing and Occupation Operation; $ 150B direct "aid" and $ 130B in "Offense" contracts
    Source: Embassy of Israel, Washington, D.C. and US Department of State.

    There is a vast plan for global censorship by US and British military contractors:



    US military contractor Pablo Breuer (left), UK defense researcher Sara-Jayne “SJ” Terp (center), and Chris Krebs, former director of the U.S. Department of Homeland Security’s Cybersecurity and Infrastructure Security Agency (DHS-CISA)

    – Documents received by investigative journalists Michael Shellenberger, Alex Gutentag and Matt Taibbi from an anonymous but “highly credible” whistleblower reveal new details about how the US censorship industrial complex – a network of more than 100 government agencies, private companies, universities and organizations non-profit – seeks to control and criminalize “wrong thinking”.
    – The documents describe how modern digital censorship programs were created and the various roles of the military, US intelligence agencies, civil society organizations and commercial media.
    They also describe the methods and techniques used, such as the creation and use of “sock puppet” accounts to spy on and direct online discussions and propagate desired narratives, and the discrediting of dissidents “as a necessary prerequisite for requiring censorship in their comparisons.”
    – Documents show that the weaponization of the financial sector originated with the Cyber Threat Intelligence League (CTIL), which specifically sought to get banks to “cut off financial services to individuals organizing gatherings or events.”
    – CTIL files also show that there was a clear intent to circumvent the First Amendment by outsourcing censorship to the private, non-governmental sector. According to the informant, “the ethic was that if we get away with it, it’s legal.”

    Documents received by investigative journalists Michael Shellenberger, Alex Gutentag and Matt Taibbi from an anonymous but “highly credible” whistleblower reveal new details about how the US censorship industrial complex – a network of more than 100 government agencies, private companies, universities and non-profit organizations – regulates and criminalizes “wrong thinking”.


    as Ursula Van der Leyen, the president of European Commission since 2019,

    stated at the WEF in Davos on January 17th, 2023 similar censorship are the most urgent and necessary policies (!) and will be implemented everywhere

    They describe the activities of an “anti-disinformation” group called the Cyber Threat Intelligence League, or CTIL, which officially began as a volunteer project of data scientists and defense and intelligence veterans, but whose tactics over time appear to have been absorbed into multiple official projects, including those of the Department of Homeland Security (DHS).

    The CTI League documents provide missing answers to key questions not addressed in the Twitter Files and Facebook Files. Together, they offer a complete picture of the rise of the “anti-disinformation” industry, or what we have called the Censorship Industrial Complex.”

    The documents describe how modern digital censorship programs were created and the various roles of the military, US intelligence agencies, civil society organizations and commercial media.

    They also describe the methods and techniques used, such as the creation and use of “sock puppet” accounts to spy on and direct online discussions and propagate desired narratives, the discrediting of dissidents, and the deliberate weaponization of the financial industry against them .

    According to the whistleblower, the CTIL was also involved in the creation of a counter-disinformation project to “avoid a repeat of 2016”, a reference to Brexit and Donald Trump’s surprise victory in the elections, two situations in which the democratic processes have actually won.

    As Jimmy Dore noted, it wasn’t about preventing the circulation of false information.

    It was about ensuring that no political outsider could ever enter the Oval Office again.

    The instruction to prevent a repeat of 2016 was a direct call to undermine, if not eliminate, the process of free and fair elections.

    Importantly, the documents admit that censorship efforts against Americans must be carried out by private sector partners, because the government does not have “legal authority” to do so.

    The new series of documents and videos reveals that 2019 was a pivotal year for the censorship industrial complex. According to Public, it was then that “US and British military and intelligence contractors, led by a former British defense researcher, Sara-Jayne ‘SJ’ Terp, developed the blanket censorship framework.”



    These contractors became co-leaders of CTIL, whose original founders were a former Israeli intelligence official, Ohad Zaidenberg, the person responsible of Microsoft security Nate Warfield, Chris Mills, another Microsoft security official, and Marc Rogers, the head of security operations at the hacker convention DEF CON.

    According to media reports , these highly trained and in-demand professionals have made the altruistic decision to offer their services to help billion-dollar hospitals with their cybersecurity, for free and with no strings attached. It wasn’t a believable cover story then, and it certainly hasn’t gotten any better.

    Within a month of CTIL’s founding in March 2020, this supposedly entirely volunteer group had grown to 1,400 “invitation-only” members in 76 countries and entered into an official partnership with Cybersecurity and Information Security Agency (CISA) of the United States Department of Homeland Security. As reported by Public:

    Parallel censorship agencies

    In spring 2020, CISA also created the Election Integrity Partnership (EIP) – a consortium composed of the Stanford Internet Observatory (SIO), the University of Washington’s Center for an Informed Public, the Atlantic’s Digital Forensic Research Lab Council and from Graphika (a social media analytics company) – and outsourced what would otherwise have been illegal and unconstitutional censorship.

    During the 2020 election cycle, EIP and CISA worked with the State Department’s Global Engagement Center (GEC) and the DHS-supported Elections Infrastructure Information Sharing and Analysis Center (EI-ISAC) to influence and monitor political discussions online. EIP coordinated the removal of unwanted content using a real-time chat application shared by DHS, EIP, and social media companies.

    At the same time, CTIL monitored and reported anti-blockade views on social media. A “law enforcement” channel was created specifically to spy on and monitor social media users posting anti-lockdown hashtags. CTIL even kept a printout detailing their Twitter biographies.

    According to Public, the CTIL has also “engaged in offensive operations to influence public opinion, discussing ways to promote ‘counter-messaging,’ co-opting hashtags, diluting unfavorable messaging, creating sock puppet accounts, and infiltrating private groups by invitation.” In February 2021, the EIP was renamed the Virality Project, at which point its censorship focus shifted from elections to COVID-related issues.

    Government infiltration and takeover

    Although CTIL member Bonnie Smalley responded to a Public question by saying that CTIL has “nothing to do with the government,” the evidence shows otherwise. At least a dozen government employees working with DHS, the FBI, and CISA were also active members of CTIL.

    According to the whistleblower, CTIL’s goal “was to become part of the federal government.” Terp’s plan called for the creation of “MisinfoSec communities” that would include the federal sector, and documents show that this goal was achieved. In April 2020, Chris Krebs, then director of CISA, also publicly announced the agency’s partnership with CTIL.

    The audience continues:“The documents also show that Terp and his colleagues, through a group called the MisinfoSec Working Group, which included Renee DiResta, head of research at the Stanford Internet Observatory, created a censorship, influence and counter-disinformation strategy called

    Adversarial Misinformation and Influence Tactics and Techniques (AMITT).

    SJ on X: "AMITT (Adversarial Misinformation and Influence Tactics and Techniques) includes the left-of-boom misinformation activities that are often missed by other analyses, where ”left of boom” covers activity before an incident

    They wrote AMITT by adapting a cybersecurity framework developed by MITER… Terp then used AMITT to develop the DISARM framework, which the World Health Organization then used to “counter anti-vaccination campaigns across Europe.”

    A key component of Terp’s work through CTIL, MisinfoSec and AMITT has been to bring the concept of “cognitive security” to the fields of cybersecurity and information security…

    The ambitions of the 2020 pioneers of the censorship industrial complex went far beyond simply requiring Twitter to place a warning label on tweets or blacklist individuals.

    The AMITT framework calls for discrediting people as a necessary prerequisite for requiring censorship of them. Invite influencers to train to spread messages. And he invites us to try to convince banks to cut financial services to individuals who organize demonstrations or events.”

    The arming of the financial sector was born with the CTIL

    Now we know where this financial sector weapon comes from. It originated with the CTIL, which hspecifically sought to induce banks to “cut financial services to individuals who organize rallies or events”.

    Clearly, as my case and that of many others demonstrates, even banks and online payment processors have been tricked into cutting off services to people who simply expressed opposing views. It’s not just demonstration organizers who are being targeted.

    Under the cover of altruism

    Although CTIL officials have repeatedly stressed that the organization was founded on purely altruistic principles, the clear goal of its leaders was to “build support for censorship among national security and cybersecurity institutions,” writes Public, and they built that support by promoting Terp’s idea of “cognitive safety.”

    The choice of the term “cognitive safety” takes on a rather sinister flavor in light of Dr. Michael Nehls’ findings that over the past four years there has been what appears to be an intentional effort to destroy autobiographical memory function in the public’s brain , thus facilitating mass indoctrination and inhibiting personal will and critical thinking.vast plan for global censorship by US and British military contractors

    The Indoctrinated Brain - By Michael Nehls (hardcover) : Target

    He presents his thesis in the book “The Indoctrinated Brain: How to Successfully Fend Off the Global Attack on Your Mental Freedom”, published in mid-December 2023.

    The whistleblower material clearly reveals that sophisticated military tactics have been turned against the American public, powerful psychological tools – the same tools that, according to Nehls, can literally alter the biological functions of the brain.

    Public cites a MisinfoSec report in which “the authors called for placing censorship efforts within ‘cybersecurity,’ while acknowledging that ‘disinformation security’ is entirely different from cybersecurity. They wrote that the third pillar of the “information environment”, after physical and cyber security, should be the “cognitive dimension”.

    Indeed, your mind – your cognition, your very ability to think independently – is the battlefield of today’s war, as Nehls proposes in his book. The scary part is that the tools used have the power to reprogram who we are.

    We are indeed “hackable animals,” as proposed by Yuval Noah Harari, and the censorship industrial complex has already hacked the brain structure of billions of people over the past four years. Gutentag also talks about it in an article dated December 3, 2023:”What was once considered a “conspiracy theory”, according to which military and intelligence forces manipulated public opinion through inorganic interventions, has now been confirmed .

    Our study of the censorship industrial complex has exposed a far-reaching plan to subvert the democratic process and engage in activities that have a basis in military techniques and that amount to attempts at thought or mind control.”

    ”It’s legal if we can get away with it”

    The CTIL files also demonstrate that there was a clear intent to circumvent the First Amendment by outsourcing censorship to the private, non-governmental sector.

    According to the informant:“The ethos was if we get away with it, it’s legal, and there were no First Amendment problems because we have a ‘public-private partnership’ – that’s the word they used to mask these problems. Private individuals can do things that public officials cannot do, and public officials can provide leadership and coordination.”

    Good news, bad news

    ”The good news is that more and more information is coming out about the U.S. government’s illegal outsourcing of censorship, and with it, legal challenges that pose roadblocks to this circumvention of the Constitution.

    The three activists also achieved other victories. In August 2022, DHS was forced to shut down the Disinformation Governance Board due to public backlash. CISA also deleted information about its national censorship work from its website and dismantled its Misinformation, Disinformation, and Malinformation (MDM) subcommittee.

    The federal government’s Select Subcommittee on Armaments is also continuing its search for the truth and will (hopefully) use all the power at its disposal to put an end to the abuses. Its latest report, “The Weaponization of ‘Disinformation’ Pseudo-Experts and Bureaucrats: How the Federal Government Partnered with Universities to Censor Americans’ Political Speech” was released on November 6, 2023.

    Unfortunately, there is a global effort underway not only to normalize, but also to legalize this type of censorship by third parties.

    In short, they are trying to restructure the censorship industry “away from a top-down government-led model” to a “competitive brokerage model” in which “content management” (read censorship) is simply outsourced to third-party organizations.

    In this way, a “legal” market for disinformation compliance is created, while the government can claim to have nothing to do with controlling the information. In essence, we are witnessing the emergence of organized corporate censorship.

    There is no clear solution to this threat other than to continue to oppose all efforts to legalize, standardize and normalize censorship. Vocally oppose, refuse to use intermediaries like NewsGuard, and boycott any company or organization that uses intermediaries or engages in censorship of any kind.”

    Claudio Resta was born in Genoa, Italy in 1958, he is a citizen of the world (Spinoza), a maverick philosopher, and an interdisciplinary expert, oh, and an artist, too.

    Grew up in a family of scientists where many sciences were represented by philosophy to psychoanalysis, from economics to history, from mathematics to physics, and where these sciences were subject to public display by their subject experts family members, and all those who they were part of could participate in a public family dialogue/debate on these subjects if they so wished. Read Full Bio

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    We See The World From All Sides and Want YOU To Be Fully Informed
    In fact, intentional disinformation is a disgraceful scourge in media today. So to assuage any possible errant incorrect information posted herein, we strongly encourage you to seek corroboration from other non-VT sources before forming an educated opinion.

    About VT - Policies & Disclosures - Comment Policy
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    https://www.vtforeignpolicy.com/2024/01/the-cyber-threat-intelligence-league/
    The Cyber Threat Intelligence League Claudio RestaJanuary 18, 2024 VT Condemns the ETHNIC CLEANSING OF PALESTINIANS by USA/Israel $ 280 BILLION US TAXPAYER DOLLARS INVESTED since 1948 in US/Israeli Ethnic Cleansing and Occupation Operation; $ 150B direct "aid" and $ 130B in "Offense" contracts Source: Embassy of Israel, Washington, D.C. and US Department of State. There is a vast plan for global censorship by US and British military contractors: US military contractor Pablo Breuer (left), UK defense researcher Sara-Jayne “SJ” Terp (center), and Chris Krebs, former director of the U.S. Department of Homeland Security’s Cybersecurity and Infrastructure Security Agency (DHS-CISA) – Documents received by investigative journalists Michael Shellenberger, Alex Gutentag and Matt Taibbi from an anonymous but “highly credible” whistleblower reveal new details about how the US censorship industrial complex – a network of more than 100 government agencies, private companies, universities and organizations non-profit – seeks to control and criminalize “wrong thinking”. – The documents describe how modern digital censorship programs were created and the various roles of the military, US intelligence agencies, civil society organizations and commercial media. They also describe the methods and techniques used, such as the creation and use of “sock puppet” accounts to spy on and direct online discussions and propagate desired narratives, and the discrediting of dissidents “as a necessary prerequisite for requiring censorship in their comparisons.” – Documents show that the weaponization of the financial sector originated with the Cyber Threat Intelligence League (CTIL), which specifically sought to get banks to “cut off financial services to individuals organizing gatherings or events.” – CTIL files also show that there was a clear intent to circumvent the First Amendment by outsourcing censorship to the private, non-governmental sector. According to the informant, “the ethic was that if we get away with it, it’s legal.” Documents received by investigative journalists Michael Shellenberger, Alex Gutentag and Matt Taibbi from an anonymous but “highly credible” whistleblower reveal new details about how the US censorship industrial complex – a network of more than 100 government agencies, private companies, universities and non-profit organizations – regulates and criminalizes “wrong thinking”. as Ursula Van der Leyen, the president of European Commission since 2019, stated at the WEF in Davos on January 17th, 2023 similar censorship are the most urgent and necessary policies (!) and will be implemented everywhere They describe the activities of an “anti-disinformation” group called the Cyber Threat Intelligence League, or CTIL, which officially began as a volunteer project of data scientists and defense and intelligence veterans, but whose tactics over time appear to have been absorbed into multiple official projects, including those of the Department of Homeland Security (DHS). The CTI League documents provide missing answers to key questions not addressed in the Twitter Files and Facebook Files. Together, they offer a complete picture of the rise of the “anti-disinformation” industry, or what we have called the Censorship Industrial Complex.” The documents describe how modern digital censorship programs were created and the various roles of the military, US intelligence agencies, civil society organizations and commercial media. They also describe the methods and techniques used, such as the creation and use of “sock puppet” accounts to spy on and direct online discussions and propagate desired narratives, the discrediting of dissidents, and the deliberate weaponization of the financial industry against them . According to the whistleblower, the CTIL was also involved in the creation of a counter-disinformation project to “avoid a repeat of 2016”, a reference to Brexit and Donald Trump’s surprise victory in the elections, two situations in which the democratic processes have actually won. As Jimmy Dore noted, it wasn’t about preventing the circulation of false information. It was about ensuring that no political outsider could ever enter the Oval Office again. The instruction to prevent a repeat of 2016 was a direct call to undermine, if not eliminate, the process of free and fair elections. Importantly, the documents admit that censorship efforts against Americans must be carried out by private sector partners, because the government does not have “legal authority” to do so. The new series of documents and videos reveals that 2019 was a pivotal year for the censorship industrial complex. According to Public, it was then that “US and British military and intelligence contractors, led by a former British defense researcher, Sara-Jayne ‘SJ’ Terp, developed the blanket censorship framework.” These contractors became co-leaders of CTIL, whose original founders were a former Israeli intelligence official, Ohad Zaidenberg, the person responsible of Microsoft security Nate Warfield, Chris Mills, another Microsoft security official, and Marc Rogers, the head of security operations at the hacker convention DEF CON. According to media reports , these highly trained and in-demand professionals have made the altruistic decision to offer their services to help billion-dollar hospitals with their cybersecurity, for free and with no strings attached. It wasn’t a believable cover story then, and it certainly hasn’t gotten any better. Within a month of CTIL’s founding in March 2020, this supposedly entirely volunteer group had grown to 1,400 “invitation-only” members in 76 countries and entered into an official partnership with Cybersecurity and Information Security Agency (CISA) of the United States Department of Homeland Security. As reported by Public: Parallel censorship agencies In spring 2020, CISA also created the Election Integrity Partnership (EIP) – a consortium composed of the Stanford Internet Observatory (SIO), the University of Washington’s Center for an Informed Public, the Atlantic’s Digital Forensic Research Lab Council and from Graphika (a social media analytics company) – and outsourced what would otherwise have been illegal and unconstitutional censorship. During the 2020 election cycle, EIP and CISA worked with the State Department’s Global Engagement Center (GEC) and the DHS-supported Elections Infrastructure Information Sharing and Analysis Center (EI-ISAC) to influence and monitor political discussions online. EIP coordinated the removal of unwanted content using a real-time chat application shared by DHS, EIP, and social media companies. At the same time, CTIL monitored and reported anti-blockade views on social media. A “law enforcement” channel was created specifically to spy on and monitor social media users posting anti-lockdown hashtags. CTIL even kept a printout detailing their Twitter biographies. According to Public, the CTIL has also “engaged in offensive operations to influence public opinion, discussing ways to promote ‘counter-messaging,’ co-opting hashtags, diluting unfavorable messaging, creating sock puppet accounts, and infiltrating private groups by invitation.” In February 2021, the EIP was renamed the Virality Project, at which point its censorship focus shifted from elections to COVID-related issues. Government infiltration and takeover Although CTIL member Bonnie Smalley responded to a Public question by saying that CTIL has “nothing to do with the government,” the evidence shows otherwise. At least a dozen government employees working with DHS, the FBI, and CISA were also active members of CTIL. According to the whistleblower, CTIL’s goal “was to become part of the federal government.” Terp’s plan called for the creation of “MisinfoSec communities” that would include the federal sector, and documents show that this goal was achieved. In April 2020, Chris Krebs, then director of CISA, also publicly announced the agency’s partnership with CTIL. The audience continues:“The documents also show that Terp and his colleagues, through a group called the MisinfoSec Working Group, which included [Renee] DiResta, head of research at the Stanford Internet Observatory, created a censorship, influence and counter-disinformation strategy called Adversarial Misinformation and Influence Tactics and Techniques (AMITT). SJ on X: "AMITT (Adversarial Misinformation and Influence Tactics and Techniques) includes the left-of-boom misinformation activities that are often missed by other analyses, where ”left of boom” covers activity before an incident They wrote AMITT by adapting a cybersecurity framework developed by MITER… Terp then used AMITT to develop the DISARM framework, which the World Health Organization then used to “counter anti-vaccination campaigns across Europe.” A key component of Terp’s work through CTIL, MisinfoSec and AMITT has been to bring the concept of “cognitive security” to the fields of cybersecurity and information security… The ambitions of the 2020 pioneers of the censorship industrial complex went far beyond simply requiring Twitter to place a warning label on tweets or blacklist individuals. The AMITT framework calls for discrediting people as a necessary prerequisite for requiring censorship of them. Invite influencers to train to spread messages. And he invites us to try to convince banks to cut financial services to individuals who organize demonstrations or events.” The arming of the financial sector was born with the CTIL Now we know where this financial sector weapon comes from. It originated with the CTIL, which hspecifically sought to induce banks to “cut financial services to individuals who organize rallies or events”. Clearly, as my case and that of many others demonstrates, even banks and online payment processors have been tricked into cutting off services to people who simply expressed opposing views. It’s not just demonstration organizers who are being targeted. Under the cover of altruism Although CTIL officials have repeatedly stressed that the organization was founded on purely altruistic principles, the clear goal of its leaders was to “build support for censorship among national security and cybersecurity institutions,” writes Public, and they built that support by promoting Terp’s idea of “cognitive safety.” The choice of the term “cognitive safety” takes on a rather sinister flavor in light of Dr. Michael Nehls’ findings that over the past four years there has been what appears to be an intentional effort to destroy autobiographical memory function in the public’s brain , thus facilitating mass indoctrination and inhibiting personal will and critical thinking.vast plan for global censorship by US and British military contractors The Indoctrinated Brain - By Michael Nehls (hardcover) : Target He presents his thesis in the book “The Indoctrinated Brain: How to Successfully Fend Off the Global Attack on Your Mental Freedom”, published in mid-December 2023. The whistleblower material clearly reveals that sophisticated military tactics have been turned against the American public, powerful psychological tools – the same tools that, according to Nehls, can literally alter the biological functions of the brain. Public cites a MisinfoSec report in which “the authors called for placing censorship efforts within ‘cybersecurity,’ while acknowledging that ‘disinformation security’ is entirely different from cybersecurity. They wrote that the third pillar of the “information environment”, after physical and cyber security, should be the “cognitive dimension”. Indeed, your mind – your cognition, your very ability to think independently – is the battlefield of today’s war, as Nehls proposes in his book. The scary part is that the tools used have the power to reprogram who we are. We are indeed “hackable animals,” as proposed by Yuval Noah Harari, and the censorship industrial complex has already hacked the brain structure of billions of people over the past four years. Gutentag also talks about it in an article dated December 3, 2023:”What was once considered a “conspiracy theory”, according to which military and intelligence forces manipulated public opinion through inorganic interventions, has now been confirmed . Our study of the censorship industrial complex has exposed a far-reaching plan to subvert the democratic process and engage in activities that have a basis in military techniques and that amount to attempts at thought or mind control.” ”It’s legal if we can get away with it” The CTIL files also demonstrate that there was a clear intent to circumvent the First Amendment by outsourcing censorship to the private, non-governmental sector. According to the informant:“The ethos was if we get away with it, it’s legal, and there were no First Amendment problems because we have a ‘public-private partnership’ – that’s the word they used to mask these problems. Private individuals can do things that public officials cannot do, and public officials can provide leadership and coordination.” Good news, bad news ”The good news is that more and more information is coming out about the U.S. government’s illegal outsourcing of censorship, and with it, legal challenges that pose roadblocks to this circumvention of the Constitution. The three activists also achieved other victories. In August 2022, DHS was forced to shut down the Disinformation Governance Board due to public backlash. CISA also deleted information about its national censorship work from its website and dismantled its Misinformation, Disinformation, and Malinformation (MDM) subcommittee. The federal government’s Select Subcommittee on Armaments is also continuing its search for the truth and will (hopefully) use all the power at its disposal to put an end to the abuses. Its latest report, “The Weaponization of ‘Disinformation’ Pseudo-Experts and Bureaucrats: How the Federal Government Partnered with Universities to Censor Americans’ Political Speech” was released on November 6, 2023. Unfortunately, there is a global effort underway not only to normalize, but also to legalize this type of censorship by third parties. In short, they are trying to restructure the censorship industry “away from a top-down government-led model” to a “competitive brokerage model” in which “content management” (read censorship) is simply outsourced to third-party organizations. In this way, a “legal” market for disinformation compliance is created, while the government can claim to have nothing to do with controlling the information. In essence, we are witnessing the emergence of organized corporate censorship. There is no clear solution to this threat other than to continue to oppose all efforts to legalize, standardize and normalize censorship. Vocally oppose, refuse to use intermediaries like NewsGuard, and boycott any company or organization that uses intermediaries or engages in censorship of any kind.” Claudio Resta was born in Genoa, Italy in 1958, he is a citizen of the world (Spinoza), a maverick philosopher, and an interdisciplinary expert, oh, and an artist, too. Grew up in a family of scientists where many sciences were represented by philosophy to psychoanalysis, from economics to history, from mathematics to physics, and where these sciences were subject to public display by their subject experts family members, and all those who they were part of could participate in a public family dialogue/debate on these subjects if they so wished. Read Full Bio Latest Articles (2023-Present) Archived Articles (2019-2022) ATTENTION READERS We See The World From All Sides and Want YOU To Be Fully Informed In fact, intentional disinformation is a disgraceful scourge in media today. So to assuage any possible errant incorrect information posted herein, we strongly encourage you to seek corroboration from other non-VT sources before forming an educated opinion. About VT - Policies & Disclosures - Comment Policy Due to the nature of uncensored content posted by VT's fully independent international writers, VT cannot guarantee absolute validity. All content is owned by the author exclusively. Expressed opinions are NOT necessarily the views of VT, other authors, affiliates, advertisers, sponsors, partners, or technicians. Some content may be satirical in nature. All images are the full responsibility of the article author and NOT VT. https://www.vtforeignpolicy.com/2024/01/the-cyber-threat-intelligence-league/
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  • BOMBSHELL! Inside mRNA Vaccines a Human Molecule Diabolically Altered | VT Foreign Policy
    donshafi911
    BOMBSHELL! Inside mRNA Vaccines a Human Molecule Diabolically Altered | VT Foreign Policy

    January 6, 2024

    VT Condemns the ETHNIC CLEANSING OF PALESTINIANS by USA/Israel
    $ 280 BILLION US TAXPAYER DOLLARS INVESTED since 1948 in US/Israeli Ethnic Cleansing and Occupation Operation; $ 150B direct "aid" and $ 130B in "Offense" contracts

    Source: Embassy of Israel, Washington, D.C. and US Department of State.

    In the cover image, the Canadian researcher Jessica Rose, author of an excellent biochemical analysis of an article from the University of Cambridge commenting a study by some of its researchers on the toxicity of manipulated human nucleoside in mRNA genetic sera

    by Fabio Giuseppe Carlo Carisio

    VERSIONE IN ITALIANO

    «Well of course! Now that we know that billions of people’s cells might be making aberrant proteins, for unknown periods of time, we can simply sweep these people under the rug, ‘fix’ the product, and keep on makin’ money. Let’s go slidin’ down the slippery sequence slope of gene therapy straight to the Gates of hell».

    With this phrase to be engraved in the history of the massive Covid vaccination campaign, the esteemed Canadian researcher, biochemist, immunologist and molecular biologist Jessica Rose (Source 1), author of multiple fundamental discoveries on the contamination of mRNA genetic sera, best describes the disturbing importance of an article published by University of Cambridge in relation to an enlightening scientific research which confirmed to the global scientific community the dangerous experimental use in the Pfizer-Biontech and Moderna mRNA vaccines of what we do not hesitate to define as the “Diabolical Molecule” because it is a biological human component modified twice in the laboratory. (Source 1).

    UPDATE! Florida State Surgeon General Calls for Halt of mRNA Vaccines due to Dangerous, Oncogenes DNA Fragments
    Author of multiple fundamental discoveries on the contamination of mRNA genetic sera, best describes the disturbing importance of an article published by University of Cambridgein relation to an enlightening scientific research which confirmed to the global scientific community the dangerous experimental use in the Pfizer-Biontech and Moderna mRNA vaccines of what we do not hesitate to define as the “Diabolical Molecule”because it is a biological human component modified twice in the laboratory.

    Billions of Dangerous Spike DNA’s Molecules inside Covid mRNA Vaccines. They can Reproduce the Toxic Protein in Human Cells for a Long Time
    This is the double alteration of Uridinetransformed into Pseudourine with the first synthetic biochemical alteration and then into N1-methylpseudouridine initialed “m1Ψ” as an acronym for N1-methyl-Ψ in which the Greek letter “Psi” was used to name Psueudoridine .

    Uridine is an organic compound, nucleoside,made up of the coupling of a molecule of ribose and one of uracil. Uracil is one of the two pyrimidine nitrogenous bases that form the nucleotides of RNA nucleic acid.



    This manipulation was designed by the Hungarian biochemist Katalin Karikó,awarded the 2023 Nobel Prize for Medicine precisely for having laid the foundations of mRNA vaccines, in order to “deceive” human cells into recognizing the synthetic mRNA as harmless human RNA …

    I apologize to the biochemistry experts for any transcription mistakes I may make trying to translate from a difficult chemical language the portentous scientific essence of the abundant technical quotations in the article published by Rose on her Substack, from which we will only extrapolate its introduction.

    Bombshell from US! FDA “Hides” Toxicity on DNA Fragments inside mRNA Vaccines despite Danger of Cancer Highlighted in its Guidance too
    Martin: “Pseudouridine Killer in the Vaccines for Depopulation”
    This analysis comes surprisingly providential as on Gospa News International we have just reported the summary of a conference by the famous patent expert David E. Martin in which he narrated in recent weeks the story of SARS-Cov-2 as a bacteriological weapon built in 58 years of military research on coronaviruses and that of mRNA vaccines, in his opinion, knowingly spread in a mass experiment for the search for vaccines against HIV-AIDS and cancer but also aimed at global depopulation.

    WUHAN-GATES – 73. Half of Century of Covert Bioweapon Development Leading to Fauci’s SARS-Cov-2 and to mRNA Lethal Vaccines
    In a very detailed article the American osteopath doctor Joseph Mercola wrote that «Martin points out that even if they don’t unleash any other bioweapons, the desired death toll may still be achieved, because they used pseudouridine in the mRNA shots, which is causing “turbo cancers”».

    Because: «Pseudouridine suppresses cancer-controlling agents and promotes oncogenic activity in the body, and this has been known since 2018, so its inclusion was hardly an accident. It’s a conspiracy, alright. But not a conspiracy theory in the dismissive sense. It’s a global conspiracy by identifiable agents who have, for nearly 60 years, plotted to commit, and profit from, the greatest genocide the world has ever seen, while hiding behind the false veneer of “public health.”».
    Well today, both the University of Cambridge and other authoritative scientists from around the world implicitly confirm that all those vaccinated with Covid mRNA with Moderna’s Spikevax and Pfizer-Biontech’s Comirnaty have been and continue to be unpaid and, above all, unaware human guinea pigs.

    Precisely because of this altered nucleoside…

    The Disturbing Article from Cambridge University
    The comment by the researcher Rose that we reported in the incipit of the article referred to the text of the University of Cambridge(Source 2) in relation to the study “N1-methylpseudouridylation of mRNA causes +1 ribosomal frameshifting” by Mulroney et al.published on December 6, 2023 by Nature after more than a month of review.



    «Researchers redesign future mRNA therapeutics to prevent potentially harmful immune responses» is the eloquent title of the scientific text published by the British university.

    «The latest developments, led by biochemist Professor Anne Willis and immunologist Dr James Thaventhiran from the MRC Toxicology Unit at the University of Cambridge, build upon previous advances to ensure the prevention of any safety issues linked with future mRNA-based therapeutics. Their report is published today in the journal Nature» we read in the unsigned article.

    «The researchers identified that bases with a chemical modification called N1-methylpseudouridine – which are currently contained in mRNA therapies – are responsible for the ‘slips’ along the mRNA sequence» adds the university website.
    In collaboration with researchers at the Universities of Kent, Oxford and Liverpool, the MRC Toxicology Unit team«tested for evidence of the production of ‘off-target’ proteins in people who received the mRNA Pfizer vaccine against COVID-19. They found an unintended immune response occurred in one third of the 21 patients in the study who were vaccinated – but with no ill-effects, in keeping with the extensive safety data available on these COVID-19 vaccines».

    SCIENCE Magazine Finally Admitted the mRNA Vaccines Dangerous Side Effects! Shots linked to Long Covid, Neurologic Damages and POTS
    Despite disturbing the article already appears biased as it is aimed at “minimizing” the adverse reactions, even lethal one, that are accumulating in pharmacovigilance systems around the world, which have been confirmed by an alarming article in the journal Science, by the regulatory bodies from all over the world (EMA, FDA, etc.) and which led Moderna and Pfizer-Biontech to include the risk of lethal myocarditis in the information leaflets of their genetic drugs…

    7 EURODEPUTATI CHIEDONO IL RITIRO DEI VACCINI COVID. Per Miocarditi Letali, Malori Improvvisi e Sicurezza Incerta nei Fragili
    British Study: “Incorrect mRNA Translation may Increase Toxicity”
    But it is the same authors of the study whose first signatory is Thomas E. Mulroney (Source 3), associate researcher of the Toxicology Unit of the MRC in Cambridge, who wrote the shocking considerations from a biochemical point of view in the conclusions.

    «We show that 1-methylΨ is a modified ribonucleotide that significantly increases +1 ribosomal frameshifting during mRNA translation and that cellular immunity to +1 frameshifted products can occur following vaccination with mRNA containing 1-methylΨ. To our knowledge, this is the first report that mRNA modification affects ribosomal frameshifting. Alongside this impact on host T cell immunity, the off-target effects of ribosomal frameshifting could include increased production of new B cell antigens».




    And they further add:

    «These findings are of particular importance to our fundamental understanding of how ribonucleotide modification affects mRNA translation, and for designing and optimizing future mRNA-based therapeutics to avoid mistranslation events that may decrease efficacy or increase toxicity».
    We will not delve further into the technical references but return to the analysis published by Jessica Rose in her Substack, making an extreme summary of it and advising professionals to read the text full of important images.

    Billions of DNA Fragments of Toxic Spike Protein and SV40 gene in the mRNA Vaccines. New Study: “They may Cause Turbo-Cancer”
    Let’s start with the comment added under the research published by Nature by her together with David Wiseman, L. Maria Gutschi, David J. Speicher, Kevin McKernan.

    Alongside the Canadian biologist they were already co-authors of the study “DNA fragments detected in the monovalent and bivalent Pfizer/BioNTech and Moderna modRNA COVID-19 vaccines from Ontario, Canada: exploratory dose-response relationship with serious adverse events” which induced the EMA to confess that Pfizer hid the use of the very dangerous SV40 gene in its vaccine, which can cause tumors.

    The same research encouraged the bioimmunologist Robert Malone to denounce the presence of the antibiotic resistance gene in the Moderna one, pointing out also that the pharmaceutical company was aware of the tumor risks of mRNA biotechnology as reported in its own patent.

    Bomba Mondiale! “NEI VACCINI COVID GENE DI RESISTENZA AGLI ANTIBIOTICI”. Studio Spagnolo lo Conferma. Ministro Schillaci lo CELA nell’Allarme Morti AMR
    We have written extensively about these topics in three investigations, one of which – on antibiotic resistance gene – is a world exclusive.

    Alarm of American Scientists for the New Research
    Let us therefore see the content of the comment by Rose and colleagues (Source 1)on Cambridge’s research:

    The paper provides evidence for the formation “off-target” or unintended proteins following vaccination with BNT162b2 due to frameshifting. Given the proposed mechanism, a similar problem is likely to exist for the Moderna product.
    While the authors have not isolated samples of these proteins from vaccinated patients or animals, their existence is evidenced by the specific cellular immune responses elicited to frameshifted proteins the authors synthesized. It is not clear why B cell – antibody responses were not studied.
    The authors state that “Although there is no evidence that frameshifted products in humans generated from BNT162b2 vaccination are associated with adverse outcomes.”
    BOMBSHELL: mRNA COVID jabs can Damage Children’s Immune Response to OTHER Viruses as well, Study finds
    It is unclear how it is possible to make this statement, given:
    • The small number of vaccinated subjects (n=21) providing samples.
    • This was not a controlled trial.
    • None of these subjects had reported undue effects of vaccination. Accordingly, the sample is subject to selection bias.
    • The toxicology of these unintended proteins must be studied.
    • The authors acknowledge the misdirected immunity “has huge potential to be harmful.”
    Translated into simpler words, no one has verified the selection methods of the samples which may have been chosen precisely because they did not have serious adverse reactions.

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    Furthermore, in the interests of expertise we read that the two Cambridge scientists Thomas E. Mulroney and Anne E. Willis «are inventors of a pending patent application (2305297.0) relating to mRNA technology» while in the information on the authors it is discovered that Alexander J Mentzer works at the Wellcome Center for Human Genetics, University of Oxford.

    Wellcome, with the Bill & Melinda Gates Foundation and the World Economic Forum, is among the founders of the Ngo CEPI(Coalition for Epidemic Preparedness Innovations) which has already launched the SKYCovion vaccine together with the London-based GSK, managed by CEO Emma Walmsley who is also director of Microsoft, and SK Bioscience.

    WUHAN-GATES – 73. BILL III A CACCIA DI CAVIE UMANE PER VACCINO COVID COREANO. “Genotossicità non Studiata” ma OMS & UK danno OK a SkyCovione con Spike Tossica e Adiuvante GSK da Pericoloso Squalene
    But let’s go back to the analysis made by Jessica Rose on the Cambridge researchers’ study: «The authors write that N1-methylpseudouridine affects the fidelity of mRNA translation via ribosome stalling that induces frameshifting. Frameshifting results in the production multiple, unique and potentially aberrant proteins».

    «The modified mRNAs for use in the COVID-19 products were codon-optimized for maximal protein expression in humans. Codon optimization, or synonymous codon replacement, rests on the idea that one can induce mutations throughout a gene of interest (like spike) based on an organism’s (like humans) codon usage bias, to increase translational efficiency and protein expression without altering the sequence of the protein. But, it is well-known that codon-optimization can lead to protein conformation, folding and stability problems».
    COVID: SCOPERTA LA PROTEINA CHE RIVELA I LETALI COAGULI DI SANGUE. Ma Nessuno Indaga sulla Correlazione coi Vaccini
    The Canadian immunologist further notes:

    «Codon optimization could affect protein conformation, folding and stability, change post-translational modification sites and even affect protein function.Different rates of translation by different tRNAs, including those that exhibit wobble base-pairing (a tRNA that can recognize multiple synonymous codons) may actually be critical for determining the rate of translation. The ribosome may slow and pause during elongation which may actually be necessary for proper protein folding. Therefore, codon optimization may disrupt the fine-tuned timing of translation and ultimately protein function».
    The Prophetic Seneff Study on Autoimmune and Neurocerebral Damage
    He then refers to other studies that had reported the dangers of this biochemical manipulation (Source 1):

    «Codon optimization can also lead to misfolding of mRNAs due to increased Guanine/Cytosine (GC content). Please read McKernan et al.’s preprint, Xia et al.’s paper and Seneff et al.’s paper to learn more about potential problems relating to codon optimization and GC content changes. The latter group write: Synonymous codon replacement also results in a change in the multifunctional regulatory and structural roles of resulting proteins».
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    The risks to the human organism are clearly highlighted:

    «There is, in fact, a significant enrichment of GC content (17% and 25% enrichments as per Pfizer and Moderna, respectively, as compared to SARS-CoV-2) as a result of the codon optimization that was done, and this can lead to “dysregulation of the G4-RNA-protein binding system and a wide range of potential disease-associated cellular pathologies including suppression of innate immunity, neurodegeneration, and malignant transformation”. Increased GC content significantly alters mRNA secondary structure as well, and this can also lead to ribosomal pausing or stalling».
    These considerations were expressed in a study published by illustrious scientists such as Stephanie Seneff, Computer Science and Artificial Intelligence Laboratory, MIT, Cambridge, MA, USA, Greg Nigh, Immersion Health, Portland, OR, USA, Anthony M. Kyriakopoulos, Nasco AD Biotechnology Laboratory, Department of Research and Development, Piraeus, Greece and Peter A. McCullough, for Health Foundation, Tucson, AZ, USA, which was the subject of enormous censorship by specialized medical journals but we published in Gospa News thanks to an excellent summary by Dr. Mercola.

    Dangerous RNA Manipulation with N1-methyl-Ψ
    Below are the quotes from Seneff et al.(Source 4) useful for understanding the connection with uridine modified in N1-methyl-Ψ: «The utilization of mRNA vaccines in the context of infectious disease has no precedent. The many alterations in the vaccine mRNA hide the mRNA from cellular defenses and promote a longer biological half-life and high production of spike protein».

    «However, the immune response to the vaccine is very different from that to a SARS-CoV-2 infection. In this paper, we present evidence that vaccination induces a profound impairment in type I interferon signaling, which has diverse adverse consequences to human health. Immune cells that have taken up the vaccine nanoparticles release into circulation large numbers of exosomes containing spike protein along with critical microRNAs that induce a signaling response in recipient cells at distant sites. We also identify potential profound disturbances in regulatory control of protein synthesis and cancer surveillance».
    The COVID Jabs’ Mechanisms of Injury: Sudden Death, Blood Cloths, Human Mad Cow and Autoimmune Diseases
    In the study entitled “Innate immune suppression by SARS-CoV-2 mRNA vaccinations: The role of G-quadruplexes, exosomes, and MicroRNAs” the scientists added:

    «These disturbances potentially have a causal link to neurodegenerative disease, myocarditis, immune thrombocytopenia, Bell’s palsy, liver disease, impaired adaptive immunity, impaired DNA damage response and tumorigenesis. We show evidence from the VAERS database supporting our hypothesis. We believe a comprehensive risk/benefit assessment of the mRNA vaccines questions them as positive contributors to public health».
    The late biologist Luc Montagnier, in a study published posthumously by his research friends Jean-Claude Perez and Claire Moret-Chalmin with a review contribution from Seneff biophysics, proved without a shadow of a doubt the correlation between killer prions caused by vaccines and rapid deaths for neurocerebral Creutzfeldt-Jacob disease, human mad cow disease.

    PRIONS as KILLERS: 25 Deaths due to a New Mad-Cow from Covid Vaccines. Shocking Research by Montagnier (RIP), Perez & Moret-Chalmin on CJD Brain Damages
    In detail Seneff and the other scientists also refer to specific alterations:

    «Impaired type I IFN signaling is linked to many disease risks, most notably cancer, as type I IFN signaling suppresses proliferation of both viruses and cancer cells by arresting the cell cycle, in part through upregulation of p53, a tumor suppressor gene, and various cyclin- dependent kinase inhibitors (Musella et al., 2017; Matsuoka et al., 1998). IFNα also induces major histocompatibility (MHC) class 1 antigen presentation by tumor cells, causing them to be more readily recognized by the cancer surveillance system (Heise et al., 2016)».
    They then delve into the problem of the uridine molecule.

    To understand its importance we report a note from Rose: «Pseudouridines (Ψs) are a normal and essential part of our biology. They have been called the 5th nucleotide, in fact, and “are a ubiquitous constituent of structural RNA (transfer, ribosomal, small nuclear (snRNA) and small nucleolar), and present in coding RNA, across the three phylogenetic domains of life”and “accounts for about 1.4% of all bases in human rRNAs”».

    “mRNA COVID-19 Vaccines are Like Gene Therapy Products” French Study highlighted Omitted Controls on Genotoxicity
    Here’s what Seneff and his colleagues wrote about vaccines:

    «A breakthrough came when it was discovered experimentally that the mRNA coding for the spike protein could be modified in specific ways that would essentially fool the human cells into recognizing it as harmless human RNA. A seminal paper by Karikó et al. (2005) demonstrated through a series of in vitro experiments that a simple modification to the mRNA such that all uridines were replaced with pseudouridine could dramatically reduce innate immune activation against exogenous mRNA».

    Cancer Risk pointed out by the Nobel Inventor of mRNA Vaccines
    Precisely for this discovery, Hungarian researcher Katalin Karikó, long-time at Biontech, recently received the Nobel Prize for Medicine together with her American colleague Drew Weissman, although both warned of the dangers of the new mRNA biotechnology.

    Medicine Nobel to mRNA Covid Vaccines’ Scientists, both Sponsored by Gates, Fauci and Zuckerberg
    In particular, on January 6, Karikó declared to the German newspaper Welt (Source 5):

    «Every day I receive many emails from people who write to me about their experiences. One woman wrote to me that two days after the vaccination she developed a large lump in her breast. Vaccination caused cancer, it was her conclusion. But the cancer was already there, only vaccination gave an extra boost to the immune system, so that the immune defense cells rushed in large numbers towards the enemy».



    The Gospa News investigations on Turbo-Cancer based now on seven published scientific studies have highlighted a very strong correlation between mRNA gene sera and the appearance or reactivation of tumor phenomena with abnormal degeneration resulting in lethal outcomes.

    TURBO-CANCER – 2. Many Lethal/Serious Cases and New Researches on Covid mRNA Vaccines Risks. Melatonin Hope…
    Karikó herself adds: «Vaccination provides a strong boost to the immune system. It can happen that a dormant infection breaks out in people with an already weakened immune system. The extent to which this is the case for shingles will need to be examined more closely».

    Gospa News did so by discovering 27 thousand cases of Herpes Zoster, in the European Union only, as adverse reactions to vaccines reported by EMA pharmacovigilance database even in children, who are more exposed to damage to the natural immune system as confirmed by recent research.

    Esclusivo! EPIDEMIA DI HERPES DOPO I VACCINI COVID. 27mila Casi nell’UE: 31 Morti da Zoster. Lo Studio: “Per danni al Sistema Immunitario”
    Let’s go back to Seneff’s conclusions:

    «Andries et al. (2015) later discovered that 1-methylpseudouridine as a replacement for uridine was even more effective than pseudouridine and could essentially abolish the TLR response to the mRNA, preventing the activation of blood-derived dendritic cells. This modification is applied in both the mRNA vaccines on the market (Park et al., 2021)».
    To put it simply, the dendritic cell plays the role of sentinel and if it senses the presence of a pathogen in the body, it stimulates the immune response of B and T lymphocytes, specific against that antigen. If its action is limited or suppressed, it may become incapable of dealing with viral or bacterial enemies but also tumor dangers.

    Critical Role of Pseudouridine in mRNA Vaccines
    A study published by Pedro Morais, Director (Pseudouridylation Technology) ProQR Therapeutics, Leiden, Netherlands, and by Department of Biochemistry and Biophysics, Center for RNA Biology, University of Rochester Medical Center, Rochester, NY, US, entitled “The Critical Contribution of Pseudouridine to mRNA COVID-19 Vaccines” highlighted the fundamental role of the laboratory alteration of this protein in the Comirnaty and Spikevax genetic sera (source 6).

    «Both consisted of N1-methyl-pseudouridine-modified mRNA encoding the SARS-COVID-19 Spike protein and were delivered with a lipid nanoparticle (LNP) formulation. Because the delivery problem of ribonucleic acids had been known for decades, the success of LNPs was quickly hailed by many as the unsung hero of COVID-19 mRNA vaccines».
    “European Medicines Agency Knew Toxicity of Pfizer Covid Vaccine”. Bombshell Study Published in US by an Italian BioChemist on Dangers mRNA-LNPs
    But the scholars, one of whom has a clear conflict of interest because he is director of the Pseudouridylation Technology project, have highlighted another very interesting fact:

    «However, the clinical trial efficacy results of the Curevac mRNA vaccine (CVnCoV) suggested that the delivery system was not the only key to the success. CVnCoV consisted of an unmodified mRNA (encoding the same spike protein as Moderna and Pfizer-BioNTech’s mRNA vaccines) and was formulated with the same LNP as Pfizer-BioNTech’s vaccine (Acuitas ALC-0315).However, its efficacy was only 48%. This striking difference in efficacy could be attributed to the presence of a critical RNA modification (N1-methyl-pseudouridine) in the Pfizer-BioNTech and Moderna’s mRNA vaccines (but not in CVnCoV)».
    “Toxic Nanoforms inside Pfizer-Biontech Covid Vaccine”. Vital Study by Italian Biochemist on US Journal of Virology highlights an Alleged Crime
    However, the same researchers highlight a significant note:

    «The intrinsic immunogenicity of non-modified mRNA was once considered a potential advantage for its use in vaccines(Ishii and Akira, 2005) as it would encode the antigen and concomitantly serve as an adjuvant while permitting a low dose. In fact, the unmodified COVID-19 mRNA vaccine candidate in late-stage clinical trials (CVnCoV, developed by Curevac) had a maximum dose of 12 µg».
    Curevac was developed by Curevac NV of Tubingen, together with the Ngo CEPI founded by Bill Gates with Wellcome and WEF, which initiated an authorization process before the CHMP committee of the European Medicines Agency (EMA) but withdrew it due to its low efficacy on October 12, 2021 (source 7) in view of the arrival of a new pharmacological product developed with GSK financed by Gates himself.

    MINISTRO SCHILLACI SPECULA SU BIG PHARMA FINANZIATA DA GATES. €700mila Investiti in Biomediche USA che Testano anche Vaccini DNA Covid
    Here is another cryptic phrase in which we talk about the “safety” of vaccines, implicitly implying that it is not clear in the current vaccines which therefore make all those who take them into “human guinea pigs”from the laboratory as the immunologist Rose clearly highlights in her final bioethical considerations.

    Rose: “Unpredictable Health Effects of Manipulated Codons”
    «Ehden Biber also wrote a great article about the pitfalls of codon optimization that you can read here. In a Nature article published in 2011 entitled: “Breaking the silence”, the author writes on the potential danger of fiddling with codons in therapeutic proteins whereby it “could have unpredictable effects on people’s health”»

    Rose wrote in her comment on the Cambridge research quoting many sentences by scientific journalist Alla Katsnelson which we report below.

    Bombshell! Texas Attorney General sues Pfizer on Covid Vaccine Efficacy and Conspiring
    In detail, the Canadian researcher adds:

    «She points to a study where the authors show that a synonymous codon change found in the most common form of cystic fibrosis results in mRNA misfolding. (Keep this in mind.) She also points out that in the context of the multi-drug resistance 1 gene (MDR1) (the gene that encodes P-glycoprotein), that a codon change may interfere with the pauses that characterize RNA passing through the ribosome, thereby changing how the growing amino acid chain folds».

    «But perhaps the most timely and spine-tingly relevant statement in this article is found at the end, and I quote: “At the moment, companies developing recombinant therapies must verify that the DNA sequence designed by their scientists is the one that’s producing their proteins, but they aren’t required to note how different that is from the native genetic code”».
    European Regulator: Pfizer Hid Dangerous Cancer Gene! It Kept Secret the SV40 DNA Sequence In COVID-19 Vaccine
    We do not have any guidance with regard to the [DNA] sequence,” Kimchi-Sarfaty notes.

    While it was the Italian bioimmunologist Mauro Mantovani who demonstrated how the “double Proline” inserted in mRNA vaccines makes the toxic Spike protein dangerously persistent in the human body.

    «That’s one piece of data that could be tracked by the system she is proposing. Such knowledge, in turn, could ultimately help define better strategies for optimization and possibly even make biologic drugs safer for people» adds Alla Katsnelson while the immunologist asks herself a question:

    «I wonder if the FDA ever took her advice to track the differences in codons and the resulting potential adverse effects?»
    Covid Vaccines Killer Pathologies in a Name Only: Spikeopathy! Huge, Chilling Study on mRNA Genic Serums’ Serious Adverse Reactions
    Therefore Rose quoted the article which we analyzed before:

    «In addition to our comment on the Nature paper, a University of Cambridge write-up entitled: Researchers redesign future mRNA therapeutics to prevent potentially harmful immune responses was penned. They make it clear that the most relevant conclusion from the Nature paper is that we can make more products similarly insanely dangerous as the ones pumped into billions of bodies because we can simply ‘reduce the production of frameshifted products’ by ‘synonymous targeting of slippery sequences’».

    So she wrote her milestone sentence:

    «Well of course! Now that we know that billions of people’s cells might be making aberrant proteins, for unknown periods of time, we can simply sweep these people under the rug, ‘fix’ the product, and keep on makin’ money. Let’s go slidin’ down the slippery sequence slope of gene therapy straight to the Gates of hell».
    Moderna AWARE that mRNA Jabs cause CANCER due to DNA Fragments. Malone Unveils Patent
    The Canadian molecular biologist concludes before going into detail about a biochemical analysis that is too technical for non-experts:

    «The manufacturers might have thought to explore options to prevent potentially harmful responses from their products prior to injecting billions of people with them. It is criminal that these products continue to be forced onto newborns and infants by mandate, to this day».
    And then she report an emblematic quote about the risks of “Fooling with Mother Nature” by an evolutionary cell biologist at the University of Chicago: “Please do not monkey with these sites; they are optimized for some reason”, in reference to codon bias in mammals.

    Fabio Giuseppe Carlo Carisio

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    MAIN SOURCES

    SOURCE 1 – JESSICA ROSE – That Substack about N1-methylpseudouridines and frameshifting

    SOURCE 2 – UNIVERSITY OF CAMBRIDGE – Researchers redesign future mRNA therapeutics to prevent potentially harmful immune responses

    SOURCE 3 – NATURE – N1-methylpseudouridylation of mRNA causes +1 ribosomal frameshifting

    SOURCE 4– PUBMED – Innate immune suppression by SARS-CoV-2 mRNA vaccinations: The role of G-quadruplexes, exosomes, and MicroRNAs

    SOURCE 5 – WELT – “Das ist der wirkliche Grund, warum man unter neuen Varianten nicht mehr so krank wird“

    SOURCE 6 – FRONTIERS IN – The Critical Contribution of Pseudouridine to mRNA COVID-19 Vaccines

    SOURCE 7 – EMA ends rolling review of CVnCoV COVID-19 vaccine following withdrawal by CureVac AG

    Fabio G. C. Carisio

    Fabio is investigative journalist since 1991. Now geopolitics, intelligence, military, SARS-Cov-2 manmade, NWO expert and Director-founder of Gospa News: a Christian Information Journal.

    His articles were published on many international media and website as SouthFront, Reseau International, Sputnik Italia, United Nation Association Westminster, Global Research, Kolozeg and more…

    Most popolar investigation on VT is:

    Rumsfeld Shady Heritage in Pandemic: GILEAD’s Intrigues with WHO & Wuhan Lab. Bio-Weapons’ Tests with CIA & Pentagon

    Fabio Giuseppe Carlo Carisio, born on 24/2/1967 in Borgosesia, started working as a reporter when he was only 19 years old in the alpine area of Valsesia, Piedmont, his birth region in Italy. After studying literature and history at the Catholic University of the Sacred Heart in Milan, he became director of the local newspaper Notizia Oggi Vercelli and specialized in judicial reporting.

    For about 15 years he is a correspondent from Northern Italy for the Italian newspapers Libero and Il Giornale, also writing important revelations on the Ustica massacre, a report on Freemasonry and organized crime.

    With independent investigations, he collaborates with Carabinieri and Guardia di Finanza in important investigations that conclude with the arrest of Camorra entrepreneurs or corrupt politicians.

    In July 2018 he found the counter-information web media Gospa News focused on geopolitics, terrorism, Middle East, and military intelligence.

    In 2020 published the book, in Italian only, WUHAN-GATES – The New World Order Plot on SARS-Cov-2 manmade focused on the cycle of investigations Wuhan-Gates

    His investigations was quoted also by The Gateway Pundit, Tasnim and others

    He worked for many years for the magazine Art & Wine as an art critic and curator.

    VETERANS TODAY OLD POSTS

    www.gospanews.net/





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    https://www.vtforeignpolicy.com/2024/01/bombshell-inside-mrna-vaccines-a-human-molecule-diabolically-altered/
    BOMBSHELL! Inside mRNA Vaccines a Human Molecule Diabolically Altered | VT Foreign Policy donshafi911 BOMBSHELL! Inside mRNA Vaccines a Human Molecule Diabolically Altered | VT Foreign Policy January 6, 2024 VT Condemns the ETHNIC CLEANSING OF PALESTINIANS by USA/Israel $ 280 BILLION US TAXPAYER DOLLARS INVESTED since 1948 in US/Israeli Ethnic Cleansing and Occupation Operation; $ 150B direct "aid" and $ 130B in "Offense" contracts Source: Embassy of Israel, Washington, D.C. and US Department of State. In the cover image, the Canadian researcher Jessica Rose, author of an excellent biochemical analysis of an article from the University of Cambridge commenting a study by some of its researchers on the toxicity of manipulated human nucleoside in mRNA genetic sera by Fabio Giuseppe Carlo Carisio VERSIONE IN ITALIANO «Well of course! Now that we know that billions of people’s cells might be making aberrant proteins, for unknown periods of time, we can simply sweep these people under the rug, ‘fix’ the product, and keep on makin’ money. Let’s go slidin’ down the slippery sequence slope of gene therapy straight to the Gates of hell». With this phrase to be engraved in the history of the massive Covid vaccination campaign, the esteemed Canadian researcher, biochemist, immunologist and molecular biologist Jessica Rose (Source 1), author of multiple fundamental discoveries on the contamination of mRNA genetic sera, best describes the disturbing importance of an article published by University of Cambridge in relation to an enlightening scientific research which confirmed to the global scientific community the dangerous experimental use in the Pfizer-Biontech and Moderna mRNA vaccines of what we do not hesitate to define as the “Diabolical Molecule” because it is a biological human component modified twice in the laboratory. (Source 1). UPDATE! Florida State Surgeon General Calls for Halt of mRNA Vaccines due to Dangerous, Oncogenes DNA Fragments Author of multiple fundamental discoveries on the contamination of mRNA genetic sera, best describes the disturbing importance of an article published by University of Cambridgein relation to an enlightening scientific research which confirmed to the global scientific community the dangerous experimental use in the Pfizer-Biontech and Moderna mRNA vaccines of what we do not hesitate to define as the “Diabolical Molecule”because it is a biological human component modified twice in the laboratory. Billions of Dangerous Spike DNA’s Molecules inside Covid mRNA Vaccines. They can Reproduce the Toxic Protein in Human Cells for a Long Time This is the double alteration of Uridinetransformed into Pseudourine with the first synthetic biochemical alteration and then into N1-methylpseudouridine initialed “m1Ψ” as an acronym for N1-methyl-Ψ in which the Greek letter “Psi” was used to name Psueudoridine . Uridine is an organic compound, nucleoside,made up of the coupling of a molecule of ribose and one of uracil. Uracil is one of the two pyrimidine nitrogenous bases that form the nucleotides of RNA nucleic acid. This manipulation was designed by the Hungarian biochemist Katalin Karikó,awarded the 2023 Nobel Prize for Medicine precisely for having laid the foundations of mRNA vaccines, in order to “deceive” human cells into recognizing the synthetic mRNA as harmless human RNA … I apologize to the biochemistry experts for any transcription mistakes I may make trying to translate from a difficult chemical language the portentous scientific essence of the abundant technical quotations in the article published by Rose on her Substack, from which we will only extrapolate its introduction. Bombshell from US! FDA “Hides” Toxicity on DNA Fragments inside mRNA Vaccines despite Danger of Cancer Highlighted in its Guidance too Martin: “Pseudouridine Killer in the Vaccines for Depopulation” This analysis comes surprisingly providential as on Gospa News International we have just reported the summary of a conference by the famous patent expert David E. Martin in which he narrated in recent weeks the story of SARS-Cov-2 as a bacteriological weapon built in 58 years of military research on coronaviruses and that of mRNA vaccines, in his opinion, knowingly spread in a mass experiment for the search for vaccines against HIV-AIDS and cancer but also aimed at global depopulation. WUHAN-GATES – 73. Half of Century of Covert Bioweapon Development Leading to Fauci’s SARS-Cov-2 and to mRNA Lethal Vaccines In a very detailed article the American osteopath doctor Joseph Mercola wrote that «Martin points out that even if they don’t unleash any other bioweapons, the desired death toll may still be achieved, because they used pseudouridine in the mRNA shots, which is causing “turbo cancers”». Because: «Pseudouridine suppresses cancer-controlling agents and promotes oncogenic activity in the body, and this has been known since 2018, so its inclusion was hardly an accident. It’s a conspiracy, alright. But not a conspiracy theory in the dismissive sense. It’s a global conspiracy by identifiable agents who have, for nearly 60 years, plotted to commit, and profit from, the greatest genocide the world has ever seen, while hiding behind the false veneer of “public health.”». Well today, both the University of Cambridge and other authoritative scientists from around the world implicitly confirm that all those vaccinated with Covid mRNA with Moderna’s Spikevax and Pfizer-Biontech’s Comirnaty have been and continue to be unpaid and, above all, unaware human guinea pigs. Precisely because of this altered nucleoside… The Disturbing Article from Cambridge University The comment by the researcher Rose that we reported in the incipit of the article referred to the text of the University of Cambridge(Source 2) in relation to the study “N1-methylpseudouridylation of mRNA causes +1 ribosomal frameshifting” by Mulroney et al.published on December 6, 2023 by Nature after more than a month of review. «Researchers redesign future mRNA therapeutics to prevent potentially harmful immune responses» is the eloquent title of the scientific text published by the British university. «The latest developments, led by biochemist Professor Anne Willis and immunologist Dr James Thaventhiran from the MRC Toxicology Unit at the University of Cambridge, build upon previous advances to ensure the prevention of any safety issues linked with future mRNA-based therapeutics. Their report is published today in the journal Nature» we read in the unsigned article. «The researchers identified that bases with a chemical modification called N1-methylpseudouridine – which are currently contained in mRNA therapies – are responsible for the ‘slips’ along the mRNA sequence» adds the university website. In collaboration with researchers at the Universities of Kent, Oxford and Liverpool, the MRC Toxicology Unit team«tested for evidence of the production of ‘off-target’ proteins in people who received the mRNA Pfizer vaccine against COVID-19. They found an unintended immune response occurred in one third of the 21 patients in the study who were vaccinated – but with no ill-effects, in keeping with the extensive safety data available on these COVID-19 vaccines». SCIENCE Magazine Finally Admitted the mRNA Vaccines Dangerous Side Effects! Shots linked to Long Covid, Neurologic Damages and POTS Despite disturbing the article already appears biased as it is aimed at “minimizing” the adverse reactions, even lethal one, that are accumulating in pharmacovigilance systems around the world, which have been confirmed by an alarming article in the journal Science, by the regulatory bodies from all over the world (EMA, FDA, etc.) and which led Moderna and Pfizer-Biontech to include the risk of lethal myocarditis in the information leaflets of their genetic drugs… 7 EURODEPUTATI CHIEDONO IL RITIRO DEI VACCINI COVID. Per Miocarditi Letali, Malori Improvvisi e Sicurezza Incerta nei Fragili British Study: “Incorrect mRNA Translation may Increase Toxicity” But it is the same authors of the study whose first signatory is Thomas E. Mulroney (Source 3), associate researcher of the Toxicology Unit of the MRC in Cambridge, who wrote the shocking considerations from a biochemical point of view in the conclusions. «We show that 1-methylΨ is a modified ribonucleotide that significantly increases +1 ribosomal frameshifting during mRNA translation and that cellular immunity to +1 frameshifted products can occur following vaccination with mRNA containing 1-methylΨ. To our knowledge, this is the first report that mRNA modification affects ribosomal frameshifting. Alongside this impact on host T cell immunity, the off-target effects of ribosomal frameshifting could include increased production of new B cell antigens». And they further add: «These findings are of particular importance to our fundamental understanding of how ribonucleotide modification affects mRNA translation, and for designing and optimizing future mRNA-based therapeutics to avoid mistranslation events that may decrease efficacy or increase toxicity». We will not delve further into the technical references but return to the analysis published by Jessica Rose in her Substack, making an extreme summary of it and advising professionals to read the text full of important images. Billions of DNA Fragments of Toxic Spike Protein and SV40 gene in the mRNA Vaccines. New Study: “They may Cause Turbo-Cancer” Let’s start with the comment added under the research published by Nature by her together with David Wiseman, L. Maria Gutschi, David J. Speicher, Kevin McKernan. Alongside the Canadian biologist they were already co-authors of the study “DNA fragments detected in the monovalent and bivalent Pfizer/BioNTech and Moderna modRNA COVID-19 vaccines from Ontario, Canada: exploratory dose-response relationship with serious adverse events” which induced the EMA to confess that Pfizer hid the use of the very dangerous SV40 gene in its vaccine, which can cause tumors. The same research encouraged the bioimmunologist Robert Malone to denounce the presence of the antibiotic resistance gene in the Moderna one, pointing out also that the pharmaceutical company was aware of the tumor risks of mRNA biotechnology as reported in its own patent. Bomba Mondiale! “NEI VACCINI COVID GENE DI RESISTENZA AGLI ANTIBIOTICI”. Studio Spagnolo lo Conferma. Ministro Schillaci lo CELA nell’Allarme Morti AMR We have written extensively about these topics in three investigations, one of which – on antibiotic resistance gene – is a world exclusive. Alarm of American Scientists for the New Research Let us therefore see the content of the comment by Rose and colleagues (Source 1)on Cambridge’s research: The paper provides evidence for the formation “off-target” or unintended proteins following vaccination with BNT162b2 due to frameshifting. Given the proposed mechanism, a similar problem is likely to exist for the Moderna product. While the authors have not isolated samples of these proteins from vaccinated patients or animals, their existence is evidenced by the specific cellular immune responses elicited to frameshifted proteins the authors synthesized. It is not clear why B cell – antibody responses were not studied. The authors state that “Although there is no evidence that frameshifted products in humans generated from BNT162b2 vaccination are associated with adverse outcomes.” BOMBSHELL: mRNA COVID jabs can Damage Children’s Immune Response to OTHER Viruses as well, Study finds It is unclear how it is possible to make this statement, given: • The small number of vaccinated subjects (n=21) providing samples. • This was not a controlled trial. • None of these subjects had reported undue effects of vaccination. Accordingly, the sample is subject to selection bias. • The toxicology of these unintended proteins must be studied. • The authors acknowledge the misdirected immunity “has huge potential to be harmful.” Translated into simpler words, no one has verified the selection methods of the samples which may have been chosen precisely because they did not have serious adverse reactions. SPIKE-DEMIC among Vaccinated: 83 % hit by PCVS Syndrome. Indian Study confirmed Gates, Big Pharma’s Health Disaster Furthermore, in the interests of expertise we read that the two Cambridge scientists Thomas E. Mulroney and Anne E. Willis «are inventors of a pending patent application (2305297.0) relating to mRNA technology» while in the information on the authors it is discovered that Alexander J Mentzer works at the Wellcome Center for Human Genetics, University of Oxford. Wellcome, with the Bill & Melinda Gates Foundation and the World Economic Forum, is among the founders of the Ngo CEPI(Coalition for Epidemic Preparedness Innovations) which has already launched the SKYCovion vaccine together with the London-based GSK, managed by CEO Emma Walmsley who is also director of Microsoft, and SK Bioscience. WUHAN-GATES – 73. BILL III A CACCIA DI CAVIE UMANE PER VACCINO COVID COREANO. “Genotossicità non Studiata” ma OMS & UK danno OK a SkyCovione con Spike Tossica e Adiuvante GSK da Pericoloso Squalene But let’s go back to the analysis made by Jessica Rose on the Cambridge researchers’ study: «The authors write that N1-methylpseudouridine affects the fidelity of mRNA translation via ribosome stalling that induces frameshifting. Frameshifting results in the production multiple, unique and potentially aberrant proteins». «The modified mRNAs for use in the COVID-19 products were codon-optimized for maximal protein expression in humans. Codon optimization, or synonymous codon replacement, rests on the idea that one can induce mutations throughout a gene of interest (like spike) based on an organism’s (like humans) codon usage bias, to increase translational efficiency and protein expression without altering the sequence of the protein. But, it is well-known that codon-optimization can lead to protein conformation, folding and stability problems». COVID: SCOPERTA LA PROTEINA CHE RIVELA I LETALI COAGULI DI SANGUE. Ma Nessuno Indaga sulla Correlazione coi Vaccini The Canadian immunologist further notes: «Codon optimization could affect protein conformation, folding and stability, change post-translational modification sites and even affect protein function.Different rates of translation by different tRNAs, including those that exhibit wobble base-pairing (a tRNA that can recognize multiple synonymous codons) may actually be critical for determining the rate of translation. The ribosome may slow and pause during elongation which may actually be necessary for proper protein folding. Therefore, codon optimization may disrupt the fine-tuned timing of translation and ultimately protein function». The Prophetic Seneff Study on Autoimmune and Neurocerebral Damage He then refers to other studies that had reported the dangers of this biochemical manipulation (Source 1): «Codon optimization can also lead to misfolding of mRNAs due to increased Guanine/Cytosine (GC content). Please read McKernan et al.’s preprint, Xia et al.’s paper and Seneff et al.’s paper to learn more about potential problems relating to codon optimization and GC content changes. The latter group write: Synonymous codon replacement also results in a change in the multifunctional regulatory and structural roles of resulting proteins». ONE in THREE Covid Vaccinated with Neurological Complications. Alarming Study from Italian National Research Council The risks to the human organism are clearly highlighted: «There is, in fact, a significant enrichment of GC content (17% and 25% enrichments as per Pfizer and Moderna, respectively, as compared to SARS-CoV-2) as a result of the codon optimization that was done, and this can lead to “dysregulation of the G4-RNA-protein binding system and a wide range of potential disease-associated cellular pathologies including suppression of innate immunity, neurodegeneration, and malignant transformation”. Increased GC content significantly alters mRNA secondary structure as well, and this can also lead to ribosomal pausing or stalling». These considerations were expressed in a study published by illustrious scientists such as Stephanie Seneff, Computer Science and Artificial Intelligence Laboratory, MIT, Cambridge, MA, USA, Greg Nigh, Immersion Health, Portland, OR, USA, Anthony M. Kyriakopoulos, Nasco AD Biotechnology Laboratory, Department of Research and Development, Piraeus, Greece and Peter A. McCullough, for Health Foundation, Tucson, AZ, USA, which was the subject of enormous censorship by specialized medical journals but we published in Gospa News thanks to an excellent summary by Dr. Mercola. Dangerous RNA Manipulation with N1-methyl-Ψ Below are the quotes from Seneff et al.(Source 4) useful for understanding the connection with uridine modified in N1-methyl-Ψ: «The utilization of mRNA vaccines in the context of infectious disease has no precedent. The many alterations in the vaccine mRNA hide the mRNA from cellular defenses and promote a longer biological half-life and high production of spike protein». «However, the immune response to the vaccine is very different from that to a SARS-CoV-2 infection. In this paper, we present evidence that vaccination induces a profound impairment in type I interferon signaling, which has diverse adverse consequences to human health. Immune cells that have taken up the vaccine nanoparticles release into circulation large numbers of exosomes containing spike protein along with critical microRNAs that induce a signaling response in recipient cells at distant sites. We also identify potential profound disturbances in regulatory control of protein synthesis and cancer surveillance». The COVID Jabs’ Mechanisms of Injury: Sudden Death, Blood Cloths, Human Mad Cow and Autoimmune Diseases In the study entitled “Innate immune suppression by SARS-CoV-2 mRNA vaccinations: The role of G-quadruplexes, exosomes, and MicroRNAs” the scientists added: «These disturbances potentially have a causal link to neurodegenerative disease, myocarditis, immune thrombocytopenia, Bell’s palsy, liver disease, impaired adaptive immunity, impaired DNA damage response and tumorigenesis. We show evidence from the VAERS database supporting our hypothesis. We believe a comprehensive risk/benefit assessment of the mRNA vaccines questions them as positive contributors to public health». The late biologist Luc Montagnier, in a study published posthumously by his research friends Jean-Claude Perez and Claire Moret-Chalmin with a review contribution from Seneff biophysics, proved without a shadow of a doubt the correlation between killer prions caused by vaccines and rapid deaths for neurocerebral Creutzfeldt-Jacob disease, human mad cow disease. PRIONS as KILLERS: 25 Deaths due to a New Mad-Cow from Covid Vaccines. Shocking Research by Montagnier (RIP), Perez & Moret-Chalmin on CJD Brain Damages In detail Seneff and the other scientists also refer to specific alterations: «Impaired type I IFN signaling is linked to many disease risks, most notably cancer, as type I IFN signaling suppresses proliferation of both viruses and cancer cells by arresting the cell cycle, in part through upregulation of p53, a tumor suppressor gene, and various cyclin- dependent kinase inhibitors (Musella et al., 2017; Matsuoka et al., 1998). IFNα also induces major histocompatibility (MHC) class 1 antigen presentation by tumor cells, causing them to be more readily recognized by the cancer surveillance system (Heise et al., 2016)». They then delve into the problem of the uridine molecule. To understand its importance we report a note from Rose: «Pseudouridines (Ψs) are a normal and essential part of our biology. They have been called the 5th nucleotide, in fact, and “are a ubiquitous constituent of structural RNA (transfer, ribosomal, small nuclear (snRNA) and small nucleolar), and present in coding RNA, across the three phylogenetic domains of life”and “accounts for about 1.4% of all bases in human rRNAs”». “mRNA COVID-19 Vaccines are Like Gene Therapy Products” French Study highlighted Omitted Controls on Genotoxicity Here’s what Seneff and his colleagues wrote about vaccines: «A breakthrough came when it was discovered experimentally that the mRNA coding for the spike protein could be modified in specific ways that would essentially fool the human cells into recognizing it as harmless human RNA. A seminal paper by Karikó et al. (2005) demonstrated through a series of in vitro experiments that a simple modification to the mRNA such that all uridines were replaced with pseudouridine could dramatically reduce innate immune activation against exogenous mRNA». Cancer Risk pointed out by the Nobel Inventor of mRNA Vaccines Precisely for this discovery, Hungarian researcher Katalin Karikó, long-time at Biontech, recently received the Nobel Prize for Medicine together with her American colleague Drew Weissman, although both warned of the dangers of the new mRNA biotechnology. Medicine Nobel to mRNA Covid Vaccines’ Scientists, both Sponsored by Gates, Fauci and Zuckerberg In particular, on January 6, Karikó declared to the German newspaper Welt (Source 5): «Every day I receive many emails from people who write to me about their experiences. One woman wrote to me that two days after the vaccination she developed a large lump in her breast. Vaccination caused cancer, it was her conclusion. But the cancer was already there, only vaccination gave an extra boost to the immune system, so that the immune defense cells rushed in large numbers towards the enemy». The Gospa News investigations on Turbo-Cancer based now on seven published scientific studies have highlighted a very strong correlation between mRNA gene sera and the appearance or reactivation of tumor phenomena with abnormal degeneration resulting in lethal outcomes. TURBO-CANCER – 2. Many Lethal/Serious Cases and New Researches on Covid mRNA Vaccines Risks. Melatonin Hope… Karikó herself adds: «Vaccination provides a strong boost to the immune system. It can happen that a dormant infection breaks out in people with an already weakened immune system. The extent to which this is the case for shingles will need to be examined more closely». Gospa News did so by discovering 27 thousand cases of Herpes Zoster, in the European Union only, as adverse reactions to vaccines reported by EMA pharmacovigilance database even in children, who are more exposed to damage to the natural immune system as confirmed by recent research. Esclusivo! EPIDEMIA DI HERPES DOPO I VACCINI COVID. 27mila Casi nell’UE: 31 Morti da Zoster. Lo Studio: “Per danni al Sistema Immunitario” Let’s go back to Seneff’s conclusions: «Andries et al. (2015) later discovered that 1-methylpseudouridine as a replacement for uridine was even more effective than pseudouridine and could essentially abolish the TLR response to the mRNA, preventing the activation of blood-derived dendritic cells. This modification is applied in both the mRNA vaccines on the market (Park et al., 2021)». To put it simply, the dendritic cell plays the role of sentinel and if it senses the presence of a pathogen in the body, it stimulates the immune response of B and T lymphocytes, specific against that antigen. If its action is limited or suppressed, it may become incapable of dealing with viral or bacterial enemies but also tumor dangers. Critical Role of Pseudouridine in mRNA Vaccines A study published by Pedro Morais, Director (Pseudouridylation Technology) ProQR Therapeutics, Leiden, Netherlands, and by Department of Biochemistry and Biophysics, Center for RNA Biology, University of Rochester Medical Center, Rochester, NY, US, entitled “The Critical Contribution of Pseudouridine to mRNA COVID-19 Vaccines” highlighted the fundamental role of the laboratory alteration of this protein in the Comirnaty and Spikevax genetic sera (source 6). «Both consisted of N1-methyl-pseudouridine-modified mRNA encoding the SARS-COVID-19 Spike protein and were delivered with a lipid nanoparticle (LNP) formulation. Because the delivery problem of ribonucleic acids had been known for decades, the success of LNPs was quickly hailed by many as the unsung hero of COVID-19 mRNA vaccines». “European Medicines Agency Knew Toxicity of Pfizer Covid Vaccine”. Bombshell Study Published in US by an Italian BioChemist on Dangers mRNA-LNPs But the scholars, one of whom has a clear conflict of interest because he is director of the Pseudouridylation Technology project, have highlighted another very interesting fact: «However, the clinical trial efficacy results of the Curevac mRNA vaccine (CVnCoV) suggested that the delivery system was not the only key to the success. CVnCoV consisted of an unmodified mRNA (encoding the same spike protein as Moderna and Pfizer-BioNTech’s mRNA vaccines) and was formulated with the same LNP as Pfizer-BioNTech’s vaccine (Acuitas ALC-0315).However, its efficacy was only 48%. This striking difference in efficacy could be attributed to the presence of a critical RNA modification (N1-methyl-pseudouridine) in the Pfizer-BioNTech and Moderna’s mRNA vaccines (but not in CVnCoV)». “Toxic Nanoforms inside Pfizer-Biontech Covid Vaccine”. Vital Study by Italian Biochemist on US Journal of Virology highlights an Alleged Crime However, the same researchers highlight a significant note: «The intrinsic immunogenicity of non-modified mRNA was once considered a potential advantage for its use in vaccines(Ishii and Akira, 2005) as it would encode the antigen and concomitantly serve as an adjuvant while permitting a low dose. In fact, the unmodified COVID-19 mRNA vaccine candidate in late-stage clinical trials (CVnCoV, developed by Curevac) had a maximum dose of 12 µg». Curevac was developed by Curevac NV of Tubingen, together with the Ngo CEPI founded by Bill Gates with Wellcome and WEF, which initiated an authorization process before the CHMP committee of the European Medicines Agency (EMA) but withdrew it due to its low efficacy on October 12, 2021 (source 7) in view of the arrival of a new pharmacological product developed with GSK financed by Gates himself. MINISTRO SCHILLACI SPECULA SU BIG PHARMA FINANZIATA DA GATES. €700mila Investiti in Biomediche USA che Testano anche Vaccini DNA Covid Here is another cryptic phrase in which we talk about the “safety” of vaccines, implicitly implying that it is not clear in the current vaccines which therefore make all those who take them into “human guinea pigs”from the laboratory as the immunologist Rose clearly highlights in her final bioethical considerations. Rose: “Unpredictable Health Effects of Manipulated Codons” «Ehden Biber also wrote a great article about the pitfalls of codon optimization that you can read here. In a Nature article published in 2011 entitled: “Breaking the silence”, the author writes on the potential danger of fiddling with codons in therapeutic proteins whereby it “could have unpredictable effects on people’s health”» Rose wrote in her comment on the Cambridge research quoting many sentences by scientific journalist Alla Katsnelson which we report below. Bombshell! Texas Attorney General sues Pfizer on Covid Vaccine Efficacy and Conspiring In detail, the Canadian researcher adds: «She points to a study where the authors show that a synonymous codon change found in the most common form of cystic fibrosis results in mRNA misfolding. (Keep this in mind.) She also points out that in the context of the multi-drug resistance 1 gene (MDR1) (the gene that encodes P-glycoprotein), that a codon change may interfere with the pauses that characterize RNA passing through the ribosome, thereby changing how the growing amino acid chain folds». «But perhaps the most timely and spine-tingly relevant statement in this article is found at the end, and I quote: “At the moment, companies developing recombinant therapies must verify that the DNA sequence designed by their scientists is the one that’s producing their proteins, but they aren’t required to note how different that is from the native genetic code”». European Regulator: Pfizer Hid Dangerous Cancer Gene! It Kept Secret the SV40 DNA Sequence In COVID-19 Vaccine We do not have any guidance with regard to the [DNA] sequence,” Kimchi-Sarfaty notes. While it was the Italian bioimmunologist Mauro Mantovani who demonstrated how the “double Proline” inserted in mRNA vaccines makes the toxic Spike protein dangerously persistent in the human body. «That’s one piece of data that could be tracked by the system she is proposing. Such knowledge, in turn, could ultimately help define better strategies for optimization and possibly even make biologic drugs safer for people» adds Alla Katsnelson while the immunologist asks herself a question: «I wonder if the FDA ever took her advice to track the differences in codons and the resulting potential adverse effects?» Covid Vaccines Killer Pathologies in a Name Only: Spikeopathy! Huge, Chilling Study on mRNA Genic Serums’ Serious Adverse Reactions Therefore Rose quoted the article which we analyzed before: «In addition to our comment on the Nature paper, a University of Cambridge write-up entitled: Researchers redesign future mRNA therapeutics to prevent potentially harmful immune responses was penned. They make it clear that the most relevant conclusion from the Nature paper is that we can make more products similarly insanely dangerous as the ones pumped into billions of bodies because we can simply ‘reduce the production of frameshifted products’ by ‘synonymous targeting of slippery sequences’». So she wrote her milestone sentence: «Well of course! Now that we know that billions of people’s cells might be making aberrant proteins, for unknown periods of time, we can simply sweep these people under the rug, ‘fix’ the product, and keep on makin’ money. Let’s go slidin’ down the slippery sequence slope of gene therapy straight to the Gates of hell». Moderna AWARE that mRNA Jabs cause CANCER due to DNA Fragments. Malone Unveils Patent The Canadian molecular biologist concludes before going into detail about a biochemical analysis that is too technical for non-experts: «The manufacturers might have thought to explore options to prevent potentially harmful responses from their products prior to injecting billions of people with them. It is criminal that these products continue to be forced onto newborns and infants by mandate, to this day». And then she report an emblematic quote about the risks of “Fooling with Mother Nature” by an evolutionary cell biologist at the University of Chicago: “Please do not monkey with these sites; they are optimized for some reason”, in reference to codon bias in mammals. Fabio Giuseppe Carlo Carisio © COPYRIGHT GOSPA NEWS prohibition of reproduction without authorization follow Fabio Carisio Gospa News director on Twitter follow Gospa News on Telegram MAIN SOURCES SOURCE 1 – JESSICA ROSE – That Substack about N1-methylpseudouridines and frameshifting SOURCE 2 – UNIVERSITY OF CAMBRIDGE – Researchers redesign future mRNA therapeutics to prevent potentially harmful immune responses SOURCE 3 – NATURE – N1-methylpseudouridylation of mRNA causes +1 ribosomal frameshifting SOURCE 4– PUBMED – Innate immune suppression by SARS-CoV-2 mRNA vaccinations: The role of G-quadruplexes, exosomes, and MicroRNAs SOURCE 5 – WELT – “Das ist der wirkliche Grund, warum man unter neuen Varianten nicht mehr so krank wird“ SOURCE 6 – FRONTIERS IN – The Critical Contribution of Pseudouridine to mRNA COVID-19 Vaccines SOURCE 7 – EMA ends rolling review of CVnCoV COVID-19 vaccine following withdrawal by CureVac AG Fabio G. C. Carisio Fabio is investigative journalist since 1991. Now geopolitics, intelligence, military, SARS-Cov-2 manmade, NWO expert and Director-founder of Gospa News: a Christian Information Journal. His articles were published on many international media and website as SouthFront, Reseau International, Sputnik Italia, United Nation Association Westminster, Global Research, Kolozeg and more… Most popolar investigation on VT is: Rumsfeld Shady Heritage in Pandemic: GILEAD’s Intrigues with WHO & Wuhan Lab. Bio-Weapons’ Tests with CIA & Pentagon Fabio Giuseppe Carlo Carisio, born on 24/2/1967 in Borgosesia, started working as a reporter when he was only 19 years old in the alpine area of Valsesia, Piedmont, his birth region in Italy. After studying literature and history at the Catholic University of the Sacred Heart in Milan, he became director of the local newspaper Notizia Oggi Vercelli and specialized in judicial reporting. For about 15 years he is a correspondent from Northern Italy for the Italian newspapers Libero and Il Giornale, also writing important revelations on the Ustica massacre, a report on Freemasonry and organized crime. With independent investigations, he collaborates with Carabinieri and Guardia di Finanza in important investigations that conclude with the arrest of Camorra entrepreneurs or corrupt politicians. In July 2018 he found the counter-information web media Gospa News focused on geopolitics, terrorism, Middle East, and military intelligence. In 2020 published the book, in Italian only, WUHAN-GATES – The New World Order Plot on SARS-Cov-2 manmade focused on the cycle of investigations Wuhan-Gates His investigations was quoted also by The Gateway Pundit, Tasnim and others He worked for many years for the magazine Art & Wine as an art critic and curator. VETERANS TODAY OLD POSTS www.gospanews.net/ ATTENTION READERS We See The World From All Sides and Want YOU To Be Fully Informed In fact, intentional disinformation is a disgraceful scourge in media today. So to assuage any possible errant incorrect information posted herein, we strongly encourage you to seek corroboration from other non-VT sources before forming an educated opinion. About VT - Policies & Disclosures - Comment Policy Due to the nature of uncensored content posted by VT's fully independent international writers, VT cannot guarantee absolute validity. All content is owned by the author exclusively. Expressed opinions are NOT necessarily the views of VT, other authors, affiliates, advertisers, sponsors, partners, or technicians. Some content may be satirical in nature. All images are the full responsibility of the article author and NOT VT. https://www.vtforeignpolicy.com/2024/01/bombshell-inside-mrna-vaccines-a-human-molecule-diabolically-altered/
    WWW.VTFOREIGNPOLICY.COM
    BOMBSHELL! Inside mRNA Vaccines a Human Molecule Diabolically Altered
    In the cover image, the Canadian researcher Jessica Rose, author of an excellent biochemical analysis of an article from the University of Cambridge commenting a study by some of its researchers on the toxicity of manipulated human nucleoside in mRNA genetic sera by Fabio Giuseppe Carlo Carisio VERSIONE IN ITALIANO «Well of course! Now that we know that...
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  • To Save Gaza, Invoke the Genocide Convention
    The ICC is a "puppet institution". What's needed is a country to invoke the Genocide Convention at the International Court of Justice. Here's how, with argument, phone numbers, addresses and emails.

    Sam Husseini

    [Addendum: RootsAction and World Beyond War have put out the action alert “It’s Time to Invoke the Genocide Convention”. This full piece has been posted on X/Twitter with thread containing handles for various national leaders who can be petitioned.]

    Some of the greatest successes in recent human history have combined protest movements with strong diplomatic moves.

    In February 1998, the Clinton administration seemed poised to inflict a massive attack on Iraq, but vocal opposition from the US public, especially at a CNN town hall meeting in Ohio, combined by UN Secretary General Kofi Annan going to Iraq, repelled the US government attack.

    The following year, in the Battle of Seattle, combined protests in the streets and delegations from the global south finding their backbone resulted in the World Trade Organization’s plans collapsing. This was a major setback for global corporate interests.

    There is now effectively a global movement, largely based around mass protests, to stop Israel’s genocide of Palestinians in Gaza.

    Several countries, including South Africa, Bangladesh, Bolivia, Comoros, Djibouti as well as Colombia and Algeria and Turkey have moved for the International Criminal Court to prosecute Israeli officials.

    The problem is that ICC has been dragging its heels for years on prosecuting Israelis. It has been called a “white man’s court” after only going after Africans, and, after letting Israel off the hook during an earlier assault on Gaza, “a hoax”. Some of these nations have called Israel’s war crimes “genocide”. They should act on their words and invoke the relevant treaty. Other nations that have been especially critical of Israel are Pakistan, Brazil, Chile, Belize, Jordan, Chad, Honduras, Bahrain, Venezuela, Iran, and Cuba.

    The International Court of Justice, also called the World Court, in contrast has ruled against Israel. But so far these rulings have been advisory opinions. It ruled against Israel in a case regarding its wall in 2004. In another case before it, is expected to rule against Israel’s long term policies.

    But what can be done now, Prof. Francis Boyle, who successfully represented the Bosnians before the World Court, argues is to use emergency processes to give more teeth to the World Court. This can be done by invoking the Genocide Convention. This is outlined by Boyle, noted by UN whistleblower Craig Mokhiber, backed by Nobel Peace Prize winner Mairead Maguire, and written about by myself. And most recently by Craig Murray, now a human rights activist who was the British ambassador to Uzbekistan and Rector of the University of Dundee.

    Murray just wrote the piece “Activating the Genocide Convention” which states: “There are 149 states party to the Genocide Convention. Every one of them has the right to call out the genocide in progress in Gaza and report it to the United Nations. In the event that another state party disputes the claim of genocide — and Israel, the United States and the United Kingdom are all states party — then the International Court of Justice [also called the World Court] is required to adjudicate on ‘the responsibility of a State for genocide.'”

    Murray quotes from the Genocide Convention and cites evidence that Israel is conducting genocide and that the US and British governments are at minimum complicit in that. He then states: “The International Court of Justice is the most respected of international institutions; while the United States has repudiated its compulsory jurisdiction, the United Kingdom has not and the EU positively accepts it.

    “If the International Court of Justice makes a determination of genocide, then the International Criminal Court does not have to determine that genocide has happened. This is important because unlike the august and independent ICJ, the ICC is very much a western government puppet institution which will wiggle out of action if it can. But a determination of the ICJ of genocide and of complicity in genocide would reduce the ICC’s task to determining which individuals bear the responsibility. That is a prospect which can indeed alter the calculations of politicians.

    “It is also the fact that a reference for genocide would force the western media to address the issue and use the term, rather than just pump out propaganda about Hamas fighting bases in hospitals. …

    “I am afraid the question of why Palestine has not invoked the Genocide Convention takes us somewhere very dark. … It is Fatah who occupy the Palestinian seat at the United Nations, and the decision for Palestine to call into play the Genocide Convention lies with Mahmoud Abbas. It is more and more difficult daily to support Abbas. He seems extraordinarily passive, and the suspicion that he is more concerned with refighting the Palestinian civil war than with resisting the genocide is impossible to shake. By invoking the Genocide Convention he could put himself and Fatah back at the centre of the narrative. But he does nothing. I do not want to believe that corruption and a Blinken promise of inheriting Gaza are Mahmoud’s motivators. But at the moment, I cannot grab on to any other explanation to believe in.”

    Thus speeches from Abbas and allied Palestinians figures should be viewed extremely skeptically. It is also very odd, to say the very least, that Francesca Albanese, Special Rapporteur on the situation of human rights in the Palestinian Territory occupied since 1967, and other officials put out a statement “Gaza: UN experts call on international community to prevent genocide against the Palestinian people” — but make no mention whatever of the Genocide Convention.

    As Murray writes: “Any one of the 139 states party could invoke the Genocide Convention against Israel and its co-conspirators. Those states include Iran, Russia, Libya, Malaysia, Bolivia, Venezuela, Brazil, Afghanistan, Cuba, Ireland, Iceland, Jordan, South Africa, Turkey and Qatar. But not one of these states has called out the genocide [by invoking the Convention]. Why?

    “It is not because the Genocide Convention is a dead letter. It is not. It was invoked against Serbia by Bosnia and Herzegovina and the ICJ ruled against Serbia with regard to the massacre at Srebrenica.” Murray notes that this helped lead to prosecutions.

    He adds: “Some states may simply not have thought of it. For Arab states in particular, the fact that Palestine itself has not invoked the Genocide Convention may provide an excuse. EU states can hide behind bloc unanimity.

    “But I am afraid that the truth is that no state cares sufficiently about the thousands of Palestinian children already killed and thousands more who will shortly be killed, to introduce another factor of hostility in their relationship with the United States. Just as at [the recent] summit in Saudi Arabia, where Islamic countries could not agree [on] an oil and gas boycott of Israel, the truth is that those in power really do not care about a genocide in Gaza. They care about their own interests.

    “It just needs one state to invoke the Genocide Convention and change the narrative and the international dynamic. That will only happen through the power of the people in pressing the idea on their governments. This is where everybody can do a little something to add to the pressure. Please do what you can.”

    What can you do? Urge countries which have been critical of Israel to invoke the Genocide Convention at the International Court of Justice. Get groups and influential people to make this a primary ask.

    Protests in NYC should include visits and vigils to the missions of those countries. Activists who have been arrested for protesting against Israel’s slaughter can ask UN officials from countries critical of Israel to invoke the Genocide Convention.

    Palestinians in Ramallah may be able to directly contact the representatives of various countries to Palestine.

    This can be done anywhere. Protests in London can respectfully appeal to the embassies of various countries critical of Israel.

    We need to keep pressing directly against the US and Israeli governments, but their hearts are like stone. If we reach other states to invoke the Genocide Convention, it may be a key stop in curtailing the slaughter.

    Moreover, it could be a turning point in global relations. Should a positive emergency ruling by the International Court of Justice be forthcoming, it would dramatically isolate the US and Israel at the UN. The US would of course try to block anything at the UN Security Council. But with a World Court ruling, Boyle argues, the stage would be set for the General Assembly to assert itself using the Uniting for Peace procedure. Combined with sustained protests, like the WTO and other critical confrontations, the costs of continuing the slaughter could become unsustainable. Moreover, a World Court ruling could facilitate other legal efforts, like universal jurisdiction.

    For all that to happen, a country needs to step forward and invoke the Genocide Convention.

    Make no mistake; any nation that does this may well be targeted in insidious ways by the US and by Israel. Any such nation should be afforded every bit of support people of goodwill can muster.

    Here's a website that seems to list all the embassies and other diplomatic missions around the world. People from anywhere can be emailing, calling and going to these embassies and missions, urging these countries to use every legal mechanism to pressure Israel to stop, including invoking the Genocide Convention: embassy-worldwide.com.

    A friend extracted emails of missions to the UN:

    info@afghanistan-un.org
    mission.newyork@mfa.gov.al
    officeofthepr.albania@mfa.gov.al
    algeriamission.ny@gmail.com
    contact@andorraun.org
    theangolamission@angolaun.org
    unmission@ab.gov.ag
    jackley.peters@ab.gov.ag
    enaun@mrecic.gov.ar
    armenia@missionun.org
    australiaun@dfat.gov.au
    new-york-ov@bmeia.gv.at
    mission@azerbaijanun.org
    mission@bahamasny.com
    newyork.mission@mofa.gov.bh
    bangladeshatun@gmail.com
    bdpmny@gmail.com
    prun@foreign.gov.bb
    barbados@un.int
    usaun@mfa.gov.by
    newyorkun@diplobel.fed.be
    blzun@belizemission.com
    blzun@aol.com
    onu.newyork@gouv.bj
    beninewyork@gmail.com
    bhutanmission@pmbny.bt
    missionboliviaun@gmail.com
    bihun@mvp.gov.ba
    botswana@un.int
    distri.delbrasonu@itamaraty.gov.br
    bruneiunmission@protonmail.com
    mission.newyork@mfa.bg
    miperfaso.ny@burkina-onu.org
    ambabunewyork@yahoo.fr
    cvpm.unny@mnec.gov.cv
    cambodia@un.int
    cameroon.mission@yahoo.com
    canada.un@international.gc.ca
    repercaf.ny@gmail.com
    chadmission.un@gmail.com
    chile.un@minrel.gob.cl
    chinesemission@yahoo.com
    colombia@colombiaun.org
    comores.nu@gmail.com
    cgbrazzadel60@gmail.com
    miscr-onu@rree.go.cr
    cotedivoiremission@yahoo.com
    cromiss.un@mvep.hr
    cuba_onu@cubanmission.com
    unmission@mfa.gov.cy
    un.newyork@embassy.mzv.cz
    dprk.un@verizon.net
    missiondrc@gmail.com
    nycmis@um.dk
    djibouti@nyct.net
    dominicaun@gmail.com
    drmun1114@gmail.com
    onunewyork@cancilleria.gob.ec
    mission@egyptmissionny.com
    elsalvador@un.int
    info@equatorialguineaun.org
    general@eritreaun.org
    mission.newyork@mfa.ee
    eswatini@un.int
    eswatinimissionunny@yahoo.com
    ethiopia@un.int
    mission@fijiprun.org
    sanomat.yke@gov.fi
    france@franceonu.org
    info@gabonunmission.com
    gambia_un@hotmail.com
    geomission.un@mfa.gov.ge
    info@new-york-un.diplo.de
    ghanaperm@aol.com
    grdel.un@mfa.gr
    gmun@mofa.gov.gd
    onunewyork@minex.gob.gt
    missionofguinea.un@gmail.com
    guinebissauonu@gmail.com
    pmny@mission.gov.gy
    mphonu.newyork@diplomatie.ht
    ny.honduras@hnun.org
    hungaryun.ny@mfa.gov.hu
    unmission@mfa.is
    india.newyorkpmi@mea.gov.in
    ptri@indonesiaun.org
    iranunny@mfa.gov.ir
    iraq.mission@iraqmission-un.com
    newyorkpmun@dfa.ie
    uninfo@newyork.mfa.gov.il
    info.italyun@esteri.it
    info.unmissionny@mfaft.gov.jm
    p-m-j@dn.mofa.go.jp
    missionun@jordanmissionun.com
    unkazmission@gmail.com
    info@kenyaun.org
    kimission.newyork@mfa.gov.ki
    kuwait@kuwaitmissionun.org
    kyrgyzstan.un.ny@mfa.gov.kg
    lao.pr.ny@gmail.com
    mission.un-ny@mfa.gov.lv
    contact@lebanonun.org
    lesothonewyork@gmail.com
    liberiamission@pmun.gov.lr
    mission@libya-un.gov.ly
    newyork@llv.li
    lithuaniaun@gmail.com
    newyork.rp@mae.etat.lu
    repermad.ny@gmail.com
    malawinewyork@aol.com
    malawiu@aol.com
    mwnewyorkun@kln.gov.my
    info@maldivesmission.com
    miperma@malionu.com
    malta-un.newyork@gov.mt
    marshallislands@rmiunmission.org
    mauritaniamission@gmail.com
    mauritiusmissionnyc@gmail.com
    onuusr1@sre.gob.mx
    fsmun@fsmgov.org
    monaco.un@gmail.com
    mongolianmission@twcmetrobiz.com
    unnewyork.montenegro@gmail.com
    morocco.un@maec.gov.ma
    mozambique.unmission@gmail.com
    myanmarmission@verizon.net
    info@namibiaunmission.org
    nauru@un.int
    nepalmissionusa@gmail.com
    nyv@minbuza.nl
    nzpmun@gmail.com
    nicaraguaunny@yahoo.com
    nigermission@ymail.com
    permny@nigeriaunmission.org
    newyork@mfa.gov.mk
    delun@mfa.no
    oman@un.int
    pakistan@pakun.org
    mission@palauun.org
    emb@panama-un.org
    pngun@pngmission.org
    paraguay.un@mre.gov.py
    onuper@unperu.org
    newyork.pm@nypm.org
    newyork.pm@dfa.gov.ph
    poland.un@msz.gov.pl
    portugal.nu@mne.pt
    pmun@mofa.gov.qa
    korea.un@mofa.go.kr
    unmoldova@mfa.gov.md
    newyork-onu@mae.ro
    press@russiaun.ru
    ambanewyork@minaffet.gov.rw
    ambanewyork@gmail.com
    sknmission@aol.com
    info@stluciamission.org
    svgmission@gmail.com
    ambassadorassistantsvg@gmail.com
    samoa@samoanymission.ws
    sanmarinoun@gmail.com
    rdstppmun@gmail.com
    correspondence@ksamission-gov.net
    senegal.mission@yahoo.fr
    info@serbiamissionun.org
    pr.office@serbiamissionun.org
    seychellesmissionun@gmail.com
    seychellesmission@sycun.org
    sierraleone@pmun.net
    singaporeun@outlook.com
    un.newyork@mzv.sk
    slomission.newyork@gov.si
    simun@solomons.com
    somalia@unmission.gov.so
    pmun.newyork@dirco.gov.za
    info@rssun-nyc.org
    rep.nuevayorkonu@maec.es
    prun.newyork@mfa.gov.lk
    mail@slmission.com
    sudan@sudanmission.org
    suriname_un@proton.me
    representationen.new-york@gov.se
    newyork.un@eda.admin.ch
    syrianmission-ny@sar-un.org
    tajikistanunmission@gmail.com
    thaimission.ny@gmail.com
    timorleste.unmission@gmail.com
    togo.mission@togounmission.org
    tongaunmission@gmail.com
    pmun-ny@trinbago.org
    tunisia@un.int
    tunisiamission@usa.com
    tr-delegation.newyork@mfa.gov.tr
    turkmenistan.un@mfa.gov.tm
    tuvalu.unmission@gov.tv
    admin@ugandaunny.com
    uno_us@mfa.gov.ua
    nyunprm@mofaic.gov.ae
    nyunprm@uaeun.org
    ukmissionny@gmail.com
    tanzania.un@nje.go.tz
    usun.newyork@state.gov
    urudeleg@mrree.gub.uy
    uzbekistan.un@gmail.com
    vanunmis@aol.com
    misionvenezuelaonu@gmail.com
    info@vietnam-un.org
    yemenmissionny@gmail.com
    un@grz.gov.zm
    info@zambiamissionun.com
    zimnewyork@gmail.com
    office@holyseemission.org
    admin@palestinemissionun.org
    aumission_ny@yahoo.com
    ny.un@las.int
    aalco@un.int
    cari.per.obs.un@gmail.com
    ccampos@sgsica-ny.org
    newyork@commonwealth.int
    gccny@gccsg.org
    ceeaceccasom@gmail.com
    kjawara-njai@ecowas.int
    ecowasmission.ny@gmail.com
    bfaedda@eplo.int
    delegation-new-york@eeas.europa.eu
    amparo.morales@filac.org
    jonathan.granoff@iaca.int
    dijana.duric@iaca.int
    un@iccwbo.org
    nyoffice@interpol.int
    newyork@idlo.int
    unobserver@idea.int
    reper.new-york@francophonie.org
    nyoffice@irena.org
    iucn@un.int
    internationalyouthorganization@un.int
    uncontact@oecd.org
    oic.un.ny@gmail.com
    pam.unny@pam.int
    srao@ppdsec.org
    rgarvey@ppdsec.org
    south@southcentre.int
    nyinfo@upeace.org
    ny-office@ipu.org
    newyork@icrc.org
    newyork.delegation@ifrc.org
    ioc-unobserver@olympic.org
    un.mission.ny@orderofmalta.int
    faolon-director@fao.org
    iaeany@un.org
    liaisonofficeny@icc-cpi.int
    ifad.ny@ifad.org
    newyork@ilo.org
    rpowell@imf.org
    jlammens@imf.org
    unofficeny@iom.int
    seaun@un.org
    itlos@itlos.org
    newyork@unesco.org
    office.newyork@unido.org
    whonewyork@who.int
    newyork.office@wipo.int
    ola.zahran@wipo.int
    lpaterson@wmo.int
    laura.paterson@un.org

    Emails of embassies to and from Palestine via this page.

    aeoalg@caramail.org
    alembac@ucomgh.com
    alestine@intnet.dj
    aliman@icon.co.zw
    ambpal@eunet.rs
    ambpal@eunet.yu
    auemb@mofa-gov.ps
    austrep@palnet.com
    bremb@mofa-gov.ps
    chinaemb_ps@mfa.gov.cn
    clemb@mofa-gov.ps
    cyprusoffice@palnet.com
    del.palestine@wanadoo.fr
    deleg.palestinienne@beon.be
    elian@freemail.hu
    em.alasad_asad@hotmail.com
    embagoda.palestine@mad.servicom.es
    embassy@palestineindia.com
    embassyofpalestine.portugal@gmail.com
    embassyofpalestine@gmail.com
    embpalnic@turbonett.com.in
    empaltr@gmail.com
    eosopmet@omantel.net.com
    falastin@hellasnet.gr
    fiemb@mofa-gov.ps
    gdpalestine@swissonline.ch
    info@gdp.ie
    info@plo.swieden.org
    iqemb@mofa-gov.ps
    jerusalem@mianet.com.ar
    jerusalem@telesat.com.co
    jorrep@palnet.com
    kwemb@mofa-gov.ps
    lbemb@mofa-gov.ps
    maemb@mofa-gov.ps
    ngemb@mofa-gov.ps
    pal.damas@gmail.com
    pal_embassy@yahoo.com
    palango@netangola.com
    palastinelo@hotmail.com
    palemb.no@outlook.com
    palemb1@yemen.net
    palembassy_ukraine@hotmail.com
    palembs@qatar.net.qa
    palembtn@yahoo.com
    palestcz@mbox.vol.cz
    palestin@spidernet.com
    palestine@dsi.net.pk
    palestine@paltsts-jp.com
    palestine_bel_emb@hotmail.com
    palestine_emb_abuja@yahoo.com
    palestine_emb_mozambique@yahoo.com
    palestinead@hotmail.com
    palestinebg@yahoo.com
    palestinegd@gmail.com
    palestinekorea@hotmail.com
    pgd@planet.nl
    plemb@mofa-gov.ps
    plo@neda.net
    plomission1@aol.com
    plosrilanka@hotmail.com
    ramallah@embassy.mzv.cz
    repkon@ramdk.org
    roem@mofa.ps
    roi_gaza@mtcgaza.com
    saemb@mofa-gov.ps
    sanomat.ram@formin.fi
    sdemb@mofa-gov.ps
    sifmagaz@palnet.com
    skemb@mofa-gov.ps
    snemb@mofa-gov.ps
    vnemb@mofa.pna.ps
    zaemb@mofa-gov.ps
    zmemb@mofa-gov.ps

    https://open.substack.com/pub/husseini/p/to-save-gaza-invoke-the-genocide?r=29hg4d&utm_medium=ios&utm_campaign=post
    To Save Gaza, Invoke the Genocide Convention The ICC is a "puppet institution". What's needed is a country to invoke the Genocide Convention at the International Court of Justice. Here's how, with argument, phone numbers, addresses and emails. Sam Husseini [Addendum: RootsAction and World Beyond War have put out the action alert “It’s Time to Invoke the Genocide Convention”. This full piece has been posted on X/Twitter with thread containing handles for various national leaders who can be petitioned.] Some of the greatest successes in recent human history have combined protest movements with strong diplomatic moves. In February 1998, the Clinton administration seemed poised to inflict a massive attack on Iraq, but vocal opposition from the US public, especially at a CNN town hall meeting in Ohio, combined by UN Secretary General Kofi Annan going to Iraq, repelled the US government attack. The following year, in the Battle of Seattle, combined protests in the streets and delegations from the global south finding their backbone resulted in the World Trade Organization’s plans collapsing. This was a major setback for global corporate interests. There is now effectively a global movement, largely based around mass protests, to stop Israel’s genocide of Palestinians in Gaza. Several countries, including South Africa, Bangladesh, Bolivia, Comoros, Djibouti as well as Colombia and Algeria and Turkey have moved for the International Criminal Court to prosecute Israeli officials. The problem is that ICC has been dragging its heels for years on prosecuting Israelis. It has been called a “white man’s court” after only going after Africans, and, after letting Israel off the hook during an earlier assault on Gaza, “a hoax”. Some of these nations have called Israel’s war crimes “genocide”. They should act on their words and invoke the relevant treaty. Other nations that have been especially critical of Israel are Pakistan, Brazil, Chile, Belize, Jordan, Chad, Honduras, Bahrain, Venezuela, Iran, and Cuba. The International Court of Justice, also called the World Court, in contrast has ruled against Israel. But so far these rulings have been advisory opinions. It ruled against Israel in a case regarding its wall in 2004. In another case before it, is expected to rule against Israel’s long term policies. But what can be done now, Prof. Francis Boyle, who successfully represented the Bosnians before the World Court, argues is to use emergency processes to give more teeth to the World Court. This can be done by invoking the Genocide Convention. This is outlined by Boyle, noted by UN whistleblower Craig Mokhiber, backed by Nobel Peace Prize winner Mairead Maguire, and written about by myself. And most recently by Craig Murray, now a human rights activist who was the British ambassador to Uzbekistan and Rector of the University of Dundee. Murray just wrote the piece “Activating the Genocide Convention” which states: “There are 149 states party to the Genocide Convention. Every one of them has the right to call out the genocide in progress in Gaza and report it to the United Nations. In the event that another state party disputes the claim of genocide — and Israel, the United States and the United Kingdom are all states party — then the International Court of Justice [also called the World Court] is required to adjudicate on ‘the responsibility of a State for genocide.'” Murray quotes from the Genocide Convention and cites evidence that Israel is conducting genocide and that the US and British governments are at minimum complicit in that. He then states: “The International Court of Justice is the most respected of international institutions; while the United States has repudiated its compulsory jurisdiction, the United Kingdom has not and the EU positively accepts it. “If the International Court of Justice makes a determination of genocide, then the International Criminal Court does not have to determine that genocide has happened. This is important because unlike the august and independent ICJ, the ICC is very much a western government puppet institution which will wiggle out of action if it can. But a determination of the ICJ of genocide and of complicity in genocide would reduce the ICC’s task to determining which individuals bear the responsibility. That is a prospect which can indeed alter the calculations of politicians. “It is also the fact that a reference for genocide would force the western media to address the issue and use the term, rather than just pump out propaganda about Hamas fighting bases in hospitals. … “I am afraid the question of why Palestine has not invoked the Genocide Convention takes us somewhere very dark. … It is Fatah who occupy the Palestinian seat at the United Nations, and the decision for Palestine to call into play the Genocide Convention lies with Mahmoud Abbas. It is more and more difficult daily to support Abbas. He seems extraordinarily passive, and the suspicion that he is more concerned with refighting the Palestinian civil war than with resisting the genocide is impossible to shake. By invoking the Genocide Convention he could put himself and Fatah back at the centre of the narrative. But he does nothing. I do not want to believe that corruption and a Blinken promise of inheriting Gaza are Mahmoud’s motivators. But at the moment, I cannot grab on to any other explanation to believe in.” Thus speeches from Abbas and allied Palestinians figures should be viewed extremely skeptically. It is also very odd, to say the very least, that Francesca Albanese, Special Rapporteur on the situation of human rights in the Palestinian Territory occupied since 1967, and other officials put out a statement “Gaza: UN experts call on international community to prevent genocide against the Palestinian people” — but make no mention whatever of the Genocide Convention. As Murray writes: “Any one of the 139 states party could invoke the Genocide Convention against Israel and its co-conspirators. Those states include Iran, Russia, Libya, Malaysia, Bolivia, Venezuela, Brazil, Afghanistan, Cuba, Ireland, Iceland, Jordan, South Africa, Turkey and Qatar. But not one of these states has called out the genocide [by invoking the Convention]. Why? “It is not because the Genocide Convention is a dead letter. It is not. It was invoked against Serbia by Bosnia and Herzegovina and the ICJ ruled against Serbia with regard to the massacre at Srebrenica.” Murray notes that this helped lead to prosecutions. He adds: “Some states may simply not have thought of it. For Arab states in particular, the fact that Palestine itself has not invoked the Genocide Convention may provide an excuse. EU states can hide behind bloc unanimity. “But I am afraid that the truth is that no state cares sufficiently about the thousands of Palestinian children already killed and thousands more who will shortly be killed, to introduce another factor of hostility in their relationship with the United States. Just as at [the recent] summit in Saudi Arabia, where Islamic countries could not agree [on] an oil and gas boycott of Israel, the truth is that those in power really do not care about a genocide in Gaza. They care about their own interests. “It just needs one state to invoke the Genocide Convention and change the narrative and the international dynamic. That will only happen through the power of the people in pressing the idea on their governments. This is where everybody can do a little something to add to the pressure. Please do what you can.” What can you do? Urge countries which have been critical of Israel to invoke the Genocide Convention at the International Court of Justice. Get groups and influential people to make this a primary ask. Protests in NYC should include visits and vigils to the missions of those countries. Activists who have been arrested for protesting against Israel’s slaughter can ask UN officials from countries critical of Israel to invoke the Genocide Convention. Palestinians in Ramallah may be able to directly contact the representatives of various countries to Palestine. This can be done anywhere. Protests in London can respectfully appeal to the embassies of various countries critical of Israel. We need to keep pressing directly against the US and Israeli governments, but their hearts are like stone. If we reach other states to invoke the Genocide Convention, it may be a key stop in curtailing the slaughter. Moreover, it could be a turning point in global relations. Should a positive emergency ruling by the International Court of Justice be forthcoming, it would dramatically isolate the US and Israel at the UN. The US would of course try to block anything at the UN Security Council. But with a World Court ruling, Boyle argues, the stage would be set for the General Assembly to assert itself using the Uniting for Peace procedure. Combined with sustained protests, like the WTO and other critical confrontations, the costs of continuing the slaughter could become unsustainable. Moreover, a World Court ruling could facilitate other legal efforts, like universal jurisdiction. For all that to happen, a country needs to step forward and invoke the Genocide Convention. Make no mistake; any nation that does this may well be targeted in insidious ways by the US and by Israel. Any such nation should be afforded every bit of support people of goodwill can muster. Here's a website that seems to list all the embassies and other diplomatic missions around the world. People from anywhere can be emailing, calling and going to these embassies and missions, urging these countries to use every legal mechanism to pressure Israel to stop, including invoking the Genocide Convention: embassy-worldwide.com. A friend extracted emails of missions to the UN: info@afghanistan-un.org mission.newyork@mfa.gov.al officeofthepr.albania@mfa.gov.al algeriamission.ny@gmail.com contact@andorraun.org theangolamission@angolaun.org unmission@ab.gov.ag jackley.peters@ab.gov.ag enaun@mrecic.gov.ar armenia@missionun.org australiaun@dfat.gov.au new-york-ov@bmeia.gv.at mission@azerbaijanun.org mission@bahamasny.com newyork.mission@mofa.gov.bh bangladeshatun@gmail.com bdpmny@gmail.com prun@foreign.gov.bb barbados@un.int usaun@mfa.gov.by newyorkun@diplobel.fed.be blzun@belizemission.com blzun@aol.com onu.newyork@gouv.bj beninewyork@gmail.com bhutanmission@pmbny.bt missionboliviaun@gmail.com bihun@mvp.gov.ba botswana@un.int distri.delbrasonu@itamaraty.gov.br bruneiunmission@protonmail.com mission.newyork@mfa.bg miperfaso.ny@burkina-onu.org ambabunewyork@yahoo.fr cvpm.unny@mnec.gov.cv cambodia@un.int cameroon.mission@yahoo.com canada.un@international.gc.ca repercaf.ny@gmail.com chadmission.un@gmail.com chile.un@minrel.gob.cl chinesemission@yahoo.com colombia@colombiaun.org comores.nu@gmail.com cgbrazzadel60@gmail.com miscr-onu@rree.go.cr cotedivoiremission@yahoo.com cromiss.un@mvep.hr cuba_onu@cubanmission.com unmission@mfa.gov.cy un.newyork@embassy.mzv.cz dprk.un@verizon.net missiondrc@gmail.com nycmis@um.dk djibouti@nyct.net dominicaun@gmail.com drmun1114@gmail.com onunewyork@cancilleria.gob.ec mission@egyptmissionny.com elsalvador@un.int info@equatorialguineaun.org general@eritreaun.org mission.newyork@mfa.ee eswatini@un.int eswatinimissionunny@yahoo.com ethiopia@un.int mission@fijiprun.org sanomat.yke@gov.fi france@franceonu.org info@gabonunmission.com gambia_un@hotmail.com geomission.un@mfa.gov.ge info@new-york-un.diplo.de ghanaperm@aol.com grdel.un@mfa.gr gmun@mofa.gov.gd onunewyork@minex.gob.gt missionofguinea.un@gmail.com guinebissauonu@gmail.com pmny@mission.gov.gy mphonu.newyork@diplomatie.ht ny.honduras@hnun.org hungaryun.ny@mfa.gov.hu unmission@mfa.is india.newyorkpmi@mea.gov.in ptri@indonesiaun.org iranunny@mfa.gov.ir iraq.mission@iraqmission-un.com newyorkpmun@dfa.ie uninfo@newyork.mfa.gov.il info.italyun@esteri.it info.unmissionny@mfaft.gov.jm p-m-j@dn.mofa.go.jp missionun@jordanmissionun.com unkazmission@gmail.com info@kenyaun.org kimission.newyork@mfa.gov.ki kuwait@kuwaitmissionun.org kyrgyzstan.un.ny@mfa.gov.kg lao.pr.ny@gmail.com mission.un-ny@mfa.gov.lv contact@lebanonun.org lesothonewyork@gmail.com liberiamission@pmun.gov.lr mission@libya-un.gov.ly newyork@llv.li lithuaniaun@gmail.com newyork.rp@mae.etat.lu repermad.ny@gmail.com malawinewyork@aol.com malawiu@aol.com mwnewyorkun@kln.gov.my info@maldivesmission.com miperma@malionu.com malta-un.newyork@gov.mt marshallislands@rmiunmission.org mauritaniamission@gmail.com mauritiusmissionnyc@gmail.com onuusr1@sre.gob.mx fsmun@fsmgov.org monaco.un@gmail.com mongolianmission@twcmetrobiz.com unnewyork.montenegro@gmail.com morocco.un@maec.gov.ma mozambique.unmission@gmail.com myanmarmission@verizon.net info@namibiaunmission.org nauru@un.int nepalmissionusa@gmail.com nyv@minbuza.nl nzpmun@gmail.com nicaraguaunny@yahoo.com nigermission@ymail.com permny@nigeriaunmission.org newyork@mfa.gov.mk delun@mfa.no oman@un.int pakistan@pakun.org mission@palauun.org emb@panama-un.org pngun@pngmission.org paraguay.un@mre.gov.py onuper@unperu.org newyork.pm@nypm.org newyork.pm@dfa.gov.ph poland.un@msz.gov.pl portugal.nu@mne.pt pmun@mofa.gov.qa korea.un@mofa.go.kr unmoldova@mfa.gov.md newyork-onu@mae.ro press@russiaun.ru ambanewyork@minaffet.gov.rw ambanewyork@gmail.com sknmission@aol.com info@stluciamission.org svgmission@gmail.com ambassadorassistantsvg@gmail.com samoa@samoanymission.ws sanmarinoun@gmail.com rdstppmun@gmail.com correspondence@ksamission-gov.net senegal.mission@yahoo.fr info@serbiamissionun.org pr.office@serbiamissionun.org seychellesmissionun@gmail.com seychellesmission@sycun.org sierraleone@pmun.net singaporeun@outlook.com un.newyork@mzv.sk slomission.newyork@gov.si simun@solomons.com somalia@unmission.gov.so pmun.newyork@dirco.gov.za info@rssun-nyc.org rep.nuevayorkonu@maec.es prun.newyork@mfa.gov.lk mail@slmission.com sudan@sudanmission.org suriname_un@proton.me representationen.new-york@gov.se newyork.un@eda.admin.ch syrianmission-ny@sar-un.org tajikistanunmission@gmail.com thaimission.ny@gmail.com timorleste.unmission@gmail.com togo.mission@togounmission.org tongaunmission@gmail.com pmun-ny@trinbago.org tunisia@un.int tunisiamission@usa.com tr-delegation.newyork@mfa.gov.tr turkmenistan.un@mfa.gov.tm tuvalu.unmission@gov.tv admin@ugandaunny.com uno_us@mfa.gov.ua nyunprm@mofaic.gov.ae nyunprm@uaeun.org ukmissionny@gmail.com tanzania.un@nje.go.tz usun.newyork@state.gov urudeleg@mrree.gub.uy uzbekistan.un@gmail.com vanunmis@aol.com misionvenezuelaonu@gmail.com info@vietnam-un.org yemenmissionny@gmail.com un@grz.gov.zm info@zambiamissionun.com zimnewyork@gmail.com office@holyseemission.org admin@palestinemissionun.org aumission_ny@yahoo.com ny.un@las.int aalco@un.int cari.per.obs.un@gmail.com ccampos@sgsica-ny.org newyork@commonwealth.int gccny@gccsg.org ceeaceccasom@gmail.com kjawara-njai@ecowas.int ecowasmission.ny@gmail.com bfaedda@eplo.int delegation-new-york@eeas.europa.eu amparo.morales@filac.org jonathan.granoff@iaca.int dijana.duric@iaca.int un@iccwbo.org nyoffice@interpol.int newyork@idlo.int unobserver@idea.int reper.new-york@francophonie.org nyoffice@irena.org iucn@un.int internationalyouthorganization@un.int uncontact@oecd.org oic.un.ny@gmail.com pam.unny@pam.int srao@ppdsec.org rgarvey@ppdsec.org south@southcentre.int nyinfo@upeace.org ny-office@ipu.org newyork@icrc.org newyork.delegation@ifrc.org ioc-unobserver@olympic.org un.mission.ny@orderofmalta.int faolon-director@fao.org iaeany@un.org liaisonofficeny@icc-cpi.int ifad.ny@ifad.org newyork@ilo.org rpowell@imf.org jlammens@imf.org unofficeny@iom.int seaun@un.org itlos@itlos.org newyork@unesco.org office.newyork@unido.org whonewyork@who.int newyork.office@wipo.int ola.zahran@wipo.int lpaterson@wmo.int laura.paterson@un.org Emails of embassies to and from Palestine via this page. aeoalg@caramail.org alembac@ucomgh.com alestine@intnet.dj aliman@icon.co.zw ambpal@eunet.rs ambpal@eunet.yu auemb@mofa-gov.ps austrep@palnet.com bremb@mofa-gov.ps chinaemb_ps@mfa.gov.cn clemb@mofa-gov.ps cyprusoffice@palnet.com del.palestine@wanadoo.fr deleg.palestinienne@beon.be elian@freemail.hu em.alasad_asad@hotmail.com embagoda.palestine@mad.servicom.es embassy@palestineindia.com embassyofpalestine.portugal@gmail.com embassyofpalestine@gmail.com embpalnic@turbonett.com.in empaltr@gmail.com eosopmet@omantel.net.com falastin@hellasnet.gr fiemb@mofa-gov.ps gdpalestine@swissonline.ch info@gdp.ie info@plo.swieden.org iqemb@mofa-gov.ps jerusalem@mianet.com.ar jerusalem@telesat.com.co jorrep@palnet.com kwemb@mofa-gov.ps lbemb@mofa-gov.ps maemb@mofa-gov.ps ngemb@mofa-gov.ps pal.damas@gmail.com pal_embassy@yahoo.com palango@netangola.com palastinelo@hotmail.com palemb.no@outlook.com palemb1@yemen.net palembassy_ukraine@hotmail.com palembs@qatar.net.qa palembtn@yahoo.com palestcz@mbox.vol.cz palestin@spidernet.com palestine@dsi.net.pk palestine@paltsts-jp.com palestine_bel_emb@hotmail.com palestine_emb_abuja@yahoo.com palestine_emb_mozambique@yahoo.com palestinead@hotmail.com palestinebg@yahoo.com palestinegd@gmail.com palestinekorea@hotmail.com pgd@planet.nl plemb@mofa-gov.ps plo@neda.net plomission1@aol.com plosrilanka@hotmail.com ramallah@embassy.mzv.cz repkon@ramdk.org roem@mofa.ps roi_gaza@mtcgaza.com saemb@mofa-gov.ps sanomat.ram@formin.fi sdemb@mofa-gov.ps sifmagaz@palnet.com skemb@mofa-gov.ps snemb@mofa-gov.ps vnemb@mofa.pna.ps zaemb@mofa-gov.ps zmemb@mofa-gov.ps https://open.substack.com/pub/husseini/p/to-save-gaza-invoke-the-genocide?r=29hg4d&utm_medium=ios&utm_campaign=post
    OPEN.SUBSTACK.COM
    To Save Gaza, Invoke the Genocide Convention
    The ICC is a "puppet institution". What's needed is a country to invoke the Genocide Convention at the International Court of Justice. Here's how, with argument, phone numbers, addresses and emails.
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  • To Save Gaza, Invoke the Genocide Convention

    The ICC is a "puppet institution". What's needed is a country to invoke the Genocide Convention at the International Court of Justice. Here's how, with argument, phone numbers, addresses and emails.
    Sam Husseini





    [Addendum: RootsAction and World Beyond War have put out the action alert “It’s Time to Invoke the Genocide Convention”. This full piece has been posted on X/Twitter with threadcontaining handles for various national leaders who can be petitioned.]

    Some of the greatest successes in recent human history have combined protest movements with strong diplomatic moves.

    In February 1998, the Clinton administration seemed poised to inflict a massive attack on Iraq, but vocal opposition from the US public, especially at a CNN town hall meeting in Ohio, combined by UN Secretary General Kofi Annangoing to Iraq, repelled the US government attack.

    The following year, in the Battle of Seattle, combined protests in the streets and delegations from the global south finding their backbone resulted in the World Trade Organization’s plans collapsing. This was a major setback for global corporate interests.

    There is now effectively a global movement, largely based around mass protests, to stop Israel’s genocide of Palestinians in Gaza.

    Several countries, including South Africa, Bangladesh, Bolivia, Comoros, Djibouti as well as Colombia and Algeria and Turkey have moved for the International Criminal Court to prosecute Israeli officials.

    The problem is that ICC has been dragging its heels for years on prosecuting Israelis. It has been called a “white man’s court” after only going after Africans, and, after letting Israel off the hook during an earlier assault on Gaza, “a hoax”. Some of these nations have called Israel’s war crimes “genocide”. They should act on their words and invoke the relevant treaty. Other nations that have been especially critical of Israel are Pakistan, Brazil, Chile, Belize, Jordan, Chad, Honduras, Bahrain, Venezuela, Iran, and Cuba.

    The International Court of Justice, also called the World Court, in contrast has ruled against Israel. But so far these rulings have been advisory opinions. It ruled against Israel in a case regarding its wall in 2004. In another case before it, is expected to rule against Israel’s long term policies.

    But what can be done now, Prof. Francis Boyle, who successfully represented the Bosnians before the World Court, argues is to use emergency processes to give more teeth to the World Court. This can be done by invoking the Genocide Convention. This is outlined by Boyle, noted by UN whistleblower Craig Mokhiber, backed by Nobel Peace Prize winner Mairead Maguire, and written about by myself. And most recently by Craig Murray, now a human rights activist who was the British ambassador to Uzbekistan and Rector of the University of Dundee.

    Murray just wrote the piece “Activating the Genocide Convention” which states: “There are 149 states party to the Genocide Convention. Every one of them has the right to call out the genocide in progress in Gaza and report it to the United Nations. In the event that another state party disputes the claim of genocide — and Israel, the United States and the United Kingdom are all states party — then the International Court of Justice [also called the World Court] is required to adjudicate on ‘the responsibility of a State for genocide.'”

    Murray quotes from the Genocide Convention and cites evidence that Israel is conducting genocide and that the US and British governments are at minimum complicit in that. He then states: “The International Court of Justice is the most respected of international institutions; while the United States has repudiated its compulsory jurisdiction, the United Kingdom has not and the EU positively accepts it.



    “If the International Court of Justice makes a determination of genocide, then the International Criminal Court does not have to determine that genocide has happened. This is important because unlike the august and independent ICJ, the ICC is very much a western government puppet institution which will wiggle out of action if it can. But a determination of the ICJ of genocide and of complicity in genocide would reduce the ICC’s task to determining which individuals bear the responsibility. That is a prospect which can indeed alter the calculations of politicians.



    “It is also the fact that a reference for genocide would force the western media to address the issue and use the term, rather than just pump out propaganda about Hamas fighting bases in hospitals. …

    “I am afraid the question of why Palestine has not invoked the Genocide Convention takes us somewhere very dark. … It is Fatah who occupy the Palestinian seat at the United Nations, and the decision for Palestine to call into play the Genocide Convention lies with Mahmoud Abbas. It is more and more difficult daily to support Abbas. He seems extraordinarily passive, and the suspicion that he is more concerned with refighting the Palestinian civil war than with resisting the genocide is impossible to shake. By invoking the Genocide Convention he could put himself and Fatah back at the centre of the narrative. But he does nothing. I do not want to believe that corruption and a Blinken promise of inheriting Gaza are Mahmoud’s motivators. But at the moment, I cannot grab on to any other explanation to believe in.”

    Thus speeches from Abbas and allied Palestinians figures should be viewed extremely skeptically. It is also very odd, to say the very least, that Francesca Albanese, Special Rapporteur on the situation of human rights in the Palestinian Territory occupied since 1967, and other officials put out a statement “Gaza: UN experts call on international community to prevent genocide against the Palestinian people” — but make no mention whatever of the Genocide Convention.



    As Murray writes: “Any one of the 139 states party could invoke the Genocide Convention against Israel and its co-conspirators. Those states include Iran, Russia, Libya, Malaysia, Bolivia, Venezuela, Brazil, Afghanistan, Cuba, Ireland, Iceland, Jordan, South Africa, Turkey and Qatar. But not one of these states has called out the genocide [by invoking the Convention]. Why?

    “It is not because the Genocide Convention is a dead letter. It is not. It was invoked against Serbia by Bosnia and Herzegovina and the ICJ ruled against Serbia with regard to the massacre at Srebrenica.” Murray notes that this helped lead to prosecutions.



    He adds: “Some states may simply not have thought of it. For Arab states in particular, the fact that Palestine itself has not invoked the Genocide Convention may provide an excuse. EU states can hide behind bloc unanimity.



    “But I am afraid that the truth is that no state cares sufficiently about the thousands of Palestinian children already killed and thousands more who will shortly be killed, to introduce another factor of hostility in their relationship with the United States. Just as at [the recent] summit in Saudi Arabia, where Islamic countries could not agree [on] an oil and gas boycott of Israel, the truth is that those in power really do not care about a genocide in Gaza. They care about their own interests.



    “It just needs one state to invoke the Genocide Convention and change the narrative and the international dynamic. That will only happen through the power of the people in pressing the idea on their governments. This is where everybody can do a little something to add to the pressure. Please do what you can.”

    What can you do? Urge countries which have been critical of Israel to invoke the Genocide Convention at the International Court of Justice. Get groups and influential people to make this a primary ask.

    Protests in NYC should include visits and vigils to the missions of those countries. Activists who have been arrested for protesting against Israel’s slaughter can ask UN officials from countries critical of Israel to invoke the Genocide Convention.

    Palestinians in Ramallah may be able to directly contact the representatives of various countries to Palestine.

    This can be done anywhere. Protests in London can respectfully appeal to the embassies of various countries critical of Israel.

    We need to keep pressing directly against the US and Israeli governments, but their hearts are like stone. If we reach other states to invoke the Genocide Convention, it may be a key stop in curtailing the slaughter.

    Moreover, it could be a turning point in global relations. Should a positive emergency ruling by the International Court of Justice be forthcoming, it would dramatically isolate the US and Israel at the UN. The US would of course try to block anything at the UN Security Council. But with a World Court ruling, Boyle argues, the stage would be set for the General Assembly to assert itself using the Uniting for Peace procedure. Combined with sustained protests, like the WTO and other critical confrontations, the costs of continuing the slaughter could become unsustainable. Moreover, a World Court ruling could facilitate other legal efforts, like universal jurisdiction.

    For all that to happen, a country needs to step forward and invoke the Genocide Convention.

    Make no mistake; any nation that does this may well be targeted in insidious ways by the US and by Israel. Any such nation should be afforded every bit of support people of goodwill can muster.

    Here's a website that seems to list all the embassies and other diplomatic missions around the world. People from anywhere can be emailing, calling and going to these embassies and missions, urging these countries to use every legal mechanism to pressure Israel to stop, including invoking the Genocide Convention: embassy-worldwide.com.

    A friend extracted emails of missions to the UN:

    info@afghanistan-un.org

    mission.newyork@mfa.gov.al

    officeofthepr.albania@mfa.gov.al

    algeriamission.ny@gmail.com

    contact@andorraun.org

    theangolamission@angolaun.org

    unmission@ab.gov.ag

    jackley.peters@ab.gov.ag

    enaun@mrecic.gov.ar

    armenia@missionun.org

    australiaun@dfat.gov.au

    new-york-ov@bmeia.gv.at

    mission@azerbaijanun.org

    mission@bahamasny.com

    newyork.mission@mofa.gov.bh

    bangladeshatun@gmail.com

    bdpmny@gmail.com

    prun@foreign.gov.bb

    barbados@un.int

    usaun@mfa.gov.by

    newyorkun@diplobel.fed.be

    blzun@belizemission.com

    blzun@aol.com

    onu.newyork@gouv.bj

    beninewyork@gmail.com

    bhutanmission@pmbny.bt

    missionboliviaun@gmail.com

    bihun@mvp.gov.ba

    botswana@un.int

    distri.delbrasonu@itamaraty.gov.br

    bruneiunmission@protonmail.com

    mission.newyork@mfa.bg

    miperfaso.ny@burkina-onu.org

    ambabunewyork@yahoo.fr

    cvpm.unny@mnec.gov.cv

    cambodia@un.int

    cameroon.mission@yahoo.com

    canada.un@international.gc.ca

    repercaf.ny@gmail.com

    chadmission.un@gmail.com

    chile.un@minrel.gob.cl

    chinesemission@yahoo.com

    colombia@colombiaun.org

    comores.nu@gmail.com

    cgbrazzadel60@gmail.com

    miscr-onu@rree.go.cr

    cotedivoiremission@yahoo.com

    cromiss.un@mvep.hr

    cuba_onu@cubanmission.com

    unmission@mfa.gov.cy

    un.newyork@embassy.mzv.cz

    dprk.un@verizon.net

    missiondrc@gmail.com

    nycmis@um.dk

    djibouti@nyct.net

    dominicaun@gmail.com

    drmun1114@gmail.com

    onunewyork@cancilleria.gob.ec

    mission@egyptmissionny.com

    elsalvador@un.int

    info@equatorialguineaun.org

    general@eritreaun.org

    mission.newyork@mfa.ee

    eswatini@un.int

    eswatinimissionunny@yahoo.com

    ethiopia@un.int

    mission@fijiprun.org

    sanomat.yke@gov.fi

    france@franceonu.org

    info@gabonunmission.com

    gambia_un@hotmail.com

    geomission.un@mfa.gov.ge

    info@new-york-un.diplo.de

    ghanaperm@aol.com

    grdel.un@mfa.gr

    gmun@mofa.gov.gd

    onunewyork@minex.gob.gt

    missionofguinea.un@gmail.com

    guinebissauonu@gmail.com

    pmny@mission.gov.gy

    mphonu.newyork@diplomatie.ht

    ny.honduras@hnun.org

    hungaryun.ny@mfa.gov.hu

    unmission@mfa.is

    india.newyorkpmi@mea.gov.in

    ptri@indonesiaun.org

    iranunny@mfa.gov.ir

    iraq.mission@iraqmission-un.com

    newyorkpmun@dfa.ie

    uninfo@newyork.mfa.gov.il

    info.italyun@esteri.it

    info.unmissionny@mfaft.gov.jm

    p-m-j@dn.mofa.go.jp

    missionun@jordanmissionun.com

    unkazmission@gmail.com

    info@kenyaun.org

    kimission.newyork@mfa.gov.ki

    kuwait@kuwaitmissionun.org

    kyrgyzstan.un.ny@mfa.gov.kg

    lao.pr.ny@gmail.com

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    Urge Governments to Invoke the Genocide Convention to Stop the War on Gaza

    https://worldbeyondwar.org/gaza-genocide/
    To Save Gaza, Invoke the Genocide Convention The ICC is a "puppet institution". What's needed is a country to invoke the Genocide Convention at the International Court of Justice. Here's how, with argument, phone numbers, addresses and emails. Sam Husseini [Addendum: RootsAction and World Beyond War have put out the action alert “It’s Time to Invoke the Genocide Convention”. This full piece has been posted on X/Twitter with threadcontaining handles for various national leaders who can be petitioned.] Some of the greatest successes in recent human history have combined protest movements with strong diplomatic moves. In February 1998, the Clinton administration seemed poised to inflict a massive attack on Iraq, but vocal opposition from the US public, especially at a CNN town hall meeting in Ohio, combined by UN Secretary General Kofi Annangoing to Iraq, repelled the US government attack. The following year, in the Battle of Seattle, combined protests in the streets and delegations from the global south finding their backbone resulted in the World Trade Organization’s plans collapsing. This was a major setback for global corporate interests. There is now effectively a global movement, largely based around mass protests, to stop Israel’s genocide of Palestinians in Gaza. Several countries, including South Africa, Bangladesh, Bolivia, Comoros, Djibouti as well as Colombia and Algeria and Turkey have moved for the International Criminal Court to prosecute Israeli officials. The problem is that ICC has been dragging its heels for years on prosecuting Israelis. It has been called a “white man’s court” after only going after Africans, and, after letting Israel off the hook during an earlier assault on Gaza, “a hoax”. Some of these nations have called Israel’s war crimes “genocide”. They should act on their words and invoke the relevant treaty. Other nations that have been especially critical of Israel are Pakistan, Brazil, Chile, Belize, Jordan, Chad, Honduras, Bahrain, Venezuela, Iran, and Cuba. The International Court of Justice, also called the World Court, in contrast has ruled against Israel. But so far these rulings have been advisory opinions. It ruled against Israel in a case regarding its wall in 2004. In another case before it, is expected to rule against Israel’s long term policies. But what can be done now, Prof. Francis Boyle, who successfully represented the Bosnians before the World Court, argues is to use emergency processes to give more teeth to the World Court. This can be done by invoking the Genocide Convention. This is outlined by Boyle, noted by UN whistleblower Craig Mokhiber, backed by Nobel Peace Prize winner Mairead Maguire, and written about by myself. And most recently by Craig Murray, now a human rights activist who was the British ambassador to Uzbekistan and Rector of the University of Dundee. Murray just wrote the piece “Activating the Genocide Convention” which states: “There are 149 states party to the Genocide Convention. Every one of them has the right to call out the genocide in progress in Gaza and report it to the United Nations. In the event that another state party disputes the claim of genocide — and Israel, the United States and the United Kingdom are all states party — then the International Court of Justice [also called the World Court] is required to adjudicate on ‘the responsibility of a State for genocide.'” Murray quotes from the Genocide Convention and cites evidence that Israel is conducting genocide and that the US and British governments are at minimum complicit in that. He then states: “The International Court of Justice is the most respected of international institutions; while the United States has repudiated its compulsory jurisdiction, the United Kingdom has not and the EU positively accepts it. “If the International Court of Justice makes a determination of genocide, then the International Criminal Court does not have to determine that genocide has happened. This is important because unlike the august and independent ICJ, the ICC is very much a western government puppet institution which will wiggle out of action if it can. But a determination of the ICJ of genocide and of complicity in genocide would reduce the ICC’s task to determining which individuals bear the responsibility. That is a prospect which can indeed alter the calculations of politicians. “It is also the fact that a reference for genocide would force the western media to address the issue and use the term, rather than just pump out propaganda about Hamas fighting bases in hospitals. … “I am afraid the question of why Palestine has not invoked the Genocide Convention takes us somewhere very dark. … It is Fatah who occupy the Palestinian seat at the United Nations, and the decision for Palestine to call into play the Genocide Convention lies with Mahmoud Abbas. It is more and more difficult daily to support Abbas. He seems extraordinarily passive, and the suspicion that he is more concerned with refighting the Palestinian civil war than with resisting the genocide is impossible to shake. By invoking the Genocide Convention he could put himself and Fatah back at the centre of the narrative. But he does nothing. I do not want to believe that corruption and a Blinken promise of inheriting Gaza are Mahmoud’s motivators. But at the moment, I cannot grab on to any other explanation to believe in.” Thus speeches from Abbas and allied Palestinians figures should be viewed extremely skeptically. It is also very odd, to say the very least, that Francesca Albanese, Special Rapporteur on the situation of human rights in the Palestinian Territory occupied since 1967, and other officials put out a statement “Gaza: UN experts call on international community to prevent genocide against the Palestinian people” — but make no mention whatever of the Genocide Convention. As Murray writes: “Any one of the 139 states party could invoke the Genocide Convention against Israel and its co-conspirators. Those states include Iran, Russia, Libya, Malaysia, Bolivia, Venezuela, Brazil, Afghanistan, Cuba, Ireland, Iceland, Jordan, South Africa, Turkey and Qatar. But not one of these states has called out the genocide [by invoking the Convention]. Why? “It is not because the Genocide Convention is a dead letter. It is not. It was invoked against Serbia by Bosnia and Herzegovina and the ICJ ruled against Serbia with regard to the massacre at Srebrenica.” Murray notes that this helped lead to prosecutions. He adds: “Some states may simply not have thought of it. For Arab states in particular, the fact that Palestine itself has not invoked the Genocide Convention may provide an excuse. EU states can hide behind bloc unanimity. “But I am afraid that the truth is that no state cares sufficiently about the thousands of Palestinian children already killed and thousands more who will shortly be killed, to introduce another factor of hostility in their relationship with the United States. Just as at [the recent] summit in Saudi Arabia, where Islamic countries could not agree [on] an oil and gas boycott of Israel, the truth is that those in power really do not care about a genocide in Gaza. They care about their own interests. “It just needs one state to invoke the Genocide Convention and change the narrative and the international dynamic. That will only happen through the power of the people in pressing the idea on their governments. This is where everybody can do a little something to add to the pressure. Please do what you can.” What can you do? Urge countries which have been critical of Israel to invoke the Genocide Convention at the International Court of Justice. Get groups and influential people to make this a primary ask. Protests in NYC should include visits and vigils to the missions of those countries. Activists who have been arrested for protesting against Israel’s slaughter can ask UN officials from countries critical of Israel to invoke the Genocide Convention. Palestinians in Ramallah may be able to directly contact the representatives of various countries to Palestine. This can be done anywhere. Protests in London can respectfully appeal to the embassies of various countries critical of Israel. We need to keep pressing directly against the US and Israeli governments, but their hearts are like stone. If we reach other states to invoke the Genocide Convention, it may be a key stop in curtailing the slaughter. Moreover, it could be a turning point in global relations. Should a positive emergency ruling by the International Court of Justice be forthcoming, it would dramatically isolate the US and Israel at the UN. The US would of course try to block anything at the UN Security Council. But with a World Court ruling, Boyle argues, the stage would be set for the General Assembly to assert itself using the Uniting for Peace procedure. Combined with sustained protests, like the WTO and other critical confrontations, the costs of continuing the slaughter could become unsustainable. Moreover, a World Court ruling could facilitate other legal efforts, like universal jurisdiction. For all that to happen, a country needs to step forward and invoke the Genocide Convention. Make no mistake; any nation that does this may well be targeted in insidious ways by the US and by Israel. Any such nation should be afforded every bit of support people of goodwill can muster. Here's a website that seems to list all the embassies and other diplomatic missions around the world. People from anywhere can be emailing, calling and going to these embassies and missions, urging these countries to use every legal mechanism to pressure Israel to stop, including invoking the Genocide Convention: embassy-worldwide.com. A friend extracted emails of missions to the UN: info@afghanistan-un.org mission.newyork@mfa.gov.al officeofthepr.albania@mfa.gov.al algeriamission.ny@gmail.com contact@andorraun.org theangolamission@angolaun.org unmission@ab.gov.ag jackley.peters@ab.gov.ag enaun@mrecic.gov.ar armenia@missionun.org australiaun@dfat.gov.au new-york-ov@bmeia.gv.at mission@azerbaijanun.org mission@bahamasny.com newyork.mission@mofa.gov.bh bangladeshatun@gmail.com bdpmny@gmail.com prun@foreign.gov.bb barbados@un.int usaun@mfa.gov.by newyorkun@diplobel.fed.be blzun@belizemission.com blzun@aol.com onu.newyork@gouv.bj beninewyork@gmail.com bhutanmission@pmbny.bt missionboliviaun@gmail.com bihun@mvp.gov.ba botswana@un.int distri.delbrasonu@itamaraty.gov.br bruneiunmission@protonmail.com mission.newyork@mfa.bg miperfaso.ny@burkina-onu.org ambabunewyork@yahoo.fr cvpm.unny@mnec.gov.cv cambodia@un.int cameroon.mission@yahoo.com canada.un@international.gc.ca repercaf.ny@gmail.com chadmission.un@gmail.com chile.un@minrel.gob.cl chinesemission@yahoo.com colombia@colombiaun.org comores.nu@gmail.com cgbrazzadel60@gmail.com miscr-onu@rree.go.cr cotedivoiremission@yahoo.com cromiss.un@mvep.hr cuba_onu@cubanmission.com unmission@mfa.gov.cy un.newyork@embassy.mzv.cz dprk.un@verizon.net missiondrc@gmail.com nycmis@um.dk djibouti@nyct.net dominicaun@gmail.com drmun1114@gmail.com onunewyork@cancilleria.gob.ec mission@egyptmissionny.com elsalvador@un.int info@equatorialguineaun.org general@eritreaun.org mission.newyork@mfa.ee eswatini@un.int eswatinimissionunny@yahoo.com ethiopia@un.int mission@fijiprun.org sanomat.yke@gov.fi france@franceonu.org info@gabonunmission.com gambia_un@hotmail.com geomission.un@mfa.gov.ge info@new-york-un.diplo.de ghanaperm@aol.com grdel.un@mfa.gr gmun@mofa.gov.gd onunewyork@minex.gob.gt missionofguinea.un@gmail.com guinebissauonu@gmail.com pmny@mission.gov.gy mphonu.newyork@diplomatie.ht ny.honduras@hnun.org hungaryun.ny@mfa.gov.hu unmission@mfa.is india.newyorkpmi@mea.gov.in ptri@indonesiaun.org iranunny@mfa.gov.ir iraq.mission@iraqmission-un.com newyorkpmun@dfa.ie uninfo@newyork.mfa.gov.il info.italyun@esteri.it info.unmissionny@mfaft.gov.jm p-m-j@dn.mofa.go.jp missionun@jordanmissionun.com unkazmission@gmail.com info@kenyaun.org kimission.newyork@mfa.gov.ki kuwait@kuwaitmissionun.org kyrgyzstan.un.ny@mfa.gov.kg lao.pr.ny@gmail.com mission.un-ny@mfa.gov.lv contact@lebanonun.org lesothonewyork@gmail.com liberiamission@pmun.gov.lr mission@libya-un.gov.ly newyork@llv.li lithuaniaun@gmail.com newyork.rp@mae.etat.lu repermad.ny@gmail.com malawinewyork@aol.com malawiu@aol.com mwnewyorkun@kln.gov.my info@maldivesmission.com miperma@malionu.com malta-un.newyork@gov.mt marshallislands@rmiunmission.org mauritaniamission@gmail.com mauritiusmissionnyc@gmail.com onuusr1@sre.gob.mx fsmun@fsmgov.org monaco.un@gmail.com mongolianmission@twcmetrobiz.com unnewyork.montenegro@gmail.com morocco.un@maec.gov.ma mozambique.unmission@gmail.com myanmarmission@verizon.net info@namibiaunmission.org nauru@un.int nepalmissionusa@gmail.com nyv@minbuza.nl nzpmun@gmail.com nicaraguaunny@yahoo.com nigermission@ymail.com permny@nigeriaunmission.org newyork@mfa.gov.mk delun@mfa.no oman@un.int pakistan@pakun.org mission@palauun.org emb@panama-un.org pngun@pngmission.org paraguay.un@mre.gov.py onuper@unperu.org newyork.pm@nypm.org newyork.pm@dfa.gov.ph poland.un@msz.gov.pl portugal.nu@mne.pt pmun@mofa.gov.qa korea.un@mofa.go.kr unmoldova@mfa.gov.md newyork-onu@mae.ro press@russiaun.ru ambanewyork@minaffet.gov.rw ambanewyork@gmail.com sknmission@aol.com info@stluciamission.org svgmission@gmail.com ambassadorassistantsvg@gmail.com samoa@samoanymission.ws sanmarinoun@gmail.com rdstppmun@gmail.com correspondence@ksamission-gov.net senegal.mission@yahoo.fr info@serbiamissionun.org pr.office@serbiamissionun.org seychellesmissionun@gmail.com seychellesmission@sycun.org sierraleone@pmun.net singaporeun@outlook.com un.newyork@mzv.sk slomission.newyork@gov.si simun@solomons.com somalia@unmission.gov.so pmun.newyork@dirco.gov.za info@rssun-nyc.org rep.nuevayorkonu@maec.es prun.newyork@mfa.gov.lk mail@slmission.com sudan@sudanmission.org suriname_un@proton.me representationen.new-york@gov.se newyork.un@eda.admin.ch syrianmission-ny@sar-un.org tajikistanunmission@gmail.com thaimission.ny@gmail.com timorleste.unmission@gmail.com togo.mission@togounmission.org tongaunmission@gmail.com pmun-ny@trinbago.org tunisia@un.int tunisiamission@usa.com tr-delegation.newyork@mfa.gov.tr turkmenistan.un@mfa.gov.tm tuvalu.unmission@gov.tv admin@ugandaunny.com uno_us@mfa.gov.ua nyunprm@mofaic.gov.ae nyunprm@uaeun.org ukmissionny@gmail.com tanzania.un@nje.go.tz usun.newyork@state.gov urudeleg@mrree.gub.uy uzbekistan.un@gmail.com vanunmis@aol.com misionvenezuelaonu@gmail.com info@vietnam-un.org yemenmissionny@gmail.com un@grz.gov.zm info@zambiamissionun.com zimnewyork@gmail.com office@holyseemission.org admin@palestinemissionun.org aumission_ny@yahoo.com ny.un@las.int aalco@un.int cari.per.obs.un@gmail.com ccampos@sgsica-ny.org newyork@commonwealth.int gccny@gccsg.org ceeaceccasom@gmail.com kjawara-njai@ecowas.int ecowasmission.ny@gmail.com bfaedda@eplo.int delegation-new-york@eeas.europa.eu amparo.morales@filac.org jonathan.granoff@iaca.int dijana.duric@iaca.int un@iccwbo.org nyoffice@interpol.int newyork@idlo.int unobserver@idea.int reper.new-york@francophonie.org nyoffice@irena.org iucn@un.int internationalyouthorganization@un.int uncontact@oecd.org oic.un.ny@gmail.com pam.unny@pam.int srao@ppdsec.org rgarvey@ppdsec.org south@southcentre.int nyinfo@upeace.org ny-office@ipu.org newyork@icrc.org newyork.delegation@ifrc.org ioc-unobserver@olympic.org un.mission.ny@orderofmalta.int faolon-director@fao.org iaeany@un.org liaisonofficeny@icc-cpi.int ifad.ny@ifad.org newyork@ilo.org rpowell@imf.org jlammens@imf.org unofficeny@iom.int seaun@un.org itlos@itlos.org newyork@unesco.org office.newyork@unido.org whonewyork@who.int newyork.office@wipo.int ola.zahran@wipo.int lpaterson@wmo.int laura.paterson@un.org Emails of embassies to and from Palestine via this page. aeoalg@caramail.org alembac@ucomgh.com alestine@intnet.dj aliman@icon.co.zw ambpal@eunet.rs ambpal@eunet.yu auemb@mofa-gov.ps austrep@palnet.com bremb@mofa-gov.ps chinaemb_ps@mfa.gov.cn clemb@mofa-gov.ps cyprusoffice@palnet.com del.palestine@wanadoo.fr deleg.palestinienne@beon.be elian@freemail.hu em.alasad_asad@hotmail.com embagoda.palestine@mad.servicom.es embassy@palestineindia.com embassyofpalestine.portugal@gmail.com embassyofpalestine@gmail.com embpalnic@turbonett.com.in empaltr@gmail.com eosopmet@omantel.net.com falastin@hellasnet.gr fiemb@mofa-gov.ps gdpalestine@swissonline.ch info@gdp.ie info@plo.swieden.org iqemb@mofa-gov.ps jerusalem@mianet.com.ar jerusalem@telesat.com.co jorrep@palnet.com kwemb@mofa-gov.ps lbemb@mofa-gov.ps maemb@mofa-gov.ps ngemb@mofa-gov.ps pal.damas@gmail.com pal_embassy@yahoo.com palango@netangola.com palastinelo@hotmail.com palemb.no@outlook.com palemb1@yemen.net palembassy_ukraine@hotmail.com palembs@qatar.net.qa palembtn@yahoo.com palestcz@mbox.vol.cz palestin@spidernet.com palestine@dsi.net.pk palestine@paltsts-jp.com palestine_bel_emb@hotmail.com palestine_emb_abuja@yahoo.com palestine_emb_mozambique@yahoo.com palestinead@hotmail.com palestinebg@yahoo.com palestinegd@gmail.com palestinekorea@hotmail.com pgd@planet.nl plemb@mofa-gov.ps plo@neda.net plomission1@aol.com plosrilanka@hotmail.com ramallah@embassy.mzv.cz repkon@ramdk.org roem@mofa.ps roi_gaza@mtcgaza.com saemb@mofa-gov.ps sanomat.ram@formin.fi sdemb@mofa-gov.ps sifmagaz@palnet.com skemb@mofa-gov.ps snemb@mofa-gov.ps vnemb@mofa.pna.ps zaemb@mofa-gov.ps zmemb@mofa-gov.ps Urge Governments to Invoke the Genocide Convention to Stop the War on Gaza https://worldbeyondwar.org/gaza-genocide/
    WORLDBEYONDWAR.ORG
    GENOCIDE - World BEYOND War
    Let's use the law to stop the killing in Gaza. #WorldBEYONDWar
    2 Kommentare 0 Anteile 30572 Ansichten
  • Human Serum Albumin is human cells from aborted fetus (diploid cells). Injecting this into the body producing autoimmune conditions.

    https://www.westonaprice.org/health-topics/vaccinations/adjuvants-in-vaccines/#gsc.tab=0

    See also:
    https://journals.plos.org/plosone/article?id=10.1371/journal.pone.0104426
    Human Serum Albumin is human cells from aborted fetus (diploid cells). Injecting this into the body producing autoimmune conditions. https://www.westonaprice.org/health-topics/vaccinations/adjuvants-in-vaccines/#gsc.tab=0 See also: https://journals.plos.org/plosone/article?id=10.1371/journal.pone.0104426
    WWW.WESTONAPRICE.ORG
    Adjuvants in Vaccines
    The Toxic Ingredients in Innoculations Most people who vaccinate their children do not realize the kind of ingredients contained in vaccines—and even if they do know, they may […]
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    0 Kommentare 1 Anteile 728 Ansichten
  • Did Israel build a bunker under al-Shifa hospital?
    Ali Abunimah 16 November 2023



    Israel’s ongoing assault on al-Shifa hospital – where 7,000 people are currently besieged in desperate conditions – may be part of its attempt to prove its claims that Hamas operates a sophisticated command bunker under the hospital.
    That James Bond villain-like lair was depicted in an animation released by the Israeli army last month.

    Israel has never offered any evidence for its claims. But as I explain in the video at the top of this article recorded on Wednesday, its assertions go back to at least 2009.



    That year, The New York Times reported that “The Israeli intelligence chief, Yuval Diskin, in a report to the Israeli cabinet, said that the Gaza-based leadership of Hamas was in underground housing beneath the No. 2 building of al Shifa hospital, the largest in Gaza. That allegation cannot be confirmed.”
    Also in 2009, Haaretz reported that “Senior Hamas officials in Gaza are hiding out in a ‘bunker’ built by Israel, intelligence officials suspect.”

    “Many are believed to be in the basements of the al-Shifa hospital complex in Gaza City, which was refurbished during Israel’s occupation of the Gaza Strip,” the Tel Aviv newspaper added.

    And in 2014, the pro-Israel publication Tablet asserted that “The Israelis are so sure about the location of the Hamas bunker … not because they are trying to score propaganda points, or because it has been repeatedly mentioned in passing by Western reporters – but because they built it.”

    “Back in 1983, when Israel still ruled Gaza, they built a secure underground operating room and tunnel network beneath al-Shifa hospital – which is one among several reasons why Israeli security sources are so sure that there is a main Hamas command bunker in or around the large cement basement beneath the area of Building 2 of the hospital,” Tablet added.

    Israel claims it destroyed underground infrastructure in 2021

    During its assault on Gaza in May 2021, Israel heavily bombed the area around al-Shifa, perpetrating what came to be known as the al-Wihda Street massacre.

    “The air raids turned one of the busiest streets in Gaza, and the main access point to the strip’s chief hospital al-Shifa, into a crater-marked moonscape,” Britain’s The Independent reported at the time.

    “In place of apartment blocks are mangled heaps of concrete fringed with curls of iron rebar and scraps of belongings.”

    When challenged over the death and devastation its attacks caused to apartment buildings and their civilian residents near al-Shifa, the Israeli military claimed that it was attacking “underground military infrastructure” that was located under the road.

    “The underground military facilities collapsed causing the foundations of the civilian houses above them to collapse as well leading to unintended casualties,” the army added.

    Israel never presented any evidence to support these claims.

    But now, as it besieges and attacks the hospital again, Israel expects the world to believe that Hamas would keep its main command center in exactly the location Israeli and American newspapers have said it is in for years, and which Israel asserted in 2021 had been substantially destroyed.

    Still, given Israel’s propensity to lie, it may well “discover” an underground facility which Israel itself built, and try to present it to the world as vindication of its accusations.

    Israel releases more videos

    On Thursday evening, the Israeli military released a video showing a cache of weapons displayed on the ground in an outdoor area, that it claims was found in al-Shifa hospital.

    The military offered no evidence that the weapons – about a half dozen rifles, some magazines, hand grenades and what appears to be a drill – were found inside the hospital.



    It also released a video showing what it claims is the entrance to a tunnel near the hospital. The brief video shows a hole in the ground surrounded by overturned earth and rubble, making it difficult to discern what is depicted.
    Earlier this month, Israel claimed to have found the entrance to a Hamas tunnel near the Qatari-funded Sheikh Hamad hospital. The opening was in fact a water reservoir for the hospital.





    Biden admits “indiscriminate bombing” by Israel

    Trapped inside al-Shifa, some 7,000 people face a catastrophic situation and a slow death, without a water supply, food, medicine, medical oxygen, fuel or electricity.

    On Thursday, Israel continued to lay siege to al-Shifa as its troops ransacked buildings and bulldozers carried out excavations around the hospital and its grounds, including severing the main water line.

    This comes as US President Joe Biden continued to push Israel’s claims that Hamas uses the hospital as a command center.

    He also repeated previously debunked atrocity propaganda that Hamas fighters beheaded and burned dozens of Israeli babies on 7 October.

    And despite other comments Wednesday evening that show Biden to be out of touch with the realities of the situation, he did inadvertently admit that Israel has been bombing Gaza indiscriminately.

    Defending what he claimed was a careful Israeli assault on al-Shifa, the president said “this is a different story than I believe was occurring before, an indiscriminate bombing.”

    This admission means there can be no doubt that Biden has been arming Israel while knowing it is indiscriminately killing civilians, including thousands of children – a confession that will be of great interest to those trying to hold him legally accountable for war crimes and stop the slaughter in Gaza.



    Patients dying

    Speaking with Al Jazeera Arabic on Thursday, al-Shifa hospital’s director Dr. Muhammad Abu Salmiya said that one dialysis patient had died earlier in the day and four others faced imminent death.

    In total the hospital is caring for 45 patients who require dialysis – something they can’t receive with no electricity to run the machines.



    Two of some 650 injured people had died because staff could not provide effective treatment. Wounds he said are becoming seriously infected, some with maggots.
    Of 39 premature babies in the hospital, three had died in recent days, according to Abu Salmiya.

    With no electricity or fuel, incubators have stopped functioning. Purified water to make special formula for the babies has run out, so staff are using ordinary water and some of the infants are now sick with diarrhea, infections and fever.



    Thousands of displaced people, many of them children, have no food and are suffering from worsening desperation and hunger.
    Meanwhile, according to Dr. Abu Salmiya, the hospital compound is besieged from all sides by tanks and bulldozers, but no one can see clearly what they are doing.

    He said that anyone who tries to move between hospital buildings is shot at by snipers or drones.

    Israelis refuse to speak

    According to Dr. Abu Salmiya, hospital administrators tried to send a delegation to speak with the Israeli military and ask for food, water, fuel, medicine and other urgent relief supplies.

    On Wednesday, Israel presented a few guns and other equipment it claims to have found in one al-Shifa hospital building.

    The so-called evidence did not corroborate Israel’s longstanding claims that Hamas has a sophisticated command bunker under the hospital.

    It was met with the same widespread skepticism and derision as the farcical “evidence” of Hamas activity that Israel offered after it raided the Rantisi children’s hospital days earlier.

    Over the 48 hours that Israeli forces have occupied parts of the al-Shifa compound, no shots have been fired at them, according to Dr. Abu Salmiya.

    Palestinian resistance groups have firmly denied they use hospitals for military activities and have regularly called for impartial international bodies to visit the hospitals and investigate Israel’s claims.

    “Israeli soldiers briefly exchanged fire with gunmen outside the hospital before going in, a senior military official said, but more than 12 hours after it began, the operation appeared more like a police raid than a pitched battle,” The New York Times reported on Wednesday.

    The newspaper quoted a witness inside the hospital recounting that the Israelis “are digging and excavating and breaking tiles and looking.”

    While there is a particular focus on al-Shifa, Israel is also now laying siege to al-Ahli hospital in Gaza City.



    Biden repeats Israeli lies

    On Wednesday evening, President Joe Biden repeated Israeli assertions that Hamas has a major command center located under al-Shifa hospital.

    “Here’s the situation,” Biden told reporters after meeting with China’s President Xi Jinping in San Francisco. “You have a circumstance where the first war crime is being committed by Hamas by having their headquarters, their military hidden under a hospital. And that’s a fact. That’s what’s happened.”

    Administration officials have made similar assertions in recent days but have adamantly declined to offer any evidence for them. Nonetheless, they are a green light for Israel’s attack on al-Shifa.

    “We’ve discussed the need for them to be incredibly careful,” Biden added. “You have a circumstance where you know there is a fair number of Hamas terrorists. Hamas has already said publicly that they plan on attacking Israel again like they did before, to where they were cutting babies’ heads off to burn – burning women and children alive.”

    Last month Biden notoriously stated that he had seen photos corroborating Israeli claims that Palestinian fighters had beheaded dozens of beheaded babies, before the White House had to admit the president had been shown no such photos.

    Israel has presented no evidence for that claim and many of its other assertions. Meanwhile there’s a growing body of evidence that Israeli forces killed many of their own civilians on and after 7 October.

    Defending Israel’s actions at al-Shifa, Biden asserted, “they’re also bringing in incubators. They’re bringing in other – other means to help the people in the hospital, and they’ve given the doctors and – I’m told – the doctors and nurses and personnel an opportunity to get out of harm’s way.”

    Were Biden well-informed, he would know that al-Shifa and other hospitals in Gaza do not lack incubators, but the electricity and fuel to power them.

    Notably, al-Shifa director Abu Salmiya told Al Jazeera earlier that the Israelis had delivered no supplies to the hospital – in spite of propaganda by the Israeli army designed to market its attack on the hospital as a “humanitarian” operation.

    Abu Salmiya said that despite the dire circumstances, the medical staff would not abandon their patients and would stay there and die with them if it came to that.

    Operation Al-Aqsa Flood
    al-Shifa Hospital


    https://electronicintifada.net/blogs/ali-abunimah/did-israel-build-bunker-under-al-shifa-hospital

    👇https://donshafi911.blogspot.com/2023/11/did-israel-build-bunker-under-al-shifa.html
    Did Israel build a bunker under al-Shifa hospital? Ali Abunimah 16 November 2023 Israel’s ongoing assault on al-Shifa hospital – where 7,000 people are currently besieged in desperate conditions – may be part of its attempt to prove its claims that Hamas operates a sophisticated command bunker under the hospital. That James Bond villain-like lair was depicted in an animation released by the Israeli army last month. Israel has never offered any evidence for its claims. But as I explain in the video at the top of this article recorded on Wednesday, its assertions go back to at least 2009. That year, The New York Times reported that “The Israeli intelligence chief, Yuval Diskin, in a report to the Israeli cabinet, said that the Gaza-based leadership of Hamas was in underground housing beneath the No. 2 building of al Shifa hospital, the largest in Gaza. That allegation cannot be confirmed.” Also in 2009, Haaretz reported that “Senior Hamas officials in Gaza are hiding out in a ‘bunker’ built by Israel, intelligence officials suspect.” “Many are believed to be in the basements of the al-Shifa hospital complex in Gaza City, which was refurbished during Israel’s occupation of the Gaza Strip,” the Tel Aviv newspaper added. And in 2014, the pro-Israel publication Tablet asserted that “The Israelis are so sure about the location of the Hamas bunker … not because they are trying to score propaganda points, or because it has been repeatedly mentioned in passing by Western reporters – but because they built it.” “Back in 1983, when Israel still ruled Gaza, they built a secure underground operating room and tunnel network beneath al-Shifa hospital – which is one among several reasons why Israeli security sources are so sure that there is a main Hamas command bunker in or around the large cement basement beneath the area of Building 2 of the hospital,” Tablet added. Israel claims it destroyed underground infrastructure in 2021 During its assault on Gaza in May 2021, Israel heavily bombed the area around al-Shifa, perpetrating what came to be known as the al-Wihda Street massacre. “The air raids turned one of the busiest streets in Gaza, and the main access point to the strip’s chief hospital al-Shifa, into a crater-marked moonscape,” Britain’s The Independent reported at the time. “In place of apartment blocks are mangled heaps of concrete fringed with curls of iron rebar and scraps of belongings.” When challenged over the death and devastation its attacks caused to apartment buildings and their civilian residents near al-Shifa, the Israeli military claimed that it was attacking “underground military infrastructure” that was located under the road. “The underground military facilities collapsed causing the foundations of the civilian houses above them to collapse as well leading to unintended casualties,” the army added. Israel never presented any evidence to support these claims. But now, as it besieges and attacks the hospital again, Israel expects the world to believe that Hamas would keep its main command center in exactly the location Israeli and American newspapers have said it is in for years, and which Israel asserted in 2021 had been substantially destroyed. Still, given Israel’s propensity to lie, it may well “discover” an underground facility which Israel itself built, and try to present it to the world as vindication of its accusations. Israel releases more videos On Thursday evening, the Israeli military released a video showing a cache of weapons displayed on the ground in an outdoor area, that it claims was found in al-Shifa hospital. The military offered no evidence that the weapons – about a half dozen rifles, some magazines, hand grenades and what appears to be a drill – were found inside the hospital. It also released a video showing what it claims is the entrance to a tunnel near the hospital. The brief video shows a hole in the ground surrounded by overturned earth and rubble, making it difficult to discern what is depicted. Earlier this month, Israel claimed to have found the entrance to a Hamas tunnel near the Qatari-funded Sheikh Hamad hospital. The opening was in fact a water reservoir for the hospital. Biden admits “indiscriminate bombing” by Israel Trapped inside al-Shifa, some 7,000 people face a catastrophic situation and a slow death, without a water supply, food, medicine, medical oxygen, fuel or electricity. On Thursday, Israel continued to lay siege to al-Shifa as its troops ransacked buildings and bulldozers carried out excavations around the hospital and its grounds, including severing the main water line. This comes as US President Joe Biden continued to push Israel’s claims that Hamas uses the hospital as a command center. He also repeated previously debunked atrocity propaganda that Hamas fighters beheaded and burned dozens of Israeli babies on 7 October. And despite other comments Wednesday evening that show Biden to be out of touch with the realities of the situation, he did inadvertently admit that Israel has been bombing Gaza indiscriminately. Defending what he claimed was a careful Israeli assault on al-Shifa, the president said “this is a different story than I believe was occurring before, an indiscriminate bombing.” This admission means there can be no doubt that Biden has been arming Israel while knowing it is indiscriminately killing civilians, including thousands of children – a confession that will be of great interest to those trying to hold him legally accountable for war crimes and stop the slaughter in Gaza. Patients dying Speaking with Al Jazeera Arabic on Thursday, al-Shifa hospital’s director Dr. Muhammad Abu Salmiya said that one dialysis patient had died earlier in the day and four others faced imminent death. In total the hospital is caring for 45 patients who require dialysis – something they can’t receive with no electricity to run the machines. Two of some 650 injured people had died because staff could not provide effective treatment. Wounds he said are becoming seriously infected, some with maggots. Of 39 premature babies in the hospital, three had died in recent days, according to Abu Salmiya. With no electricity or fuel, incubators have stopped functioning. Purified water to make special formula for the babies has run out, so staff are using ordinary water and some of the infants are now sick with diarrhea, infections and fever. Thousands of displaced people, many of them children, have no food and are suffering from worsening desperation and hunger. Meanwhile, according to Dr. Abu Salmiya, the hospital compound is besieged from all sides by tanks and bulldozers, but no one can see clearly what they are doing. He said that anyone who tries to move between hospital buildings is shot at by snipers or drones. Israelis refuse to speak According to Dr. Abu Salmiya, hospital administrators tried to send a delegation to speak with the Israeli military and ask for food, water, fuel, medicine and other urgent relief supplies. On Wednesday, Israel presented a few guns and other equipment it claims to have found in one al-Shifa hospital building. The so-called evidence did not corroborate Israel’s longstanding claims that Hamas has a sophisticated command bunker under the hospital. It was met with the same widespread skepticism and derision as the farcical “evidence” of Hamas activity that Israel offered after it raided the Rantisi children’s hospital days earlier. Over the 48 hours that Israeli forces have occupied parts of the al-Shifa compound, no shots have been fired at them, according to Dr. Abu Salmiya. Palestinian resistance groups have firmly denied they use hospitals for military activities and have regularly called for impartial international bodies to visit the hospitals and investigate Israel’s claims. “Israeli soldiers briefly exchanged fire with gunmen outside the hospital before going in, a senior military official said, but more than 12 hours after it began, the operation appeared more like a police raid than a pitched battle,” The New York Times reported on Wednesday. The newspaper quoted a witness inside the hospital recounting that the Israelis “are digging and excavating and breaking tiles and looking.” While there is a particular focus on al-Shifa, Israel is also now laying siege to al-Ahli hospital in Gaza City. Biden repeats Israeli lies On Wednesday evening, President Joe Biden repeated Israeli assertions that Hamas has a major command center located under al-Shifa hospital. “Here’s the situation,” Biden told reporters after meeting with China’s President Xi Jinping in San Francisco. “You have a circumstance where the first war crime is being committed by Hamas by having their headquarters, their military hidden under a hospital. And that’s a fact. That’s what’s happened.” Administration officials have made similar assertions in recent days but have adamantly declined to offer any evidence for them. Nonetheless, they are a green light for Israel’s attack on al-Shifa. “We’ve discussed the need for them to be incredibly careful,” Biden added. “You have a circumstance where you know there is a fair number of Hamas terrorists. Hamas has already said publicly that they plan on attacking Israel again like they did before, to where they were cutting babies’ heads off to burn – burning women and children alive.” Last month Biden notoriously stated that he had seen photos corroborating Israeli claims that Palestinian fighters had beheaded dozens of beheaded babies, before the White House had to admit the president had been shown no such photos. Israel has presented no evidence for that claim and many of its other assertions. Meanwhile there’s a growing body of evidence that Israeli forces killed many of their own civilians on and after 7 October. Defending Israel’s actions at al-Shifa, Biden asserted, “they’re also bringing in incubators. They’re bringing in other – other means to help the people in the hospital, and they’ve given the doctors and – I’m told – the doctors and nurses and personnel an opportunity to get out of harm’s way.” Were Biden well-informed, he would know that al-Shifa and other hospitals in Gaza do not lack incubators, but the electricity and fuel to power them. Notably, al-Shifa director Abu Salmiya told Al Jazeera earlier that the Israelis had delivered no supplies to the hospital – in spite of propaganda by the Israeli army designed to market its attack on the hospital as a “humanitarian” operation. Abu Salmiya said that despite the dire circumstances, the medical staff would not abandon their patients and would stay there and die with them if it came to that. Operation Al-Aqsa Flood al-Shifa Hospital https://electronicintifada.net/blogs/ali-abunimah/did-israel-build-bunker-under-al-shifa-hospital 👇https://donshafi911.blogspot.com/2023/11/did-israel-build-bunker-under-al-shifa.html
    ELECTRONICINTIFADA.NET
    Did Israel build a bunker under al-Shifa hospital?
    Joe Biden repeats Israeli lies, further fueling genocide in Gaza.
    0 Kommentare 0 Anteile 11013 Ansichten
  • The Immune System and Vaccines are Complicated ⋆ Brownstone Institute
    The Immune System and Vaccines are Complicated
    SHARE | PRINT | EMAIL
    Vaccines are a complicated area, which is because the immune system is immensely complicated. Targeted vaccines have ancillary effects, and it is not possible to predict what they are.

    Professor Peter Aaby’s group has done ground-breaking research on the effects of vaccines in randomized trials and in field studies. His team discovered that all live, attenuated vaccines decrease total mortality whereas some non-live vaccines increase total mortality. There are also gender differences, and the sequence of vaccinations is important. It is best to end with a live vaccine.

    My rule of thumb is that if a vaccine is part of the official vaccination program in some countries and not in others of similar standing, it is not important to get vaccinated. An example is the rotavirus vaccine against diarrhoea, which is not on the childhood program in Denmark even though we had a strong lobby group promoting it.

    The Measles Vaccines
    The measles vaccines are a good example that live, attenuated vaccines decrease total mortality much more than what is possible based on their targeted effect, in this case on preventing measles. In a randomised trial in Bissau, for example, children vaccinated against measles at age 6 months had 70 percent lower mortality than unvaccinated children, and this reduction was not due to prevention of measles infection. The WHO has estimated that there were 128,000 measles deaths globally in 2021, mostly among unvaccinated or under-vaccinated children under the age of 5 years.

    If we do not vaccinate our children against measles, it will lead to many deaths and cases of severe brain damage that could have been avoided. We have a joint responsibility towards each other to ensure we get vaccinated because herd immunity is important. Measles is highly contagious, and to prevent the occurrence of measles epidemics, vaccinating about 95 percent of the population is necessary.

    Annual Influenza Jabs are not Needed
    People all over the world, particularly the elderly, are being nudged by the authorities to get an annual vaccination against influenza, but it is not at all obvious that this is a good idea. In fact, there are several reasons to be skeptical.

    First, the preventive effect is small. Twenty-nine people would need to be vaccinated to avoid one case of influenza-like illness and 71 people to avoid one case of influenza, and the vaccination does not reduce hospital admissions or days off work.

    Second, as the virus mutates quite rapidly, the effect obtained by vaccination will likely be smaller than in the randomized trials.

    Third, the vaccine has negative effects on the immune system. Canadian researchers showed in four different studies that people who received a seasonal influenza vaccine in 2008 had an increased risk of getting infected with another strain in 2009.

    Fourth, all vaccines cause harms, which can potentially be serious. Pandemrix, one of the influenza vaccines used during the 2009-2010 pandemic, caused narcolepsy in children and adolescents with a certain tissue type. Up to several years after vaccination of children and adolescents, people may suddenly start falling asleep while engaging in their normal activities, and there is no cure.

    Fifth, we should always consider the likelihood of getting infected without vaccination. Influenza pandemics are uncommon and rarely involve large portions of the population. In any given year, the likelihood of acquiring influenza if unvaccinated is therefore very small. I never had an influenza vaccination, and my wife, a professor in clinical microbiology, never had one, and together, we have perhaps had influenza twice for 135 years. But we don’t know. When people say they have influenza, it usually just means an influenza-like illness of which there are many, which vaccination does not protect against.

    Some fundamentalists, particularly in the United States and Australia, have mandated influenza vaccination of healthcare workers to protect patients. This violation of informed consent is deeply troubling and unethical. Moreover, a large review about vaccination of healthcare workers caring for elderly people did not find an effect on laboratory-proven influenza, lower respiratory tract infection, hospitalisation, death due to lower respiratory tract illness, or all-cause mortality.

    A researcher mentioned that, “to focus exclusively on the risk posed by unvaccinated workers – treating them as outcasts or, worse, terminating their employment – while overlooking the risk posed by vaccinated workers, potentially jeopardizes patients.” Indeed. Vaccination may provide staff with a false sense of security that might reduce their level of handwashing and potentially increase, rather than decrease, the risk of infecting patients.

    HPV Vaccines: Not a Simple Issue
    When the HPV vaccines were suspected of causing serious neurological harms – postural orthostatic tachycardia syndrome (POTS), complex regional pain syndrome (CRPS), and chronic fatigue syndrome – the European Drug Agency cleared the vaccines. However, they did not investigate the issues themselves but let the manufacturers do it for them.

    My research group examined the clinical study reports submitted to the European Medicines Agency and found a significant increase in serious neurological harms. This was surprising because almost everyone in the control groups had been treated with a hepatitis vaccine or a strongly immunogenic adjuvant, which might also cause harms, making it difficult to detect the harms of the HPV vaccines.

    The Cochrane review of the HPV vaccines was incomplete and ignored important evidence of bias. The authors overlooked several adverse events and failed to mention that some of the included trials did not report serious adverse events for the whole trial period. For example, three Gardasil trials with a total of 21,441 girls or women with up to four years follow-up only reported serious adverse events occurring within 14 days post-vaccination even though it takes years in many patients before serious neurological harms get diagnosed.

    The Cochrane authors found more deaths in the HPV vaccine groups than in the comparator groups, and the death rate was significantly increased in women above age 25, risk ratio 2.36 (95 percent confidence interval 1.10 to 5.03). They considered this a chance occurrence since there was no pattern in the causes of death or in the time between vaccine administration and death.

    However, deaths are often miscoded. For example, traumatic head injury and drowning in a bathtub have been described, and this could have been caused by a syncope or near syncope, which is a recognized vaccine harm that can occur at any time. The serious neurological harms seem to be caused by an autoimmune reaction.

    The drug companies, EMA and Cochrane called the trials placebo-controlled, which they weren’t. I find it shocking that vaccines are not tested against placebo or no treatment because this makes it impossible to ever know with certainty what the rare but serious harms are. There is no good reason why vaccines – which are preventative drugs – are not tested in the same rigorous way as other drugs.

    EMA declared that the adjuvants used in the vaccines to boost the immune response are safe, but the five references provided in support of this view were either non-accessible or irrelevant. Furthermore, nothing is safe if it is active. GlaxoSmithKline has stated that its aluminum-based comparator might cause harms, and the clinical study reports show that this is also the case for Merck’s adjuvant.

    The decision-making is not straightforward. The official propaganda has made women believe that cervical cancer is a major threat to their lives, but this cancer only contributes 0.5 percent of all deaths. Thus, very few women can benefit from the HPV vaccines, and since they do not protect against all HPV types, regular screening is still recommended even for women who are vaccinated. As the precursors to cancer are very slow-growing, women can avoid getting cervical cancer if they go to screening. This is more effective than getting vaccinated, but it comes with a price, e.g. conization for cancer precursors increases the risk of preterm birth.

    COVID-19 Vaccines: A Mess
    The story of the COVID-19 vaccines is officially touted as one of success but what stands out is a story of massive deceit and lack of scientific evidence behind many of the recommendations.

    The randomized trials that led to emergency approval of the vaccines showed that only one of 50 severe cases of COVID-19 occurred in the vaccine groups. This makes it likely that the vaccines have saved lives, and meta-analyses of the trials showed that the adenovirus vector vaccines, but not the mRNA vaccines, decreased total mortality significantly.

    The hype has been extreme, however. Among those that have claimed 100 percent efficacy of the vaccines are the FDA, US presidential advisor Anthony Fauci, the Australian government, Science Magazine, Reuters, CNN, US National Public Radio, The Hill, Sky News, Pfizer, Moderna, AstraZeneca, and Johnson & Johnson. The efficacy is closer to 50 percent and many people, including me, have become infected despite having received two or more doses of the vaccine.

    Officials, including US President Joe Biden, once claimed that the vaccines were 100 percent protective against transmission to other people, but now it is widely acknowledged that there is no evidence that the vaccines can prevent transmission.

    The information on the website of the US Centers for Disease Control and Prevention (CDC) is particularly misleading. The CDC uses industry jargon when claiming that the vaccines are “safe and effective.” It states that “Adults and children may have some side effects from a COVID-19 vaccine, including pain, redness or swelling at the injection site, tiredness, headache, muscle pain, chills, fever, and nausea. These side effects typically resolve after a few days.  Serious side effects are rare but may occur.”

    The link to serious side effects does not lead to any mention of what those are. But we know that the vaccines kill some people, e.g. because they can cause myocarditis, most commonly in young males, and thromboses.

    The CDC recommends “everyone ages 6 months and older get an updated COVID-19 vaccine to protect against serious illness.” However, children tolerate the infection very well and it is likely harmful to vaccine children against COVID-19. Moreover, boosters may be harmful at any age but this is not popular information either. Facebook censored research and an interview with top vaccine researcher Professor Christine Stabell Benn even though the European Medicines Agency was also worried that COVID-19 vaccine boosters might be “overloading people’s immune systems and leading to fatigue.”

    Facebook also censored research that showed that the mRNA COVID-19 vaccines could weaken the immune response and make cells of the immune system “lazy” when it comes to fighting off viral and bacterial infections. Facebook called this research “false information.”

    The Cochrane Collaboration, which has the logo “Trusted information,” did not provide trusted information. The Cochrane authors used industry jargon in the title of their review, “Efficacy and safety of COVID‐19 vaccines,” even though I convinced Cochrane many years ago that we should talk about benefits and harms of the interventions we study, in agreement with the CONSORT guidelines for good reporting of harms in trials, which I coauthored in 2004.

    The Cochrane authors concluded that there is little or no difference in serious adverse events compared to placebo whereas Peter Doshi and colleagues who reanalysed the pivotal mRNA trials found that one additional serious adverse event occurred for every 800 people vaccinated with an mRNA vaccine. Their article, published four months before the Cochrane review, was not cited in it.

    When I studied the pivotal randomised trials, which were published in the New England Journal of Medicine and in the Lancet, I found that essential data on serious and severe harms were missing (see also my freely available book, The Chinese virus: killed millions and scientific freedom).

    Doshi et al.’s criticism of the Cochrane review, which is published within the review itself, is so substantial that it is fair to call the Cochrane review a politically expedient garbage in, garbage out exercise.

    There can be no doubt that the COVID-19 vaccines are much overused and partly to the wrong people. Now that most of us have had the infection, recommending booster after booster seems to be a particularly bad idea.

    Childhood Vaccines
    The childhood vaccination programs differ a lot from country to country. In the US, 17 vaccines are recommended, in Denmark only 10.

    Since vaccinations can weaken the immune system and since some non-live vaccines increase total mortality, it is reasonable to ask if the many vaccinations in the US could result in net harm.

    It is very important to study this possibility, but I am only aware of two researchers who have done it. They did several studies and found that those nations that require more vaccines for their infants have higher infant mortality, neonatal mortality, and under age five mortality. I find this an alarm signal that should lead to other studies as a matter of urgency.

    Censorship
    Censorship is detrimental for scientific debate and scientific advances, and it is harmful for the patients. But for vaccines, it is all over the place.

    Peter Aaby, one of the world’s top vaccine researchers, lectured about vaccines at the opening symposium for my Institute for Scientific Freedom in March 2019. In early November 2021, YouTube removed the video of his lecture. Everything he said was correct and important for people who want to understand what vaccines do. We appealed this outrageous act of censorship, but to no avail, and I therefore uploaded his lecture on my own website.

    In February 2022, a US lawyer wrote a 3-page letter to Susan Wojcicki, Chief Operating Officer, Legal Support, YouTube, asking her to restore Professor Aaby’s video about the beneficial and harmful effects of vaccines so that a healthy conversation surrounding medical science could continue. The lawyer received an automated message saying that the video had violated YouTube’s Community Guidelines, adding that “If you think a Community Guidelines strike was applied to your account in error, you can appeal it.” The lawyer appealed and received no reply.

    In July 2022, Christine Stabel Benn uploaded a videocast with Peter Aaby on YouTube about his research in Africa, which mainly addressed his discovery of the beneficial non-specific effects of measles vaccines. But Aaby also mentioned his interactions with the WHO related to the introduction of a high-titre measles vaccine, which he and his colleagues’ studies had shown increased mortality in girls.

    Initially, the WHO did not react, but when American colleagues confirmed Aaby’s findings in Haiti, the high-titre vaccine was withdrawn. It has been estimated that this vaccine would have cost around 0.5 million lives per year in Africa alone. It is an important lesson that a highly beneficial vaccine that has saved millions of lives can kill millions if used in too high doses. But YouTube quickly removed the videocast due to “inappropriate content.” Censorship kills. It is as simple as that.

    In September 2022, I was interviewed by enGrama in Spain for an hour about organised crime in psychiatry and the drug industry. I spoke about COVID-19 for 5 minutes, which made YouTube instantly eliminate the whole interview. This was utterly ridiculous. What I said was true, but YouTube even refused to allow the interviewers to download their own video. Later, they succeeded to reproduce it via the YouTube Studio and it is now up again, but without the forbidden 5 minutes. I have described verbatim what they were about.

    I was convinced – and still am – that the pandemic was caused by a laboratory leak in Wuhan and that the virus was manufactured there; that repeated vaccinations could weaken the immune response; and that the vaccines can cause serious harm, even death. All of which is considered taboo by social media.

    In September 2023, I launched an evidence-based podcast channel, Broken Medical Science, in collaboration with documentary filmmaker Janus Bang. To avoid censorship, we have our own server but also publish the episodes on social media. I interviewed Professor Martin Kulldorff, one of the authors of the Great Barrington Declaration, about “The harmful effects of lockdowns, facemask mandates, censorship, and scientific dishonesty,” and Christine Stabell Benn about “Vaccines, a complicated area. Some decrease total mortality, some increase it, and COVID-19 vaccines are overused.”

    Within 7 minutes after we uploaded these episodes on YouTube, they got this label: “COVID-19 vaccine. Learn about vaccine progress from the WHO.” But some of the WHO’s information was questionable, which we addressed in our newsletter:

    What are the benefits of getting vaccinated against COVID-19?

    One should always ask what the benefits and harms are, of any intervention. The vaccines have killed some people because of myocarditis and thromboses.

    Getting vaccinated could save your life. COVID-19 vaccines have saved millions of lives.

    What is the evidence for this? The vaccines are not particularly effective because the virus mutates.

    Consider continuing to practice protective and preventive behaviours such as keeping a distance, wearing a mask in crowded and poorly ventilated spaces.

    The randomized trials have not found any effect of face masks.

    Even if you have had COVID-19, the WHO still recommends that you get vaccinated after infection because vaccination enhances your protection against severe outcomes of future COVID-19 infection, and you may be protected for longer. Furthermore, hybrid immunity resulting from vaccine and infection may provide superior protection against existing variants of concern.

    This has not been documented, and many researchers doubt that it is correct.

    To ensure optimal protection, it is important to receive COVID-19 vaccine doses and boosters recommended to you by your health authority.

    It has not been documented that boosters are beneficial, and the European Medicines Agency has warned that boosters may be harmful, as they may weaken the immune system.

    In both cases, within a couple of hours, YouTube removed the link to the WHO, with no explanation. We speculate that perhaps YouTube is worried about their reputation. I had interviewed two of the most knowledgeable people in the world about vaccines who, to some extent, contradicted the WHO’s recommendations, based on solid science.

    It is time to change the paradigm about vaccines, and to study them more thoroughly – and their combinations – before they are possibly allowed onto the market.

    A Final Word about Censorship
    My deputy director, PhD Maryanne Demasi, and I have been unable to publish our systematic review of serious harms of the COVID-19 vaccines in a medical journal. This is not because I don’t know how to do research and publish it in good journals. I have published over 100 papers in “the big five” (BMJ, Lancet, JAMA, Annals of Internal Medicine and New England Journal of Medicine) and my scientific works have been cited over 190,000 times.


    Published under a Creative Commons Attribution 4.0 International License
    For reprints, please set the canonical link back to the original Brownstone Institute Article and Author.

    Dr. Peter Gøtzsche co-founded the Cochrane Collaboration, once considered the world’s preeminent independent medical research organization. In 2010 Gøtzsche was named Professor of Clinical Research Design and Analysis at the University of Copenhagen. Gøtzsche has published more than 97 papers in the “big five” medical journals (JAMA, Lancet, New England Journal of Medicine, British Medical Journal, and Annals of Internal Medicine). Gøtzsche has also authored books on medical issues including Deadly Medicines and Organized Crime. Following many years of being an outspoken critic of the corruption of science by pharmaceutical companies, Gøtzsche’s membership on the governing board of Cochrane was terminated by its Board of Trustees in September, 2018. Four board resigned in protest.


    https://brownstone.org/articles/the-immune-system-and-vaccines-are-complicated/
    The Immune System and Vaccines are Complicated ⋆ Brownstone Institute The Immune System and Vaccines are Complicated SHARE | PRINT | EMAIL Vaccines are a complicated area, which is because the immune system is immensely complicated. Targeted vaccines have ancillary effects, and it is not possible to predict what they are. Professor Peter Aaby’s group has done ground-breaking research on the effects of vaccines in randomized trials and in field studies. His team discovered that all live, attenuated vaccines decrease total mortality whereas some non-live vaccines increase total mortality. There are also gender differences, and the sequence of vaccinations is important. It is best to end with a live vaccine. My rule of thumb is that if a vaccine is part of the official vaccination program in some countries and not in others of similar standing, it is not important to get vaccinated. An example is the rotavirus vaccine against diarrhoea, which is not on the childhood program in Denmark even though we had a strong lobby group promoting it. The Measles Vaccines The measles vaccines are a good example that live, attenuated vaccines decrease total mortality much more than what is possible based on their targeted effect, in this case on preventing measles. In a randomised trial in Bissau, for example, children vaccinated against measles at age 6 months had 70 percent lower mortality than unvaccinated children, and this reduction was not due to prevention of measles infection. The WHO has estimated that there were 128,000 measles deaths globally in 2021, mostly among unvaccinated or under-vaccinated children under the age of 5 years. If we do not vaccinate our children against measles, it will lead to many deaths and cases of severe brain damage that could have been avoided. We have a joint responsibility towards each other to ensure we get vaccinated because herd immunity is important. Measles is highly contagious, and to prevent the occurrence of measles epidemics, vaccinating about 95 percent of the population is necessary. Annual Influenza Jabs are not Needed People all over the world, particularly the elderly, are being nudged by the authorities to get an annual vaccination against influenza, but it is not at all obvious that this is a good idea. In fact, there are several reasons to be skeptical. First, the preventive effect is small. Twenty-nine people would need to be vaccinated to avoid one case of influenza-like illness and 71 people to avoid one case of influenza, and the vaccination does not reduce hospital admissions or days off work. Second, as the virus mutates quite rapidly, the effect obtained by vaccination will likely be smaller than in the randomized trials. Third, the vaccine has negative effects on the immune system. Canadian researchers showed in four different studies that people who received a seasonal influenza vaccine in 2008 had an increased risk of getting infected with another strain in 2009. Fourth, all vaccines cause harms, which can potentially be serious. Pandemrix, one of the influenza vaccines used during the 2009-2010 pandemic, caused narcolepsy in children and adolescents with a certain tissue type. Up to several years after vaccination of children and adolescents, people may suddenly start falling asleep while engaging in their normal activities, and there is no cure. Fifth, we should always consider the likelihood of getting infected without vaccination. Influenza pandemics are uncommon and rarely involve large portions of the population. In any given year, the likelihood of acquiring influenza if unvaccinated is therefore very small. I never had an influenza vaccination, and my wife, a professor in clinical microbiology, never had one, and together, we have perhaps had influenza twice for 135 years. But we don’t know. When people say they have influenza, it usually just means an influenza-like illness of which there are many, which vaccination does not protect against. Some fundamentalists, particularly in the United States and Australia, have mandated influenza vaccination of healthcare workers to protect patients. This violation of informed consent is deeply troubling and unethical. Moreover, a large review about vaccination of healthcare workers caring for elderly people did not find an effect on laboratory-proven influenza, lower respiratory tract infection, hospitalisation, death due to lower respiratory tract illness, or all-cause mortality. A researcher mentioned that, “to focus exclusively on the risk posed by unvaccinated workers – treating them as outcasts or, worse, terminating their employment – while overlooking the risk posed by vaccinated workers, potentially jeopardizes patients.” Indeed. Vaccination may provide staff with a false sense of security that might reduce their level of handwashing and potentially increase, rather than decrease, the risk of infecting patients. HPV Vaccines: Not a Simple Issue When the HPV vaccines were suspected of causing serious neurological harms – postural orthostatic tachycardia syndrome (POTS), complex regional pain syndrome (CRPS), and chronic fatigue syndrome – the European Drug Agency cleared the vaccines. However, they did not investigate the issues themselves but let the manufacturers do it for them. My research group examined the clinical study reports submitted to the European Medicines Agency and found a significant increase in serious neurological harms. This was surprising because almost everyone in the control groups had been treated with a hepatitis vaccine or a strongly immunogenic adjuvant, which might also cause harms, making it difficult to detect the harms of the HPV vaccines. The Cochrane review of the HPV vaccines was incomplete and ignored important evidence of bias. The authors overlooked several adverse events and failed to mention that some of the included trials did not report serious adverse events for the whole trial period. For example, three Gardasil trials with a total of 21,441 girls or women with up to four years follow-up only reported serious adverse events occurring within 14 days post-vaccination even though it takes years in many patients before serious neurological harms get diagnosed. The Cochrane authors found more deaths in the HPV vaccine groups than in the comparator groups, and the death rate was significantly increased in women above age 25, risk ratio 2.36 (95 percent confidence interval 1.10 to 5.03). They considered this a chance occurrence since there was no pattern in the causes of death or in the time between vaccine administration and death. However, deaths are often miscoded. For example, traumatic head injury and drowning in a bathtub have been described, and this could have been caused by a syncope or near syncope, which is a recognized vaccine harm that can occur at any time. The serious neurological harms seem to be caused by an autoimmune reaction. The drug companies, EMA and Cochrane called the trials placebo-controlled, which they weren’t. I find it shocking that vaccines are not tested against placebo or no treatment because this makes it impossible to ever know with certainty what the rare but serious harms are. There is no good reason why vaccines – which are preventative drugs – are not tested in the same rigorous way as other drugs. EMA declared that the adjuvants used in the vaccines to boost the immune response are safe, but the five references provided in support of this view were either non-accessible or irrelevant. Furthermore, nothing is safe if it is active. GlaxoSmithKline has stated that its aluminum-based comparator might cause harms, and the clinical study reports show that this is also the case for Merck’s adjuvant. The decision-making is not straightforward. The official propaganda has made women believe that cervical cancer is a major threat to their lives, but this cancer only contributes 0.5 percent of all deaths. Thus, very few women can benefit from the HPV vaccines, and since they do not protect against all HPV types, regular screening is still recommended even for women who are vaccinated. As the precursors to cancer are very slow-growing, women can avoid getting cervical cancer if they go to screening. This is more effective than getting vaccinated, but it comes with a price, e.g. conization for cancer precursors increases the risk of preterm birth. COVID-19 Vaccines: A Mess The story of the COVID-19 vaccines is officially touted as one of success but what stands out is a story of massive deceit and lack of scientific evidence behind many of the recommendations. The randomized trials that led to emergency approval of the vaccines showed that only one of 50 severe cases of COVID-19 occurred in the vaccine groups. This makes it likely that the vaccines have saved lives, and meta-analyses of the trials showed that the adenovirus vector vaccines, but not the mRNA vaccines, decreased total mortality significantly. The hype has been extreme, however. Among those that have claimed 100 percent efficacy of the vaccines are the FDA, US presidential advisor Anthony Fauci, the Australian government, Science Magazine, Reuters, CNN, US National Public Radio, The Hill, Sky News, Pfizer, Moderna, AstraZeneca, and Johnson & Johnson. The efficacy is closer to 50 percent and many people, including me, have become infected despite having received two or more doses of the vaccine. Officials, including US President Joe Biden, once claimed that the vaccines were 100 percent protective against transmission to other people, but now it is widely acknowledged that there is no evidence that the vaccines can prevent transmission. The information on the website of the US Centers for Disease Control and Prevention (CDC) is particularly misleading. The CDC uses industry jargon when claiming that the vaccines are “safe and effective.” It states that “Adults and children may have some side effects from a COVID-19 vaccine, including pain, redness or swelling at the injection site, tiredness, headache, muscle pain, chills, fever, and nausea. These side effects typically resolve after a few days.  Serious side effects are rare but may occur.” The link to serious side effects does not lead to any mention of what those are. But we know that the vaccines kill some people, e.g. because they can cause myocarditis, most commonly in young males, and thromboses. The CDC recommends “everyone ages 6 months and older get an updated COVID-19 vaccine to protect against serious illness.” However, children tolerate the infection very well and it is likely harmful to vaccine children against COVID-19. Moreover, boosters may be harmful at any age but this is not popular information either. Facebook censored research and an interview with top vaccine researcher Professor Christine Stabell Benn even though the European Medicines Agency was also worried that COVID-19 vaccine boosters might be “overloading people’s immune systems and leading to fatigue.” Facebook also censored research that showed that the mRNA COVID-19 vaccines could weaken the immune response and make cells of the immune system “lazy” when it comes to fighting off viral and bacterial infections. Facebook called this research “false information.” The Cochrane Collaboration, which has the logo “Trusted information,” did not provide trusted information. The Cochrane authors used industry jargon in the title of their review, “Efficacy and safety of COVID‐19 vaccines,” even though I convinced Cochrane many years ago that we should talk about benefits and harms of the interventions we study, in agreement with the CONSORT guidelines for good reporting of harms in trials, which I coauthored in 2004. The Cochrane authors concluded that there is little or no difference in serious adverse events compared to placebo whereas Peter Doshi and colleagues who reanalysed the pivotal mRNA trials found that one additional serious adverse event occurred for every 800 people vaccinated with an mRNA vaccine. Their article, published four months before the Cochrane review, was not cited in it. When I studied the pivotal randomised trials, which were published in the New England Journal of Medicine and in the Lancet, I found that essential data on serious and severe harms were missing (see also my freely available book, The Chinese virus: killed millions and scientific freedom). Doshi et al.’s criticism of the Cochrane review, which is published within the review itself, is so substantial that it is fair to call the Cochrane review a politically expedient garbage in, garbage out exercise. There can be no doubt that the COVID-19 vaccines are much overused and partly to the wrong people. Now that most of us have had the infection, recommending booster after booster seems to be a particularly bad idea. Childhood Vaccines The childhood vaccination programs differ a lot from country to country. In the US, 17 vaccines are recommended, in Denmark only 10. Since vaccinations can weaken the immune system and since some non-live vaccines increase total mortality, it is reasonable to ask if the many vaccinations in the US could result in net harm. It is very important to study this possibility, but I am only aware of two researchers who have done it. They did several studies and found that those nations that require more vaccines for their infants have higher infant mortality, neonatal mortality, and under age five mortality. I find this an alarm signal that should lead to other studies as a matter of urgency. Censorship Censorship is detrimental for scientific debate and scientific advances, and it is harmful for the patients. But for vaccines, it is all over the place. Peter Aaby, one of the world’s top vaccine researchers, lectured about vaccines at the opening symposium for my Institute for Scientific Freedom in March 2019. In early November 2021, YouTube removed the video of his lecture. Everything he said was correct and important for people who want to understand what vaccines do. We appealed this outrageous act of censorship, but to no avail, and I therefore uploaded his lecture on my own website. In February 2022, a US lawyer wrote a 3-page letter to Susan Wojcicki, Chief Operating Officer, Legal Support, YouTube, asking her to restore Professor Aaby’s video about the beneficial and harmful effects of vaccines so that a healthy conversation surrounding medical science could continue. The lawyer received an automated message saying that the video had violated YouTube’s Community Guidelines, adding that “If you think a Community Guidelines strike was applied to your account in error, you can appeal it.” The lawyer appealed and received no reply. In July 2022, Christine Stabel Benn uploaded a videocast with Peter Aaby on YouTube about his research in Africa, which mainly addressed his discovery of the beneficial non-specific effects of measles vaccines. But Aaby also mentioned his interactions with the WHO related to the introduction of a high-titre measles vaccine, which he and his colleagues’ studies had shown increased mortality in girls. Initially, the WHO did not react, but when American colleagues confirmed Aaby’s findings in Haiti, the high-titre vaccine was withdrawn. It has been estimated that this vaccine would have cost around 0.5 million lives per year in Africa alone. It is an important lesson that a highly beneficial vaccine that has saved millions of lives can kill millions if used in too high doses. But YouTube quickly removed the videocast due to “inappropriate content.” Censorship kills. It is as simple as that. In September 2022, I was interviewed by enGrama in Spain for an hour about organised crime in psychiatry and the drug industry. I spoke about COVID-19 for 5 minutes, which made YouTube instantly eliminate the whole interview. This was utterly ridiculous. What I said was true, but YouTube even refused to allow the interviewers to download their own video. Later, they succeeded to reproduce it via the YouTube Studio and it is now up again, but without the forbidden 5 minutes. I have described verbatim what they were about. I was convinced – and still am – that the pandemic was caused by a laboratory leak in Wuhan and that the virus was manufactured there; that repeated vaccinations could weaken the immune response; and that the vaccines can cause serious harm, even death. All of which is considered taboo by social media. In September 2023, I launched an evidence-based podcast channel, Broken Medical Science, in collaboration with documentary filmmaker Janus Bang. To avoid censorship, we have our own server but also publish the episodes on social media. I interviewed Professor Martin Kulldorff, one of the authors of the Great Barrington Declaration, about “The harmful effects of lockdowns, facemask mandates, censorship, and scientific dishonesty,” and Christine Stabell Benn about “Vaccines, a complicated area. Some decrease total mortality, some increase it, and COVID-19 vaccines are overused.” Within 7 minutes after we uploaded these episodes on YouTube, they got this label: “COVID-19 vaccine. Learn about vaccine progress from the WHO.” But some of the WHO’s information was questionable, which we addressed in our newsletter: What are the benefits of getting vaccinated against COVID-19? One should always ask what the benefits and harms are, of any intervention. The vaccines have killed some people because of myocarditis and thromboses. Getting vaccinated could save your life. COVID-19 vaccines have saved millions of lives. What is the evidence for this? The vaccines are not particularly effective because the virus mutates. Consider continuing to practice protective and preventive behaviours such as keeping a distance, wearing a mask in crowded and poorly ventilated spaces. The randomized trials have not found any effect of face masks. Even if you have had COVID-19, the WHO still recommends that you get vaccinated after infection because vaccination enhances your protection against severe outcomes of future COVID-19 infection, and you may be protected for longer. Furthermore, hybrid immunity resulting from vaccine and infection may provide superior protection against existing variants of concern. This has not been documented, and many researchers doubt that it is correct. To ensure optimal protection, it is important to receive COVID-19 vaccine doses and boosters recommended to you by your health authority. It has not been documented that boosters are beneficial, and the European Medicines Agency has warned that boosters may be harmful, as they may weaken the immune system. In both cases, within a couple of hours, YouTube removed the link to the WHO, with no explanation. We speculate that perhaps YouTube is worried about their reputation. I had interviewed two of the most knowledgeable people in the world about vaccines who, to some extent, contradicted the WHO’s recommendations, based on solid science. It is time to change the paradigm about vaccines, and to study them more thoroughly – and their combinations – before they are possibly allowed onto the market. A Final Word about Censorship My deputy director, PhD Maryanne Demasi, and I have been unable to publish our systematic review of serious harms of the COVID-19 vaccines in a medical journal. This is not because I don’t know how to do research and publish it in good journals. I have published over 100 papers in “the big five” (BMJ, Lancet, JAMA, Annals of Internal Medicine and New England Journal of Medicine) and my scientific works have been cited over 190,000 times. Published under a Creative Commons Attribution 4.0 International License For reprints, please set the canonical link back to the original Brownstone Institute Article and Author. Dr. Peter Gøtzsche co-founded the Cochrane Collaboration, once considered the world’s preeminent independent medical research organization. In 2010 Gøtzsche was named Professor of Clinical Research Design and Analysis at the University of Copenhagen. Gøtzsche has published more than 97 papers in the “big five” medical journals (JAMA, Lancet, New England Journal of Medicine, British Medical Journal, and Annals of Internal Medicine). Gøtzsche has also authored books on medical issues including Deadly Medicines and Organized Crime. Following many years of being an outspoken critic of the corruption of science by pharmaceutical companies, Gøtzsche’s membership on the governing board of Cochrane was terminated by its Board of Trustees in September, 2018. Four board resigned in protest. https://brownstone.org/articles/the-immune-system-and-vaccines-are-complicated/
    BROWNSTONE.ORG
    The Immune System and Vaccines are Complicated ⋆ Brownstone Institute
    Vaccines are a complicated area, which is because the immune system is immensely complicated. Targeted vaccines have ancillary effects, and it is not possible to predict what they are.
    0 Kommentare 0 Anteile 19498 Ansichten
  • Vuoristonäköala: Viihtyisä Yksiö Torreblanca Altassa, Fuengirolassa

    Rauhallisuus ja näkymät vuorille:
    Yksiö sijaitsee Torreblancan yläosassa, Fuengirolassa. Pohjoiseen suuntautuva asunto jakautuu olohuoneen ja pienen oleskelutilan välillä. Kylpyhuone on hyvänkokoinen ja siinä on suihkualusta.
    Asunnossa on kaksi vuodesohvaa, viileä/lämmin ilmastointi, televisio ja yhteisöllinen pysäköintialue.
    Muutaman metrin päässä on bussipysäkki (linja 5), joka vie Los Bolichesin keskustaan ja kulkee 15 minuutin välein. Ranta on noin 2 kilometrin päässä, noin 5 minuutin ajomatkan päässä.

    https://www.bluehorse.es/fi/yksio-sijainti-fuengirola-los-boliches-torreblanca-hissi-fi1114490.html
    Vuoristonäköala: Viihtyisä Yksiö Torreblanca Altassa, Fuengirolassa Rauhallisuus ja näkymät vuorille: Yksiö sijaitsee Torreblancan yläosassa, Fuengirolassa. Pohjoiseen suuntautuva asunto jakautuu olohuoneen ja pienen oleskelutilan välillä. Kylpyhuone on hyvänkokoinen ja siinä on suihkualusta. Asunnossa on kaksi vuodesohvaa, viileä/lämmin ilmastointi, televisio ja yhteisöllinen pysäköintialue. Muutaman metrin päässä on bussipysäkki (linja 5), joka vie Los Bolichesin keskustaan ja kulkee 15 minuutin välein. Ranta on noin 2 kilometrin päässä, noin 5 minuutin ajomatkan päässä. https://www.bluehorse.es/fi/yksio-sijainti-fuengirola-los-boliches-torreblanca-hissi-fi1114490.html
    WWW.BLUEHORSE.ES
    Loma-asunnot Yksiö sijainti...
    Rauhallisuus ja näkymät vuorille: Yksiö sijaitsee Torreblancan yläosassa, Fuengirolassa. Pohjoiseen suuntautuva asunto jakautuu olohuoneen ja pienen oleskelutilan välillä. Kylpyhuone on hyvänkokoinen ja siinä on suihkualusta. Asunnossa on kaksi vuodesohvaa, viileä/lämmin ilmastointi, televisio
    0 Kommentare 0 Anteile 2438 Ansichten
  • What media reports fail to tell you about October 7
    Alison Weir November 13, 2023 bbc, Gaza, hamas
    What media reports fail to tell you about October 7
    BBC's Lucy Williamson is taken by the Israeli military to view kibbutz damage.regurgitating Israeli claims. (photo)
    It is journalistic malpractice for the media to still be repeating so credulously the Israeli military’s account of that day, including alleged Hamas atrocities that turned out to be fiction

    Media neglected to report much key information, e.g. Israeli military commanders had ordered the shelling of kibbutz houses in order to eliminate the “terrorists along with the hostages”… once Israeli special forces arrived: “They eliminated everyone, including the hostages”

    Are the images of charred bodies evidence that Israeli civilians and Hamas fighters burned alongside each other, after they were engulfed in flames caused by Israeli shelling of the houses?

    While this article focuses on BBC coverage, it’s analysis applies equally to US media. Some news coverage, in fact, has been considerably worse

    By Jonathan Cook, reposted from Jonathan Cook Substack, Nov 2, 2023.

    The BBC’s Lucy Williamson was taken once again this week to view the terrible destruction at a kibbutz community just outside Gaza attacked on October 7. As we have been shown so many times before, the Israeli homes were riddled with automatic fire, both inside and out. Sections of concrete wall had holes in them, or had collapsed entirely. And parts of the buildings that were still standing were deeply charred. It looked like a small snapshot of the current horrors in Gaza.

    There is a possible reason for those similarities – one that the BBC is studiously failing to report, despite mounting evidence from a variety of sources, including the Israeli media. Instead the BBC is sticking resolutely to a narrative crafted for them, and the rest of the western media, by the Israeli military: that Hamas alone caused all this destruction.

    Simply repeating that narrative without any caveats has by now reached the level of journalistic malpractice. And yet that is precisely what the BBC does night after night.

    Just a cursory look at the wreckage in the various kibbutz communities that were attacked that day should raise questions in the mind of any good reporter. Were Palestinian militants in a position to actually inflict physical damage to that degree and extent with the kind of light weapons they carried?

    And if not, who else was in a position to wreak such havoc other than Israel?

    A separate question that good journalists ought to be asking is this: What was the purpose of such damage? What did the Palestinian militants hope to achieve by it?

    The implicit answer the media is supplying is also the answer the Israeli military wants western publics to hear: that Hamas engaged in an orgy of gratuitious killing and savagery because … well, let’s say the quiet part out loud: because Palestinians are inherently savage.

    With that as the implicit narrative, western politicians have been handed a licence to cheerlead Israel as it murders a Palestinian child in Gaza every few minutes. Savages only understand the language of savagery, after all.

    Brutal tango

    For this reason alone, any journalist who wishes to avoid colluding in the genocide unfolding in Gaza ought to be increasingly wary of simply repeating the Israeli military’s claims about what happened on October 7. Certainly, they should not credulously regurgitate the latest agitprop from the IDF press office, as the BBC is so evidently doing.

    What we know from a growing body of evidence gleaned from the Israeli media and Israeli eyewitnesses – carefully laid out, for example, in this report from Max Blumenthal – is that the Israeli military was completely blindsided by that day’s events. Heavy artillery, including tanks and attack helicopters, was called in to deal with Hamas. That appears to have been a straightforward decision in regard to the military bases Hamas had overrun.

    Israel has a long-standing policy of seeking to prevent Israeli soldiers from being taken captive – chiefly, because of the high price Israeli society insists on paying to ensure soldiers are returned. For decades, the military’s so-called “Hannibal procedure” has directed Israeli troops to kill fellow soldiers rather than allow them to be taken captive. For the same reason, Hamas expends a great deal of energy in trying to find innovative ways to seize soldiers.

    The two sides are essentially engaged in a brutal tango in which each understands the other’s dance moves.

    Given Hamas’ situation, effectively managing the Israeli-controlled concentration camp of Gaza, it has limited resistance strategies available to it. Capturing Israeli soldiers maximises its leverage. They can be traded for the release of many of the thousands of Palestinian political prisoners held in jails inside Israel, in breach of international law. In addition, in the negotiations, Hamas usually hopes to win an easing of Israel’s 16-year siege of Gaza.

    To avert this scenario, Israeli commanders reportedly called in the attack helicopters on the military bases overwhelmed by Hamas on October 7. The helicopters appear to have fired indiscriminately, despite the risk posed to the Israeli soldiers in the base who were still alive. Israel’s was a scorched-earth policy to stop Hamas achieving its aims. That may, in part, explain the very large proportion of Israeli soldiers among the 1,300 killed that day.

    Charred bodies

    But what about the situation in the kibbutz communities? By the time the army arrived and was in position, Hamas was well dug in. It had taken the inhabitants as hostages inside their own homes. Israeli eyewitness testimony and media reports suggest Hamas was almost certainly trying to negotiate safe passage back into Gaza, using the Israeli civilians as human shields. The civilians were the Hamas fighters’ only ticket out, and they could be converted later into bargaining chips for the release of Palestinian prisoners.

    [YouTube and others are suppressing the video below – see this]

    The evidence – from Israeli media reports and eyewitnesses, as well as a host of visual clues from the crime scene itself – tell a far more complex story than the one presented nightly on the BBC.

    Did the Israeli military fire into the Hamas-controlled civilian homes in the same fashion as it had fired into its own military bases, and with the same disregard for the safety of Israelis inside? Was the goal in each case to prevent at all costs Hamas taking hostages whose release would require a very high price from Israel?

    Kibbutz Be’eri has been a favoured destination for BBC reporters keen to illustrate Hamas’ barbarity. It is where Lucy Williamson headed again this week. And yet none of her reporting highlighted comments made to the Israeli Haaretz newspaper by Tuval Escapa, the kibbutz’s security coordinator. He said Israeli military commanders had ordered the “shelling [of] houses on their occupants in order to eliminate the terrorists along with the hostages”.

    That echoed the testimony of Yasmin Porat, who sought shelter in Be’eri from the nearby Nova music festival. She told Israeli Radio that once Israeli special forces arrived: “They eliminated everyone, including the hostages because there was very, very heavy crossfire.”

    Are the images of charred bodies presented by Williamson, accompanied by a warning of their graphic, upsetting nature, incontrovertible proof that Hamas behaved like monsters, bent on the most twisted kind of vengeance? Or might those blackened remains be evidence that Israeli civilians and Hamas fighters burned alongside each other, after they were engulfed in flames caused by Israeli shelling of the houses?

    Israel will not agree to an independent investigation so a definitive answer will never be forthcoming. But that does not absolve the media of their professional and moral duty to be cautious.

    Consider for a moment the stark contrast in the western media’s treatment of events on October 7 and its treatment of the strike on the car park at Al-Ahli Baptist Hospital in northern Gaza on October 17, in which hundreds of Palestinians were reported killed.
    In the case of Al-Ahli, the media were only too ready to cast aside all the evidence that the hospital had been hit by an Israeli strike immediately Israel contested the claim. Instead journalists hurriedly amplified Israel’s counter-allegation that a Palestinian rocket had fallen on the hospital. Most of the media moved on after concluding “The truth may never be clear”, or even less credibly, that Palestinian militants were the most likely culprits.

    In telling contrast, the western media have not been willing to raise even a single question about what happened on October 7. They have enthusiastically attributed every horror that day to Hamas. They have ignored the reality of utter chaos that reigned for many hours and the potential for poor, desperate and morally dubious decision-making by the Israeli military.

    In fact, the media have gone much further. In advancing the narrative of “Hamas as savages”, they have promoted obvious fictions, such as the story that “Hamas beheaded 40 babies”. That piece of fake news was even taken up briefly by US President Joe Biden, before it was quietly walked back by his officials.


    Similarly, it is still a popular throwaway line among the western commentariat that “Hamas carried out rapes”, though once again the allegation is evidence-free so far.

    We should be clear. If Israel had serious evidence for either of these claims, it would be aggressively promoting it. Instead, it is doing the next best thing: letting innuendo gently sink into the audience’s subconscious, settling there as a prejudice that cannot be interrogated.

    Hamas undoubtedly committed war crimes on October 7 – not least, by taking civilians as human shields. But that kind of crime is one we are familiar with, one “ordinary” enough that the Israel military has been regularly documented carrying it out too. The practice of Israeli soldiers taking Palestinians as human shields goes under various names, such as the “neighbour procedure” and the “early warning procedure”.

    Worse atrocities may have happened too, especially given the unexpected scale of Hamas’ success in breaking out of Gaza. Large numbers of Palestinians escaped the enclave, some of them doubtless armed civilians with no connection to the operation. In such circumstances, it would be surprising if there were no examples of the headline-grabbing atrocities being committed.

    The issue is whether such atrocities were planned and systematic, as Israel claims and the western media repeats, or examples of rogue actions by individuals or groups. If the latter, Israel would be in no position to judge. Israel’s own history is littered with examples of such crimes, including the documented case of an Israeli army unit taking captive a Bedouin girl in 1949 and repeatedly gang-raping her.

    Savagery would certainly not be a uniquely Hamas trait. Following the October 7 attack, videos have been emerging of systematic abuses of any Hamas fighters captured, whether alive or dead. Images show them being beaten and tortured in public for the gratification of onlookers, when there is clearly not even the pretence of information gathering. Others show the bodies of Hamas fighters being defiled and mutilated.

    No one can claim the moral high ground here.

    What the media’s uncritical promotion of Israel’s “Hamas as savages” narrative has achieved is something sinister – and all too familiar from the West’s long colonial history. It has been used to demonise a whole people, presenting them either as barbarians or as the willing protectors and enablers of barbarism.

    The “savages” narrative is being weaponised by Israel to justify its mounting campaign of atrocities in Gaza. Which is why it is so important that journalists don’t simply allow themselves to be spoonfed. Far too much is at stake.

    Hamas committed war crimes on October 7 on a scale that is unprecedented for any Palestinian group. But there is little more than Israeli narrative spin so far to suggest that there was an unparalleled depravity to Hamas’ actions. Certainly from what we know, it is hard to see that anything Hamas did that day was worse, or more savage, than what Israel has been doing daily in Gaza for weeks.

    And Israel’s actions – from bombing Palestinian families to starving them of food and water – has the blessing of every major western politician.

    Jonathan Cook is an independent British journalist who has covered the Israel-Palestine beat for 20+ years. He is a winner of the Martha Gellhorn Special Prize for Journalism. He was formerly with the Guardian and Observer newspapers.

    RELATED:

    More Palestinians killed in past 34 days than in the past 22 years combined
    A Synopsis of the Israel/Palestine Conflict
    Gaza-Israel: Latest news and statistics (the first 25 days)
    It’s not just Gaza – Israel is also killing scores in the West Bank
    Israeli communities near Gaza are on stolen land, former owners consigned to the Gaza ghetto
    The Israeli strike on Al Ahli Hospital days BEFORE the famous blast
    WATCH: What was happening in Gaza BEFORE the Hamas attack that the media didn’t tell you?
    Gideon Levy: Israel Can’t Imprison Two Million Gazans Without Paying a Cruel Price
    Palestinians inspect damage to their homes caused by Israeli air strikes on October 13, 2023, in Gaza City
    Palestinians inspect damage to their homes caused by Israeli air strikes on October 13, 2023, in Gaza City (photo)


    https://israelpalestinenews.org/what-media-reports-fail-to-tell-you-about-october-7/
    What media reports fail to tell you about October 7 Alison Weir November 13, 2023 bbc, Gaza, hamas What media reports fail to tell you about October 7 BBC's Lucy Williamson is taken by the Israeli military to view kibbutz damage.regurgitating Israeli claims. (photo) It is journalistic malpractice for the media to still be repeating so credulously the Israeli military’s account of that day, including alleged Hamas atrocities that turned out to be fiction Media neglected to report much key information, e.g. Israeli military commanders had ordered the shelling of kibbutz houses in order to eliminate the “terrorists along with the hostages”… once Israeli special forces arrived: “They eliminated everyone, including the hostages” Are the images of charred bodies evidence that Israeli civilians and Hamas fighters burned alongside each other, after they were engulfed in flames caused by Israeli shelling of the houses? While this article focuses on BBC coverage, it’s analysis applies equally to US media. Some news coverage, in fact, has been considerably worse By Jonathan Cook, reposted from Jonathan Cook Substack, Nov 2, 2023. The BBC’s Lucy Williamson was taken once again this week to view the terrible destruction at a kibbutz community just outside Gaza attacked on October 7. As we have been shown so many times before, the Israeli homes were riddled with automatic fire, both inside and out. Sections of concrete wall had holes in them, or had collapsed entirely. And parts of the buildings that were still standing were deeply charred. It looked like a small snapshot of the current horrors in Gaza. There is a possible reason for those similarities – one that the BBC is studiously failing to report, despite mounting evidence from a variety of sources, including the Israeli media. Instead the BBC is sticking resolutely to a narrative crafted for them, and the rest of the western media, by the Israeli military: that Hamas alone caused all this destruction. Simply repeating that narrative without any caveats has by now reached the level of journalistic malpractice. And yet that is precisely what the BBC does night after night. Just a cursory look at the wreckage in the various kibbutz communities that were attacked that day should raise questions in the mind of any good reporter. Were Palestinian militants in a position to actually inflict physical damage to that degree and extent with the kind of light weapons they carried? And if not, who else was in a position to wreak such havoc other than Israel? A separate question that good journalists ought to be asking is this: What was the purpose of such damage? What did the Palestinian militants hope to achieve by it? The implicit answer the media is supplying is also the answer the Israeli military wants western publics to hear: that Hamas engaged in an orgy of gratuitious killing and savagery because … well, let’s say the quiet part out loud: because Palestinians are inherently savage. With that as the implicit narrative, western politicians have been handed a licence to cheerlead Israel as it murders a Palestinian child in Gaza every few minutes. Savages only understand the language of savagery, after all. Brutal tango For this reason alone, any journalist who wishes to avoid colluding in the genocide unfolding in Gaza ought to be increasingly wary of simply repeating the Israeli military’s claims about what happened on October 7. Certainly, they should not credulously regurgitate the latest agitprop from the IDF press office, as the BBC is so evidently doing. What we know from a growing body of evidence gleaned from the Israeli media and Israeli eyewitnesses – carefully laid out, for example, in this report from Max Blumenthal – is that the Israeli military was completely blindsided by that day’s events. Heavy artillery, including tanks and attack helicopters, was called in to deal with Hamas. That appears to have been a straightforward decision in regard to the military bases Hamas had overrun. Israel has a long-standing policy of seeking to prevent Israeli soldiers from being taken captive – chiefly, because of the high price Israeli society insists on paying to ensure soldiers are returned. For decades, the military’s so-called “Hannibal procedure” has directed Israeli troops to kill fellow soldiers rather than allow them to be taken captive. For the same reason, Hamas expends a great deal of energy in trying to find innovative ways to seize soldiers. The two sides are essentially engaged in a brutal tango in which each understands the other’s dance moves. Given Hamas’ situation, effectively managing the Israeli-controlled concentration camp of Gaza, it has limited resistance strategies available to it. Capturing Israeli soldiers maximises its leverage. They can be traded for the release of many of the thousands of Palestinian political prisoners held in jails inside Israel, in breach of international law. In addition, in the negotiations, Hamas usually hopes to win an easing of Israel’s 16-year siege of Gaza. To avert this scenario, Israeli commanders reportedly called in the attack helicopters on the military bases overwhelmed by Hamas on October 7. The helicopters appear to have fired indiscriminately, despite the risk posed to the Israeli soldiers in the base who were still alive. Israel’s was a scorched-earth policy to stop Hamas achieving its aims. That may, in part, explain the very large proportion of Israeli soldiers among the 1,300 killed that day. Charred bodies But what about the situation in the kibbutz communities? By the time the army arrived and was in position, Hamas was well dug in. It had taken the inhabitants as hostages inside their own homes. Israeli eyewitness testimony and media reports suggest Hamas was almost certainly trying to negotiate safe passage back into Gaza, using the Israeli civilians as human shields. The civilians were the Hamas fighters’ only ticket out, and they could be converted later into bargaining chips for the release of Palestinian prisoners. [YouTube and others are suppressing the video below – see this] The evidence – from Israeli media reports and eyewitnesses, as well as a host of visual clues from the crime scene itself – tell a far more complex story than the one presented nightly on the BBC. Did the Israeli military fire into the Hamas-controlled civilian homes in the same fashion as it had fired into its own military bases, and with the same disregard for the safety of Israelis inside? Was the goal in each case to prevent at all costs Hamas taking hostages whose release would require a very high price from Israel? Kibbutz Be’eri has been a favoured destination for BBC reporters keen to illustrate Hamas’ barbarity. It is where Lucy Williamson headed again this week. And yet none of her reporting highlighted comments made to the Israeli Haaretz newspaper by Tuval Escapa, the kibbutz’s security coordinator. He said Israeli military commanders had ordered the “shelling [of] houses on their occupants in order to eliminate the terrorists along with the hostages”. That echoed the testimony of Yasmin Porat, who sought shelter in Be’eri from the nearby Nova music festival. She told Israeli Radio that once Israeli special forces arrived: “They eliminated everyone, including the hostages because there was very, very heavy crossfire.” Are the images of charred bodies presented by Williamson, accompanied by a warning of their graphic, upsetting nature, incontrovertible proof that Hamas behaved like monsters, bent on the most twisted kind of vengeance? Or might those blackened remains be evidence that Israeli civilians and Hamas fighters burned alongside each other, after they were engulfed in flames caused by Israeli shelling of the houses? Israel will not agree to an independent investigation so a definitive answer will never be forthcoming. But that does not absolve the media of their professional and moral duty to be cautious. Consider for a moment the stark contrast in the western media’s treatment of events on October 7 and its treatment of the strike on the car park at Al-Ahli Baptist Hospital in northern Gaza on October 17, in which hundreds of Palestinians were reported killed. In the case of Al-Ahli, the media were only too ready to cast aside all the evidence that the hospital had been hit by an Israeli strike immediately Israel contested the claim. Instead journalists hurriedly amplified Israel’s counter-allegation that a Palestinian rocket had fallen on the hospital. Most of the media moved on after concluding “The truth may never be clear”, or even less credibly, that Palestinian militants were the most likely culprits. In telling contrast, the western media have not been willing to raise even a single question about what happened on October 7. They have enthusiastically attributed every horror that day to Hamas. They have ignored the reality of utter chaos that reigned for many hours and the potential for poor, desperate and morally dubious decision-making by the Israeli military. In fact, the media have gone much further. In advancing the narrative of “Hamas as savages”, they have promoted obvious fictions, such as the story that “Hamas beheaded 40 babies”. That piece of fake news was even taken up briefly by US President Joe Biden, before it was quietly walked back by his officials. Similarly, it is still a popular throwaway line among the western commentariat that “Hamas carried out rapes”, though once again the allegation is evidence-free so far. We should be clear. If Israel had serious evidence for either of these claims, it would be aggressively promoting it. Instead, it is doing the next best thing: letting innuendo gently sink into the audience’s subconscious, settling there as a prejudice that cannot be interrogated. Hamas undoubtedly committed war crimes on October 7 – not least, by taking civilians as human shields. But that kind of crime is one we are familiar with, one “ordinary” enough that the Israel military has been regularly documented carrying it out too. The practice of Israeli soldiers taking Palestinians as human shields goes under various names, such as the “neighbour procedure” and the “early warning procedure”. Worse atrocities may have happened too, especially given the unexpected scale of Hamas’ success in breaking out of Gaza. Large numbers of Palestinians escaped the enclave, some of them doubtless armed civilians with no connection to the operation. In such circumstances, it would be surprising if there were no examples of the headline-grabbing atrocities being committed. The issue is whether such atrocities were planned and systematic, as Israel claims and the western media repeats, or examples of rogue actions by individuals or groups. If the latter, Israel would be in no position to judge. Israel’s own history is littered with examples of such crimes, including the documented case of an Israeli army unit taking captive a Bedouin girl in 1949 and repeatedly gang-raping her. Savagery would certainly not be a uniquely Hamas trait. Following the October 7 attack, videos have been emerging of systematic abuses of any Hamas fighters captured, whether alive or dead. Images show them being beaten and tortured in public for the gratification of onlookers, when there is clearly not even the pretence of information gathering. Others show the bodies of Hamas fighters being defiled and mutilated. No one can claim the moral high ground here. What the media’s uncritical promotion of Israel’s “Hamas as savages” narrative has achieved is something sinister – and all too familiar from the West’s long colonial history. It has been used to demonise a whole people, presenting them either as barbarians or as the willing protectors and enablers of barbarism. The “savages” narrative is being weaponised by Israel to justify its mounting campaign of atrocities in Gaza. Which is why it is so important that journalists don’t simply allow themselves to be spoonfed. Far too much is at stake. Hamas committed war crimes on October 7 on a scale that is unprecedented for any Palestinian group. But there is little more than Israeli narrative spin so far to suggest that there was an unparalleled depravity to Hamas’ actions. Certainly from what we know, it is hard to see that anything Hamas did that day was worse, or more savage, than what Israel has been doing daily in Gaza for weeks. And Israel’s actions – from bombing Palestinian families to starving them of food and water – has the blessing of every major western politician. Jonathan Cook is an independent British journalist who has covered the Israel-Palestine beat for 20+ years. He is a winner of the Martha Gellhorn Special Prize for Journalism. He was formerly with the Guardian and Observer newspapers. RELATED: More Palestinians killed in past 34 days than in the past 22 years combined A Synopsis of the Israel/Palestine Conflict Gaza-Israel: Latest news and statistics (the first 25 days) It’s not just Gaza – Israel is also killing scores in the West Bank Israeli communities near Gaza are on stolen land, former owners consigned to the Gaza ghetto The Israeli strike on Al Ahli Hospital days BEFORE the famous blast WATCH: What was happening in Gaza BEFORE the Hamas attack that the media didn’t tell you? Gideon Levy: Israel Can’t Imprison Two Million Gazans Without Paying a Cruel Price Palestinians inspect damage to their homes caused by Israeli air strikes on October 13, 2023, in Gaza City Palestinians inspect damage to their homes caused by Israeli air strikes on October 13, 2023, in Gaza City (photo) https://israelpalestinenews.org/what-media-reports-fail-to-tell-you-about-october-7/
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    What media reports fail to tell you about October 7
    It's journalistic malpractice for media to repeat the Israeli military's accounts, including alleged atrocities that turned out to be fiction
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