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  • 12 Israeli sensor technologies that will rock your world
    No more canaries in mines: Today’s sensors provide key information on everything from digital health to airport safety.

    By Brian Blum
    Sensors translate physical phenomena to a measurable signal. Photo courtesy of Consumer Physics/SCiO
    Sensors are the hidden brain in everything from precision agriculture to connected cars, home appliances to security systems, smart cities to digital health.

    “A sensor is anything that translates a physical phenomenon to a measurable signal or other information. For example, in the past they used canaries as sensors for poisonous gas in mines,” explains Amichai Yifrach, an Israeli expert in military and civilian sensor development and currently the CTO of ag-tech startup Flux.

    “Using that definition, Israel is on the cutting edge of technology in all aspects of sensors,” he tells ISRAEL21c. “A lot of it is related to our capabilities in sensing things that others cannot, especially in relation to border security and airport control.”

    Historically, Israel’s edge in sensor technology comes from defense needs and much of the sector is still focused on military applications, with companies such as Elbit Systems, Rafael Advanced Defense Systems and Seraphim Optronics in the lead.

    YOU CAN GET ISRAEL21c NEWS DELIVERED STRAIGHT TO YOUR INBOX.

    But as in many other fields, knowhow from the military gave a huge boost to Israel’s civilian sensor industry. “On the consumer side, we’re strong in image processing and algorithms. We have very good chemists, too,” says Yifrach.

    “Sensors will be more and more important in water quality, air quality and even food quality, like for makers of wine, beer or balsamic vinegar,” Yifrach predicts. “Processes that follow chemical or physical properties need sensing to deduct valuable information for future quality or efficiency of the process. It all comes down to monitoring and controlling processes for quality.”

    ISRAEL21c chose a dozen Israeli sensor pioneers to illustrate the country’s strength in this powerful sector.

    Sensifree
    Sensifree specializes in low-power, contact-free, electromagnetic sensors that accurately collect a range of continuous biometric data without the need to touch the human body. Its first product, a contactless heartrate sensor for wearable devices such as watches, fitness trackers and smart clothing, will be followed by a cuff-free blood-pressure sensor.

    Based in California with R&D in Petah Tikva, Sensifree recently won $5 million in Series A financing, bringing its total funding since launching its revolutionary RF-based biometric sensor technology to $7 million.

    MS Technologies
    Based in Herzliya Pituah, MS Tech designs and manufactures nanotechnology detection and diagnostic sensors. Major airlines use its hand-held, non-radioactive explosives and narcotics detectors for carry-on baggage inspection, air-cargo screening and passenger security checks in several airports. Other industries that use MS Tech sensor technologies include food safety and product inspection, biomedical diagnostics, fire and smoke detection, water and air monitoring and aerospace.

    https://www.youtube.com/watch?v=id4Q4SIYmRs

    ContinUse Biometrics
    ContinUse of Tel Aviv received a strategic investment from the multinational corporation Tyco to develop nanotechnology sensors that will be embedded into a range of construction and smart-home solutions.

    ContinUse Biometrics’ biometric no-contact sensor — based on technology developed over a decade by Bar-Ilan and Valencia universities — can detect heartbeat, blood pressure, breathing pace, glucose level, oxygen saturation and alcohol levels in the blood of a fully dressed person without touching the person. This data can be used to authenticate identity and manage access for security and smart-home applications, workplaces and sensitive facilities.

    Vayyar
    Vayyar sensors could make every cellphone or tablet a full 3D imaging system. Based in Yehud, Vayyar uses low-power radio transmissions to scan objects in a fraction of a second and create an enhanced imaging experience. One of the applications is better detection of irregularities in an object being examined, for example to detect tumors on mammograms or bacteria in milk bottling. The company recently won the Fast Pitch Contest sponsored by the Global Electronics Industry Association in Tel Aviv.

    https://www.youtube.com/watch?v=TLjUK-teB8o

    Elfi-Tech
    Elfi-Tech of Rehovot has introduced several sensor products for noninvasive measurements of physiological and blood parameters for use in fitness, wellness and first-line diagnostics apps. Its proprietary mDLS sensor module was integrated into Samsung’s Simband wearable open platform, and now the company is collaborating with pharma and medical-device industry to integrate mDLS into patient-monitoring devices. Elfi-Tech also is working with companies in the big-data analytics space on its new Data Logger device, which collects and analyzes mass amounts of cardiovascular health data from a single wearable.



    Accurate Sensors Technologies
    Started in 1994 as 3T, Accurate Sensors Technologies manufactures no-contact temperature-measurement solutions for extreme conditions, such as digital infrared thermometers. Headquartered in Misgav, the company also makes plug-and-play pyrometers — instruments for measuring high temperatures in furnaces and kilns – for the aluminum industry.



    Neteera Technologies
    Founded in January 2015 in partnership with Yissum Research Development Company of the Hebrew University of Jerusalem, Neteera is developing novel Terahertz imaging and sensing devices, of unprecedented resolution, size, cost-effectiveness and reliability.

    Neteera’s technology is revolutionary as it allows for multiple applications such as all-weather and night imaging for automotive and surveillance applications; weapons, explosives and contraband detection; medical imaging; manufacturing and quality control; monitoring of human physiological and biometric indicators and more.

    Occipital
    Occipital’s Structure Sensor is touted as the world’s first 3D sensor for mobile devices, adding 3D scanning, large-scale reconstruction and augmented-reality (AR) capabilities to new or existing iOS devices.

    Named a Popular Science “Best of What’s New” gadget for 2013, and recognized with a 2014 CES Innovations award, the Structure Sensor hardware platform gives developers the ability to easily create applications such as 3D mapping of indoor spaces, AR games, body scanning for fitness tracking and virtual clothes fitting, and 3D object scanning for easy 3D content creation.

    Occipital’s Structure Sensor can be used for object and body scans. Photo: courtesy
    Occipital’s Structure Sensor can be used for object and body scans. Photo: courtesy
    Consumer Physics
    Consumer Physics’ soon-to-be-released SCiO device uses optical sensors to read the chemical makeup of just about anything without touching it: for example, the fat in a piece of cake, the ripeness of fruit, the ingredients in medicines, the properties of cosmetics and precious stones.



    Nexense
    Ramat Gan-based Nexense makes a sensor system worn as a chest strap or wristwatch to monitor various physical parameters during sleep for the treatment of snoring and sleep apnea. The product, already approved in Europe and Israel, counts GE Healthcare among its investors and is expected to go public in 2017.

    EarlySense
    EarlySense uses an under-bed sensor system for continuous monitoring of patient vital signs and movement in hospitals and other healthcare settings. Without ever touching the patient, EarlySense helps the clinical team manage early detection of patient deterioration, fall prevention and prevention of bedsores.

    EarlySense goes under the patient’s bed. Photo: courtesy
    EarlySense goes under the patient’s bed. Photo: courtesy
    Saturas
    Saturas, founded in 2013 in the Trendlines incubator program, has developed a system of miniature implanted sensors and wireless transponders for determining the water status of fruit trees easily and inexpensively. According to CEO Anat Halgoa Solomon, the system (to be available in 2018) could save farmers up to 20 percent on water usage.

    Among many other sensor-based ag-tech companies in Israel are Phytech, AutoAgronom, CropX, GreenIQ and Flux.


    ISRAEL'S CIVILIAN BIOSENSOR INDUSTRY

    "Sensors are the hidden brain in everything from precision agriculture to connected cars, home appliances to security systems, smart cities to digital health."

    “Sensors will be more and more important in water quality, air quality and even food quality, like for makers of wine, beer or balsamic vinegar"

    https://www.israel21c.org/12-israeli-sensor-technologies-that-will-rock-your-world/

    https://donshafi911.blogspot.com/2024/02/12-israeli-sensor-technologies-that.html
    12 Israeli sensor technologies that will rock your world No more canaries in mines: Today’s sensors provide key information on everything from digital health to airport safety. By Brian Blum Sensors translate physical phenomena to a measurable signal. Photo courtesy of Consumer Physics/SCiO Sensors are the hidden brain in everything from precision agriculture to connected cars, home appliances to security systems, smart cities to digital health. “A sensor is anything that translates a physical phenomenon to a measurable signal or other information. For example, in the past they used canaries as sensors for poisonous gas in mines,” explains Amichai Yifrach, an Israeli expert in military and civilian sensor development and currently the CTO of ag-tech startup Flux. “Using that definition, Israel is on the cutting edge of technology in all aspects of sensors,” he tells ISRAEL21c. “A lot of it is related to our capabilities in sensing things that others cannot, especially in relation to border security and airport control.” Historically, Israel’s edge in sensor technology comes from defense needs and much of the sector is still focused on military applications, with companies such as Elbit Systems, Rafael Advanced Defense Systems and Seraphim Optronics in the lead. YOU CAN GET ISRAEL21c NEWS DELIVERED STRAIGHT TO YOUR INBOX. But as in many other fields, knowhow from the military gave a huge boost to Israel’s civilian sensor industry. “On the consumer side, we’re strong in image processing and algorithms. We have very good chemists, too,” says Yifrach. “Sensors will be more and more important in water quality, air quality and even food quality, like for makers of wine, beer or balsamic vinegar,” Yifrach predicts. “Processes that follow chemical or physical properties need sensing to deduct valuable information for future quality or efficiency of the process. It all comes down to monitoring and controlling processes for quality.” ISRAEL21c chose a dozen Israeli sensor pioneers to illustrate the country’s strength in this powerful sector. Sensifree Sensifree specializes in low-power, contact-free, electromagnetic sensors that accurately collect a range of continuous biometric data without the need to touch the human body. Its first product, a contactless heartrate sensor for wearable devices such as watches, fitness trackers and smart clothing, will be followed by a cuff-free blood-pressure sensor. Based in California with R&D in Petah Tikva, Sensifree recently won $5 million in Series A financing, bringing its total funding since launching its revolutionary RF-based biometric sensor technology to $7 million. MS Technologies Based in Herzliya Pituah, MS Tech designs and manufactures nanotechnology detection and diagnostic sensors. Major airlines use its hand-held, non-radioactive explosives and narcotics detectors for carry-on baggage inspection, air-cargo screening and passenger security checks in several airports. Other industries that use MS Tech sensor technologies include food safety and product inspection, biomedical diagnostics, fire and smoke detection, water and air monitoring and aerospace. https://www.youtube.com/watch?v=id4Q4SIYmRs ContinUse Biometrics ContinUse of Tel Aviv received a strategic investment from the multinational corporation Tyco to develop nanotechnology sensors that will be embedded into a range of construction and smart-home solutions. ContinUse Biometrics’ biometric no-contact sensor — based on technology developed over a decade by Bar-Ilan and Valencia universities — can detect heartbeat, blood pressure, breathing pace, glucose level, oxygen saturation and alcohol levels in the blood of a fully dressed person without touching the person. This data can be used to authenticate identity and manage access for security and smart-home applications, workplaces and sensitive facilities. Vayyar Vayyar sensors could make every cellphone or tablet a full 3D imaging system. Based in Yehud, Vayyar uses low-power radio transmissions to scan objects in a fraction of a second and create an enhanced imaging experience. One of the applications is better detection of irregularities in an object being examined, for example to detect tumors on mammograms or bacteria in milk bottling. The company recently won the Fast Pitch Contest sponsored by the Global Electronics Industry Association in Tel Aviv. https://www.youtube.com/watch?v=TLjUK-teB8o Elfi-Tech Elfi-Tech of Rehovot has introduced several sensor products for noninvasive measurements of physiological and blood parameters for use in fitness, wellness and first-line diagnostics apps. Its proprietary mDLS sensor module was integrated into Samsung’s Simband wearable open platform, and now the company is collaborating with pharma and medical-device industry to integrate mDLS into patient-monitoring devices. Elfi-Tech also is working with companies in the big-data analytics space on its new Data Logger device, which collects and analyzes mass amounts of cardiovascular health data from a single wearable. Accurate Sensors Technologies Started in 1994 as 3T, Accurate Sensors Technologies manufactures no-contact temperature-measurement solutions for extreme conditions, such as digital infrared thermometers. Headquartered in Misgav, the company also makes plug-and-play pyrometers — instruments for measuring high temperatures in furnaces and kilns – for the aluminum industry. Neteera Technologies Founded in January 2015 in partnership with Yissum Research Development Company of the Hebrew University of Jerusalem, Neteera is developing novel Terahertz imaging and sensing devices, of unprecedented resolution, size, cost-effectiveness and reliability. Neteera’s technology is revolutionary as it allows for multiple applications such as all-weather and night imaging for automotive and surveillance applications; weapons, explosives and contraband detection; medical imaging; manufacturing and quality control; monitoring of human physiological and biometric indicators and more. Occipital Occipital’s Structure Sensor is touted as the world’s first 3D sensor for mobile devices, adding 3D scanning, large-scale reconstruction and augmented-reality (AR) capabilities to new or existing iOS devices. Named a Popular Science “Best of What’s New” gadget for 2013, and recognized with a 2014 CES Innovations award, the Structure Sensor hardware platform gives developers the ability to easily create applications such as 3D mapping of indoor spaces, AR games, body scanning for fitness tracking and virtual clothes fitting, and 3D object scanning for easy 3D content creation. Occipital’s Structure Sensor can be used for object and body scans. Photo: courtesy Occipital’s Structure Sensor can be used for object and body scans. Photo: courtesy Consumer Physics Consumer Physics’ soon-to-be-released SCiO device uses optical sensors to read the chemical makeup of just about anything without touching it: for example, the fat in a piece of cake, the ripeness of fruit, the ingredients in medicines, the properties of cosmetics and precious stones. Nexense Ramat Gan-based Nexense makes a sensor system worn as a chest strap or wristwatch to monitor various physical parameters during sleep for the treatment of snoring and sleep apnea. The product, already approved in Europe and Israel, counts GE Healthcare among its investors and is expected to go public in 2017. EarlySense EarlySense uses an under-bed sensor system for continuous monitoring of patient vital signs and movement in hospitals and other healthcare settings. Without ever touching the patient, EarlySense helps the clinical team manage early detection of patient deterioration, fall prevention and prevention of bedsores. EarlySense goes under the patient’s bed. Photo: courtesy EarlySense goes under the patient’s bed. Photo: courtesy Saturas Saturas, founded in 2013 in the Trendlines incubator program, has developed a system of miniature implanted sensors and wireless transponders for determining the water status of fruit trees easily and inexpensively. According to CEO Anat Halgoa Solomon, the system (to be available in 2018) could save farmers up to 20 percent on water usage. Among many other sensor-based ag-tech companies in Israel are Phytech, AutoAgronom, CropX, GreenIQ and Flux. ISRAEL'S CIVILIAN BIOSENSOR INDUSTRY "Sensors are the hidden brain in everything from precision agriculture to connected cars, home appliances to security systems, smart cities to digital health." “Sensors will be more and more important in water quality, air quality and even food quality, like for makers of wine, beer or balsamic vinegar" https://www.israel21c.org/12-israeli-sensor-technologies-that-will-rock-your-world/ https://donshafi911.blogspot.com/2024/02/12-israeli-sensor-technologies-that.html
    WWW.ISRAEL21C.ORG
    12 Israeli sensor technologies that will rock your world - ISRAEL21c
    No more canaries in mines: Today's sensors provide key information on everything from digital health to airport safety.
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  • "For god's sake, stop complying. Start rebelling. They are out to get you if you do not resist."

    German MEP, Christine Anderson: The so-called "pandemic" was a beta test—conducted by unelected globalists—to see how easy it would be to seize totalitarian control, under the pretext of a global "emergency".

    "The goal, ultimately, is to transform our free and democratic societies into totalitarian societies. Their goal is to strip each and every one of us of our fundamental rights, of freedom, democracy, the rule of law. They want to get rid of all of this."

    "In the entire history of mankind, there has never been a political elite concerned about the well being of regular people, and it isn't any different now."

    Credit: @AndersonAfDMdEP

    Source: youtube.com/watch?v=4MIS18…

    Follow my backup account: @wide_awake_news

    Subscribe to me on Telegram: t.me/realwideawakem…

    Subscribe to my newsletter, for daily email updates: wide-awake-media.com


    https://x.com/wideawake_media/status/1757756893664104781?s=46
    "For god's sake, stop complying. Start rebelling. They are out to get you if you do not resist." German MEP, Christine Anderson: The so-called "pandemic" was a beta test—conducted by unelected globalists—to see how easy it would be to seize totalitarian control, under the pretext of a global "emergency". "The goal, ultimately, is to transform our free and democratic societies into totalitarian societies. Their goal is to strip each and every one of us of our fundamental rights, of freedom, democracy, the rule of law. They want to get rid of all of this." "In the entire history of mankind, there has never been a political elite concerned about the well being of regular people, and it isn't any different now." Credit: @AndersonAfDMdEP Source: youtube.com/watch?v=4MIS18… Follow my backup account: @wide_awake_news Subscribe to me on Telegram: t.me/realwideawakem… Subscribe to my newsletter, for daily email updates: wide-awake-media.com https://x.com/wideawake_media/status/1757756893664104781?s=46
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  • An easy and proven way to Build good habits!!!
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  • Digital wallets (Cryptocurrency Wallets): digital wallets are a crucial tool in the world of digital currencies, as they contribute to the safe and efficient storage and management of digital assets. Many investors and traders offer different types of digital wallets that meet their needs and preferences. In this article, we will review the main types of digital wallets and their features:

    Paper wallets (Paper Wallets):
    Paper wallets are one of the safest ways to store digital currencies.
    The private key and the public address are generated on a sheet of paper or document.
    They do not require an internet connection, which minimizes the risk of electronic hacking.

    Hot wallets (Hot Wallets):
    It works online and remains connected to the network.
    They include web wallets, mobile wallets, software.
    Suitable for daily transactions and efficient trading.

    Cold Wallets (Cold Wallets):
    It saves without an internet connection, which strengthens its security.
    Top wallets include external devices such as USB, and paper wallets.
    They are used to store digital currencies for long periods without the risk of hacking online.

    Hardware Wallets (Hardware Wallets):
    A small device that securely holds encryption keys.
    They are considered among the most secure wallets, as it is very difficult to hack them.
    They are usually used for long-term storage of digital currencies.

    Software Wallets (Software Wallets):
    They are considered easy to use and are available for various systems.
    They are installed on personal devices or mobile phones.
    It provides flexibility in accessing and controlling digital assets.

    Multi-Asset wallets (Multi-Asset Wallets):
    Supports storage and management of several types of digital currencies.
    It provides users with the ability to easily navigate between various assets.

    Ultimately, users choose the type of digital wallet according to their individual needs and the level of security they would like to achieve. Investors should also consider security updates and precautionary measures to ensure that their digital assets are protected from security threats.
    Digital wallets (Cryptocurrency Wallets): digital wallets are a crucial tool in the world of digital currencies, as they contribute to the safe and efficient storage and management of digital assets. Many investors and traders offer different types of digital wallets that meet their needs and preferences. In this article, we will review the main types of digital wallets and their features: Paper wallets (Paper Wallets): Paper wallets are one of the safest ways to store digital currencies. The private key and the public address are generated on a sheet of paper or document. They do not require an internet connection, which minimizes the risk of electronic hacking. Hot wallets (Hot Wallets): It works online and remains connected to the network. They include web wallets, mobile wallets, software. Suitable for daily transactions and efficient trading. Cold Wallets (Cold Wallets): It saves without an internet connection, which strengthens its security. Top wallets include external devices such as USB, and paper wallets. They are used to store digital currencies for long periods without the risk of hacking online. Hardware Wallets (Hardware Wallets): A small device that securely holds encryption keys. They are considered among the most secure wallets, as it is very difficult to hack them. They are usually used for long-term storage of digital currencies. Software Wallets (Software Wallets): They are considered easy to use and are available for various systems. They are installed on personal devices or mobile phones. It provides flexibility in accessing and controlling digital assets. Multi-Asset wallets (Multi-Asset Wallets): Supports storage and management of several types of digital currencies. It provides users with the ability to easily navigate between various assets. Ultimately, users choose the type of digital wallet according to their individual needs and the level of security they would like to achieve. Investors should also consider security updates and precautionary measures to ensure that their digital assets are protected from security threats.
    0 Comments 0 Shares 2944 Views
  • 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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  • Will Disease X be Leaked in 2025?

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    New Year Donation Drive: Global Research Is Committed to the “Unspoken Truth”

    ***

    The WHO’s pandemic treaty is the gateway to a global, top-down totalitarian regime, a one world government. The reason we can be sure there will be additional pandemics, whether manufactured using either fear and hype alone or an actual bioweapon created for this very purpose, is because the takeover plan, aka The Great Reset, is based on the premise that we need global biosecurity surveillance and centralized response

    A new contagion will likely be born in 2025, and media are already preparing us for it

    January 15-19, 2024, global leaders met at the World Economic Forum’s (WEF) Davos summit where the key topic of discussion was “Preparing for Disease X,” a hypothetical new pandemic predicted to kill 20 times more people than COVID-19

    In August 2023, a new vaccine research facility was set up in Wiltshire, England, to begin work on a vaccine against the unknown “Disease X”

    The U.S. Congress introduced the “Disease X Act of 2023” (H.R.3832) in June 2023. The bill calls for the establishment of a BARDA program to develop “medical countermeasures for viral threats with pandemic potential.” The bill was referred to the Subcommittee on Health in early June 2023 but has not yet been passed

    *



    The COVID-19 pandemic allowed for an unprecedented shift in power and wealth distribution across the world and, as predicted, it was not to be a one-off event. A new contagion will likely be born in 2025, and media are already preparing us for it.

    January 15-19, 2024, global leaders met at the World Economic Forum’s (WEF) Davos summit where the key topic of discussion was “Preparing for Disease X,”1 a hypothetical new pandemic predicted to emerge in 2025 and kill 20 times more people than COVID-19.2 As reported by the Mirror:3

    “The World Health Organization (WHO) has warned of a potential Disease X since 2017, a term indicating an unknown pathogen that could cause a serious international epidemic …

    Public speakers at the ‘Preparing for Disease X’ event next Wednesday [January 17, 2024] include Tedros Adhanom Ghebreyesus, director-general of the WHO, Brazilian minister of health Nisia Trindade Lima, and Michel Demaré, chair of the board at AstraZeneca.

    In their first post-pandemic meeting held in November 2022, the WHO brought over 300 scientists to consider which of over 25 virus families and bacteria could potentially create another pandemic.

    The list the team came up with included: the Ebola virus, the Marburg virus disease, Covid-19, SARS, and the Middle East respiratory syndrome coronavirus (MERS-CoV). Others included lassa fever, nipah and henipaviral diseases, zift Valley fever, and zika — as well as the unknown pathogen that would cause ‘Disease X.’”

    I’ve interviewed Meryl Nass about how the WHO is trying to take over aspects of everyone’s lives. She just published an important piece over the weekend, Why Is Davos So Interested in Disease? about how the WEF and the WHO have become partners to terrify the world.

    Alexis Baden-Mayer, Esq., political director for the Organic Consumers Association, did some digging into the participants of this WEF event, and the two things they all have in common are 1) dumping the AstraZeneca COVID shot on the developing world (primarily India and Brazil) after rich countries rejected it due to its admitted blood clotting risk, and 2) pushing for the implementation of medical AI systems that will eliminate doctors along with patient choice and privacy.

    Practice Runs or Responsible Planning?

    In a January 11, 2024, tweet, Fox News analyst and former assistant secretary for public affairs for the U.S. Treasury Department, Monica Crowley, wrote:4

    “From the same people who brought you COVID-19 now comes Disease X: Next week in Davos, the unelected globalists at the World Economic Forum will hold a panel on a future pandemic 20x deadlier than COVID …

    Just in time for the election, a new contagion to allow them to implement a new WHO treaty, lock down again, restrict free speech and destroy more freedoms. Sound far-fetched? So did what happened in 2020. When your enemies tell you what they’re planning and what they’re planning FOR, believe them. And get ready.”

    Dr. Stuart Ray, vice chair of medicine for data integrity and analytics at Johns Hopkins’ Department of Medicine, dismissed such warnings, telling Fortune magazine5 that “Coordination of public health response is not conspiracy, it’s simply responsible planning.”

    I’d be willing to believe him if it wasn’t for a now-obvious trend: Whatever the globalists claim will happen actually does happen at a remarkable frequency, and their prognostic capabilities become easier to explain when you consider that most lethal pandemics have been caused by manmade viruses, the products of gain-of-function research. It’s pretty easy to predict a new viral outbreak if you have said virus waiting in the wings.

    With that in mind, recent research from China certainly raises concern, to say the least. According to a January 3, 2024, preprint,6 a SARS-CoV-2-related pangolin coronavirus — described as a “cell culture-adapted mutant” called GX_P2V that was first cultured in 2017 — was found to kill 100% of the humanized mice (ACE2-transgenic mice) infected with it.7

    The primary cause of death was brain inflammation. According to the authors, “this is the first report showing that a SARS-CoV-2-related pangolin coronavirus can cause 100% mortality in hACE2 mice, suggesting a risk for GX_P2V to spill over into humans.”

    However, if this virus mutated as a result of passaging through cell cultures, then it’s not likely to emerge in the wild. It’s another unnatural lab creation, so rather than saying it may spill over from pangolins to humans, it would be more accurate to admit that it may pose a (rather serious) risk to humans were a lab escape to occur.

    COVID Dress Rehearsals

    In 2017, Johns Hopkins Center of Health Security held a coronavirus pandemic simulation called the SPARS Pandemic 2025-2028 scenario.8 Importantly, the exercise stressed “communication dilemmas concerning medical countermeasures that could plausibly emerge” in a pandemic scenario.

    Then, in October 2019, less than three months before the COVID-19 outbreak, the Bill & Melinda Gates Foundation in collaboration with Johns Hopkins and the World Economic Forum hosted Event 201.

    The name itself suggests it may have been a continuation of the SPARS Pandemic exercise. College courses are numbered based on their prerequisites. A 101 course does not require any prior knowledge whereas 201 courses require prior familiarity with the topic at hand.

    As in the SPARS Pandemic scenario, Event 201 involved an outbreak of a highly infectious coronavirus, and the primary (if not sole) focus of the exercise was, again, how to control information and keep “misinformation” in check, not how to effectively discover and share remedies.

    Social media censorship played a prominent role in the Event 201 plan, and in the real-world events of 2020 through the present, accurate information about vaccine development, production and injury has indeed been effectively suppressed around the world, thanks to social media companies and Google’s censoring of opposing viewpoints.

    In March 2021, an outbreak of “an unusual strain of monkeypox virus” was simulated.9 In late July the following year, the WHO director-general declared that a multi-country outbreak of monkeypox constituted a public health emergency of international concern,10 against his own advisory group.

    ‘Catastrophic Contagion’ Exercise

    Considering both of these simulations, SPARS (“Event 101”?) and Event 201, foreshadowed what eventually occurred in real life during COVID, when Gates hosts yet another pandemic exercise, it’s worth paying attention to the details.

    October 23, 2022, Gates, Johns Hopkins and the WHO cohosted “a global challenge exercise” dubbed “Catastrophic Contagion,”11,12 involving a fictional pathogen called “severe epidemic enterovirus respiratory syndrome 2025” (SEERS-25).

    Enterovirus D6813 is typically associated with cold and flu-like illness in infants, children and teens. In rare cases, it’s also been known to cause viral meningitis and acute flaccid myelitis, a neurological condition resulting in muscle weakness and loss of reflexes in one or more extremities.

    Enteroviruses A71 and A6 are known to cause hand, foot and mouth disease,14 while poliovirus, the prototypical enterovirus, causes polio (poliomyelitis), a potentially life-threatening type of paralysis that primarily affects children under age 5. So, the virus they modeled in this simulation appears to be something similar to enterovirus D68, but worse.

    Vaccine Drug Trials Begin for Deadly Nipah Virus

    One known virus that bears some resemblance to the fictional SEERS-25 is the Nipah virus. This virus has a kill rate of about 75%,15 and survivors oftentimes face long-term neurological issues stemming from the infection. Nipah is also said to affect children to a greater degree than adults.16

    Incidentally, human trials for a vaccine against the deadly Nipah virus were recently launched.17Volunteers received their first shots in early January 2024. The experimental injection uses the same viral vector technology used to produce AstraZeneca’s COVID shot.

    The trial is reportedly being carried out by the University of Oxford in an undisclosed area where Nipah is actively infecting victims. (India seems to be indicated, as an outbreak in Kerala killed two people and hospitalized three in September 2023.18)

    The disease is thought to spread via interaction with infected animals such as goats, pigs, cats and horses. It may also spread via tainted blood products and food. Symptoms can emerge anywhere from a few days after exposure to as long as 45 days.

    Initial symptoms include fever, headache and respiratory illness, which can rapidly progress to encephalitis (brain swelling), seizures and coma within just a couple of days. According to the WHO, pigs are known to be “highly contagious” during the incubation period, and it’s possible that humans may be as well, although that has yet to be confirmed.

    Training African Leaders to Go Along with the Narrative

    Tellingly, the Catastrophic Contagion exercise focused on getting leadership in African countries involved and trained in following the script. African nations went “off script” more often than others during the COVID pandemic, and didn’t follow in the footsteps of developed nations when it came to pushing the jabs.

    As a result, vaccine makers now face the problem of having a huge control group, as the COVID jab uptake on the African continent was only 6%,19 yet it fared far better than developed nations in terms of COVID-19 infections and related deaths.20

    The Catastrophic Contagion exercise predicts SEERS-25 will kill 20 million people worldwide, including 15 million children, and many who survive the infection will be left with paralysis and/or brain damage. In other words, the “cue” given is that the next pandemic may target children rather than the elderly, as was the case with COVID-19.

    Vaccine Against Unknown ‘X’ Pathogen Is Already in the Works


    In August 2023, a new vaccine research facility was set up in Wiltshire, England, fully staffed with more 200 scientists, to begin work on a vaccine against the unknown “Disease X.” As reported by Metro:21

    “It took 362 days to develop the Covid-19 vaccine. But the Vaccine Development and Evaluation Centre team wants to reduce that time to 100 days. Scientists at the facility will develop a range of prototype vaccines and tests.

    The new lab is a part of a global effort to respond to global health threats. The UK and other G7 countries signed up to the ‘100 Days Mission’ in 2021. The government has invested £65 million into the lab.

    Professor Dame Jenny Harries, the head of the UK Health Security Agency, said the new facility would ‘ensure that we prepare so that if we have a new Disease X, a new pathogen, we have as much of that work in advance as possible.’”

    In the U.S., Congress also introduced the “Disease X Act of 2023” (H.R.383222) back in June 2023. The bill calls for the establishment of a BARDA program to develop “medical countermeasures for viral threats with pandemic potential.” The bill was referred to the Subcommittee on Health in early June 2023 but has not yet been passed.

    The Disease X Act amends a section of the Public Health Service Act with two new clauses that call for “the identification and development of platform manufacturing technologies needed for advanced development and manufacturing of medical countermeasures for viral families which have significant potential to cause a pandemic,” and “advanced research and development of flexible medical countermeasures against priority respiratory virus families and other respiratory viral pathogens with a significant potential to cause a pandemic, with both pathogen-specific and pathogen-agnostic approaches …”

    Needless to say, since it’s impossible to customize vaccines using the conventional method of growing viruses in eggs or some other cell media in 100 days, it seems inevitable that all these efforts are about the expansion of gene-based technologies. This, despite the fact that the mRNA technology used for the COVID jabs has proven to be disastrous from a safety standpoint, and ineffective to boot.

    Why Manufactured Pandemics Will Continue

    At this point, it’s quite clear that “biosecurity” is the chosen means by which the globalist cabal intends to seize power over the world. The WHO is working on securing sole power over pandemic response globally through its international pandemic treaty which, if implemented, will eradicate the sovereignty of all member nations.

    The WHO’s pandemic treaty is the gateway to a global, top-down totalitarian regime, a one world government. Ultimately, the WHO intends to dictate all health care. But to secure that power, they will need more pandemics. COVID-19 alone was not enough to get everyone onboard with a centralized pandemic response unit, and they probably knew that from the start.

    So, the reason we can be sure there will be additional pandemics, whether manufactured using either fear and hype alone or an actual bioweapon created for this very purpose, is because the takeover plan, aka The Great Reset, is based on the premise that we need global biosecurity surveillance and centralized response.

    Biosecurity, in turn, is the justification for an international vaccine passport, which the G20 has signed on to, and that passport will also be your digital identification. That digital ID, then, will be tied to your social credit score, personal carbon footprint tracker, medical records, educational records, work records, social media presence, purchase records, your bank accounts and a programmable central bank digital currency (CBDC).

    Once all these pieces are fully connected, you’ll be in a digital prison, and the ruling cabal — whether officially a one world government by then or not — will have total control over your life from cradle to grave.

    We’re Already Suffering Under a Pseudo-One World Government

    We actually already have a pseudo-one world government, in the form of Bill Gates’ nongovernmental organizations (NGOs). They are making health care decisions that should be left to individual nations and/or states, and they’re making decisions that will line their own pockets, regardless of what happens to the public health-wise.

    They coordinate and synchronize pandemic communication during simulated practice runs, and then, when the real-world situation emerges that fits the bill, the preplanned script is played out more or less verbatim.

    Between the G20 declaration to implement an international vaccine passport under the auspice of the WHO, and the WHO’s pandemic treaty, everything is lined up to take control of the next pandemic, and in so doing, further securing the foundation for a one world government.

    As discussed in my 2021 article, “COVID-19 Dress Rehearsals and Proof of the Plan,” the pandemic measures rolled out for COVID-19 were the culmination of decades of careful planning to radically and permanently alter the governance and social structures of the world.

    The medical system has been used in the past to drive forward a New World Order agenda — now rebranded as “The Great Reset” — and it’s now being used to implement the final stages of that longstanding plan. COVID-19 was a real-world practice run, and showed just how effectively a pandemic can be used to shift the balance of power, and strip the global population of its wealth and individual freedoms.

    So, there’s no doubt in my mind that additional pandemics will be declared, because they’re the means to the globalists’ ends. To prevent this global coup, we need everyone to speak and share the truth to the point that you’re able. Only then will our voices outnumber the voices of the propaganda machine.

    Door To Freedom (doortofreedom.org), an organization founded by Dr. Meryl Nass, has a poster that explains how the pandemic treaty and International Health Regulations (IHR) amendments will change life as we know it and strip us of every vestige of freedom. Please download this poster and share it with everyone you know. Also put it up on public billboards and places where communities share information.

    *

    Note to readers: Please click the share button above. Follow us on Instagram and Twitter and subscribe to our Telegram Channel. Feel free to repost and share widely Global Research articles.

    Notes

    1, 21 Metro January 15, 2024

    2, 3 Mirror January 13, 2024

    4 Twitter/X Monica Crowley January 11, 2024

    5 Fortune January 12, 2024

    6 ResearchGate January 2024 DOI: 10.1101/2024.01.03.574008

    7 MSN January 15, 2024

    8 SPARS Pandemic Scenario

    9 NTI Paper November 2021

    10 UN News July 23, 2022

    11 Catastrophic Contagion

    12 Catastrophic Contagion Videos

    13 CDC Enterovirus D68

    14 CDC Enteroviruses

    15 Forbes September 15, 2023

    16 Intractable & Rare Diseases Research February 2019; 8(1): 1-8

    17 Forbes January 11, 2024

    18 BBC September 14, 2023

    19 First Post November 19, 2021

    20 Yahoo News November 19, 2021

    22 HR 3832 The Disease X Act of 2023

    Featured image source

    https://www.globalresearch.ca/will-disease-x-leaked-2025/5847210

    https://donshafi911.blogspot.com/2024/01/will-disease-x-be-leaked-in-2025-all.html
    Will Disease X be Leaked in 2025? All Global Research articles can be read in 51 languages by activating the Translate Website button below the author’s name (only available in desktop version). To receive Global Research’s Daily Newsletter (selected articles), click here. Click the share button above to email/forward this article to your friends and colleagues. Follow us on Instagram and Twitter and subscribe to our Telegram Channel. Feel free to repost and share widely Global Research articles. New Year Donation Drive: Global Research Is Committed to the “Unspoken Truth” *** The WHO’s pandemic treaty is the gateway to a global, top-down totalitarian regime, a one world government. The reason we can be sure there will be additional pandemics, whether manufactured using either fear and hype alone or an actual bioweapon created for this very purpose, is because the takeover plan, aka The Great Reset, is based on the premise that we need global biosecurity surveillance and centralized response A new contagion will likely be born in 2025, and media are already preparing us for it January 15-19, 2024, global leaders met at the World Economic Forum’s (WEF) Davos summit where the key topic of discussion was “Preparing for Disease X,” a hypothetical new pandemic predicted to kill 20 times more people than COVID-19 In August 2023, a new vaccine research facility was set up in Wiltshire, England, to begin work on a vaccine against the unknown “Disease X” The U.S. Congress introduced the “Disease X Act of 2023” (H.R.3832) in June 2023. The bill calls for the establishment of a BARDA program to develop “medical countermeasures for viral threats with pandemic potential.” The bill was referred to the Subcommittee on Health in early June 2023 but has not yet been passed * The COVID-19 pandemic allowed for an unprecedented shift in power and wealth distribution across the world and, as predicted, it was not to be a one-off event. A new contagion will likely be born in 2025, and media are already preparing us for it. January 15-19, 2024, global leaders met at the World Economic Forum’s (WEF) Davos summit where the key topic of discussion was “Preparing for Disease X,”1 a hypothetical new pandemic predicted to emerge in 2025 and kill 20 times more people than COVID-19.2 As reported by the Mirror:3 “The World Health Organization (WHO) has warned of a potential Disease X since 2017, a term indicating an unknown pathogen that could cause a serious international epidemic … Public speakers at the ‘Preparing for Disease X’ event next Wednesday [January 17, 2024] include Tedros Adhanom Ghebreyesus, director-general of the WHO, Brazilian minister of health Nisia Trindade Lima, and Michel Demaré, chair of the board at AstraZeneca. In their first post-pandemic meeting held in November 2022, the WHO brought over 300 scientists to consider which of over 25 virus families and bacteria could potentially create another pandemic. The list the team came up with included: the Ebola virus, the Marburg virus disease, Covid-19, SARS, and the Middle East respiratory syndrome coronavirus (MERS-CoV). Others included lassa fever, nipah and henipaviral diseases, zift Valley fever, and zika — as well as the unknown pathogen that would cause ‘Disease X.’” I’ve interviewed Meryl Nass about how the WHO is trying to take over aspects of everyone’s lives. She just published an important piece over the weekend, Why Is Davos So Interested in Disease? about how the WEF and the WHO have become partners to terrify the world. Alexis Baden-Mayer, Esq., political director for the Organic Consumers Association, did some digging into the participants of this WEF event, and the two things they all have in common are 1) dumping the AstraZeneca COVID shot on the developing world (primarily India and Brazil) after rich countries rejected it due to its admitted blood clotting risk, and 2) pushing for the implementation of medical AI systems that will eliminate doctors along with patient choice and privacy. Practice Runs or Responsible Planning? In a January 11, 2024, tweet, Fox News analyst and former assistant secretary for public affairs for the U.S. Treasury Department, Monica Crowley, wrote:4 “From the same people who brought you COVID-19 now comes Disease X: Next week in Davos, the unelected globalists at the World Economic Forum will hold a panel on a future pandemic 20x deadlier than COVID … Just in time for the election, a new contagion to allow them to implement a new WHO treaty, lock down again, restrict free speech and destroy more freedoms. Sound far-fetched? So did what happened in 2020. When your enemies tell you what they’re planning and what they’re planning FOR, believe them. And get ready.” Dr. Stuart Ray, vice chair of medicine for data integrity and analytics at Johns Hopkins’ Department of Medicine, dismissed such warnings, telling Fortune magazine5 that “Coordination of public health response is not conspiracy, it’s simply responsible planning.” I’d be willing to believe him if it wasn’t for a now-obvious trend: Whatever the globalists claim will happen actually does happen at a remarkable frequency, and their prognostic capabilities become easier to explain when you consider that most lethal pandemics have been caused by manmade viruses, the products of gain-of-function research. It’s pretty easy to predict a new viral outbreak if you have said virus waiting in the wings. With that in mind, recent research from China certainly raises concern, to say the least. According to a January 3, 2024, preprint,6 a SARS-CoV-2-related pangolin coronavirus — described as a “cell culture-adapted mutant” called GX_P2V that was first cultured in 2017 — was found to kill 100% of the humanized mice (ACE2-transgenic mice) infected with it.7 The primary cause of death was brain inflammation. According to the authors, “this is the first report showing that a SARS-CoV-2-related pangolin coronavirus can cause 100% mortality in hACE2 mice, suggesting a risk for GX_P2V to spill over into humans.” However, if this virus mutated as a result of passaging through cell cultures, then it’s not likely to emerge in the wild. It’s another unnatural lab creation, so rather than saying it may spill over from pangolins to humans, it would be more accurate to admit that it may pose a (rather serious) risk to humans were a lab escape to occur. COVID Dress Rehearsals In 2017, Johns Hopkins Center of Health Security held a coronavirus pandemic simulation called the SPARS Pandemic 2025-2028 scenario.8 Importantly, the exercise stressed “communication dilemmas concerning medical countermeasures that could plausibly emerge” in a pandemic scenario. Then, in October 2019, less than three months before the COVID-19 outbreak, the Bill & Melinda Gates Foundation in collaboration with Johns Hopkins and the World Economic Forum hosted Event 201. The name itself suggests it may have been a continuation of the SPARS Pandemic exercise. College courses are numbered based on their prerequisites. A 101 course does not require any prior knowledge whereas 201 courses require prior familiarity with the topic at hand. As in the SPARS Pandemic scenario, Event 201 involved an outbreak of a highly infectious coronavirus, and the primary (if not sole) focus of the exercise was, again, how to control information and keep “misinformation” in check, not how to effectively discover and share remedies. Social media censorship played a prominent role in the Event 201 plan, and in the real-world events of 2020 through the present, accurate information about vaccine development, production and injury has indeed been effectively suppressed around the world, thanks to social media companies and Google’s censoring of opposing viewpoints. In March 2021, an outbreak of “an unusual strain of monkeypox virus” was simulated.9 In late July the following year, the WHO director-general declared that a multi-country outbreak of monkeypox constituted a public health emergency of international concern,10 against his own advisory group. ‘Catastrophic Contagion’ Exercise Considering both of these simulations, SPARS (“Event 101”?) and Event 201, foreshadowed what eventually occurred in real life during COVID, when Gates hosts yet another pandemic exercise, it’s worth paying attention to the details. October 23, 2022, Gates, Johns Hopkins and the WHO cohosted “a global challenge exercise” dubbed “Catastrophic Contagion,”11,12 involving a fictional pathogen called “severe epidemic enterovirus respiratory syndrome 2025” (SEERS-25). Enterovirus D6813 is typically associated with cold and flu-like illness in infants, children and teens. In rare cases, it’s also been known to cause viral meningitis and acute flaccid myelitis, a neurological condition resulting in muscle weakness and loss of reflexes in one or more extremities. Enteroviruses A71 and A6 are known to cause hand, foot and mouth disease,14 while poliovirus, the prototypical enterovirus, causes polio (poliomyelitis), a potentially life-threatening type of paralysis that primarily affects children under age 5. So, the virus they modeled in this simulation appears to be something similar to enterovirus D68, but worse. Vaccine Drug Trials Begin for Deadly Nipah Virus One known virus that bears some resemblance to the fictional SEERS-25 is the Nipah virus. This virus has a kill rate of about 75%,15 and survivors oftentimes face long-term neurological issues stemming from the infection. Nipah is also said to affect children to a greater degree than adults.16 Incidentally, human trials for a vaccine against the deadly Nipah virus were recently launched.17Volunteers received their first shots in early January 2024. The experimental injection uses the same viral vector technology used to produce AstraZeneca’s COVID shot. The trial is reportedly being carried out by the University of Oxford in an undisclosed area where Nipah is actively infecting victims. (India seems to be indicated, as an outbreak in Kerala killed two people and hospitalized three in September 2023.18) The disease is thought to spread via interaction with infected animals such as goats, pigs, cats and horses. It may also spread via tainted blood products and food. Symptoms can emerge anywhere from a few days after exposure to as long as 45 days. Initial symptoms include fever, headache and respiratory illness, which can rapidly progress to encephalitis (brain swelling), seizures and coma within just a couple of days. According to the WHO, pigs are known to be “highly contagious” during the incubation period, and it’s possible that humans may be as well, although that has yet to be confirmed. Training African Leaders to Go Along with the Narrative Tellingly, the Catastrophic Contagion exercise focused on getting leadership in African countries involved and trained in following the script. African nations went “off script” more often than others during the COVID pandemic, and didn’t follow in the footsteps of developed nations when it came to pushing the jabs. As a result, vaccine makers now face the problem of having a huge control group, as the COVID jab uptake on the African continent was only 6%,19 yet it fared far better than developed nations in terms of COVID-19 infections and related deaths.20 The Catastrophic Contagion exercise predicts SEERS-25 will kill 20 million people worldwide, including 15 million children, and many who survive the infection will be left with paralysis and/or brain damage. In other words, the “cue” given is that the next pandemic may target children rather than the elderly, as was the case with COVID-19. Vaccine Against Unknown ‘X’ Pathogen Is Already in the Works In August 2023, a new vaccine research facility was set up in Wiltshire, England, fully staffed with more 200 scientists, to begin work on a vaccine against the unknown “Disease X.” As reported by Metro:21 “It took 362 days to develop the Covid-19 vaccine. But the Vaccine Development and Evaluation Centre team wants to reduce that time to 100 days. Scientists at the facility will develop a range of prototype vaccines and tests. The new lab is a part of a global effort to respond to global health threats. The UK and other G7 countries signed up to the ‘100 Days Mission’ in 2021. The government has invested £65 million into the lab. Professor Dame Jenny Harries, the head of the UK Health Security Agency, said the new facility would ‘ensure that we prepare so that if we have a new Disease X, a new pathogen, we have as much of that work in advance as possible.’” In the U.S., Congress also introduced the “Disease X Act of 2023” (H.R.383222) back in June 2023. The bill calls for the establishment of a BARDA program to develop “medical countermeasures for viral threats with pandemic potential.” The bill was referred to the Subcommittee on Health in early June 2023 but has not yet been passed. The Disease X Act amends a section of the Public Health Service Act with two new clauses that call for “the identification and development of platform manufacturing technologies needed for advanced development and manufacturing of medical countermeasures for viral families which have significant potential to cause a pandemic,” and “advanced research and development of flexible medical countermeasures against priority respiratory virus families and other respiratory viral pathogens with a significant potential to cause a pandemic, with both pathogen-specific and pathogen-agnostic approaches …” Needless to say, since it’s impossible to customize vaccines using the conventional method of growing viruses in eggs or some other cell media in 100 days, it seems inevitable that all these efforts are about the expansion of gene-based technologies. This, despite the fact that the mRNA technology used for the COVID jabs has proven to be disastrous from a safety standpoint, and ineffective to boot. Why Manufactured Pandemics Will Continue At this point, it’s quite clear that “biosecurity” is the chosen means by which the globalist cabal intends to seize power over the world. The WHO is working on securing sole power over pandemic response globally through its international pandemic treaty which, if implemented, will eradicate the sovereignty of all member nations. The WHO’s pandemic treaty is the gateway to a global, top-down totalitarian regime, a one world government. Ultimately, the WHO intends to dictate all health care. But to secure that power, they will need more pandemics. COVID-19 alone was not enough to get everyone onboard with a centralized pandemic response unit, and they probably knew that from the start. So, the reason we can be sure there will be additional pandemics, whether manufactured using either fear and hype alone or an actual bioweapon created for this very purpose, is because the takeover plan, aka The Great Reset, is based on the premise that we need global biosecurity surveillance and centralized response. Biosecurity, in turn, is the justification for an international vaccine passport, which the G20 has signed on to, and that passport will also be your digital identification. That digital ID, then, will be tied to your social credit score, personal carbon footprint tracker, medical records, educational records, work records, social media presence, purchase records, your bank accounts and a programmable central bank digital currency (CBDC). Once all these pieces are fully connected, you’ll be in a digital prison, and the ruling cabal — whether officially a one world government by then or not — will have total control over your life from cradle to grave. We’re Already Suffering Under a Pseudo-One World Government We actually already have a pseudo-one world government, in the form of Bill Gates’ nongovernmental organizations (NGOs). They are making health care decisions that should be left to individual nations and/or states, and they’re making decisions that will line their own pockets, regardless of what happens to the public health-wise. They coordinate and synchronize pandemic communication during simulated practice runs, and then, when the real-world situation emerges that fits the bill, the preplanned script is played out more or less verbatim. Between the G20 declaration to implement an international vaccine passport under the auspice of the WHO, and the WHO’s pandemic treaty, everything is lined up to take control of the next pandemic, and in so doing, further securing the foundation for a one world government. As discussed in my 2021 article, “COVID-19 Dress Rehearsals and Proof of the Plan,” the pandemic measures rolled out for COVID-19 were the culmination of decades of careful planning to radically and permanently alter the governance and social structures of the world. The medical system has been used in the past to drive forward a New World Order agenda — now rebranded as “The Great Reset” — and it’s now being used to implement the final stages of that longstanding plan. COVID-19 was a real-world practice run, and showed just how effectively a pandemic can be used to shift the balance of power, and strip the global population of its wealth and individual freedoms. So, there’s no doubt in my mind that additional pandemics will be declared, because they’re the means to the globalists’ ends. To prevent this global coup, we need everyone to speak and share the truth to the point that you’re able. Only then will our voices outnumber the voices of the propaganda machine. Door To Freedom (doortofreedom.org), an organization founded by Dr. Meryl Nass, has a poster that explains how the pandemic treaty and International Health Regulations (IHR) amendments will change life as we know it and strip us of every vestige of freedom. Please download this poster and share it with everyone you know. Also put it up on public billboards and places where communities share information. * Note to readers: Please click the share button above. Follow us on Instagram and Twitter and subscribe to our Telegram Channel. Feel free to repost and share widely Global Research articles. Notes 1, 21 Metro January 15, 2024 2, 3 Mirror January 13, 2024 4 Twitter/X Monica Crowley January 11, 2024 5 Fortune January 12, 2024 6 ResearchGate January 2024 DOI: 10.1101/2024.01.03.574008 7 MSN January 15, 2024 8 SPARS Pandemic Scenario 9 NTI Paper November 2021 10 UN News July 23, 2022 11 Catastrophic Contagion 12 Catastrophic Contagion Videos 13 CDC Enterovirus D68 14 CDC Enteroviruses 15 Forbes September 15, 2023 16 Intractable & Rare Diseases Research February 2019; 8(1): 1-8 17 Forbes January 11, 2024 18 BBC September 14, 2023 19 First Post November 19, 2021 20 Yahoo News November 19, 2021 22 HR 3832 The Disease X Act of 2023 Featured image source https://www.globalresearch.ca/will-disease-x-leaked-2025/5847210 https://donshafi911.blogspot.com/2024/01/will-disease-x-be-leaked-in-2025-all.html
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    All Global Research articles can be read in 51 languages by activating the Translate Website button below the author’s name (only available in desktop version). To receive Global Research’s Daily Newsletter (selected articles), click here. Click the share button above to email/forward this article to your friends and colleagues. Follow us on Instagram and Twitter and subscribe to our Telegram Channel. Feel …
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  • The Truth About HPV Vaccination, Part 3: Can It Prevent Cervical Cancer?
    There are no valid studies showing the vaccine for the human papillomavirus, or HPV, prevents cervical cancer. However, there are studies suggesting the vaccine could increase the risk of cancer.

    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 third 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 and Part 2 here.

    In part 1 and part 2 of this series, we discussed the human papillomavirus (HPV) vaccine and its links to ovarian insufficiency and autoimmune disease.

    In part 3, we turn to questions regarding the effectiveness of the vaccine to prevent cervical cancer, and the limitations of relevant clinical trials to detect such a type of effect.

    Summary of key facts

    There are multiple obstacles in designing a valid clinical trial to prove the HPV vaccine could prevent cervical cancer, e.g. long lead time, lack of adequate informed consent, complexity between HPV infection and cervical cancer and the negative impact of girls’ sexual behavior, which may worsen the risks of cervical cancer.
    Most of the HPV’s interventional clinical trials have too short a follow-up time to draw a concrete conclusion.
    In a large Swedish observational trial, which is treated as the most convincing study to prove the HPV vaccine’s effects on cervical cancer, a few confounding factors were not adequately balanced between the HPV vaccination group versus the unvaccinated group.
    The National Cancer Institute’s Surveillance, Epidemiology, and End Results Program (SEER) data and another U.S. study found the HPV vaccine has no effects in reducing cancer rates.
    Two other registry-based studies in Australia and the U.K. suggest that HPV vaccination is associated with increased cervical cancer rates in certain age groups.
    Long lead time from HPV infection to cervical cancer

    Typically, there is a long period from HPV infection to cervical epithelium abnormalities, then cervical cancer.

    HPV infections usually last 12–18 months and are eventually cleared by the immune system.

    Fewer than 10% of HPV infections are persistent.

    There are two types of precancerous cervical lesions, low-grade or high-grade. Low-grade cervical neoplasia grade 1 (CIN1) is usually transient and resolves naturally within one to two years.

    Only a few persistent infections progress to the clinically meaningful high-grade, CIN2 or 3. Meanwhile, the median time from CIN2/3 to transition to cancer is estimated to be 23.5 years.

    Among those with weakened immune systems, HPV-related cancer might progress more quickly.

    In a review of the natural history of HPV infection, the complex pathway from infection to cancer is elucidated, including what is known (purple boxes) and where uncertainty remains (blue boxes).



    Difficulty running clinical trials for the HPV vaccine

    Because of the long lead time from HPV infection to cervical cancer, a prospective, randomized controlled trial is not easily designed and feasibly implemented.

    Lack of long-term follow-up is a common issue for most clinical trials to prove the HPV vaccine’s effectiveness in preventing cervical cancer.

    For example, a 2007 study found that Gardasil was effective in reducing HPV-associated cervical precancerous lesions rate by 20%.

    This study followed their subjects for only an average of three years after administration of the first dose.

    Furthermore, due to the complex uncertainties in the natural history between HPV infection and cervical cancer, it is not easy to claim the effectiveness of the HPV vaccine.

    A randomized trial is designed to balance the two groups — vaccine and placebo — so that any unmeasured confounding variables which might influence the outcome of the trial are distributed evenly.

    However, if the treatment group knows they got the vaccine, might their behaviors change? Might they be less risk-averse, thinking they have some protection?

    For example, girls might think they are vaccinated and “protected” from cervical cancer and may tend to initiate sexual intercourse at a younger age or engage in sexual activities with more partners.

    However, sexual intercourse at a young age, multiple sexual partners and oral contraceptive use are associated with an increased risk of cervical cancer in women.

    In other words, HPV vaccination may offer some protection if offered before sexual activity is initiated, but it may also be associated with increased behavioral risk factors.

    Whether the benefits of vaccination outweigh any risks is therefore a multifactorial question deserving of careful longitudinal study.

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

    Order Now

    Systemic analysis of 12 clinical trials on HPV vaccine efficacy

    In 2020, a Queen Mary University study led by Dr. Claire Rees reviewed 12 randomized clinical trials for Cervarix and Gardasil. The investigators found that the trials did not include populations representative of the vaccination target groups, and the trial design may have overstated vaccine efficacy.

    For example, one trial design generated evidence that the vaccine prevents CIN1. But this is not meaningful because these lesions usually resolve on their own.

    Furthermore, the study accessed efficacy against low-grade precancerous lesions. But this is not necessarily suggestive of efficacy against the more serious but much less frequent high-grade lesions.

    Finally, the cytology screenings were done every six to 12 months instead of every 36 months (normal screening interval), meaning the efficacy of the vaccine may have been overestimated, as low-grade lesions could go away spontaneously.

    All this is to say the HPV vaccine may be effective at preventing more serious lesions which lead to cervical cancer, but it is hard to know because of these poorly designed trials.

    Nothing is conclusive without a larger trial powered to detect a difference in rates of more serious cervical changes according to the typical screening schedule. However, such a trial has not yet been performed.

    Swedish nationwide health registry study

    A nationwide Swedish health registry-based study followed 1,672,983 women for 12 years to assess the association between HPV vaccination and the risk of cervical cancer.

    In this study, the cumulative incidence of cervical cancer was 47 cases per 100,000 women vaccinated and 94 per 100,000 unvaccinated, suggesting that HPV4 vaccination was associated with a reduced risk of 49 to 63% of invasive cervical cancer at the population level.

    Even though the results are positive, the study researchers raised a few concerns themselves.

    First, HPV-vaccinated women could have been generally healthier than unvaccinated women. This is known as “healthy volunteer bias.”

    Second, a mother’s history of cervical cancer might be associated with both vaccination uptake and underlying risk of cervical cancer as well as screening rates.

    Third, lifestyle and health factors such as smoking, sexual intercourse at a young age, multiple sexual partners, oral contraceptive use and obesity are reportedly associated with the risk of cervical cancer.

    These factors have not been thoroughly analyzed by this study and could have contributed to the data.

    Furthermore, parental education level and annual household income level may be interconnected with lifestyle factors such as smoking status.

    Strengths of this study include its size, duration and outcome of interest being invasive cancer, not low-grade lesions. However, it is impossible to exclude the relationship between lifestyle factors, vaccination uptake and cervical cancer.

    Only a randomized controlled trial (RCT) could balance the two groups on these unmeasured — but related — risk factors.

    However even if the risk factors (sexual behaviors) are fully balanced at baseline with an RCT, it is hard to keep them still balanced during the whole study course after HPV vaccination.

    No association found in a U.S. database

    Meanwhile, researchers found no association between vaccination and cancer mortality in the U.S.

    According to the National Cancer Institute’s SEER program, the incidence of deaths from cervical cancer before Gardasil’s introduction in the U.S. had been steadily declining for years and, in 2006, was 2.4 per 100,000 women.

    The data from 2016–2020 is 2.2 per 100,000 women — essentially unchanged.

    In a cross-sectional study using a nationally representative sample of U.S. adults aged 20–59 years, among 9,891 participants, the researchers did not find an association between HPV vaccination and HPV-related cancers.

    Increase in cervical cancer after HPV vaccine rollout: Australia

    In Australia, government data similarly reveal an increase in cervical cancer rates in certain age groups of women following the implementation of the Gardasil vaccine.

    Thirteen years after Gardasil was recommended for teenagers and young adults, there has been a 30% increase in 30- to 34-year-old women (4.9 cases/100,000 compared to 6.6 cases/100,000 in 2020) being diagnosed with cervical cancer.

    Even though the rates decreased in other age groups, the abnormal increase in the 30–34 age group needs an explanation.



    Several factors should be considered.

    First, this database does not tell the stage of cancer. More cancer diagnosed at an early stage may result in a cancer-rate increase.

    Second, decreasing cancer rates could be caused by declines in screening rates, perhaps due to the pandemic and/or a reluctance to get tested.

    Third, Australia has an increasing proportion of immigrants from South Asia, and these cultural factors may influence the cervical cancer-screening rate.

    A study of South Asian women living in Australia found that almost half had never had a previous screening test.

    Cervical cancer rates rise after HPV vaccination in the UK

    In the U.K., HPV vaccination was introduced in 2008 for girls aged 12–13 with catch-up for those aged 14–18. Many expected cervical cancer rates in women aged 20–24 to fall by 2014 as the vaccinated cohorts entered their 20s.

    However, in 2016 national statistics showed a worrying and substantial 70% increase in the rate of cervical cancer at ages 20 to 24 (i.e. from 2.7 in 2012 to 4.6 per 100,000 in 2014).

    While the author would consider it to be too early to draw conclusions regarding vaccine efficacy in protecting against cancer, this merits further study.

    Accordingly, an analysis was conducted in the U.K. in 2018 in response to public interest regarding this increase in cervical cancer.

    Researchers from Queen Mary University and King’s College London found that it was attributable to an increase in the proportion of women first screened at age 24.5 years.

    The increase was limited to stage I cervical cancer. But there was no evidence of a lack of screening leading to increasing rates.

    While the researchers considered it too early to conclude vaccine efficacy in protecting against cancer, these findings merit further study.

    Could HPV vaccines make HPV infections worse?

    Besides the vaccine’s unclear effectiveness in cancer prevention, studies further suggest the suppression of the HPV strains targeted by the vaccine may induce more virulent strains.

    For example, a 2015 study found that vaccinated young adult women had a higher prevalence of high-risk HPV types other than types 16 and 18, putting them at risk for more aggressive cervical and other HPV-related cancers.

    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.

    https://childrenshealthdefense.org/defender/truth-hpv-vaccine-part-3-et/


    https://donshafi911.blogspot.com/2024/01/the-truth-about-hpv-vaccination-part-3.html
    The Truth About HPV Vaccination, Part 3: Can It Prevent Cervical Cancer? There are no valid studies showing the vaccine for the human papillomavirus, or HPV, prevents cervical cancer. However, there are studies suggesting the vaccine could increase the risk of cancer. 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 third 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 and Part 2 here. In part 1 and part 2 of this series, we discussed the human papillomavirus (HPV) vaccine and its links to ovarian insufficiency and autoimmune disease. In part 3, we turn to questions regarding the effectiveness of the vaccine to prevent cervical cancer, and the limitations of relevant clinical trials to detect such a type of effect. Summary of key facts There are multiple obstacles in designing a valid clinical trial to prove the HPV vaccine could prevent cervical cancer, e.g. long lead time, lack of adequate informed consent, complexity between HPV infection and cervical cancer and the negative impact of girls’ sexual behavior, which may worsen the risks of cervical cancer. Most of the HPV’s interventional clinical trials have too short a follow-up time to draw a concrete conclusion. In a large Swedish observational trial, which is treated as the most convincing study to prove the HPV vaccine’s effects on cervical cancer, a few confounding factors were not adequately balanced between the HPV vaccination group versus the unvaccinated group. The National Cancer Institute’s Surveillance, Epidemiology, and End Results Program (SEER) data and another U.S. study found the HPV vaccine has no effects in reducing cancer rates. Two other registry-based studies in Australia and the U.K. suggest that HPV vaccination is associated with increased cervical cancer rates in certain age groups. Long lead time from HPV infection to cervical cancer Typically, there is a long period from HPV infection to cervical epithelium abnormalities, then cervical cancer. HPV infections usually last 12–18 months and are eventually cleared by the immune system. Fewer than 10% of HPV infections are persistent. There are two types of precancerous cervical lesions, low-grade or high-grade. Low-grade cervical neoplasia grade 1 (CIN1) is usually transient and resolves naturally within one to two years. Only a few persistent infections progress to the clinically meaningful high-grade, CIN2 or 3. Meanwhile, the median time from CIN2/3 to transition to cancer is estimated to be 23.5 years. Among those with weakened immune systems, HPV-related cancer might progress more quickly. In a review of the natural history of HPV infection, the complex pathway from infection to cancer is elucidated, including what is known (purple boxes) and where uncertainty remains (blue boxes). Difficulty running clinical trials for the HPV vaccine Because of the long lead time from HPV infection to cervical cancer, a prospective, randomized controlled trial is not easily designed and feasibly implemented. Lack of long-term follow-up is a common issue for most clinical trials to prove the HPV vaccine’s effectiveness in preventing cervical cancer. For example, a 2007 study found that Gardasil was effective in reducing HPV-associated cervical precancerous lesions rate by 20%. This study followed their subjects for only an average of three years after administration of the first dose. Furthermore, due to the complex uncertainties in the natural history between HPV infection and cervical cancer, it is not easy to claim the effectiveness of the HPV vaccine. A randomized trial is designed to balance the two groups — vaccine and placebo — so that any unmeasured confounding variables which might influence the outcome of the trial are distributed evenly. However, if the treatment group knows they got the vaccine, might their behaviors change? Might they be less risk-averse, thinking they have some protection? For example, girls might think they are vaccinated and “protected” from cervical cancer and may tend to initiate sexual intercourse at a younger age or engage in sexual activities with more partners. However, sexual intercourse at a young age, multiple sexual partners and oral contraceptive use are associated with an increased risk of cervical cancer in women. In other words, HPV vaccination may offer some protection if offered before sexual activity is initiated, but it may also be associated with increased behavioral risk factors. Whether the benefits of vaccination outweigh any risks is therefore a multifactorial question deserving of careful longitudinal study. RFK Jr. and Brian Hooker Vax-Unvax RFK Jr. and Brian Hooker’s New Book: “Vax-Unvax” Order Now Systemic analysis of 12 clinical trials on HPV vaccine efficacy In 2020, a Queen Mary University study led by Dr. Claire Rees reviewed 12 randomized clinical trials for Cervarix and Gardasil. The investigators found that the trials did not include populations representative of the vaccination target groups, and the trial design may have overstated vaccine efficacy. For example, one trial design generated evidence that the vaccine prevents CIN1. But this is not meaningful because these lesions usually resolve on their own. Furthermore, the study accessed efficacy against low-grade precancerous lesions. But this is not necessarily suggestive of efficacy against the more serious but much less frequent high-grade lesions. Finally, the cytology screenings were done every six to 12 months instead of every 36 months (normal screening interval), meaning the efficacy of the vaccine may have been overestimated, as low-grade lesions could go away spontaneously. All this is to say the HPV vaccine may be effective at preventing more serious lesions which lead to cervical cancer, but it is hard to know because of these poorly designed trials. Nothing is conclusive without a larger trial powered to detect a difference in rates of more serious cervical changes according to the typical screening schedule. However, such a trial has not yet been performed. Swedish nationwide health registry study A nationwide Swedish health registry-based study followed 1,672,983 women for 12 years to assess the association between HPV vaccination and the risk of cervical cancer. In this study, the cumulative incidence of cervical cancer was 47 cases per 100,000 women vaccinated and 94 per 100,000 unvaccinated, suggesting that HPV4 vaccination was associated with a reduced risk of 49 to 63% of invasive cervical cancer at the population level. Even though the results are positive, the study researchers raised a few concerns themselves. First, HPV-vaccinated women could have been generally healthier than unvaccinated women. This is known as “healthy volunteer bias.” Second, a mother’s history of cervical cancer might be associated with both vaccination uptake and underlying risk of cervical cancer as well as screening rates. Third, lifestyle and health factors such as smoking, sexual intercourse at a young age, multiple sexual partners, oral contraceptive use and obesity are reportedly associated with the risk of cervical cancer. These factors have not been thoroughly analyzed by this study and could have contributed to the data. Furthermore, parental education level and annual household income level may be interconnected with lifestyle factors such as smoking status. Strengths of this study include its size, duration and outcome of interest being invasive cancer, not low-grade lesions. However, it is impossible to exclude the relationship between lifestyle factors, vaccination uptake and cervical cancer. Only a randomized controlled trial (RCT) could balance the two groups on these unmeasured — but related — risk factors. However even if the risk factors (sexual behaviors) are fully balanced at baseline with an RCT, it is hard to keep them still balanced during the whole study course after HPV vaccination. No association found in a U.S. database Meanwhile, researchers found no association between vaccination and cancer mortality in the U.S. According to the National Cancer Institute’s SEER program, the incidence of deaths from cervical cancer before Gardasil’s introduction in the U.S. had been steadily declining for years and, in 2006, was 2.4 per 100,000 women. The data from 2016–2020 is 2.2 per 100,000 women — essentially unchanged. In a cross-sectional study using a nationally representative sample of U.S. adults aged 20–59 years, among 9,891 participants, the researchers did not find an association between HPV vaccination and HPV-related cancers. Increase in cervical cancer after HPV vaccine rollout: Australia In Australia, government data similarly reveal an increase in cervical cancer rates in certain age groups of women following the implementation of the Gardasil vaccine. Thirteen years after Gardasil was recommended for teenagers and young adults, there has been a 30% increase in 30- to 34-year-old women (4.9 cases/100,000 compared to 6.6 cases/100,000 in 2020) being diagnosed with cervical cancer. Even though the rates decreased in other age groups, the abnormal increase in the 30–34 age group needs an explanation. Several factors should be considered. First, this database does not tell the stage of cancer. More cancer diagnosed at an early stage may result in a cancer-rate increase. Second, decreasing cancer rates could be caused by declines in screening rates, perhaps due to the pandemic and/or a reluctance to get tested. Third, Australia has an increasing proportion of immigrants from South Asia, and these cultural factors may influence the cervical cancer-screening rate. A study of South Asian women living in Australia found that almost half had never had a previous screening test. Cervical cancer rates rise after HPV vaccination in the UK In the U.K., HPV vaccination was introduced in 2008 for girls aged 12–13 with catch-up for those aged 14–18. Many expected cervical cancer rates in women aged 20–24 to fall by 2014 as the vaccinated cohorts entered their 20s. However, in 2016 national statistics showed a worrying and substantial 70% increase in the rate of cervical cancer at ages 20 to 24 (i.e. from 2.7 in 2012 to 4.6 per 100,000 in 2014). While the author would consider it to be too early to draw conclusions regarding vaccine efficacy in protecting against cancer, this merits further study. Accordingly, an analysis was conducted in the U.K. in 2018 in response to public interest regarding this increase in cervical cancer. Researchers from Queen Mary University and King’s College London found that it was attributable to an increase in the proportion of women first screened at age 24.5 years. The increase was limited to stage I cervical cancer. But there was no evidence of a lack of screening leading to increasing rates. While the researchers considered it too early to conclude vaccine efficacy in protecting against cancer, these findings merit further study. Could HPV vaccines make HPV infections worse? Besides the vaccine’s unclear effectiveness in cancer prevention, studies further suggest the suppression of the HPV strains targeted by the vaccine may induce more virulent strains. For example, a 2015 study found that vaccinated young adult women had a higher prevalence of high-risk HPV types other than types 16 and 18, putting them at risk for more aggressive cervical and other HPV-related cancers. 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. https://childrenshealthdefense.org/defender/truth-hpv-vaccine-part-3-et/ https://donshafi911.blogspot.com/2024/01/the-truth-about-hpv-vaccination-part-3.html
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    The Truth About HPV Vaccination, Part 3: Can It Prevent Cervical Cancer?
    There are no valid studies showing the vaccine for the human papillomavirus, or HPV, prevents cervical cancer. However, there are studies suggesting the vaccine could increase the risk of cancer.
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  • The Truth About HPV Vaccination, Part 1: How Safe Is It, Really?
    This first installment in a multi-part series about the human papillomavirus, or HPV, vaccine explores peer-reviewed scientific literature that reveals serious safety concerns about a vaccine widely regarded as safe.

    The Epoch Times

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

    By Yuhong Dong

    The decline of public trust in COVID-19 vaccines significantly impacts vaccination rates against routine childhood diseases. This multiple-part series explores the international research done over the past two decades on the human papillomavirus (HPV) vaccine — believed to be one of the most effective vaccines developed to date.

    Summary of Key Facts

    This multiple-part series offers a thorough analysis of concerns raised about HPV vaccination following the global HPV campaign, which commenced in 2006.
    In the U.S., the HPV vaccine was reported to have a disproportionately higher percentage of adverse events of fainting and blood clots in the veins. The U.S. Food and Drug Administration (FDA) acknowledges that fainting can happen following the HPV vaccine, and recommends sitting or lying down to get the shot, then waiting for 15 minutes afterward.
    International scientists found that the Centers for Disease Control and Prevention’s (CDC) Vaccine Adverse Event Reporting System (VAERS) logged a substantial increase in reports of premature ovarian failure from 1.4 per year before 2006 to 22.2 per year after the HPV vaccine approval, yielding a Proportional Reporting Ratio of 46.1.
    The HPV vaccine is widely regarded as one of the most effective vaccines developed to date. Nevertheless, safety issues have been raised following its approval, and in response, additional research has been published and litigation has been brought on behalf of those with a vaccine injury.

    In this HPV vaccine series, Parts I and II explain how the vaccine works and the evidence suggesting there may be legitimate safety concerns. The remaining parts present questions about real-world vaccine effectiveness and identify specific ingredients which may pose harm.

    The information presented here is drawn from peer-reviewed scientific literature from the U.S., Australia, Denmark, Sweden, France and Japan, as well as statistics published by public health agencies in each of these countries.

    More than 100 hours of research and internal peer review among scientists with experience in infectious diseases, virology, clinical trials and vaccine epidemiology have been invested in presenting this summary of the evidence.

    Large registry-based studies have identified plausible associations between HPV vaccination and autoimmune conditions, including premature ovarian insufficiency or premature ovarian failure, Guillain-Barré syndrome (GBS), postural orthostatic tachycardia syndrome and chronic regional pain syndrome.

    While it is easy to be enthusiastic about recent advances in human vaccine technology, we should keep in mind that achieving real and lasting good health is much more than just the absence of a certain virus.

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

    Order Now

    What is HPV?

    According to the CDC, HPV is the most common sexually transmitted infection in the U.S.

    HPV is a small DNA virus infecting human cutaneous epithelial cells in the mucosa and skin. More than 150 strains of the HPV virus have been identified.

    HPV infection is so common that the majority of sexually active people will get it at some point in their lives, even if they have only one or very few sexual partners. It can spread through sexual intercourse and oral sex. It can also pass between people through skin-to-skin contact, even by people who have no symptoms.

    HPV infection causes genital warts, some of which can turn into cancer. For the most part, however, HPV infection is benign. More than 90% of HPV infections cause no clinical symptoms and are self-limited, meaning the virus is cleared by the body via natural immunological defenses.

    HPV-associated cancers

    High-risk HPV types (types 16, 18 and others) can cause cervical cell abnormalities that are precursors to cancers.

    Type 16 is associated with approximately 50% of cervical cancers worldwide, and types 16 and 18 together are linked to 66% of cervical cancers.

    An additional five high-risk types, 31, 33, 45, 52 and 58, are linked with another 15% of cervical cancers and 11% of all HPV-associated cancers.

    Infection with a high-risk HPV type is associated with a higher chance of the development of cervical cancer but, by itself, HPV infection is not the sole risk factor to cause cancer. There are many other reasons, as discussed in this paper.

    Given the prevalence of infection, it is unsurprising that globally, cervical cancer is the fourth most common cancer in women. In 2018, an estimated 570,000 women were diagnosed with cervical cancer worldwide and more than 300,000 died of the disease.

    In the U.S., nearly 50,000 new HPV-associated cancers occur annually, with women infected at a slightly higher rate than men.

    But in 9 out of 10 cases, HPV goes away within two years without causing health problems.

    Only persistent HPV infections may lead to cancer. These infections evade the immune system’s innate cell-mediated defenses.

    The incidence of cervical cancer can be controlled as a result of the implementation of routine testing and screening, including Pap and DNA tests.

    HPV vaccines

    Three HPV vaccines — bivalent HPV vaccine (Cervarix, 2vHPV), quadrivalent HPV vaccine (Gardasil, 4vHPV or HPV4) and 9-valent HPV vaccine (Gardasil 9, 9vHPV) — have been licensed by the FDA.

    The HPV vaccine uses recombinant technology to assemble the shell of the virus — L1 capsid protein. These viral-like particles do not contain the virus genome and are not infectious.

    Cervarix, developed by GlaxoSmithKline, is a bivalent vaccine against HPV types 16 and 18, that was pulled from the U.S. market in 2016 due to “very low market demand.”

    Merck’s original Gardasil vaccine was designed to prevent infections from four strains (types 6, 11, 16 and 18).

    On June 8, 2006, after the FDA’s fast-tracked review, Gardasil was approved for use in females ages 9 to 26 for the prevention of cervical, vulvar and vaginal cancers.

    According to the label accompanying the vaccine, the ingredients in Merck’s first Gardasil vaccine were proteins of HPV, amorphous aluminum hydroxyphosphate sulfate, yeast protein, sodium chloride, L-histidine, polysorbate 80, sodium borate and water for injection.

    On Oct. 16, 2009, the FDA approved Gardasil (HPV4) for use in boys ages 9 through 26 for the prevention of genital warts caused by HPV types 6 and 11, but not for cancer.

    In 2010, it approved Gardasil for the prevention of anal cancer in males and females ages 9 to 26.

    Four years later, the FDA approved an updated vaccine, Merck’s Gardasil 9, for use in girls ages 9 to 26 and boys ages 9 to 15 for the prevention of cervical, vaginal and anal cancers.

    Gardasil 9 contains the same ingredients as Gardasil, but offers protection against nine HPV strains, adding five additional types (HPV types 31, 33, 45, 52 and 58).

    The current HPV vaccination schedule recommended by the CDC is two doses for both boys and girls aged 11 or 12. However, it is approved for children as young as 9. The second dose is given 6 to 12 months after the first.

    For those aged 15 and above, a three-dose schedule is implemented at one- to two-month and six-month intervals, although antibody-level studies suggest that two doses are sufficient.

    The vaccine prompts the body to produce neutralizing antibodies against HPV. Antibody responses appear to peak seven months after the first dose (or one month after the third dose). The vaccine-induced antibody levels appear to be 10 to 100 times higher than those after natural infection.

    The high vaccine effectiveness (90 to 98%) against the fast-growing, abnormal cells which may cause precancerous lesions in people ages 16 to 26 suggested that the best timing for vaccination was to give it to patients before they became sexually active.

    HPV VAERS reports from 2 large countries

    U.S. HPV vaccine adverse events

    On Aug. 19, 2009, the Journal of the American Medical Association published an article authored by scientists from the FDA and CDC that reviewed the safety data for Gardasil for adverse events reported to VAERS between June 2006 through December 2008.

    During that time, there were 12,424 reports of adverse events. Of these, 772 (6.2%) were serious.

    VAERS is a passive surveillance system, which is subject to multiple limitations, including underreporting, unconfirmed diagnosis, lack of denominator data and no unbiased comparison groups.

    Nevertheless, it is a useful and important tool for detecting postmarket safety issues with vaccines.

    A disproportionately high percentage of Gardasil VAERS reports were of syncope (fainting) and venous thromboembolic events (blood clots in the veins) compared with other vaccines. There were 8.2 syncope events per 100,000 HPV doses and 0.2 venous thromboembolic events per 100,000 HPV doses reported, respectively.

    The Gardasil package insert includes a warning about fainting, fever, dizziness, nausea and headaches (page 1) and notes at least the following adverse reactions reported during postmarketing surveillance (section 6.2): Guillain-Barré syndrome, transverse myelitis, motor neuron disease, venous thromboembolic events, pancreatitis and autoimmune disorders.

    Australia HPV vaccines adverse events

    In 2007, Australia reported an annual adverse drug reaction rate of 7.3/100,000, the highest since 2003, representing an 85% increase from 2006.

    Per the analysis of the Adverse Drug Reactions System database by the Australian Department of Health and Aging, this increase was “almost entirely due to” reports following the national rollout of the three-dose HPV vaccination program for young females in April 2007; 705 of the 1,538 adverse drug reactions reported that year were from the Gardasil vaccine.

    1 vaccine adverse events australia chart
    In Australia, the ADR increase in 2007 was almost entirely due to the three-dose HPV vaccination program for females aged 12 to 26 years in April 2007. Credit: Australian Government Department of Health and Aged Care.
    Moreover, though people may take different vaccines other than HPV, the HPV vaccine was the only suspected vaccine to cause adverse reactions in 96% of records. Twenty-nine percent had causality ratings of “certain” or “probable” and 6% were defined as “serious.”

    2 vaccine types vaccine suspected chart
    In these HPV-induced ADRs, 674 were suspected to be related to HPV vaccines, 203 had causality ratings of “certain” or “probable,” and 43 were defined as “serious.” Credit: Australian Government Department of Health and Aged Care.
    Japan withdraws recommendation, vaccine acceptance plunged

    In 2013, the Japanese raised concerns about a variety of widely reported post-vaccination serious adverse events. This led the government to suspend recommending the HPV vaccine for six years. Vaccine acceptance of HPV in Japan plunged significantly after 2013, from 42.9% to 14.3%, or from 65.4% to 3.9%.

    Researchers around the world also started to investigate HPV safety. A World Health Organization (WHO) position paper released on July 14, 2017, concluded that the HPV vaccines were “extremely safe.”

    The same report estimated approximately 1.7 cases of anaphylaxis per million HPV doses, that no association with GBS was found, and that syncope (fainting) was “established as a common anxiety or stress-related reaction to the injection.”

    In the spring of 2022, Japan announced it was relaunching its HPV vaccination drive. Mainstream news outlets reported that for thousands of women, the cost of caution may have led to preventable HPV-induced cancers and an estimated 5,000 to 5,700 deaths.

    However, a true risk-benefit analysis would also consider the number of serious adverse events prevented by putting the program on hold. The question remains: Was Japan’s caution warranted, or should their national vaccination program have continued?

    Ovarian insufficiency

    Concerns that the vaccine may be negatively affecting fertility have been detailed in the scientific literature.

    In 2014, a peer-reviewed case series describing premature ovarian failure among Australian women following HPV vaccination was published in the Journal of Investigative Medicine.

    This prompted other researchers to systematically examine the VAERS data to see if there was a connection between premature ovarian failure and Gardasil. Their study found a “potential safety signal” and concluded that “further investigations are warranted.”

    VAERS analysis on ovarian failure

    Two recent publications based on VAERS reports (first study, second study) found that events with a probable autoimmune background were significantly more frequent after HPV vaccination compared to other vaccinations.

    The team of international scientists that did the second study evaluated reports between 1990 and 2018. They found that among the 228,341 premature ovarian failure reports, 0.1% was considered to be associated with HPV vaccination with a median age of 15 years and the time to onset was 20.5 days following vaccination.

    The primary symptoms were amenorrhea (80.4%) and premature menopause (15.3%).

    Most strikingly, the mean number of premature ovarian failure cases increased significantly from 1.4 per year prior to 2006 to 22.2 per year after the HPV vaccine was approved, with a proportional reporting ratio of 46.

    The investigators noted that the WHO and CDC declared the HPV vaccine safe regardless of lacking adequate research into safety concerns.

    For example, the authors note that in a CDC-sponsored VAERS study, 17 cases of premature ovarian failure were identified but 15 were excluded due to insufficient information to confirm the diagnosis. A separate observational study using the Vaccine Safety Datalink found no increased risk.

    But this study was too underpowered to detect a signal. In addition, a cross-sectional survey study using National Health and Nutrition Examination Survey data relied on an inaccurate measurement of premature ovarian failure and self-reported HPV vaccination.

    In summary, the researchers detected a strong safety signal even after accounting for a potential upswing in reports due to media coverage after the product launch (they refer to this as “notoriety bias”).

    Because VAERS is a passive reporting system, the data may be incomplete and are often unconfirmed by physicians. Therefore, this study cannot provide a definitive link between HPV vaccination and premature ovarian insufficiency or premature ovarian failure but does generate a hypothetical link.

    The authors of the second study conclude by insisting that “this signal warrants well-designed and appropriate epidemiological research.” They note that “if the signal is confirmed, the risk is small compared to the lifetime risk of cervical cancer.”

    However, the benefit-risk profile on an individual level is not uniform.

    Given the health impacts of premature ovarian insufficiency and premature ovarian failure — some of which may be irreversible — and the declining mortality rate for cervical cancer even in the prevaccine era, the risk-benefit profile for HPV vaccination remains unclear.

    3 case reports on ovarian insufficiency

    In the 2014 investigation mentioned above, a general practitioner in Australia noticed that three girls developed premature ovarian insufficiency following HPV4 vaccination.

    As a result of vaccination, each of the girls (ages 16, 16 and 18) had been prescribed oral contraception to treat menstrual cycle irregularities. Typically, women present with amenorrhea (no periods) or oligomenorrhea (infrequent periods) as the initial symptom of premature ovarian insufficiency.

    One girl had irregular periods following three doses of HPV vaccination. She then became amenorrheic and was diagnosed with premature ovarian insufficiency.

    Another girl’s periods were “like clockwork” until after the third HPV dose, which she received at age 15. Her first cycle after being vaccinated for the third time started two weeks late, and her next cycle was two months late. The final cycle began nine months later. The patient had no family history of early menopause.

    She was diagnosed with premature ovarian failure at 16. Lab work found hormone levels consistent with those of postmenopausal women, but her bone mineral density was normal.

    The authors of this case series noted that in preclinical studies of HPV4, the five-week-old rats only conceived one litter and the only available toxicology studies appear to be on the male rodent reproductive system.

    However, only two of three doses were administered prior to mating, and the overall fecundity was 95%, slightly lower than the control rats (98%) that received no vaccination prior to mating.

    The dose tolerance recommendations were based on an average weight of 50 kilograms for an adolescent girl but failed to take into account that HPV4 is administered to girls ages 9 to 13 years, who range in weight from 28 to 46 kilograms.

    Danish retrospective cohort study finds no link

    A 2021 study also evaluated premature ovarian insufficiency in a nationwide cohort of nearly 1 million Danish females ages 11 to 34 years.

    The researchers used Cox proportional hazard regression to detect an increased risk of premature ovarian insufficiency diagnosis by HPV4 vaccination status during the years 2007-2016. The hazard ratio for premature ovarian insufficiency (vaccinated versus unvaccinated) was 0.96.

    One limitation was that data on age at menarche (first menstruation) and oral contraceptive use were not available. Girls who had not yet reached menarche would not be at risk for premature ovarian insufficiency, of course.

    The authors excluded girls under age 15 in a sensitivity analysis and still found no signal, concluding that no association was found between HPV4 vaccination and premature ovarian insufficiency.

    Reprinted with permission from The Epoch Times. Dr. Yuhong Dong, a medical doctor who also holds a doctorate in infectious diseases from China, is the chief scientific officer and co-founder of a Swiss biotech company and a 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/hpv-vaccine-safety-concerns-part-1-et/


    https://donshafi911.blogspot.com/2024/01/the-truth-about-hpv-vaccination-part-1.html
    The Truth About HPV Vaccination, Part 1: How Safe Is It, Really? This first installment in a multi-part series about the human papillomavirus, or HPV, vaccine explores peer-reviewed scientific literature that reveals serious safety concerns about a vaccine widely regarded as safe. The Epoch Times Miss a day, miss a lot. Subscribe to The Defender's Top News of the Day. It's free. By Yuhong Dong The decline of public trust in COVID-19 vaccines significantly impacts vaccination rates against routine childhood diseases. This multiple-part series explores the international research done over the past two decades on the human papillomavirus (HPV) vaccine — believed to be one of the most effective vaccines developed to date. Summary of Key Facts This multiple-part series offers a thorough analysis of concerns raised about HPV vaccination following the global HPV campaign, which commenced in 2006. In the U.S., the HPV vaccine was reported to have a disproportionately higher percentage of adverse events of fainting and blood clots in the veins. The U.S. Food and Drug Administration (FDA) acknowledges that fainting can happen following the HPV vaccine, and recommends sitting or lying down to get the shot, then waiting for 15 minutes afterward. International scientists found that the Centers for Disease Control and Prevention’s (CDC) Vaccine Adverse Event Reporting System (VAERS) logged a substantial increase in reports of premature ovarian failure from 1.4 per year before 2006 to 22.2 per year after the HPV vaccine approval, yielding a Proportional Reporting Ratio of 46.1. The HPV vaccine is widely regarded as one of the most effective vaccines developed to date. Nevertheless, safety issues have been raised following its approval, and in response, additional research has been published and litigation has been brought on behalf of those with a vaccine injury. In this HPV vaccine series, Parts I and II explain how the vaccine works and the evidence suggesting there may be legitimate safety concerns. The remaining parts present questions about real-world vaccine effectiveness and identify specific ingredients which may pose harm. The information presented here is drawn from peer-reviewed scientific literature from the U.S., Australia, Denmark, Sweden, France and Japan, as well as statistics published by public health agencies in each of these countries. More than 100 hours of research and internal peer review among scientists with experience in infectious diseases, virology, clinical trials and vaccine epidemiology have been invested in presenting this summary of the evidence. Large registry-based studies have identified plausible associations between HPV vaccination and autoimmune conditions, including premature ovarian insufficiency or premature ovarian failure, Guillain-Barré syndrome (GBS), postural orthostatic tachycardia syndrome and chronic regional pain syndrome. While it is easy to be enthusiastic about recent advances in human vaccine technology, we should keep in mind that achieving real and lasting good health is much more than just the absence of a certain virus. RFK Jr. and Brian Hooker Vax-Unvax RFK Jr. and Brian Hooker’s New Book: “Vax-Unvax” Order Now What is HPV? According to the CDC, HPV is the most common sexually transmitted infection in the U.S. HPV is a small DNA virus infecting human cutaneous epithelial cells in the mucosa and skin. More than 150 strains of the HPV virus have been identified. HPV infection is so common that the majority of sexually active people will get it at some point in their lives, even if they have only one or very few sexual partners. It can spread through sexual intercourse and oral sex. It can also pass between people through skin-to-skin contact, even by people who have no symptoms. HPV infection causes genital warts, some of which can turn into cancer. For the most part, however, HPV infection is benign. More than 90% of HPV infections cause no clinical symptoms and are self-limited, meaning the virus is cleared by the body via natural immunological defenses. HPV-associated cancers High-risk HPV types (types 16, 18 and others) can cause cervical cell abnormalities that are precursors to cancers. Type 16 is associated with approximately 50% of cervical cancers worldwide, and types 16 and 18 together are linked to 66% of cervical cancers. An additional five high-risk types, 31, 33, 45, 52 and 58, are linked with another 15% of cervical cancers and 11% of all HPV-associated cancers. Infection with a high-risk HPV type is associated with a higher chance of the development of cervical cancer but, by itself, HPV infection is not the sole risk factor to cause cancer. There are many other reasons, as discussed in this paper. Given the prevalence of infection, it is unsurprising that globally, cervical cancer is the fourth most common cancer in women. In 2018, an estimated 570,000 women were diagnosed with cervical cancer worldwide and more than 300,000 died of the disease. In the U.S., nearly 50,000 new HPV-associated cancers occur annually, with women infected at a slightly higher rate than men. But in 9 out of 10 cases, HPV goes away within two years without causing health problems. Only persistent HPV infections may lead to cancer. These infections evade the immune system’s innate cell-mediated defenses. The incidence of cervical cancer can be controlled as a result of the implementation of routine testing and screening, including Pap and DNA tests. HPV vaccines Three HPV vaccines — bivalent HPV vaccine (Cervarix, 2vHPV), quadrivalent HPV vaccine (Gardasil, 4vHPV or HPV4) and 9-valent HPV vaccine (Gardasil 9, 9vHPV) — have been licensed by the FDA. The HPV vaccine uses recombinant technology to assemble the shell of the virus — L1 capsid protein. These viral-like particles do not contain the virus genome and are not infectious. Cervarix, developed by GlaxoSmithKline, is a bivalent vaccine against HPV types 16 and 18, that was pulled from the U.S. market in 2016 due to “very low market demand.” Merck’s original Gardasil vaccine was designed to prevent infections from four strains (types 6, 11, 16 and 18). On June 8, 2006, after the FDA’s fast-tracked review, Gardasil was approved for use in females ages 9 to 26 for the prevention of cervical, vulvar and vaginal cancers. According to the label accompanying the vaccine, the ingredients in Merck’s first Gardasil vaccine were proteins of HPV, amorphous aluminum hydroxyphosphate sulfate, yeast protein, sodium chloride, L-histidine, polysorbate 80, sodium borate and water for injection. On Oct. 16, 2009, the FDA approved Gardasil (HPV4) for use in boys ages 9 through 26 for the prevention of genital warts caused by HPV types 6 and 11, but not for cancer. In 2010, it approved Gardasil for the prevention of anal cancer in males and females ages 9 to 26. Four years later, the FDA approved an updated vaccine, Merck’s Gardasil 9, for use in girls ages 9 to 26 and boys ages 9 to 15 for the prevention of cervical, vaginal and anal cancers. Gardasil 9 contains the same ingredients as Gardasil, but offers protection against nine HPV strains, adding five additional types (HPV types 31, 33, 45, 52 and 58). The current HPV vaccination schedule recommended by the CDC is two doses for both boys and girls aged 11 or 12. However, it is approved for children as young as 9. The second dose is given 6 to 12 months after the first. For those aged 15 and above, a three-dose schedule is implemented at one- to two-month and six-month intervals, although antibody-level studies suggest that two doses are sufficient. The vaccine prompts the body to produce neutralizing antibodies against HPV. Antibody responses appear to peak seven months after the first dose (or one month after the third dose). The vaccine-induced antibody levels appear to be 10 to 100 times higher than those after natural infection. The high vaccine effectiveness (90 to 98%) against the fast-growing, abnormal cells which may cause precancerous lesions in people ages 16 to 26 suggested that the best timing for vaccination was to give it to patients before they became sexually active. HPV VAERS reports from 2 large countries U.S. HPV vaccine adverse events On Aug. 19, 2009, the Journal of the American Medical Association published an article authored by scientists from the FDA and CDC that reviewed the safety data for Gardasil for adverse events reported to VAERS between June 2006 through December 2008. During that time, there were 12,424 reports of adverse events. Of these, 772 (6.2%) were serious. VAERS is a passive surveillance system, which is subject to multiple limitations, including underreporting, unconfirmed diagnosis, lack of denominator data and no unbiased comparison groups. Nevertheless, it is a useful and important tool for detecting postmarket safety issues with vaccines. A disproportionately high percentage of Gardasil VAERS reports were of syncope (fainting) and venous thromboembolic events (blood clots in the veins) compared with other vaccines. There were 8.2 syncope events per 100,000 HPV doses and 0.2 venous thromboembolic events per 100,000 HPV doses reported, respectively. The Gardasil package insert includes a warning about fainting, fever, dizziness, nausea and headaches (page 1) and notes at least the following adverse reactions reported during postmarketing surveillance (section 6.2): Guillain-Barré syndrome, transverse myelitis, motor neuron disease, venous thromboembolic events, pancreatitis and autoimmune disorders. Australia HPV vaccines adverse events In 2007, Australia reported an annual adverse drug reaction rate of 7.3/100,000, the highest since 2003, representing an 85% increase from 2006. Per the analysis of the Adverse Drug Reactions System database by the Australian Department of Health and Aging, this increase was “almost entirely due to” reports following the national rollout of the three-dose HPV vaccination program for young females in April 2007; 705 of the 1,538 adverse drug reactions reported that year were from the Gardasil vaccine. 1 vaccine adverse events australia chart In Australia, the ADR increase in 2007 was almost entirely due to the three-dose HPV vaccination program for females aged 12 to 26 years in April 2007. Credit: Australian Government Department of Health and Aged Care. Moreover, though people may take different vaccines other than HPV, the HPV vaccine was the only suspected vaccine to cause adverse reactions in 96% of records. Twenty-nine percent had causality ratings of “certain” or “probable” and 6% were defined as “serious.” 2 vaccine types vaccine suspected chart In these HPV-induced ADRs, 674 were suspected to be related to HPV vaccines, 203 had causality ratings of “certain” or “probable,” and 43 were defined as “serious.” Credit: Australian Government Department of Health and Aged Care. Japan withdraws recommendation, vaccine acceptance plunged In 2013, the Japanese raised concerns about a variety of widely reported post-vaccination serious adverse events. This led the government to suspend recommending the HPV vaccine for six years. Vaccine acceptance of HPV in Japan plunged significantly after 2013, from 42.9% to 14.3%, or from 65.4% to 3.9%. Researchers around the world also started to investigate HPV safety. A World Health Organization (WHO) position paper released on July 14, 2017, concluded that the HPV vaccines were “extremely safe.” The same report estimated approximately 1.7 cases of anaphylaxis per million HPV doses, that no association with GBS was found, and that syncope (fainting) was “established as a common anxiety or stress-related reaction to the injection.” In the spring of 2022, Japan announced it was relaunching its HPV vaccination drive. Mainstream news outlets reported that for thousands of women, the cost of caution may have led to preventable HPV-induced cancers and an estimated 5,000 to 5,700 deaths. However, a true risk-benefit analysis would also consider the number of serious adverse events prevented by putting the program on hold. The question remains: Was Japan’s caution warranted, or should their national vaccination program have continued? Ovarian insufficiency Concerns that the vaccine may be negatively affecting fertility have been detailed in the scientific literature. In 2014, a peer-reviewed case series describing premature ovarian failure among Australian women following HPV vaccination was published in the Journal of Investigative Medicine. This prompted other researchers to systematically examine the VAERS data to see if there was a connection between premature ovarian failure and Gardasil. Their study found a “potential safety signal” and concluded that “further investigations are warranted.” VAERS analysis on ovarian failure Two recent publications based on VAERS reports (first study, second study) found that events with a probable autoimmune background were significantly more frequent after HPV vaccination compared to other vaccinations. The team of international scientists that did the second study evaluated reports between 1990 and 2018. They found that among the 228,341 premature ovarian failure reports, 0.1% was considered to be associated with HPV vaccination with a median age of 15 years and the time to onset was 20.5 days following vaccination. The primary symptoms were amenorrhea (80.4%) and premature menopause (15.3%). Most strikingly, the mean number of premature ovarian failure cases increased significantly from 1.4 per year prior to 2006 to 22.2 per year after the HPV vaccine was approved, with a proportional reporting ratio of 46. The investigators noted that the WHO and CDC declared the HPV vaccine safe regardless of lacking adequate research into safety concerns. For example, the authors note that in a CDC-sponsored VAERS study, 17 cases of premature ovarian failure were identified but 15 were excluded due to insufficient information to confirm the diagnosis. A separate observational study using the Vaccine Safety Datalink found no increased risk. But this study was too underpowered to detect a signal. In addition, a cross-sectional survey study using National Health and Nutrition Examination Survey data relied on an inaccurate measurement of premature ovarian failure and self-reported HPV vaccination. In summary, the researchers detected a strong safety signal even after accounting for a potential upswing in reports due to media coverage after the product launch (they refer to this as “notoriety bias”). Because VAERS is a passive reporting system, the data may be incomplete and are often unconfirmed by physicians. Therefore, this study cannot provide a definitive link between HPV vaccination and premature ovarian insufficiency or premature ovarian failure but does generate a hypothetical link. The authors of the second study conclude by insisting that “this signal warrants well-designed and appropriate epidemiological research.” They note that “if the signal is confirmed, the risk is small compared to the lifetime risk of cervical cancer.” However, the benefit-risk profile on an individual level is not uniform. Given the health impacts of premature ovarian insufficiency and premature ovarian failure — some of which may be irreversible — and the declining mortality rate for cervical cancer even in the prevaccine era, the risk-benefit profile for HPV vaccination remains unclear. 3 case reports on ovarian insufficiency In the 2014 investigation mentioned above, a general practitioner in Australia noticed that three girls developed premature ovarian insufficiency following HPV4 vaccination. As a result of vaccination, each of the girls (ages 16, 16 and 18) had been prescribed oral contraception to treat menstrual cycle irregularities. Typically, women present with amenorrhea (no periods) or oligomenorrhea (infrequent periods) as the initial symptom of premature ovarian insufficiency. One girl had irregular periods following three doses of HPV vaccination. She then became amenorrheic and was diagnosed with premature ovarian insufficiency. Another girl’s periods were “like clockwork” until after the third HPV dose, which she received at age 15. Her first cycle after being vaccinated for the third time started two weeks late, and her next cycle was two months late. The final cycle began nine months later. The patient had no family history of early menopause. She was diagnosed with premature ovarian failure at 16. Lab work found hormone levels consistent with those of postmenopausal women, but her bone mineral density was normal. The authors of this case series noted that in preclinical studies of HPV4, the five-week-old rats only conceived one litter and the only available toxicology studies appear to be on the male rodent reproductive system. However, only two of three doses were administered prior to mating, and the overall fecundity was 95%, slightly lower than the control rats (98%) that received no vaccination prior to mating. The dose tolerance recommendations were based on an average weight of 50 kilograms for an adolescent girl but failed to take into account that HPV4 is administered to girls ages 9 to 13 years, who range in weight from 28 to 46 kilograms. Danish retrospective cohort study finds no link A 2021 study also evaluated premature ovarian insufficiency in a nationwide cohort of nearly 1 million Danish females ages 11 to 34 years. The researchers used Cox proportional hazard regression to detect an increased risk of premature ovarian insufficiency diagnosis by HPV4 vaccination status during the years 2007-2016. The hazard ratio for premature ovarian insufficiency (vaccinated versus unvaccinated) was 0.96. One limitation was that data on age at menarche (first menstruation) and oral contraceptive use were not available. Girls who had not yet reached menarche would not be at risk for premature ovarian insufficiency, of course. The authors excluded girls under age 15 in a sensitivity analysis and still found no signal, concluding that no association was found between HPV4 vaccination and premature ovarian insufficiency. Reprinted with permission from The Epoch Times. Dr. Yuhong Dong, a medical doctor who also holds a doctorate in infectious diseases from China, is the chief scientific officer and co-founder of a Swiss biotech company and a 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/hpv-vaccine-safety-concerns-part-1-et/ https://donshafi911.blogspot.com/2024/01/the-truth-about-hpv-vaccination-part-1.html
    CHILDRENSHEALTHDEFENSE.ORG
    The Truth About HPV Vaccination, Part 1: How Safe Is It, Really?
    This first installment in a multi-part series about the human papillomavirus, or HPV, vaccine explores peer-reviewed scientific literature that reveals serious safety concerns about a vaccine widely regarded as safe.
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  • Can 2 Cheap Meds, 1 Vitamin & Baking Soda Kill Any Cancer?
    Ivermectin, Fenbendazole, Vit C and Sodium Bicarb. But don't worry your cancer is safe because the FDA would never allow it.

    Dr. Syed Haider
    Cancer Treatment Options | Houston Methodist
    Cancer rates have skyrocketed in the past century for a number of reasons not least of which is the incredibly large number of toxins spewed into the environment and incorporated into our food supplies. And now with most of humanity exposed to the cancerous spike protein there is likely to be even further acceleration. Those exposed to the fallout from the East Palestine Ohio train wreck, which may spread quite widely along the eastern seaboard, are particularly at risk of developing cancer in the coming months and years from the ingition of the vinyl chloride cargo and it’s toxic breakdown products, especially dioxins.

    This post is not meant to be an exhaustive treatise on the prevention and treatment of cancer, but only to explain as simply as possible the scientific theory behind Adam Gaertner’s anti-cancer protocol, which combines 4 simple and cheap therapies that have been separately used and studied for a wide variety of human cancers with mixed results, but together have powerful synergistic effects that may, it is hoped, effectively eliminate any cancer. And at the end his simple 3 week protocol is included.

    Before we begin I also have to say that I have seen many people beat end stage cancer using drastic elimination diets and a modifed Gerson juicing protocol. And of course I have known many who decided on chemotherapy, radiation and surgery. Both paths are extremely difficult and require a lot of commitment and sacrifice. Perhaps the following protocol can help more people more easily overcome cancer.

    And after cancer is beaten, it pays to address the root causes because those who overcome cancer are often prone to an even more aggressive recurrence, especially if they persist in the unhealthy exposures and lifestyle habits that triggered it in the first place.

    WHAT IS CANCER?

    All tissues are made up of individual cellular building blocks that work together to accomplish a joint function. For example liver cells are like millions of workmen that all together make up the liver. Normally tissues maintain just the right amount of helpful worker cells. As old cells die off, new ones take their place.

    Cancers arise from cells in normal tissues that start to grow uncontrollably - the old workmen don't want to die and instead find a way to become immortal. They also don't want to work anymore and begin using up resources like the nutrients and oxygen coming into the tissue via the blood. These immortal cells also multiply very quickly and if left unchecked can destroy the normal cells and then the entire organ ceases to function. Not only that but they also enter the bloodstream and travel to other distant organs and take up new residence and continue to multiply out of control.


    Just as there are a tiny percentage of psychopaths and criminals in every society, who attempt to murder others and appropriate all the resources for themselves, there are cancer cells in everyone's bodies all the time that would like nothing better than to take over.

    Thank you for reading Dr. Syed Haider. This post is public so feel free to share it.

    Share

    And just as nations utilize a police force and military to maintain the peace, our bodies utilize specialized immune system processes and immune cells to keep the cancer cells in check - to continuously search them out and put them to death.

    However, when these defenses fail due to exposure to various carcinogens or simply old age, cancerous cells can gain a foothold and destroy us.

    DEFENSES AGAINST CANCER

    Intracellular Cytosolic Immunity

    Think of a cell like a 3D sphere. Inside the sphere there is another smaller sphere, which is the nucleus and holds the genetic material or DNA. Everything outside the nucleus is called the cytoplasm.

    Steph's Nature and Science
    Each individual cell has an internal immune system, called the cytosolic immune system that will monitor the cells health, and if the cell becomes cancerous will kill it in a process of cellular suicide termed apoptosis.

    You can imagine this as a person's conscience.

    Think of a horror movie scenario where someone becomes bitten by a mindless zombie and begins to change into a zombie themselves, feeling the first stirrings of hunger for the blood of those around them. Knowing they are doomed and wanting to preserve the lives of their loved ones they commit suicide rather than becoming a monster.

    In this way our own first line of defense against cancer is a system of internal checks and balances that will lead to cellular suicide or apoptosis.

    The checks and balances are a system of pro-suicide (pro-apoptotic) and anti-suicide (anti-apoptotic) pathways: p53 tumor suppressor gene, G1/S checkpoint, Hippo, TGF-β, Wnt signaling, Notch signaling, and PI3K/AKT signaling.

    Within these extremely complex pathways made up of numerous interacting chemical messengers there are just a small handful of signals that can lead to cellular death: caspases, apoptosis inducing factor (AIF), endonucleases, granzymes, BH3-interacting domain death agonist (Bid), Death receptor 5 (DR5), Fas-associated protein with death domain (FADD).

    A vast majority of cancers arise due to mutations affecting these critical cytosolic immunity pathways.

    So the conscience of the cell, its own internal checks and balances, become distorted and do not trigger suicide as they should when the cell begins transforming into a cancer cell.

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    The mutations work by producing malformed proteins that do not do their usual job of triggering cellular suicide.

    Usually malformed proteins would themselves be destroyed by the intracellular “chaperone” and “proteasome” systems - these are both meant to protect our cells from mutations.

    The reason this does not happen in the case of most cancers is that most cancers also stimulate an internal process that makes them more resistant to the chaperone and proteasome systems - by way of the production of heat shock protein 90 (hsp90).

    Ivermectin

    Doctors Sue FDA For Prohibiting Use Of Ivermectin To Treat Covid
    Ivermectin, the horse and cow and human drug, has traditionally been used as an antiparasitic (e.g. scabies), but also has antiviral and anti-inflammatory activities. It binds to hsp90 and other heat shock proteins blocking their ability to stabilize mutated checkpoint proteins. It likewise suppresses a number of the anti-apoptotic pathway especially TGF-β, as well as increasing the expression of p53 tumor suppressor gene pro-apoptotic pathway.

    So in effect ivermectin helps the cancer cell reestablish the ability to detect that it is cancerous and thereby trigger an internal process of suicide.

    Unfortunately not every cancer utilizes the pathways ivermectin targets.

    And as a result of the relatively rapid replication rate of cancerous cells, and the evolutionary imperative to survive, additional mutations are often present across the tumor mass. As a result, ivermectin may be effective against only 90% of a given tumor mass; however, if the 90% is killed in this way, the remaining 10% will, by default, not be able to be corrected, leading to relapse, with the remainder becoming harder to treat - as the 10% left over multiplies and becomes the entire 100% of tumor.

    Extracellular Natural Killer Cell Immunity

    Immense Immunology Insight: Girl, if we were lymphocytes... You'd be a ...
    Another arm of the immune system that protects against cancer is outside the cancer cell itself. We can think of this like the police force that keeps an eye out for dangerous cancer cells.

    Our internal police force uses markers to identify healthy cells and unhealthy cells as well as foreign intruders like bacteria and viruses.

    The markers our immune system uses for identification are called antigens - little bits of cells.

    Most of our immune cells are trained to recognize foreign particles that do not belong and destroy them - like crazy immigration agent death squads.

    But the Natural Killer (NK) cells are trained to check for what is supposed to be present - self-antigens - markers that indicate normal cells, kind of like ID cards.

    In policing terms: NK cells wander the streets and demand everyone's papers, regardless of any evidence of a crime, and immediately execute anyone who cannot prove they belong.

    "Ihre Papiere, bitte!" (Episode 48) | #FSCK 'Em All!
    The rapid rate of replication of cancerous cells places them under heavy evolutionary pressure; those cells that do not express self-antigens will be targeted and destroyed by the NK cells, whereas those that do may not be - so some cancer cells develop the ability to forge their own papers and pass themselves off as normal law abiding residents, rather than dangerous alien invaders.

    Those wily ones will multiply while the others die off, and eventually the entire tumor mass is comprised of cells that can trick the NK cells into leaving them alone by presenting proper identification, even though they will still be presenting other signs of being foreign - like devil horns growing out of their heads - “it’s just part of my mardi gras outfit officer”.

    While this is very bad news it does open up an avenue of treatment via T cell activation.

    T cell Immunity

    CD 4 T cells are also called helper T cells, they aid other immune cells via the release of cytokine messengers. CD 8 T cells are also called cytotoxic T cells. Cyto for cell, toxic for toxic - i.e. they kill cancer cells.

    T cells like NK cells detect self antigens and will ignore those that present them, but they also look for non self antigens (like those devil horns) as well as an additional costimulatory signal to trigger their death squad role.

    It’s like they not only check your papers, but they check to make sure those horns are actually real and they make you pass a lie detector test. If they find real horns and sense signs of stress during the lie detector test they have enough evidence to declare you guilty and execute you.

    Geek Comic for November 17th - You can Beat the Lie Detector Test Because…
    If they just find the horns, but no signs of stress, they let you go on your way.

    Cancer cells can’t avoid making weird mutated horn-like proteins, but they can figure out how to pass the lie detector test by muting their stress signals.

    The way to bypass that is by subjecting them to so much stress that their ability to mute the signs of stress breaks down, and at the same time triggering more foreign proteins and stopping proliferation would also be helpful, which brings us to the other 3 therapies.

    Fenbendazole, Sodium Bicarbonate & Vitamin C

    Fenbendazole

    Panacur Granules 22.2% [Fenbendazole] (1 lb)
    Humans are not listed on the side panel
    Fenbendazole is not FDA approved for use in humans, but is commonly used as an antiparasitic medication in animals, and has been studied in some human cancer studies, where it appears to be safe. It has multiple effects against cancer cells. Most significantly, it can lead to the influence the MAPK pathway to activate cellular suicide or apoptosis.

    It destabilizes cellular protein structures called microtubules that are essential to cell division.

    It also disrupts cancer cell energy production by blocking the breakdown of sugar (glycolysis) which is like crude oil for cells and also blocking the ability of mitochondria, the energy refining factories of cells from using the crude oil to produce the cellular equivalent of electricity, i.e. ATP - the universal bioenergy molecule.

    This collection of actions may not be applicable for all cancers, however a sizable proportion are affected; as such metabolic disruption occurs which then leads to production of cellular stress signals.

    An important manifestation of this is CD80, a costimulatory signal that in combination with T Cell Receptor binding to a foreign antigen, activates CD8 T-cells; alternatively if the antigen is self, it will inhibit them, as well as activate dormant NK cells in the area.

    Share

    So what’s happening here is if the cancer cell has non self antigens (those devil horns) the stress signals (failed lie detector test) will activate CD8 cytotoxic T cells to kill it.

    If however the cancer cell shows a normal self antigen to the T cell along with the stress signals, the T cell will stand down but the same stress signals may still activate nearby NK cells.

    Thereby some of the tumor cells will be destroyed releasing many new antigens into the area, both self and non self. These new antigens will be recognized by nearby immune cells and train them to better detect the remaining tumor cells. This triggers a far more robust immune activation and ends up in effectively nuking the area - destroying all remaining tumor as well as some friendlies and innocent bystanders mixed up in the fray.

    Sodium Bicarbonate

    Alkaline Diet for Cancer : Comprehensive Nutrional Guide to Cure and ...
    The mechanism of sodium bicarbonate action is easy to understand, based on the Warburg effect: decreasing acidity (increasing the pH or alkalinity) outside the cancer cells impairs their ability to maintain a highly alkaline environment within themselves. That alters cancer cells' metabolism, prompting similar immune system reactions as previously discussed and igniting further cascades.

    Unfortunately, if sodium bicarbonate is used without other agents from the protocol, tumors promptly become resistant and cancer-fighting benefits decrease to mere prolongation of life expectancy instead of complete elimination.

    Vitamin C

    Best Linus Pauling Cancer Vitamin C - Your Best Life
    When ascorbic acid is used in large quantities, along with the reduced form dehydroascorbate (DHA), it induces intense oxidative stress within cancerous cells; if that stress is insufficient to destroy the cell outright, it triggers the release of numerous cytokines, including our friend CD80, which initiates the cascade described above involving CD8 cytotoxic T cells.

    Not all forms of cancer are responsive to this pathway and sodium bicarbonate is capable of directly counteracting it.

    As a potent immunomodulator vitamin C even has the potential to disrupt the inflammatory response involved in targeting a significant-sized tumor.

    So it’s important to carefully balance the two options, and not use both simultaneously. The alkalization brought about by sodium bicarbonate won't last for particularly long; therefore, employing one after another in alternating fashion will likely provide more benefits than using just one of them at a time.

    In a Nutshell

    The following are four therapeutic pathways that, when used together, cause cancerous cells to undergo both apoptosis and loss of immune evasion features so the immune system can identify and attack them.

    Ivermectin inhibits mutant checkpoint and cascade transduction proteins, particularly PI3K, reduces TAM anti-apoptotic signaling, and increases expression of the tumor suppressor p53 by binding to the hsp90 protein.

    In addition to modulating the MAPK pathway, fenbendazole destabilizes microtubules, inhibits glycolytic metabolism, inhibits mitochondrial oxidative phosphorylation, and reduces anti-apoptotic PD-L1 expression feedback loops.

    Through alkalization of the cytosolic tumor environment, sodium bicarbonate induces metabolic stress.

    Vitamin C triggers oxidative stress and cytokine production.

    In this method, cytosolic apoptosis signaling cascades are promoted, and effector CD8 and NK cells are infiltrated into a tumor mass through adaptive recognition of foreign antigens and inhibition of anti-apoptotic pathways in order to achieve complete remission through both self-destruct signaling pathways as well as inflammatory immune destruction of cancerous cells.

    The Proposed Protocol

    Unlike most traditional cytotoxic cancer therapies that destroy both cancer cells as well as regular cells and especially the body's immune system cells, this protocol stimulates the body's own innate and adaptive immune system to fight off cancer.

    NLRP3 and STING enhance immune attack on cancer | Cancer Biology
    This protocol should not be used in combination with most mainstream cancer treatments, such as chemotherapy or radiotherapy, due to their ability to impair the immune system that the protocol depends on.

    It is likely to be most potent at the early stages of disease; further progress of the condition will prolong duration of treatment needed.

    A healthy immune system takes time to ramp up the necessary response, so the protocol is based on the time required for each drug to take effect, safety data, bioavailability, and elimination time.

    Day 1:

    Ivermectin: 1 mg/kg by mouth

    Fenbendazole: 1000mg by mouth

    Sodium Bicarbonate: 1 tsp morning and evening dissolved in 1 quart of water

    Day 2:

    Ascorbic acid: 50 mg/kg by mouth, two doses, 8 hours apart or 20g IV, once

    Day 3:

    Repeat Day 1

    Day 4:

    Repeat Day 2

    Days 5 to 10:

    Fenbendazole, 200mg by mouth daily

    Alternate sodium bicarbonate and ascorbic acid every other day beginning with sodium bicarb on day 5, then vitamin C on day 6, etc.

    Day 11:

    Ivermectin: 1 mg/kg by mouth

    Fenbendazole: 1000 mg by mouth

    Sodium Bicarbonate: 1 tsp morning and evening dissolved in 1 quart of water

    Days 12 to 20:

    Sodium Bicarbonate: 1 tsp morning and evening dissolved in 1 quart of water

    Day 20:

    Imaging: Check progress. Significant reduction or complete elimination of tumor mass should have occurred by this time, if not repeat the protocol.

    At this time the US FDA has not approved this protocol for study or for use in humans.

    It is unlikely that any pharmaceutical company will spend the millions of dollars it would take to prove this protocol in large randomized controlled trials because none of the four therapeutics are under patent and therefore cannot be effectively monetized.

    Even if some billionaire decided to back this protocol, Big Pharma would move heaven and earth to prove it doesn’t work as they did with ivermectin and hydroxychloroquine for COVID.

    Let me know below if you know of anyone who has utilized these 4 therapeutics together.

    And finally beating cancer inside us is a great first step to healing our world, but next we need to beat the cancerous psychopaths who are destroying our societies. If not we will go the way of Rome and a new civilization will rise from our ashes.


    I believe in the Judeo Christian ethic of working hard and giving back without big government. My online clinic, mygotodoc.com, exemplifies that by charging a fee that is well worth the service, but also offering free medical answers and (asynchronous) care for anyone that needs it.

    The same applies at my free online Summit Long COVID Reset, exclusive weekly content, including live Q&As and much more released on my video subscription platform, and in my course, Phoenix for Healing Long Haul and Lean Vitality - all are available for a fee or for free by request.

    So thank you to everyone who finds this written content valuable and supports it by being a paid subscriber (even though there are currently no paid subscriber benefits aside from a warm fuzzy feeling that you did something good). You are helping enable the significant amount of time and effort it takes to write. If you have the means also please consider donating to help support the care of those cannot afford it at mygotodoc.com/donation.

    If you are a free subscriber thanks for being here, and please also consider supporting my efforts in any way you can, but especially by sharing my posts widely.

    https://blog.mygotodoc.com/p/can-2-cheap-meds-1-vitamin-and-baking
    Can 2 Cheap Meds, 1 Vitamin & Baking Soda Kill Any Cancer? Ivermectin, Fenbendazole, Vit C and Sodium Bicarb. But don't worry your cancer is safe because the FDA would never allow it. Dr. Syed Haider Cancer Treatment Options | Houston Methodist Cancer rates have skyrocketed in the past century for a number of reasons not least of which is the incredibly large number of toxins spewed into the environment and incorporated into our food supplies. And now with most of humanity exposed to the cancerous spike protein there is likely to be even further acceleration. Those exposed to the fallout from the East Palestine Ohio train wreck, which may spread quite widely along the eastern seaboard, are particularly at risk of developing cancer in the coming months and years from the ingition of the vinyl chloride cargo and it’s toxic breakdown products, especially dioxins. This post is not meant to be an exhaustive treatise on the prevention and treatment of cancer, but only to explain as simply as possible the scientific theory behind Adam Gaertner’s anti-cancer protocol, which combines 4 simple and cheap therapies that have been separately used and studied for a wide variety of human cancers with mixed results, but together have powerful synergistic effects that may, it is hoped, effectively eliminate any cancer. And at the end his simple 3 week protocol is included. Before we begin I also have to say that I have seen many people beat end stage cancer using drastic elimination diets and a modifed Gerson juicing protocol. And of course I have known many who decided on chemotherapy, radiation and surgery. Both paths are extremely difficult and require a lot of commitment and sacrifice. Perhaps the following protocol can help more people more easily overcome cancer. And after cancer is beaten, it pays to address the root causes because those who overcome cancer are often prone to an even more aggressive recurrence, especially if they persist in the unhealthy exposures and lifestyle habits that triggered it in the first place. WHAT IS CANCER? All tissues are made up of individual cellular building blocks that work together to accomplish a joint function. For example liver cells are like millions of workmen that all together make up the liver. Normally tissues maintain just the right amount of helpful worker cells. As old cells die off, new ones take their place. Cancers arise from cells in normal tissues that start to grow uncontrollably - the old workmen don't want to die and instead find a way to become immortal. They also don't want to work anymore and begin using up resources like the nutrients and oxygen coming into the tissue via the blood. These immortal cells also multiply very quickly and if left unchecked can destroy the normal cells and then the entire organ ceases to function. Not only that but they also enter the bloodstream and travel to other distant organs and take up new residence and continue to multiply out of control. Just as there are a tiny percentage of psychopaths and criminals in every society, who attempt to murder others and appropriate all the resources for themselves, there are cancer cells in everyone's bodies all the time that would like nothing better than to take over. Thank you for reading Dr. Syed Haider. This post is public so feel free to share it. Share And just as nations utilize a police force and military to maintain the peace, our bodies utilize specialized immune system processes and immune cells to keep the cancer cells in check - to continuously search them out and put them to death. However, when these defenses fail due to exposure to various carcinogens or simply old age, cancerous cells can gain a foothold and destroy us. DEFENSES AGAINST CANCER Intracellular Cytosolic Immunity Think of a cell like a 3D sphere. Inside the sphere there is another smaller sphere, which is the nucleus and holds the genetic material or DNA. Everything outside the nucleus is called the cytoplasm. Steph's Nature and Science Each individual cell has an internal immune system, called the cytosolic immune system that will monitor the cells health, and if the cell becomes cancerous will kill it in a process of cellular suicide termed apoptosis. You can imagine this as a person's conscience. Think of a horror movie scenario where someone becomes bitten by a mindless zombie and begins to change into a zombie themselves, feeling the first stirrings of hunger for the blood of those around them. Knowing they are doomed and wanting to preserve the lives of their loved ones they commit suicide rather than becoming a monster. In this way our own first line of defense against cancer is a system of internal checks and balances that will lead to cellular suicide or apoptosis. The checks and balances are a system of pro-suicide (pro-apoptotic) and anti-suicide (anti-apoptotic) pathways: p53 tumor suppressor gene, G1/S checkpoint, Hippo, TGF-β, Wnt signaling, Notch signaling, and PI3K/AKT signaling. Within these extremely complex pathways made up of numerous interacting chemical messengers there are just a small handful of signals that can lead to cellular death: caspases, apoptosis inducing factor (AIF), endonucleases, granzymes, BH3-interacting domain death agonist (Bid), Death receptor 5 (DR5), Fas-associated protein with death domain (FADD). A vast majority of cancers arise due to mutations affecting these critical cytosolic immunity pathways. So the conscience of the cell, its own internal checks and balances, become distorted and do not trigger suicide as they should when the cell begins transforming into a cancer cell. 2 Zombie Stocks Coming Back from the Dead | Nasdaq The mutations work by producing malformed proteins that do not do their usual job of triggering cellular suicide. Usually malformed proteins would themselves be destroyed by the intracellular “chaperone” and “proteasome” systems - these are both meant to protect our cells from mutations. The reason this does not happen in the case of most cancers is that most cancers also stimulate an internal process that makes them more resistant to the chaperone and proteasome systems - by way of the production of heat shock protein 90 (hsp90). Ivermectin Doctors Sue FDA For Prohibiting Use Of Ivermectin To Treat Covid Ivermectin, the horse and cow and human drug, has traditionally been used as an antiparasitic (e.g. scabies), but also has antiviral and anti-inflammatory activities. It binds to hsp90 and other heat shock proteins blocking their ability to stabilize mutated checkpoint proteins. It likewise suppresses a number of the anti-apoptotic pathway especially TGF-β, as well as increasing the expression of p53 tumor suppressor gene pro-apoptotic pathway. So in effect ivermectin helps the cancer cell reestablish the ability to detect that it is cancerous and thereby trigger an internal process of suicide. Unfortunately not every cancer utilizes the pathways ivermectin targets. And as a result of the relatively rapid replication rate of cancerous cells, and the evolutionary imperative to survive, additional mutations are often present across the tumor mass. As a result, ivermectin may be effective against only 90% of a given tumor mass; however, if the 90% is killed in this way, the remaining 10% will, by default, not be able to be corrected, leading to relapse, with the remainder becoming harder to treat - as the 10% left over multiplies and becomes the entire 100% of tumor. Extracellular Natural Killer Cell Immunity Immense Immunology Insight: Girl, if we were lymphocytes... You'd be a ... Another arm of the immune system that protects against cancer is outside the cancer cell itself. We can think of this like the police force that keeps an eye out for dangerous cancer cells. Our internal police force uses markers to identify healthy cells and unhealthy cells as well as foreign intruders like bacteria and viruses. The markers our immune system uses for identification are called antigens - little bits of cells. Most of our immune cells are trained to recognize foreign particles that do not belong and destroy them - like crazy immigration agent death squads. But the Natural Killer (NK) cells are trained to check for what is supposed to be present - self-antigens - markers that indicate normal cells, kind of like ID cards. In policing terms: NK cells wander the streets and demand everyone's papers, regardless of any evidence of a crime, and immediately execute anyone who cannot prove they belong. "Ihre Papiere, bitte!" (Episode 48) | #FSCK 'Em All! The rapid rate of replication of cancerous cells places them under heavy evolutionary pressure; those cells that do not express self-antigens will be targeted and destroyed by the NK cells, whereas those that do may not be - so some cancer cells develop the ability to forge their own papers and pass themselves off as normal law abiding residents, rather than dangerous alien invaders. Those wily ones will multiply while the others die off, and eventually the entire tumor mass is comprised of cells that can trick the NK cells into leaving them alone by presenting proper identification, even though they will still be presenting other signs of being foreign - like devil horns growing out of their heads - “it’s just part of my mardi gras outfit officer”. While this is very bad news it does open up an avenue of treatment via T cell activation. T cell Immunity CD 4 T cells are also called helper T cells, they aid other immune cells via the release of cytokine messengers. CD 8 T cells are also called cytotoxic T cells. Cyto for cell, toxic for toxic - i.e. they kill cancer cells. T cells like NK cells detect self antigens and will ignore those that present them, but they also look for non self antigens (like those devil horns) as well as an additional costimulatory signal to trigger their death squad role. It’s like they not only check your papers, but they check to make sure those horns are actually real and they make you pass a lie detector test. If they find real horns and sense signs of stress during the lie detector test they have enough evidence to declare you guilty and execute you. Geek Comic for November 17th - You can Beat the Lie Detector Test Because… If they just find the horns, but no signs of stress, they let you go on your way. Cancer cells can’t avoid making weird mutated horn-like proteins, but they can figure out how to pass the lie detector test by muting their stress signals. The way to bypass that is by subjecting them to so much stress that their ability to mute the signs of stress breaks down, and at the same time triggering more foreign proteins and stopping proliferation would also be helpful, which brings us to the other 3 therapies. Fenbendazole, Sodium Bicarbonate & Vitamin C Fenbendazole Panacur Granules 22.2% [Fenbendazole] (1 lb) Humans are not listed on the side panel Fenbendazole is not FDA approved for use in humans, but is commonly used as an antiparasitic medication in animals, and has been studied in some human cancer studies, where it appears to be safe. It has multiple effects against cancer cells. Most significantly, it can lead to the influence the MAPK pathway to activate cellular suicide or apoptosis. It destabilizes cellular protein structures called microtubules that are essential to cell division. It also disrupts cancer cell energy production by blocking the breakdown of sugar (glycolysis) which is like crude oil for cells and also blocking the ability of mitochondria, the energy refining factories of cells from using the crude oil to produce the cellular equivalent of electricity, i.e. ATP - the universal bioenergy molecule. This collection of actions may not be applicable for all cancers, however a sizable proportion are affected; as such metabolic disruption occurs which then leads to production of cellular stress signals. An important manifestation of this is CD80, a costimulatory signal that in combination with T Cell Receptor binding to a foreign antigen, activates CD8 T-cells; alternatively if the antigen is self, it will inhibit them, as well as activate dormant NK cells in the area. Share So what’s happening here is if the cancer cell has non self antigens (those devil horns) the stress signals (failed lie detector test) will activate CD8 cytotoxic T cells to kill it. If however the cancer cell shows a normal self antigen to the T cell along with the stress signals, the T cell will stand down but the same stress signals may still activate nearby NK cells. Thereby some of the tumor cells will be destroyed releasing many new antigens into the area, both self and non self. These new antigens will be recognized by nearby immune cells and train them to better detect the remaining tumor cells. This triggers a far more robust immune activation and ends up in effectively nuking the area - destroying all remaining tumor as well as some friendlies and innocent bystanders mixed up in the fray. Sodium Bicarbonate Alkaline Diet for Cancer : Comprehensive Nutrional Guide to Cure and ... The mechanism of sodium bicarbonate action is easy to understand, based on the Warburg effect: decreasing acidity (increasing the pH or alkalinity) outside the cancer cells impairs their ability to maintain a highly alkaline environment within themselves. That alters cancer cells' metabolism, prompting similar immune system reactions as previously discussed and igniting further cascades. Unfortunately, if sodium bicarbonate is used without other agents from the protocol, tumors promptly become resistant and cancer-fighting benefits decrease to mere prolongation of life expectancy instead of complete elimination. Vitamin C Best Linus Pauling Cancer Vitamin C - Your Best Life When ascorbic acid is used in large quantities, along with the reduced form dehydroascorbate (DHA), it induces intense oxidative stress within cancerous cells; if that stress is insufficient to destroy the cell outright, it triggers the release of numerous cytokines, including our friend CD80, which initiates the cascade described above involving CD8 cytotoxic T cells. Not all forms of cancer are responsive to this pathway and sodium bicarbonate is capable of directly counteracting it. As a potent immunomodulator vitamin C even has the potential to disrupt the inflammatory response involved in targeting a significant-sized tumor. So it’s important to carefully balance the two options, and not use both simultaneously. The alkalization brought about by sodium bicarbonate won't last for particularly long; therefore, employing one after another in alternating fashion will likely provide more benefits than using just one of them at a time. In a Nutshell The following are four therapeutic pathways that, when used together, cause cancerous cells to undergo both apoptosis and loss of immune evasion features so the immune system can identify and attack them. Ivermectin inhibits mutant checkpoint and cascade transduction proteins, particularly PI3K, reduces TAM anti-apoptotic signaling, and increases expression of the tumor suppressor p53 by binding to the hsp90 protein. In addition to modulating the MAPK pathway, fenbendazole destabilizes microtubules, inhibits glycolytic metabolism, inhibits mitochondrial oxidative phosphorylation, and reduces anti-apoptotic PD-L1 expression feedback loops. Through alkalization of the cytosolic tumor environment, sodium bicarbonate induces metabolic stress. Vitamin C triggers oxidative stress and cytokine production. In this method, cytosolic apoptosis signaling cascades are promoted, and effector CD8 and NK cells are infiltrated into a tumor mass through adaptive recognition of foreign antigens and inhibition of anti-apoptotic pathways in order to achieve complete remission through both self-destruct signaling pathways as well as inflammatory immune destruction of cancerous cells. The Proposed Protocol Unlike most traditional cytotoxic cancer therapies that destroy both cancer cells as well as regular cells and especially the body's immune system cells, this protocol stimulates the body's own innate and adaptive immune system to fight off cancer. NLRP3 and STING enhance immune attack on cancer | Cancer Biology This protocol should not be used in combination with most mainstream cancer treatments, such as chemotherapy or radiotherapy, due to their ability to impair the immune system that the protocol depends on. It is likely to be most potent at the early stages of disease; further progress of the condition will prolong duration of treatment needed. A healthy immune system takes time to ramp up the necessary response, so the protocol is based on the time required for each drug to take effect, safety data, bioavailability, and elimination time. Day 1: Ivermectin: 1 mg/kg by mouth Fenbendazole: 1000mg by mouth Sodium Bicarbonate: 1 tsp morning and evening dissolved in 1 quart of water Day 2: Ascorbic acid: 50 mg/kg by mouth, two doses, 8 hours apart or 20g IV, once Day 3: Repeat Day 1 Day 4: Repeat Day 2 Days 5 to 10: Fenbendazole, 200mg by mouth daily Alternate sodium bicarbonate and ascorbic acid every other day beginning with sodium bicarb on day 5, then vitamin C on day 6, etc. Day 11: Ivermectin: 1 mg/kg by mouth Fenbendazole: 1000 mg by mouth Sodium Bicarbonate: 1 tsp morning and evening dissolved in 1 quart of water Days 12 to 20: Sodium Bicarbonate: 1 tsp morning and evening dissolved in 1 quart of water Day 20: Imaging: Check progress. Significant reduction or complete elimination of tumor mass should have occurred by this time, if not repeat the protocol. At this time the US FDA has not approved this protocol for study or for use in humans. It is unlikely that any pharmaceutical company will spend the millions of dollars it would take to prove this protocol in large randomized controlled trials because none of the four therapeutics are under patent and therefore cannot be effectively monetized. Even if some billionaire decided to back this protocol, Big Pharma would move heaven and earth to prove it doesn’t work as they did with ivermectin and hydroxychloroquine for COVID. Let me know below if you know of anyone who has utilized these 4 therapeutics together. And finally beating cancer inside us is a great first step to healing our world, but next we need to beat the cancerous psychopaths who are destroying our societies. If not we will go the way of Rome and a new civilization will rise from our ashes. I believe in the Judeo Christian ethic of working hard and giving back without big government. My online clinic, mygotodoc.com, exemplifies that by charging a fee that is well worth the service, but also offering free medical answers and (asynchronous) care for anyone that needs it. The same applies at my free online Summit Long COVID Reset, exclusive weekly content, including live Q&As and much more released on my video subscription platform, and in my course, Phoenix for Healing Long Haul and Lean Vitality - all are available for a fee or for free by request. So thank you to everyone who finds this written content valuable and supports it by being a paid subscriber (even though there are currently no paid subscriber benefits aside from a warm fuzzy feeling that you did something good). You are helping enable the significant amount of time and effort it takes to write. If you have the means also please consider donating to help support the care of those cannot afford it at mygotodoc.com/donation. If you are a free subscriber thanks for being here, and please also consider supporting my efforts in any way you can, but especially by sharing my posts widely. https://blog.mygotodoc.com/p/can-2-cheap-meds-1-vitamin-and-baking
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    Can 2 Cheap Meds, 1 Vitamin & Baking Soda Kill Any Cancer?
    Ivermectin, Fenbendazole, Vit C and Sodium Bicarb. But don't worry your cancer is safe because the FDA would never allow it.
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  • MMR Vaccine Debate Heats Up as Media Claim ‘Vaccine Hesitancy’ to Blame for Recent Outbreaks
    As major news outlets linked reports of measles cases in the U.S. and U.K. to declining vaccine rates, experts told The Defender that case numbers in the U.S. have been extremely low for decades and the very minor variations in vaccination rates do not make a difference.

    Brenda Baletti, Ph.D.
    mmr vaccine media outbreaks feature
    Miss a day, miss a lot. Subscribe to The Defender's Top News of the Day. It's free.

    Measles outbreaks are in the news again.

    In the U.S., local health departments and media reported about 16 cases of measles between December 2023 and January. The outbreaks occurred in Philadelphia, New Jersey, Georgia and Washington.

    In the United Kingdom, the UK Health Security Agency reported 209 cases between January and November 2023 and about 319 cases between October 2023 and the present.

    Media blamed international travel and declining vaccination rates among children as “probably” behind the outbreaks.

    But Dr. Liz Mumper, a pediatrician, told The Defender it doesn’t make sense to assume the unvaccinated are to blame. She said cyclical outbreaks still occur even in populations with nearly 100% vaccination, such as college students.

    Dr. Paul Thomas, a retired pediatrician and author of “The Vaccine-Friendly Plan: Dr. Paul’s Safe and Effective Approach to Immunity and Health-from Pregnancy Through Your Child’s Teen Years Paperback,” told The Defender some cases of measles are reported every year. Despite the hype around the recent outbreaks, he said, “There have not been any significant measles outbreaks in the U.S. for decades.”

    The largest recent national spike in measles cases occurred in 2019 when 1,274 cases were reported, according to the Centers for Disease Control and Prevention (CDC). It was the worst year for measles in the U.S. since 1992.

    Since 2019, the number of cases reported has been significantly lower: In 2020, there were 13 cases, in 2021, 49 cases, in 2022 there were 121 cases and in 2023, there were 56 cases. The post-2019 numbers also tend to be lower than the numbers from 2000-2018, which averaged around 200 per year.


    Credit: Centers for Disease Control and Prevention
    Measles is a contagious childhood viral disease characterized by a cough, runny nose and fever, followed by a generalized rash.

    It was declared to be eliminated in the U.S. in 2000 — meaning there was no continuous transmission.

    Mortality from measles in the U.S. declined significantly during the 20th century — 98% from 1900 to 1963, before the measles vaccine was introduced — due to advances in living conditions, healthcare and nutrition, according to Physicians for Informed Consent.

    Since 2000, there have been only four measles deaths in the Americas — three in 2000 and one in 2022, according to a November 2023 CDC report.

    The overwhelming majority of the approximately 130,000 measles deaths annually occur in countries in the global south that have weak health infrastructures, according to the World Health Organization (WHO). Those deaths, along with measles hospitalizations in the global north, are associated with vitamin A deficiency.

    “Measles can be deadly if a child does not have access to safe water and medical care,” Mumper said. “In developed countries, fatalities from measles are very rare.”

    Effective treatments include vitamin A in high doses and attention to hydration status, Mumper said.

    “Many natural methods to help the body fight viruses, like extra vitamin D and vitamin C are effective but not widely recommended by mainstream medicine,” she added.

    Prior to the introduction of the vaccine in the U.S. in 1963, most people contracted measles and gained lifetime immunity, and the number of deaths had dropped to 0.9 per 100,000 for children under age 10.

    The vaccines significantly reduced the number of reported measles cases, with efficacy rates that can be upwards of 95%, Thomas said. However, he added immunity from the vaccines wanes over time.

    “From a mechanistic standpoint, the lifelong 100% natural immunity comes when measles is caught through respiratory spread. Giving a vaccine by injection may be an inherently poor substitute for Mother Nature,” Mumper said.

    Approximately 83% of children globally received one dose of the measles, mumps and rubella (MMR) vaccine by their first birthday in 2022.

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    Hotez, Offit blame the ‘anti-vaxers’ for measles outbreaks

    Although case numbers have declined in the U.S. since 2020, and the recently reported cases were either among adults or children who may be too young to have completed the MMR vaccine schedule, news reports about the outbreaks consistently link them to lower post-pandemic vaccination rates among kindergarteners.

    The CDC recommends two doses of the MMR vaccine, with the first dose at 12 to 15 months old and the second dose between ages 4 and 6.

    The agency reported that from the 2019-20 school year to the 2021-22 school year vaccination rates for state-required vaccines among kindergarten children declined from approximately 95% to approximately 93%, and the exemption rate increased to 3.0%.

    CDC data going back to 2011 show that rates typically vary from year-to-year, but consistently stay above 93%.

    Thomas said the drop has been minimal and “given the loss of immunity in both children and adults in the vaccinated, this minor reduction in MMR uptake by children is not going to make a difference [in infection rates].”

    Dr. Peter Hotez, a go-to “expert” for mainstream media on vaccines — and a vaccine developer and patent holder himself, who has repeatedly smeared vaccine safety advocates as “anti-science aggressors” — told ABC and CBS News that he thought the sporadic outbreaks were likely a result of lowered vaccination rates and that they were going to get worse.

    “We’re just seeing now, this is the tip of the iceberg,” Hotez said. “We’re going to be seeing this in communities across the United States in the coming weeks and months because of the spillover of the U.S. anti-vaccine movement of childhood immunizations.”

    According to ABC — quoting Hotez, Dr. Paul Offit and the Mayo Clinic’s Dr. Gregory Poland — this is due to vaccine “misinformation” linking vaccines and autism, combined with the politicization of the COVID-19 vaccines, which Hotez said caused “an acceleration of anti-vaccine sentiments.”

    Hotez has been making these arguments for years, writing a New York Times op-ed in 2020 claiming there is no link between vaccines and autism and blaming unvaccinated people for infectious disease outbreaks.

    Offit said given the vaccine’s efficacy, it was “unconscionable” for parents to forgo vaccination for their children.

    But there is a significant and growing body of evidence suggesting the MMR vaccine can cause autism in certain susceptible children. That includes evidence that U.S. Department of Justice lawyers suppressed testimony by their own expert witness making the link, and evidence from whistleblower William Thompson, Ph.D., that the CDC covered up its own data showing a link between vaccines and autism.

    In a Substack post from 2022, Dr. Peter McCullough evaluated a study on the “Association Between Vaccine Refusal and Vaccine-Preventable Diseases in the United States,” namely measles and pertussis.

    The study indicated that since measles was declared eradicated in 2000, there have been 18 published studies of 1,416 measles cases — 43.2% of the cases occurred in vaccinated people and no hospitalizations or deaths were reported.

    McCullough concluded:

    “Large fractions of ‘preventable disease outbreaks’ involving measles and pertussis occur because vaccines fail to provide adequate protection. Given the neuropsychiatric concerns over the MMR vaccine and the stochastic risk of allergic/immunologic reactions to any injection including components of (DTaP, Tdap) or MMR, the parental movement for vaccine choice is well justified.

    “For measles and pertussis, the vaccines convey imperfect protection and breakthrough infection (vaccine failure) should receive considerable ‘blame’ by public health researchers.”

    Mumper said the vaccine schedule has changed, lowering efficacy. “Vaccine efficacy was calculated to be ~94% when the first dose was given at 15 months,” she said.

    “Now babies are scheduled to get the first dose at 12 months (only 85% efficacy) and their second dose at kindergarten.”

    Mumper added, “People with different genotypes respond differently to MMR vaccines, so there is variable measles transmission depending on the individual’s immune response. Up to 10% of the population does not develop enough protective antibodies.”

    New outbreaks lead push for adults to get another MMR

    Derek Gatherer, Ph.D., a lecturer in biomedical and life sciences at Lancaster University who is funded by the U.K. government to study “vaccine hesitancy,” said the solution to the problem of measles outbreaks is more vaccination — for adults.

    Gatherer published a recent article in The Conversation blaming the vaccine-hesitant for the outbreaks. He argued that even adults who are already vaccinated should consider getting more MMR jabs.

    “Measles is the most infectious disease known to science — adults should consider getting another MMR vaccine,” he declared.

    Gatherer conceded that the measles risk to adults is extremely small, but said “adult MMR is still worthwhile as it goes beyond just protecting the person who receives the vaccination,” stopping asymptomatic infections from spreading.

    Thomas said it is not common to recommend booster shots to adults for illnesses they were vaccinated for as children. “However,” he added, “the pharmaceutical industry, backed by the CDC, has been looking at the adult population as an untapped resource to expand market share and penetration.”

    Reports of cases rising in the UK

    In the U.K., measles was considered eliminated in 2016, but it resurfaced in 2018.

    U.K. MMR vaccination rates average 85%, down from a peak of 88.6% in 2014, with some locations reporting rates as low as 74%.

    According to The Guardian, “Most experts agree that misinformation about the MMR jab is very unlikely to play a significant role in declining vaccination rates.

    “It is too easy to blame anti-vaccine sentiment for the measles outbreaks,” Helen Bedford, professor of children’s health at the University College London Great Ormond Street Institute of Child Health told the paper. “Although some mistrust of vaccines may play a small part, research shows that parental vaccine confidence remains high.”

    Experts there pointed to pandemic disruptions in vaccination, concerns among Muslim and Jewish communities about the use of porcine gelatin in the vaccine, and also the fact that because the disease is so rare, people are less concerned about possible risks.

    England’s National Health Service is launching an MMR vaccination campaign, the BBC reported, contacting 4 million parents via text, email or letter to inform them their child has not had one or two doses of the vaccine.




    🚨 MMR Vaccine Debate Heats Up as Media Claim ‘Vaccine Hesitancy’ to Blame for Recent Outbreaks
    “Many natural methods to help the body fight viruses, like extra vitamin D + vitamin C are effective but not widely recommended by mainstream medicine." — Dr. Liz Mumper
    https://childrenshealthdefense.org/defender/mmr-vaccine-media-measles-outbreaks
    MMR Vaccine Debate Heats Up as Media Claim ‘Vaccine Hesitancy’ to Blame for Recent Outbreaks As major news outlets linked reports of measles cases in the U.S. and U.K. to declining vaccine rates, experts told The Defender that case numbers in the U.S. have been extremely low for decades and the very minor variations in vaccination rates do not make a difference. Brenda Baletti, Ph.D. mmr vaccine media outbreaks feature Miss a day, miss a lot. Subscribe to The Defender's Top News of the Day. It's free. Measles outbreaks are in the news again. In the U.S., local health departments and media reported about 16 cases of measles between December 2023 and January. The outbreaks occurred in Philadelphia, New Jersey, Georgia and Washington. In the United Kingdom, the UK Health Security Agency reported 209 cases between January and November 2023 and about 319 cases between October 2023 and the present. Media blamed international travel and declining vaccination rates among children as “probably” behind the outbreaks. But Dr. Liz Mumper, a pediatrician, told The Defender it doesn’t make sense to assume the unvaccinated are to blame. She said cyclical outbreaks still occur even in populations with nearly 100% vaccination, such as college students. Dr. Paul Thomas, a retired pediatrician and author of “The Vaccine-Friendly Plan: Dr. Paul’s Safe and Effective Approach to Immunity and Health-from Pregnancy Through Your Child’s Teen Years Paperback,” told The Defender some cases of measles are reported every year. Despite the hype around the recent outbreaks, he said, “There have not been any significant measles outbreaks in the U.S. for decades.” The largest recent national spike in measles cases occurred in 2019 when 1,274 cases were reported, according to the Centers for Disease Control and Prevention (CDC). It was the worst year for measles in the U.S. since 1992. Since 2019, the number of cases reported has been significantly lower: In 2020, there were 13 cases, in 2021, 49 cases, in 2022 there were 121 cases and in 2023, there were 56 cases. The post-2019 numbers also tend to be lower than the numbers from 2000-2018, which averaged around 200 per year. Credit: Centers for Disease Control and Prevention Measles is a contagious childhood viral disease characterized by a cough, runny nose and fever, followed by a generalized rash. It was declared to be eliminated in the U.S. in 2000 — meaning there was no continuous transmission. Mortality from measles in the U.S. declined significantly during the 20th century — 98% from 1900 to 1963, before the measles vaccine was introduced — due to advances in living conditions, healthcare and nutrition, according to Physicians for Informed Consent. Since 2000, there have been only four measles deaths in the Americas — three in 2000 and one in 2022, according to a November 2023 CDC report. The overwhelming majority of the approximately 130,000 measles deaths annually occur in countries in the global south that have weak health infrastructures, according to the World Health Organization (WHO). Those deaths, along with measles hospitalizations in the global north, are associated with vitamin A deficiency. “Measles can be deadly if a child does not have access to safe water and medical care,” Mumper said. “In developed countries, fatalities from measles are very rare.” Effective treatments include vitamin A in high doses and attention to hydration status, Mumper said. “Many natural methods to help the body fight viruses, like extra vitamin D and vitamin C are effective but not widely recommended by mainstream medicine,” she added. Prior to the introduction of the vaccine in the U.S. in 1963, most people contracted measles and gained lifetime immunity, and the number of deaths had dropped to 0.9 per 100,000 for children under age 10. The vaccines significantly reduced the number of reported measles cases, with efficacy rates that can be upwards of 95%, Thomas said. However, he added immunity from the vaccines wanes over time. “From a mechanistic standpoint, the lifelong 100% natural immunity comes when measles is caught through respiratory spread. Giving a vaccine by injection may be an inherently poor substitute for Mother Nature,” Mumper said. Approximately 83% of children globally received one dose of the measles, mumps and rubella (MMR) vaccine by their first birthday in 2022. RFK Jr. and Brian Hooker Vax-Unvax RFK Jr. and Brian Hooker’s New Book: “Vax-Unvax” Order Now Hotez, Offit blame the ‘anti-vaxers’ for measles outbreaks Although case numbers have declined in the U.S. since 2020, and the recently reported cases were either among adults or children who may be too young to have completed the MMR vaccine schedule, news reports about the outbreaks consistently link them to lower post-pandemic vaccination rates among kindergarteners. The CDC recommends two doses of the MMR vaccine, with the first dose at 12 to 15 months old and the second dose between ages 4 and 6. The agency reported that from the 2019-20 school year to the 2021-22 school year vaccination rates for state-required vaccines among kindergarten children declined from approximately 95% to approximately 93%, and the exemption rate increased to 3.0%. CDC data going back to 2011 show that rates typically vary from year-to-year, but consistently stay above 93%. Thomas said the drop has been minimal and “given the loss of immunity in both children and adults in the vaccinated, this minor reduction in MMR uptake by children is not going to make a difference [in infection rates].” Dr. Peter Hotez, a go-to “expert” for mainstream media on vaccines — and a vaccine developer and patent holder himself, who has repeatedly smeared vaccine safety advocates as “anti-science aggressors” — told ABC and CBS News that he thought the sporadic outbreaks were likely a result of lowered vaccination rates and that they were going to get worse. “We’re just seeing now, this is the tip of the iceberg,” Hotez said. “We’re going to be seeing this in communities across the United States in the coming weeks and months because of the spillover of the U.S. anti-vaccine movement of childhood immunizations.” According to ABC — quoting Hotez, Dr. Paul Offit and the Mayo Clinic’s Dr. Gregory Poland — this is due to vaccine “misinformation” linking vaccines and autism, combined with the politicization of the COVID-19 vaccines, which Hotez said caused “an acceleration of anti-vaccine sentiments.” Hotez has been making these arguments for years, writing a New York Times op-ed in 2020 claiming there is no link between vaccines and autism and blaming unvaccinated people for infectious disease outbreaks. Offit said given the vaccine’s efficacy, it was “unconscionable” for parents to forgo vaccination for their children. But there is a significant and growing body of evidence suggesting the MMR vaccine can cause autism in certain susceptible children. That includes evidence that U.S. Department of Justice lawyers suppressed testimony by their own expert witness making the link, and evidence from whistleblower William Thompson, Ph.D., that the CDC covered up its own data showing a link between vaccines and autism. In a Substack post from 2022, Dr. Peter McCullough evaluated a study on the “Association Between Vaccine Refusal and Vaccine-Preventable Diseases in the United States,” namely measles and pertussis. The study indicated that since measles was declared eradicated in 2000, there have been 18 published studies of 1,416 measles cases — 43.2% of the cases occurred in vaccinated people and no hospitalizations or deaths were reported. McCullough concluded: “Large fractions of ‘preventable disease outbreaks’ involving measles and pertussis occur because vaccines fail to provide adequate protection. Given the neuropsychiatric concerns over the MMR vaccine and the stochastic risk of allergic/immunologic reactions to any injection including components of (DTaP, Tdap) or MMR, the parental movement for vaccine choice is well justified. “For measles and pertussis, the vaccines convey imperfect protection and breakthrough infection (vaccine failure) should receive considerable ‘blame’ by public health researchers.” Mumper said the vaccine schedule has changed, lowering efficacy. “Vaccine efficacy was calculated to be ~94% when the first dose was given at 15 months,” she said. “Now babies are scheduled to get the first dose at 12 months (only 85% efficacy) and their second dose at kindergarten.” Mumper added, “People with different genotypes respond differently to MMR vaccines, so there is variable measles transmission depending on the individual’s immune response. Up to 10% of the population does not develop enough protective antibodies.” New outbreaks lead push for adults to get another MMR Derek Gatherer, Ph.D., a lecturer in biomedical and life sciences at Lancaster University who is funded by the U.K. government to study “vaccine hesitancy,” said the solution to the problem of measles outbreaks is more vaccination — for adults. Gatherer published a recent article in The Conversation blaming the vaccine-hesitant for the outbreaks. He argued that even adults who are already vaccinated should consider getting more MMR jabs. “Measles is the most infectious disease known to science — adults should consider getting another MMR vaccine,” he declared. Gatherer conceded that the measles risk to adults is extremely small, but said “adult MMR is still worthwhile as it goes beyond just protecting the person who receives the vaccination,” stopping asymptomatic infections from spreading. Thomas said it is not common to recommend booster shots to adults for illnesses they were vaccinated for as children. “However,” he added, “the pharmaceutical industry, backed by the CDC, has been looking at the adult population as an untapped resource to expand market share and penetration.” Reports of cases rising in the UK In the U.K., measles was considered eliminated in 2016, but it resurfaced in 2018. U.K. MMR vaccination rates average 85%, down from a peak of 88.6% in 2014, with some locations reporting rates as low as 74%. According to The Guardian, “Most experts agree that misinformation about the MMR jab is very unlikely to play a significant role in declining vaccination rates. “It is too easy to blame anti-vaccine sentiment for the measles outbreaks,” Helen Bedford, professor of children’s health at the University College London Great Ormond Street Institute of Child Health told the paper. “Although some mistrust of vaccines may play a small part, research shows that parental vaccine confidence remains high.” Experts there pointed to pandemic disruptions in vaccination, concerns among Muslim and Jewish communities about the use of porcine gelatin in the vaccine, and also the fact that because the disease is so rare, people are less concerned about possible risks. England’s National Health Service is launching an MMR vaccination campaign, the BBC reported, contacting 4 million parents via text, email or letter to inform them their child has not had one or two doses of the vaccine. 🚨 MMR Vaccine Debate Heats Up as Media Claim ‘Vaccine Hesitancy’ to Blame for Recent Outbreaks “Many natural methods to help the body fight viruses, like extra vitamin D + vitamin C are effective but not widely recommended by mainstream medicine." — Dr. Liz Mumper https://childrenshealthdefense.org/defender/mmr-vaccine-media-measles-outbreaks
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    MMR Vaccine Debate Heats Up as Media Claim ‘Vaccine Hesitancy’ to Blame for Recent Outbreaks
    As major news outlets linked reports of measles cases in the U.S. and U.K. to declining vaccine rates, experts told The Defender that case numbers in the U.S. have been extremely low for decades and the very minor variations in vaccination rates do not make a difference.
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    EU Votes on Resolution To List “Hate Speech” as a Crime
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    🤡 https://www.who.int/europe/news/item/16-01-2024-covid-19-vaccinations-have-saved-more-than-1.4-million-lives-in-the-who-european-region--a-new-study-finds
    Absent an objective definition, it’s easy to imagine the last one functioning as a blank check to cover whatever anyone might be offended by. EU Votes on Resolution To List “Hate Speech” as a Crime https://ift.tt/2B1UH0N - FOLLOW: @reclaimthenet 🤡 https://www.who.int/europe/news/item/16-01-2024-covid-19-vaccinations-have-saved-more-than-1.4-million-lives-in-the-who-european-region--a-new-study-finds
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