• COVID Vaccine Gene Could Integrate Into Human Cancer Cells: Researcher
    What Mr. McKernan and his team have found contradicts the latest arguments from fact-checkers.

    COVID Vaccine Gene Could Integrate Into Human Cancer Cells: Researcher
    (CROCOTHERY/Shutterstock)
    Following his discovery of DNA contamination in COVID-19 mRNA vaccines, genomic researcher Kevin McKernan has recently found that the DNA in these vaccines can potentially integrate into human DNA.

    The COVID-19 vaccine spike sequence was detected in two types of chromosomes in cancer cell lines following exposure to the COVID-19 mRNA vaccine. Mr. McKernan’s findings, which he presents on his Substack blog, haven’t been peer-reviewed.
    These are expected to be “rare events,” but they can happen, Mr. McKernan told The Epoch Times.
    DNA Integration

    Since the introduction of the COVID-19 mRNA vaccines, some members of the public have been concerned that the vaccines may modify human DNA by combining their sequences with the human genome.

    Story continues below advertisement

    “Fact-checkers” refuted this, saying mRNA cannot be changed into DNA. Yet Mr. McKernan’s earlier work shows that DNA in the vaccine vials may be capable of changing human DNA.
    Ulrike Kämmerer, a professor of human biology at the University Hospital of Würzburg in Germany, conducted earlier stages of this research.

    Exposing breast and ovarian human cancer cells to Pfizer and Moderna mRNA vaccines, Ms. Kämmerer found that about half of the cells expressed the COVID-19 spike protein on their cellular surface, indicating that they had absorbed the vaccines.

    Mr. McKernan then performed gene sequencing and found that these cells and their descendant cells contained vaccine DNA.

    Story continues below advertisement

    After this, he tested to see whether any vaccine DNA combined with the cancer cell DNA, a process known as DNA integration. Integration is more of a concern in healthy cells than cancer cells because it disrupts cells’ genetic stability and integrity, increasing cancer risk.

    However, because cancer cells already have unstable DNA, the effects of DNA integration are less clear.

    Currently, in biomedical research, most experiments are carried out in cancer cell lines, as they are easier to obtain, experiment on, and maintain in the laboratory.

    Mr. McKernan detected vaccine DNA sequences on two chromosomes in the cancer cell lines: chromosome 9 and chromosome 12. The sequencing machine detected both instances of integration twice. It is important to get two readings of the DNA integration to ensure that the integration is not a result of misreading or random error, he said.

    Story continues below advertisement

    “The integration of ‘vaccine’ genetic information into the genome of cells was not such a surprise for me—more the confirmation of what we had to expect, unfortunately,” he told The Epoch Times.

    Mr. McKernan said it is unsurprising that integration was detected on only two chromosomes with two readings of each integration. This is because integration is rare, and the genes must be sequenced many times to get more sensitive results.

    The current findings are still preliminary, he said. More tests are also needed to determine whether DNA integration could be passed on to descendant cancer cells and whether this may affect cancer patients.

    Also, since the test was conducted in cancer cells and not in healthy human cells, it does not suggest the same integration would occur in healthy human cells.

    Story continues below advertisement

    However, Hiroshi Arakawa, a researcher at the Institute of Molecular Oncology who has a doctorate in molecular biology and immunology, wrote in his blog that “what happens in cultured cells can also occur in normal cells” after examining Mr. McKernan’s data.
    His review of Mr. McKernan’s data also found signs of DNA integration at chromosomes 9 and 12.

    “A wide variety of abnormalities can occur [in normal cells] depending on the site of genome integration,” Mr. Arakawa said.
    Not Random Events

    The two integration events into chromosome 9 occurred at the same place, as did the integration events into chromosome 12.

    Mr. McKernan said the odds of this occurring are one in 3 billion, highlighting that where the DNA integrates may not be random.

    Story continues below advertisement

    “There’s likely hotspots for this,” he told The Epoch Times, highlighting that in the human genome, jumping genes—short segments of DNA sequences—tend to “jump” into highly activated areas of DNA.

    Highly activated DNA tends to play important roles in the human body.

    The DNA integration into chromosome 12 occurred within the FAIM2 gene. Once activated, this gene creates a protein involved in programmed cell death. Since cancer cells evade cell death, the integration at chromosome 12 may be a survival-driven change.
    Vaccine DNA Is Active in the Cells

    Mr. McKernan said he believes that vaccine DNA is highly active in cancer cells. His sequencing machine detected the DNA of cancer cells 30 times but detected spike DNA 3,000 times.

    Not only did he detect much higher levels of vaccine DNA, but he also detected new variants in certain segments of the vaccine DNA.

    Story continues below advertisement

    These new DNA variations were not observed in unvaccinated cancer cells nor in the vaccine not exposed to the cancer cells.

    Mr. McKernan said he believes that these new gene variants likely occurred because the cancer cell made copies of the vaccine DNA and created small errors.

    What he and his team have found contradicts the latest arguments from fact-checkers claiming that the DNA from the mRNA vaccines cannot get into the cell, nor can it be active, he said.
    DNA Contamination From mRNA Vaccine Manufacturing

    DNA is present in the COVID-19 mRNA vaccines because of the manufacturing process.
    This has been verified by the U.S. Food and Drug Administration (FDA), Health Canada, and the European Medicines Agency.
    The mRNA vaccines are made from DNA; some of this DNA persists in the final product because of insufficient clearance.
    Initially, Pfizer reported that it would use a PCR machine to produce the DNA for its mRNA vaccine. The PCR machine first makes many copies of DNA, which is then sequenced into RNA.

    However, because this process wouldn’t be fast enough to meet demands, the vaccine manufacturers switched to using bacteria to mass-produce DNA as the template for the mRNA vaccine.

    In this process, vaccine manufacturers introduce bacterial DNA containing the vaccine spike sequences. The bacteria make many copies of this spike DNA as they divide. This spike DNA is then harvested and transcribed into mRNA in a machine. The mRNA is then packaged into lipid nanoparticles for use in vaccination.

    However, some bacterial DNA containing spike protein and other sequences could be packaged into lipid nanoparticles during the process, which would then be transported into cells during vaccination. Mr. McKernan’s earlier works have demonstrated this.
    Works by molecular virologist David Speicher have shown that the amount of DNA in the mRNA vaccine vials is higher than the FDA’s allowable threshold of 10 nanograms per vaccine dose.
    Mr. McKernan highlighted that compared with previous vaccines, mainly composed of naked DNA that had difficulty entering the cells, the DNA carried in the mRNA vaccines presents greater health risks, as it is packed into lipid nanoparticles and delivered straight into the cells.

    https://www.theepochtimes.com/health/covid-vaccine-gene-could-integrate-into-human-cancer-cells-researcher-5604184
    COVID Vaccine Gene Could Integrate Into Human Cancer Cells: Researcher What Mr. McKernan and his team have found contradicts the latest arguments from fact-checkers. COVID Vaccine Gene Could Integrate Into Human Cancer Cells: Researcher (CROCOTHERY/Shutterstock) Following his discovery of DNA contamination in COVID-19 mRNA vaccines, genomic researcher Kevin McKernan has recently found that the DNA in these vaccines can potentially integrate into human DNA. The COVID-19 vaccine spike sequence was detected in two types of chromosomes in cancer cell lines following exposure to the COVID-19 mRNA vaccine. Mr. McKernan’s findings, which he presents on his Substack blog, haven’t been peer-reviewed. These are expected to be “rare events,” but they can happen, Mr. McKernan told The Epoch Times. DNA Integration Since the introduction of the COVID-19 mRNA vaccines, some members of the public have been concerned that the vaccines may modify human DNA by combining their sequences with the human genome. Story continues below advertisement “Fact-checkers” refuted this, saying mRNA cannot be changed into DNA. Yet Mr. McKernan’s earlier work shows that DNA in the vaccine vials may be capable of changing human DNA. Ulrike Kämmerer, a professor of human biology at the University Hospital of Würzburg in Germany, conducted earlier stages of this research. Exposing breast and ovarian human cancer cells to Pfizer and Moderna mRNA vaccines, Ms. Kämmerer found that about half of the cells expressed the COVID-19 spike protein on their cellular surface, indicating that they had absorbed the vaccines. Mr. McKernan then performed gene sequencing and found that these cells and their descendant cells contained vaccine DNA. Story continues below advertisement After this, he tested to see whether any vaccine DNA combined with the cancer cell DNA, a process known as DNA integration. Integration is more of a concern in healthy cells than cancer cells because it disrupts cells’ genetic stability and integrity, increasing cancer risk. However, because cancer cells already have unstable DNA, the effects of DNA integration are less clear. Currently, in biomedical research, most experiments are carried out in cancer cell lines, as they are easier to obtain, experiment on, and maintain in the laboratory. Mr. McKernan detected vaccine DNA sequences on two chromosomes in the cancer cell lines: chromosome 9 and chromosome 12. The sequencing machine detected both instances of integration twice. It is important to get two readings of the DNA integration to ensure that the integration is not a result of misreading or random error, he said. Story continues below advertisement “The integration of ‘vaccine’ genetic information into the genome of cells was not such a surprise for me—more the confirmation of what we had to expect, unfortunately,” he told The Epoch Times. Mr. McKernan said it is unsurprising that integration was detected on only two chromosomes with two readings of each integration. This is because integration is rare, and the genes must be sequenced many times to get more sensitive results. The current findings are still preliminary, he said. More tests are also needed to determine whether DNA integration could be passed on to descendant cancer cells and whether this may affect cancer patients. Also, since the test was conducted in cancer cells and not in healthy human cells, it does not suggest the same integration would occur in healthy human cells. Story continues below advertisement However, Hiroshi Arakawa, a researcher at the Institute of Molecular Oncology who has a doctorate in molecular biology and immunology, wrote in his blog that “what happens in cultured cells can also occur in normal cells” after examining Mr. McKernan’s data. His review of Mr. McKernan’s data also found signs of DNA integration at chromosomes 9 and 12. “A wide variety of abnormalities can occur [in normal cells] depending on the site of genome integration,” Mr. Arakawa said. Not Random Events The two integration events into chromosome 9 occurred at the same place, as did the integration events into chromosome 12. Mr. McKernan said the odds of this occurring are one in 3 billion, highlighting that where the DNA integrates may not be random. Story continues below advertisement “There’s likely hotspots for this,” he told The Epoch Times, highlighting that in the human genome, jumping genes—short segments of DNA sequences—tend to “jump” into highly activated areas of DNA. Highly activated DNA tends to play important roles in the human body. The DNA integration into chromosome 12 occurred within the FAIM2 gene. Once activated, this gene creates a protein involved in programmed cell death. Since cancer cells evade cell death, the integration at chromosome 12 may be a survival-driven change. Vaccine DNA Is Active in the Cells Mr. McKernan said he believes that vaccine DNA is highly active in cancer cells. His sequencing machine detected the DNA of cancer cells 30 times but detected spike DNA 3,000 times. Not only did he detect much higher levels of vaccine DNA, but he also detected new variants in certain segments of the vaccine DNA. Story continues below advertisement These new DNA variations were not observed in unvaccinated cancer cells nor in the vaccine not exposed to the cancer cells. Mr. McKernan said he believes that these new gene variants likely occurred because the cancer cell made copies of the vaccine DNA and created small errors. What he and his team have found contradicts the latest arguments from fact-checkers claiming that the DNA from the mRNA vaccines cannot get into the cell, nor can it be active, he said. DNA Contamination From mRNA Vaccine Manufacturing DNA is present in the COVID-19 mRNA vaccines because of the manufacturing process. This has been verified by the U.S. Food and Drug Administration (FDA), Health Canada, and the European Medicines Agency. The mRNA vaccines are made from DNA; some of this DNA persists in the final product because of insufficient clearance. Initially, Pfizer reported that it would use a PCR machine to produce the DNA for its mRNA vaccine. The PCR machine first makes many copies of DNA, which is then sequenced into RNA. However, because this process wouldn’t be fast enough to meet demands, the vaccine manufacturers switched to using bacteria to mass-produce DNA as the template for the mRNA vaccine. In this process, vaccine manufacturers introduce bacterial DNA containing the vaccine spike sequences. The bacteria make many copies of this spike DNA as they divide. This spike DNA is then harvested and transcribed into mRNA in a machine. The mRNA is then packaged into lipid nanoparticles for use in vaccination. However, some bacterial DNA containing spike protein and other sequences could be packaged into lipid nanoparticles during the process, which would then be transported into cells during vaccination. Mr. McKernan’s earlier works have demonstrated this. Works by molecular virologist David Speicher have shown that the amount of DNA in the mRNA vaccine vials is higher than the FDA’s allowable threshold of 10 nanograms per vaccine dose. Mr. McKernan highlighted that compared with previous vaccines, mainly composed of naked DNA that had difficulty entering the cells, the DNA carried in the mRNA vaccines presents greater health risks, as it is packed into lipid nanoparticles and delivered straight into the cells. https://www.theepochtimes.com/health/covid-vaccine-gene-could-integrate-into-human-cancer-cells-researcher-5604184
    WWW.THEEPOCHTIMES.COM
    COVID Vaccine Gene Could Integrate Into Human Cancer Cells: Researcher
    What Mr. McKernan and his team have found contradicts the latest arguments from fact-checkers.
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  • Subject: Fw: Dr Mike Yeadon: Introductory statement about serious crimes per Mark Sexton communication
    To: Ben.Bates@met.police.uk <Ben.Bates@met.police.uk>
    Cc: Mark Sexton

    Dear Ben Bates,

    I have been asked by former policeman, Mark Sexton (copied) to introduce myself to you & to indicate the fields in which I have unequivocal evidence of criminal activity.

    Let me begin my outlining my credentials to have realised that the areas I will outline were incorrect in the first place.

    My name is Dr Mike Yeadon. I am the most senior, former “big pharma” & biotech research executive speaking out about several serious crimes in relation to what I call the “Covid era”.

    My original training was in Biochemistry & Toxicology, in which I was awarded the strongest first class joint honours degree that the School of Biomedical Sciences had ever awarded at the time (1985, University of Surrey).

    Part of my undergraduate training involved research placements at the Chemical Defence Establishment, Porton Down, Wiltshire, where I was a small cog in the long term development of injected antidotes for nerve gas poisoning to protect British troops. I also worked at the then Central Laboratory of the Forensic Sciences Service, Aldermaston, Berkshire, adjacent to the Atomic Weapons Research Establishment. While with the Forensic Science Service, I received training on several precision analytical methods including mass spectrometry, then a highly technically complex method.
    As far as I recall, I had security clearance for both establishments. Porton Down, then as now, is a top security facility with an international reputation.

    My PhD, in the field of Pharmacology was “On the effect of opiates on respiratory function” (1988) and this was sponsored by the MOD.

    After securing my PhD, which gave me a sound training in several additional subdisciplines of biology, chemistry & drug metabolism, I joined the pharmaceutical industry.

    I spent 24years with “big pharma”, starting at Wellcome Research Laboratories, where I briefly worked alongside a Dr Patrick Vallance (who became Chief Scientific Advisor to the British Government).

    For the longest period, I was in charge of Pfizer’s global research in the field of Allergic & Respiratory Disease Therapeutics. I left Pfizer in 2011, having reached the level of Vice President, because the company had decided to exit their large R&D base in Kent. The parting was cordial. Before leaving, I sought to find new homes for the portfolio of exploratory medicines I had helped create & was gratified that Mylan U.K. Ltd, the world’s second largest generics company, acquired much of my former portfolio soon after I had left.

    I later founded & lead as CEO a highly successful biotechnology company, Ziarco Pharma Ltd. Pfizer and four other venture capital firms were investors in my company, which was acquired by Novartis Pharmaceuticals, in 2017.

    My accomplishments are considered by some to have been unusual. So much so that a former Pfizer board member & previously worldwide head of R&D, Dr John LaMattina, wrote up my last venture in Forbes, a leading business magazine (February 2017).
    https://www.forbes.com/sites/johnlamattina/2017/03/15/turning-pfizer-discards-into-novartis-gold-the-story-of-ziarco/

    In summary, I have had a very strong training in multiple disciplines and over 30 years leadership experience in the field of inventing and testing new medicines for respiratory illnesses. I have an excellent analytical background and I can claim to be at least the equal of anyone advising the government in science.

    I have no history of “conspiracy theory” or political campaigns or protests. I don’t believe I made a single public comment on anything prior to 2020.

    My accomplishments in applied biomedical sciences qualify me to be taken seriously.
    I ask that the evidence I marshall is evaluated thoroughly. I am confident in my assessments, which have been tested by dozens of others, internationally well known scientists and doctors.

    👉 https://t.me/DrMikeYeadon
    Subject: Fw: Dr Mike Yeadon: Introductory statement about serious crimes per Mark Sexton communication To: Ben.Bates@met.police.uk <Ben.Bates@met.police.uk> Cc: Mark Sexton Dear Ben Bates, I have been asked by former policeman, Mark Sexton (copied) to introduce myself to you & to indicate the fields in which I have unequivocal evidence of criminal activity. Let me begin my outlining my credentials to have realised that the areas I will outline were incorrect in the first place. My name is Dr Mike Yeadon. I am the most senior, former “big pharma” & biotech research executive speaking out about several serious crimes in relation to what I call the “Covid era”. My original training was in Biochemistry & Toxicology, in which I was awarded the strongest first class joint honours degree that the School of Biomedical Sciences had ever awarded at the time (1985, University of Surrey). Part of my undergraduate training involved research placements at the Chemical Defence Establishment, Porton Down, Wiltshire, where I was a small cog in the long term development of injected antidotes for nerve gas poisoning to protect British troops. I also worked at the then Central Laboratory of the Forensic Sciences Service, Aldermaston, Berkshire, adjacent to the Atomic Weapons Research Establishment. While with the Forensic Science Service, I received training on several precision analytical methods including mass spectrometry, then a highly technically complex method. As far as I recall, I had security clearance for both establishments. Porton Down, then as now, is a top security facility with an international reputation. My PhD, in the field of Pharmacology was “On the effect of opiates on respiratory function” (1988) and this was sponsored by the MOD. After securing my PhD, which gave me a sound training in several additional subdisciplines of biology, chemistry & drug metabolism, I joined the pharmaceutical industry. I spent 24years with “big pharma”, starting at Wellcome Research Laboratories, where I briefly worked alongside a Dr Patrick Vallance (who became Chief Scientific Advisor to the British Government). For the longest period, I was in charge of Pfizer’s global research in the field of Allergic & Respiratory Disease Therapeutics. I left Pfizer in 2011, having reached the level of Vice President, because the company had decided to exit their large R&D base in Kent. The parting was cordial. Before leaving, I sought to find new homes for the portfolio of exploratory medicines I had helped create & was gratified that Mylan U.K. Ltd, the world’s second largest generics company, acquired much of my former portfolio soon after I had left. I later founded & lead as CEO a highly successful biotechnology company, Ziarco Pharma Ltd. Pfizer and four other venture capital firms were investors in my company, which was acquired by Novartis Pharmaceuticals, in 2017. My accomplishments are considered by some to have been unusual. So much so that a former Pfizer board member & previously worldwide head of R&D, Dr John LaMattina, wrote up my last venture in Forbes, a leading business magazine (February 2017). https://www.forbes.com/sites/johnlamattina/2017/03/15/turning-pfizer-discards-into-novartis-gold-the-story-of-ziarco/ In summary, I have had a very strong training in multiple disciplines and over 30 years leadership experience in the field of inventing and testing new medicines for respiratory illnesses. I have an excellent analytical background and I can claim to be at least the equal of anyone advising the government in science. I have no history of “conspiracy theory” or political campaigns or protests. I don’t believe I made a single public comment on anything prior to 2020. My accomplishments in applied biomedical sciences qualify me to be taken seriously. I ask that the evidence I marshall is evaluated thoroughly. I am confident in my assessments, which have been tested by dozens of others, internationally well known scientists and doctors. 👉 https://t.me/DrMikeYeadon
    WWW.FORBES.COM
    Turning Pfizer Discards Into Novartis Gold: The Story Of Ziarco
    Mike was told in the fall of 2010 that Pfizer was closing the Allergy & Respiratory diseases programs and his own role as the CSO of this group was being eliminated. Rather than seek employment elsewhere, Mike had others ideas.
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  • Carmen Leitch - A Tropical Fruit With a Antimicrobial Effects:

    https://www.labroots.com/trending/microbiology/26800/tropical-fruit-antimicrobial-effects

    #BlighiaSapida #Okpu #TropicalFruit #Antimicrobial #AntibioticResistance #Antibiotic #Disease #Pathogenicity #Medicine #PlantBiology #Microbiology #Biology
    Carmen Leitch - A Tropical Fruit With a Antimicrobial Effects: https://www.labroots.com/trending/microbiology/26800/tropical-fruit-antimicrobial-effects #BlighiaSapida #Okpu #TropicalFruit #Antimicrobial #AntibioticResistance #Antibiotic #Disease #Pathogenicity #Medicine #PlantBiology #Microbiology #Biology
    WWW.LABROOTS.COM
    A Tropical Fruit With a Antimicrobial Effects | Microbiology
    Tens of thousands of people die from antibiotic resistant infections very year, and these pathogenic microbes present a growing threat to public health. | Microbiology
    0 Commentarii 0 Distribuiri 599 Views
  • RT - Scientists discover Chernobyl ‘super worms’:

    https://www.rt.com/news/593982-chernobyl-worms-radiation-study/

    #OscheiusTipulae #Nematode #Extremophile #ChernobylExclusionZone #Chernobyl #Radiation #DNADamage #Genetics #Biology
    RT - Scientists discover Chernobyl ‘super worms’: https://www.rt.com/news/593982-chernobyl-worms-radiation-study/ #OscheiusTipulae #Nematode #Extremophile #ChernobylExclusionZone #Chernobyl #Radiation #DNADamage #Genetics #Biology
    WWW.RT.COM
    Scientists discover Chernobyl ‘super worms’
    Nematodes from the vicinity of the stricken nuclear power plant showed no signs of radiation damage to their DNA, according to a new study
    0 Commentarii 0 Distribuiri 464 Views
  • Xinhua - New plant species discovered in SW China:

    http://en.people.cn/n3/2024/0220/c90000-20134899.html

    #LeptomischusBracteosus #Leptomischus #Rubiaceae #YunnanProvince #Botany #PlantBiology #Biology
    Xinhua - New plant species discovered in SW China: http://en.people.cn/n3/2024/0220/c90000-20134899.html #LeptomischusBracteosus #Leptomischus #Rubiaceae #YunnanProvince #Botany #PlantBiology #Biology
    New plant species discovered in SW China - People's Daily Online
    KUNMING, Feb. 19 (Xinhua) -- Chinese researchers have found a new plant species of the Rubiaceae fam
    0 Commentarii 0 Distribuiri 764 Views
  • America's COVID Response Was Based on Lies
    Almost all of America's leaders have gradually pulled back their COVID mandates, requirements, and closures—even in states like California, which had imposed the most stringent and longest-lasting restrictions on the public. At the same time, the media has been gradually acknowledging the ongoing release of studies that totally refute the purported reasons behind those restrictions. This overt reversal is falsely portrayed as "learned" or "new evidence." Little acknowledgement of error is to be found. We have seen no public apology for promulgating false information, or for the vilification and delegitimization of policy experts and medical scientists like myself who spoke out correctly about data, standard knowledge about viral infections and pandemics, and fundamental biology.

    The historical record is critical. We have seen a macabre Orwellian attempt to rewrite history and to blame the failure of widespread lockdowns on the lockdowns' critics, alongside absurd denials of officials' own incessant demands for them. In the Trump administration, Dr. Deborah Birx was formally in charge of the medical side of the White House's coronavirus task force during the pandemic's first year. In that capacity, she authored all written federal policy recommendations to governors and states and personally advised each state's public health officials during official visits, often with Vice President Mike Pence, who oversaw the entire task force. Upon the inauguration of President Joe Biden, Dr. Anthony Fauci became chief medical advisor and ran the Biden pandemic response.

    We must acknowledge the abject failure of the Birx-Fauci policies. They were enacted, but they failed to stop the dying, failed to stop the infection from spreading, and inflicted massive damage and destruction particularly on lower-income families and on America's children.

    More than 1 million American deaths have been attributed to that virus. Even after draconian measures, including school closures, stoppage of non-COVID medical care, business shutdowns, personal restrictions, and then the continuation of many restrictions and mandates in the presence of a vaccine, there was an undeniable failure—over two presidential administrations—to stop cases from rapidly escalating.

    Numerous experts—including John Ioannidis, David Katz, and myself—called for targeted protection, a safer alternative to widespread lockdowns, in national media beginning in March of 2020. That proposal was rejected. History's biggest public health policy failure came at the hands of those who recommended the lockdowns and those who implemented them, not those who advised otherwise.

    White House COVID task force
    WASHINGTON, DC - APRIL 09: White House coronavirus response coordinator Deborah Birx speaks as (L-R) National Institute of Allergy and Infectious Diseases Director Anthony Fauci, U.S. Vice President Mike Pence and Labor Secretary Eugene Scalia... Alex Wong/Getty Images
    Your daily briefing of everything you need to know

    The tragic failure of reckless, unprecedented lockdowns that were contrary to established pandemic science, and the added massive harms of those policies on children, the elderly, and lower-income families, are indisputable and well-documented in numerous studies. This was the biggest, the most tragic, and the most unethical breakdown of public health leadership in modern history.

    In a democracy, indeed in any ethical and free society, the truth is essential. The American people need to hear the truth—the facts, free from the political distortions, misrepresentations, and censorship. The first step is to clearly state the harsh truth in the starkest possible terms. Lies were told. Those lies harmed the public. Those lies were directly contrary to the evidence, to decades of knowledge on viral pandemics, and to long-established fundamental biology.

    Here are the 10 biggest falsehoods—known for years to be false, not recently learned or proven to be so—promoted by America's public health leaders, elected and unelected officials, and now-discredited academics:

    1. SARS-CoV-2 coronavirus has a far higher fatality rate than the flu by several orders of magnitude.

    2. Everyone is at significant risk to die from this virus.

    3. No one has any immunological protection, because this virus is completely new.

    4. Asymptomatic people are major drivers of the spread.

    5. Locking down—closing schools and businesses, confining people to their homes, stopping non-COVID medical care, and eliminating travel—will stop or eliminate the virus.

    6. Masks will protect everyone and stop the spread.

    7. The virus is known to be naturally occurring, and claiming it originated in a lab is a conspiracy theory.

    8. Teachers are at especially high risk.

    9. COVID vaccines stop the spread of the infection.

    10. Immune protection only comes from a vaccine.

    None of us are so naïve as to expect a direct apology from critics at my employer, Stanford University, or in government, academic public health, and the media. But to ensure that this never happens again, government leaders, power-driven officials, and influential academics and advisors often harboring conflicts of interest must be held accountable. Personally, I remain highly skeptical that any government investigation or commission can avoid politicization. Regardless of their intention, all such government-run inquiries will at least be perceived as politically motivated and their conclusions will be rejected outright by many. Those investigations must proceed, though, if only to seek the truth, to teach our children that truth matters, and to remember G.K. Chesterton's critical lesson that "Right is right, even if nobody does it. Wrong is wrong, even if everybody is wrong about it."

    Scott W. Atlas, MD is the Robert Wesson Senior Fellow in health policy at Stanford University's Hoover Institution, Co-Director of the Global Liberty Institute, Founding Fellow of Hillsdale's Academy for Science & Freedom, and author of A Plague Upon Our House: My Fight at the Trump White House to Stop COVID from Destroying America (Bombardier Press, 2022).

    The views expressed in this article are the writer's own.

    Read more
    How Fauci Fooled America
    Untangling America from the Never-Ending COVID 'State of Emergency'
    We Need a COVID Commission

    https://www.newsweek.com/america-covid-response-was-based-lies-opinion-1785177


    https://donshafi911.blogspot.com/2024/01/americas-covid-response-was-based-on.html
    America's COVID Response Was Based on Lies Almost all of America's leaders have gradually pulled back their COVID mandates, requirements, and closures—even in states like California, which had imposed the most stringent and longest-lasting restrictions on the public. At the same time, the media has been gradually acknowledging the ongoing release of studies that totally refute the purported reasons behind those restrictions. This overt reversal is falsely portrayed as "learned" or "new evidence." Little acknowledgement of error is to be found. We have seen no public apology for promulgating false information, or for the vilification and delegitimization of policy experts and medical scientists like myself who spoke out correctly about data, standard knowledge about viral infections and pandemics, and fundamental biology. The historical record is critical. We have seen a macabre Orwellian attempt to rewrite history and to blame the failure of widespread lockdowns on the lockdowns' critics, alongside absurd denials of officials' own incessant demands for them. In the Trump administration, Dr. Deborah Birx was formally in charge of the medical side of the White House's coronavirus task force during the pandemic's first year. In that capacity, she authored all written federal policy recommendations to governors and states and personally advised each state's public health officials during official visits, often with Vice President Mike Pence, who oversaw the entire task force. Upon the inauguration of President Joe Biden, Dr. Anthony Fauci became chief medical advisor and ran the Biden pandemic response. We must acknowledge the abject failure of the Birx-Fauci policies. They were enacted, but they failed to stop the dying, failed to stop the infection from spreading, and inflicted massive damage and destruction particularly on lower-income families and on America's children. More than 1 million American deaths have been attributed to that virus. Even after draconian measures, including school closures, stoppage of non-COVID medical care, business shutdowns, personal restrictions, and then the continuation of many restrictions and mandates in the presence of a vaccine, there was an undeniable failure—over two presidential administrations—to stop cases from rapidly escalating. Numerous experts—including John Ioannidis, David Katz, and myself—called for targeted protection, a safer alternative to widespread lockdowns, in national media beginning in March of 2020. That proposal was rejected. History's biggest public health policy failure came at the hands of those who recommended the lockdowns and those who implemented them, not those who advised otherwise. White House COVID task force WASHINGTON, DC - APRIL 09: White House coronavirus response coordinator Deborah Birx speaks as (L-R) National Institute of Allergy and Infectious Diseases Director Anthony Fauci, U.S. Vice President Mike Pence and Labor Secretary Eugene Scalia... Alex Wong/Getty Images Your daily briefing of everything you need to know The tragic failure of reckless, unprecedented lockdowns that were contrary to established pandemic science, and the added massive harms of those policies on children, the elderly, and lower-income families, are indisputable and well-documented in numerous studies. This was the biggest, the most tragic, and the most unethical breakdown of public health leadership in modern history. In a democracy, indeed in any ethical and free society, the truth is essential. The American people need to hear the truth—the facts, free from the political distortions, misrepresentations, and censorship. The first step is to clearly state the harsh truth in the starkest possible terms. Lies were told. Those lies harmed the public. Those lies were directly contrary to the evidence, to decades of knowledge on viral pandemics, and to long-established fundamental biology. Here are the 10 biggest falsehoods—known for years to be false, not recently learned or proven to be so—promoted by America's public health leaders, elected and unelected officials, and now-discredited academics: 1. SARS-CoV-2 coronavirus has a far higher fatality rate than the flu by several orders of magnitude. 2. Everyone is at significant risk to die from this virus. 3. No one has any immunological protection, because this virus is completely new. 4. Asymptomatic people are major drivers of the spread. 5. Locking down—closing schools and businesses, confining people to their homes, stopping non-COVID medical care, and eliminating travel—will stop or eliminate the virus. 6. Masks will protect everyone and stop the spread. 7. The virus is known to be naturally occurring, and claiming it originated in a lab is a conspiracy theory. 8. Teachers are at especially high risk. 9. COVID vaccines stop the spread of the infection. 10. Immune protection only comes from a vaccine. None of us are so naïve as to expect a direct apology from critics at my employer, Stanford University, or in government, academic public health, and the media. But to ensure that this never happens again, government leaders, power-driven officials, and influential academics and advisors often harboring conflicts of interest must be held accountable. Personally, I remain highly skeptical that any government investigation or commission can avoid politicization. Regardless of their intention, all such government-run inquiries will at least be perceived as politically motivated and their conclusions will be rejected outright by many. Those investigations must proceed, though, if only to seek the truth, to teach our children that truth matters, and to remember G.K. Chesterton's critical lesson that "Right is right, even if nobody does it. Wrong is wrong, even if everybody is wrong about it." Scott W. Atlas, MD is the Robert Wesson Senior Fellow in health policy at Stanford University's Hoover Institution, Co-Director of the Global Liberty Institute, Founding Fellow of Hillsdale's Academy for Science & Freedom, and author of A Plague Upon Our House: My Fight at the Trump White House to Stop COVID from Destroying America (Bombardier Press, 2022). The views expressed in this article are the writer's own. Read more How Fauci Fooled America Untangling America from the Never-Ending COVID 'State of Emergency' We Need a COVID Commission https://www.newsweek.com/america-covid-response-was-based-lies-opinion-1785177 https://donshafi911.blogspot.com/2024/01/americas-covid-response-was-based-on.html
    WWW.NEWSWEEK.COM
    America's COVID Response Was Based on Lies
    We have seen an Orwellian attempt to rewrite history and to blame the failure of widespread lockdowns on the lockdowns' critics.
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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.

    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
    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
    BLOG.MYGOTODOC.COM
    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.
    Angry
    1
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  • Xinhua - New gecko species discovered in China:

    http://en.people.cn/n3/2024/0125/c90000-20126757.html

    #GekkoKaiyai #Gekko #Kaiyai #Gecko #DabieMountains #AnhuiProvince #MitochondrialDNA #AnimalBiology #Biology
    Xinhua - New gecko species discovered in China: http://en.people.cn/n3/2024/0125/c90000-20126757.html #GekkoKaiyai #Gekko #Kaiyai #Gecko #DabieMountains #AnhuiProvince #MitochondrialDNA #AnimalBiology #Biology
    New gecko species discovered in China - People's Daily Online
    HEFEI, Jan. 25 (Xinhua) -- Chinese researchers have discovered a new species of gecko, which they ha
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  • Environmental Filaments UV Light Fluorescence Darkfield Microscopy
    Ana Maria Mihalcea, MD, PhD

    Image: Environmental filaments collected in regular light and under UV light

    I was visited by Dr. Justin Coy, a former Defense Department Contractor who has been following and validating my research. He brought me an environmental filament sample and a UV flashlight - 365nm. In this post, I am documenting the darkfield microscopy of these filaments and experiments with UV light. He was suspecting Luciferase to be present in the filaments and asked me to take a look. From my research there are metal nanoparticles in the filaments and they can cause fluorescence. Luciferase is used in in molecular biology that uses the luciferase enzyme and a substrate (such as luciferin) to study gene regulation at the level of transcription. I do not think that is the mechanism of the fluorescence of the polymers as other mechanisms using metals have been described in the literature and since Clifford Carnicoms analysis showed huge amounts of metals in the filaments that could be plausible.

    There have been developments of bright orange proteins fused with Luciferase in biological systems - this remains a question for further research and discovery.

    Novel NanoLuc substrates enable bright two-population bioluminescence imaging in animals

    We know that embedded Quantum Dot technology can make filaments emit different light and filaments found in the blood have been shown to have bifringence. We also know that UV light can be used as an energy source by nano sensors which can embed themselves in the self assembly polymers. Karl C has done some remarkable microscopy research showing this unusual light emission which I posted here: Extraordinary Microscopy Of Self Assembly Nanotechnology - A Request For Funding Help For Karl C


    Here are different images of the filaments analyzed by me observing how they change with normal light and then UV light:


    Image: Darkfield Microscopy: UV light off left, UV light on right


    Image above: normal light


    Image: UV light

    I then wanted to see if different aspects of the filament react differently to UV light, and they appear to. Some areas are more luminescent then others.


    Image: UV light on, both pictures.

    Below you can see a closer view of the filament under UV light, and there being very specific region that react to the UV light more:


    Off the orange appearing filament a white one came forth. Magnification of 2000x on the right shows a central cavitation of the filament


    Below you can see the orange environmental filament compared to a "self assembly nanotechnology hydrogel” filament from shedding in C19 unvaccinated blood with many visible Quantum Dot like structures seen embedded. The filament composition look the same except the colors differ.


    Here are different areas of the filament that have enormous glow under UV light, magnification 2000x:


    Here is an area of the filament with UV light:


    Same without UV light:


    Here are some research articles on fluorescent polymers:

    New 'smart' polymer glows brighter when stretched

    Spider fossils glow under UV light, a clue to their remarkable preservation

    Plastics shine bright to warn of invisible cracks Damage to polymers ruptures microcapsules, releasing fluorescent molecules

    I have been speaking about spider silk which is a polyamide protein and recently did microscopy on an environmental filament found:

    Spider Silk Polymer Sprayed Via Geoengineering Operations From California - Darkfield Microscopy Analysis

    This article explains that if metals are introduced the the nanofibers, florescence can be achieved:

    Optical fluorescent spider silk electrospun nanofibers with embedded cerium oxide nanoparticles

    The work demonstrates an electrospun nanocomposite of recombinant spider silk protein (rSSp) nanofibers with embedded cerium oxide (ceria) nanoparticles. RSSP (MaSp1) has been produced, extracted from goat milk, and fabricated into nanofibers using an electrospinning process. The resulting electrospun nanofibers have a mean diameter of ∼50 nm. Furthermore, ceria nanoparticles of mean diameter 10 nm were added in the spinning dope to be embedded within the generated nanofibers. These nanoparticles show certain optical activity due to optical trivaliant cerium ions, associated with formed oxygen vacancies. The formed nanocomposite shows promising mechanical properties such as the Young's modulus, elasticity (or elongation at break), and toughness. In addition, the electrospun mat becomes fluorescent with 520-nm emission upon exposure to UV light, due to excitation of the optically active ceria nanoparticles. Also, the formed nanocomposite shows a decay of its electric resistance over time upon exposure to cyclic loads at different humidity conditions. The synthesized nanocomposite can be utilized in different biomedical, textile, and sensing applications.

    We do know that these polymers are used for transhumanist surveillance and synthetic biology. Here they used spider silk as an inspiration. Note how they describe that these polymers can wrap around nerves, muscles and hearts and be the next generation tissue electronic interface:

    Polymer films inspired by spider silk connect biological tissues and electronic devices

    Linking biological tissues with electronic devices is challenging owing to the softness of tissues and their arbitrary shapes and sizes. An innovative water-responsive, supercontractile polymer film, inspired by spider silk, allows the construction of soft, stretchable and shape-adaptive tissue–electronic interfaces.

    We designed water-responsive supercontractile polymer films composed of poly(ethylene oxide) and poly(ethylene glycol)-α-cyclodextrin inclusion complex, which are initially dry, flexible and stable under ambient conditions, contract by more than 50% of their original length within seconds (about 30% per second) after wetting and become soft (about 100 kPa) and stretchable (around 600%) hydrogel thin films thereafter. This supercontraction is attributed to the aligned microporous hierarchical structures of the films, which also facilitate electronic integration. We used this film to fabricate shape-adaptive electrode arrays that simplify the implantation procedure through supercontraction and conformally wrap around nerves, muscles and hearts of different sizes when wetted for in vivo nerve stimulation and electrophysiological signal recording. This study demonstrates that this water-responsive material can play an important part in shaping the next-generation tissue–electronics interfaces as well as broadening the biomedical application of shape-adaptive materials.

    Here is video of the microscopy UV light on in both videos:

    UV light on playing with the focus:

    I took a blood sample and applied the UV light to see what happens to the micro robots. As in my experiments with the 450nm cold laser, the robots are quite happy and seem to absorb the extra energy - if you look at the robot its light emission intensifies, and that is consistent with the WBAN article I just posted that light is an energy source for the biosensors. Energy Harvesting From The Human Body By Wireless Body Area Network - A Cause For The Electrical Conductivity Loss in Human Blood?

    https://anamihalceamdphd.substack.com/p/environmental-filaments-uv-light?utm_medium=ios
    Environmental Filaments UV Light Fluorescence Darkfield Microscopy Ana Maria Mihalcea, MD, PhD Image: Environmental filaments collected in regular light and under UV light I was visited by Dr. Justin Coy, a former Defense Department Contractor who has been following and validating my research. He brought me an environmental filament sample and a UV flashlight - 365nm. In this post, I am documenting the darkfield microscopy of these filaments and experiments with UV light. He was suspecting Luciferase to be present in the filaments and asked me to take a look. From my research there are metal nanoparticles in the filaments and they can cause fluorescence. Luciferase is used in in molecular biology that uses the luciferase enzyme and a substrate (such as luciferin) to study gene regulation at the level of transcription. I do not think that is the mechanism of the fluorescence of the polymers as other mechanisms using metals have been described in the literature and since Clifford Carnicoms analysis showed huge amounts of metals in the filaments that could be plausible. There have been developments of bright orange proteins fused with Luciferase in biological systems - this remains a question for further research and discovery. Novel NanoLuc substrates enable bright two-population bioluminescence imaging in animals We know that embedded Quantum Dot technology can make filaments emit different light and filaments found in the blood have been shown to have bifringence. We also know that UV light can be used as an energy source by nano sensors which can embed themselves in the self assembly polymers. Karl C has done some remarkable microscopy research showing this unusual light emission which I posted here: Extraordinary Microscopy Of Self Assembly Nanotechnology - A Request For Funding Help For Karl C Here are different images of the filaments analyzed by me observing how they change with normal light and then UV light: Image: Darkfield Microscopy: UV light off left, UV light on right Image above: normal light Image: UV light I then wanted to see if different aspects of the filament react differently to UV light, and they appear to. Some areas are more luminescent then others. Image: UV light on, both pictures. Below you can see a closer view of the filament under UV light, and there being very specific region that react to the UV light more: Off the orange appearing filament a white one came forth. Magnification of 2000x on the right shows a central cavitation of the filament Below you can see the orange environmental filament compared to a "self assembly nanotechnology hydrogel” filament from shedding in C19 unvaccinated blood with many visible Quantum Dot like structures seen embedded. The filament composition look the same except the colors differ. Here are different areas of the filament that have enormous glow under UV light, magnification 2000x: Here is an area of the filament with UV light: Same without UV light: Here are some research articles on fluorescent polymers: New 'smart' polymer glows brighter when stretched Spider fossils glow under UV light, a clue to their remarkable preservation Plastics shine bright to warn of invisible cracks Damage to polymers ruptures microcapsules, releasing fluorescent molecules I have been speaking about spider silk which is a polyamide protein and recently did microscopy on an environmental filament found: Spider Silk Polymer Sprayed Via Geoengineering Operations From California - Darkfield Microscopy Analysis This article explains that if metals are introduced the the nanofibers, florescence can be achieved: Optical fluorescent spider silk electrospun nanofibers with embedded cerium oxide nanoparticles The work demonstrates an electrospun nanocomposite of recombinant spider silk protein (rSSp) nanofibers with embedded cerium oxide (ceria) nanoparticles. RSSP (MaSp1) has been produced, extracted from goat milk, and fabricated into nanofibers using an electrospinning process. The resulting electrospun nanofibers have a mean diameter of ∼50 nm. Furthermore, ceria nanoparticles of mean diameter 10 nm were added in the spinning dope to be embedded within the generated nanofibers. These nanoparticles show certain optical activity due to optical trivaliant cerium ions, associated with formed oxygen vacancies. The formed nanocomposite shows promising mechanical properties such as the Young's modulus, elasticity (or elongation at break), and toughness. In addition, the electrospun mat becomes fluorescent with 520-nm emission upon exposure to UV light, due to excitation of the optically active ceria nanoparticles. Also, the formed nanocomposite shows a decay of its electric resistance over time upon exposure to cyclic loads at different humidity conditions. The synthesized nanocomposite can be utilized in different biomedical, textile, and sensing applications. We do know that these polymers are used for transhumanist surveillance and synthetic biology. Here they used spider silk as an inspiration. Note how they describe that these polymers can wrap around nerves, muscles and hearts and be the next generation tissue electronic interface: Polymer films inspired by spider silk connect biological tissues and electronic devices Linking biological tissues with electronic devices is challenging owing to the softness of tissues and their arbitrary shapes and sizes. An innovative water-responsive, supercontractile polymer film, inspired by spider silk, allows the construction of soft, stretchable and shape-adaptive tissue–electronic interfaces. We designed water-responsive supercontractile polymer films composed of poly(ethylene oxide) and poly(ethylene glycol)-α-cyclodextrin inclusion complex, which are initially dry, flexible and stable under ambient conditions, contract by more than 50% of their original length within seconds (about 30% per second) after wetting and become soft (about 100 kPa) and stretchable (around 600%) hydrogel thin films thereafter. This supercontraction is attributed to the aligned microporous hierarchical structures of the films, which also facilitate electronic integration. We used this film to fabricate shape-adaptive electrode arrays that simplify the implantation procedure through supercontraction and conformally wrap around nerves, muscles and hearts of different sizes when wetted for in vivo nerve stimulation and electrophysiological signal recording. This study demonstrates that this water-responsive material can play an important part in shaping the next-generation tissue–electronics interfaces as well as broadening the biomedical application of shape-adaptive materials. Here is video of the microscopy UV light on in both videos: UV light on playing with the focus: I took a blood sample and applied the UV light to see what happens to the micro robots. As in my experiments with the 450nm cold laser, the robots are quite happy and seem to absorb the extra energy - if you look at the robot its light emission intensifies, and that is consistent with the WBAN article I just posted that light is an energy source for the biosensors. Energy Harvesting From The Human Body By Wireless Body Area Network - A Cause For The Electrical Conductivity Loss in Human Blood? https://anamihalceamdphd.substack.com/p/environmental-filaments-uv-light?utm_medium=ios
    ANAMIHALCEAMDPHD.SUBSTACK.COM
    Environmental Filaments UV Light Fluorescence Darkfield Microscopy
    Image: Environmental filaments collected in regular light and under UV light I was visited by Dr. Justin Coy, a former Defense Department Contractor who has been following and validating my research. He brought me an environmental filament sample and a UV flashlight - 365nm. In this post, I am documenting the darkfield microscopy of these filaments and experiments with UV light. He was suspecting Luciferase to be present in the filaments and asked me to take a look. From my research there are metal nanoparticles in the filaments and they can cause fluorescence. Luciferase is used in in molecular biology that uses the
    Like
    1
    0 Commentarii 1 Distribuiri 9179 Views
  • THE MEDICAL FREEDOM SYMPOSIUM CONFERENCE at THE CONSCIOUS LIFE EXPO
    Monday, Feb.12 - 2pm-4:30pm



    FORGING THE FUTURE TERRAIN


    OF WELLNESS



    Join us for a riveting, powerful, inspiring exchange of motivational insights that will stir you to support and create the changes we need for our Medical Freedom!


    Together We Stand!


    The Supreme Court has long recognized a person's constitutionally protected liberty interest in his or her own medical autonomy, especially when those interests are secured by state laws.



    Kelly Gallagher



    Kelly Gallagher is an Award-winning filmmaker, writer, poet, international health activist, and wellness/survival expert. Hailing from Network TV, this 5x cancer “thriver” powered by her 6th pacemaker, and a prosthetic heart valve has successfully navigated both conventional and alternative wellness protocols for almost 40 years.


    Del Bigtree



    Del Bigtree inspires thousands with his unique blend of investigation, scientific expertise and solutions. As the Emmy winning producer of "The Doctors" TV series and producer of the ground-breaking documentary, Vaxxed:From Cover-up to Catastrophe, he ignited a revolution against pharmaceutical tyranny around the world. Del’s internet TV news show, The HighWire reaches out to over 100 million views. His non-profit, the Informed Consent Action Network, (ICAN), is leading worldwide investigations into drug and vaccine fraud that have already resulted in multiple winning lawsuits against US Government agencies Health and Human Services, National Institutes of Health, CDC and FDA.


    Dr. Judy Mikovits



    Dr. Judy Mikovits has been called one of the most accomplished scientist of her generation. Her 1991 doctoral thesis revolutionized the treatment of HIV/AIDS.. In 2020 Dr. Mikovits started Dr Solution, a company focused, not only on education, but on providing solutions for prevention and treatment of autoimmune/auto-inflammatory diseases resulting from viral infection, drugs and environmental toxins.. Her heart and passion is to focus on natural products chemistry and plant based drug and nutritional therapeutic protocols. Dr Mikovits is a New York Times Best selling author of the books Plague, Plague of Corruption, Ending Plague and the Truth about the Masks.


    Dr. Mikovits is featured in both "Plandemic" films.


    Dr. Jeffrey Barke



    Dr. Jeffrey Barke is a board certified primary care physician in private practice for over 25 years. He has served as an Associate Clinical Professor at U.C. Irvine and a board member of the Orange County Medical Association. Dr. Barke is the author of COVID-19: A Physicians Take on the Exaggerated Fear of Corona Virus. He is a sought after speaker on the failure of government education and all things related to COVID-19. Dr. Barke is a proud founding member of America’s Frontline Doctor.He is also the co-host of the podcast: InformedDissentMedia.com

    Steve Kirsch



    Steve Kirsch is a Silicon Valley entrepreneur, MIT graduate and philanthropist, as well the founder of the COVID-19 Early Treatment Fund and the Vaccine Safety Research Foundation. He has been featured on 60 Minutes and profiled in Forbes. Kirsch has one of the most widely read Substacks in the world.


    Dr. Byran Ardis



    Dr. Bryan Ardis is a tireless researcher, seeking to weed out deception in health and medicine and provide truth through his personal research,“The Dr. Ardis” Podcast and his product formulations. In May of 2020, Dr. Ardis blew the whistle on the deadly, toxic and experimental drug, Remdesivir. Dr Ardis has been featured in many documentaries including, “Antidote” with Jason Shurka, “Watch the Water” and “Watch the Water 2”, with Stew Peters, “COVENOM-19” with Jonathan Otto, and “Propaganda Exposed” with the Bollinger’s. The Dr. Ardis Show has a mission statement which is, “Creating Doubt in Big Pharma, and Restoring Faith in Nature!” During the intentionally created supply chain issues of the fraudulent COVID pandemic, Dr. Ardis launched his own brand of all natural supplements called ArdisLabs.com. Whether by media interviews, speaking on stages, or testifying in state capital buildings, Dr. Ardis is on a mission to protect the health of innocent human beings worldwide, and help them make sense of their symptoms


    Dr. Robert O. Young has been recognized as one of the top clinical scientists in the world specializing in cellular nutrition, biochemistry and microbiology. Dr. Young has devoted his life to researching the true causes of "disease," subsequently developing "The New Biology™" to help people balance their life. He is the author of over 100 published peer-reviewed articles and author and co-author of many books. The pH Miracle series of books have sold over 10 million copies and are gaining a widespread following in over 159 countries. He is best known for his four book series, The pH Miracle, The pH Miracle for Diabetes, The pH Miracle for Weight Loss and The pH Miracle for Cancer.


    Last year Dr. Young and his co-author Tom Ballantyne, Jr. published 3 new books, “Truth vs Deception – Liberty vs. Tyranny - Facts vs, Fiction - Science vs, Scientism, Part 1, 2 and 3 based on the premise that if we are to remain free, we must learn the truth on what is going on around us, and not just from the media, government, etc.


    While author's Dr. Robert Young and T. M. Ballantyne, Jr. (the "Truth Author," so-named by Dr. Young) will discuss the facts surrounding what Sasha Stone has called "Covidiocy," and its attendant "vaccines," along with the third book in the series, 'Let Freedom Ring', about child trafficking and its attendant evils, released in late October of 2023 (3 1/2 months ago), the underlying theme of the series is exactly what the title indicates: How to discern truth and avoid deception.


    As the goal of the conference is "to create a new world based on new paradigms in various areas of life," we will address how truth liberates us from the captivity of deception."


    "Given that the key to both health and happiness is right-thinking, we posit that only by recognizing and embracing actual truth can our thoughts achieve those ends. We maintain that the ultimate aim of our existence, both now and hereafter, is that we "might have joy."


    Authors Young and Ballantyne


    T. M. Ballantyne, Jr.



    https://consciouslifeexpo.com/dr-robert-young-2024/...

    PRESS CONTACT:


    Dawna Shuman, Lighthouse Public Relations


    dslighthousepr@aol.com/Cell: 818-632-3297

    I wonder why I'm never invited to panels?

    https://www.drrobertyoung.com/post/the-medical-freedom-symposiumpost-conference-at-the-conscious-life-expo
    THE MEDICAL FREEDOM SYMPOSIUM CONFERENCE at THE CONSCIOUS LIFE EXPO Monday, Feb.12 - 2pm-4:30pm FORGING THE FUTURE TERRAIN OF WELLNESS Join us for a riveting, powerful, inspiring exchange of motivational insights that will stir you to support and create the changes we need for our Medical Freedom! Together We Stand! The Supreme Court has long recognized a person's constitutionally protected liberty interest in his or her own medical autonomy, especially when those interests are secured by state laws. Kelly Gallagher Kelly Gallagher is an Award-winning filmmaker, writer, poet, international health activist, and wellness/survival expert. Hailing from Network TV, this 5x cancer “thriver” powered by her 6th pacemaker, and a prosthetic heart valve has successfully navigated both conventional and alternative wellness protocols for almost 40 years. Del Bigtree Del Bigtree inspires thousands with his unique blend of investigation, scientific expertise and solutions. As the Emmy winning producer of "The Doctors" TV series and producer of the ground-breaking documentary, Vaxxed:From Cover-up to Catastrophe, he ignited a revolution against pharmaceutical tyranny around the world. Del’s internet TV news show, The HighWire reaches out to over 100 million views. His non-profit, the Informed Consent Action Network, (ICAN), is leading worldwide investigations into drug and vaccine fraud that have already resulted in multiple winning lawsuits against US Government agencies Health and Human Services, National Institutes of Health, CDC and FDA. Dr. Judy Mikovits Dr. Judy Mikovits has been called one of the most accomplished scientist of her generation. Her 1991 doctoral thesis revolutionized the treatment of HIV/AIDS.. In 2020 Dr. Mikovits started Dr Solution, a company focused, not only on education, but on providing solutions for prevention and treatment of autoimmune/auto-inflammatory diseases resulting from viral infection, drugs and environmental toxins.. Her heart and passion is to focus on natural products chemistry and plant based drug and nutritional therapeutic protocols. Dr Mikovits is a New York Times Best selling author of the books Plague, Plague of Corruption, Ending Plague and the Truth about the Masks. Dr. Mikovits is featured in both "Plandemic" films. Dr. Jeffrey Barke Dr. Jeffrey Barke is a board certified primary care physician in private practice for over 25 years. He has served as an Associate Clinical Professor at U.C. Irvine and a board member of the Orange County Medical Association. Dr. Barke is the author of COVID-19: A Physicians Take on the Exaggerated Fear of Corona Virus. He is a sought after speaker on the failure of government education and all things related to COVID-19. Dr. Barke is a proud founding member of America’s Frontline Doctor.He is also the co-host of the podcast: InformedDissentMedia.com Steve Kirsch Steve Kirsch is a Silicon Valley entrepreneur, MIT graduate and philanthropist, as well the founder of the COVID-19 Early Treatment Fund and the Vaccine Safety Research Foundation. He has been featured on 60 Minutes and profiled in Forbes. Kirsch has one of the most widely read Substacks in the world. Dr. Byran Ardis Dr. Bryan Ardis is a tireless researcher, seeking to weed out deception in health and medicine and provide truth through his personal research,“The Dr. Ardis” Podcast and his product formulations. In May of 2020, Dr. Ardis blew the whistle on the deadly, toxic and experimental drug, Remdesivir. Dr Ardis has been featured in many documentaries including, “Antidote” with Jason Shurka, “Watch the Water” and “Watch the Water 2”, with Stew Peters, “COVENOM-19” with Jonathan Otto, and “Propaganda Exposed” with the Bollinger’s. The Dr. Ardis Show has a mission statement which is, “Creating Doubt in Big Pharma, and Restoring Faith in Nature!” During the intentionally created supply chain issues of the fraudulent COVID pandemic, Dr. Ardis launched his own brand of all natural supplements called ArdisLabs.com. Whether by media interviews, speaking on stages, or testifying in state capital buildings, Dr. Ardis is on a mission to protect the health of innocent human beings worldwide, and help them make sense of their symptoms Dr. Robert O. Young has been recognized as one of the top clinical scientists in the world specializing in cellular nutrition, biochemistry and microbiology. Dr. Young has devoted his life to researching the true causes of "disease," subsequently developing "The New Biology™" to help people balance their life. He is the author of over 100 published peer-reviewed articles and author and co-author of many books. The pH Miracle series of books have sold over 10 million copies and are gaining a widespread following in over 159 countries. He is best known for his four book series, The pH Miracle, The pH Miracle for Diabetes, The pH Miracle for Weight Loss and The pH Miracle for Cancer. Last year Dr. Young and his co-author Tom Ballantyne, Jr. published 3 new books, “Truth vs Deception – Liberty vs. Tyranny - Facts vs, Fiction - Science vs, Scientism, Part 1, 2 and 3 based on the premise that if we are to remain free, we must learn the truth on what is going on around us, and not just from the media, government, etc. While author's Dr. Robert Young and T. M. Ballantyne, Jr. (the "Truth Author," so-named by Dr. Young) will discuss the facts surrounding what Sasha Stone has called "Covidiocy," and its attendant "vaccines," along with the third book in the series, 'Let Freedom Ring', about child trafficking and its attendant evils, released in late October of 2023 (3 1/2 months ago), the underlying theme of the series is exactly what the title indicates: How to discern truth and avoid deception. As the goal of the conference is "to create a new world based on new paradigms in various areas of life," we will address how truth liberates us from the captivity of deception." "Given that the key to both health and happiness is right-thinking, we posit that only by recognizing and embracing actual truth can our thoughts achieve those ends. We maintain that the ultimate aim of our existence, both now and hereafter, is that we "might have joy." Authors Young and Ballantyne T. M. Ballantyne, Jr. https://consciouslifeexpo.com/dr-robert-young-2024/... PRESS CONTACT: Dawna Shuman, Lighthouse Public Relations dslighthousepr@aol.com/Cell: 818-632-3297 I wonder why I'm never invited to panels? https://www.drrobertyoung.com/post/the-medical-freedom-symposiumpost-conference-at-the-conscious-life-expo
    WWW.DRROBERTYOUNG.COM
    THE MEDICAL FREEDOM SYMPOSIUM CONFERENCE at THE CONSCIOUS LIFE EXPO
    Monday, Feb.12 - 2pm-4:30pm FORGING THE FUTURE TERRAIN OF WELLNESS Join us for a riveting, powerful, inspiring exchange of motivational insights that will stir you to support and create the changes we need for our Medical Freedom! Together We Stand! The Supreme Court has long recognized a person's constitutionally protected liberty interest in his or her own medical autonomy, especially when those interests are secured by state laws. Kelly Gallagher Kelly Gallagher is an Award-winning filmmaker,
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  • Snake Venom Key Ingredient In “Covid-19 Vaccine” Patents
    April 14, 2022 by Dr. Ariyana Love
    By Dr. Ariyana Love, ND

    The world premier documentary Watch The Water aired on Red Voice Media this week. Dr. Bryan Ardis dropped a bombshell during his interview with Stew Peters about one of the greatest conspiracy truths of all time. The intentional poisoning of the world’s population through our municipal water supply using snake venom.

    Please see: VenomTech company announces massive library of SNAKE VENOM peptides for pharmaceutical development; “nanocarriers” stabilize snake venom in WATER (PubMed)

    SNAKE VENOM PATENTS

    Most snake venoms contain proteolytic enzymes. I found Snake venom in ten Covid-19 vaccine patents listed as “venom” and “proteolytic” (enzyme).

    Snake venom is being recently touted as an “anti-HIV” drug, since January 2022. There’s six PLA2s from Snake Venoms patents “against HIV”. These synthetically derived snake venoms are marketed under the guise of being “antiviral” and as a preventive treatment for HIV infection.

    The study claims snake venom works to “protect against Lentiviruses” through the “destruction of the viral membrane.” However, this is a lie because we know the Lentiviruses are a lab generated, chimeric mRNA bioweapon containing SARS, MERS, HIV 1-3 and SRV-1 (AIDS), as I documented in my article entitled, Transgenic Hydras & Parasites A Biological Weapons System For Rapid Human Cloning.

    In actuality, snake venom is being used to destroy the human cell membrane not the “viral membrane”, so that nanoparticles can enter the cell and code your genome. This PubMed study proves that HIV is being encoded into people’s cells to produce a new cell line persistently. So snake venom assists mRNA to clone your cells. The J&J patent also mentions “RNA Replicons” which are forever replicating proteins.

    Our Satanic “elites” have programmed the AI to create bioweapons far more complex than humans could ever come up with and the AI came up with 40,000 of the most deadly bioweapons to date.

    THE SPIKE PROTEIN

    The ACE2 protein acts as an anti-inflammatory, keeping immune cells from inflicting damage on the body’s own cells. The ACE2 receptor helps muscles contract and acts as a messenger between nerves, muscles and cells. It’s crucial in your cell signaling processes.

    The ACE2 molecule acts as a gateway, preventing toxins from entering your cells. The mainstream narrative says that SARS-CoV-2 or the “spike protein”, attaches to human cells and blocks the ACE2 receptors. Snake venoms are postsynaptic neurotoxins, meaning they block the Ace2 receptors. So, I think we’ve identified the “spike protein”.

    Snake venom latches onto ACE2 proteins and they get knocked out of commission. This destroys the body’s cell signaling function and enables the nanotech weapons system to enter the cells and reach the nucleus, where the mRNA is reverse-transcribed and integrated into the human genome.

    Snake venom causes paralysis, the loss of muscle function and respiratory failure. It also causes inflammation, cytokine storms and induces auto-immune illness. Studies say snake venom triggers irreversible intracellular alterations, organ failure and continued cell death.

    Heart and lung cells are covered with these ACE2 surface proteins which could explain why there’s so many reports of acute Myocardial injury following “Covid-19 vaccination”. I am receiving a lot of reports from my clients of prolonged stomach pain from these lethal jabs, another causation of snake venom which affects your digestion.

    Speaking of digestion, the Food and Agriculture Organization of the US approved the use of snake venom in food last year (2021). According to the FAO/WHO the PLA2 enzyme (snake venom) complies with the General Specifications and Considerations for Enzyme Preparations Used in Food Processing. They’re using a combination of snake venom and a genetically modified Streptomyces violaceoruber bacteria (strain pChi). In other words, it will alter your genome.

    Notice the conflict of interest in this safety study that declares the pChi strain is not harmful for consumption. The study does admit that this bacterial strain modifies your genome. I don’t believe that any level of genetic modification of humans is at all safe.

    CROTOXIN

    60% of snake venom consists of a neurotoxic substance called Crotoxin. It was the first proteinic toxin to be crystallized into protein crystallization. Once crystallized it can be used in structural biology. You can even buy Crotoxin online.

    ORGANOIDS

    Organoids are being grown a lab to mass produce snake venom. Organoids of snake glands can produce snake venom artificially, without the entire snake.

    MONOCLONAL ANTIBODIES

    Monoclonal antibodies were funded and developed by DARPA and Bill Gates. All monoclonal antibody patents reveal this is a mRNA “vaccine” that codes your cells with HIV-1. Just like the “Covid-19 vaccines”, monoclonal antibodies never underwent clinical safety trials. They’ve never been approved for use on humans and were passed under the Emergency Use Authorization.

    In his interview with Mike Adams, Dr. Bryan Ardis mentioned a study funded by Fauci and the NIH that proved monoclonal antibodies are in fact, unsafe. They specifically target and destroy your T-cells (killer cells) through cytotoxicity. Thermo Fisher’s monoclonal antibodies actually contain snake venom (PLA2)!

    Please read: Monoclonal Antibodies Is Experimental Gene Therapy – Patent Review

    All monoclonal antibodies contain Hydroxychloroquine or chloroquine in “some embodiments”. This explains why some people report feeling better after using monoclonal antibodies at first and that’s enough to fool doctors but later they become extremely fatigued. The long-term effects are still unknown but they cannot be good. When your immune system is destroyed, your body cannot fight off disease.

    NANOBODIES

    The Oxford patent mentions “Nanobodies” and says that “antibodies have been replaced with Nanobodies”. The whole purpose of the “Covid-19 vaccines” was to invoke an “antibody response”. Now that lie too is exposed. The nanotechnology is being programmed to kill.

    ANTIDOTE

    There are breakthrough medicines and supplements that work antidotally against all poisons, including snake venom. In the Dr. Bryan Ardis interview with Dr. Braun, he mentioned the power of redox molecules against snake poison.

    A peer-reviewed study from 2018, shows that Melatonin inhibits snake venom and antivenom induced oxidative stress:

    “Besides antibodies, molecules like melatonin are reported to underlie the antivenom effect. The study of such was established in Egyptian cobra (Naja haje) venom using a rat model; the vital organs, like kidney, liver and heart, of the rat were protected from the venomous effect.”

    Contact me on Telegram for information on where you can obtain the redox molecule supplement that enables your body to remove all poisons and restores all of your body system functions.

    Also, follow my Telegram channel here.

    Watch my latest interview with Stew Peters at Red Voice Media, here.

    Here's the synthetic snake venom patents I documented and found in the Covid-19 vaccines.

    https://ambassadorlove.blog/2022/04/14/snake-venom-key-ingredient-in-covid-19-vaccine-patents/
    Snake Venom Key Ingredient In “Covid-19 Vaccine” Patents April 14, 2022 by Dr. Ariyana Love By Dr. Ariyana Love, ND The world premier documentary Watch The Water aired on Red Voice Media this week. Dr. Bryan Ardis dropped a bombshell during his interview with Stew Peters about one of the greatest conspiracy truths of all time. The intentional poisoning of the world’s population through our municipal water supply using snake venom. Please see: VenomTech company announces massive library of SNAKE VENOM peptides for pharmaceutical development; “nanocarriers” stabilize snake venom in WATER (PubMed) SNAKE VENOM PATENTS Most snake venoms contain proteolytic enzymes. I found Snake venom in ten Covid-19 vaccine patents listed as “venom” and “proteolytic” (enzyme). Snake venom is being recently touted as an “anti-HIV” drug, since January 2022. There’s six PLA2s from Snake Venoms patents “against HIV”. These synthetically derived snake venoms are marketed under the guise of being “antiviral” and as a preventive treatment for HIV infection. The study claims snake venom works to “protect against Lentiviruses” through the “destruction of the viral membrane.” However, this is a lie because we know the Lentiviruses are a lab generated, chimeric mRNA bioweapon containing SARS, MERS, HIV 1-3 and SRV-1 (AIDS), as I documented in my article entitled, Transgenic Hydras & Parasites A Biological Weapons System For Rapid Human Cloning. In actuality, snake venom is being used to destroy the human cell membrane not the “viral membrane”, so that nanoparticles can enter the cell and code your genome. This PubMed study proves that HIV is being encoded into people’s cells to produce a new cell line persistently. So snake venom assists mRNA to clone your cells. The J&J patent also mentions “RNA Replicons” which are forever replicating proteins. Our Satanic “elites” have programmed the AI to create bioweapons far more complex than humans could ever come up with and the AI came up with 40,000 of the most deadly bioweapons to date. THE SPIKE PROTEIN The ACE2 protein acts as an anti-inflammatory, keeping immune cells from inflicting damage on the body’s own cells. The ACE2 receptor helps muscles contract and acts as a messenger between nerves, muscles and cells. It’s crucial in your cell signaling processes. The ACE2 molecule acts as a gateway, preventing toxins from entering your cells. The mainstream narrative says that SARS-CoV-2 or the “spike protein”, attaches to human cells and blocks the ACE2 receptors. Snake venoms are postsynaptic neurotoxins, meaning they block the Ace2 receptors. So, I think we’ve identified the “spike protein”. Snake venom latches onto ACE2 proteins and they get knocked out of commission. This destroys the body’s cell signaling function and enables the nanotech weapons system to enter the cells and reach the nucleus, where the mRNA is reverse-transcribed and integrated into the human genome. Snake venom causes paralysis, the loss of muscle function and respiratory failure. It also causes inflammation, cytokine storms and induces auto-immune illness. Studies say snake venom triggers irreversible intracellular alterations, organ failure and continued cell death. Heart and lung cells are covered with these ACE2 surface proteins which could explain why there’s so many reports of acute Myocardial injury following “Covid-19 vaccination”. I am receiving a lot of reports from my clients of prolonged stomach pain from these lethal jabs, another causation of snake venom which affects your digestion. Speaking of digestion, the Food and Agriculture Organization of the US approved the use of snake venom in food last year (2021). According to the FAO/WHO the PLA2 enzyme (snake venom) complies with the General Specifications and Considerations for Enzyme Preparations Used in Food Processing. They’re using a combination of snake venom and a genetically modified Streptomyces violaceoruber bacteria (strain pChi). In other words, it will alter your genome. Notice the conflict of interest in this safety study that declares the pChi strain is not harmful for consumption. The study does admit that this bacterial strain modifies your genome. I don’t believe that any level of genetic modification of humans is at all safe. CROTOXIN 60% of snake venom consists of a neurotoxic substance called Crotoxin. It was the first proteinic toxin to be crystallized into protein crystallization. Once crystallized it can be used in structural biology. You can even buy Crotoxin online. ORGANOIDS Organoids are being grown a lab to mass produce snake venom. Organoids of snake glands can produce snake venom artificially, without the entire snake. MONOCLONAL ANTIBODIES Monoclonal antibodies were funded and developed by DARPA and Bill Gates. All monoclonal antibody patents reveal this is a mRNA “vaccine” that codes your cells with HIV-1. Just like the “Covid-19 vaccines”, monoclonal antibodies never underwent clinical safety trials. They’ve never been approved for use on humans and were passed under the Emergency Use Authorization. In his interview with Mike Adams, Dr. Bryan Ardis mentioned a study funded by Fauci and the NIH that proved monoclonal antibodies are in fact, unsafe. They specifically target and destroy your T-cells (killer cells) through cytotoxicity. Thermo Fisher’s monoclonal antibodies actually contain snake venom (PLA2)! Please read: Monoclonal Antibodies Is Experimental Gene Therapy – Patent Review All monoclonal antibodies contain Hydroxychloroquine or chloroquine in “some embodiments”. This explains why some people report feeling better after using monoclonal antibodies at first and that’s enough to fool doctors but later they become extremely fatigued. The long-term effects are still unknown but they cannot be good. When your immune system is destroyed, your body cannot fight off disease. NANOBODIES The Oxford patent mentions “Nanobodies” and says that “antibodies have been replaced with Nanobodies”. The whole purpose of the “Covid-19 vaccines” was to invoke an “antibody response”. Now that lie too is exposed. The nanotechnology is being programmed to kill. ANTIDOTE There are breakthrough medicines and supplements that work antidotally against all poisons, including snake venom. In the Dr. Bryan Ardis interview with Dr. Braun, he mentioned the power of redox molecules against snake poison. A peer-reviewed study from 2018, shows that Melatonin inhibits snake venom and antivenom induced oxidative stress: “Besides antibodies, molecules like melatonin are reported to underlie the antivenom effect. The study of such was established in Egyptian cobra (Naja haje) venom using a rat model; the vital organs, like kidney, liver and heart, of the rat were protected from the venomous effect.” Contact me on Telegram for information on where you can obtain the redox molecule supplement that enables your body to remove all poisons and restores all of your body system functions. Also, follow my Telegram channel here. Watch my latest interview with Stew Peters at Red Voice Media, here. Here's the synthetic snake venom patents I documented and found in the Covid-19 vaccines. https://ambassadorlove.blog/2022/04/14/snake-venom-key-ingredient-in-covid-19-vaccine-patents/
    AMBASSADORLOVE.BLOG
    Snake Venom Key Ingredient In “Covid-19 Vaccine” Patents
    By Dr. Ariyana Love, ND The world premier documentary Watch The Water aired on Red Voice Media this week. Dr. Bryan Ardis dropped a bombshell during his interview with Stew Peters about one of the …
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  • Terrifying! New LETHAL BIO-WEAPON SARS-COV-3 Built and Hid by CHINA’s ARMY | VT Foreign Policy
    January 24, 2024
    VT Condemns the ETHNIC CLEANSING OF PALESTINIANS by USA/Israel

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

    by Fabio Giuseppe Carlo Carisio

    VERSIONE IN ITALIANO

    The news is much more alarming than the mysterious and lethal Virus with which Bill Gates and his accomplices at the World Economic Forum have continued to threaten humanity for almost a year to push all governments to accept the Pandemic Treaty of the World Health Organization (financed by Bill & Melinda Gates Foundation), the international Vaccine Passport following the example of the European Union’s Green Pass and, consequently, a new wave of mandatory vaccinations to implement the global immunization plan launched by the Microsoft’s tycoon in 1999 in the Congress Center of Rockefeller in the Villa Serbelloni in Bellagio (Como).

    Perhaps it could be this new version of SARS-Cov-2, engineered in a laboratory at Being University and so powerful that it can be defined as SARS-Cov-3 due to its multiple mutations, the mysterious Disease X!

    Indeed after the investigation by Gospa News (published in Italian only), the study was modified, making the most alarming parts disappear…

    The suspicion comes from 4 disturbing circumstances that make the new, very dangerous Chinese research a real BIO-WEAPON capable of threatening all of humanity.

    It was developed with the help of military doctors of PLA: People’s Liberation Army of China.
    The laboratory experiments showed a lethality of 100% on humanized mice
    The research was carried out based on previous virological tests conducted by zoologist Shi Zhengli of the Wuhan Institute of Virology
    On January 21, 2024, the authors have modified the study by eliminating any terrifying reference to the 100% mortality on humanized mice, two days after the publication of the Gospa News investigation! Fortunately we have preserved both the screenshots and the original PDF study…
    A first study was published on December 18, 2022 in the specialized journal Emerging Microbes & Infections and on the same date also on PubMed, the library of the National Institute for Health (NIH) of the US Department of Health, but only in the update of a few days ago the lethality of the laboratory genotype of SARS-Cov-2 called GX_P2V was made known when the new research was relaunched the first time on January 4th in pre-print by BioRxivwhere it has yet to be subjected to peer review.

    The Abstract of the research up to January 21st was as brief as it was chilling:

    «SARS-CoV-2-related pangolin coronavirus GX_P2V(short_3UTR) can cause 100% mortality in human ACE2-transgenic mice, potentially attributable to late-stage brain infection. This underscores a spillover risk of GX_P2V into humans and provides a unique model for understanding the pathogenic mechanisms of SARS-CoV-2-related viruses».


    The study published on January 4th from which the role of a military doctor from the Beijing General Hospital of the PLA army can be deduced and, alongside, the study modified on January 21st with a new title and a new Abstract from which the alarm about 100% lethality in humanized mice disappeared
    The updated study instead appears with a new, less alarming title “An infection and pathogenesis mouse model of SARS-CoV-2-related pangolin coronavirus GX_P2V(short_3UTR)” has also been sweetened in the ABSTRACT from which any reference to the VERY HIGH LETHALITY of the virus created in the laboratory DISAPPEARS:

    «SARS-CoV-2-related pangolin coronavirus GX_P2V(short_3UTR) is highly attenuated, but can cause mortality in a specifically designed human ACE2-transgenic mouse model, making it an invaluable surrogate model for evaluating the efficacy of drugs and vaccines against SARS-CoV-2».

    Even more so after this SELF-CENSORSHIP, the previous original document that we wrote about takes on importance and on which we believe it is our duty to focus even if the researchers will obviously be able to claim that they are wrong…

    The study by Lai Wei et al. was conducted by Beijing Advanced Innovation Center for Soft Matter Science and Engineering, College of Life Science and Technology, Beijing University of Chemical Technology (China), with the collaboration of State Key Laboratory of Pharmaceutical Biotechnology, Medical School, Nanjing University, but also with Research Center for Clinical Medicine, The Fifth Medical Center of PLA General Hospital, Beijing, where the military doctor Shengdong Luo, present in both studies, and his colleague Weiwei Chen work.

    The latter is one of the various military hospitals that have taken the place of civilian facilities since 2016 as confirmed by a photo of the inauguration found on the internet.


    One of Beijing’s civilian hospitals converted into a military facility in 2016
    One of the most disturbing aspects of this research is the fact that it derives from the previous study published in 2022 which highlighted only research aimed at producing a vaccine. While this new in-depth study has in fact transformed the study into the typology products defined in the US as “Dual Use Research of Concern (DURC)”where the dual utility consists precisely in the use as a vaccine or as a bio-weapon.

    From the “Smoking Gun” of Artificial SARS-Cov-2 to Beijing’s New Bio-Weapon

    This new and very dangerous experiment brings us back to the studies on chimeric coronaviruses at the Wuhan Institute of Virology where the scientist Shi Zhengli infected SARS strains with HIV plasmids since 2004 thanks to the funding of the Episars project of the European Commission chaired by Romano Prodi to experiment with an artificial enhancement of the wild virus which culminated in the so-called “smoking gun” on the origin of SARS-Cov-2 of Covid 19.

    «When I first saw the furin cleavage site in the viral sequence (of SARS-Cov-2 – ed.), with its arginine codons, I told my wife that it was the smoking gun for the origin of the virus”.

    This is what Dr. David Baltimore, a renowned American virologist and co-discoverer of reverse transcriptase, stated in support of the thesis (now much more than a theory) of the artificial origin of the pandemic pathogen which, to summarize it in a simple way , attaches itself to human cells and becomes lethal precisely thanks to that criticality in furin.

    Proof of this laboratory alteration emerged from a 2016 study, which remained almost unknown until recently, which was financed by the virologist Antony Fauci (former director of the American National Institute of Allergy and Infectious Diseases – NIAID) and conducted by US scientists, Wuhan researchers and Chinese medical doctors as revealed by the dossier of the US Senate Health Committee which not only ascertained the high probability of the artificial origin of SARS-Cov-2 but highlighted the role of American researchers…

    It is now known that Fauci himself admitted before the American Congress that the theory of the virus built in the laboratory is not a conspiracy as he instead claimed in a study on natural origins published shortly after some Indian scientists from the Kusuma School of Biology in New Delhi discovered the anomalous HIV sequences and reported them in a paper published in ResearchGate.

    But “they were then forced to withdraw” according to the late biologist Luc Montagnier, who was the first to publish research on artificial origin together with his biomathematician friend Jean-Claude Perez whom Gospa News interviewed exclusively a few months ago.

    In our investigations of the Wuhan-Gates cycle (in homage to Bill Gates who financed the Wuhan projects through EcoHealthAliance) we highlighted how the collaboration between the US and China started on biological weapons by former presidents Bill Clinton and Jiang Zemin was fundamental to the Predict-2 project on chimeric coronavirus researches funded by the Obama-Biden administration.

    This is why we have embraced the thesis of the patent expert David E. Martin who supported something very serious: according to him, in fact, the SARS-Cov-2 built between China and the US (but probably with contributions also in Canada, the United Kingdom and Ukraine) was allegedly intentionally released by the United States of America. In fact, it has brought to light too many intrigues between the research of Moderna Big Pharma (also financed by Gates and Fauci) and the Pentagon’s military agency DARPA.

    So China (led by Xi Jinping disliked by the Shanghai Clan of Jiang Zemin’s political heirs and his son who strengthened the Wuhan Institute of Virology) would have suffered, for the second time after the SARS of 2003 also built in a laboratory according to Martin and Russian genomics experts, the dispersal of the virus likely occurred during the World Military Games in Wuhan in October 2019.

    This is why, as reported recently by the Wall Street Journal, on the basis of documents obtained from the United States Department of Health, Chinese researchers isolated and mapped the Covid-19 virus at the end of December 2019, at least two weeks before Beijing revealed the details of the deadly virus to the world. According to the US newspaper, a Chinese researcher in Beijing uploaded an almost complete sequence of the structure of Covid into a database managed by the American government on December 28, 2019, while China shared the sequence of the virus with the World Health Organization (WHO) only 11 January 2020.

    In light of these considerations, the new experimentation also conducted by Chinese military doctors takes on an even more disturbing plot. So much so as to fuel the suspicion that Beijing has built a deadly bio-weapon ready to be spread in a global bacteriological war should new Western-inspired pandemics appear.

    Chinese research for a new attenuated vaccine against Covid-19

    Now that we have analyzed the historical and geopolitical context, let’s briefly summarize the peculiarities of the two different studies on SARS-CoV-2 GX_P2V, the one for the 2022 vaccine and the one for the 2023 bioweapon.


    The first research by Beijing University for a new anti-Covid vaccine – link at the bottom of the page
    «SARS-CoV-2 related coronaviruses (SARS-CoV-2r) from Guangdong and Guangxi pangolins have been implicated in the emergence of SARS-CoV-2 and future pandemics. We previously reported the culture of a SARS-CoV-2r GX_P2V from Guangxi pangolins. Here we report the GX_P2V isolate rapidly adapted to Vero cells by acquiring two genomic mutations: an alanine to valine substitution in the nucleoprotein and a 104-nucleotide deletion in the hypervariable region (HVR) of the 3′-terminus untranslated region (3′-UTR)».

    This is what we read in the Abstract on PubMed of December 2022 regarding the research by Shanshan Lu et al. entitled “Induction of significant neutralizing antibodies against SARS-CoV-2 by a highly attenuated pangolin coronavirus variant with a 104nt deletion at the 3′-UTR”.

    «We further report the characterization of the GX_P2V variant (renamed GX_P2V(short_3UTR)) in in vitro and in vivo infection models. In cultured Vero, BGM and Calu-3 cells, GX_P2V(short_3UTR) had similar robust replication kinetics, and consistently produced minimum cell damage. GX_P2V(short_3UTR) infected golden hamsters and BALB/c mice but was highly attenuated. Golden hamsters infected intranasally had a short duration of productive infection in pulmonary, not extrapulmonary, tissues».

    The Abstract then goes into the specifics of the development of an antidote against Covid based not on the new and controversial biotechnology of mRNA gene sera but on that of traditional vaccines:

    «These productive infections induced neutralizing antibodies against pseudoviruses of GX_P2V and SARS-CoV-2. Collectively, our data show that the GX_P2V(short_3UTR) is highly attenuated in in vitro and in vivo infection models. Attenuation of the variant is likely partially due to the 104-nt deletion in the HVR in the 3′-UTR. This study furthers our understanding of pangolin coronaviruses pathogenesis and provides novel insights for the design of live attenuated vaccines against SARS-CoV-2».

    The Army Laboratory Experiment for a Bacteriological Weapon

    The recently published study with the already extremely alarming title “Lethal Infection of Human ACE2- Transgenic Mice Caused by SARS-CoV-2-related Pangolin Coronavirus GX_P2V(short_3UTR)” had a different impact, before it was altered on January 21 to mitigate its hazard…

    This work was supported by NSFC-MFST project (China–Mongolia) (grant number 32161143027), National Key R&D Program of China (2021YFC2301804) and Biosafety Special Program (No. 19SWAQ 13).

    «Two SARS-CoV-2-related pangolin coronaviruses, GD/2019 and GX/2017, were identified prior to the COVID-19 outbreak (1,2). The respective isolates, termed pCoV-GD01 and GX_P2V, were cultured in 2020 and 2017, respectively (2,3). The infectivity and pathogenicity of these isolates have been studied (4–6). The pCoV-GD01 isolate, which has higher homology with SARS-CoV-2, can infect and cause disease in both golden hamsters and hACE2 mice (4)».

    We read in the pre-print research by Lai Wei et al.:

    «In contrast, while GX_P2V can also infect both species, it does not appear to cause obvious disease in these animals (5,6). We previously reported that the early passaged GX_P2V isolate was actually a cell culture-adapted mutant, named GX_P2V(short_3UTR), which possesses a 104-nucleotide deletion at the 3’-UTR (6). In this study, we cloned this mutant, considering the propensity of coronaviruses to undergo rapid adaptive mutation in cell culture, and assessed its pathogenicity in hACE2 mice. We found that the GX_P2V(short_3UTR) clone can infect hACE2 mice, with high viral loads detected in both lung and brain tissues. This infection resulted in 100% mortality in the hACE2 mice. We surmise that the cause of death may be linked to the occurrence of late brain infection».


    The cover of the study published on January 4 on BiorXiv before the modification on January 21, 2024 – link at the bottom of the page
    Then they also recall that these SARS-CoV-2, GD/2019 and GX/2017 studies were initially carried out by the well-known scientist from the Wuhan Institute of Virology:

    «To the best of our knowledge, 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. Our findings are evidently inconsistent with those of Zhengli Shiet al. (5), who tested the virulence of GX_P2V in two different hACE2 mouse models».

    The discussion then becomes very technical and evidence of expert biochemists or virologists:

    «It is important to note that we did not isolate the wild-type GX_P2V strain. The study by Zhengli Shi et al tested the GX_P2V(short_3UTR) variant that we reported. However, the adaptative evolutionary changes of this variant during their laboratory culture remain understudied. In fact, according to additional infection experiments, the uncloned GX_P2V(short_3UTR) also resulted in 100% mortality in hACE2 mice. Due to the propensity of coronaviruses to undergo adaptive mutation during passage culture, we cloned and analyzed mutations in GX_P2V(short_3UTR), focusing specifically on the pathogenicity of the cloned strains. The high pathogenicity mechanism of GX_P2V C7 in hACE2 mice, in the absence of the wild-type GX_P2V control, requires further investigation».

    And the conclusion doesn’t suggest anything good…

    «Compared to the original sequence of GX_P2V(short_3UTR), GX_P2V C7 has two amino acid mutations in the spike protein. Given the close relationship between coronavirus virulence and spike protein mutations (7), it is possible that GX_P2V C7 has undergone a virulence-enhancing mutation. However, it is important to note that our hACE2 mouse model may be relatively unique. The company has not yet published a paper on this hACE2 mouse model, but our results suggest that hACE2 may be highly expressed in the mouse brain. Additionally, according to the data provided by the company, these hACE2 mice have abnormal physiology, as indicated by relatively reduced serum triglyceride, cholesterol, and lipase levels, compared to those of wild-type C57BL/6J mice. In summary, our study provides a unique perspective on the pathogenicity of GX_P2V and offers a distinct alternative model for understanding the pathogenic mechanisms of SARS-CoV-2-related coronaviruses».

    The scientific explanation is cloaked by a strong emphasis on virulence which may also appear as a “threat” on the possibility of transforming these GX_P2V genotypes into a real bacteriological weapon.

    Fabio Giuseppe Carlo Carisio
    © COPYRIGHT GOSPA NEWS
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    MAIN SOURCES

    PUBMED – Induction of significant neutralizing antibodies against SARS-CoV-2 by a highly attenuated pangolin coronavirus variant with a 104nt deletion at the 3′-UTR’

    BIORXIV – Lethal Infection of Human ACE2-Transgenic Mice Caused by SARS-CoV-2-related Pangolin Coronavirus GX_P2V(short_3UTR)

    To receive the COMPLETE PDF OF THE ORIGINAL DISTURBING RESEARCH, subscribe to the Gospa News Newsletter and write to redazione@gospanews.net

    GOSPA NEWS – WUHAN-GATES DOSSIER

    GOSPA NEWS – COVID-19 DOSSIER

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

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

    Most popolar investigation on VT is:

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

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

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

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

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

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

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

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

    VETERANS TODAY OLD POSTS

    www.gospanews.net/


    ATTENTION READERS

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    https://www.vtforeignpolicy.com/2024/01/terrifying-new-lethal-bio-weapon-sars-cov-3-built-and-hid-by-chinas-army/
    Terrifying! New LETHAL BIO-WEAPON SARS-COV-3 Built and Hid by CHINA’s ARMY | VT Foreign Policy January 24, 2024 VT Condemns the ETHNIC CLEANSING OF PALESTINIANS by USA/Israel $ 280 BILLION US TAXPAYER DOLLARS INVESTED since 1948 in US/Israeli Ethnic Cleansing and Occupation Operation; $ 150B direct "aid" and $ 130B in "Offense" contracts Source: Embassy of Israel, Washington, D.C. and US Department of State. by Fabio Giuseppe Carlo Carisio VERSIONE IN ITALIANO The news is much more alarming than the mysterious and lethal Virus with which Bill Gates and his accomplices at the World Economic Forum have continued to threaten humanity for almost a year to push all governments to accept the Pandemic Treaty of the World Health Organization (financed by Bill & Melinda Gates Foundation), the international Vaccine Passport following the example of the European Union’s Green Pass and, consequently, a new wave of mandatory vaccinations to implement the global immunization plan launched by the Microsoft’s tycoon in 1999 in the Congress Center of Rockefeller in the Villa Serbelloni in Bellagio (Como). Perhaps it could be this new version of SARS-Cov-2, engineered in a laboratory at Being University and so powerful that it can be defined as SARS-Cov-3 due to its multiple mutations, the mysterious Disease X! Indeed after the investigation by Gospa News (published in Italian only), the study was modified, making the most alarming parts disappear… The suspicion comes from 4 disturbing circumstances that make the new, very dangerous Chinese research a real BIO-WEAPON capable of threatening all of humanity. It was developed with the help of military doctors of PLA: People’s Liberation Army of China. The laboratory experiments showed a lethality of 100% on humanized mice The research was carried out based on previous virological tests conducted by zoologist Shi Zhengli of the Wuhan Institute of Virology On January 21, 2024, the authors have modified the study by eliminating any terrifying reference to the 100% mortality on humanized mice, two days after the publication of the Gospa News investigation! Fortunately we have preserved both the screenshots and the original PDF study… A first study was published on December 18, 2022 in the specialized journal Emerging Microbes & Infections and on the same date also on PubMed, the library of the National Institute for Health (NIH) of the US Department of Health, but only in the update of a few days ago the lethality of the laboratory genotype of SARS-Cov-2 called GX_P2V was made known when the new research was relaunched the first time on January 4th in pre-print by BioRxivwhere it has yet to be subjected to peer review. The Abstract of the research up to January 21st was as brief as it was chilling: «SARS-CoV-2-related pangolin coronavirus GX_P2V(short_3UTR) can cause 100% mortality in human ACE2-transgenic mice, potentially attributable to late-stage brain infection. This underscores a spillover risk of GX_P2V into humans and provides a unique model for understanding the pathogenic mechanisms of SARS-CoV-2-related viruses». The study published on January 4th from which the role of a military doctor from the Beijing General Hospital of the PLA army can be deduced and, alongside, the study modified on January 21st with a new title and a new Abstract from which the alarm about 100% lethality in humanized mice disappeared The updated study instead appears with a new, less alarming title “An infection and pathogenesis mouse model of SARS-CoV-2-related pangolin coronavirus GX_P2V(short_3UTR)” has also been sweetened in the ABSTRACT from which any reference to the VERY HIGH LETHALITY of the virus created in the laboratory DISAPPEARS: «SARS-CoV-2-related pangolin coronavirus GX_P2V(short_3UTR) is highly attenuated, but can cause mortality in a specifically designed human ACE2-transgenic mouse model, making it an invaluable surrogate model for evaluating the efficacy of drugs and vaccines against SARS-CoV-2». Even more so after this SELF-CENSORSHIP, the previous original document that we wrote about takes on importance and on which we believe it is our duty to focus even if the researchers will obviously be able to claim that they are wrong… The study by Lai Wei et al. was conducted by Beijing Advanced Innovation Center for Soft Matter Science and Engineering, College of Life Science and Technology, Beijing University of Chemical Technology (China), with the collaboration of State Key Laboratory of Pharmaceutical Biotechnology, Medical School, Nanjing University, but also with Research Center for Clinical Medicine, The Fifth Medical Center of PLA General Hospital, Beijing, where the military doctor Shengdong Luo, present in both studies, and his colleague Weiwei Chen work. The latter is one of the various military hospitals that have taken the place of civilian facilities since 2016 as confirmed by a photo of the inauguration found on the internet. One of Beijing’s civilian hospitals converted into a military facility in 2016 One of the most disturbing aspects of this research is the fact that it derives from the previous study published in 2022 which highlighted only research aimed at producing a vaccine. While this new in-depth study has in fact transformed the study into the typology products defined in the US as “Dual Use Research of Concern (DURC)”where the dual utility consists precisely in the use as a vaccine or as a bio-weapon. From the “Smoking Gun” of Artificial SARS-Cov-2 to Beijing’s New Bio-Weapon This new and very dangerous experiment brings us back to the studies on chimeric coronaviruses at the Wuhan Institute of Virology where the scientist Shi Zhengli infected SARS strains with HIV plasmids since 2004 thanks to the funding of the Episars project of the European Commission chaired by Romano Prodi to experiment with an artificial enhancement of the wild virus which culminated in the so-called “smoking gun” on the origin of SARS-Cov-2 of Covid 19. «When I first saw the furin cleavage site in the viral sequence (of SARS-Cov-2 – ed.), with its arginine codons, I told my wife that it was the smoking gun for the origin of the virus”. This is what Dr. David Baltimore, a renowned American virologist and co-discoverer of reverse transcriptase, stated in support of the thesis (now much more than a theory) of the artificial origin of the pandemic pathogen which, to summarize it in a simple way , attaches itself to human cells and becomes lethal precisely thanks to that criticality in furin. Proof of this laboratory alteration emerged from a 2016 study, which remained almost unknown until recently, which was financed by the virologist Antony Fauci (former director of the American National Institute of Allergy and Infectious Diseases – NIAID) and conducted by US scientists, Wuhan researchers and Chinese medical doctors as revealed by the dossier of the US Senate Health Committee which not only ascertained the high probability of the artificial origin of SARS-Cov-2 but highlighted the role of American researchers… It is now known that Fauci himself admitted before the American Congress that the theory of the virus built in the laboratory is not a conspiracy as he instead claimed in a study on natural origins published shortly after some Indian scientists from the Kusuma School of Biology in New Delhi discovered the anomalous HIV sequences and reported them in a paper published in ResearchGate. But “they were then forced to withdraw” according to the late biologist Luc Montagnier, who was the first to publish research on artificial origin together with his biomathematician friend Jean-Claude Perez whom Gospa News interviewed exclusively a few months ago. In our investigations of the Wuhan-Gates cycle (in homage to Bill Gates who financed the Wuhan projects through EcoHealthAliance) we highlighted how the collaboration between the US and China started on biological weapons by former presidents Bill Clinton and Jiang Zemin was fundamental to the Predict-2 project on chimeric coronavirus researches funded by the Obama-Biden administration. This is why we have embraced the thesis of the patent expert David E. Martin who supported something very serious: according to him, in fact, the SARS-Cov-2 built between China and the US (but probably with contributions also in Canada, the United Kingdom and Ukraine) was allegedly intentionally released by the United States of America. In fact, it has brought to light too many intrigues between the research of Moderna Big Pharma (also financed by Gates and Fauci) and the Pentagon’s military agency DARPA. So China (led by Xi Jinping disliked by the Shanghai Clan of Jiang Zemin’s political heirs and his son who strengthened the Wuhan Institute of Virology) would have suffered, for the second time after the SARS of 2003 also built in a laboratory according to Martin and Russian genomics experts, the dispersal of the virus likely occurred during the World Military Games in Wuhan in October 2019. This is why, as reported recently by the Wall Street Journal, on the basis of documents obtained from the United States Department of Health, Chinese researchers isolated and mapped the Covid-19 virus at the end of December 2019, at least two weeks before Beijing revealed the details of the deadly virus to the world. According to the US newspaper, a Chinese researcher in Beijing uploaded an almost complete sequence of the structure of Covid into a database managed by the American government on December 28, 2019, while China shared the sequence of the virus with the World Health Organization (WHO) only 11 January 2020. In light of these considerations, the new experimentation also conducted by Chinese military doctors takes on an even more disturbing plot. So much so as to fuel the suspicion that Beijing has built a deadly bio-weapon ready to be spread in a global bacteriological war should new Western-inspired pandemics appear. Chinese research for a new attenuated vaccine against Covid-19 Now that we have analyzed the historical and geopolitical context, let’s briefly summarize the peculiarities of the two different studies on SARS-CoV-2 GX_P2V, the one for the 2022 vaccine and the one for the 2023 bioweapon. The first research by Beijing University for a new anti-Covid vaccine – link at the bottom of the page «SARS-CoV-2 related coronaviruses (SARS-CoV-2r) from Guangdong and Guangxi pangolins have been implicated in the emergence of SARS-CoV-2 and future pandemics. We previously reported the culture of a SARS-CoV-2r GX_P2V from Guangxi pangolins. Here we report the GX_P2V isolate rapidly adapted to Vero cells by acquiring two genomic mutations: an alanine to valine substitution in the nucleoprotein and a 104-nucleotide deletion in the hypervariable region (HVR) of the 3′-terminus untranslated region (3′-UTR)». This is what we read in the Abstract on PubMed of December 2022 regarding the research by Shanshan Lu et al. entitled “Induction of significant neutralizing antibodies against SARS-CoV-2 by a highly attenuated pangolin coronavirus variant with a 104nt deletion at the 3′-UTR”. «We further report the characterization of the GX_P2V variant (renamed GX_P2V(short_3UTR)) in in vitro and in vivo infection models. In cultured Vero, BGM and Calu-3 cells, GX_P2V(short_3UTR) had similar robust replication kinetics, and consistently produced minimum cell damage. GX_P2V(short_3UTR) infected golden hamsters and BALB/c mice but was highly attenuated. Golden hamsters infected intranasally had a short duration of productive infection in pulmonary, not extrapulmonary, tissues». The Abstract then goes into the specifics of the development of an antidote against Covid based not on the new and controversial biotechnology of mRNA gene sera but on that of traditional vaccines: «These productive infections induced neutralizing antibodies against pseudoviruses of GX_P2V and SARS-CoV-2. Collectively, our data show that the GX_P2V(short_3UTR) is highly attenuated in in vitro and in vivo infection models. Attenuation of the variant is likely partially due to the 104-nt deletion in the HVR in the 3′-UTR. This study furthers our understanding of pangolin coronaviruses pathogenesis and provides novel insights for the design of live attenuated vaccines against SARS-CoV-2». The Army Laboratory Experiment for a Bacteriological Weapon The recently published study with the already extremely alarming title “Lethal Infection of Human ACE2- Transgenic Mice Caused by SARS-CoV-2-related Pangolin Coronavirus GX_P2V(short_3UTR)” had a different impact, before it was altered on January 21 to mitigate its hazard… This work was supported by NSFC-MFST project (China–Mongolia) (grant number 32161143027), National Key R&D Program of China (2021YFC2301804) and Biosafety Special Program (No. 19SWAQ 13). «Two SARS-CoV-2-related pangolin coronaviruses, GD/2019 and GX/2017, were identified prior to the COVID-19 outbreak (1,2). The respective isolates, termed pCoV-GD01 and GX_P2V, were cultured in 2020 and 2017, respectively (2,3). The infectivity and pathogenicity of these isolates have been studied (4–6). The pCoV-GD01 isolate, which has higher homology with SARS-CoV-2, can infect and cause disease in both golden hamsters and hACE2 mice (4)». We read in the pre-print research by Lai Wei et al.: «In contrast, while GX_P2V can also infect both species, it does not appear to cause obvious disease in these animals (5,6). We previously reported that the early passaged GX_P2V isolate was actually a cell culture-adapted mutant, named GX_P2V(short_3UTR), which possesses a 104-nucleotide deletion at the 3’-UTR (6). In this study, we cloned this mutant, considering the propensity of coronaviruses to undergo rapid adaptive mutation in cell culture, and assessed its pathogenicity in hACE2 mice. We found that the GX_P2V(short_3UTR) clone can infect hACE2 mice, with high viral loads detected in both lung and brain tissues. This infection resulted in 100% mortality in the hACE2 mice. We surmise that the cause of death may be linked to the occurrence of late brain infection». The cover of the study published on January 4 on BiorXiv before the modification on January 21, 2024 – link at the bottom of the page Then they also recall that these SARS-CoV-2, GD/2019 and GX/2017 studies were initially carried out by the well-known scientist from the Wuhan Institute of Virology: «To the best of our knowledge, 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. Our findings are evidently inconsistent with those of Zhengli Shiet al. (5), who tested the virulence of GX_P2V in two different hACE2 mouse models». The discussion then becomes very technical and evidence of expert biochemists or virologists: «It is important to note that we did not isolate the wild-type GX_P2V strain. The study by Zhengli Shi et al tested the GX_P2V(short_3UTR) variant that we reported. However, the adaptative evolutionary changes of this variant during their laboratory culture remain understudied. In fact, according to additional infection experiments, the uncloned GX_P2V(short_3UTR) also resulted in 100% mortality in hACE2 mice. Due to the propensity of coronaviruses to undergo adaptive mutation during passage culture, we cloned and analyzed mutations in GX_P2V(short_3UTR), focusing specifically on the pathogenicity of the cloned strains. The high pathogenicity mechanism of GX_P2V C7 in hACE2 mice, in the absence of the wild-type GX_P2V control, requires further investigation». And the conclusion doesn’t suggest anything good… «Compared to the original sequence of GX_P2V(short_3UTR), GX_P2V C7 has two amino acid mutations in the spike protein. Given the close relationship between coronavirus virulence and spike protein mutations (7), it is possible that GX_P2V C7 has undergone a virulence-enhancing mutation. However, it is important to note that our hACE2 mouse model may be relatively unique. The company has not yet published a paper on this hACE2 mouse model, but our results suggest that hACE2 may be highly expressed in the mouse brain. Additionally, according to the data provided by the company, these hACE2 mice have abnormal physiology, as indicated by relatively reduced serum triglyceride, cholesterol, and lipase levels, compared to those of wild-type C57BL/6J mice. In summary, our study provides a unique perspective on the pathogenicity of GX_P2V and offers a distinct alternative model for understanding the pathogenic mechanisms of SARS-CoV-2-related coronaviruses». The scientific explanation is cloaked by a strong emphasis on virulence which may also appear as a “threat” on the possibility of transforming these GX_P2V genotypes into a real bacteriological weapon. Fabio Giuseppe Carlo Carisio © COPYRIGHT GOSPA NEWS prohibition of reproduction without authorization follow Fabio Carisio Gospa News director on Twitter follow Gospa News on Telegram Subscribe to the Gospa News Newsletter to read the news as soon as it is published MAIN SOURCES PUBMED – Induction of significant neutralizing antibodies against SARS-CoV-2 by a highly attenuated pangolin coronavirus variant with a 104nt deletion at the 3′-UTR’ BIORXIV – Lethal Infection of Human ACE2-Transgenic Mice Caused by SARS-CoV-2-related Pangolin Coronavirus GX_P2V(short_3UTR) To receive the COMPLETE PDF OF THE ORIGINAL DISTURBING RESEARCH, subscribe to the Gospa News Newsletter and write to redazione@gospanews.net GOSPA NEWS – WUHAN-GATES DOSSIER GOSPA NEWS – COVID-19 DOSSIER Fabio G. C. Carisio Fabio is investigative journalist since 1991. Now geopolitics, intelligence, military, SARS-Cov-2 manmade, NWO expert and Director-founder of Gospa News: a Christian Information Journal. His articles were published on many international media and website as SouthFront, Reseau International, Sputnik Italia, United Nation Association Westminster, Global Research, Kolozeg and more… Most popolar investigation on VT is: Rumsfeld Shady Heritage in Pandemic: GILEAD’s Intrigues with WHO & Wuhan Lab. Bio-Weapons’ Tests with CIA & Pentagon Fabio Giuseppe Carlo Carisio, born on 24/2/1967 in Borgosesia, started working as a reporter when he was only 19 years old in the alpine area of Valsesia, Piedmont, his birth region in Italy. After studying literature and history at the Catholic University of the Sacred Heart in Milan, he became director of the local newspaper Notizia Oggi Vercelli and specialized in judicial reporting. For about 15 years he is a correspondent from Northern Italy for the Italian newspapers Libero and Il Giornale, also writing important revelations on the Ustica massacre, a report on Freemasonry and organized crime. With independent investigations, he collaborates with Carabinieri and Guardia di Finanza in important investigations that conclude with the arrest of Camorra entrepreneurs or corrupt politicians. In July 2018 he found the counter-information web media Gospa News focused on geopolitics, terrorism, Middle East, and military intelligence. In 2020 published the book, in Italian only, WUHAN-GATES – The New World Order Plot on SARS-Cov-2 manmade focused on the cycle of investigations Wuhan-Gates His investigations was quoted also by The Gateway Pundit, Tasnim and others He worked for many years for the magazine Art & Wine as an art critic and curator. VETERANS TODAY OLD POSTS www.gospanews.net/ ATTENTION READERS We See The World From All Sides and Want YOU To Be Fully Informed In fact, intentional disinformation is a disgraceful scourge in media today. So to assuage any possible errant incorrect information posted herein, we strongly encourage you to seek corroboration from other non-VT sources before forming an educated opinion. About VT - Policies & Disclosures - Comment Policy Due to the nature of uncensored content posted by VT's fully independent international writers, VT cannot guarantee absolute validity. All content is owned by the author exclusively. Expressed opinions are NOT necessarily the views of VT, other authors, affiliates, advertisers, sponsors, partners, or technicians. Some content may be satirical in nature. All images are the full responsibility of the article author and NOT VT. https://www.vtforeignpolicy.com/2024/01/terrifying-new-lethal-bio-weapon-sars-cov-3-built-and-hid-by-chinas-army/
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    Terrifying! New LETHAL BIO-WEAPON SARS-COV-3 Built and Hid by CHINA’s ARMY
    by Fabio Giuseppe Carlo Carisio VERSIONE IN ITALIANO The news is much more alarming than the mysterious and lethal Virus with which Bill Gates and his accomplices at the World Economic Forum have continued to threaten humanity for almost a year to push all governments to accept the Pandemic Treaty of the World Health Organization...
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  • Moderna’s influence over the US and UK governments is more than most realise
    Rhoda WilsonJanuary 3, 2024
    The sheer sprawl, corruption, influence and involvement of Moderna in politics and the wider medical industry is staggering. It is difficult to convey and harder to comprehend, The Underdog writes.

    Months before a pandemic was declared in 2020, World Economic Forum Young Global Leader and CEO of Moderna Stéphane Bancel told his staff that there was going to be a pandemic and Moderna would need to manufacture a billion doses of vaccine the “next year,” being 2021.

    How did Bancel know?

    A recent article written by The Underdog may provide some insight which lays out his/her findings relating to Moderna infiltrating the USA and UK governments as well as academia.

    The Underdog is a non de plume for someone who self-describes as a citizen journalist and publishes articles on a Substack page titled ‘The Daily Beagle’.

    In the USA, Moderna took control of the FDA and Operation Warp Speed, and influenced NIH and BARDA, The Underdog says. Adding that Moderna controls the UK government through Installed Prime Minister Rishi Sunak.

    As well as governments, The Underdog surmises that Moderna has compromised academics in universities in the USA and Canada.

    For previous articles we’ve published that relate to and complement The Underdog’s article, please see ‘Rishi Sunak, Thélème and Moderna’ and various other articles HERE.

    Let’s not lose touch…Your Government and Big Tech are actively trying to censor the information reported by The Exposé to serve their own needs. Subscribe now to make sure you receive the latest uncensored news in your inbox…

    Murderous Moderna’s Infiltration of Politics

    By The Underdog

    Murder, They Wrote

    Let us clarify murderous: a peer-reviewed study found that myocarditis in under 40-year-old males was higher in those who had taken all vaccines, and those who had taken a second dose of mRNA-1273, the Moderna covid injection.

    It was so bad that Sweden, Norway, and Finland suspended the use of the Moderna vaccine in young people, as noted in the British Medical Journal (“BMJ”).

    As previously known, the US National Institutes of Health (“NIH”) and their corrupt cohorts attempted to censor evidence that myocarditis has a fatality rate of 50% within 5 years. So it isn’t unreasonable to assert Moderna has in all likelihood murdered at least 50% of those with myocarditis caused by the Moderna injections; of which will include children.

    Like in an attempt to discourage people from getting the poisonous shots without declaring that they’re harmful and recalling them, Moderna recently jacked up the price of their injections to $130. A reminder Moderna produced injections that contained stainless steel contaminants.


    It cost only $2.85 to manufacture and despite this, the US government paid $15 to $26 a dose. Why?

    Moderna Have Infiltrated the Government

    Seems pretty incredulous, but no.

    Moderna Is Part of WEF

    Stéphane Bancel was “elected” 2009 Young Global Leader by the World Economic Forum (“WEF”).


    Bancel was founding chief executive officer for Moderna and joined Flagship Pioneering in 2013.

    Noubar Afeyan, co-founder of Moderna and CEO of Flagship Pioneering, “received a Technology Pioneer 2012 award from the World Economic Forum”.

    Noubar also “served as Chairman of the Global Agenda Council on Chemicals, Advanced Materials and Biotechnology of the World Economic Forum as well as being a member of the Meta-Council on Emerging Technologies.”

    Moderna Took Control of Operation Warp Speed

    Moncef Slaoui, owning 82,508 Moderna shares on 21 February 2020, stepped down from Moderna, divested his stake, and went on to lead Operation Warp Speed. As it just so happened, the US government spent over $4 billion on Moderna, twice as much as any other pharmaceutical company:


    During this time of taking fat wads of government cash, Moderna also received heavy investment from hedge funds in September 2020.

    Moderna Influenced NIH, BARDA

    The NIH in December 2020 bragged how they worked with Moderna in a partnership, along with BARDA (Biomedical Advanced Research and Development Authority) and NIAID (National Institute of Allergy and Infectious Diseases) Vaccine Research Centre to develop the myocarditis inducing mRNA-1273 injection:

    Factoring in that the NIH deleted evidence of the myocarditis fatality rate implicating firms such as Moderna and the NIH itself, this shouldn’t be surprising.

    Moderna ultimately got into a fight with NIH over mRNA patents, with Moderna insisting they did everything. Current NIH director Francis Collins remarked the NIH played “a major role in the development of the vaccine,” in which Moderna received approximately $10 billion in government funding.

    Moderna paid the NIH their bribe patent money, to the tune of $400 million, just under half a billion, but held dispute over another patent. To try to appease the NIH, Moderna offered co-ownership of the vaccine patent with NIH.

    Curiously, an NIH employee, Philip Leder, worked on mRNA research decades before NIH’s agreement with Moderna. They conveniently died in 2020.

    Moderna Took Control of the FDA


    Stephan Hahn
    Stephen Hahn, former FDA Commissioner who insisted he’d fast-track the covid-19 injections, left the FDA to go join Flagship Pioneering after approving the injections. He claimed Donald Trump told him “to authorise a covid-19 vaccine or go.”


    Flagship Pioneering are a venture capital firm that financed and kickstarted Moderna. The CEO of Flagship Pioneering, Noubar Afeyan, also co-founded Moderna. So, they’re essentially one and the same.

    Moderna LLC was the successor in interest to Moderna Therapeutics, Inc., a Delaware corporation incorporated in 2009 as Newco LS18, Inc. by Flagship Pioneering.

    SEC EDGAR filing on Moderna LLCnone
    One of the founding investors of Moderna, Bob Langer, also previously worked on the FDA’s advisory board according to his own biography, serving as both a member and later the chairman:

    It is likely Bob retained contacts within the FDA even after leaving.

    Moderna Control the UK Government

    This isn’t hyperbole. We wish it were.

    The UK government signed a memorandum of understanding with Flagship Pioneering:

    This includes a spin-off company called Quotient Therapeutics:

    The UK government also formed an unusually aggressive and expansive 10-year contract with Moderna, worth at least £1 billion for a “new vaccine centre” – despite the fact these are genetic modification injections.


    This was agreed during Rishi Sunak’s tenure as Prime Minister.

    Moderna de facto Control the Prime Minister

    The investment will benefit current unelected pharmaceutical bureaucrat Rishi Sunak, who is the Prime Minister of the United Kingdom (read as: Moderna have influence of the UK government).


    Unelected Prime Minister Rishi Sunak
    Rishi was also formerly Chancellor of the Exchequer (read as: controlled the UK government purse strings) back in 2020, and allocated even more funds to the vaccine industry during that time. He bragged how it was a “success.” For his bank account, we surmise.

    How will he benefit? Rishi Sunak co-founded a firm called Thélème Partners LLP (aka. Thélème) back in 2009, registered in the Cayman Islands, along with co-founder and former French Navy Patrick Degorce, after they previously met at The Children’s Investment Fund (“TCIF”). TCIF was run by billionaire Chris Hohn.


    Rishi Sunak appointed Thélème partner John Sheridan as an advisor to government during his time as Chancellor of the Exchequer.

    Thélème started with an initial investment fund of £536m, and were early backers of Moderna. Thélème co-founder Degorce invested in Moderna over a decade ago, meaning their rise was also Rishi Sunak’s rise.

    Thélème are Moderna’s single largest hedge fund investor, despite Thélème cutting their exposure by 11%. On 30 September 2023, Thélème disclosed ownership of 6,897,612 shares of Moderna, Inc. (US:MRNA) valued at $712,454,343 USD, more than half a billion.

    The name Thélème is likely based upon the French ‘Abbaye de Thélème’, an idea invented by French monk Rabelais, who gives his vision of an “ideal and utopian abbey.”

    The “Thelemites of the Abbey” follow “do what thou wilt”. Occultist Aleister Crowley declared a so-called “Theleme religion” whose central belief was “do what thou wilt”, even remarking “There is no law beyond do what thou wilt.”

    Unsurprisingly, Moderna plant Rishi Sunak did whatever he wanted and declined to say that he did not profit from the Moderna injections. He claims to have left the firm in 2013 and that his finances are in a so-called “blind trust,” along with 10 other ministers. There’s no legal definition of a “blind trust” so this is pure theatre.


    Given he’s the original founder of Thélème, he no doubt has shares and investments and still stands to profit from Moderna’s success, explaining why he gave Flagship Pioneering favourable treatment and Moderna a 10-year contract on a plate. This is the same Rishi who tried to “break banks” during the 2008 collapse.

    On another note…

    Moderna Have Compromised Academia

    Bear in mind academic institutions are involved in peer-reviewed processes, clinical research and more, so this has wider, damning ramifications. Moderna were formed within the heart of academia.

    Moderna Have Control In MIT


    Noubar Afeyan
    Noubar Afeyan, CEO of Flagship Pioneering, studied at MIT (Massachusetts Institute of Technology). He was recently installed in MIT Corporation’s board of trustees.


    The purpose of the trust? (Emphasis added):

    […] to see that the Institute adheres to the purposes for which it was chartered and that its integrity and financial resources are preserved for future generations as well as for current purposes. […]

    “About the Corporation”, MIT Corporation pagenone
    Control of the finances. And integrity.

    During the founding period of Moderna, Noubar Afeyan joined the likes of MIT Bob Langer. Langer, since investing in Moderna, has now become a billionaire as a result.

    MIT Mandates the Covid-19 Injection, That MIT Based Modern Just Happens to Sell

    Profitably for MIT-inspired Moderna, during Moderna’s rise, MIT adopted a vaccine mandate, one where MIT reported there were still covid-19 cases anyway and that they weren’t mild:

    They huffed the copium and tried to argue there were no Omicron-related hospitalisations (Omicron is deemed the mildest of the covid-19 set), but conveniently omitted Alpha, Delta, and the others, implying there were other variant hospitalisations (read as: The injections they mandated for profits, didn’t work).

    Noubar Afeyan and MIT’s Bob Langer are also joined by investor Derrick Rossi (Harvard), after they learn they can reprogram human cells and reverse them back into pluripotent stem cells based on Harvard Derrick Rossi’s research. Notice it involves using mRNA to change human cells (read as: Modify their DNA).

    Rossi is head of the Harvard Department of Stem Cell and Regenerative Biology. Current Moderna CEO Stéphane Bancel also studied at Harvard.

    Rossi approached Harvard faculty member Timothy Springer asking him to invest in Moderna, which he did so. In April 2021, Timothy Springer was declared a billionaire by Cord Magazine. Back patting their own, Timothy Springer went on to receive a Lasker award, and a Robert Koch prize.

    The Koch brothers also finances MIT Bob Langer’s lab:

    In a surprise to no-one, Harvard also mandated the injection from which they stand to profit.

    This included for Harvard staff, flushing out anyone critical of the financial abuses by the vaccine industry.


    Bearing in mind the majority of Moderna directed Operation Warp Speed financing went to Moderna, the majority of the injections that would have been available would have also been primarily Moderna, guaranteeing their selfish, harmful, murderous profit

    Remember: Those below the age of 40 are adversely affected by myocarditis, and the majority of students on campus would be below that age; 50% fatality rate within 5 years for myocarditis.

    University of Toronto, As Well – Maybe Even the Canadian Government?

    The Academia orgy was apparently not big enough, and the University of Toronto wanted some, giving Derrick Rossi an “honorary degree”.


    University of Toronto are particularly interesting because they’re one of a handful of “kingmaker universities” in Canada.

    When investigating Acuitas Therapeutics, The Daily Beagle remarked:

    The only University with more Canadian Prime Ministers is University of Toronto, with Arthur Meighen, W.L. Mackenzie King, Lester B. Pearson, and Paul Martin.

    It is very likely a lot of ministers for the Canadian government also come from the University of Toronto. So, the University of Toronto’s corrupt love-in with Moderna implies Moderna also has influence over the Canadian government.

    And in surprise to no-one, the University of Toronto also anti-competitively mandated the emergency authorisation injections:


    You know, the same injections Health Canada admitted contained plasmid DNA, the same kind Moderna used in partnership with Aldevron.

    What is it with academic universities mandating the injections from which they stand to benefit financially?

    Moderna are in Bed with Multiple Major Pharmaceutical Companies

    To give you an idea how deep this shell game goes, did you know that AstraZeneca are one of the key initial investors in Moderna and a major shareholder? So it doesn’t matter to them if their AstraZeneca injection becomes the fall guy for mRNA shots – they profit either way!

    And guess what they focused on? Heart disease and cancer (any time you see the word ‘oncology’, think cancer).

    Moderna Clearly Expects a Lot of Cancer

    Moderna went batshit and agreed a lot of partnerships with major pharmaceutical firms and fired up a lot of oncology (cancer) related spin-offs.

    Even in their own timeline, they spun-off ‘Onkaido Therapeutics’ to research cancer, partnered with Merck to advocate “personalised” cancer vaccines, and then produced mRNA injections, mRNA-4157, for tumours.


    They also launched ‘Caperna LLC’, again focusing on personalised cancer vaccines.

    Flagship Pioneering (Moderna) Gets into Bed with Pfizer


    Moderna love-in Flagship Pioneering got into bed with Pfizer to do a $100 million drug discovery jaunt in July 2023. What type of drugs, they mysteriously didn’t say. Pfizer said their breakthroughs would “change patients’ lives”. They didn’t say for the better.

    This isn’t forgetting that earlier in 2023 Pfizer bought out Seagan for a whopping $43 billion in order to develop cancer drugs.


    Flagship Pioneering (Moderna) Gets into Bed With Novo Nordisk

    The target? Heart disease and “rare diseases” (it’s only “rare”):

    Established in 2022, after it was found the Moderna injections cause myocarditis. Convenient.

    The Daily Beagle Smells a Rat – Merck Again

    Despite being rightly lambasted for making a harmful, murderous product and taking a beating with stocks and shares, on about 12 December 2023, Moderna started to mysteriously climb, and The Daily Beagle smelled a rat.


    And a rat it was. On the 14 December Moderna and Merck bragged their little jaunt into personalised cancer vaccines – vaguely worded as “a powerful new cancer therapy” – was “in the works.” We wonder if it’s as “safe and effective” as the myocarditis inducing covid-19 injections.

    What a great way to profit. Introduce DNA with transfection agents that cause insertational mutagensis (read as: Cause foreign DNA to enter your DNA and cause cancer), then profit from the resulting spike in cancer cases.


    Cancer, Cancer Everywhere

    Moderna’s entire theme seems to be primarily cancer focused. Besides the partnerships with AstraZeneca, Pfizer, Merck, Novo Nordisk, Aldevron, NIH and more, it turns out Moderna is even more focused on cancer (somehow).

    Take former FDA commissioner Stephen Hahn, for example, the man who betrayed the American public for a cushy job at Flagship Pioneering:


    He specialises in oncology (cancer), having been part of the National Cancer Institute, American Association for Cancer Research, and American Society for Radiation Oncology. Conveniently this also means Moderna has influence over cancer research (read as: No investigating any Moderna-related causes of cancer).

    University of Texas Cancer Corruption

    In another tangled web of cancer-related corruption, MD Anderson Cancer Centre are owned by the Koch brothers. Koch financed the likes of Moderna’s Bob Langer’s lab and gave Moderna investor Timothy Springer a monetary award.

    MD Anderson Cancer Centre, were involved in controversy when the President, Ronald DePinho, was found to own stocks in Aveo Oncology, a company whose drugs University of Texas would be assessing in clinical trial, at none other than… the MD Anderson Cancer Centre.

    We bet it is exciting … for your bank account.

    Unsurprisingly, the corrupt University of Texas investigated itself and found itself innocent, using the meaningless term “blind trust” with zero transparency on the arrangement. University of Texas wheeled out the usual nonsense that financial conflicts of interest were somehow in the patients’ best interests.


    Surely they mean the best interests of the investors, University of Texas itself! And what safeguards? You kept the stocks and the clinical trial.

    Any Cure for The Cancer That Is Corruption?

    Apparently not.

    Even now, Moderna CEO Stéphane Bancel is somehow selling off 40,000 shares a pop via automatic sells, without somehow reducing the total number of shares he holds (???):


    Apparently Moderna can just print itself as many shares for profit as it wants, on account of how many departments and institutions it controls.

    Oh, and to top it off, Moderna are even in bed with charities. Oxfam America (you know, of Oxfam child rapists fame) filed a SEC complaint that Moderna had committed fraud and misled investors (read as: Oxfam America is an investor in Moderna).

    Tip of the Iceberg

    Phew, that’s a lot to go over. No doubt there’s more, however we’ll be cutting it here for now as it is a lot to go over. It is surprising how much influence and control Moderna have consolidated in such a short space of time, and no doubt corruption is rife abounds elsewhere too.



    https://expose-news.com/2024/01/03/modernas-influence-over-the-us-and-uk
    Moderna’s influence over the US and UK governments is more than most realise Rhoda WilsonJanuary 3, 2024 The sheer sprawl, corruption, influence and involvement of Moderna in politics and the wider medical industry is staggering. It is difficult to convey and harder to comprehend, The Underdog writes. Months before a pandemic was declared in 2020, World Economic Forum Young Global Leader and CEO of Moderna Stéphane Bancel told his staff that there was going to be a pandemic and Moderna would need to manufacture a billion doses of vaccine the “next year,” being 2021. How did Bancel know? A recent article written by The Underdog may provide some insight which lays out his/her findings relating to Moderna infiltrating the USA and UK governments as well as academia. The Underdog is a non de plume for someone who self-describes as a citizen journalist and publishes articles on a Substack page titled ‘The Daily Beagle’. In the USA, Moderna took control of the FDA and Operation Warp Speed, and influenced NIH and BARDA, The Underdog says. Adding that Moderna controls the UK government through Installed Prime Minister Rishi Sunak. As well as governments, The Underdog surmises that Moderna has compromised academics in universities in the USA and Canada. For previous articles we’ve published that relate to and complement The Underdog’s article, please see ‘Rishi Sunak, Thélème and Moderna’ and various other articles HERE. Let’s not lose touch…Your Government and Big Tech are actively trying to censor the information reported by The Exposé to serve their own needs. Subscribe now to make sure you receive the latest uncensored news in your inbox… Murderous Moderna’s Infiltration of Politics By The Underdog Murder, They Wrote Let us clarify murderous: a peer-reviewed study found that myocarditis in under 40-year-old males was higher in those who had taken all vaccines, and those who had taken a second dose of mRNA-1273, the Moderna covid injection. It was so bad that Sweden, Norway, and Finland suspended the use of the Moderna vaccine in young people, as noted in the British Medical Journal (“BMJ”). As previously known, the US National Institutes of Health (“NIH”) and their corrupt cohorts attempted to censor evidence that myocarditis has a fatality rate of 50% within 5 years. So it isn’t unreasonable to assert Moderna has in all likelihood murdered at least 50% of those with myocarditis caused by the Moderna injections; of which will include children. Like in an attempt to discourage people from getting the poisonous shots without declaring that they’re harmful and recalling them, Moderna recently jacked up the price of their injections to $130. A reminder Moderna produced injections that contained stainless steel contaminants. It cost only $2.85 to manufacture and despite this, the US government paid $15 to $26 a dose. Why? Moderna Have Infiltrated the Government Seems pretty incredulous, but no. Moderna Is Part of WEF Stéphane Bancel was “elected” 2009 Young Global Leader by the World Economic Forum (“WEF”). Bancel was founding chief executive officer for Moderna and joined Flagship Pioneering in 2013. Noubar Afeyan, co-founder of Moderna and CEO of Flagship Pioneering, “received a Technology Pioneer 2012 award from the World Economic Forum”. Noubar also “served as Chairman of the Global Agenda Council on Chemicals, Advanced Materials and Biotechnology of the World Economic Forum as well as being a member of the Meta-Council on Emerging Technologies.” Moderna Took Control of Operation Warp Speed Moncef Slaoui, owning 82,508 Moderna shares on 21 February 2020, stepped down from Moderna, divested his stake, and went on to lead Operation Warp Speed. As it just so happened, the US government spent over $4 billion on Moderna, twice as much as any other pharmaceutical company: During this time of taking fat wads of government cash, Moderna also received heavy investment from hedge funds in September 2020. Moderna Influenced NIH, BARDA The NIH in December 2020 bragged how they worked with Moderna in a partnership, along with BARDA (Biomedical Advanced Research and Development Authority) and NIAID (National Institute of Allergy and Infectious Diseases) Vaccine Research Centre to develop the myocarditis inducing mRNA-1273 injection: Factoring in that the NIH deleted evidence of the myocarditis fatality rate implicating firms such as Moderna and the NIH itself, this shouldn’t be surprising. Moderna ultimately got into a fight with NIH over mRNA patents, with Moderna insisting they did everything. Current NIH director Francis Collins remarked the NIH played “a major role in the development of the vaccine,” in which Moderna received approximately $10 billion in government funding. Moderna paid the NIH their bribe patent money, to the tune of $400 million, just under half a billion, but held dispute over another patent. To try to appease the NIH, Moderna offered co-ownership of the vaccine patent with NIH. Curiously, an NIH employee, Philip Leder, worked on mRNA research decades before NIH’s agreement with Moderna. They conveniently died in 2020. Moderna Took Control of the FDA Stephan Hahn Stephen Hahn, former FDA Commissioner who insisted he’d fast-track the covid-19 injections, left the FDA to go join Flagship Pioneering after approving the injections. He claimed Donald Trump told him “to authorise a covid-19 vaccine or go.” Flagship Pioneering are a venture capital firm that financed and kickstarted Moderna. The CEO of Flagship Pioneering, Noubar Afeyan, also co-founded Moderna. So, they’re essentially one and the same. Moderna LLC was the successor in interest to Moderna Therapeutics, Inc., a Delaware corporation incorporated in 2009 as Newco LS18, Inc. by Flagship Pioneering. SEC EDGAR filing on Moderna LLCnone One of the founding investors of Moderna, Bob Langer, also previously worked on the FDA’s advisory board according to his own biography, serving as both a member and later the chairman: It is likely Bob retained contacts within the FDA even after leaving. Moderna Control the UK Government This isn’t hyperbole. We wish it were. The UK government signed a memorandum of understanding with Flagship Pioneering: This includes a spin-off company called Quotient Therapeutics: The UK government also formed an unusually aggressive and expansive 10-year contract with Moderna, worth at least £1 billion for a “new vaccine centre” – despite the fact these are genetic modification injections. This was agreed during Rishi Sunak’s tenure as Prime Minister. Moderna de facto Control the Prime Minister The investment will benefit current unelected pharmaceutical bureaucrat Rishi Sunak, who is the Prime Minister of the United Kingdom (read as: Moderna have influence of the UK government). Unelected Prime Minister Rishi Sunak Rishi was also formerly Chancellor of the Exchequer (read as: controlled the UK government purse strings) back in 2020, and allocated even more funds to the vaccine industry during that time. He bragged how it was a “success.” For his bank account, we surmise. How will he benefit? Rishi Sunak co-founded a firm called Thélème Partners LLP (aka. Thélème) back in 2009, registered in the Cayman Islands, along with co-founder and former French Navy Patrick Degorce, after they previously met at The Children’s Investment Fund (“TCIF”). TCIF was run by billionaire Chris Hohn. Rishi Sunak appointed Thélème partner John Sheridan as an advisor to government during his time as Chancellor of the Exchequer. Thélème started with an initial investment fund of £536m, and were early backers of Moderna. Thélème co-founder Degorce invested in Moderna over a decade ago, meaning their rise was also Rishi Sunak’s rise. Thélème are Moderna’s single largest hedge fund investor, despite Thélème cutting their exposure by 11%. On 30 September 2023, Thélème disclosed ownership of 6,897,612 shares of Moderna, Inc. (US:MRNA) valued at $712,454,343 USD, more than half a billion. The name Thélème is likely based upon the French ‘Abbaye de Thélème’, an idea invented by French monk Rabelais, who gives his vision of an “ideal and utopian abbey.” The “Thelemites of the Abbey” follow “do what thou wilt”. Occultist Aleister Crowley declared a so-called “Theleme religion” whose central belief was “do what thou wilt”, even remarking “There is no law beyond do what thou wilt.” Unsurprisingly, Moderna plant Rishi Sunak did whatever he wanted and declined to say that he did not profit from the Moderna injections. He claims to have left the firm in 2013 and that his finances are in a so-called “blind trust,” along with 10 other ministers. There’s no legal definition of a “blind trust” so this is pure theatre. Given he’s the original founder of Thélème, he no doubt has shares and investments and still stands to profit from Moderna’s success, explaining why he gave Flagship Pioneering favourable treatment and Moderna a 10-year contract on a plate. This is the same Rishi who tried to “break banks” during the 2008 collapse. On another note… Moderna Have Compromised Academia Bear in mind academic institutions are involved in peer-reviewed processes, clinical research and more, so this has wider, damning ramifications. Moderna were formed within the heart of academia. Moderna Have Control In MIT Noubar Afeyan Noubar Afeyan, CEO of Flagship Pioneering, studied at MIT (Massachusetts Institute of Technology). He was recently installed in MIT Corporation’s board of trustees. The purpose of the trust? (Emphasis added): […] to see that the Institute adheres to the purposes for which it was chartered and that its integrity and financial resources are preserved for future generations as well as for current purposes. […] “About the Corporation”, MIT Corporation pagenone Control of the finances. And integrity. During the founding period of Moderna, Noubar Afeyan joined the likes of MIT Bob Langer. Langer, since investing in Moderna, has now become a billionaire as a result. MIT Mandates the Covid-19 Injection, That MIT Based Modern Just Happens to Sell Profitably for MIT-inspired Moderna, during Moderna’s rise, MIT adopted a vaccine mandate, one where MIT reported there were still covid-19 cases anyway and that they weren’t mild: They huffed the copium and tried to argue there were no Omicron-related hospitalisations (Omicron is deemed the mildest of the covid-19 set), but conveniently omitted Alpha, Delta, and the others, implying there were other variant hospitalisations (read as: The injections they mandated for profits, didn’t work). Noubar Afeyan and MIT’s Bob Langer are also joined by investor Derrick Rossi (Harvard), after they learn they can reprogram human cells and reverse them back into pluripotent stem cells based on Harvard Derrick Rossi’s research. Notice it involves using mRNA to change human cells (read as: Modify their DNA). Rossi is head of the Harvard Department of Stem Cell and Regenerative Biology. Current Moderna CEO Stéphane Bancel also studied at Harvard. Rossi approached Harvard faculty member Timothy Springer asking him to invest in Moderna, which he did so. In April 2021, Timothy Springer was declared a billionaire by Cord Magazine. Back patting their own, Timothy Springer went on to receive a Lasker award, and a Robert Koch prize. The Koch brothers also finances MIT Bob Langer’s lab: In a surprise to no-one, Harvard also mandated the injection from which they stand to profit. This included for Harvard staff, flushing out anyone critical of the financial abuses by the vaccine industry. Bearing in mind the majority of Moderna directed Operation Warp Speed financing went to Moderna, the majority of the injections that would have been available would have also been primarily Moderna, guaranteeing their selfish, harmful, murderous profit Remember: Those below the age of 40 are adversely affected by myocarditis, and the majority of students on campus would be below that age; 50% fatality rate within 5 years for myocarditis. University of Toronto, As Well – Maybe Even the Canadian Government? The Academia orgy was apparently not big enough, and the University of Toronto wanted some, giving Derrick Rossi an “honorary degree”. University of Toronto are particularly interesting because they’re one of a handful of “kingmaker universities” in Canada. When investigating Acuitas Therapeutics, The Daily Beagle remarked: The only University with more Canadian Prime Ministers is University of Toronto, with Arthur Meighen, W.L. Mackenzie King, Lester B. Pearson, and Paul Martin. It is very likely a lot of ministers for the Canadian government also come from the University of Toronto. So, the University of Toronto’s corrupt love-in with Moderna implies Moderna also has influence over the Canadian government. And in surprise to no-one, the University of Toronto also anti-competitively mandated the emergency authorisation injections: You know, the same injections Health Canada admitted contained plasmid DNA, the same kind Moderna used in partnership with Aldevron. What is it with academic universities mandating the injections from which they stand to benefit financially? Moderna are in Bed with Multiple Major Pharmaceutical Companies To give you an idea how deep this shell game goes, did you know that AstraZeneca are one of the key initial investors in Moderna and a major shareholder? So it doesn’t matter to them if their AstraZeneca injection becomes the fall guy for mRNA shots – they profit either way! And guess what they focused on? Heart disease and cancer (any time you see the word ‘oncology’, think cancer). Moderna Clearly Expects a Lot of Cancer Moderna went batshit and agreed a lot of partnerships with major pharmaceutical firms and fired up a lot of oncology (cancer) related spin-offs. Even in their own timeline, they spun-off ‘Onkaido Therapeutics’ to research cancer, partnered with Merck to advocate “personalised” cancer vaccines, and then produced mRNA injections, mRNA-4157, for tumours. They also launched ‘Caperna LLC’, again focusing on personalised cancer vaccines. Flagship Pioneering (Moderna) Gets into Bed with Pfizer Moderna love-in Flagship Pioneering got into bed with Pfizer to do a $100 million drug discovery jaunt in July 2023. What type of drugs, they mysteriously didn’t say. Pfizer said their breakthroughs would “change patients’ lives”. They didn’t say for the better. This isn’t forgetting that earlier in 2023 Pfizer bought out Seagan for a whopping $43 billion in order to develop cancer drugs. Flagship Pioneering (Moderna) Gets into Bed With Novo Nordisk The target? Heart disease and “rare diseases” (it’s only “rare”): Established in 2022, after it was found the Moderna injections cause myocarditis. Convenient. The Daily Beagle Smells a Rat – Merck Again Despite being rightly lambasted for making a harmful, murderous product and taking a beating with stocks and shares, on about 12 December 2023, Moderna started to mysteriously climb, and The Daily Beagle smelled a rat. And a rat it was. On the 14 December Moderna and Merck bragged their little jaunt into personalised cancer vaccines – vaguely worded as “a powerful new cancer therapy” – was “in the works.” We wonder if it’s as “safe and effective” as the myocarditis inducing covid-19 injections. What a great way to profit. Introduce DNA with transfection agents that cause insertational mutagensis (read as: Cause foreign DNA to enter your DNA and cause cancer), then profit from the resulting spike in cancer cases. Cancer, Cancer Everywhere Moderna’s entire theme seems to be primarily cancer focused. Besides the partnerships with AstraZeneca, Pfizer, Merck, Novo Nordisk, Aldevron, NIH and more, it turns out Moderna is even more focused on cancer (somehow). Take former FDA commissioner Stephen Hahn, for example, the man who betrayed the American public for a cushy job at Flagship Pioneering: He specialises in oncology (cancer), having been part of the National Cancer Institute, American Association for Cancer Research, and American Society for Radiation Oncology. Conveniently this also means Moderna has influence over cancer research (read as: No investigating any Moderna-related causes of cancer). University of Texas Cancer Corruption In another tangled web of cancer-related corruption, MD Anderson Cancer Centre are owned by the Koch brothers. Koch financed the likes of Moderna’s Bob Langer’s lab and gave Moderna investor Timothy Springer a monetary award. MD Anderson Cancer Centre, were involved in controversy when the President, Ronald DePinho, was found to own stocks in Aveo Oncology, a company whose drugs University of Texas would be assessing in clinical trial, at none other than… the MD Anderson Cancer Centre. We bet it is exciting … for your bank account. Unsurprisingly, the corrupt University of Texas investigated itself and found itself innocent, using the meaningless term “blind trust” with zero transparency on the arrangement. University of Texas wheeled out the usual nonsense that financial conflicts of interest were somehow in the patients’ best interests. Surely they mean the best interests of the investors, University of Texas itself! And what safeguards? You kept the stocks and the clinical trial. Any Cure for The Cancer That Is Corruption? Apparently not. Even now, Moderna CEO Stéphane Bancel is somehow selling off 40,000 shares a pop via automatic sells, without somehow reducing the total number of shares he holds (???): Apparently Moderna can just print itself as many shares for profit as it wants, on account of how many departments and institutions it controls. Oh, and to top it off, Moderna are even in bed with charities. Oxfam America (you know, of Oxfam child rapists fame) filed a SEC complaint that Moderna had committed fraud and misled investors (read as: Oxfam America is an investor in Moderna). Tip of the Iceberg Phew, that’s a lot to go over. No doubt there’s more, however we’ll be cutting it here for now as it is a lot to go over. It is surprising how much influence and control Moderna have consolidated in such a short space of time, and no doubt corruption is rife abounds elsewhere too. https://expose-news.com/2024/01/03/modernas-influence-over-the-us-and-uk
    EXPOSE-NEWS.COM
    Moderna’s influence over the US and UK governments is more than most realise
    The sheer sprawl, corruption, influence and involvement of Moderna in politics and the wider medical industry is staggering. It is difficult to convey and harder to comprehend, The Underdog writes.…
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  • Health benefits of the Sun: Vitamin D can reduce the risk of cancer by as much as 67%
    Rhoda WilsonDecember 28, 2023
    Vitamin D is involved in the biology of all cells in your body, including your immune cells. A large number of studies have shown raising your vitamin D level can significantly reduce your risk of cancer.

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

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

    Higher Vitamin D Levels Lower Cancer Risk

    By Dr. Joseph Mercola

    This article was originally published on 10 April 2017.

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

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

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

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

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

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

    Research Again Concludes Vitamin D Lowers Cancer Risk

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

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

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

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

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

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

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

    Vitamin D Status Is Strongly Correlated with Cancer Risk

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

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

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

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

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

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

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

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

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

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

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

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

    How to Minimise Your Risk of Skin Cancer from Sun Exposure

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

    Sources and References

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

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




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

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

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

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

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

    Project Defuse detailed plans to investigate and manipulate coronaviruses with the potential to infect humans — but experts insist it is not a smoking gun

    "The documents form a grant proposal from 2018 for a pre-pandemic collaboration between US and Chinese scientists. The proposal described how coronaviruses could be found, combined and cultured with the ability to infect human cells. The stated idea was to find ways to protect against the emergence of zoonotic viruses.

    The proposal of more than a thousand pages, released after a freedom of information request, outlines the full details of the plans. Michael Lin, associate professor of neurobiology and bioengineering at Stanford University, called the full document “quite shocking.”

    Lin said that it did not constitute a recipe to make Sars-CoV-2, as some have claimed. “However,” he wrote on Twitter/X, “the intention was to identify natural viruses with features that would help them infect cells. So it may be not much of a difference functionally.”

    Proponents of the “lab leak hypothesis” argue that even if the original proposal was rejected by the US funding agency Darpa, it could have been carried out anyway in China, perhaps using updated protocols.

    Cummings said the latest release showed that scientists “planned to engineer changes that match just what we see in Covid and it’s unarguable that the US and UK governments have covered this up”.

    Writing on his blog, he said: “In spring 2020 Whitehall’s top scientists and the top intelligence officials walked into the PM’s office and told the PM and me that lab leak ‘is definitely false’ and ‘a conspiracy theory’.”

    He added that one of his own advisors, James Phillips, formerly a neuroscientist, said at the time that their confidence was misplaced. Cummings implied that his subsequent attempts to expose what he called the “monumentally false advice” Johnson received on this topic were redacted by the Covid Inquiry." Tom Whipple

    https://www.thetimes.co.uk/article/rejected-wuhan-research-project-hints-at-origins-of-pandemic-znpwzgm2k

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    Rejected Wuhan research project hints at origins of pandemic Project Defuse detailed plans to investigate and manipulate coronaviruses with the potential to infect humans — but experts insist it is not a smoking gun "The documents form a grant proposal from 2018 for a pre-pandemic collaboration between US and Chinese scientists. The proposal described how coronaviruses could be found, combined and cultured with the ability to infect human cells. The stated idea was to find ways to protect against the emergence of zoonotic viruses. The proposal of more than a thousand pages, released after a freedom of information request, outlines the full details of the plans. Michael Lin, associate professor of neurobiology and bioengineering at Stanford University, called the full document “quite shocking.” Lin said that it did not constitute a recipe to make Sars-CoV-2, as some have claimed. “However,” he wrote on Twitter/X, “the intention was to identify natural viruses with features that would help them infect cells. So it may be not much of a difference functionally.” Proponents of the “lab leak hypothesis” argue that even if the original proposal was rejected by the US funding agency Darpa, it could have been carried out anyway in China, perhaps using updated protocols. Cummings said the latest release showed that scientists “planned to engineer changes that match just what we see in Covid and it’s unarguable that the US and UK governments have covered this up”. Writing on his blog, he said: “In spring 2020 Whitehall’s top scientists and the top intelligence officials walked into the PM’s office and told the PM and me that lab leak ‘is definitely false’ and ‘a conspiracy theory’.” He added that one of his own advisors, James Phillips, formerly a neuroscientist, said at the time that their confidence was misplaced. Cummings implied that his subsequent attempts to expose what he called the “monumentally false advice” Johnson received on this topic were redacted by the Covid Inquiry." Tom Whipple https://www.thetimes.co.uk/article/rejected-wuhan-research-project-hints-at-origins-of-pandemic-znpwzgm2k ➡️ Boost RobinMG 🚀
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    Rejected Wuhan research project hints at origins of pandemic
    Project Defuse detailed plans to investigate and manipulate coronaviruses with the potential to infect humans — but experts insist it is not a smoking gun
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