• https://www.zerohedge.com/medical/those-who-are-vaxxed-and-boosted-may-have-immune-imprinting-ignores-new-jabs
    https://www.zerohedge.com/medical/those-who-are-vaxxed-and-boosted-may-have-immune-imprinting-ignores-new-jabs
    WWW.ZEROHEDGE.COM
    Those Who Are 'Vaxxed And Boosted' May Have 'Immune Imprinting' That Ignores New Jabs
    Immune imprinting occurs when previous exposures leave such a strong immune memory that the body continues to produce antibodies targeting the past experience.
    Angry
    1
    0 Comments 0 Shares 86 Views
  • DNA contamination in Covid vaccines DOES get into human cells, new evidence shows
    It also appears that the contamination enters the cell nucleus and integrates with human DNA

    Rebekah Barnett
    Regulators and fact checkers claim that plasmid DNA contamination in the mRNA Covid vaccines can’t change your genomic DNA, but new evidence suggests that it actually can.

    The fact checkers assert that DNA contamination poses no risk to your genomic DNA because your body will naturally destroy any contaminant DNA before it even gets into the cells.

    Even if the contaminant DNA could get into cells, there’s no way it can enter the cell nucleus, where genomic integration events occur, they say.

    And even if the contaminant DNA could enter the nucleus, which it can’t, it still couldn’t genomically integrate unless specific enzymes are present, they say.

    However, results from independent lab testing conducted on ovarian cancer cell lines show that contaminant DNA from Pfizer’s Covid vaccine not only crossed into the cells, but that it survived multiple cell divisions. This is suggestive that the contaminant DNA is able to transfect (enter) the cell nucleus, and that it integrated with the human cell DNA.

    TLDR

    1. Scientists claim that Pfizer vaccine contaminant DNA has been detected in ovarian cancer cell line DNA, but they do not yet know if it’s chromosomal (heritable) or extra-chromosomal DNA (not heritable)

    2. This is an in vitro (in a lab dish) finding, and needs to be replicated in vivo (in a human patient)

    3. As the finding is specific to cancer cell lines, it is not generalisable, but scientists say it may give an indication of what cancer patients in remission could experience after mRNA Covid vaccination

    4. This finding calls into question fact checker claims that mRNA Covid vaccine DNA contamination can't enter cells, can't enter the nucleus, and cannot integrate with human DNA.
    Last year, Boston-based genomics scientist Kevin McKernan made the shocking discovery that the mRNA Covid vaccines are contaminated with excessive levels of plasmid DNA, an artefact of the vaccine production process.

    McKernan’s findings were soon confirmed by multiple independent labs around the world for both the Pfizer and Moderna mono- and bi-valent vaccines, including lots approved for children, with one Canadian study led by Dr David Speicher concluding that there are “billions to hundreds of billions of DNA molecules per dose.”

    Scientists including McKernan, University of South Carolina cancer genomics scientist Dr Phillip Buckhaults, and Dr Wafik El-Diery, head of the Cancer Centre at Brown University, expressed concerns that fragments of plasmid DNA contamination could cause adverse events, autoimmune problems and cancers in some patients.

    But perhaps most significantly, there is also a theoretical risk of the contaminant DNA integrating with patients’ chromosomal DNA and modifying the human genome. This is of particular concern with the Pfizer vaccine, which contains an SV40 enhancer sequence, used in gene therapies “to drive DNA into the nucleus,” explains McKernan.

    While regulators have taken a ‘wait and see’ approach, independent scientists, including McKernan, have been more proactive, initiating experiments testing for evidence of genomic integration.

    Now, the first results are in.

    In an experiment conducted together with German molecular biologist Dr Ulrike Kämmerer, McKernan has detected vaccine contaminant DNA in ovarian cancer cell lines treated with Pfizer’s Covid vaccine.

    The scientists found a chimeric combination of human ovarian cell line DNA and spike sequence DNA derived from the contaminating plasmid at at least one, and possibly two sites.

    “If anything, this work has put to bed the question regarding if this contaminant DNA gets into the cell, and the chimeric human and contaminant spike DNA sequences imply it has entered the nucleus,” McKernan says.

    “The PCR and sequencing data both demonstrate the vaccine is getting into the cell and surviving cell passaging. It is likely bioactive and being partially replicated.”

    To reach this finding, Dr Kämmerer first treated ovarian cancer cell lines with mRNA Covid vaccines, using cells treated with AstraZeneca and Janssen vaccines as controls.

    The cells were then ‘passaged’, meaning they were left to divide and replicate numerous times. This has the effect of “rinsing away residual vaccine,” explains McKernan.

    Immunohistochemistry (IHC) was then performed, a staining process that Dr Kämmerer used to detect levels of spike protein expression produced by the vaccine modified-RNA.

    This was to confirm that the lipid nanoparticles (LNPs) carrying mod-RNA and plasmid DNA contamination “did their job and delivered the payload,” says McKernan. Measuring how many cells expressed spike protein also allowed the scientists to determine how much of the vaccine to treat the cells with.


    Immunohistochemistry performed with Pfizer top left, AstraZeneca top right as a control. Source: Kevin McKernan’s Substack
    Cell lines were then sent in cold storage to McKernan’s Boston lab, where his team used qPCR to screen which samples to sequence the cell line DNA.

    “What we found is, [contaminant] DNA that is getting transfected into ovarian cancer cell lines is replicating in the cells,” says McKernan, noting that the ratio of vaccine contaminant DNA to human cell DNA was “higher than we expected.”

    Chimeric sequences of human and vaccine contaminant DNA were detected at two sites: chromosomes 9 and 12, with the evidence for the latter being the strongest. “But we don't know if it's extra-chromosomal or whether it's chromosomal because of the Illumina (short read) method we used to sequence,” explains McKernan.


    Source: Kevin McKernan’s Substack
    Extra-chromosomal DNA is not part of the chromosome, and is therefore less likely to replicate and to be heritable. Chromosomal DNA, on the other hand, is heritable and more likely to be replicated. A third category, mitochondrial DNA, is heritable, but only from the maternal line.

    You can read a detailed account of methods and findings via McKernan’s Substack article, ‘Vaccine targeted qPCR of Cancer Cell Lines treated with BNT162b2.’

    ‘Major advance,’ but clinical implications are limited

    McKernan emphasises that these findings cannot be generalised, stating that “it is too early to make comments on the clinical implications.”

    “The study is performed in ovarian cancer cell lines. It is not performed in patient cells, but this is a proxy for what might happen in an ovarian cancer patient who's in remission,” says McKernan, especially as there is evidence that the LNPs go to the ovaries.

    The risk for patients in this scenario is that integration events with contaminant DNA might cause aberrant cell growth, which poses a risk to immune suppression of new cancer cells.

    McKernan notes that his experiment only picked up on putative integration events that persisted after multiple cell replications. That is to say, the scientists were not able to detect integration events that may have occurred, but then died off immediately.

    At the moment, no one knows how many integration events might be occurring, or what effect that would have on patients. “The unknowns are just exponential,” says McKernan.

    The cancer cell line experiment can be said to be “a microcosm of genome integration of contaminated DNA,” said Japanese molecular oncology scientist Hiroshi Arakawa, in his own analysis of McKernan and Dr Kämmerer’s experiment, published to his popular science blog on which he shares critical views on Covid vaccine safety.

    Akira calls the two possible integrations observed in Dr Kämmerer’s experiment a “major advance” laying the ground for further experimentation. “What happens in cultured cells can also occur in normal cells, and a wide variety of abnormalities can occur depending on the site of genome integration,” such as “the induction of cancer or malignant transformation,” he wrote (translated from Japanese to English).

    LNPs deliver contaminant DNA straight to the cells

    A key assumption underlying claims that mRNA Covid vaccine contamination cannot enter the cell nucleus, and cannot genomically integrate with host DNA, is that the contamination will never make it into dividing cells, which would be required for integration to occur.

    This is based on the assumption that the LNPs containing both mod-RNA and contaminant DNA mostly stay in the muscle at the injection site. As muscle cells do not divide, there’s no problem, the logic goes.

    This is misleading, however, as Pfizer’s own biodistribution data shows that the LNPs enter the blood and every major organ system, including the ovaries, as mentioned above. While it is true that muscle cells don’t divide, LNPs distributed around the body can transfect any number of dividing cells in various organ systems.


    Table 4-2. shows biodistribution of LNPs, Pfizer Nonclinical Evaluation Report, 2021
    From there, it’s only a matter of time before the LNP contents get into the cell nucleus, says McKernan. “In any dividing cell, the nucleus dissolves. So, when people say the DNA can get into the cytoplasm [inside the cell membrane] but won't get into the nucleus, well, in any dividing cell, it will end up getting into the nucleus.”

    It is possible that the dissolution of the cell nucleus during division is the mechanism underlying McKernan and Dr Kämmerer’s observed passaging of contaminant DNA, but further research will be required to confirm or disprove this hypothesis.

    Because of the effectiveness of LNPs in delivering their contents into cells, McKernan, Dr Buckhaults and Dr Speicher have questioned the suitability of the current regulatory limits on contaminant DNA in vaccines, which were set prior to the introduction of LNP technology in vaccines.

    Regulators unconcerned

    I sent McKernan’s Substack article documenting the new DNA integration findings to Australia’s drug regulator, the Therapeutic Goods Administration, for comment.

    The TGA did not address the new findings, but a spokesperson from the TGA responded,

    “The Department of Health and Aged Care has every confidence in the safety, quality and efficacy of the various approved COVID-19 vaccines for use in Australia. The TGA’s assessment of all vaccines is based upon high quality evidence, including studies and reviews published in peer-reviewed scientific and clinical journals.”

    However, when asked previously to provide evidence for its position that Covid vaccines pose no risk of DNA integration, the TGA provided no peer-reviewed scientific evidence to support its claims.

    Instead, the TGA provided links to a Mayo Clinic fact page with no scientific citations, an article by the discredited RMIT FactLab, and a scientific commentary article suggesting that in vitro findings cannot be generalised.

    Furthermore, TGA has not been forthcoming with the evidence it does hold. When asked to release Covid vaccine batch testing results under Freedom of Information, the regulator provided all 74 pages - fully redacted.

    In the US, the Food and Drug Administration (FDA) denied that contaminant DNA in the mRNA vaccines can enter the nucleus or pose any threat to patients’ genomic DNA, in a response to concerns raised by Florida Surgeon General, Dr Joseph A. Ladapo in December of last year.

    Additionally, the FDA misleadingly refuted the presence of SV40 proteins in the vaccines, when in fact Dr Ladapo raised concerns over the presence of an SV40 enchancer sequence in the Pfizer vaccine, as confirmed by Health Canada and numerous independent laboratories.

    Such ham-fisted mischaracterisation of a gene therapy sequence by the FDA is suggestive of either gross incompetence, or a disinformation play. Both are concerning.

    Science journalist Maryanne Demasi reported, in November last year, that the FDA shut down her enquiries into the DNA contamination matter, refusing to confirm if it found levels of DNA that exceeded acceptable levels, or if it was investigating further.

    The presence of contamination has been officially acknowledged by the European Medicines Agency (EMA) and Health Canada, with the latter also acknowledging the presence of the SV40 enhancer sequence, though both regulators deny that the amounts exceed regulatory limits, or that the DNA contamination poses any risk.

    ‘No excuse’ for ignoring ‘screaming hot signal’

    Instead of denying excessive DNA levels and deferring to manufacturers’ reported test results, regulators should run their own qPCR testing on batch lots, says McKernan.

    Then, “they would see what everyone else is seeing, which is that sometimes the CT scores come out as low as 13… that’s a screaming hot signal.”

    “As a reference, the Covid test would call people positive at 33-35,” McKernan explains. “That’s a million-fold difference (20 CTs). A million-fold less Covid RNA and you're positive and quarantined. But you can inject a million-fold more past your mucosa?”

    There’s “no excuse” for regulators to not sequence every vaccine lot, says McKernan, when the costs for doing so have dropped dramatically in recent years.

    “DNA sequencing costs have dropped 100,000 fold in the last decade. They have relaxed the DNA contamination limits 1000-fold in this time frame. It likely only costs $1,000 in reagents for millions-to-billions of dollars worth of product.”


    Source: National Human Genome Research Institute
    DNA sequencing by regulatory agencies is important not just for measuring quantities, says McKernan, but also for determining the type of DNA contamination.

    “Not all DNA is created equal. Some is designed to replicate - when it gets into a cell, it can make more of itself. It's a massive loophole in the regulations that they don't do sequencing. But it's never been cheaper. You can precisely know the nature of the DNA in every single vial.”

    Scientists pick up regulators’ slack

    In the absence of any regulatory appetite for investigating the risks of DNA contamination in the mRNA Covid shots, and particularly the risk of genomic integration, independent scientists have taken the baton.

    “We are writing up our findings and will publish a preprint soon,” says McKernan, who is planning further testing in partnership with Dr Kämmerer. “We’re doing more experiments first. We need to sequence deeper to find out if the integration events are in chromosomal or extra-chromosomal DNA.”

    Dr Buckhaults is also running his own experiment, calling for de-identified samples of tumours or fresh blood from pathology and hematology labs. These samples will be tested for the presence of plasmid DNA contamination, with whole genome sequencing to then be carried out on positive samples to identify genomic integration sites.

    In an email outlining his experiment, Dr Buckhaults told me that he intends to report his findings in a peer-reviewed publication, predicting that the work could take “a few months to a year,” depending on how fast samples come in.

    “I am hopeful to prove my concerns are unwarranted by accumulating a lot of negative data, and of course negative data takes the most time to collect,” he said.

    McKernan says he is aware of other labs running tests for contaminant plasmid DNA integration, but cannot disclose the details at present.

    Decentralisation the future of science?

    McKernan says he has experienced some pushback for publishing his methods and findings in real time via Substack, X, and preprints. But, he believes that making his data available as quickly as possible is a way for the field of science to regain public trust.

    “Many will criticize our disclosure of preliminary findings but we feel this is an insult to the intelligence of the average person,” says McKernan.

    “It's a form of scientific elitism that implies people can't handle the truth and will be scared like sheep if given a glimpse of how the true scientific process is performed. Scientists are 90% of the time wrong but only publish the times when they are right. There is no journal of negative results.“

    In light of the prospect that most published research findings are false (as famously asserted in a 2005 article by Professor John Ioannidis), McKernan questions the value of peer-review, instead favouring replication or refutation in the real world.


    Source: X
    For this reason, McKernan says he has not prioritised peer-reviewed publication for his DNA contamination findings, but is rather focusing on conducting more experiments and releasing the data as he goes - even when it’s incomplete, or requires further experimentation.

    “We were not expecting to find any integration events at this depth of coverage, but they are evident to anyone who downloads our public reads. To not speak to obvious evidence in such data would be irresponsible even when such evidence doesn't 100% answer a given question,” says McKernan.

    Dr Buckhaults takes a somewhat different view. After sharing his initial plasmid DNA contamination findings in a South Carolina Senate hearing in September last year, the video recording broke the internet.

    Believing the hearing to have been private, Dr Buckhaults was alarmed that the widespread distribution of his testimony may have caused “unintended, harmful side effects.” He requested that YouTube take down his testimony video, which is now defunct.


    Source: X
    In our correspondence, Dr Buckhaults stressed that while more research is warranted, he is of the opinion that the public “should not overreact to the news of the plasmid DNA contamination. It's serious enough that scientists need to hustle and figure out if it's causing any health problems now or down the road, but it's not cause for the general public to be alarmed.”

    But, “The reality is that`transfection experiments with contaminated DNA' have been carried out on vast numbers of people around the world in the name of vaccination,” writes Arakawa.

    Perhaps the experiment participants will be the ones to decide if they should be alarmed, or not.

    The FDA was contacted for comment about Dr Kämmerer and McKernan’s new findings, but they did not respond by publication deadline. This article will be updated if comment is received.

    View Kevin McKernan’s write up of his DNA integration experiment (in partnership with Dr Kämmerer) here. Scroll down for links to sequencing data files.

    Pathology and hematology labs wishing to send samples to Dr Buckhaults are invited to contact him at the University of South Carolina.

    Update 23 March 2024: This article was edited to add mention of the Dr David Speicher et al. finding of “billions to hundreds of billions of DNA molecules per dose” of the mRNA vaccines, and the scientists’ concerns that regulatory limits on DNA contamination have not taken LNP transfection into account.


    To support my work, make a one-off contribution to DDU via my Kofi account and/or subscribe. Thanks!

    Follow me on X

    Follow me on Instagram

    1
    From an article I wrote for Umbrella News on this topic last year:

    The TGA maintains that allegations put forward in the case about the potential for mRNA vaccines to alter the recipient’s DNA are unfounded. A spokesperson for the TGA told Umbrella News,

    “COVID-19 vaccines do not alter a person’s DNA. The mRNA in the vaccines does not enter the nucleus of cells and is not integrated into the human genome. Thus, the mRNA does not cause genetic damage or affect the offspring of vaccinated individuals.”

    “The TGA continues to monitor the scientific literature associated with the SARS – CoV-2 virus and the various COVID-19 vaccines approved for use in Australia.”

    With reference to the specific studies cited in the case materials, the TGA pointed Umbrella News to an RMIT ABC Fact Check post from 2022 purporting to ‘debunk’ claims that mRNA jabs are genotoxic. This is the same site that ‘debunked’ claims that COVID vaccines can cause menstrual disruption, before peer-reviewed scientific studies proved that they can and do (the post has not been corrected).

    As evidence that it is “well established” that vaccine mRNA and protein do not enter the nucleus, the TGA provided a link to a Mayo Clinic fact page which provides no studies or scientific evidence in support of its claims.

    The TGA did provide one commentary article published in a scientific journal which pointed out that the in vitro liver cell line study cannot be extrapolated to generalise about in vivo findings (in a human, not a dish) without further research being undertaken.

    Additionally, RMIT FactLab was suspended by Facebook in August 2023 after an uproar over its blatantly biased and factually dubious ‘fact checking’ of media articles relating to the Voice referendum campaign. It also transpired that RMIT FactLab had falsely represented its accreditation with the International Fact-Checking Network as current, when it had in fact lapsed.


    https://news.rebekahbarnett.com.au/p/dna-contamination-in-covid-vaccines
    DNA contamination in Covid vaccines DOES get into human cells, new evidence shows It also appears that the contamination enters the cell nucleus and integrates with human DNA Rebekah Barnett Regulators and fact checkers claim that plasmid DNA contamination in the mRNA Covid vaccines can’t change your genomic DNA, but new evidence suggests that it actually can. The fact checkers assert that DNA contamination poses no risk to your genomic DNA because your body will naturally destroy any contaminant DNA before it even gets into the cells. Even if the contaminant DNA could get into cells, there’s no way it can enter the cell nucleus, where genomic integration events occur, they say. And even if the contaminant DNA could enter the nucleus, which it can’t, it still couldn’t genomically integrate unless specific enzymes are present, they say. However, results from independent lab testing conducted on ovarian cancer cell lines show that contaminant DNA from Pfizer’s Covid vaccine not only crossed into the cells, but that it survived multiple cell divisions. This is suggestive that the contaminant DNA is able to transfect (enter) the cell nucleus, and that it integrated with the human cell DNA. TLDR 1. Scientists claim that Pfizer vaccine contaminant DNA has been detected in ovarian cancer cell line DNA, but they do not yet know if it’s chromosomal (heritable) or extra-chromosomal DNA (not heritable) 2. This is an in vitro (in a lab dish) finding, and needs to be replicated in vivo (in a human patient) 3. As the finding is specific to cancer cell lines, it is not generalisable, but scientists say it may give an indication of what cancer patients in remission could experience after mRNA Covid vaccination 4. This finding calls into question fact checker claims that mRNA Covid vaccine DNA contamination can't enter cells, can't enter the nucleus, and cannot integrate with human DNA. Last year, Boston-based genomics scientist Kevin McKernan made the shocking discovery that the mRNA Covid vaccines are contaminated with excessive levels of plasmid DNA, an artefact of the vaccine production process. McKernan’s findings were soon confirmed by multiple independent labs around the world for both the Pfizer and Moderna mono- and bi-valent vaccines, including lots approved for children, with one Canadian study led by Dr David Speicher concluding that there are “billions to hundreds of billions of DNA molecules per dose.” Scientists including McKernan, University of South Carolina cancer genomics scientist Dr Phillip Buckhaults, and Dr Wafik El-Diery, head of the Cancer Centre at Brown University, expressed concerns that fragments of plasmid DNA contamination could cause adverse events, autoimmune problems and cancers in some patients. But perhaps most significantly, there is also a theoretical risk of the contaminant DNA integrating with patients’ chromosomal DNA and modifying the human genome. This is of particular concern with the Pfizer vaccine, which contains an SV40 enhancer sequence, used in gene therapies “to drive DNA into the nucleus,” explains McKernan. While regulators have taken a ‘wait and see’ approach, independent scientists, including McKernan, have been more proactive, initiating experiments testing for evidence of genomic integration. Now, the first results are in. In an experiment conducted together with German molecular biologist Dr Ulrike Kämmerer, McKernan has detected vaccine contaminant DNA in ovarian cancer cell lines treated with Pfizer’s Covid vaccine. The scientists found a chimeric combination of human ovarian cell line DNA and spike sequence DNA derived from the contaminating plasmid at at least one, and possibly two sites. “If anything, this work has put to bed the question regarding if this contaminant DNA gets into the cell, and the chimeric human and contaminant spike DNA sequences imply it has entered the nucleus,” McKernan says. “The PCR and sequencing data both demonstrate the vaccine is getting into the cell and surviving cell passaging. It is likely bioactive and being partially replicated.” To reach this finding, Dr Kämmerer first treated ovarian cancer cell lines with mRNA Covid vaccines, using cells treated with AstraZeneca and Janssen vaccines as controls. The cells were then ‘passaged’, meaning they were left to divide and replicate numerous times. This has the effect of “rinsing away residual vaccine,” explains McKernan. Immunohistochemistry (IHC) was then performed, a staining process that Dr Kämmerer used to detect levels of spike protein expression produced by the vaccine modified-RNA. This was to confirm that the lipid nanoparticles (LNPs) carrying mod-RNA and plasmid DNA contamination “did their job and delivered the payload,” says McKernan. Measuring how many cells expressed spike protein also allowed the scientists to determine how much of the vaccine to treat the cells with. Immunohistochemistry performed with Pfizer top left, AstraZeneca top right as a control. Source: Kevin McKernan’s Substack Cell lines were then sent in cold storage to McKernan’s Boston lab, where his team used qPCR to screen which samples to sequence the cell line DNA. “What we found is, [contaminant] DNA that is getting transfected into ovarian cancer cell lines is replicating in the cells,” says McKernan, noting that the ratio of vaccine contaminant DNA to human cell DNA was “higher than we expected.” Chimeric sequences of human and vaccine contaminant DNA were detected at two sites: chromosomes 9 and 12, with the evidence for the latter being the strongest. “But we don't know if it's extra-chromosomal or whether it's chromosomal because of the Illumina (short read) method we used to sequence,” explains McKernan. Source: Kevin McKernan’s Substack Extra-chromosomal DNA is not part of the chromosome, and is therefore less likely to replicate and to be heritable. Chromosomal DNA, on the other hand, is heritable and more likely to be replicated. A third category, mitochondrial DNA, is heritable, but only from the maternal line. You can read a detailed account of methods and findings via McKernan’s Substack article, ‘Vaccine targeted qPCR of Cancer Cell Lines treated with BNT162b2.’ ‘Major advance,’ but clinical implications are limited McKernan emphasises that these findings cannot be generalised, stating that “it is too early to make comments on the clinical implications.” “The study is performed in ovarian cancer cell lines. It is not performed in patient cells, but this is a proxy for what might happen in an ovarian cancer patient who's in remission,” says McKernan, especially as there is evidence that the LNPs go to the ovaries. The risk for patients in this scenario is that integration events with contaminant DNA might cause aberrant cell growth, which poses a risk to immune suppression of new cancer cells. McKernan notes that his experiment only picked up on putative integration events that persisted after multiple cell replications. That is to say, the scientists were not able to detect integration events that may have occurred, but then died off immediately. At the moment, no one knows how many integration events might be occurring, or what effect that would have on patients. “The unknowns are just exponential,” says McKernan. The cancer cell line experiment can be said to be “a microcosm of genome integration of contaminated DNA,” said Japanese molecular oncology scientist Hiroshi Arakawa, in his own analysis of McKernan and Dr Kämmerer’s experiment, published to his popular science blog on which he shares critical views on Covid vaccine safety. Akira calls the two possible integrations observed in Dr Kämmerer’s experiment a “major advance” laying the ground for further experimentation. “What happens in cultured cells can also occur in normal cells, and a wide variety of abnormalities can occur depending on the site of genome integration,” such as “the induction of cancer or malignant transformation,” he wrote (translated from Japanese to English). LNPs deliver contaminant DNA straight to the cells A key assumption underlying claims that mRNA Covid vaccine contamination cannot enter the cell nucleus, and cannot genomically integrate with host DNA, is that the contamination will never make it into dividing cells, which would be required for integration to occur. This is based on the assumption that the LNPs containing both mod-RNA and contaminant DNA mostly stay in the muscle at the injection site. As muscle cells do not divide, there’s no problem, the logic goes. This is misleading, however, as Pfizer’s own biodistribution data shows that the LNPs enter the blood and every major organ system, including the ovaries, as mentioned above. While it is true that muscle cells don’t divide, LNPs distributed around the body can transfect any number of dividing cells in various organ systems. Table 4-2. shows biodistribution of LNPs, Pfizer Nonclinical Evaluation Report, 2021 From there, it’s only a matter of time before the LNP contents get into the cell nucleus, says McKernan. “In any dividing cell, the nucleus dissolves. So, when people say the DNA can get into the cytoplasm [inside the cell membrane] but won't get into the nucleus, well, in any dividing cell, it will end up getting into the nucleus.” It is possible that the dissolution of the cell nucleus during division is the mechanism underlying McKernan and Dr Kämmerer’s observed passaging of contaminant DNA, but further research will be required to confirm or disprove this hypothesis. Because of the effectiveness of LNPs in delivering their contents into cells, McKernan, Dr Buckhaults and Dr Speicher have questioned the suitability of the current regulatory limits on contaminant DNA in vaccines, which were set prior to the introduction of LNP technology in vaccines. Regulators unconcerned I sent McKernan’s Substack article documenting the new DNA integration findings to Australia’s drug regulator, the Therapeutic Goods Administration, for comment. The TGA did not address the new findings, but a spokesperson from the TGA responded, “The Department of Health and Aged Care has every confidence in the safety, quality and efficacy of the various approved COVID-19 vaccines for use in Australia. The TGA’s assessment of all vaccines is based upon high quality evidence, including studies and reviews published in peer-reviewed scientific and clinical journals.” However, when asked previously to provide evidence for its position that Covid vaccines pose no risk of DNA integration, the TGA provided no peer-reviewed scientific evidence to support its claims. Instead, the TGA provided links to a Mayo Clinic fact page with no scientific citations, an article by the discredited RMIT FactLab, and a scientific commentary article suggesting that in vitro findings cannot be generalised. Furthermore, TGA has not been forthcoming with the evidence it does hold. When asked to release Covid vaccine batch testing results under Freedom of Information, the regulator provided all 74 pages - fully redacted. In the US, the Food and Drug Administration (FDA) denied that contaminant DNA in the mRNA vaccines can enter the nucleus or pose any threat to patients’ genomic DNA, in a response to concerns raised by Florida Surgeon General, Dr Joseph A. Ladapo in December of last year. Additionally, the FDA misleadingly refuted the presence of SV40 proteins in the vaccines, when in fact Dr Ladapo raised concerns over the presence of an SV40 enchancer sequence in the Pfizer vaccine, as confirmed by Health Canada and numerous independent laboratories. Such ham-fisted mischaracterisation of a gene therapy sequence by the FDA is suggestive of either gross incompetence, or a disinformation play. Both are concerning. Science journalist Maryanne Demasi reported, in November last year, that the FDA shut down her enquiries into the DNA contamination matter, refusing to confirm if it found levels of DNA that exceeded acceptable levels, or if it was investigating further. The presence of contamination has been officially acknowledged by the European Medicines Agency (EMA) and Health Canada, with the latter also acknowledging the presence of the SV40 enhancer sequence, though both regulators deny that the amounts exceed regulatory limits, or that the DNA contamination poses any risk. ‘No excuse’ for ignoring ‘screaming hot signal’ Instead of denying excessive DNA levels and deferring to manufacturers’ reported test results, regulators should run their own qPCR testing on batch lots, says McKernan. Then, “they would see what everyone else is seeing, which is that sometimes the CT scores come out as low as 13… that’s a screaming hot signal.” “As a reference, the Covid test would call people positive at 33-35,” McKernan explains. “That’s a million-fold difference (20 CTs). A million-fold less Covid RNA and you're positive and quarantined. But you can inject a million-fold more past your mucosa?” There’s “no excuse” for regulators to not sequence every vaccine lot, says McKernan, when the costs for doing so have dropped dramatically in recent years. “DNA sequencing costs have dropped 100,000 fold in the last decade. They have relaxed the DNA contamination limits 1000-fold in this time frame. It likely only costs $1,000 in reagents for millions-to-billions of dollars worth of product.” Source: National Human Genome Research Institute DNA sequencing by regulatory agencies is important not just for measuring quantities, says McKernan, but also for determining the type of DNA contamination. “Not all DNA is created equal. Some is designed to replicate - when it gets into a cell, it can make more of itself. It's a massive loophole in the regulations that they don't do sequencing. But it's never been cheaper. You can precisely know the nature of the DNA in every single vial.” Scientists pick up regulators’ slack In the absence of any regulatory appetite for investigating the risks of DNA contamination in the mRNA Covid shots, and particularly the risk of genomic integration, independent scientists have taken the baton. “We are writing up our findings and will publish a preprint soon,” says McKernan, who is planning further testing in partnership with Dr Kämmerer. “We’re doing more experiments first. We need to sequence deeper to find out if the integration events are in chromosomal or extra-chromosomal DNA.” Dr Buckhaults is also running his own experiment, calling for de-identified samples of tumours or fresh blood from pathology and hematology labs. These samples will be tested for the presence of plasmid DNA contamination, with whole genome sequencing to then be carried out on positive samples to identify genomic integration sites. In an email outlining his experiment, Dr Buckhaults told me that he intends to report his findings in a peer-reviewed publication, predicting that the work could take “a few months to a year,” depending on how fast samples come in. “I am hopeful to prove my concerns are unwarranted by accumulating a lot of negative data, and of course negative data takes the most time to collect,” he said. McKernan says he is aware of other labs running tests for contaminant plasmid DNA integration, but cannot disclose the details at present. Decentralisation the future of science? McKernan says he has experienced some pushback for publishing his methods and findings in real time via Substack, X, and preprints. But, he believes that making his data available as quickly as possible is a way for the field of science to regain public trust. “Many will criticize our disclosure of preliminary findings but we feel this is an insult to the intelligence of the average person,” says McKernan. “It's a form of scientific elitism that implies people can't handle the truth and will be scared like sheep if given a glimpse of how the true scientific process is performed. Scientists are 90% of the time wrong but only publish the times when they are right. There is no journal of negative results.“ In light of the prospect that most published research findings are false (as famously asserted in a 2005 article by Professor John Ioannidis), McKernan questions the value of peer-review, instead favouring replication or refutation in the real world. Source: X For this reason, McKernan says he has not prioritised peer-reviewed publication for his DNA contamination findings, but is rather focusing on conducting more experiments and releasing the data as he goes - even when it’s incomplete, or requires further experimentation. “We were not expecting to find any integration events at this depth of coverage, but they are evident to anyone who downloads our public reads. To not speak to obvious evidence in such data would be irresponsible even when such evidence doesn't 100% answer a given question,” says McKernan. Dr Buckhaults takes a somewhat different view. After sharing his initial plasmid DNA contamination findings in a South Carolina Senate hearing in September last year, the video recording broke the internet. Believing the hearing to have been private, Dr Buckhaults was alarmed that the widespread distribution of his testimony may have caused “unintended, harmful side effects.” He requested that YouTube take down his testimony video, which is now defunct. Source: X In our correspondence, Dr Buckhaults stressed that while more research is warranted, he is of the opinion that the public “should not overreact to the news of the plasmid DNA contamination. It's serious enough that scientists need to hustle and figure out if it's causing any health problems now or down the road, but it's not cause for the general public to be alarmed.” But, “The reality is that`transfection experiments with contaminated DNA' have been carried out on vast numbers of people around the world in the name of vaccination,” writes Arakawa. Perhaps the experiment participants will be the ones to decide if they should be alarmed, or not. The FDA was contacted for comment about Dr Kämmerer and McKernan’s new findings, but they did not respond by publication deadline. This article will be updated if comment is received. View Kevin McKernan’s write up of his DNA integration experiment (in partnership with Dr Kämmerer) here. Scroll down for links to sequencing data files. Pathology and hematology labs wishing to send samples to Dr Buckhaults are invited to contact him at the University of South Carolina. Update 23 March 2024: This article was edited to add mention of the Dr David Speicher et al. finding of “billions to hundreds of billions of DNA molecules per dose” of the mRNA vaccines, and the scientists’ concerns that regulatory limits on DNA contamination have not taken LNP transfection into account. To support my work, make a one-off contribution to DDU via my Kofi account and/or subscribe. Thanks! Follow me on X Follow me on Instagram 1 From an article I wrote for Umbrella News on this topic last year: The TGA maintains that allegations put forward in the case about the potential for mRNA vaccines to alter the recipient’s DNA are unfounded. A spokesperson for the TGA told Umbrella News, “COVID-19 vaccines do not alter a person’s DNA. The mRNA in the vaccines does not enter the nucleus of cells and is not integrated into the human genome. Thus, the mRNA does not cause genetic damage or affect the offspring of vaccinated individuals.” “The TGA continues to monitor the scientific literature associated with the SARS – CoV-2 virus and the various COVID-19 vaccines approved for use in Australia.” With reference to the specific studies cited in the case materials, the TGA pointed Umbrella News to an RMIT ABC Fact Check post from 2022 purporting to ‘debunk’ claims that mRNA jabs are genotoxic. This is the same site that ‘debunked’ claims that COVID vaccines can cause menstrual disruption, before peer-reviewed scientific studies proved that they can and do (the post has not been corrected). As evidence that it is “well established” that vaccine mRNA and protein do not enter the nucleus, the TGA provided a link to a Mayo Clinic fact page which provides no studies or scientific evidence in support of its claims. The TGA did provide one commentary article published in a scientific journal which pointed out that the in vitro liver cell line study cannot be extrapolated to generalise about in vivo findings (in a human, not a dish) without further research being undertaken. Additionally, RMIT FactLab was suspended by Facebook in August 2023 after an uproar over its blatantly biased and factually dubious ‘fact checking’ of media articles relating to the Voice referendum campaign. It also transpired that RMIT FactLab had falsely represented its accreditation with the International Fact-Checking Network as current, when it had in fact lapsed. https://news.rebekahbarnett.com.au/p/dna-contamination-in-covid-vaccines
    NEWS.REBEKAHBARNETT.COM.AU
    DNA contamination in Covid vaccines DOES get into human cells, new evidence shows
    It also appears that the contamination enters the cell nucleus and integrates with human DNA
    Angry
    1
    0 Comments 1 Shares 3507 Views
  • Sending This Notice of Liability To Your Doctors May Wake Them Up And Stop Them Causing More Harm
    Feel free to adapt this letter template as you see fit

    Dr Tess Lawrie, MBBCh, PhD​
    This is just a quick post to share a letter that we have drafted with the help of a valued solicitor as a first notice of liability to your doctor or vaccinating health practitioner.


    We felt it was best to keep to a page so that it will be read!

    This text for this full Letter Template to Doctors and Health Practitioners administering, promoting or facilitating Covid-19 injections can be found and copied below

    Feel free to copy, paste and adapt as you see fit. If you want to add links, for example to the DNA contamination independent expert hearing, please share suggestions to others in the comments below. Let us know what your doctor’s response too!

    Sharing with paid subscribers today and all for free tomorrow! Thank you so much for supporting our work. We could not do it without you.

    I hope this template inspires you to get active! We are not helpless. There are many things one can do. Your actions today will help others.


    Share

    [Enter Address]

    [Enter Date]

    Dear Sir/Madam/Doctor

    Re: Administration of SARS CoV2 vaccines:

    I write to put you on notice that your practice/NHS Trust/clinic may be liable for gross negligence in administering the SARS CoV2 vaccine.

    A clinician has to obtain free and informed consent before carrying out any medical procedure. A failure to obtain free and informed consent can be both a breach of the duty of care as well as a battery. To obtain a patient’s consent a clinician has to advise the patient of the material risks of the procedure. Material risks will vary from person to person. A doctor is under a legal obligation to inform patients of material risks so that patients can then decide autonomously whether they wish to run those material risks.

    The reason why the practice is at risk is that in relation to the mRNA vaccines, patients have not been advised of the following:

    The long term material risks of SARS CoV2 vaccines are unknown. The mRNA platform is a gene therapy where material risks are identified over a period up to 15 years. Patients have not been advised that the vaccine is a gene therapy.

    Follow up studies are awaited on medium term material risks.

    The Pfizer vaccine that is being rolled out uses a different manufacturing process, process two, to the vaccine that was authorised which was developed via process one. There has been no large RCT of process two vaccines and material risks are only being identified during the roll out.

    SV40 plasmids have been found in Pfizer SARS CoV2 vaccines. At least two regulators have now acknowledged the presence of SV40. SV40 inhibits cancer suppressing cells and promotes cancer forming cells.

    In the circumstances I would be grateful if you would confirm in writing that patients are being advised by your clinicians about the known material risks, including plasmid contamination, and the fact that there are unknown material risks relating to gene therapies and that such material risks are identified over time.

    Yours sincerely

    [insert name]

    Thanks for your collaboration to make a better world!

    Value Exchange

    If you find value in these Substack articles and videos, please recommend it to others. All proceeds from paid subscriptions go to the work of the World Council for Health. You can also make a one-off donation or become a regular monthly donor in 2024 to support our expanding WCH team and humanitarian work.

    Share A Better Way with Dr Tess Lawrie




    WCH Notice of Liability to Covid Vaccinators

    The World Council for Health have put together a useful template Notice of Liability for the public to use to educate and serve on those healthcare professionals who are still vaccinating people with the Covid-19 jabs.

    "This text for this full Letter Template to Doctors and Health Practitioners administering, promoting or facilitating Covid-19 injections can be found and copied below. Feel free to copy, paste and adapt as you see fit. If you want to add links"

    https://drtesslawrie.substack.com/p/this-notice-of-liability-to-your
    Sending This Notice of Liability To Your Doctors May Wake Them Up And Stop Them Causing More Harm Feel free to adapt this letter template as you see fit Dr Tess Lawrie, MBBCh, PhD​ This is just a quick post to share a letter that we have drafted with the help of a valued solicitor as a first notice of liability to your doctor or vaccinating health practitioner. We felt it was best to keep to a page so that it will be read! This text for this full Letter Template to Doctors and Health Practitioners administering, promoting or facilitating Covid-19 injections can be found and copied below Feel free to copy, paste and adapt as you see fit. If you want to add links, for example to the DNA contamination independent expert hearing, please share suggestions to others in the comments below. Let us know what your doctor’s response too! Sharing with paid subscribers today and all for free tomorrow! Thank you so much for supporting our work. We could not do it without you. I hope this template inspires you to get active! We are not helpless. There are many things one can do. Your actions today will help others. Share [Enter Address] [Enter Date] Dear Sir/Madam/Doctor Re: Administration of SARS CoV2 vaccines: I write to put you on notice that your practice/NHS Trust/clinic may be liable for gross negligence in administering the SARS CoV2 vaccine. A clinician has to obtain free and informed consent before carrying out any medical procedure. A failure to obtain free and informed consent can be both a breach of the duty of care as well as a battery. To obtain a patient’s consent a clinician has to advise the patient of the material risks of the procedure. Material risks will vary from person to person. A doctor is under a legal obligation to inform patients of material risks so that patients can then decide autonomously whether they wish to run those material risks. The reason why the practice is at risk is that in relation to the mRNA vaccines, patients have not been advised of the following: The long term material risks of SARS CoV2 vaccines are unknown. The mRNA platform is a gene therapy where material risks are identified over a period up to 15 years. Patients have not been advised that the vaccine is a gene therapy. Follow up studies are awaited on medium term material risks. The Pfizer vaccine that is being rolled out uses a different manufacturing process, process two, to the vaccine that was authorised which was developed via process one. There has been no large RCT of process two vaccines and material risks are only being identified during the roll out. SV40 plasmids have been found in Pfizer SARS CoV2 vaccines. At least two regulators have now acknowledged the presence of SV40. SV40 inhibits cancer suppressing cells and promotes cancer forming cells. In the circumstances I would be grateful if you would confirm in writing that patients are being advised by your clinicians about the known material risks, including plasmid contamination, and the fact that there are unknown material risks relating to gene therapies and that such material risks are identified over time. Yours sincerely [insert name] Thanks for your collaboration to make a better world! Value Exchange If you find value in these Substack articles and videos, please recommend it to others. All proceeds from paid subscriptions go to the work of the World Council for Health. You can also make a one-off donation or become a regular monthly donor in 2024 to support our expanding WCH team and humanitarian work. Share A Better Way with Dr Tess Lawrie WCH Notice of Liability to Covid Vaccinators The World Council for Health have put together a useful template Notice of Liability for the public to use to educate and serve on those healthcare professionals who are still vaccinating people with the Covid-19 jabs. "This text for this full Letter Template to Doctors and Health Practitioners administering, promoting or facilitating Covid-19 injections can be found and copied below. Feel free to copy, paste and adapt as you see fit. If you want to add links" https://drtesslawrie.substack.com/p/this-notice-of-liability-to-your
    Like
    1
    0 Comments 0 Shares 2395 Views
  • WCH Notice of Liability to Covid Vaccinators

    The World Council for Health have put together a useful template Notice of Liability for the public to use to educate and serve on those healthcare professionals who are still vaccinating people with the Covid-19 jabs.

    "This text for this full Letter Template to Doctors and Health Practitioners administering, promoting or facilitating Covid-19 injections can be found and copied below. Feel free to copy, paste and adapt as you see fit. If you want to add links"

    https://drtesslawrie.substack.com/p/this-notice-of-liability-to-your
    WCH Notice of Liability to Covid Vaccinators The World Council for Health have put together a useful template Notice of Liability for the public to use to educate and serve on those healthcare professionals who are still vaccinating people with the Covid-19 jabs. "This text for this full Letter Template to Doctors and Health Practitioners administering, promoting or facilitating Covid-19 injections can be found and copied below. Feel free to copy, paste and adapt as you see fit. If you want to add links" https://drtesslawrie.substack.com/p/this-notice-of-liability-to-your
    Like
    1
    0 Comments 0 Shares 598 Views
  • Lawsuit Claiming COVID-19 Jab Is a 'Biological Weapon' Docketed by Florida Supreme Court
    Writ of mandamus calls for halt in distribution of COVID vaccine "weapons of mass destruction."

    Jon Fleetwood

    In an extraordinary legal move, the Florida Supreme Court has accepted into its system a writ of mandamus that presents a grave portrayal of COVID-19 vaccines, characterizing them as “biological weapons” and “weapons of mass destruction.”

    Share Jon Fleetwood


    Follow Jon Fleetwood on Instagram @realjonfleetwood / Twitter @JonMFleetwood


    A ‘writ of mandamus’ is a court order compelling a party to perform a specific legal duty.

    The petitioner, Joseph Sansone (MS, PhD), brings the action with serious accusations regarding the vaccines’ safety, efficacy, and legality.

    The case was docketed on Monday under the case number SC2024-0327.

    Dr. Sansone’s petition pulls no punches, declaring that “COVID-19 injections have caused countless deaths, permanent injury, and disability.”

    He demands immediate action, stating that “the COVID-19 injections are dangerous” and that it is therefore “the duty of the Governor and Attorney General to act immediately to prohibit their distribution.”

    The urgency of the matter is underscored as Sansone argues it “is incumbent on this Court to compel the Governor and Attorney General to act immediately.”

    A critical aspect of the petition revolves around the scrutiny of the mainstream public health campaign concerning coronavirus jabs.

    According to the writ, “A massive mass media and government campaign promoting ‘COVID-19 vaccines’ as safe and effective ‘vaccines’ to prevent infection targeted Florida’s population of approximately 22 million people. This campaign narrative was false and misleading and has led to numerous deaths, permanent injury, and disability.”

    Share Jon Fleetwood


    Follow Jon Fleetwood on Instagram @realjonfleetwood / Twitter @JonMFleetwood


    Sansone’s claim extends to the foundation of the vaccine’s approval process through the U.S. Food and Drug Administration (FDA).

    “It is well-established that the FDA clinical trials for the COVID-19 injections were not designed to clinically or statistically demonstrate that the COVID-19 nanoparticle injections prevent infection, prevent transmission, or protect against disease, hospitalizations, and death,” he states.

    The foundation of Sansone’s argument hinges on the belief that these shots, due to “shedding,” whereby components of the vaccine are shed from the vaccinated onto the unvaccinated, “pose a risk of harm, including death and disability, to all Floridians whether ‘vaccinated’ or ‘unvaccinated.’”

    He goes further, saying, “Every Floridian, including members of this Court, and likely the Respondents, were lied to—COVID-19 injections are not safe, nor are they effective.”

    Also central to the writ’s claim is the assertion that “COVID-19 injections containing engineered mRNA nanoparticle technologies meet the legal definition of biological weapons” and “meet the exact criteria of weapons of mass destruction.”

    “The facts of this case evidenced above demonstrate nanotechnology present in the COVID-19 injections which do qualify as a device designed and intended to cause harm, as does the use of such technology, and or a biological agent, resulting in death or harm. Repeatedly distributing a biological agent or device causing harm in mass, especially after it is well known to cause harm, qualifies it as a weapon of mass destruction and a biological weapon.”

    The legal statutes cited in the petition are broad and encompassing, aiming to leverage “Biological Weapons 18 USC § 175; Weapons and Firearms § 790.166 Fla. Stat. (2023); Federal Crime of Treason 18 USC § 2381; Treason § 876.32 Fla. Stat. (2023); Domestic Terrorism, 18 USC § 2331, Terrorism § 775.30 Fla. Stat. (2023); Murder § 782.04 (1)(a) Fla. Stat. (2023); and Genocide 18 USC §1091.”

    Through these laws, Sansone seeks an order to “immediately prohibit the distribution, promotion, access and administration of COVID-19 injections, mRNA nanoparticle injections, and all mRNA products in the State of Florida.”

    Share Jon Fleetwood


    Follow Jon Fleetwood on Instagram @realjonfleetwood / Twitter @JonMFleetwood


    This stance is supported by resolutions from “approximately 10 Florida Republican County Political Parties,” calling for a ban on the injections and analysis of their contents.

    Dr. Francis Boyle, a key figure in the drafting of the Biological Weapons Convention of 1972, is cited as endorsing the resolution, adding significant weight to Sansone’s arguments.

    Sansone’s argument crescendos as he suggests that the stakes involve “the future existence of the human race itself.”

    He firmly believes he has a “clear legal right to the requested relief,” positioning his request not just as a legal challenge but as a plea to “protect the public from biological and technological weapons of mass destruction and remove them from the market.”

    Citing the fact that, “Since February 21, 2023, approximately 10 Florida Republican County Political Parties, representing millions of people, have passed resolutions declaring Covid 19 injections and mRNA injections biological and technological weapons,” the writ paints a dire picture of the possible threat posed by COVID jabs.

    Sansone identifies himself as a victim, stating he “has been targeted with biological and technological weapons of mass destruction,” and expresses his advocacy not only for his rights but for “the millions of Floridians that have been targeted, including friends and family members.”

    The petition also makes clear its aim of “not demanding the prosecution of individuals.”

    Rather, the mandamus “simply seeks to compel the Governor and Attorney General to enforce the law and protect the public from biological and technological weapons of mass destruction and remove them from the market.”

    This legal challenge marks a pivotal moment, thrusting the Florida Supreme Court into the center of a highly charged debate over public health, vaccine safety, and the legal categorization of these interventions.

    As the court prepares to deliberate on this unprecedented case, the outcome could set a significant legal and ethical precedent concerning the response to pandemics and the regulation of vaccines.

    You can read the full lawsuit here:

    Share Jon Fleetwood


    Follow Jon Fleetwood on Instagram @realjonfleetwood / Twitter @JonMFleetwood


    https://telegra.ph/Lawsuit-Claiming-COVID-19-Jab-Is-a-Biological-Weapon-Docketed-by-Florida-Supreme-Court-03-11


    🔴 Lawsuit Claiming COVID-19 Jab Is a 'Biological Weapon' Docketed by Florida Supreme Court

    In an extraordinary legal move, the Florida Supreme Court has accepted a writ of mandamus that characterizes Covid-19 vaccines as “biological weapons” and “weapons of mass destruction.”

    A ‘writ of mandamus’ is a court order compelling a party to perform a specific legal duty. The petitioner, Joseph Sansone (MS, PhD), brings the action with serious accusations regarding the vaccines’ safety, efficacy, and legality.

    The case was docketed on Monday under the case number SC2024-0327.
    Dr. Sansone’s petition pulls no punches, declaring that “COVID-19 injections have caused countless deaths, permanent injury, and disability.”

    He demands immediate action, stating that “the COVID-19 injections are dangerous” and that it is therefore “the duty of the Governor and Attorney General to act immediately to prohibit their distribution.”

    https://jonfleetwood.substack.com/p/lawsuit-claiming-covid-19-jab-is
    Lawsuit Claiming COVID-19 Jab Is a 'Biological Weapon' Docketed by Florida Supreme Court Writ of mandamus calls for halt in distribution of COVID vaccine "weapons of mass destruction." Jon Fleetwood In an extraordinary legal move, the Florida Supreme Court has accepted into its system a writ of mandamus that presents a grave portrayal of COVID-19 vaccines, characterizing them as “biological weapons” and “weapons of mass destruction.” Share Jon Fleetwood Follow Jon Fleetwood on Instagram @realjonfleetwood / Twitter @JonMFleetwood A ‘writ of mandamus’ is a court order compelling a party to perform a specific legal duty. The petitioner, Joseph Sansone (MS, PhD), brings the action with serious accusations regarding the vaccines’ safety, efficacy, and legality. The case was docketed on Monday under the case number SC2024-0327. Dr. Sansone’s petition pulls no punches, declaring that “COVID-19 injections have caused countless deaths, permanent injury, and disability.” He demands immediate action, stating that “the COVID-19 injections are dangerous” and that it is therefore “the duty of the Governor and Attorney General to act immediately to prohibit their distribution.” The urgency of the matter is underscored as Sansone argues it “is incumbent on this Court to compel the Governor and Attorney General to act immediately.” A critical aspect of the petition revolves around the scrutiny of the mainstream public health campaign concerning coronavirus jabs. According to the writ, “A massive mass media and government campaign promoting ‘COVID-19 vaccines’ as safe and effective ‘vaccines’ to prevent infection targeted Florida’s population of approximately 22 million people. This campaign narrative was false and misleading and has led to numerous deaths, permanent injury, and disability.” Share Jon Fleetwood Follow Jon Fleetwood on Instagram @realjonfleetwood / Twitter @JonMFleetwood Sansone’s claim extends to the foundation of the vaccine’s approval process through the U.S. Food and Drug Administration (FDA). “It is well-established that the FDA clinical trials for the COVID-19 injections were not designed to clinically or statistically demonstrate that the COVID-19 nanoparticle injections prevent infection, prevent transmission, or protect against disease, hospitalizations, and death,” he states. The foundation of Sansone’s argument hinges on the belief that these shots, due to “shedding,” whereby components of the vaccine are shed from the vaccinated onto the unvaccinated, “pose a risk of harm, including death and disability, to all Floridians whether ‘vaccinated’ or ‘unvaccinated.’” He goes further, saying, “Every Floridian, including members of this Court, and likely the Respondents, were lied to—COVID-19 injections are not safe, nor are they effective.” Also central to the writ’s claim is the assertion that “COVID-19 injections containing engineered mRNA nanoparticle technologies meet the legal definition of biological weapons” and “meet the exact criteria of weapons of mass destruction.” “The facts of this case evidenced above demonstrate nanotechnology present in the COVID-19 injections which do qualify as a device designed and intended to cause harm, as does the use of such technology, and or a biological agent, resulting in death or harm. Repeatedly distributing a biological agent or device causing harm in mass, especially after it is well known to cause harm, qualifies it as a weapon of mass destruction and a biological weapon.” The legal statutes cited in the petition are broad and encompassing, aiming to leverage “Biological Weapons 18 USC § 175; Weapons and Firearms § 790.166 Fla. Stat. (2023); Federal Crime of Treason 18 USC § 2381; Treason § 876.32 Fla. Stat. (2023); Domestic Terrorism, 18 USC § 2331, Terrorism § 775.30 Fla. Stat. (2023); Murder § 782.04 (1)(a) Fla. Stat. (2023); and Genocide 18 USC §1091.” Through these laws, Sansone seeks an order to “immediately prohibit the distribution, promotion, access and administration of COVID-19 injections, mRNA nanoparticle injections, and all mRNA products in the State of Florida.” Share Jon Fleetwood Follow Jon Fleetwood on Instagram @realjonfleetwood / Twitter @JonMFleetwood This stance is supported by resolutions from “approximately 10 Florida Republican County Political Parties,” calling for a ban on the injections and analysis of their contents. Dr. Francis Boyle, a key figure in the drafting of the Biological Weapons Convention of 1972, is cited as endorsing the resolution, adding significant weight to Sansone’s arguments. Sansone’s argument crescendos as he suggests that the stakes involve “the future existence of the human race itself.” He firmly believes he has a “clear legal right to the requested relief,” positioning his request not just as a legal challenge but as a plea to “protect the public from biological and technological weapons of mass destruction and remove them from the market.” Citing the fact that, “Since February 21, 2023, approximately 10 Florida Republican County Political Parties, representing millions of people, have passed resolutions declaring Covid 19 injections and mRNA injections biological and technological weapons,” the writ paints a dire picture of the possible threat posed by COVID jabs. Sansone identifies himself as a victim, stating he “has been targeted with biological and technological weapons of mass destruction,” and expresses his advocacy not only for his rights but for “the millions of Floridians that have been targeted, including friends and family members.” The petition also makes clear its aim of “not demanding the prosecution of individuals.” Rather, the mandamus “simply seeks to compel the Governor and Attorney General to enforce the law and protect the public from biological and technological weapons of mass destruction and remove them from the market.” This legal challenge marks a pivotal moment, thrusting the Florida Supreme Court into the center of a highly charged debate over public health, vaccine safety, and the legal categorization of these interventions. As the court prepares to deliberate on this unprecedented case, the outcome could set a significant legal and ethical precedent concerning the response to pandemics and the regulation of vaccines. You can read the full lawsuit here: Share Jon Fleetwood Follow Jon Fleetwood on Instagram @realjonfleetwood / Twitter @JonMFleetwood https://telegra.ph/Lawsuit-Claiming-COVID-19-Jab-Is-a-Biological-Weapon-Docketed-by-Florida-Supreme-Court-03-11 🔴 Lawsuit Claiming COVID-19 Jab Is a 'Biological Weapon' Docketed by Florida Supreme Court In an extraordinary legal move, the Florida Supreme Court has accepted a writ of mandamus that characterizes Covid-19 vaccines as “biological weapons” and “weapons of mass destruction.” A ‘writ of mandamus’ is a court order compelling a party to perform a specific legal duty. The petitioner, Joseph Sansone (MS, PhD), brings the action with serious accusations regarding the vaccines’ safety, efficacy, and legality. The case was docketed on Monday under the case number SC2024-0327. Dr. Sansone’s petition pulls no punches, declaring that “COVID-19 injections have caused countless deaths, permanent injury, and disability.” He demands immediate action, stating that “the COVID-19 injections are dangerous” and that it is therefore “the duty of the Governor and Attorney General to act immediately to prohibit their distribution.” https://jonfleetwood.substack.com/p/lawsuit-claiming-covid-19-jab-is
    JONFLEETWOOD.SUBSTACK.COM
    Lawsuit Claiming COVID-19 Jab Is a 'Biological Weapon' Docketed by Florida Supreme Court
    Writ of mandamus calls for halt in distribution of COVID vaccine "weapons of mass destruction."
    Like
    1
    0 Comments 0 Shares 3640 Views
  • Biologist prof. dr. Ulrike Kammerer: COVID jabs contain spider silk gene sequence



    https://www.brighteon.com/57cdd548-bd1a-46e9-aba9-265aca741464
    Biologist prof. dr. Ulrike Kammerer: COVID jabs contain spider silk gene sequence https://www.brighteon.com/57cdd548-bd1a-46e9-aba9-265aca741464
    Like
    1
    1 Comments 1 Shares 363 Views
  • Largest Covid-19 vaccine study yet finds links to health conditions
    Published: 12:31pm, 19 Feb, 2024

    Vaccines that protect against severe illness, death and lingering long Covid-19 symptoms from a coronavirus infection were linked to small increases in neurological, blood, and heart-related conditions in the largest global vaccine safety study to date.

    The rare events – identified early in the pandemic – included a higher risk of heart-related inflammation from mRNA shots made by Pfizer Inc, BioNTech SE, and Moderna Inc, and an increased risk of a type of blood clot in the brain after immunisation with viral-vector vaccines such as the one developed by the University of Oxford and made by AstraZeneca Plc.

    The viral-vector jabs were also tied to an increased risk of Guillain-Barre syndrome, a neurological disorder in which the immune system mistakenly attacks the peripheral nervous system.

    https://www.scmp.com/news/world/united-states-canada/article/3252387/largest-covid-19-vaccine-study-yet-finds-links-health-conditions
    Largest Covid-19 vaccine study yet finds links to health conditions Published: 12:31pm, 19 Feb, 2024 Vaccines that protect against severe illness, death and lingering long Covid-19 symptoms from a coronavirus infection were linked to small increases in neurological, blood, and heart-related conditions in the largest global vaccine safety study to date. The rare events – identified early in the pandemic – included a higher risk of heart-related inflammation from mRNA shots made by Pfizer Inc, BioNTech SE, and Moderna Inc, and an increased risk of a type of blood clot in the brain after immunisation with viral-vector vaccines such as the one developed by the University of Oxford and made by AstraZeneca Plc. The viral-vector jabs were also tied to an increased risk of Guillain-Barre syndrome, a neurological disorder in which the immune system mistakenly attacks the peripheral nervous system. https://www.scmp.com/news/world/united-states-canada/article/3252387/largest-covid-19-vaccine-study-yet-finds-links-health-conditions
    WWW.SCMP.COM
    Largest Covid-19 vaccine study yet finds links to health conditions
    More than 13.5 billion doses of Covid vaccines have been administered globally over the past three years. A small proportion were injured by the shots, stoking debate about their benefits versus harms.
    Angry
    1
    0 Comments 0 Shares 2740 Views
  • Private Cancer Care And Jabs Get A Royal Promotion - UK Column News - 14th February 2024

    - Sky News (YouTube): King Charles expresses 'heartfelt thanks' to public in first message since cancer diagnosis
    - Guardian: Surge in UK cancer patients going private revealed as King Charles starts treatment
    - Tony Blair Institute for Global Change: Why the UK Government Must Act Urgently to Become a Global Leader in Cutting-Edge Cancer Treatment
    - 5 News (YouTube 2023): BioNTech to start cancer vaccine trials in the UK from September
    - WEF (2022): FIRST Cancer Care: Leveraging Fourth Industrial Revolution technologies for cancer care
    - The World Economic Forum: What is the UN Summit of the Future in 2024?
    - Cancer Research UK: Early Detection and Diagnosis of Cancer Roadmap
    - Queen Mary University of London: Cancer Behavioural Science Group
    - UCL: Behavioural Science and Early Diagnosis of Cancer Group
    - University College London: Christian Von Wagner Profile
    “Prof Christian von Wagner is Programme lead of the UCL MSc Health psychology and has a long standing research interest in behavioural approaches early diagnosis of colorectal cancer”
    - King's College London: Cancer Behavioural Science Unit
    - The House of Commons Library: Cancer statistics for England
    - UK Column Article (2022): NHS Long Term Plan and Mental Health Implementation Plan: Phoenix or dinosaur?
    - GOV.UK: Children and Young People Cancer Taskforce launched to save lives

    Sources: www.ukcolumn.org/video/uk-column-news-14th-february-2024
    Private Cancer Care And Jabs Get A Royal Promotion - UK Column News - 14th February 2024 - Sky News (YouTube): King Charles expresses 'heartfelt thanks' to public in first message since cancer diagnosis - Guardian: Surge in UK cancer patients going private revealed as King Charles starts treatment - Tony Blair Institute for Global Change: Why the UK Government Must Act Urgently to Become a Global Leader in Cutting-Edge Cancer Treatment - 5 News (YouTube 2023): BioNTech to start cancer vaccine trials in the UK from September - WEF (2022): FIRST Cancer Care: Leveraging Fourth Industrial Revolution technologies for cancer care - The World Economic Forum: What is the UN Summit of the Future in 2024? - Cancer Research UK: Early Detection and Diagnosis of Cancer Roadmap - Queen Mary University of London: Cancer Behavioural Science Group - UCL: Behavioural Science and Early Diagnosis of Cancer Group - University College London: Christian Von Wagner Profile “Prof Christian von Wagner is Programme lead of the UCL MSc Health psychology and has a long standing research interest in behavioural approaches early diagnosis of colorectal cancer” - King's College London: Cancer Behavioural Science Unit - The House of Commons Library: Cancer statistics for England - UK Column Article (2022): NHS Long Term Plan and Mental Health Implementation Plan: Phoenix or dinosaur? - GOV.UK: Children and Young People Cancer Taskforce launched to save lives Sources: www.ukcolumn.org/video/uk-column-news-14th-february-2024
    Like
    1
    0 Comments 0 Shares 4482 Views 0
  • There's also a ton of information from the IEC regarding international Standards surrounding Biodigital convergence.

    Quantum Dots are programmable graphene oxide nanoparticles which serve many functions, including biometric data harvesting (spying).

    The demons want to build their Smart Cities from this material!

    https://ambassadorlove.blog/2021/12/17/quantum-dots-dna-barcoding-nano-razors-the-israeli-state/


    Quantum Dots, DNA Barcoding, Nano-Razors & The Israeli State
    December 17, 2021 by Dr. Ariyana Love
    December 2, 2021
    By Dr. Ariyana Love, ND

    In my latest interview with Stew Peter’s, I brought evidence confirming that Dr. Andreas Noack, the good doctor who risked his life to warn humanity of the extreme dangers of the death jab, is in fact deceased.

    Days after Dr. Noack’s mysterious death, a video was leaked revealing Graphene Hydroxide nano-razors inside the Pfizer death jab, under Dark Field Microscopy. The sample is loaded with Graphene Hydroxide.

    You will see an individual Microsphere releasing it’s payload of nanoscale Graphene Hydroxide which looks exactly like razorblades when zoomed in on the individual shiny specs. See more images here.

    LEAKED FOOTAGE: GRAPHENE HYDROXIDE NANO-RAZORBLADES – DARK FIELD MICROSCOPY

    An English translation of this video can be found in the article entitled, Dr. Ariyana Discusses Nano-Biosensors/Nanorazors and Dr. Noack’s Death After He Located Graphene Hydroxide in the COVID Vaccine.

    MICROSPHERES & MICROBUBBLES

    Microbeads and Microspheres are listed as an active ingredient in the Pfizer death jab patent. Microspheres and Microbubbles are listed in the Moderna death jab patent.

    Microspheres and Microbubbles are micrometer size devices approximately equal in size to a red blood cell, according to the NIH. That’s about the width of a Human hair.


    Microbubbles and Microspheres (bottom right)
    Microspheres and Microbubbles are made from Poly(lactic-co-glycolic) acid (PLGA). PLGA is a copolymer made from Graphene Oxide (GO). Graphene Oxide-PLGA nanofibers are used in a host of Food and Drug Administration (FDA) approved “therapeutic” devices. However, the ingredients of these devices are cytotoxic, meaning they destroy cells.

    Graphene Oxide PLGA Toxicity induces an inflammatory response and deadly cytokine storm reaction, according to animal studies. The FDA should be investigated for this.

    Microspheres are coated with gold nanoparticles. Microspheres are used for scaffolding, which is artificial tissue engineering inside the Human body. PubMed writes, “Scaffolds are materials that have been engineered to cause desirable cellular interactions to contribute to the formation of new functional tissues for medical purposes. Cells are often ‘seeded’ into these structures capable of supporting three-dimensional tissue formation.”

    This technology is being used for DNA-based tissue engineering and “scaffolding” of Humans, without their Informed Consent. See more scaffolding images from a Slovakian study of the death jab, here.

    Microbubbles contain one or more “viral vectors coding CRISPR-Cas-9 system“. It’s a “state-of-the-art” drug and chemical delivery method. They contain lab enhanced chimeric proteins of the messenger RNA/DNA. Microbubbles have a lipid and nickel-coated quartz substrate. They contain a drug and chemical payload in the outer, lipid-coating and another payload on the inside.

    Graphene Oxide Nanotubes enable Microbubbles to self-replicate via electrical pulse. They interlink by electrodes. Microbubbles were designed to break through the blood/brain barrier and deliver their drug and chemical payload into brain cells. Ultrasound is used to help Microbubbles breach the blood/brain barrier. Here’s a video animation of how microbubbles / microspheres work to deliver drugs into the brain.

    This gene delivery technology was funded and developed for the purpose of treating sick people, not healthy people. It was intended to be used as a treatment for cancer, not as a medical intervention for our healthy kids.

    The Microbubble and Microsphere devices carry drug and chemical payloads for controlled release of encapsulated DNA. It’s targeted drug delivery can be unloaded over an extended period of time. This is very important to understand. They can be formulated for “sustained release” and programmed to release it’s payload at a later date, over a period of days, weeks, months or years, as the Moderna patent specifies.


    Moderna patent US10703789B2 delayed drug release
    QUANTOM DOTS & MICROBEADS

    Atomic scale nanometer devices called Quantum Dots and Microbeads, are also components of the death jab weapons system. They are found in the Pfizer and Moderna patents.

    These nanoscale technological devices are 1000 times smaller than a micrometer. Quantum Dots have nothing to do with plastic particles, these are carbon based nanocrystals, 10-50 atoms thick, and made from Graphene.

    Quantom Dots are used for DNA barcoding of Humans using CRISPR-Cas-9 technology. They are super conductors made for bio-imaging and bio-tracking of Humans. They too were developed for “therapeutic” use, to eradicate cancers, not to enslave Humans.

    Quantum Dots are artificial, color based, bioluminescent marker genes. They use three colors taken from the enzymatic proteins of insects (Luciferase), glow worms and jellyfish. The chimeric proteins are being barcoded onto Human genes to make them trackable, programmable and encoded, so Human cells will light up, enabling the NWO oligarchs to monitor your every move.

    I discussed Quantum Dots and more with Stew Peters on December 9th, 2021.

    Dr. Ariyana Love on Stew Peters Show, Dec. 9, 2021
    Microbead patent US20110017493A1, verifies that Microbeads “carbon based” (made from Graphene) and Microbead patent ES2784361T3/en specifies that it’s used to create molecular barcodes in Humans.

    Thermo Ficher sells Microbeads and markets them as Dynabeads and SPIONs. See SPIONS here.

    THE ISRAELI STATE

    This technology was developed at the Hebrew University in occupied Jerusalem. The Quantum Dot patent WO201413562A1 is owned by Yissum, a Hebrew University company owned by the Israeli state and co-owned by Nanosys, a Silicon Valley based company. These two companies are sublicensing the technology, worldwide.

    Yissum business partners include Google, Intel, Johnson & Johnson, Merck, Microsoft, and many more, while Samsung has a partnership with Nanosys.

    Moderna’s patents are owned by Israel. Pfizer patents are owned by Israel. Pfizer CEO is in bed with Israel. Moderna is partnered with Israel in medical maleficence.

    Moderna’s CEO Stephane Bancel, wants every man, women and child injected with Moderna’s poison #DeathJab, including INFANTS!


    Is it clear to you now who it is that has the greatest vested interest in branding and enslaving Humans like cattle? The cloning of insect DNA (Luciferase) into Humans is called cross-species genomics. This is the process of manually adding DNA from insects into Humans by transfection, a process also known as cloning, in order to change the genetic makeup of cells. It works by deleting one or more gene from the Human host and encodes Human cells to express the new genetic trait of an insect. Is that what you want to become?


    BIOCHIP & HYDROGEL

    Dr. Pablo Campra mentioned that nano-biosensors are in the death jabs. They can be found in the DARPA patent US7427497B2/en which lists “T-shaped micro-fluidic Biochips”.


    Hydrogels contain the entire mRNA weapons system. They need us saturated with their cloning technology in order to succeed in genetically modifying Humans to the point of patent eligibility. They will do so by injections, masks, nasal swabs, hand sanitizer, aerial spraying, and any other means necessary to achieve their end goal.

    We are in fact being saturated with Graphene Oxide Hydrogels. They’re being inserted into our food, clothing, hair and make-up products, household cleaners, alcohol, pharmaceutical drugs, sanitary items, water supply, etc.

    Ethylene Oxide in masks and on PCR swabs, is in fact Graphene Oxide, Poly(ethylene oxide) Graphene Nanoribbons. The bad news is that Fauci and the NIH funded mRNA nanotechnology which is skin-penetrating and can be dispensed via aerial spraying, as reported by InfoWars. The good news is this weapons system can also be expelled through the skin, if you know how to properly detox. The key to protecting yourself from this biological attack is to boost your immune system and remain on a continued Protocol.

    PROTOCOL

    There is a special natural supplement that disables the operating system, kills the parasites, and removes Graphene and other metals, effectively expelling them from your body. This supplement increases endogenous glutathione by 800%, repairs damage to your cells and to your DNA, and turns genes on, according to scientific research. This medical breakthrough is being used now by doctors who are able to reverse the coagulation cascade in just minutes. You will find this supplement in my Protocol here.

    https://donshafi911.blogspot.com/2024/02/quantum-dots-dna-barcoding-nano-razors.html
    There's also a ton of information from the IEC regarding international Standards surrounding Biodigital convergence. Quantum Dots are programmable graphene oxide nanoparticles which serve many functions, including biometric data harvesting (spying). The demons want to build their Smart Cities from this material! https://ambassadorlove.blog/2021/12/17/quantum-dots-dna-barcoding-nano-razors-the-israeli-state/ Quantum Dots, DNA Barcoding, Nano-Razors & The Israeli State December 17, 2021 by Dr. Ariyana Love December 2, 2021 By Dr. Ariyana Love, ND In my latest interview with Stew Peter’s, I brought evidence confirming that Dr. Andreas Noack, the good doctor who risked his life to warn humanity of the extreme dangers of the death jab, is in fact deceased. Days after Dr. Noack’s mysterious death, a video was leaked revealing Graphene Hydroxide nano-razors inside the Pfizer death jab, under Dark Field Microscopy. The sample is loaded with Graphene Hydroxide. You will see an individual Microsphere releasing it’s payload of nanoscale Graphene Hydroxide which looks exactly like razorblades when zoomed in on the individual shiny specs. See more images here. LEAKED FOOTAGE: GRAPHENE HYDROXIDE NANO-RAZORBLADES – DARK FIELD MICROSCOPY An English translation of this video can be found in the article entitled, Dr. Ariyana Discusses Nano-Biosensors/Nanorazors and Dr. Noack’s Death After He Located Graphene Hydroxide in the COVID Vaccine. MICROSPHERES & MICROBUBBLES Microbeads and Microspheres are listed as an active ingredient in the Pfizer death jab patent. Microspheres and Microbubbles are listed in the Moderna death jab patent. Microspheres and Microbubbles are micrometer size devices approximately equal in size to a red blood cell, according to the NIH. That’s about the width of a Human hair. Microbubbles and Microspheres (bottom right) Microspheres and Microbubbles are made from Poly(lactic-co-glycolic) acid (PLGA). PLGA is a copolymer made from Graphene Oxide (GO). Graphene Oxide-PLGA nanofibers are used in a host of Food and Drug Administration (FDA) approved “therapeutic” devices. However, the ingredients of these devices are cytotoxic, meaning they destroy cells. Graphene Oxide PLGA Toxicity induces an inflammatory response and deadly cytokine storm reaction, according to animal studies. The FDA should be investigated for this. Microspheres are coated with gold nanoparticles. Microspheres are used for scaffolding, which is artificial tissue engineering inside the Human body. PubMed writes, “Scaffolds are materials that have been engineered to cause desirable cellular interactions to contribute to the formation of new functional tissues for medical purposes. Cells are often ‘seeded’ into these structures capable of supporting three-dimensional tissue formation.” This technology is being used for DNA-based tissue engineering and “scaffolding” of Humans, without their Informed Consent. See more scaffolding images from a Slovakian study of the death jab, here. Microbubbles contain one or more “viral vectors coding CRISPR-Cas-9 system“. It’s a “state-of-the-art” drug and chemical delivery method. They contain lab enhanced chimeric proteins of the messenger RNA/DNA. Microbubbles have a lipid and nickel-coated quartz substrate. They contain a drug and chemical payload in the outer, lipid-coating and another payload on the inside. Graphene Oxide Nanotubes enable Microbubbles to self-replicate via electrical pulse. They interlink by electrodes. Microbubbles were designed to break through the blood/brain barrier and deliver their drug and chemical payload into brain cells. Ultrasound is used to help Microbubbles breach the blood/brain barrier. Here’s a video animation of how microbubbles / microspheres work to deliver drugs into the brain. This gene delivery technology was funded and developed for the purpose of treating sick people, not healthy people. It was intended to be used as a treatment for cancer, not as a medical intervention for our healthy kids. The Microbubble and Microsphere devices carry drug and chemical payloads for controlled release of encapsulated DNA. It’s targeted drug delivery can be unloaded over an extended period of time. This is very important to understand. They can be formulated for “sustained release” and programmed to release it’s payload at a later date, over a period of days, weeks, months or years, as the Moderna patent specifies. Moderna patent US10703789B2 delayed drug release QUANTOM DOTS & MICROBEADS Atomic scale nanometer devices called Quantum Dots and Microbeads, are also components of the death jab weapons system. They are found in the Pfizer and Moderna patents. These nanoscale technological devices are 1000 times smaller than a micrometer. Quantum Dots have nothing to do with plastic particles, these are carbon based nanocrystals, 10-50 atoms thick, and made from Graphene. Quantom Dots are used for DNA barcoding of Humans using CRISPR-Cas-9 technology. They are super conductors made for bio-imaging and bio-tracking of Humans. They too were developed for “therapeutic” use, to eradicate cancers, not to enslave Humans. Quantum Dots are artificial, color based, bioluminescent marker genes. They use three colors taken from the enzymatic proteins of insects (Luciferase), glow worms and jellyfish. The chimeric proteins are being barcoded onto Human genes to make them trackable, programmable and encoded, so Human cells will light up, enabling the NWO oligarchs to monitor your every move. I discussed Quantum Dots and more with Stew Peters on December 9th, 2021. Dr. Ariyana Love on Stew Peters Show, Dec. 9, 2021 Microbead patent US20110017493A1, verifies that Microbeads “carbon based” (made from Graphene) and Microbead patent ES2784361T3/en specifies that it’s used to create molecular barcodes in Humans. Thermo Ficher sells Microbeads and markets them as Dynabeads and SPIONs. See SPIONS here. THE ISRAELI STATE This technology was developed at the Hebrew University in occupied Jerusalem. The Quantum Dot patent WO201413562A1 is owned by Yissum, a Hebrew University company owned by the Israeli state and co-owned by Nanosys, a Silicon Valley based company. These two companies are sublicensing the technology, worldwide. Yissum business partners include Google, Intel, Johnson & Johnson, Merck, Microsoft, and many more, while Samsung has a partnership with Nanosys. Moderna’s patents are owned by Israel. Pfizer patents are owned by Israel. Pfizer CEO is in bed with Israel. Moderna is partnered with Israel in medical maleficence. Moderna’s CEO Stephane Bancel, wants every man, women and child injected with Moderna’s poison #DeathJab, including INFANTS! Is it clear to you now who it is that has the greatest vested interest in branding and enslaving Humans like cattle? The cloning of insect DNA (Luciferase) into Humans is called cross-species genomics. This is the process of manually adding DNA from insects into Humans by transfection, a process also known as cloning, in order to change the genetic makeup of cells. It works by deleting one or more gene from the Human host and encodes Human cells to express the new genetic trait of an insect. Is that what you want to become? BIOCHIP & HYDROGEL Dr. Pablo Campra mentioned that nano-biosensors are in the death jabs. They can be found in the DARPA patent US7427497B2/en which lists “T-shaped micro-fluidic Biochips”. Hydrogels contain the entire mRNA weapons system. They need us saturated with their cloning technology in order to succeed in genetically modifying Humans to the point of patent eligibility. They will do so by injections, masks, nasal swabs, hand sanitizer, aerial spraying, and any other means necessary to achieve their end goal. We are in fact being saturated with Graphene Oxide Hydrogels. They’re being inserted into our food, clothing, hair and make-up products, household cleaners, alcohol, pharmaceutical drugs, sanitary items, water supply, etc. Ethylene Oxide in masks and on PCR swabs, is in fact Graphene Oxide, Poly(ethylene oxide) Graphene Nanoribbons. The bad news is that Fauci and the NIH funded mRNA nanotechnology which is skin-penetrating and can be dispensed via aerial spraying, as reported by InfoWars. The good news is this weapons system can also be expelled through the skin, if you know how to properly detox. The key to protecting yourself from this biological attack is to boost your immune system and remain on a continued Protocol. PROTOCOL There is a special natural supplement that disables the operating system, kills the parasites, and removes Graphene and other metals, effectively expelling them from your body. This supplement increases endogenous glutathione by 800%, repairs damage to your cells and to your DNA, and turns genes on, according to scientific research. This medical breakthrough is being used now by doctors who are able to reverse the coagulation cascade in just minutes. You will find this supplement in my Protocol here. https://donshafi911.blogspot.com/2024/02/quantum-dots-dna-barcoding-nano-razors.html
    0 Comments 0 Shares 14555 Views
  • GMO PARASITES

    Pine needle oil and turpentine 100% pure gum spirits is the most effective and fast acting medicines for destroying Bill Gates GMO parasites found in the SEQ: ID NO 1 from the Covid jabs.

    See video #1:
    https://rumble.com/v1nuvlg-mega-bombs-deadly-gmo-parasites-are-the-mrna-vectors-patent-review-with-dr..html

    See video #2:
    https://rumble.com/v1ns3ls-deadly-gmo-parasites-are-the-mrna-vectors-patent-review-with-dr.-young-and-.html
    GMO PARASITES Pine needle oil and turpentine 100% pure gum spirits is the most effective and fast acting medicines for destroying Bill Gates GMO parasites found in the SEQ: ID NO 1 from the Covid jabs. See video #1: https://rumble.com/v1nuvlg-mega-bombs-deadly-gmo-parasites-are-the-mrna-vectors-patent-review-with-dr..html See video #2: https://rumble.com/v1ns3ls-deadly-gmo-parasites-are-the-mrna-vectors-patent-review-with-dr.-young-and-.html
    Like
    1
    0 Comments 0 Shares 1060 Views
  • The COVID-19 Vaccine Antigen Is ANTHRAX
    Dr. Ariyana Love
    By Dr. Ariyana Love

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

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

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

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

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

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

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

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


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


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

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

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


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


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

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

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

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

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

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

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

    SPIKE PROTEIN IS AEROSOLIZED ANTHRAX

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

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

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

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

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

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

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

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

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

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

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

    ALHYDROGEL

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

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

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

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

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

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

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

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

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

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

    Alhydrogel was improved and transformed into the Nanoalum adjuvant.

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

    Alhydrogel is also carried in the lipid coating of nanoparticles.

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


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


    ANTHRAX SYMPTOMS AND TREATMENT

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

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

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


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


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

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

    Anthrax also coagulates the blood.

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

    Read more here and here.

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

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


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

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

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

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

    Heroine users in Europe have been tested with Injection Anthrax.

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

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

    TREATMENT

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

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

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

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

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

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


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

    The Covid-19 Vaccine Antigen Is ANTHRAX

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


    https://donshafi911.blogspot.com/2024/02/the-covid-19-vaccine-antigen-is-anthrax.html
    The COVID-19 Vaccine Antigen Is ANTHRAX Dr. Ariyana Love By Dr. Ariyana Love Covid-19 vaccines use self-replicating, programmable nanotechnology and synthetic, modified RNA (modRNA) otherwise known as Spike Protein. We are told that a vaccine antigen is used in the Covid-19 technology to “evoke an immune response” but what if the Covid-19 vaccine antigen is ANTHRAX? “…hardly any natural pathogens are really well suited to being biowarfare agents from a military point of view. Such a bioweapon must fulfill a variety of demands: it needs to be produced in large amounts, it must act fast, it must be environmentally robust, and the disease must be treatable… only a minority of natural pathogens are suitable for military purposes. “Anthrax is of course the first choice because the causative agent, B. anthracis, fulfills nearly all of these specifications.” Anthrax was developed by Russia in 1950. According to the NIH, the USSR’s ‘invisible anthrax’ was created by introducing an “alien gene” into the highly deadly Bacillus Anthracis bacteria. This means that Cross-Species-Genomics capability was acquired by governments before 1950. A lethal bacterium and an alien gene were genetically altered and blended together to produce the deadly bioweapon known as Anthrax. Russia’s Anthrax could be treated with antibiotics even several days after exposure, and thus it met the requirements under the Biological Weapons Convention. A bioweapon of choice, Anthony Fauci decided to increase Anthrax lethality and the NIH began genetic attenuation before 2006. Through GAIN-and-LOSS-of-Function the NIH produced a more drastic and deadly Anthrax that’s resistant to antibiotics and more. According to a University of Minnesota publication, the United States D.O.D smuggled shipments of live B anthracis spores from the Army’s Dugway Proving Ground in Utah, to other labs in the United States and abroad (Source: USA Today). The U.S. Army sent shipments of live samples of Anthrax to 86 labs outside the U.S. over a period of 10 years (Source: The Daily Beast). Transfers of samples of live B anthracis and the H5N1 influenza bioweapon were sent from CDC labs to other labs. CDC correspondence released under the Freedom of Information Act shows that labs studying bioterror pathogens “have failed over and over to comply with important safety and security regulations.” The D.O.D. tried to cover for the CDC, claiming “system failure” was to blame for the lab leaks, but we already know that the D.O.D spearheaded this “Covid-19 vaccine” roll-out. Please see: Aerosolized inoculation of Anthrax – Aerosolized Intratracheal Inoculation of Recombinant Protective Antigen (rPA) Vaccine Provides In 2007, Anthony Fauci created the H7N9 bioweapon, otherwise known as the “influenza vaccine.” The NIH, CCP and the Israeli state collaborated through GAIN-and-LOSS-of-Function to produce the H7N9 “flu vaccine” and the new and improved “Aerosolized Anthrax Vaccine”. Ofir Israeli from the Israel Institute of Biological Research, sequenced the Bacillus anthracis V770-NP1-R Strain in 2014, creating a synthetic chemical bioweapon. The Israeli state oversaw the animal trials for the Anthrax “vaccine” and told us it was safe and effective. Meanwhile, the Israeli company called Sanofi Pasteur developed the first H7N9 “vaccine” and trialed it for the NIH in 2014. Also in 2014, the NIH developed the H7N9 “influenza vaccine” to be droplet transmissible. Simultaneously, in 2014 China achieved a 99% transmissibility of the H7N9 “flu vaccine”. China also trialed the first aerosolized intratracheal Anthrax “vaccine” on mice. The study revealed severe side effects. PLEASE SEE: NIH Using DEAD CORPSES To Make “Virus”; Gain Of Function Weaponized Dead Corpses The Israeli state, NIH and China turned their new and improved Anthrax bioweapon into an attenuated antigen to be used in vaccines under the guise of “evoking an immune response” and “vaccine immunity.” The nations have been intentionally poisoned with biowarfare. In March 2022, the Russian military discovered that the Covid-19 bioweapons are being developed in U.S. biolabs in Ukraine. This includes the plague, Ebola, Filoviruses’, Anthrax and more. Anthrax causes hemorrhaging. So does Ebola and Marburg. Ebola is used in the J&J and Sinovax jabs, while Filovirus is used in Moderna. Ebola and Marburg are both Anthrax. H7N9 is used in all “flu vaccines” while Anthrax is being used as a “vaccine adjuvant” in all Covid-19 jabs and swabs. Through Loss-Of-Function, genetic deletions were performed inside the B. anthracis bacteria to improve replication of the bacteria in vivo. This ensured hospital protocols would not work to stop the Anthrax from replicating inside the human body after inoculation due to it being antibiotic resistant. The B. anthracis bacteria was also genetically modified to survive in insect hosts so as not to sporulate before it’s injected into the human host by a Bill Gates GMO mosquito which is part of DARPA’s weaponized insect project called The Sentinels. Incidentally, the CDC owns the Anthrax isolate patent that was funded by the U.S. Government. This is treason. The CDC also says that a bioterrorist attack would most likely be Anthrax. Please see: Malaria Parasites In “Vaccines” Target Placenta, Kill Babies In Utero SPIKE PROTEIN IS AEROSOLIZED ANTHRAX There are 232 B. anthracis genomes that are currently available in the GenBank database. There’s an Anthrax “vaccine” for cattle and two strains are licensed for use in humans. There exist two patents for an “Aerosolized Anthrax Vaccine.” The first Anthrax “vaccine” patent for humans is partly owned by the U.S. Government. The second is a “Recombinant Anthrax Vaccine”. “The spores of the toxigenic, nonencapsulated B. anthracis STI-1 strain and the cell-free PA-based “vaccines” consisting of aluminum hydroxide-adsorbed supernatant material from cultures of the toxigenic, nonencapsulated B. anthracis strain V770-NPI-R or alum-precipitated culture filtrate from the Sterne strain. Each of these Anthrax toxins are being used for “cellular entry in humans“. The LF is a metalloprotease recently shown to cleave the amino termini of the mitogen-activated protein kinase kinases 1 and 2, which results in their inactivation.” The above quote from the Recombinant Anthrax Vaccine patent reveals that the poisonous Anthrax “antigen” is being used to genetically modify the genome of humans (cellular entry into humans). By cleaving to the amino termini, protein kinases 1 and 2 are inactivated. This is accomplished by genetic deletions. The molecular basis of Anthrax “vaccines” includes “spores and DNA plasmids” that are entering human cells. The following quote about the Anthrax “protective antigen” is particularly revealing: “PA (protective antigen) is the common receptor binding domain of the toxins and can interact with the two different effector domains, EF and LF, to mediate their entry into target cells (14).” Anthrax is being used to “regulate gene expression by binding to DNA sequences and modulating transcriptional activity through their effector domains”. Pharma has essentially found a way to encode any synthetic proteins into the human genome from any species they want, including bacteria. The “Aerosolized Anthrax Antigen” is being encoded into target cells to make those cells produce the chemical drug called Anthrax. This is how the Anthrax “vaccine” is aerosolized. Once a person is inoculated with the Covid-19 bioweapon through subcutaneous injection or nasopharyngeal delivery with contaminated PCR swabs, the weapon system will begin genetic deletions and encoding the genome of target cells with the Anthrax spike protein. A person begins producing the toxic spike protein and shedding Anthrax into the air, exposing everyone to Inhalation Anthrax. It’s a weapon system that is intentionally aerosolized. This study admits that the Anthrax spores from B. anthracis STI-1 strain and B. anthracis strain V770-NPI-R used in the “aerosolized Anthrax vaccines” are toxigenic. The Sterne strain which is used to inoculate our food supply (animals) is also genotoxic. This NIH study explains how a “replicon” of the Bacillus anthracis bacteria was cloned into an Escherichia coli (E. coli) “vector” using cross-species-genomics. These two bacteria were synthetically fused together to enhance lethality. ALHYDROGEL According to the “aerosolized Anthrax vaccine” patents, the so-called “vaccine adjuvant” used is a DARPA weapon system called Alhydrogel. Hydrogel technology was developed over many years during a collaboration between DARPA and Profusa, a private biotech company specializing in the development of tissue-integrated biosensors. In 2018, DARPA published a video revealing their intention to use this biosensing technology for both military and public health. In the Alhydrogel invention, Anthrax was fused together into a nanogel called Alhydrogel, consisting of fibrous nanoparticles (Nanofibers) that are “antigen specific to CD4+ T cells”. In layman’s terms, the nanorobots are intentionally programmed to target and alter the genome of CD4-T cells, inducing cell death. This essential part of our immune system (T-cells) stop foreign invaders from entering our cells. Destroying our T-cells enables the government’s operating system to take root in the body and quicken death. Alhydrogel is infused with 750 μg of aluminum, making it magnetic. Nanofibers are used for self-assembly and electrospinning, for tissue engineering and delivery of drugs and chemicals into the brain. Being magnetic and nanotech based, the Alhydrogel can replicate everywhere in the body and wire a new neural network. Astonishingly, Alhydrogel is already the most widely used vaccine adjuvant! There are many Alhydrogel patents that contain toxic cocktails that will overwhelm anyone’s immune system. This Alhydrogel patent demonstrates it’s use of the B anthracis bacteria, E. coli, N. gonorrhoeae, Chlamydia, Staphylococcus, TB and more. It also contains the H5N1 influenza bioweapon, RNA, DNA synthesis and Polysorbate 80 for Blood Brain Barrier (BBB) permeability. This begs the question, where do venereal diseases come from? This Nature article reveals that 2% Alhydrogel is used in all Covid-19 “vaccines”. Previously, aluminum salts were the only adjuvants licensed for vaccine use in humans in the U.S. In recent decades, nanoparticle adjuvants in hydrated gels were introduced. The article continues by saying that the “influenza vaccine” was the first to use Alhydrogel. “Aluminum salt-based adjuvants such as alhydrogel have been a mainstay of vaccines for decades” boasts Christopher B. Fox and colleagues at the Infectious Disease Research Institute in Seattle, USA. Both nanoparticles and Anthrax have been used in vaccines for decades already, without the Informed Consent of the public. Alhydrogel was improved and transformed into the Nanoalum adjuvant. Here, we introduce a top-down manufacturing process—high-pressure microfluidization—to generate aluminum oxyhydroxide nanoparticles, hereupon referred to as nanoalum, using the clinically approved Alhydrogel adjuvant as the precursor. Alhydrogel is also carried in the lipid coating of nanoparticles. The “Aerosolized Anthrax Vaccines” also contain SEQ ID NO: 1 which is owned by the Pirbright Institute (Bill & Melinda Gates). SEQ ID NO: 1 contains the world’s most deadly genetically modified parasites. Please see: MEGA BOMBS! GMO Parasites Are The mRNA Vector! ANTHRAX SYMPTOMS AND TREATMENT Anthrax has been deployed on the population by three methods; injection, inhalation and skin penetration. The mortality rate for Anthrax varies depending on the method of exposure. It’s approximately 20% fatality for cutaneous Anthrax and 25–75% for Gastrointestinal Anthrax. Inhalation Anthrax is by far the worst with a fatality rate that is 80% or higher. Inhalation Anthrax is what we’re all being exposed to from the Covid-19 jabs and contaminated PCR swabs. Antibiotics constitute the mainstay of treatment against Anthrax, despite the fact that they won’t work to stop its replication due to the NIH, China and Israel’s GAIN-and-LOSS-of-Function enhancements (antibiotic resistance). Pharmaceutical experimental genotoxic drugs such as Oblitoxaximab and Raxibacumab are being touted as Anthrax treatments but these are monoclonal antibodies. We know from the monoclonal antibody patents that they’re also the “mRNA vaccine” weapon system. Anytime you inject recombinant proteins or modRNA into humans, it’s extremely toxic and will be rejected by our immune system 100% of the time. Please read: Monoclonal Antibodies Is mRNA Gene Knockdown Tech, Encoding HIV – Patent Review Pharma wants us to believe that the only known effective “prevention” against Anthrax is the Anthrax “vaccine”. However, the Anthrax “vaccine” inoculation given to U.S. military troops was a horrific disaster. U.S. Army statistics that were never published, show the Anthrax “vaccine” induces turbo cancers. The toxicological harms of Anthrax are many. It causes severe heart issues. Could this be a contributing factor to Myocarditis and Pericarditis? Anthrax also coagulates the blood. “Pathophysiological changes associated with anthrax lethal toxin included loss of plasma proteins, decreased platelet count, slower clotting times, fibrin deposits in tissue sections, and gross and histopathological evidence of hemorrhage. These findings suggest that blood vessel leakage and hemorrhage lead to disseminating intravascular coagulation and/or circulatory shock as an underlying pathophysiological mechanism.” Read more here and here. Anthrax induces hemorrhaging. So this explains all the excessive bleeding people have experienced over the last 4 years, following Covid-19 inoculation and from aerosolized exposure, otherwise known as the “shedding” phenomenon. This is a result of Inhalation Anthrax. It becomes clear that the newly dubbed “White Lung Syndrome” and the Chinese ‘pneumonia’ outbreak is none other than Inhalation Anthrax. Mycoplasma pneumonia is on the rise, and it’s listed on Pfizer’s internal documentation as a known Adverse Effect of the Covid-19 inoculation. This study reveals that Mycoplasma Pneumonia is aerosolized. WHO also confirms this phenomenon is Mycoplasma Pneumonia. All naturally occurring bacterium have cell walls. Mycoplasmas are spherical to filamentous cells with no cell walls. It’s genetically manipulated in a laboratory by GAIN-of-Function for the purpose of enhancing replication inside the human body, making it more lethal. Mice “treated” with anthrax lethal toxin (LT) exhibit hemorrhage and liver damage. Monocyte procoagulant responses to anthrax peptidoglycan are reinforced by proinflammatory cytokine signaling and histological lesions in the spleen. Anthrax has already been tested on the public. According to the NIH, Anthrax spores were intentionally released into “some environments” in NYC during 9/11. According to the NIH, the FBI launched an investigation called “Amerithrax”. It was “one of the largest and most complex (investigation) in the history of law enforcement”, according to the FBI. Heroine users in Europe have been tested with Injection Anthrax. Our skies are sprayed with smart dust and chemicals daily. Our governments have launched an all-out war against their constituents. We are being poisoned in a myriad of ways, so please keep this in mind: “Anthrax is easy to produce in large quantities, highly lethal, relatively easy to develop as a weapon, easily spread over a large area, easily stored and dangerous for a long time. Given appropriate weather and wind conditions, 50 kilograms of aerosolised anthrax spores released from an aircraft along a 2 kilometer line could create a lethal cloud of anthrax spores that would extend beyond 20 kilometers downwind. The aerosol cloud would be colorless, odorless and invisible following its release. Given the small size of the spores, people indoors would receive the same amount of exposure as on the street. There are currently no atmospheric warning systems to detect an aerosol cloud of anthrax spores. The first sign of a bioterrorist attack would most likely be patients presenting with symptoms of inhalation anthrax. A 1970 analysis by World Health Organization concluded that the release of aerosolized anthrax upwind to a population of 5,000,000 could lead to an estimated 250,000 casualties, of whom as many as 100,000 could be expected to die. A later analysis, by the Office of Technology Assessment of the U.S. Congress estimated that 130,000 to 3 million deaths could occur following the release of 100 kilograms of aerosolized anthrax over Washington D.C., making such an attack as lethal as a hydrogen bomb.” TREATMENT If you have been inoculated with Covid-19 or PCR swabbed, and you are suffering from heart pain, unusual bleeding, skin rashes and abrasions, it could be Injection Anthrax. If you are “unvaccinated” and hemorrhaging from being around “vaccinated”, then you may have been exposed to Inhalation Anthrax. Many doctors, including myself, have documented persistent bleeding rectally, violent bleeding vaginally, nasally and in the eyes. Since October 4th, I have received many reports of a red eye syndrome where the entire eye is blood-red. This makes sense because eye tissue is more sensitive. If you have been exposed to Inhalation Anthrax, you may feel hot and severely flushed, and you may break out in big, red splotches on your skin, followed by a completely red eye in the morning. Although they don’t get much attention, “anti-toxins have long been considered an essential ‘adjunctive’ therapy, and remain so”, according to the NIH. Anti-toxins are the natural medicines that detox poisons. In other words, you need an effective natural medicine detox protocol. I have been successfully detoxing people from the Covid-19 bioweapons for three years. Since I began treating people presenting with Anthrax poisoning with strong antibacterials, my clients are experiencing quicker detox results. If you would like to schedule a consultation with me, please do so through my online booking system. Please follow me on Telegram @drloveariyana and X @drloveariyana. If you would like to donate to my research, please do so here. UPDATE: My Anthrax article is now fully edited and published on Substack. Please review and SHARE. The Covid-19 Vaccine Antigen Is ANTHRAX Read more: https://open.substack.com/pub/drloveariyana/p/the-covid-19-vaccine-antigen-is-anthrax?r=2juwfo&utm_campaign=post&utm_medium=web&showWelcomeOnShare=true https://donshafi911.blogspot.com/2024/02/the-covid-19-vaccine-antigen-is-anthrax.html
    Angry
    1
    1 Comments 1 Shares 17334 Views
  • BOMBSHELL STUDY: WE NOW HAVE 100% SCIENTIFIC PROOF WHY THE JABBED ARE DYING SUDDENLY

    Dr. Chris Shoemaker with Jim Ferguson.
    Hearts are having to work MUCH harder for people who have had two Covid-19 Jabs or more.

    A September 2023 published study in which multiple major study centers from around the world participating in comparing non-vaccinated hearts to those who have been vaccinated - what they found was astounding -- a 47% INCREASE effort going on in the Cardiac Cells of vaccinated people compared to unvaccinated people .

    They found that this elevation persisted for at least SIX Months.

    Was this study Valid?

    YES. They took 5,000 patients worldwide and they meticulously (screened) got this down to 1,000 so this would be a valid, verifiable study in which 700 were double jabbed and 300 were non-jabbed. This was a legitimate elevation and strain on the heart muscle.

    It was confirmed with P Value <.0001.

    The Unvaxxed had no elevation in cardiac effort for the next six months.

    Now we have a scientific reason why people are dying suddenly 6 months to a year after the shots.

    “This terrible, nefarious thing, in which lots are different one place to another, that’s a plan. They didn’t accidentally make one lot worse than the other. It was purposely done. It didn’t happen by accident!”

    The development of these controversial vaccines is now linked to the Defense Advanced Research Projects Agency (DARPA) and the Department of Defense. Furthermore, a shocking 33% of the substances used in these COVID vaccines are purported to be DNA-altering elements, having permanent effects on the bodies of those inoculated.

    The global rise in cases of Myocarditis, an inflammation of the heart muscle, has been tied to these vaccine developments, pointing to a massive health crisis. These revelations call into question the safety, ethics, and motivations behind the global vaccination drive, sparking urgent calls for accountability and transparency.

    https://www.bitchute.com/video/M9j8lWmHAXeA/
    BOMBSHELL STUDY: WE NOW HAVE 100% SCIENTIFIC PROOF WHY THE JABBED ARE DYING SUDDENLY Dr. Chris Shoemaker with Jim Ferguson. Hearts are having to work MUCH harder for people who have had two Covid-19 Jabs or more. A September 2023 published study in which multiple major study centers from around the world participating in comparing non-vaccinated hearts to those who have been vaccinated - what they found was astounding -- a 47% INCREASE effort going on in the Cardiac Cells of vaccinated people compared to unvaccinated people . They found that this elevation persisted for at least SIX Months. Was this study Valid? YES. They took 5,000 patients worldwide and they meticulously (screened) got this down to 1,000 so this would be a valid, verifiable study in which 700 were double jabbed and 300 were non-jabbed. This was a legitimate elevation and strain on the heart muscle. It was confirmed with P Value <.0001. The Unvaxxed had no elevation in cardiac effort for the next six months. Now we have a scientific reason why people are dying suddenly 6 months to a year after the shots. “This terrible, nefarious thing, in which lots are different one place to another, that’s a plan. They didn’t accidentally make one lot worse than the other. It was purposely done. It didn’t happen by accident!” The development of these controversial vaccines is now linked to the Defense Advanced Research Projects Agency (DARPA) and the Department of Defense. Furthermore, a shocking 33% of the substances used in these COVID vaccines are purported to be DNA-altering elements, having permanent effects on the bodies of those inoculated. The global rise in cases of Myocarditis, an inflammation of the heart muscle, has been tied to these vaccine developments, pointing to a massive health crisis. These revelations call into question the safety, ethics, and motivations behind the global vaccination drive, sparking urgent calls for accountability and transparency. https://www.bitchute.com/video/M9j8lWmHAXeA/
    Like
    1
    0 Comments 1 Shares 3655 Views
  • Dr. David Cartland
    is one of the few Medical Doctors to speak up against the Covid-19 Jabs. He testifies to the overwhelming number of vaxxine injured people he's seeing now in hospitals. He implores other medical professionals to speak out about what they're seeing.

    https://x.com/CartlandDavid/status/1754470254867001550?s=20
    Dr. David Cartland is one of the few Medical Doctors to speak up against the Covid-19 Jabs. He testifies to the overwhelming number of vaxxine injured people he's seeing now in hospitals. He implores other medical professionals to speak out about what they're seeing. https://x.com/CartlandDavid/status/1754470254867001550?s=20
    Like
    1
    0 Comments 1 Shares 987 Views
  • DIRE WARNING TO THE WORLD FROM BIO-WARFARE EXPERT PROFESSOR FRANCIS BOYLE

    Dire warning to the world from bio-warfare expert Professor Francis Boyle
    Biowarfare is modern day genocide and jabs are the method of deployment. Both the bioweapon, spike protein and the mRNA delivery system are
    harmful to humans.
    According to Professor Francis Boyle all BSL-3 and BSL-4 labs need to be shut down immediately. They serve no purpose but
    to develop offensive biological weapons. He says the Frankenstein shots are a Nuremberg crime against humanity.
    Listen to the podcast, as Professor Francis Boyle reveals the antidote
    they were working on for SARS-COV-2, a virus that had HIV inserts and gain of function. We ask Professor Boyle if biological weapons have been genetically targeted. Professor Boyle also reveals who is funding both the vaccine development and the biological weapons research, and how that research made it’s way to China, where it was leaked months earlier than officially reported.
    Professor Francis Boyle’s credentials are extensive. He also drafted the S.993 - Biological Weapons Anti-Terrorism Act of 1989 that made it a
    felony, punishable by lifetime imprisonment for any one working on US soil, to be involved in biological weapons development. https://rumble.com/v4739z9-smbpassionshare.localdataworkvideo-pod-castprofessor-boylerendersfracis-boy.html
    Francis Boyle is a professor of international law at the University of Illinois College of Law. He received an AB (1971) in Political Science from the University of Chicago, then a JD degree magna cum laude from Harvard Law School, and AM and PhD degrees in Political Science from Harvard University. He practiced tax and international tax with Bingham, Dana & Gould.
    Quotes from the interview

    "Yes, and as you correctly pointed out. This is like flying AIDS""I don't call them vaccines. They are frankenshots. Everyone is making
    money and that's what is behind this and in addition, many of these people believe in eugenics. That the fewer human beings, the better."
    "These so called vaccines, frankenshots give people live particles,
    cells of covid19 which is an offensive biological warfare weapon with gain of function properties to make it more lethal, and more infectious. And HIV in there too!"

    Professor Boyle and others have been working to get criminal indictments for all those involved in the bioweapons deployment both in the lab of
    the weaponized virus and the frankenshots. https://rumble.com/v4739z9-smbpassionshare.localdataworkvideo-pod-castprofessor-boylerendersfracis-boy.html JANUARY / 3 / 2024 = Archbishop Carlo Vigano = ON THE GLOBAL DEPOPULATION PLAN EXPOSED . Archbishop Vigano: For the past four years, we have been witnessing the implementation of a criminal plan of world depopulation, achieved through the creation of a false pandemic and imposition of her false vaccine, which you now know to be a biological weapon of mass destruction https://rumble.com/v44yj43-archbishop-carlo-vigan.html

    https://www.bitchute.com/video/DeXfOzDWkKyb/
    DIRE WARNING TO THE WORLD FROM BIO-WARFARE EXPERT PROFESSOR FRANCIS BOYLE Dire warning to the world from bio-warfare expert Professor Francis Boyle Biowarfare is modern day genocide and jabs are the method of deployment. Both the bioweapon, spike protein and the mRNA delivery system are harmful to humans. According to Professor Francis Boyle all BSL-3 and BSL-4 labs need to be shut down immediately. They serve no purpose but to develop offensive biological weapons. He says the Frankenstein shots are a Nuremberg crime against humanity. Listen to the podcast, as Professor Francis Boyle reveals the antidote they were working on for SARS-COV-2, a virus that had HIV inserts and gain of function. We ask Professor Boyle if biological weapons have been genetically targeted. Professor Boyle also reveals who is funding both the vaccine development and the biological weapons research, and how that research made it’s way to China, where it was leaked months earlier than officially reported. Professor Francis Boyle’s credentials are extensive. He also drafted the S.993 - Biological Weapons Anti-Terrorism Act of 1989 that made it a felony, punishable by lifetime imprisonment for any one working on US soil, to be involved in biological weapons development. https://rumble.com/v4739z9-smbpassionshare.localdataworkvideo-pod-castprofessor-boylerendersfracis-boy.html Francis Boyle is a professor of international law at the University of Illinois College of Law. He received an AB (1971) in Political Science from the University of Chicago, then a JD degree magna cum laude from Harvard Law School, and AM and PhD degrees in Political Science from Harvard University. He practiced tax and international tax with Bingham, Dana & Gould. Quotes from the interview "Yes, and as you correctly pointed out. This is like flying AIDS""I don't call them vaccines. They are frankenshots. Everyone is making money and that's what is behind this and in addition, many of these people believe in eugenics. That the fewer human beings, the better." "These so called vaccines, frankenshots give people live particles, cells of covid19 which is an offensive biological warfare weapon with gain of function properties to make it more lethal, and more infectious. And HIV in there too!" Professor Boyle and others have been working to get criminal indictments for all those involved in the bioweapons deployment both in the lab of the weaponized virus and the frankenshots. https://rumble.com/v4739z9-smbpassionshare.localdataworkvideo-pod-castprofessor-boylerendersfracis-boy.html JANUARY / 3 / 2024 = Archbishop Carlo Vigano = ON THE GLOBAL DEPOPULATION PLAN EXPOSED . Archbishop Vigano: For the past four years, we have been witnessing the implementation of a criminal plan of world depopulation, achieved through the creation of a false pandemic and imposition of her false vaccine, which you now know to be a biological weapon of mass destruction https://rumble.com/v44yj43-archbishop-carlo-vigan.html https://www.bitchute.com/video/DeXfOzDWkKyb/
    0 Comments 0 Shares 7534 Views
  • Here's my bio. Everything is here. I never lied to anyone as the defamation story goes. When people ask my qualifications I always tell them. This is who I am and was before 2019 brought us Event 201 and the Covid-19 democide.

    I will be updating everything soon and starting a Substack.

    https://ambassadorlove.blog/2023/09/24/dr-ariyana-love-nd-bio/



    Dr. Ariyana Love Bio
    September 24, 2023 by Dr. Ariyana Love
    Dr. Ariyana Love is an official Goodwill Ambassador to Palestine. She’s a second-generation natural doctor, investigative journalist, medical and patent researcher, and founder of an international foundation revitalizing traditional Homeopathic medicines.

    Dr. Love uses world renown disease reversing (anti-aging) protocols that detox and reverse vaxx and swab injuries. She is currently advocating for client retribution and compensation.

    Dr. Love’s father, Dr. Eric Love, founded the first natural healing school in Northern California in 1981. Prior to training through the International Association of Homeopathy (Dad’s institute) in her early 20’s, she was certified in various healing modalities from Heartwood Institute of the Healing Arts School. With 18+ years of training and experience in the field of natural medicine and nutrition, she’s currently being mentored by scientist, Dr. Robert O. Young, and Biotech expert, Dr. Judy Mikovitz.

    Dr. Love studied Motion Picture Video (film) at Montana State University and worked in Hollywood for about a year, before opting out of Hollywood and into corporate finance. Mentored in upper-level business management, she spearheaded a financial consulting company with Omega Financial and moved to Finland with her team in 1998, to acquire advanced technologies.

    Dr. Love’s elder son was vaccine injured at the age of two. He was diagnosed with High Functioning Autism (Asperger) at age 7. She applied her medical knowledge and designed a dietary protocol that resulted in a total reversal of her son’s debilitating symptoms by the time he was 8. All of his allergies also disappeared.

    In 2010, Dr. Love began homeschooling on a Native American reservation in the mountains of Northern California, where she lived with the indigenous Hoopa and Karook tribes. She studied traditional Native American Medicine and learned the Brickstitch weave from a generational teacher. Designing beautiful earring patterns is a favorite hobby. She and her sons also learned to track, hunt, skin, fish and forage.

    Dr. Love is originally from the Emerald Triangle in Northern California, where she grew up along the Sequoia/Redwood coast. She has traveled the world learning traditional medicine from indigenous people and harvesting the purest medicines from nature reserves, such as the pine tree and chaparral.

    Dr. Love pilgrimaged to the holy land of Palestine in 2012, and lived in a traditional Palestinian village in the Occupied West Bank for close to a year. She studied the root of Authentic World Judaism, Orthodox Christianity and Islam, and grew a heart felt appreciation for the Palestinian culture and their traditions. She discovered Palestine’s superior harvesting techniques and the many medicinal applications from the blessed olive tree, as well as other herbs and plants from the Middle East.

    Dr. Love’s Ministry in Palestine activated her calling. Witnessing the injustice of Apartheid inspired her journalism and Human Rights Defending. In 2013, she was invited to train with Roger Landry from the The Liberty Beacon (TLB) news network. She Directed and built two successful news channels from the ground up before she was politically targeted and de-platformed across social media, beginning in 2017.

    Dr. Love has been on the front lines in independent media, leading record-breaking campaigns in defense of political prisoners. She collaborated with Palestinian media professionals for 8 years, documenting and publishing Zionist occupation war crimes. Eventually the Palestinian Authorities (PA) and Gaza authorities awarded her with an official Goodwill Ambassador to Palestine role through the International Commission to Support Palestinian Rights (ICSPR).

    Julian Assange invited Dr. Love to join WikiLeaks from Belmarsh Prison, in 2019.

    Dr. Love was the first person in the world to read and document all the experimental modRNA “vaccine” patents and report them on Stew Peters Show. She applied her medical knowledge and research skills and designed protocols to naturally chelate heavy metals, cancel nanotech and detox the body from all poisons. Her protocols stop spike protein replication and restore the body’s original design. She’s been detoxing people successfully from jabs and swabs since October of 2020. She applies the Terrain theory to reverse cellular and DNA damage, brain injury, autoimmunity and essentially all diseases because the root cause is always the same.

    Dr. Love’s detox and health protocols are highly sought after worldwide. She is mentored by scientist Dr. Robert Young and Biotech expert, Dr. Judy Mikovitz. Her work is published in Global Research and used by medical and legal teams and natural law tribunals.
    Here's my bio. Everything is here. I never lied to anyone as the defamation story goes. When people ask my qualifications I always tell them. This is who I am and was before 2019 brought us Event 201 and the Covid-19 democide. I will be updating everything soon and starting a Substack. https://ambassadorlove.blog/2023/09/24/dr-ariyana-love-nd-bio/ Dr. Ariyana Love Bio September 24, 2023 by Dr. Ariyana Love Dr. Ariyana Love is an official Goodwill Ambassador to Palestine. She’s a second-generation natural doctor, investigative journalist, medical and patent researcher, and founder of an international foundation revitalizing traditional Homeopathic medicines. Dr. Love uses world renown disease reversing (anti-aging) protocols that detox and reverse vaxx and swab injuries. She is currently advocating for client retribution and compensation. Dr. Love’s father, Dr. Eric Love, founded the first natural healing school in Northern California in 1981. Prior to training through the International Association of Homeopathy (Dad’s institute) in her early 20’s, she was certified in various healing modalities from Heartwood Institute of the Healing Arts School. With 18+ years of training and experience in the field of natural medicine and nutrition, she’s currently being mentored by scientist, Dr. Robert O. Young, and Biotech expert, Dr. Judy Mikovitz. Dr. Love studied Motion Picture Video (film) at Montana State University and worked in Hollywood for about a year, before opting out of Hollywood and into corporate finance. Mentored in upper-level business management, she spearheaded a financial consulting company with Omega Financial and moved to Finland with her team in 1998, to acquire advanced technologies. Dr. Love’s elder son was vaccine injured at the age of two. He was diagnosed with High Functioning Autism (Asperger) at age 7. She applied her medical knowledge and designed a dietary protocol that resulted in a total reversal of her son’s debilitating symptoms by the time he was 8. All of his allergies also disappeared. In 2010, Dr. Love began homeschooling on a Native American reservation in the mountains of Northern California, where she lived with the indigenous Hoopa and Karook tribes. She studied traditional Native American Medicine and learned the Brickstitch weave from a generational teacher. Designing beautiful earring patterns is a favorite hobby. She and her sons also learned to track, hunt, skin, fish and forage. Dr. Love is originally from the Emerald Triangle in Northern California, where she grew up along the Sequoia/Redwood coast. She has traveled the world learning traditional medicine from indigenous people and harvesting the purest medicines from nature reserves, such as the pine tree and chaparral. Dr. Love pilgrimaged to the holy land of Palestine in 2012, and lived in a traditional Palestinian village in the Occupied West Bank for close to a year. She studied the root of Authentic World Judaism, Orthodox Christianity and Islam, and grew a heart felt appreciation for the Palestinian culture and their traditions. She discovered Palestine’s superior harvesting techniques and the many medicinal applications from the blessed olive tree, as well as other herbs and plants from the Middle East. Dr. Love’s Ministry in Palestine activated her calling. Witnessing the injustice of Apartheid inspired her journalism and Human Rights Defending. In 2013, she was invited to train with Roger Landry from the The Liberty Beacon (TLB) news network. She Directed and built two successful news channels from the ground up before she was politically targeted and de-platformed across social media, beginning in 2017. Dr. Love has been on the front lines in independent media, leading record-breaking campaigns in defense of political prisoners. She collaborated with Palestinian media professionals for 8 years, documenting and publishing Zionist occupation war crimes. Eventually the Palestinian Authorities (PA) and Gaza authorities awarded her with an official Goodwill Ambassador to Palestine role through the International Commission to Support Palestinian Rights (ICSPR). Julian Assange invited Dr. Love to join WikiLeaks from Belmarsh Prison, in 2019. Dr. Love was the first person in the world to read and document all the experimental modRNA “vaccine” patents and report them on Stew Peters Show. She applied her medical knowledge and research skills and designed protocols to naturally chelate heavy metals, cancel nanotech and detox the body from all poisons. Her protocols stop spike protein replication and restore the body’s original design. She’s been detoxing people successfully from jabs and swabs since October of 2020. She applies the Terrain theory to reverse cellular and DNA damage, brain injury, autoimmunity and essentially all diseases because the root cause is always the same. Dr. Love’s detox and health protocols are highly sought after worldwide. She is mentored by scientist Dr. Robert Young and Biotech expert, Dr. Judy Mikovitz. Her work is published in Global Research and used by medical and legal teams and natural law tribunals.
    AMBASSADORLOVE.BLOG
    Dr. Ariyana Love Bio
    Dr. Ariyana Love is an official Goodwill Ambassador to Palestine. She’s a second-generation natural doctor, investigative journalist, medical and patent researcher, and founder of an internat…
    0 Comments 0 Shares 14207 Views
More Results