Carmen Leitch - A Mysterious Plasmid is Found at High Levels in the Human Gut:

https://www.labroots.com/trending/genetics-and-genomics/27029/mysterious-plasmid-found-levels-human-gut

#Plasmid #PBI143 #Metagenome #Gastrointestinal #Gut #Microbiology #Biology

SV40, a DNA Altering, Carcinogenic Contaminant, found in Pfizer’s COVID-19 Vaccines
The ExposéMarch 17, 2024
It’s not just the spike protein and the mRNA that are a problem. Both Pfizer and Moderna covid injections also have DNA contamination and Pfizer’s covid injection contains SV40 promoters.

Microbiologist Kevin McKernan pioneered research on testing some of the covid vaccine vials and discovered unacceptable levels of double-stranded DNA plasmids floating around. This is DNA contamination. He found the contamination in Pfizer and Moderna vials.

During an interview with Peter Sweden, Sasha Latypova said that DNA contamination is “a huge problem because this is replication competent plasmid, it can then invade human cells, it can invade the bacterial cells that live in your gut. So, they go into the bacteria they replicate there, they replicate antibiotic-resistant genes…it can cause sepsis, it can cause cancer, all sorts of issues.”

The World Council for Health (“WCH”) stated that a red line has been crossed. “DNA contamination of mRNA ‘vaccines’ poses a risk to everyone on the planet,” WCH said. “Replicable DNA, so-called plasmids, in both the monovalent and bivalent vaccines, which should not be there at all … We can only speculate how it will end, but what needs to happen today after the publication of the paper by McKernan et al (2023) is an immediate stop of the ‘covid-19 vaccine’ program.”

In Pfizer’s mRNA injection, McKernan also discovered Simian Virus 40 (“SV40”) promoters which are tied to cancer development in humans. He emphasised that the SV40 found is a viral piece, it is not the whole virus. However, it still presents a risk of driving cancer.

SV40 or Simian Virus 40 was the 40th virus found in rhesus monkey kidney cells when these cells were used to make the polio vaccine. This virus contaminated both the inactivated polio vaccine (“IPV”) and the oral or “live” polio vaccine (“OPV”) developed by Dr. Albert Sabin. When it was discovered that SV40 was an animal carcinogen that had found its way into the polio vaccines, a federal law was passed in 1961 that required that no vaccines contain this virus.

Kanekoa The Great tweeted two audio/video transcripts. One of a recent interview with McKernan explaining his discoveries and another of a Japanese professor expressing his concerns about these discoveries. We have republished these transcripts below.

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DNA Contamination and SV40 Discovered

McKernan joined Conservative Review with Daniel Horowitz on Friday to warn that there is no quality control in the manufacturing process of these vaccines. If his findings turn out to be widespread, it could portend an even greater risk for anaphylaxis, blood clotting, developing resistance to antibiotics, gene integration risk, and long-term production of spike protein within the body. You can listen to an audio of the interview on Apple podcasts HERE.

During the interview, McKernan said:

“It’s in both Moderna and Pfizer. We looked at the bivalent vaccines for both Moderna and Pfizer and only the monovalent vaccines for Pfizer because we didn’t have access to monovalent vaccines for Moderna. In all three cases, the vaccines contain double-stranded DNA contamination. If you sequence that DNA, you’ll find that it matches what looks to be an expression vector that’s used to make the RNA…

“Whenever we see DNA contamination, like from plasmids, ending up in any injectable, the first thing people think about is whether there’s any E. coli endotoxin present because that creates anaphylaxis for the injected. And, of course, your viewers and listeners are probably aware there’s a lot of anaphylaxis going on, not only on TV but in the VAERS database. You can see people get injected with this and drop. That could be the background from this E. coli process of manufacturing the DNA…

“At least on the Pfizer side of things, it has what’s known as an SV40 promoter. This is an oncogenic virus piece. It’s not the entire virus. However, the small piece is known to drive very aggressive gene expression. And the concern that people, even at the FDA, have noted in the past whenever injecting double-stranded DNA is that these things can then integrate into the genome. If you’re not careful with how you manufacture these things, and you have excess amounts of this DNA, your concern for genome integration goes up…

“If you get an SV40 promoter in front of an oncogene, you will end up with a high expression of a gene that can drive cancer, it will be a very rare event, but you don’t need many of these cells to be hit with something like this for it to take off. SV40 actually plagued, granted it was the full viral genome, not just the promoter, but this has plagued previous vaccine programs. The polio vaccine is one of them that they were concerned that this may have contributed to cancer from that vaccine. So, there’s a history of being concerned over SV40.

“Having the promoter inside some of these vectors isn’t necessary. It seems to be superfluous oversight they could have eliminated, yet it’s still there because they ran this out the door so quickly, they didn’t really have time to get rid of superfluous parts of the plasmid. So, that piece of DNA is something we really need to pay attention to. We’ve made quantitative PCR assays to hunt for this. So several researchers around the globe are now running these assays to look for how much of this DNA is floating around after people have been vaccinated.”

Further reading:

Sequencing the Pfizer monovalent mRNA vaccines also reveals dual copy 72-bp SV40 Promoter, Anandamide (Kevin McKernan), 12 April 2023
dsDNA variance in Pfizer Docs, Anandamide (Kevin McKernan), 20 May 2023
McKernan, K., Helbert, Y., Kane, L. T., & McLaughlin, S. (2023, April 10). Sequencing of bivalent Moderna and Pfizer mRNA vaccines reveals nanogram to microgram quantities of expression vector dsDNA per dose. https://doi.org/10.31219/osf.io/b9t7m
Plasmid DNA is a Known Pfizer Ingredient – NOT a Contaminant, Karen Kingston, 14 April 2023
Japanese Professor Expresses Concern

Japanese Professor Murakami of Tokyo University expressed his concerns over the alarming discovery of SV40 promoters McKernan had made. He said:

“The Pfizer vaccine has a staggering problem. I have made an amazing finding. This figure is an enlarged view of Pfizer’s vaccine sequence. As you can see, the Pfizer vaccine sequence contains part of the SV40 sequence here. This sequence is known as a promoter. Roughly speaking, the promoter causes increased expression of the gene. The problem is that the sequence is present in a well-known carcinogenic virus.

“The question is why such a sequence that is derived from a cancer virus is present in Pfizer’s vaccine. There should be absolutely no need for such a carcinogenic virus sequence in the vaccine. This sequence is totally unnecessary for producing the mRNA vaccine. It is a problem that such a sequence is solidly contained in the vaccine. This is not the only problem. If a sequence like this is present in the DNA, the DNA is easily migrated to the nucleus.

“So, it means that the DNA can easily enter the genome. This is such an alarming problem. It is essential to remove the sequence. However, Pfizer produced the vaccine without removing the sequence. That is outrageously malicious. This kind of promoter sequence is completely unnecessary for the production of the mRNA vaccine. In fact, SV40 is a promoter of cancer viruses.”


https://expose-news.com/2024/03/17/sv40-a-dna-altering-carcinogenic-contaminant-found-in-pfizers-covid-19-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.


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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

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!

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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.

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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

BREAKING: Integration of corona vaccine-contaminated DNA into the human cell line genome
2nd Smartest Guy in the World
This important article further establishes that the Modified mRNA “vaccines” integrate into the cells. While these contaminated cells do not express the entire spike protein, but, rather, only part of it, the net effect is that the DNA of the “vaccinated” is irrevocably altered.

Any type of integration into the genome, especially when being assaulted by millions of different random sequences from the “vaccine,” will inevitably cause mutations and other damage to the genome, irrespective if the entire spike protein is expressed, or not.

This DNA contamination ultimately results in the plethora of slow kill bioweapon adverse events that we are now seeing in surging amounts, not limited to prion diseases, turbo cancers, SADS, and so on and so forth.

The below is translated from Japanese, and it is a rather technical read, but well worth your time.


by Mao Arakawa (Okudo Hirokushi)

The essence of the corona vaccine contaminated DNA problem is the possibility of altering the human genome. To validate this possibility, Dr. Ulrike Kaemmerer conducted an experiment to administer the corona vaccine to MCF7 and OVCAR-3 cancer cell lines. Dr. McKernan, consulted by Dr. Kaemmerer, conducted an experiment to detect contaminated DNA from these cell lines. He reports on his blog the first case of contaminated DNA integration into the cancer cell line genome. (2SG: yesterdays article entitled, UPDATE: Doctors Warn mRNA "Vaccines" Could Spur Epidemic of Prion Brain Diseases addresses this.)

I was interested, so I attempted to recreate the DNA recombinant event that Dr. McKernan identified. In this article, I will show the results of my analysis.

Nepetalactone Newsletter

Vaccine targeted qPCR of Cancer Cell Lines treated with BNT162b2

Ulrike Kaemmerer has treated MCF7 and OvCar3 cancer cell lines with various vaccines. Once transfected they performed cell passaging on these transfected cell lines to dilute out the residual vaccine and identify cells which were transfected. They performed Immunohistochemistry (IHC) on these cells and documented spike expression levels…

Read more

14 days ago · 109 likes · 22 comments · Anandamide

image
Figure 1
Dr. Kaemmerer administered the corona vaccine from Pfizer and AstraZeneca to the ovarian tumor cell line OVCAR-3 and, after subculture, confirmed the expression of the spikutanpak by immunohistochemical staining. Deep Sequencing comes at a high cost; therefore, preliminary experiments are required in advance to perform DNA detection experiments. Dr. McKernan first screened post-vaccination cells with qPCR and targeted qPCR-positive cells for deep sequencing.

Contaminated DNA that is not integrated into the genome is diluted with subculture. In fact, the Ct value of the vector was Ct 30.28 in the first generation, but it was 34.72 in the second generation. The difference in 4Ct is 16 times the difference, and that is the lower concentration in the second passage. Dr. McKernan extracted DNA from two cells subcultured and performed deep sequencing. Sequence data detected SV40, replication origin and spiked DNA. Spike DNA was detected in the full genomic shotgun library of vaccine-treated samples with 3000x coverage. (Coverage means the percentage of the total base pair or locus of the genome covered by sequencing.) Since the coverage in the human genome was 30 times, we can see that the DNA with a large number of copies of the genome was invading the cell.

As a result, strangely, SNP (monobasic polymorphism) was detected in deep sequencing at the origin of the vaccine plasmid replication (F1 and SV40). This SNP does not exist in the vaccine. In other words, it seems that plasmids are mutating in cells. Also, the coverage of deep sequencing in the replication origin area is higher than average, and the number of copies observed is relatively high, which means that the DNA embedded in the cell may be duplicated and mutated. I mean. Originally, plasmids and SV40 DNA replication require specific enzymes not owned by human cells. Experiments such as the introduction of large amounts of microDNA fragments containing replication points into cells are not usually performed in molecular genetics. It is possible that unexpected DNA replication is occurring within the cell.

A total of two genomic integrations were observed in the vaccinated cell line from the analysis of Deep Sequencing by Dr. McKernan. Individual arrays of deep sequencing are called 「 leads 」. It was very interesting data, so I tried to re-parse the lead myself.

image
Figure 2
Figure 2 is a lead showing genomic integration in Dr. McKernan's Deep Sequencing Analysis. The subject of the analysis is Genome Integration Leads 1 and 2. You can also read a lot of information from short array data. This time in comparison with the human genomeblat searchTo find homologyblast searchI used it.

Now, after that, it will be my own re-parse.

image
Figure 3
The top of the array in Figure 3 is the lead. As you can tell by aligning this lead with the 12th chromosome (black) and the spike gene (red) of the Pfizer Corona vaccine, the 12th chromosome (black) is on the way to the spike gene (red). I am switching. And there is a short identical array (here GAGAG) in the place of switching. You can see that the end-recombination (MMEJ, Microhomology-mediated end joining) mediated by microhomology (microhomology) recombinates the contaminated DNA and human genome. Since MMEJ involves multiple intracellular DNA repair enzymes, this recombination is an artifact (mistake product) in the test tube. Instead, gene recombination may have occurred in cells.

Genome integration occurs on the long arm of chromosome 12, and the FAIM2 gene is present at this locus. FAIM2 is a gene that has been suggested to be associated with cancer malignancy. Recombinations occur on introns (arrays that do not encode proteins), but I do not know how such mutations also affect gene expression.

image
Figure 4
Another example of genomic integration is Figure 4. If you align this lead with chromosome 9 (black) and spike gene (red), you can see that in the lead, chromosome 9 (black) is switching to the spike gene (red) on the way. There is a short identical array (here TCTGCCCT) in the place where this example also switches. After all, it is believed that the contaminated DNA and the human genome were recombined using microhomology. Since there are multiple pathways for DNA repair, which repair pathway is used when foreign DNA is taken into the genome is case-by-case.

Part of the lead had an Illumina adapter array left. Adapter arrays are arrays granted to PCR amplify and sequence DNA for deep sequencing. Originally, the adapter array is removed during parsing, but often the removal is inadequate and remains in the lead.

Integration of contaminated DNA into the genome is occurring near Centromea. Let's talk a little about Centromea. Two chromosomes with the same genetic information that can be done after DNA replication are chromatids (sister chromatids). The chromatids are connected until the chromosomes are distributed during cell division, but the region on the connected DNA is Centromea. As such, Centromea is an important area for chromosome separation and distribution.

image
Figure 5
Figure 5 is about the DNA fragments of the spike gene integrated into the genome. On the Pfizer Corona vaccine spike gene, the sequence found in the genome integrated lead was written in red. Due to lead length limitations, the actual integrated array will be even larger. The integrated sequence is part of the spike gene, and it is not possible to make a full-length spike sequence. However, it is unpredictable how contaminated DNA will be inserted into any area of the genome and have any effect.

image
Figure 6
Nucleotype (cario type) means the size, shape, and number of chromosomes. Human chromosomes consist of a total of 46 22 pairs of autosomal and one pair of sex chromosomes. The autosomal is assigned the number 1 chromosome, number 2 chromosome,, number 22 chromosome and number in order of size. The integrated site of contaminated DNA is the FAIM2 locus on the long arm of chromosome 9 and near Centromea on chromosome 12.

The genomic integration observed this time is the first two cases in cultured cell experiments, but the specific identification of recombinant sequences with the human genome of contaminated DNA is a major advance. Further verification experiments will be advanced in the future. Genome integration, as in Figure 6, does not know which locus actually occurs on the genome. This is exactly the 「 shotgun attack on the genome 」. What happens in cultured cells can also occur in normal cells, with a wide variety of alterations depending on the site of genomic integration. The first predicted catabolism is cancer induction and malignancy. And then, the ones that manifest themselves over time are various genetic diseases.

What is known as a factor that causes genomic damage is, for example, radiation exposure, but genomic modification by contaminated DNA is different in that it is due to fragments of artificially created genes, and random mutations which are akin to radiation. But it is fundamentally different in nature. This experiment in cultured cells epitomizes genomic integration of contaminated DNA. This is a real problem that a large number of humans around the world, under the name of vaccination, are now experiencing a「 transfection human body experiment 」of contaminated DNA.

The genomic modification of humanity is a direct consequence of the largest experiment in history of mRNA drug substance harm, and in the future it may be etched in history as the「 original sin 」of humanity.


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Original Social Engineering Sin
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BREAKING: Integration of corona vaccine-contaminated DNA into the human cell line genome




https://www.2ndsmartestguyintheworld.com/p/breaking-integration-of-corona-vaccine

https://telegra.ph/BREAKING-Integration-of-corona-vaccine-contaminated-DNA-into-the-human-cell-line-genome-03-11

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

Scientists Call for Global Moratorium on mRNA Vaccines, Immediate Removal From Childhood Schedule
A review paper published last week in the journal Cureus is the first peer-reviewed paper to call for a global moratorium on the COVID-19 mRNA vaccines. The authors say that reanalyzed data from the vaccine makers’ trials and high rates of serious post-injection injuries indicate the mRNA gene therapy vaccines should not have been authorized for use.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

Here are six takeaways from the review:

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

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

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

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

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

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

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

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

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

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2. Steps were taken in trials to overestimate vaccine efficacy

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

And millions of AEs have been reported to those systems.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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


https://donshafi911.blogspot.com/2024/01/scientists-call-for-global-moratorium.html

Researchers urge governments to endorse a global moratorium on mRNA injections in a newly released science paper
Rhoda WilsonJanuary 26, 2024
In a paper published on Wednesday, researchers re-analysed the Pfizer covid “vaccine” phase 3 trial data and found more serious adverse events among those in the vaccine group.

This is not what published reports from Pfizer’s phase 3 trials said. “Many key trial findings were either misreported or omitted entirely from published reports,” the researchers said.

Seven researchers – M. Nathaniel Mead, Stephanie Seneff, Russ Wolfinger, Jessica Rose, Kris Denhaerynck, Steve Kirsch and Peter A. McCullough – set out to re-analyse Pfizer’s trial data because:

our understanding of covid vaccinations and their impact on health and mortality has evolved substantially since the first vaccine rollouts; and,
problems with the methods, execution, and reporting of the pivotal phase 3 trials have emerged.
On Wednesday, they published their findings in a peer-reviewed paper titled ‘Covid-19 mRNA Vaccines: Lessons Learned from the Registrational Trials and Global Vaccination Campaign’. The paper was published in Cureus, a journal of medical science.

“Re-analysis of the Pfizer trial data identified statistically significant increases in serious adverse events (SAEs) in the vaccine group,” the researchers wrote.

Adding, “Numerous SAEs were identified following the Emergency Use Authorisation (EUA), including death, cancer, cardiac events, and various autoimmune, haematological, reproductive, and neurological disorders.”

The EUA the researchers are referring to is the authorisation granted to Pfizer by the US Food and Drugs Administration (“FDA”).

As the paper noted, Pfizer’s covid “vaccines” never underwent adequate safety and toxicological testing according to previously established scientific standards. It goes on to detail the absolute risk reduction, the underreporting of harms during trials, the shifting narratives and illusions of protection, quality control and manufacturing process-related impurities, the biological mechanisms underlying adverse events (“AEs”) and why, based on how our immune systems work, the vaccine is ineffective.

Concluding their comprehensive review, the researchers wrote:

Given the extensive, well-documented SAEs and unacceptably high harm-to-reward ratio, we urge governments to endorse a global moratorium on the modified mRNA products until all relevant questions pertaining to causality, residual DNA, and aberrant protein production are answered.

Mead M, Seneff S, Wolfinger R, et al. (January 24, 2024) COVID-19 mRNA Vaccines: Lessons Learned from the Registrational Trials and Global Vaccination Campaign. Cureus 16(1): e52876. doi:10.7759/cureus.52876none
Let’s not lose touch…Your Government and Big Tech are actively trying to censor the information reported by The Exposé to serve their own needs. Subscribe now to make sure you receive the latest uncensored news in your inbox…

The paper noted that the gene therapy products (“GTPs”) vaccine platform has been studied for over 30 years as an experimental cancer treatment, with the terms “gene therapy” and “mRNA vaccination” often used interchangeably.

“Although we employ the terms ‘vaccine’ and ‘vaccination’ throughout this paper, the covid-19 mRNA products are also accurately termed gene therapy products (GTPs) because, in essence, this was a case of GTP technology being applied to vaccination,” they wrote.

As such, throughout their analysis, the terms “vaccines” and “vaccinations” are used interchangeably with injections, inoculations, biologicals, or simply, products.

The following are some excerpts from the paper. You can read the full paper HERE.

Serious Harms Revealed after EUA was Granted

In this narrative review, we revisit the registrational trials and review analyses of the AEs from these trials and other relevant studies. Most of the revelations have only recently come to light, due to the past few years of extensive censorship of healthcare professionals and research scientists who challenged the prevailing narrative set forth by the vaccine enterprise.

Despite the rhetoric, no large randomised double-blind placebo-controlled trials have ever demonstrated reductions in SARS-CoV-2 transmission, hospitalisation or death.

The study designs for the pivotal trials that led to the EUA were never intended to determine whether the mRNA inoculations could help prevent severe disease or premature death.

It was only after the EUA that the serious biological consequences of rushing the trials became evident, with numerous cardiovascular, neurological, reproductive, haematological, malignant, and autoimmune SAEs identified and published in the peer-reviewed medical literature.

Moreover, the covid mRNA vaccines produced via Process 1 and evaluated in the trials were not the same products eventually distributed worldwide; all of the covid-19 mRNA products released to the public were produced via Process 2 and have been shown to have varying degrees of DNA contamination.

The process-related impurities were absent from the covid-19 mRNA products used in the registrational trials. Virtually all doses used in those trials originated from “clinical batches” produced using what is known as Process 1. As a post-authorisation emergency supply measure for global distribution, however, a method much more suitable for mass production known as Process 2 was devised utilising bacterial plasmid DNA.

The failure of regulatory authorities to heretofore disclose process-related impurities (e.g., SV40) has further increased concerns regarding safety and quality control oversight of mRNA vaccine manufacturing processes.

Incentives Played a Key Role in Undermining Scientific Evaluation

Political and financial incentives may have played a key role in undermining the scientific evaluation process leading up to the EUA.

Before the pandemic, the US National Institutes of Health invested $116 million (35%) in mRNA vaccine technology, the Biomedical Advanced Research and Development Authority (“BARDA”) had invested $148 million (44%), while the Department of Defence (“DOD”) contributed $72 million (21%) to mRNA vaccine development.

BARDA and the DOD also collaborated closely in the co-development of Moderna’s mRNA vaccine, dedicating over $18 billion, which included guaranteed vaccine purchases. This entailed pre-purchasing hundreds of millions of mRNA vaccine doses, alongside direct financial support for the clinical trials and the expansion of Moderna’s manufacturing capabilities.

Once the pandemic began, $29.2 billion – 92% of which came from US public funds – was dedicated to the purchase of covid-19 mRNA products; another $2.2 billion (7%) was channelled into supporting clinical trials, and $108 million (less than 1%) was allocated for manufacturing and basic research.

Using US taxpayer money to purchase so many doses in advance would suggest that, before the EUA process, US federal agencies were strongly biased toward successful outcomes for the registrational trials.

Established Vaccine Testing Period Abolished

Before the rapid authorisation process, no vaccine had been permitted for market release without undergoing a testing period of at least four years. Previous timeframes for phase 3 trial testing averaged 10 years. Health departments have stated that 10-15 years is the normal timeframe for evaluating vaccine safety.

The previously established 10-15-year timeframe for clinical evaluation of vaccines was deemed necessary to ensure adequate time for monitoring the development of AEs such as cancers and autoimmune disorders.

Pfizer’s covid vaccine completed the process in seven months.

Established Safety Standards Abolished

With the covid vaccines, safety was never assessed in a manner commensurate with previously established scientific standards, as numerous safety testing and toxicology protocols typically followed by the FDA were sidestepped.

Historical accounts bear witness to instances where vaccines were prematurely introduced to the market under immense pressure, only to reveal disabling or even fatal AEs later on. Examples include the 1955 contamination of polio vaccines, instances of Guillain-Barré syndrome observed in flu vaccine recipients in 1976, and the connection between narcolepsy and a specific flu vaccine in 2009.

Against this backdrop, it is not surprising that so many medical and public health experts voiced concerns about covid mRNA vaccines bypassing the normal safety testing process.

Concerns about inadequate safety testing extend beyond the usual regulatory approval standards and practices.

As there were no specific regulations at the time of the rapid approval process, regulatory agencies quickly “adapted” the products, generalised the definition of “vaccine” to accommodate them, and then authorised them for EUA for the first time ever against a viral disease.

Due to the GTPs’ reclassification as vaccines, none of their components have been thoroughly evaluated for safety. The main concern, in a nutshell, is that the covid mRNA products may transform body cells into viral protein factories that have no off-switch – i.e., no built-in mechanism to stop or regulate such proliferation – with the spike protein (“S-protein”) being generated for prolonged periods, causing chronic, systemic inflammation and immune dysfunction.

When the S-protein enters the bloodstream and disseminates systemically, it may become a contributing factor to diverse AEs in susceptible people.

Enforce a Global Moratorium

Given the well-documented SAEs and unacceptable harm-to-reward ratio, we urge governments to endorse and enforce a global moratorium on these modified mRNA products until all relevant questions pertaining to causality, residual DNA, and aberrant protein production are answered.



https://expose-news.com/2024/01/26/researchers-urge-a-global-moratorium-on-mrna/

Terrifying! New LETHAL BIO-WEAPON SARS-COV-3 Built and Hid by CHINA’s ARMY | VT Foreign Policy
January 24, 2024
VT Condemns the ETHNIC CLEANSING OF PALESTINIANS by USA/Israel

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

by Fabio Giuseppe Carlo Carisio

VERSIONE IN ITALIANO

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

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

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

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

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

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

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


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

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

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

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

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


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

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

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

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

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

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

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

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

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

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

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

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

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

Chinese research for a new attenuated vaccine against Covid-19

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


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

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

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

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

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

The Army Laboratory Experiment for a Bacteriological Weapon

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

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

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

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

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


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

«To the best of our knowledge, this is the first report showing that a SARS-CoV-2-related pangolin coronavirus can cause 100% mortality in hACE2 mice, suggesting a risk for GX_P2V to spill over into humans. Our findings are evidently inconsistent with those of Zhengli Shiet al. (5), who tested the virulence of GX_P2V in two different hACE2 mouse models».

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

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

And the conclusion doesn’t suggest anything good…

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

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

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

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

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

Most popolar investigation on VT is:

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

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

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

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

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

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

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

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

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Moderna’s influence over the US and UK governments is more than most realise
Rhoda WilsonJanuary 3, 2024
The sheer sprawl, corruption, influence and involvement of Moderna in politics and the wider medical industry is staggering. It is difficult to convey and harder to comprehend, The Underdog writes.

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

How did Bancel know?

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

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

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

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

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

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

Murderous Moderna’s Infiltration of Politics

By The Underdog

Murder, They Wrote

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

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

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

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


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

Moderna Have Infiltrated the Government

Seems pretty incredulous, but no.

Moderna Is Part of WEF

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


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

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

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

Moderna Took Control of Operation Warp Speed

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


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

Moderna Influenced NIH, BARDA

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

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

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

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

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

Moderna Took Control of the FDA


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


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

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

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

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

Moderna Control the UK Government

This isn’t hyperbole. We wish it were.

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

This includes a spin-off company called Quotient Therapeutics:

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


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

Moderna de facto Control the Prime Minister

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


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

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


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

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

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

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

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

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


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

On another note…

Moderna Have Compromised Academia

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

Moderna Have Control In MIT


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


The purpose of the trust? (Emphasis added):

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

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

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

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

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

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

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

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

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

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

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

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


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

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

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

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


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

When investigating Acuitas Therapeutics, The Daily Beagle remarked:

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

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

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


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

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

Moderna are in Bed with Multiple Major Pharmaceutical Companies

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

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

Moderna Clearly Expects a Lot of Cancer

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

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


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

Flagship Pioneering (Moderna) Gets into Bed with Pfizer


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

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


Flagship Pioneering (Moderna) Gets into Bed With Novo Nordisk

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

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

The Daily Beagle Smells a Rat – Merck Again

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


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

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


Cancer, Cancer Everywhere

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

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


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

University of Texas Cancer Corruption

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

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

We bet it is exciting … for your bank account.

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


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

Any Cure for The Cancer That Is Corruption?

Apparently not.

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


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

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

Tip of the Iceberg

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



https://expose-news.com/2024/01/03/modernas-influence-over-the-us-and-uk

#PlasmidGate: Biotechnician raises plasmid DNA contamination in covid injections during Austrian TV talk show
Rhoda WilsonDecember 17, 2023
Two days after German television station MDR aired a report about foreign DNA contamination found in vials of covid injection, a panellist on a popular Austrian talk show spoke about PlasmidGate; vaccines contaminated with plasmid DNA.

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On Thursday, Austrian television station Servus TV aired its talk show ‘Talk on Hanger-7’ titled ‘Corona instead of Christmas: Is there a threat of compulsory measures again?’ to discuss whether there is a looming threat of covid restrictions being re-implemented in light of the new Pirola variant of covid reportedly being on the rise.

Monitoring of wastewater, it is claimed, suggests a record-breaking wave of covid in the country and the number of sick days due to colds and flu is higher than ever. Of course, neither of those is a good enough reason to mandate restrictions which cost lives and livelihoods, and destroy the economy.

According to a survey conducted in 2021, about 33% of the Austrian population watch a Servus TV programme at least once a week to keep up to date with covid.

It’s not unusual for Servus TV to challenge the official narrative. For example, the director of Servus TV Ferdinand Wegscheider in his commentary series ‘Der Wegscheider’ explained that the covid injections were “insufficiently tested” and contained “genetically modified substances.” He also mentioned ivermectin as a treatment and regularly speaks of the “plandemic.” Microbiologist Sucharit Bhakdi is a frequent guest on Servus TV.

Michael Fleischhacker hosted the discussion on Talk on Hanger-7 on Thursday. Guests included epidemiologist Klaus Stöhr, medical journalist Werner Bartens, psychoneuroimmunologist Christian Schubert, medical historian Daniela Angetter-Pfeiffer and biotechnician and former VP of German Pharmaceutical firm Boehringer Ingelheim Dr. Monika Henninger-Erber.

The original talk show is in German and Servus TV is not available outside of Europe. However, Aussie17 managed to obtain a clip and has added English subtitles to it (see below).

During the discussion, Dr. Henninger-Erber spoke about PlasmidGate. In February, microbiologist Kevin McKernan pioneered research on testing some of the covid-19 vaccine vials and discovered unacceptable levels of double-stranded DNA plasmids floating around. This is DNA contamination. He found the contamination in Pfizer and Moderna vials. Since then, several laboratories around the world have confirmed his findings.

In September, Professor Dr. Phillip Buckhaults testified in the South Carolina Senate that his team had found 200 billion pieces of DNA contaminating a single dose of Pfizer’s covid injection.

“Before you ever say that you are calling on people to get vaccinated again, you should think carefully [and] look at what you have learned in the last few years. And you learned, for example, back in February, this year it was published for the first time that the vaccine was contaminated, namely with plasmid DNA,” Dr. Henninger-Erber said during Talk on Hanger-7 on Thursday.

“PlasmidGate … that’s not just any idea that someone has, but this is real data from laboratories, repeatedly shown that we are there have a huge problem,” she said.

Bartens is a Covidian who, according to the programme description, defends the measures politicians have taken and thinks little of populist demands to come to terms with covid. He is the one in the video below with grey hair, wearing a blue shirt and who is looking very uncomfortable with what Dr. Henninger-Erber was saying.

Talk on Hanger-7: Corona instead of Christmas: Is there a threat of compulsory measures again? 14 December 2023
Source: Aussie17 on Twitter


https://expose-news.com/2023/12/17/plasmidgate-biotechnician-raises-plasmid-dna-contamination-in-covid-injections-during-austrian-tv-talk-show/

The Pfizer COVID-19 “vaccines” forced on humanity were not the same ones used in Pfizer’s clinical trials.

There was a “bait-and-switch.” The public received vials contaminated with plasmid DNA.

Florida Surgeon General Dr. Joseph Ladapo says there is “zero question” that the mRNA shots could change people’s DNA.

Moreover, he said, “I think it’s probably likely that that is, in fact, happening.”

https://x.com/vigilantfox/status/1747324110558896154?s=46

Breaking: Florida Will be the First Jurisdiction to Halt COVID-19 mRNA Vaccines
Surgeon General Dr. Joseph Ladapo calls for halt on Jan. 3, 2024. Alberta must be second! Reasons for halting these failed pharma products


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***

Important Report by Dr. William Makis.

The State of Florida has called for a halt of the use of mRNA Covid-19 Vaccines, setting a precedent for the implementation of similar decisions not only across the United States, but Worldwide.

The evidence is overwhelming.

Read the letter of Florida State Surgeon General Joseph A. Ladapo below

We call upon people across the United States to pressure State officials to cancel the mRNA Covid-19 once and for all.

The evidence of mortality and morbidity resulting from vaccine inoculation both present (official data) and future (e.g. undetected microscopic blood clots) is overwhelming.

The official data (mortality and morbidity) as well as numerous scientific studies confirm the nature of the Covid-19 mRNA vaccine which is being imposed on all humanity.

Our thanks to Dr. William Makis

Michel Chossudovsky, Global Research, January 5, 2024

*



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There are many additional reasons to halt COVID-19 Vaccines (beyond DNA Contamination) and I present some of them in this article:

Immune System Damage

COVID-19 mRNA Vaccines damage the immune system and each additional dose causes additional immune damage, increasing the risk of COVID-19 infection and other infections and complications of infections (such as sepsis, septic shock).

This is illustrated in the Shrestha et al. study published April 19, 2023 (source), which showed that among 51,017 Cleveland Clinic healthcare employees, those who took more COVID-19 vaccines had higher risk of COVID-19 infection:

Cumulative incidence of coronavirus disease 2019 (COVID-19) for study participants stratified by the number of COVID-19 vaccine doses previously received. Day 0 was 12 September 2022, the date the bivalent vaccine was first offered to employees. Point estimates and 95% confidence intervals are jittered along the x-axis to improve visibility.

On Sep. 13, 2023 – Florida Surgeon General recommended against COVID-19 boosters for individuals under age 65, due to “safety and efficacy concerns.”

Image

WHO VigiAccess Database documents 5,273,122 adverse events associated with COVID-19 Vaccines as of Jan. 4, 2024.



WHO VigiAccess – most adverse events are in highly COVID-19 mRNA Vaccinated countries and 65% of the adverse events are suffered by women.



WHO VigiAccess – Over 180,000 pediatric adverse events have been reported.



Dec. 9, 2023 – My article on 25 babies age 0-2 who died after Pfizer or Moderna COVID-19 mRNA Vaccine, Flu Vaccine, or died from SIDS
Oct. 24, 2023 – My article on 68 children ages 0-12 who died after COVID-19 mRNA Vaccination.
Nov. 3, 2023 – My article on 60 teenagers ages 13-19 who died suddenly since May 2023.
WHO VigiAccess – 13,621 pregnancy complications including 6390 spontaneous abortions.



On May 10, 2023 – Florida Surgeon General wrote to FDA Commissioner about COVID-19 Vaccine adverse events including 3% myocardial injury risk identified in two studies (researchers from Thailand, Switzerland).

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If Florida Becomes First Jurisdiction to Halt COVID-19 Vaccines, Then Alberta, Canada Must be Second

Health Canada has admitted DNA Contamination.

“Although the full DNA sequence of the Pfizer plasmid was provided at the time of initial filing, the sponsor did not specifically identify SV40 sequence…the residual plasmid DNA is present in the final product as DNA fragments…the original risk benefit analysis that supported the initial approval of the Pfizer vaccine continues to be valid.”

First email received from Health Canada on July 19, 2023.

Second email from Health Canada received on July 28, 2023.

Third email received from Health Canada on Aug. 10, 2023.

Fourth and last email received from Health Canada on Aug. 18, 2023.

Canadian Pre-print by University of Guelph Molecular Virologist Dr.David Speicher PhD confirms DNA contamination of Pfizer & Moderna mRNA Vaccines:

“Using previously published primer and probe sequences, quantitative polymerase chain reaction (qPCR) and Qubit® fluorometry was performed on an additional 27 mRNA vials obtained in Canada.



Over 180 Canadian doctors (COVID-19 Vaccinated) have died suddenly & unexpectedly since COVID-19 vaccine rollout.

I testified to the National Citizens Inquiry and gave extensive documentation on COVID-19 Vaccinated Canadian doctor sudden deaths

On Nov.28, 2023 – FINAL REPORT was released – my extensive data on Canadian doctor deaths can be downloaded on pages 148-150 of the report (HERE)
Canadian doctors have 54% excess mortality in 2022
Canadian Medical Association responded to my letters and data by deleting all Canadian doctor deaths and data from their own website for the years 2022 and prior



Canadian children dying suddenly during record flu season Nov. 2022 – Feb. 2023 with record pediatric influenza deaths.

Feb. 27, 2023 – My article on 96 Canadian Children dying suddenly during a 3 month period Nov.2022 to Feb. 2023


My Take…

I believe Florida will be the first jurisdiction to halt all COVID-19 mRNA Vaccines, hopefully in the next few weeks or months.

I also believe that Alberta, Canada CAN AND SHOULD be the second jurisdiction to halt COVID-19 mRNA Vaccines, at the very least in children under the age of 19.

Alberta Premier Danielle Smith can lean heavily on the following:

Following Florida’s leadership that puts people ahead of pharmaceutical profits
Health Canada’s admission on DNA contamination and its failure to address it
The DNA contamination work done in Canada by Dr.David Speicher PhD at University of Guelph
The National Citizen’s Inquiry Final Report of Nov. 28, 2023 (which includes my data on Canadian doctor deaths)
“Unknown cause of death” being the #1 cause of death in Alberta since 2021
Statistics Canada “Deaths 2022” Report of Nov. 27, 2023 showing 16,043 deaths of “Unspecified cause” in 2022.


She cannot rely on the following:

Government of Canada’s COVID-19 Vaccine Adverse event reporting system which is completely broken and non-functional
Doctors have been repeatedly threatened by Colleges of Physicians and Surgeons throughout Canada – they are not allowed to report adverse events for COVID-19 Vaccines or they will lose their medical license.
Mainstream peer-reviewed research on COVID-19 Vaccine Adverse events is almost entirely fraudulent.
Alberta Healthcare Officials, Public Health Officials and Alberta Health Services Executives who have spent the last 3 years burying evidence of COVID-19 mRNA Vaccine Injuries and Deaths.
I hope to see COVID-19 Vaccines halted in Florida and Alberta, Canada as soon as possible.

*

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Dr. William Makis is a Canadian physician with expertise in Radiology, Oncology and Immunology. Governor General’s Medal, University of Toronto Scholar. Author of 100+ peer-reviewed medical publications.

The Worldwide Corona Crisis, Global Coup d’Etat Against Humanity

by Michel Chossudovsky

Michel Chossudovsky reviews in detail how this insidious project “destroys people’s lives”. He provides a comprehensive analysis of everything you need to know about the “pandemic” — from the medical dimensions to the economic and social repercussions, political underpinnings, and mental and psychological impacts.

“My objective as an author is to inform people worldwide and refute the official narrative which has been used as a justification to destabilize the economic and social fabric of entire countries, followed by the imposition of the “deadly” COVID-19 “vaccine”. This crisis affects humanity in its entirety: almost 8 billion people. We stand in solidarity with our fellow human beings and our children worldwide. Truth is a powerful instrument.”

Reviews

This is an in-depth resource of great interest if it is the wider perspective you are motivated to understand a little better, the author is very knowledgeable about geopolitics and this comes out in the way Covid is contextualized. —Dr. Mike Yeadon

In this war against humanity in which we find ourselves, in this singular, irregular and massive assault against liberty and the goodness of people, Chossudovsky’s book is a rock upon which to sustain our fight. –Dr. Emanuel Garcia

In fifteen concise science-based chapters, Michel traces the false covid pandemic, explaining how a PCR test, producing up to 97% proven false positives, combined with a relentless 24/7 fear campaign, was able to create a worldwide panic-laden “plandemic”; that this plandemic would never have been possible without the infamous DNA-modifying Polymerase Chain Reaction test – which to this day is being pushed on a majority of innocent people who have no clue. His conclusions are evidenced by renown scientists. —Peter Koenig

Professor Chossudovsky exposes the truth that “there is no causal relationship between the virus and economic variables.” In other words, it was not COVID-19 but, rather, the deliberate implementation of the illogical, scientifically baseless lockdowns that caused the shutdown of the global economy. –David Skripac

A reading of Chossudovsky’s book provides a comprehensive lesson in how there is a global coup d’état under way called “The Great Reset” that if not resisted and defeated by freedom loving people everywhere will result in a dystopian future not yet imagined. Pass on this free gift from Professor Chossudovsky before it’s too late. You will not find so much valuable information and analysis in one place. –Edward Curtin

ISBN: 978-0-9879389-3-0, Year: 2022, PDF Ebook, Pages: 164, 15 Chapters

Price: $11.50 FREE COPY! Click here (docsend) and download.

We encourage you to support the eBook project by making a donation through Global Research’s DonorBox “Worldwide Corona Crisis” Campaign Page.

https://www.globalresearch.ca/florida-first-jurisdiction-halt-covid-19-mrna-vaccines/5845239

The article discusses concerns that contamination in the COVID-19 mRNA vaccines, specifically residual DNA from the manufacturing process, could help explain the recent rise in cancer rates and autoimmune diseases. Pathologist Dr. Ryan Cole explains that while the initial Pfizer vaccine trials used a very controlled synthetic mRNA production process, when they scaled up manufacturing for billions of doses they switched to a less precise method involving bacteria and plasmids, without properly cleaning the residual DNA. He and other experts believe this contaminated DNA could be intercalating into human DNA and causing mutations, suppressing the immune system, and driving cancers that are more aggressive and no longer responding to traditional treatments. More research is still needed, but this provides a potential mechanism for the alarming patterns doctors are observing of rapid cancer growth and previously stable cancers coming out of remission after vaccination.

https://www.theepochtimes.com/us/the-rise-in-cancers-autoimmune-diseases-the-role-of-dna-contamination-5544587

No paywall source:
https://archive.is/G0Shq


The Rise in Cancers, Autoimmune Diseases: The Role of DNA Contamination
The Rise in Cancers, Autoimmune Diseases: The Role of DNA Contamination
Pathologist Dr. Ryan Cole in Dallas, Texas on Nov. 4, 2023. (York Du/The Epoch Times)
In a recent episode of “American Thought Leaders,” host Jan Jekielek speaks with Dr. Ryan Cole, a pathologist and an expert on SARS-CoV-2 and the mechanisms of the genetic injections labeled as vaccines. Here, they discuss how these COVID-19 genetic vaccines may be related to the rise in cancers and autoimmune diseases.
Jan Jekielek: I’ve done an interview with Kevin McKernan about what’s in the vaccine vials, this contamination that multiple labs had already verified. Let’s start with that, because that’s something you’ve been covering.

Dr. Ryan Cole: Many laboratories around the world have been looking at this issue, and Kevin has been a leader in this area. When these products were made, there was the J&J, that’s an adenovirus factor, but then there was Moderna and Pfizer. These are mRNA; synthetically engineered, modified RNA.

For the trials, at least for Pfizer, there’s a synthetic PCR-type process in making up the mRNA sequence for these shots. That was given to 40,000 people, and was a deliberate, synthetic, engineered attempt at a precision-type process.

Mr. Jekielek: That’s dubbed “Process 1”?

Dr. Cole: Yes. To make a lot of this for billions of people, a second process was used, which was only tested on about 252 people instead of 40,000. That was taking this complementary DNA sequence that is the reverse pattern of the spike to make mRNA a message, and then your body would make that protein in your cells.

We did the trials on this very controlled synthetic process, but then at the last minute they snuck under the radar and said, “But we’re going to make all the rest of them using a process we’ve barely tested.” That’s what got rolled out into billions of people’s arms. It was kind of a bait and switch. Those large data sets one would want to see in terms of harms, you’re not going to find that in 250 patients.

Mr. Jekielek: They actually use E. Coli, a bacterium, to grow these plasmids of DNA, which can then be turned into the RNA, but they just didn’t clean them up.

Dr. Cole: They didn’t clean them up properly. They’re supposed to put in an enzyme that breaks down any residual DNA. Even up to the current vials of the fall booster, the XBB 1.5, Kevin and 12 other laboratories have shown there is still bacterial plasmid DNA contamination within these vials. The FDA allows up to, in gene products, 10 nanograms of DNA per dose, but that’s based on old technology.

The smaller the fragment of DNA, the greater the opportunity it has to intercalate into your own DNA as well. More testing and probes are still needed to prove this, but it explains a lot of the strange happenings we’re seeing in clots, autoimmune disease, and cancers, because we’re changing signals within cells. Human cells are meant to make human proteins. They’re not meant to make foreign proteins. When we program people’s cells to make things they’re not supposed to make, they can go haywire. They can mutate and become a target of our own immune system.

My big concern is that billions of people around the world have received a product that was contaminated, which was admitted to by the Canadian health regulatory agency.

Mr. Jekielek: It was Epoch Times reporting that caused that disclosure to happen.

Dr. Cole: Yes, well done. And my concern isn’t just these COVID shots. It’s this entire technology. A lipid nanoparticle in and of itself is an unproven product. It takes on whatever you put into it. They’re trying to create them for RSV, flu, and for many other pathogens. It still takes those little gene sequences anywhere and everywhere in the body.

In some of his autopsy findings, the late Dr. Burkhardt, a friend and mentor to me, showed spike protein in the testes, in the placenta, and in the uterus. I’ve seen some of those in the studies we were doing in my laboratory.

Mr. Jekielek: You feel this provides some explanation for these turbo cancers and this clotting we’ve been seeing.

Dr. Cole: Dr. Ute Krüger from Sweden coined the term turbo cancer. She’s a breast pathologist who was looking at the damage of these shots. She noticed increases in cancer, an uptick not only in the size of the cancers, but also in the stage of the cancers. Instead of just taking out a lesion, she was finding it had spread to lymph nodes, the liver, the bone marrow, and the brain. She was seeing cancers behave in a manner like never before. Everywhere I go, I hear oncologists and physicians telling this story.

A prominent oncologist in Texas told me, “At first I saw the clots, then the blood cancers, the leukemias, and the lymphomas. Now, I’m seeing solid tissue cancers at rates I’ve never seen. Patients that were stable or cancer-free for 1, 2, 5, or 10 years, their cancer is now back, and it’s not responding to traditional therapies.”

It’s not necessarily that the gene sequence is causing cancer. The gene sequence can cause some of the mutations that lead to cancer. But it’s also suppressing the immune system, and your immune system is what kills cancer. If your immune system is asleep, your killer cells can’t be activated

In addition, there are so many basic things our public health system isn’t addressing. Do we have a horrible diet? Are we vitamin D-deficient? Absolutely. In addition, a lot of people received a contaminated adulterated gene-based product, and we don’t know the long-term outcomes.

Mr. Jekielek: Ryan, any final thoughts as we finish up?

Dr. Cole: If we can resolve conflicts by having face-to-face conversations, the world will be a better place, and maintaining our rights to speak and think freely is more important than anything. Stay positive. Stay optimistic. Life is still good.

This interview has been edited for clarity and brevity.

#PlasmidGate: Biotechnician raises plasmid DNA contamination in covid injections during Austrian TV talk show
BY RHODA WILSON ON DECEMBER 17, 2023
https://expose-news.com/2023/12/17/plasmidgate-biotechnician-raises-plasmid-dna-contamination-in-covid-injections-during-austrian-tv-talk-show/

also see DNA Contamination of COVID jabs leading to exponential increases in cancer and potentially other conditions
Crimes against humanity have been committed by our regulators, governments and medical authorities.
https://informedchoice.substack.com/p/plasmidgate-dna-contamination-of