Yesterday, I posted a video by Dr William Makis, MD advising workers in vaxxine distribution facilities to defy the Canadian government’s order to destroy all vials of the old batches of COVID-19 vaxxines, because that would be destruction of evidence of “a very serious crime”.
Dr Makis went on to say, “These vaxxines are contaminated, there are going to be labs in the future, they are going to want to test these vaxxines, hundreds of them, maybe thousands of them – and they will pay Top-Dollar,” and that even if one were purely motivated by greed, “Then, these vaxxines are going to be your Bitcoin. They are going to be worth their weight in gold!”
What I didn’t realize when I posted the above was that the Canadian government’s announcement was related to Moderna’s admission, 10 months ago, during the US Congressional Hearing last November that a new study had found that their own vials were contaminated with billions of fragments of DNA, including strands of the same Simian Virus 40 contained in the 1950s Polio Vaccines that caused the cancer plume in those vaccinated with it, prior to the early 1960s.
Moderna also acknowleged that their own patent says that RNA is preferable to DNA in vaccines, due to risks of “insertional mutagenesis”, which might activate genes that cause cancer and inhibit tumor-suppressor genes.
These admissions were made during the US Congressional Hearing, “Injuries Caused by COVID-19 Vaccines” led by Congresswoman Marjorie Taylor Greene (R-GA).
As summarized by @VigilantFox:
• Moderna has a patent that acknowledges RNA is preferable to DNA in vaccines due to risks of insertional mutagenesis, which might activate oncogenes or inhibit tumor suppressor genes, Dr. @RWMaloneMD explained.
• A new study up for peer review has found billions of residual DNA fragments in COVID-19 mRNA vaccine vials. In other words, the vials are contaminated with DNA. These findings were not disclosed to the public.
• Additionally, Pfizer, in their documentation to regulatory bodies, omitted information about the presence of SV40 sequences in their vaccine.
• As such, the COVID shots, contaminated with DNA fragments, can cause anything associated with DNA damage — birth defects and cancers being the notable ones.
Below, is a transcript of the testimony of Dr Robert Malone during that hearing, being questioned by Congressman Thomas Massie (R-KY)
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TRANSCRIPT
Dr Robert Malone, MD: Moderna has a patent on the use of RNA for vaccines. It happens to be patent number 2019-024-0317A1. And in that, Moderna explicitly acknowledges that RNA is superior to DNA for vaccine purposes, because problems including the possibility of insertional immunogenesis, which could lead to the activation of oncogenes or the integration of tumor suppressor genes.
So FDA says they’re not aware of any concerns, but Moderna, in its own patent lays out exactly the same concerns that exist about DNA and insertional immunogenesis and genotoxicity. So Moderna knows it.
Rep Thomas Massie (R-KY): Was the DNA a contaminant?
Dr Robert Malone, MD: It is a contaminant. It is left in, because the way they make it, in process two is they purify circular DNA from bacteria…DNA makes RNA. RNA makes protein.
So they use DNA to make the RNA. And then they degrade the DNA. And then they have to purify the degraded DNA away from the RNA and the process that they’re using is apparently not very good. And this was just revealed. It was just detected, because some scientists, both in the US and in Canada, managed to get their hands on some unopened vials with clear chain of custody, sample those vials – and these are people who, their business is to do deep-sequencing on samples and rebuild information about whatever DNA they find on that.
So, they were just doing the technology that they know how to do, in their business, that they’re experts in. And they found, Lo! and behold, that there were these large numbers of DNA fragments in this RNA preparation and they could apply standard tools that they have to reconstruct what those circular plasmid DNAs look like.
None of this was disclosed to the public. And it appears that the documentation is, that there are certain sequences present that are normally not allowed in anything that’s going to go into humans – not the least of which, is an antibiotic resistance gene.
So these are going into our bodies – including an antibiotic resistance gene for kanamycin or neomycin. Normally you’re not allowed to do that, if it’s a DNA engineered for human use. And they include these sequences from simian virus 40, not the whole virus, but highly active promoter sequences, which is exactly the thing that the FDA in their older regulations said must be avoided, because it confers even more risk for insertional mutagenesis.
And what appears is that Pfizer, when they provided these documents to the FDA and to the EMA and to Health Canada, they took these standard plasmid maps that are generated through programs – that we all have access to – and they deleted the little notation that said there’s SV40 sequences in there.
And the FDA, apparently out of, I can only think, incompetence, didn’t take the raw DNA sequences, reconstruct those plasmid maps, and look at them themselves. They just took for granted what Pfizer had given them.
And now, this has all come out because of these researchers that did functionally something akin to the lot release testing that is not happening.
Rep Thomas Massie (R-KY): So there was probably somebody at Pfizer who knew what they were doing.
Dr Robert Malone, MD: Absolutely. Okay. And Moderna.
Rep Thomas Massie (R-KY): And then, what are the specific downstream diseases or bad outcomes that come from having these?
Dr Robert Malone, MD: Anything that is associated with DNA damage.
Rep Thomas Massie (R-KY): For instance, cancer?
Dr Robert Malone, MD: Birth defects and cancer being the notable ones.
Rep Thomas Massie (R-KY): Okay.
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