Covered Up: mRNA Shedding, Transmissibility and Cancer.

Recently, I found myself down a rabbit hole of FDA documents and holy smokes, guys - what I found is a real barn burner.

by Tom Renz

Recently, I found myself down a rabbit hole of FDA documents and holy smokes, guys - what I found is a real barn burner. I’m going to try and keep this as brief as possible so that the gravity of what I’m about to share isn’t lost in too many details. In my opinion, what I’ve discovered is nothing less than premeditated murder.

It’s crazy to even say that, but there’s no other conclusion that I can draw after reviewing these FDA ‘Guidance for Industry’ documents, published years before the Covid fiasco. This is the smoking gun evidence that proves they knew that the gene therapy products they masqueraded as ‘vaccines’ had the ability to shed, cause cancer and kill.

It’s Gene Therapy - Not a Vaccine.

It’s critical that people understand that the Covid-19 injections are gene therapy. The Centers for Disease Control and Prevention currently defines a “vaccine” as a preparation used to stimulate the body’s immune response against diseases. However, that definition changed in 2021 because it didn’t apply to the COVID-19 vaccines. A vaccine must contain an antigen to trigger the body’s natural immune response. Pfizer and Moderna’s mRNA vaccines do not contain antigens. The active substance used to elicit an immune response in these vaccines is the mRNA—a form of nucleic acid and the genetic material of the SARS-CoV-2 virus that provides instructions to the body for producing antigens—spike proteins (actually it is modRNA - see my previous posts - and also contaminated with DNA). 

Moreso, Moderna and Pfizer’s own SEC filings admit that they are gene therapy products. On pages 148 & 149 of Moderna’s 2019 SEC filing there is a legally mandated discussion of “risk factors” that reads as follows:

“No mRNA drug has been approved in this new potential class of medicines and may never be approved as a result of efforts by others or us. mRNA drug development has substantial clinical development and regulatory risk due to the novel and unprecedented nature of this new class of medicines.

As a potential new class of medicines, no mRNA medicines have been approved to date by the FDA or other regulatory agency… currently mRNA is considered a gene therapy product by the FDA.”

In March 2015 the U.S. Department of Health and Human Services, the FDA and the Center for Biologics Evaluation and Research published a ‘guide for industry’ entitled: “Determining the Need for and Content of Environmental Assessments for Gene Therapies, Vectored Vaccines, and Related Recombinant Viral or Microbial Products” from which I pulled the following definition of ‘gene therapy’:

It defines gene therapies as “products that mediate their effects by transcription and/or translation of transferred genetic material and/or by integrating into the host genome and that are administered as nucleic acids, viruses or genetically engineered microorganisms. The products may be used to modify cells in vivo or transferred to cells ex vivo prior to administration to the recipient.”

“For purposes of this guidance, a vectored vaccine is one that uses a virus or microbe (typically a bacterium), or a DNA plasmid to introduce DNA/RNA encoding for antigens to cells of the body. “Vector” refers to the virus microbe or DNA plasmid used as the carrier.”

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