FDA Lab with FDA Student Researchers Uncovers Excess DNA Contamination in COVID-19 Vaccines
Here’s a summary of findings by the expert panelists:
Bacterial DNA (plasmids) has been found in mRNA vaccine vials.
A cancer-promoting genetic sequence—SV40—has been found in the Covid-19 injections. This was not present in the vials used for the approval studies but has been found in all vials of the BioNTech vials disseminated for public use.
These discoveries have been confirmed in several independent laboratories worldwide.
The discovery was originally made in April 2023 by Kevin McKernan at which point regulatory bodies were contacted. No official reply has been received.
Multiple mechanisms exist in which this genetic information might be integrated into the human genome.
This DNA could instruct our bodies to produce mRNA and foreign proteins for an unknown period with potential implications for subsequent generations.
There is no constructive purpose identified for the undeclared SV40 promotor sequence, which in addition to its cancer risk, enhances the capacity to incorporate the other foreign genetic material into the recipients’ own chromosomes, potentially rendering them (and possibly even their offspring) permanently genetically modified.
There are multiple completely undeclared genetic sequences in both Moderna and Pfizer vials, with the SV40 sequence found only in the Pfizer vials. However, latent SV40 infections in a significant portion of the population could present the same SV40 risk to Moderna recipients.
Even in the absence of chromosomal integration, the DNA plasmids could generate mRNA for the spike protein toxin and other harmful proteins for prolonged and unpredictable periods of time.
Integration of foreign DNA into the human genome disrupts existing natural genetic sequences; this carries further risk of disease including cancer.
The Covid-19 vaccines qualify as GMO (genetically modified organism) products, which require approval in addition to that required for older, more traditional vaccines.
Informed consent for these products is impossible as the risks have never been formally and transparently assessed by regulators and are not fully known. Independent assessment of the emerging and available evidence has found that these products are extremely dangerous with implications for disease, death, transmission and inheritance.
An immediate moratorium on these novel genetic “vaccines” was demanded by the expert panelists.
