So is the conclusion from all this information that someone, not necessarily the originating scientists, may have deliberately contaminated the new vaccines with DNA that is far above what is leagally tolerated in the US and in Europe?
I wonder if any of these concerned scientists was smart enough to mail his concerns to the FDA “Return Receipt Requested”? At least then they would have the little green card (which so far as I know is returned by the recipient mail service before the appropriate office actually opens the mail). And they could then track who did not want to answer their questions or look at their data.
So far as concerns raised by some here that the mRNA folks were trying to prevent other competing vaccines in the USA I agree. One company, I think Moderne, tried three times to buy Astra-Zenica in the previous decade, always increasing the price offered. AZ was happy with its progress and refused. Then they were blocked from entry to the US vaccine market. The Novavax people also seemed to have quite a hard time getting their vaccine approved.
To REALLY understand the DNA contamination & also the additional issue of a cancer promoting genetic sequence - SV40 - being found in all vials of the BioNTech product, you should watch this panel of experts discussing how the contamination was found, where it was found & what it potentially means. Written summary & video at the link (& I included written summary below if you don’t have time to go to the link):
WCH Expert Panel Finds Cancer-Promoting DNA Contamination in Covid-19 Vaccines
https://worldcouncilforhealth.org/news/news-releases/dna-contamination-covid-19-vaccines/
The following internationally renowned immunologists, geneticists, specialist physicians and research scientists shared their findings with the audience:
Kevin McKernan (USA)
Dr Janci Lindsay (USA)
Prof Sucharit Bhakdi (Germany)
Assoc Prof Byram Bridle (Canada)
Dr Peter McCullough (USA)
Prof Brigitte König (Germany)
Dr Jessica Rose (Canada)
Prof Alexandra Henrion-Caude (France)
Attorney Katie Ashby-Koppens (Australia) shared the legal implications of the
deployment of unregulated GMO products as vaccines
Summary of Findings:
01 - Bacterial DNA (plasmids) has been found in mRNA vaccine vials.
02 - A cancer-promoting genetic sequence—SV40—has been found in the Covid-19 vaccines. 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.
03 - These discoveries have been confirmed in several independent laboratories worldwide.
04 - The discovery was originally made in April 2023 by Kevin McKernan at which point regulatory bodies were contacted. No official reply has been received.
05 - Multiple mechanisms exist in which this genetic information might be integrated into the human genome.
06 - This DNA could instruct our bodies to produce mRNA and foreign proteins for an unknown period with potential implications for subsequent generations.
07 - 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.
08 - 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.
09 - 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.
10 - Integration of foreign DNA into the human genome disrupts existing natural genetic sequences; this carries further risk of disease including cancer.
11 - The Covid-19 vaccines qualify as GMO (genetically modified organism) products, which require approval in addition to that required for older, more traditional vaccines.
12- Informed consent for these products is impossible as the risks of the products have never been formally and transparently assessed by regulators and are not fully known. Independent assessment of the emerging and available evidence is that these products are extremely dangerous with implications for disease, death, transmission and inheritance.
13 - An immediate moratorium on these novel genetic “vaccines” was demanded by the expert panelists.
********
Of the expert hearing, Dr Peter McCullough, Scientific Advisor to World Council for
Health, said,
“I believe today in 2023 after three years of the failed Covid 19 vaccine campaign which has been a biologic disaster for the world that the multi-hit hypothesis for oncogenesis has been fulfilled ... the Covid 19 vaccines work to impair tumor suppressor systems P53 and BRCA 1 and
2. Additionally, the genetic vaccines also impair DNA repair … they impair the bodies’ ability to repair itself.”