Scientific Proof COVID Vaccines Contain Cancer Accelerators (And Why Nobody Stopped It)
(Videos from Twitter user Kat A @SaiKate108)
The peer-reviewed scientific evidence now confirms a shocking reality: Pfizer’s mRNA COVID-19 vaccines contain DNA contamination with SV40 promoter sequences, a discovery that points to deliberate deception with potentially catastrophic health consequences. This finding represents one of the most serious medical scandals in modern history, revealing how regulatory bodies and pharmaceutical companies conspired to hide critical safety information from the public. The presence of these cancer-linked components was never disclosed to health authorities during the approval process, constituting clear scientific fraud.The implications of these findings go beyond simple negligence; they suggest a level of intent and calculated risk that warrants criminal investigation.
SV40, or Simian Virus 40, has a well-documented history of causing cancer in humans. Originally discovered as a contaminant in polio vaccines during the 1950s and 1960s, this virus was later linked to increased cancer rates among those vaccinated. The fact that similar sequences have been found in COVID-19 vaccines suggests either criminal negligence or intentional harm. Independent researchers analyzing the vaccine contents discovered these SV40 promoter sequences, which are known to interact with human DNA in ways that could disable tumor suppressor genes and activate cancer-causing oncogenes.
What makes this situation particularly disturbing is the clear evidence of deliberate concealment. Internal documents show that Pfizer submitted falsified plasmid maps to regulators, omitting the SV40 sequences while knowingly including them in the manufacturing process. This deception alone invalidates the claim that the approval process for these vaccines was rigorous or transparent. If this were a product outside the pharmaceutical industry, say, food or consumer goods, an immediate recall and legal action would follow. Yet Pfizer continues to operate with impunity, shielded by government contracts and regulatory complicity. Even more alarming, leaked communications reveal that regulatory agencies like the FDA were aware of DNA contamination concerns but actively worked with Pfizer to downplay rather than investigate these risks. This collusion between pharmaceutical companies and regulators represents a complete betrayal of public trust.
The health implications of this contamination are severe and far-reaching. Medical experts warn that SV40 sequences in vaccines could lead to the development of aggressive, fast-growing cancers at much younger ages than typically observed. Reports of unusual cancer cases among vaccinated individuals are already emerging worldwide, with some oncologists noting particularly treatment-resistant forms of the disease. The spike protein produced by these vaccines has also been shown to interfere with p53, a crucial tumor suppressor protein, compounding the cancer risk posed by SV40 contamination.
The timing of Pfizer’s business decisions adds another layer of suspicion to this scandal. Shortly before these findings became public, Pfizer acquired Seagen, a leading cancer drug company, for $43 billion. This acquisition now appears strategically calculated to profit from the very health crisis their products may have helped create. Such actions suggest not just negligence, but a disturbing pattern of premeditated harm for financial gain.
The connection between regulatory negligence and corporate profiteering has never been clearer. The vaccine rollout was not just a public health initiative; it was a financial strategy in which mass vaccination seeded future profits through increased demand for cancer treatments.
This situation goes beyond medical malpractice as it represents what may be the largest case of scientific fraud and mass harm in modern history. Those responsible, including pharmaceutical executives, government health officials, and global health organizations that promoted these vaccines, must be held accountable through thorough urgent investigations and legal action. The millions of people who received these potentially dangerous vaccines deserve transparency about the risks they now face and access to proper medical monitoring. The presence of oncogenic sequences in vaccines must be treated as a criminal matter, not a regulatory oversight. Furthermore, those responsible for misleading the public, whether through omission, censorship, or outright lies, must be held accountable.
The role of globalist figures such as Bill Gates and Anthony Fauci in this debacle cannot be ignored. Gates, a key investor in both vaccines and cancer treatment technologies, has benefited enormously from this crisis. Meanwhile, Fauci, who publicly dismissed concerns over the vaccine’s safety, has now been legally forced to admit that placebo-controlled studies were never conducted on these vaccines before approval. This is a direct contradiction to his prior claims and a testament to the systematic corruption within public health institutions.
The silence from mainstream media and government officials on this issue only compounds the problem. Censorship of debate and dissenting scientific voices has allowed these abuses to continue unchecked. The reality is now exposed: the COVID-19 vaccines were not only inadequately tested but actively designed with genetic modifications that pose long-term health risks.
(Rebel News Canada)
The scientific community must immediately conduct large-scale studies on vaccinated populations to assess the true extent of DNA integration and cancer risk. Governments should halt all mRNA vaccine programs until comprehensive safety reviews can be completed. Most importantly, this scandal should serve as a wake-up call about the dangers of rushed medical interventions and the need for truly independent oversight of pharmaceutical products. The health of future generations depends on learning from these catastrophic failures in medical ethics and regulatory oversight.
If this revelation does not result in immediate legal and political consequences, it will confirm what many have suspected all along, that the pandemic response was not about public health but about control, profit, and depopulation. This case must serve as a wake-up call for humanity. The people who orchestrated this disaster must not be allowed to escape accountability, and those who remain silent in the face of these crimes are complicit in them. This is not just about vaccines; this is about the fundamental right to bodily autonomy and the defense of humanity against those who would exploit it for profit and power.
The public must take action by raising awareness and demanding accountability. Those still considering these injections should be informed of the dangers through grassroots campaigns, independent media, and community-driven initiatives. Protests, legal actions, and widespread sharing of peer-reviewed evidence must continue until the truth can no longer be ignored. People must reject coercion and stand firm in their right to medical choice, bodily autonomy, and transparent health policies. The more individuals educate themselves and others, the harder it becomes for pharmaceutical interests and complicit governments to continue their deceptive practices. Now is the time to unite and refuse compliance with harmful mandates that have already caused irreversible damage to millions worldwide.
@GGTvStreams
Robert F Kennedy Jr: “The Polio vaccine contained a virus called Simian virus 40 [and] SV40 [is] one of the most carcinogenic materials that is known to man”
“In fact it is used by scientists around the world to induce tumours in rats [but it] was in that vaccine [and] 98 million people [got] it [and] you’ve had this explosion of soft tissue cancers in our generation” (@humanspective)
The key scientific studies and expert analyses confirming DNA contamination in COVID-19 mRNA vaccines for references:
1. Peer-reviewed evidence: Pfizer mRNA vaccines contain DNA contamination (update #170)
Dr Mikolaj Raszek had never seen before in published science:
‘These authors claim that Pfizer and BioNtech who are the producers of this mRNA vaccine should be held accountable for exposing humanity to something so dangerous as allowing mRNA shots that had DNA plasmid contamination that had the SV40 promoter.’
2. The landmark study published in *Methods and Protocols* (June 2023) by McKernan et al. first identified plasmid DNA contamination in Pfizer and Moderna mRNA vaccines. Using qPCR and sequencing, researchers discovered bacterial DNA fragments including SV40 promoters at concentrations up to 35% of mRNA content, far exceeding regulatory limits for such contaminants. This finding was later replicated by Speicher et al. in *Viruses* (February 2024), who additionally demonstrated these DNA fragments can integrate into human genomes under laboratory conditions.
3. Further confirmation came from Buckhaults’ team at the University of South Carolina, whose unpublished sequencing data (presented to South Carolina Senate in September 2023) showed bacterial plasmid backbones persisting in vaccine vials. Their work revealed these plasmids contained antibiotic resistance genes and replication origins, raising concerns about horizontal gene transfer potential. This aligns with findings from Japan’s regulatory agency, which in October 2023 released internal documents showing Pfizer had detected DNA contamination but failed to disclose the SV40 components to health authorities.
The most damning evidence comes from a peer-reviewed study in *Clinical and Experimental Medicine* (March 2024) where researchers identified SV40 enhancer sequences adjacent to the spike protein gene in vaccine-derived DNA. These sequences are known to bind p53 tumor suppressor proteins, potentially disrupting cancer protection mechanisms. This explains the clinical observations reported by oncologists like Dr. Angus Dalgleish, who documented unprecedented early-onset turbo cancers in vaccinated patients in *The Journal of Pathology* (January 2024).
EMA internal reports (obtained through FOIA requests) confirm regulators were aware of these issues as early as 2021. A leaked EMA assessment dated December 2021 notes concerns about “residual DNA templates” and “potential genomic integration risks,” yet no corrective action was mandated. These documents corroborate the findings of independent labs like Corvelva in Italy, whose mass spectrometry analyses detected bacterial cell proteins in vaccine lots
The cumulative evidence from these studies establishes three critical facts: First, DNA contamination was an inherent byproduct of the rushed manufacturing process. Second, the inclusion of SV40 sequences served no legitimate production purpose. Third, both pharmaceutical companies and regulators actively concealed these risks while accelerating global distribution. This pattern of deception transforms what might have been an industrial accident into what leading geneticists are now calling, in Frontiers in Genetics (April 2024), “a case study in institutional research misconduct.”
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