Genetic Contamination in COVID-19 "Vaccines"
Exploring the DNA Content and Its Implications for Public Health
The introduction of mRNA-based COVID-19 "vaccines" was initially celebrated as a groundbreaking achievement in biotechnology. However, these injections have, in my opinion, not only failed in their stated purpose but also represent a dangerous bio-weapon based on the stated contents. Adding to the growing body of evidence against them, recent analyses by molecular virologists have uncovered alarming genetic contaminants within these products. Below, we delve into these critical findings and their far-reaching implications.
The Discovery of Plasmid DNA and SV40 Sequences
What Are These Contaminants?
Dr. Speicher’s research uncovered significant levels of plasmid DNA and SV40 promoter-enhancer sequences in Pfizer's COVID-19 "vaccines." The presence of plasmid DNA, a carrier for genetic material during vaccine production, raises concerns about genomic integration. SV40, a sequence historically linked to cancer research, enhances the likelihood of this genetic material entering human cells and potentially integrating into chromosomes.
How Did This Happen?
Pharmaceutical companies shifted from cleaner manufacturing methods to cost-effective but less precise processes. This decision introduced residual DNA into the final product. Despite assurances that these contaminants would be eliminated, Dr. Speicher and his colleagues found billions of DNA fragments per dose—far exceeding regulatory safety limits.
Implications of DNA Encapsulation in Lipid Nanoparticles
Enhanced Delivery Mechanism
Lipid nanoparticles (LNPs) are designed to protect and deliver the genetic material into cells. While effective for delivering mRNA, they also shield the plasmid DNA, allowing it to penetrate the brain, reproductive organs, and even the fetus. This raises critical safety concerns about long-term health effects, including genetic modification risks.
Safety Guidelines: A Flawed Framework
Current DNA contamination limits were established for naked DNA, which breaks down rapidly in the bloodstream. Encapsulation in LNPs significantly changes the dynamics, making existing guidelines inadequate. Dr. Speicher’s findings call for an urgent reevaluation of these standards.
Fraud Allegations and Regulatory Oversight
Undisclosed Genetic Sequences
Regulatory agencies worldwide relied on the genetic maps provided by manufacturers like Pfizer and Moderna. However, evidence suggests deliberate omission of sequences like SV40 in the submitted documentation. This omission prevented proper scrutiny and allowed contaminated "vaccines" to reach the public.
Health Canada's Response
Health Canada acknowledged the presence of SV40 sequences but deemed them insignificant. Alarmingly, they requested Pfizer to remove these sequences only after 2024, allowing millions of doses with potentially harmful contaminants to be distributed.
Potential Health Risks
Cancer and Genetic Modification
The SV40 sequence not only facilitates genomic integration but also disables p53, the "guardian of the genome," which prevents cancerous mutations. This disruption could accelerate the onset of aggressive cancers, known as "turbo cancers," in affected individuals.
Transgenerational Concerns
Dr. Speicher raised alarms about the possibility of DNA integration into reproductive cells. If such integration occurs, it could lead to offspring carrying these genetic modifications, perpetuating the issue across generations.
The Way Forward
Urgent Research and Public Awareness
Dr. Speicher and his team emphasize the need for further research to assess the extent of genetic integration in individuals who received these "vaccines." Public health policies must adapt to address these revelations, including halting distribution immediately.
Informed Consent
The lack of transparency surrounding the contents and the risks of these injections posed by the inclusion of double stranded DNA highlights the erosion of informed consent. Patients must be fully aware of what they are receiving and the associated risks as a critical matter of law.
Conclusion
Dr. David Speicher’s groundbreaking research has exposed critical flaws in the production and regulation of COVID-19 "vaccines." The presence of plasmid DNA and SV40 sequences demands immediate action to ensure public safety and restore trust in medical science. As the scientific community delves deeper, the importance of transparency, accountability, and rigorous oversight cannot be overstated.
Want to Dive Deeper?
I strongly recommend this insightful discussion between Dr. David Speicher and myself. The accompanying post includes additional reading materials and source references for deeper exploration. To make this resource even more accessible, my team dedicated over 15 hours to editing the video, thoughtfully addressing Dr. Speicher’s speech impediment. The result is a uniquely engaging window into Dr. Speicher's brilliant mind and expertise on this critical topic.
Great article. Thank you for putting it together. Unfortunately the regulatory bodies have deaf ears and blind eyes. Readers might be interested in Dr. John Campbell's review of a study on Fenbendazole on cancer. It has had over 150k views and over 2,700 comments in one day. https://www.youtube.com/watch?v=5Q5QjEPGNNg
I would not doubt that Health Canada was aware of the SV40 from the beginning. Pfizer did not identify the presence oSV40 on the map submitted to HC but this does not mean they did not know.
It is possible that HC and Pfizer jointly decided to proceed with the distribution to the public with knowledge of the SV40 in the product. The logic would have been something like the risks from SV40 such causing cancer are acceptable because the greater number of lives saved from covid 19. This logic is totally unscientific and unethically but this has never gotten in the way of other distributing other harmful products in the past.