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The spike protein from various vaccines can bind to cancer-related genes, induce cancer pathways, and inhibit DNA repair. It can turn cells into spike factories, leading to immune system attacks and potential cancer development. Reports of increased cancers and harmful effects on organs have been observed. Military data was allegedly suppressed. This situation is seen as a crime against humanity.

Kevin McKernan recently discovered that there is contamination in the mRNA shots with cDNA, including a cancer-promoting segment called SV40. SV40 turns on cancer genes in the human body and impairs tumor suppressor systems. This means that the shots not only promote cancer through SV40 but also inhibit our ability to fight cancer. The increase in cancer rates is undeniable, but the question remains: how much of this is due to the vaccines?

Kevin McKernan discovered DNA contamination in Pfizer vaccines, specifically the simian virus 40 (SV40) promoter, which is known to cause cancer. This finding has been supported by others in North Carolina, Canada, and Europe. The presence of SV40 is linked to an increase in cancer incidence and faster tumor growth, with reports of aggressive cancers appearing unexpectedly in individuals. For example, a 92-year-old woman developed large growths at her injection site, and another case involved a woman whose breast swelled after vaccination, leading to a breast cancer diagnosis. Data indicates a significant rise in lymph node and bone marrow cancers, suggesting a troubling connection to the vaccine.

Speaker 0 argues that because it’s classified as a vaccine, they don’t have to worry about being sued. Speaker 1 counters that there is immunity from liability dependent on there having been no fraud, and asserts that there clearly was fraud, so in light of that... Speaker 0 expresses surprise at known caveats to liability. Speaker 1 confirms the caveats and says it makes the situation more interesting. Speaker 0 asks how fraud is defined in this context, noting that drugs were sold with many studies but only one was good. Speaker 1 responds, “Let's try this one,” and discusses safety testing: the insufficient amount of safety testing before release was done with mRNA vaccines produced in a process that did not involve DNA. The product injected into billions of people involved DNA plasmids, with massive contamination in the shots actually delivered, including the SV40 promoter (simian virus 40). The point is that safety testing was performed on one process, but people were injected with something different that had other components not tested, which Speaker 1 calls fraudulent. Speaker 0 asks for an explanation of the SV40 issue. Speaker 1 explains production methods: techniques to generate product using a plasmid, a circular piece of DNA, allowing vats to grow the product before coating in lipid nanoparticle, with bacteria doing the work. There is a requirement to purify DNA and set standards for residual DNA contamination. In this case, not only was quality control poor, but there was a much more painstaking way to produce the same product that did not involve DNA plasmids at all. As a result, vials given to Kevin McKernan, containing material actually injected into people, showed DNA contamination across the board. Speaker 1 states that leftover DNA includes the SV40 promoter, a genetic trigger from simian virus 40, which is carcinogenic. This promoter is left over in vials from shots actually injected into people, implying that the claims about the potential for mRNA shots to integrate into the genome were incorrect. Speaker 1 asserts that there is DNA in the vials, not just some old DNA, and that it includes the SV40 promoter, a genetic engineering tool with carcinogenic potential. Therefore, Speaker 1 concludes, this seems to be clear fraud: you can’t inject a different product into the public on the basis of safety testing conducted with a product produced by a different process.

This is not conspiracy theory. This has been published in the BMJ by Retzaf Levy, and they go through this process: one where they ran these vaccines in the trial and how they changed that when they decided to go and inject the rest of the world. This is traditionally a mortal sin in vaccine manufacturing or in any sort of biologic manufacturing. The process is the product. You change the process, you have to go through trials again. And the EMA even asked them to do that, although they failed to. They asked for another trial of 250 people once they changed the process and that data was never delivered. So this bait and switch is very important for you to understand why the trial data is of absolute zero consequence to what we're actually seeing in the field. Those numbers are a caricature of what they're actually doing with these injections. They know something. Pfizer very early on they had the data on this from their trial, they knew this was going to happen and they quickly went out and acquired cancer companies. They put $43,000,000,000 into the acquisition of C Gen and they put $2,260,000,000 to acquire Trillium Therapeutics. Trillium was focused on blood cancers that have a CD one forty seven marker on them. Okay? That is one of the markers that is known to be involved in COVID. So, they have a very interesting window on those malignancies and, they're buying up the cancer companies that are probably gonna play the biggest role in benefiting from the mess that they've created. So, in summary, the Pfizer vaccines on the market are not the same formulation as what was tested in the clinical trials. This is a big bait and switch and it's a fraud. So you can't believe anything they're saying about the vaccine efficiency, which we have seen even those numbers decay over time. This is probably why. They're not really what they trialed. They gave you something different. There is significant DNA contamination that's found. Like, 10 out of 11 studies have found this, and the ones that haven't found it have some financial conflicts. So, I think the consensus is out. 10 out of 10 out of 10 of the real studies, are finding this. Several are through peer review, which have not been easy to get through peer review. The peer review journals do not like these papers. They get beat around in peer review for months to years, but they're making their way out now. There is also significant DNA contamination now found in five peer reviewed studies that were not looking at this. They were looking at people's blood and tissue and it was accidentally in there. Other people had to go sleuth it out. We've got cancer on the rise and there's several papers that report cancer post vaccination. Like, right at the site of injection, they'll see neoplasms. Alright? There is there's something going on here. This can't be ignored saying it's a coincidence anymore. Now this is these are liability free and they're often mandated. Okay? This may be the largest carcinogenic hit ever to the human population. And we have these on childhood schedules. We're giving these to pregnant women. This has gone absolutely off the rails.

The speaker claims SV40 in literature turns on cancer genes. They further claim the spike protein impairs tumor suppressor systems P53 and BRCA, promoting cancer and inhibiting the ability to fight it. The speaker suggests cancer rates are up, and the question is how much is due to vaccines. They state that repeated shots every six months increase the chances of getting loaded with synthetic genetic material that will cause harm, including heart disease, neurologic disease, blood clotting, immunologic problems, and cancer.

When COVID-19 vaccines were sequenced, commercial annotation software highlighted functional parts of the plasmids, including antibiotic resistance genes and SV40 components. The speaker claims that Pfizer had to manually remove these annotations before submitting the plasmid map to regulators. According to the speaker, regulators received the DNA sequence, but the sponsor is obligated to annotate every open reading frame and promoter, even if their function is unknown. The speaker alleges that Pfizer intentionally removed annotations, hiding them from the FDA, which the speaker believes is a violation of guidelines. The speaker suggests the reason for hiding SV40 components is due to SV40 virus contamination in polio vaccines and its debated link to cancer. The speaker asserts that while epidemiological data is confounded by vaccine shedding, laboratory studies show SV40 is a potent oncogenic virus. The speaker claims that the vaccines contain some of the more carcinogenic components of that virus, and that these sequences are functional and have consequences.

The speaker claims that this is not conspiracy theory and cites a BMJ publication by Retzaf Levy, which describes a process in vaccine development: vaccines were trialed under one formulation, but when the decision was made to deploy them globally, the process was changed and the product injected to the rest of the world. The speaker asserts that changing the process requires new trials, yet the EMA asked for an additional trial of 250 people after the process change, and that data was never delivered. This is described as a “bait and switch,” asserted as crucial for understanding why trial data is of zero consequence to what’s seen in the field, implying that real-world outcomes do not match trial data and that the numbers from trials are a caricature of field performance. The speaker claims Pfizer had early data indicating what would happen and acted on that by acquiring cancer companies: $43,000,000,000 into the acquisition of C Gen and $2,260,000,000 to acquire Trillium Therapeutics. Trillium is described as focused on blood cancers with the CD147 marker (CD Adaptor 147) on them, a marker claimed to be known to be involved in COVID. The implication is that Pfizer is building an investment portfolio in cancer companies that would benefit from the consequences the speaker alleges they caused. In summary, the vaccines on the market are said to be not the same formulation as what was tested in clinical trials, labeling this a “bait and switch” and a fraud, and asserting that vaccine effectiveness numbers are not reliable because the products differ from trial formulations and because those numbers decay over time. The speaker alleges significant DNA contamination, stating that 10 out of 11 studies have found this, with the remaining studies allegedly constrained by financial conflicts. The claim is that consensus among real studies supports DNA contamination, with several studies through peer review, which the speaker notes is difficult for those papers to pass through peer review. It is claimed that five peer-reviewed studies not originally examining contamination found DNA in blood and tissue upon sleuthing. The speaker asserts that cancer is on the rise and that several papers report cancer post-vaccination, including neoplasms at the site of injection. The claim is that this situation cannot be dismissed as coincidence and is described as “liability free” and often mandated. The speaker posits that this may be the largest carcinogenic hit to the human population, with vaccines on childhood schedules and given to pregnant women, stating that “this has gone absolutely off the rails.”

Speaker 1 reports evidence from multiple sources, including InModia lab in Germany and John Cantazaro at NEO7 Bioscience, that Pfizer and Moderna code is reverse transcribed and inserted into human DNA. According to Speaker 1, this means individuals could carry a "stamp" of Pfizer or Moderna in their genome. The speaker suggests the body may not be editing out or repressing this code, as spike protein evidence persists for years. Transmission of spike protein producing genetic code is possible, along with fragments of code for the spike protein, SV40, and other DNA fragments. Speaker 1 raises concerns about potential health issues like blood clots, heart damage, autoimmunity, and unusual tumors. John Cantazaro's research indicates a dramatically altered genetic profile in vaccinated individuals, tilting towards neoplasm or cancer. Speaker 1 shares an anecdote about a patient who developed terminal cancer after vaccination, with Cantazaro confirming the presence of Pfizer code in the patient's genome.

The speaker claims messenger RNA vaccines with the spike protein can induce cancer in multiple ways. They allege the presence of oncogene stimulants, specifically SV40 in the Pfizer vaccine, confirmed by multiple researchers. A paper from Wurzburg purportedly confirms this and shows the vaccines convert cells to cancer. The speaker asserts the spike protein and mRNA vaccines bind to major suppressor genes like P53, BRCA, and MSH, which normally suppress cancer. Mutations in these genes can lead to earlier onset of cancer. The speaker suggests these vaccines could cause the equivalent of mutations in these genes, leading to an explosion of colorectal cancers. They advocate for an immediate ban on these vaccines and accountability for those who oppose it.

The speakers discuss how initial kidney cells from monkeys used to make vaccines inadvertently gave people simian virus 40, which can lead to rapid cancer. One speaker says that this is one of the cancer-causing issues with the shots, explaining that it's supposed to stay out of the nucleus but can get in. One speaker says the initial claim was that the shot would stay local, in the arm, and dissipate quickly, but "they know that's not true." The other speaker mentions pseudouridine, a replacement nucleotide that is hard to break down, and that there's no study showing that it can be cleared from the body. This could be why some people have high antibody levels years later.

The speaker describes the first peer-reviewed paper documenting evidence of genomic integration of mRNA vaccine genetic material in a human being. They report a case of a 31-year-old woman who developed stage four bladder cancer within a year after three mRNA shots. They say they analyzed her circulating tumor DNA and performed multiomic analysis, including transcriptomic and proteomic analysis. They report finding, “within her chromosome 19,” in the circulating tumor DNA, a 20 base pair segment matching the Pfizer DNA plasmid reference sequence. The speaker characterizes the finding as a “non human non human chimeric hybrid,” stating it transitions from human to Pfizer to human. They add that there is “about a one in a trillion chance this was just an anomaly.”

The speaker states: "We found circulating Pfizer mRNA in his exosomes three point six years after his last shot, and we also found plasmid DNA from the manufacturing process SV40 ORI segments, as well as the spike expression segments in his skin, in his Grover's disease area. He developed this skin disease after the shots." They add: "We also found vaccine spike protein and no nucleocapsid in this skin area as well." The speaker emphasizes timing: "Three point six years after his last shot, he suffered from myocarditis, pulmonary embolism, multisystem vaccination syndrome, neurological adverse events as well." They conclude: "And so the fact that we are finding this material forty three months after the last shot means we were lied to completely." The speaker claims: "We were told it would stay in the arm, it would degrade within weeks, that was wrong and we expect lawsuits to begin to flood in."

The speaker explains that there is contamination in the messenger RNA, including fragments of DNA called cDNA, with one of them being s v 40, a known cancer-promoting segment. The other speaker mentions that mainstream news reports estimate that millions of Americans had cancer due to SV 40 contamination in the past. The first speaker confirms that SV 40 turns on cancer genes and that the spike protein in the shots impairs tumor suppressor systems. They conclude that the shots promote cancer through SV 40 and suppress our ability to fight cancer. The speaker acknowledges that cancer rates are increasing, but the extent to which vaccines contribute to this is still uncertain.

Speaker 0: They argue that because the vaccine is classified as such, they don’t have to worry about being sued. They claim immunity from liability is dependent on there being no fraud, and there clearly was fraud. Speaker 1: They say there is fraud. They note that immunity from liability depends on fraud, and in light of that, it matters. They explain that there was fraud. Speaker 0: Expresses surprise and asks for caveats about fraud. Acknowledges there were caveats. Speaker 1: Confirms there is fraud and says it makes the situation more interesting. Speaker 0: Asks how fraud is defined, noting that drugs were sold with multiple studies and only one was good. Speaker 1: Responds with a point about safety testing for the mRNA vaccines. States that the insufficient safety testing was done before release, and that the product injected into billions of people involved DNA plasmids. There is massive contamination in the shots actually delivered, including the SV40 promoter from simian virus 40. The point is that safety testing for one drug was completed, but people were injected with something different that had other components that were not tested, which is described as fraudulent. Speaker 0: Requests an explanation of the SV40 issue for the audience. Speaker 1: Describes production techniques used to generate the product. Explains that a plasmid, a circular piece of DNA, was used to produce the product in vats, with bacteria performing the production, later coated in lipid nanoparticle. There is a requirement to purify DNA and set standards for DNA contamination, with limits that cannot be exceeded. In this case, the problem isn’t only poor quality control but that there was a more painstaking way to produce the same product that did not involve DNA plasmids at all. Consequently, leftover material in vials injected into people contained DNA contamination across the board. Kevin McKernan tested vials, finding DNA contamination in the samples. Speaker 1: Explains that the DNA left over includes the SV40 promoter, a genetic trigger from simian virus 40, which is known to be carcinogenic. Since this promoter is left in the vials from injections given to people, it challenges the claim that the mRNA shots could not integrate into the genome. While acknowledging that there are cellular processes such as reverse transcription, the speaker asserts that even the claim of “no DNA” is false because there is DNA in the vials, specifically DNA with the SV40 promoter, a genetic engineering tool with carcinogenic potential. The speaker concludes that this appears to be fraud: injecting a different product into the public on the basis of safety testing that was conducted with a product produced by a different process. Speaker 0: Reiterates the conclusion: you can’t inject a different product into the public on the basis of safety testing that was done with something produced by a different process.

We were surprised by the findings from a patient vaccinated four times with Pfizer. A year post-vaccination, tumors developed, and the patient died within a month. Biopsies revealed SV40 in the vaccine's origin of replication. Preliminary sequencing confirmed the presence of the Pfizer vaccine's DNA, including sequences from Spike protein. Unexpectedly, the DNA copy number in the tumors exceeded that of the human genome, indicating a significant insertional mutagenesis event. Instead of the anticipated lower mutation rates, our PCR results showed signals as strong as the original vaccine vial, suggesting the DNA is replicating within the patient. This indicates that the mammalian origin of replication in Pfizer's vaccine is active in human tumors.

A colon biopsy from a Pfizer-vaccinated individual who died a month after tumor emergence revealed SV40 in the origin of replication from the Pfizer vaccine. Preliminary sequencing suggests the presence of Pfizer's vaccine. The vaccine DNA copy number was greater than the human genome, indicating replication. PCR signals suggest the vaccine concentration is similar to or higher than the original vial, despite dilution in the body. This indicates the mammalian origin of replication in Pfizer's vaccine is active in human tumors. This finding may explain shedding, which is not supposed to occur because the COVID vaccine is not intended to alter DNA. However, evidence suggests that the vaccine may be altering DNA, making it a VGBT (genome altering) product. This could mean that spike proteins are continually created, and shedding is real.

A peer-reviewed paper confirms Pfizer's mRNA vaccine is contaminated with DNA and SV40 enhancers, considered dangerous. Pfizer used bacterial plasma DNA during mass production, leading to contamination with spike protein genes, antibiotic resistance markers, and SV40 enhancers. Researchers found 4-5 times more DNA than the safe limit. The DNA fragments could integrate into the human genome due to the SV40 enhancer. Injected vaccine samples caused super strong kidney cells to produce spike protein, excreted via exosomes, potentially spreading body-wide. The vaccines were toxic to these cells, causing pathological changes. The DNA, tucked into lipid nanoparticles, could integrate into the human genome, turning the jab into accidental gene therapy. The SV40 enhancer drags DNA into the nucleus. The study suggests the inclusion of SV40 enhancers was deliberate, not accidental, and scrubbed from regulatory paperwork. Experts theorize this contamination could be linked to an explosion of turbo cancers. The study concludes mRNA shots should be suspended until safety is determined. Another study found vaccine spike protein expressed in cerebral arteries of stroke patients for up to 17 months, accompanied by an autoimmune response.

Kevin McKernan discovered DNA contamination in Pfizer vaccines, specifically the simian virus 40 (SV40) promoter, which is known to cause cancer. This finding has been supported by other researchers and indicates a rise in aggressive cancers, with patients experiencing rapid tumor growth. Anecdotal evidence suggests a correlation between COVID-19 vaccinations and sudden cancer diagnoses, including cases of lymphadenopathy and breast cancer following vaccination. The SV40 is linked to both oncogenesis and angiogenesis, which is essential for tumor growth. Reports show significant increases in lymph node and bone marrow cancers, indicating a troubling trend in cancer rates post-vaccination.

The speaker claims to have identified 13 mechanisms by which mRNA vaccines can induce or promote cancer, asserting that even one is sufficient to warrant an immediate ban. They attribute the rise of "turbo cancers" in young people to the vaccines, despite media outlets citing diet or environmental factors. The speaker alleges government censorship prevents open discussion about vaccine risks, with editors and producers reportedly considering it a crime to undermine public confidence in them. They state the vaccines are ineffective and dangerous, with benefits existing only in statistical models. They criticize COVID modeling for being consistently inaccurate and exaggerating the severity of the pandemic. The speaker highlights a Mail on Sunday article where they and James Royal argued that the vaccines cause cancer, citing relapsed cancers and new stage four cancers in healthy individuals. They conducted a survey revealing that they were the only doctor asking patients about their vaccine history, while other doctors deny any association between the vaccines and cancer.

A scientist reports an increase in cancer cases worldwide after the rollout of experimental injections. CDC data confirms this trend, with a significant increase in cancer cases. The spike protein in these injections binds to the p53 gene, leading to cancer pathways opening up. There are numerous harmful effects caused by the spike protein, and the scientist is concerned about the lack of long-term safety studies for these products. The lipid nanoparticles in Pfizer and Moderna vaccines, not intended for human or veterinary use, have been administered to over 5 billion people. The J&J vaccine, containing a carcinogenic substance, was quietly pulled from the market. The NIH is withholding information on cancer pathways and forced the retraction of a scientific paper. These injections also affect the immune system's ability to function properly, impacting cancer prevention. The scientist apologizes for those who received these injections without informed consent and urges action at the local level to stop further harm.

The speaker discusses the presence of contamination in vaccines, specifically cDNA fragments and s p 40, which is a cancer-promoting segment of DNA. They mention that s v 40, a related virus, caused cancer in millions of Americans in the past. The speaker explains that s p 40 turns on cancer genes and that the spike protein in the vaccines impairs tumor suppressor systems. They conclude that the vaccines promote cancer and hinder our ability to fight it. The speaker acknowledges that cancer rates are increasing but questions how much of it is due to the vaccines.

A peer-reviewed paper confirms Pfizer's mRNA vaccine is contaminated with dangerous DNA and SV40 enhancers. During production, bacterial plasmid DNA led to contamination with spike protein genes, antibiotic resistance markers, and SV40 enhancers. Researchers found four to five times more DNA than the safe limit; these DNA fragments could integrate into the human genome due to the SV40 enhancer. Experiments showed the vaccines were toxic to cells, causing pathological changes and spike protein production, potentially spreading body-wide via exosomes. The DNA contamination, tucked into lipid nanoparticles, could lead to unintended gene therapy. The SV40 enhancer, deliberately added but removed from regulatory paperwork, raises questions about Pfizer's intentions. Experts theorize this contamination could be linked to an increase in "turbo cancers," coinciding with Pfizer's acquisition of a cancer drugmaker. An epidemiologist noted the study found DNA from the manufacturing process way over regulatory limits, including the cancer-promoting SV40 promoter enhancer and spike-producing DNA. A separate study found vaccine spike protein expressed in cerebral arteries of stroke patients for up to seventeen months, potentially contributing to autoimmune responses. There are now 11 independent reports that have found, DNA contamination within these shots of up to 60000% above regulatory limits.

The Pfizer vaccine is contaminated with plasma DNA, not just mRNA. This DNA is the DNA vector used as the template for the in vitro transcription reaction. This was discovered by sequencing vials of Pfizer vaccine from Colombia. It's surprising that there's any DNA in there. The speaker is alarmed about the possible consequences of this, including rare but serious side effects like death from cardiac arrest. Mixing DNA with a lipid complex allows it to enter cells and become a permanent fixture. This is a real hazard for genome modification of long-lived somatic cells, like stem cells, and could cause a sustained autoimmune attack. There is also a very real theoretical risk of future cancer in some people. The risk is not zero and it may be high enough that we ought to figure out if this is happening or not.

The speaker explains that the messenger RNA in the shots is contaminated with cDNA, including a cancer-promoting segment called s v 40. They mention that s v 40 turns on cancer genes in the human body and that the spike protein in the shots impairs tumor suppressor systems. The speaker suggests that the shots promote cancer through s v 40 and inhibit our ability to fight cancer. They also mention that cancer rates are increasing. The speaker raises the question of how much of this is due to the vaccines.