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Pfizer acquired cancer companies early on, including C Gen for $43 billion and Trillium Therapeutics for $2.26 billion, the latter focused on blood cancers with a CD147 marker, also involved in COVID. The claim is that Pfizer knew about potential issues and bought companies to benefit from them. It is alleged that the Pfizer vaccines on the market are not the same as those tested in clinical trials, constituting a bait and switch and a fraud. Vaccine efficiency claims are therefore questioned. Significant DNA contamination has been found in the vaccines in 10 out of 11 studies. Additionally, DNA contamination was found in five peer-reviewed studies that were not specifically looking for it. Reports indicate a rise in cancer, with some papers reporting neoplasms at the injection site post-vaccination. It is claimed that this cannot be ignored as coincidence. It is asserted that these liability-free and often mandated vaccines may be the largest carcinogenic hit ever to the human population, especially concerning childhood schedules and pregnant women.

Every day, just the 1% of the cells of your DNA that gets replicated stretches from here to the sun four times. If you're to line it up end by end, that's very hard to conceptualize. But it should give you a little bit of humility before you go and start monkeying with it with these vaccines that can actually alter your DNA. And that's what I'm gonna show you. Is that the vaccines had a DNA contamination in them that didn't tell you about that could in fact alter your genome. Alright? These people are vibe coding your genome. And this is a major attack surface to the human gene pool because if this thing starts to alter the lifespan of people, it's going to part you with your Bitcoin. You're gonna end up spending money in a fiat system that has no controls, has no liability, and ends up oftentimes inducing mandates to get what it wants done. Many people had have peer have gone and replicated this work. It happened on Twitter. It did not happen very quickly in the peer review system. The peer review system kinda kicked it out. Some of these papers have now been peer reviewed, but it took years for them to come to this conclusion. Now, the FDA, the EMA and the TGA have all admitted that this mistake has happened. How did it happen? There's a big bait and switch. Pfizer actually ran the trial of 22,000 people on the process on the left and after they got to the trial, they then switched to the process on the right and didn't retrial the drug. And in doing so, they left a tremendous amount of excess DNA behind in the product. So all of the vaccine efficiency numbers you've heard in the news are flawed. They're not real because that's not what actually went into the trial. What went to the public was actually something that came out of this process too. It's published now in the BMJ that this fraud happened and no one has yet been prosecuted for it. So what did they leave in there? What they left in there was something we know from the polio scandal. If you're not familiar with the polio scandal, that polio vaccines were also contaminated with something known as SV40 and it created a massive cancer wave. Now the whole virus isn't in these vaccines, but there is a very curious part of this called the SV40 region that Pfizer intentionally removed from the disclosure that they gave to the FDA. So the FDA has admitted that this SV40 material is in there. They did not spell this out to the regulators. The regulators did not find them and they're actually running cover for them saying this DNA is too little consequence to matter, it's too small, and it's not functional. But we know it's functional because Dean et al has published that this piece of DNA drives DNA straight to the nucleus. It gets used in gene therapy vectors.

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.

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.

An article in Spectator Australia reported that DNA plasmids are contaminated with SV40 promoter sequences, which are oncogenic and used in cancer development in mice. The speaker questions why this is in an RNA vaccine, as the presence of DNA means it can integrate. Despite claims that the spike protein stays at the injection site, it has been identified everywhere, including in metastases from a colorectal cancer case where spike messenger RNA from the vaccine insertion was confirmed. The speaker was refused autopsies, even with consent from relatives, including a case of explosive melanoma after a booster shot. A report in The Lancet about deaths after vaccines was pulled, allegedly due to improper peer review. The speaker claims a media channel warned them that the government had made it a crime to criticize the vaccine program on the media.

Many labs, including Medicinal Genomics, found DNA contamination in Pfizer and Moderna mRNA vaccines. Regulators like the FDA and EMA admitted to this, but downplayed its significance. The SP 40 sequences omitted by Pfizer are crucial. DNA contamination can cause insertional mutagenesis, as stated in Moderna's patents. Regulatory agencies were deceived and failed to properly address the issue. This poses a serious risk that cannot be ignored.

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 argues that after trials the vaccine process was changed and a “bait and switch” occurred, stating the EMA asked for another 250-person trial and that data was never delivered, making trial data seem irrelevant to real-world outcomes. They claim Pfizer quickly acquired cancer companies—$43B into C Gen and $2.26B into Trillium Therapeutics—because Trillium focused on blood cancers with a CD one forty seven marker on them, implying beneficiaries from the situation. They assert the Pfizer vaccines on the market are not the same formulation as tested, calling it a fraud and noting efficacy numbers decay. They report significant DNA contamination found in 10 of 11 studies, with five peer-reviewed studies confirming contamination. They mention rising cancer rates and several papers reporting cancer post-vaccination, including neoplasms at the injection site, labeling this as a liability-free, often mandated issue, potentially the largest carcinogenic hit to the population, including children and pregnant women.

Pfizer knew early on that something was going to happen, and acquired cancer companies, including C Gen for $43 billion and Trillium Therapeutics for $2.26 billion, which focused on blood cancers with a CD147 marker, also involved in COVID. The Pfizer vaccines on the market are not the same formulation as what was tested in the clinical trials, which is a bait and switch and a fraud. Significant contamination has been found in the vaccines in 10 out of 11 studies. There is also significant DNA contamination found in five peer-reviewed studies. Cancer is on the rise, with several papers reporting cancer post-vaccination, sometimes at the injection site. The vaccines may be the largest carcinogenic hit ever to the human population, and are on childhood schedules and given to pregnant women. The vaccines encode a protein sequence known to be amyloidogenic, meaning it can form amyloids or prions in the body, which may be playing a role in clotting cascades and cardiovascular issues.

The amount of DNA allowed in vaccines was loosened a thousandfold after liability waivers were granted. These limits assumed naked DNA injection, which degrades quickly. However, mRNA vaccines use lipid nanoparticles (LNPs) that also coat contaminating DNA, invalidating the old limits. Studies show DNA levels in the shots are 10 to 100 times higher than the already obsolete limits. The LNPs deliver this DNA directly into cells, changing its persistence and biological impact. Pfizer used a different, more purified product in its trials than what was injected into billions of people. The initial process included a PCR amplification step to reduce DNA background, but this was dropped for mass production due to cost. This resulted in higher levels of background plasmid DNA and potentially E. coli components like endotoxin in the shots, possibly causing anaphylactic reactions. The presence of plasmids has been confirmed, and this process change, documented in the BMJ, is a major violation of manufacturing standards. The EMA requested a new trial after the process change, but the data was never delivered, rendering the original trial data irrelevant.

Recent Pfizer data reveals DNA contamination and acknowledges that liquid nanoparticles can spread throughout the body, contradicting previous denials. Concerns are raised about potential links between mRNA vaccines and cancer, referencing a 2006 FDA document warning about long-term cancer risks associated with mRNA gene therapies. Despite the push for mRNA in flu vaccines, long-term safety studies are lacking. Evidence suggests that these therapies may indeed pose cancer risks. The speaker expresses confidence that within five years, the connection to cancer will become undeniable, citing existing documents and admissions that indicate serious risks, even if they are not openly acknowledged.

At the outset, a process was approved by the FDA for emergency use authorization. However, it was later discovered that the approved process was swapped out for one containing contaminants like DNA and a cancer-causing substance. Pfizer redacted 800 pages of the manufacturing process, hiding the fact that a carcinogen was included. This lack of transparency led to no informed consent and potential harm to individuals. The vaccine rollout included a trial with a 2.4 times higher adverse event rate, including the presence of a carcinogen.

Key points: "the vials that were in fact approved are not the vials that were given to the public." The clinical trial used "process one that used PCR to make the DNA that was going to then turn into the RNA to make the spike protein." After the trial, "they switched" to a production process that "manufactured this DNA in E. Coli," introducing endotoxin risk. "There are these plasmids that have additional DNA that were not present in the actual clinical trial." Sequencing found mixtures, including "expired" and samples that had "been tapped into." Regarding Pfizer, "the Pfizer vaccines actually had a component that was not disclosed to the regulators." "The plasmid map on the right is what was disclosed to the EMA" with "no mention of the SV40 components" now "inside this DNA sequence." "The plasma on the left is what we actually found," with components not disclosed to regulators nor to patients. Monovalent Pfizer; prior ones were the bivalent vaccines from Moderna and Pfizer.

The speaker alleges that after receiving FDA Emergency Use Authorization for a vaccine produced via "process one," manufacturers switched to "process two." This new process allegedly introduced contaminants, including foreign DNA and SV40, a cancer-causing substance. The speaker connects this alleged change to a reported increase in aggressive cancers, particularly among young people. Referencing an NIH paper, the speaker claims SV40 is a known oncogenic DNA virus that induces cancers in laboratory animals. The speaker asserts Pfizer knew they were putting a carcinogen in process two. They speculate that this is the reason Pfizer redacted 800 pages of the manufacturing process, citing trade secrets.

The speaker raises concerns about the contamination of current vaccines with DNA and the unknown consequences of this contamination. They argue that efforts should be made to eliminate DNA contamination, even if it increases production costs. The speaker mentions a researcher from MIT who accidentally discovered that mRNA vaccines were contaminated with DNA. They criticize Pfizer for testing vaccines from one process and then vaccinating billions of people with vaccines from another process, which were contaminated with DNA. The presence of DNA in the vaccines raises risks, including potential cancer development. The speaker believes it is misleading to claim that the vaccines have undergone clinical trials when they have not been properly studied. They call for more rigorous research before commercializing vaccines.

Technology was proven unsafe long before 2021. The COVID-19 vaccines contain lipid nanoparticles that carry synthetic DNA into various organs, risking genomic instability, cancers, autoimmune diseases, and hereditary disorders. Contamination levels are far above permissible limits, and we're seeing evidence in patients. Cancer-free patients are relapsing with aggressive cancers post-vaccination, including unusual and rapid tumor growth. There's a rise in blood cancers too. The vaccines also contained endotoxin, which causes shock and can lead to death. The lab-leak possibility was dismissed without investigation, leading to devastating lockdowns. The "safe and effective" mantra was a lie; these injections have caused unprecedented harm. Ethical principles were ignored, and informed consent was violated. These mRNA gene therapies shouldn't have been used on anyone. We must halt distribution, monitor cancer trends, develop testing, and research vaccine-related conditions.

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.

FDA has not performed independent inspection of mRNA shots for DNA contamination, instead relying on Pfizer and Moderna's data. "The FDA acknowledged relying solely on manufacturer submitted data for compliance without independent postproduction verification" and "stated it is discussing the issue seriously, though no timeline for action was provided." Studies since 2023, including Kevin McKernan and David Spiker, "confirmed excess plasmid DNA fragments, including s v 40 sequences in vaccine vials from multiple countries" while the FDA "maintains no evidence of harm from over 13,000,000,000 global doses." "Despite independent studies detecting DNA contamination levels up to hundreds of times above the ten nanograms per dose regulatory limit." "No independent verification of manufacturers' claims. It's like having a fox guarding the henhouse." "alarm bells, genetic fingerprint of COVID vaccine found in 31 year old cancer patients' DNA." "We have identified the first instance, first direct molecular evidence of genomic integration of mRNA vaccine genetic material" with "20 base pair" "perfect match" "chromosome 19" "non safe harbor region." "This was accompanied by severe, severe genetic dysfunction" and "it should demand the immediate withdrawal of these mRNA products." "Has anyone inside the administration begun a formal investigation... moratorium on these injections?"

Pfizer allegedly knew their trial data indicated future issues and acquired cancer companies, investing $43 billion in C Gen and $2.26 billion in Trillium Therapeutics, which focused on blood cancers with the CD147 marker, also linked to COVID. The speaker claims the Pfizer vaccines on the market differ from the clinical trial formulation, constituting a "bait and switch" and fraud, invalidating claims about vaccine efficacy. Significant DNA contamination is allegedly found in most studies, including peer-reviewed ones, even those not initially investigating it. The speaker asserts cancer rates are rising, with some papers reporting neoplasms at the injection site post-vaccination. The speaker concludes that these liability-free, often mandated vaccines may represent the largest carcinogenic event in human history, especially concerning childhood schedules and pregnant women.

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.

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.

This is not conspiracy theory. Published in the BMJ by Retzaf Levy, it describes altering the vaccine trial process. The EMA asked for another trial of 250 people after the change, but data was never delivered. This bait and switch is a key reason trial data seems irrelevant to field results. Pfizer had the data early and rapidly acquired cancer companies: $43,000,000,000 for C Gen and $2,260,000,000 for Trillium Therapeutics. Trillium focused on blood cancers with a cd one forty seven marker. Pfizer vaccines on the market are not the same formulation as what was tested; this is a fraud. Cancer post vaccination is reported, including neoplasms at the injection site and DNA contamination found in studies.

Pfizer and Moderna vaccines use two processes. The first process involves using PCR to amplify and create DNA for clinical trials. Once approved, they use circular bacterial DNA plasmid to replicate billions of mRNA DNA sample copies. However, this resulted in contaminated vaccines with junk DNA. A study found DNA fragments in Pfizer and Moderna vaccines in Ontario, Canada. Researchers tested 27 mRNA vials from 12 different lots and discovered billions to 100 billions of DNA molecules per dose, exceeding FDA and WHO guidelines by 188 to 509 times. This is a significant amount, far beyond what is acceptable.

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.