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Speaker 0 ties Operation Warp Speed to Pfizer. "They're doing a huge investment into bringing more drugs into America and also coming up with a vaccine that's to solve cancer." He states, "vaccination is the cause of cancer. I never saw a case of cancer in an unvaccinated person." He adds that people "died suddenly after taking the vaccines and boosters," and that "during 1986, government decided to put an act in to protect Pfizer, Moderna, Johnson and Johnson, and all these companies from lawsuits." He alleges the military as test subjects: "Soldiers disabled and killed by vaccinations, April. No wounds, no damages, no shots, just vaccines." He recalls 1885: "Vaccinate, vaccinate, vaccinate. There's money in it. Money in the side effects." He asks, "See those people holding down that person and vaccinating them?" Mentions Murder by Injection and The Poison Needle. Speaker 1: "No, I'm a big believer in vaccines. Polio vaccine. Big, big believer in vaccines."

Pfizer did not disclose SV40 DNA in COVID vaccine to regulators, causing concern among Health Canada officials. The presence of SV40 DNA was confirmed by Pfizer but not shared with FDA, EMA, or HC initially. Despite claims that the DNA fragment is inactive and below regulatory limits, concerns remain about potential risks. Health Canada is working with international partners to address the issue for future vaccine strains. The focus seems to be on vaccine acceptance rather than addressing health risks associated with DNA contamination. Pfizer has not responded to requests for comment.

Former vice president of Pfizer, Speaker 1, shares his insights on the events of early 2020. He noticed inconsistencies in statements made by colleagues and realized something was amiss. The simultaneous lockdowns across multiple countries convinced him that this was a coordinated effort beyond the local level. Speaker 1 accuses those in power of lying and implementing ineffective measures. He believes that the vaccines being administered are intentionally harmful, based on his extensive experience in drug design. He is unafraid of legal action and challenges them to sue him, confident that he would win.

The speaker claims Pfizer documents reveal the COVID vaccines didn't work to stop the virus a month after rollout in November 2020. They allege Pfizer knew the third most common side effect was COVID. Within months, Pfizer supposedly needed to hire 2,400 staffers to process adverse event reports. The speaker asserts Pfizer and the FDA knew in May 2021 that the vaccines caused heart damage in 35 minors within a week of injection, but this wasn't disclosed to parents until August 2021. The speaker states the CDC initially claimed the injection materials stayed at the injection site, but Pfizer knew they biodistributed throughout the body within 48 hours, settling in the brain, liver, adrenals, spleen, and ovaries. Pathologist Dr. Robert Chandler allegedly found no mechanism for the body to eliminate lipid nanoparticles from the ovaries, leading to accumulation with each injection.

Speaker 0 describes a historical sequence involving SV40, a cancer-promoting virus, claiming it was taken from the polio vaccine because humanity was being injected with it along with other substances. He says researchers irradiated the virus in a gain-of-function experiment to make it more carcinogenic, then put it in animals, processed the tumors in a blender, and irradiated the material with a linear particle accelerator to make it more aggressive, repeating the cycle until achieving the maximum killing capacity. He asserts this gain-of-function work occurred in the 1960s under the guise of killing Fidel Castro, but the effort was never used for that purpose; it was turned over to MD Anderson, and the technology supposedly disappeared. He then contends that SV40 ended up in plasmids in vaccines in February 2021 (02/21/21), implying a continued or resurfaced presence of SV40 in vaccines. He asserts that this gain-of-function activity has been ongoing for a long time and that the only survivor who can tell the story is Judith Barry Baker; he claims she was there and that nearly everyone involved was killed within a year, except for the person at the head of the operation. He mentions he will discuss this at CHD that weekend. The speaker emphasizes that gain-of-function activity is not new, suggesting that if authorities admitted they took a carcinogenic virus from the animal kingdom and made it more aggressive and mass-distributed it into humanity, and then conducted gain-of-function experiments afterward, one would see rising cancer rates following the mass vaccination programs of the 1950s and 1960s. He notes that everybody knew someone who got cancer within about twenty years of the mass vaccination program of the 1950s and 1960s.

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.

Former vice president of Pfizer, Speaker 1, shares his insights on the COVID-19 pandemic. He noticed discrepancies in what his former colleagues, including Sir Patrick Valens, were saying on television. This led him to believe that there was a supranational operation at play, orchestrated by organizations like the WHO or the World Economic Forum. He accuses these individuals of lying and claims that the pandemic response measures were ineffective and not part of any country's preparedness plans. Speaker 1 also expresses concerns about the safety of the vaccines, stating that he believes they were intentionally designed to harm people.

The speaker claims the original plan to eliminate older generations with a bioweapon failed due to incorrect tuning. They connect the arrest of Harvard professor Charles Lieber in 2019 for possessing nanobot technology to China's alleged attempt to steal this technology for bioweapon tuning. To protect the technology from China, it was supposedly redeployed to Ukraine. The speaker highlights that Pfizer was late in developing its COVID vaccine. They allege Pfizer used SV40, a cancer-causing agent, in their vaccine design, then attempted to remove the evidence before FDA approval. The speaker links this to the Cutter incident involving polio vaccines during FDR's presidency. They question how a monkey virus from the 1950s appears in COVID vaccines 75 years later, suggesting malice. The speaker recalls discussing two Pfizer patents in 2021, suspecting SV40 would be used in a vaccine, most likely Pfizer's.

The speaker claims Pfizer committed the greatest crime against humanity in recorded history due to the scale and foreknowledge of harm. She states Pfizer knew within a month of the vaccine rollout in November 2020 that it didn't work to stop COVID, referring to internal language describing "vaccine failure" and "failure of efficacy." She claims the 3rd most common side effect in the documents is COVID. According to the speaker, mandates, job losses, family separations, deaths, injuries, and sterilizations were based on a lie. The speaker asserts that society was destroyed, children's education was ruined, depression and suicide levels increased, and businesses were destroyed, all based on a lie, resulting in a massive transfer of wealth.

The polio vaccine was the first to be made from monkey organs. However, using monkeys to manufacture vaccines has always been dangerous. The vaccines were contaminated with a monkey virus, which was discovered by researcher Venice Eddy at the FDA. Her findings were suppressed and there was bias against the possibility of it being a harmful virus. Doctors Sweet and Hilleman later found the same virus and named it SV40. This was just one of many monkey viruses identified during that time.

The polio vaccine was the first to be made from monkey organs. However, using monkeys to manufacture vaccines has always been dangerous. The vaccines were contaminated with a monkey virus, which was discovered by researcher Venice Eddy at the FDA. Her findings were suppressed, and there was bias against the possibility of a nasty virus. Doctors Sweet and Hilleman later found the same virus and named it SV40. This was just one of many monkey viruses discovered during that time.

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.

Pfizer was not initially ready for Operation Warp Speed. Pfizer allegedly went to their genetic department and found SV40, using it to design their COVID jab. They then allegedly instructed scientists to remove evidence of SV40 before presenting it to the FDA for approval. SV40, a monkey virus, appeared in polio vaccines during FDR's term and is now allegedly present in COVID vaccines seventy-five years later. There are two legal definitions for BioNTech and the Pfizer jab. In 2021, the speaker discussed a documentary with Robert Malone and Robert McCullough, highlighting two Pfizer patents. The speaker suspected in 2020 that SV40 would be used in someone's jab, most likely Pfizer's. The speaker advised people not to take the jab, especially the Pfizer jab.

Speaker 1, a former vice president of Pfizer, discusses his experience in the pharmaceutical industry and his concerns about the COVID-19 pandemic. He claims that global lockdowns indicate a supranational operation orchestrated by organizations like the WHO or the World Economic Forum. He accuses public figures of lying about the virus and asserts that the vaccines are intentionally harmful. Despite facing censorship and defamation, he remains convinced that the injections were designed to cause harm and even death. He expresses worry and believes that his knowledge and experience in drug development support his claims.

Every vaccine maker except Pfizer was ready to deploy the COVID jab when Operation Warp Speed came out. Pfizer allegedly went to their genetic department and used SV40 to design their jab because they were behind. They then allegedly used a molecular tool to remove the evidence of SV40 before presenting it to the FDA for approval. SV40 was present in the Cutter incident during FDR's term in polio vaccines. The speaker questions how a monkey virus from 1951-1959 appears in COVID vaccines 75 years later, and claims Pfizer tried to remove it. The speaker believes the official story is that "they wanted to kill people." In 2021, the speaker discussed in a Clubhouse Bitcoin room a documentary with Robert Malone and Robert McCullough, focusing on two Pfizer patents. The speaker suspected in 2020 that SV40 would be used in a jab, most likely Pfizer's, and advised people not to take the Pfizer jab.

The speaker discusses the issue of DNA contamination in mRNA COVID-19 vaccines and questions the FDA's handling of the situation. They explain that normally rigorous tests are required to ensure safety, but in this case, the FDA ignored those tests. The speaker also mentions that Moderna's own patent acknowledges concerns about DNA and insertional immunogenesis. They reveal that DNA fragments, including an antibiotic resistance gene and sequences from simian virus 40, were found in the vaccines. The speaker expresses shock at the FDA's lack of transparency and highlights the potential risks associated with DNA damage, such as cancer and birth defects.

I recently heard stories of people losing their children to Pfizer injections, some experiencing immediate or gruesome deaths. The FDA knew about potential risks like cancer from as far back as 2013, but suddenly in 2020, these concerns were ignored. This seems like a premeditated crime, with regulators aware of the dangers. Military involvement in pushing these products is suspicious.

In 1951, with FDR’s polio story in the background, Jonas Salk develops a polio vaccine and distributes it to four pharmaceutical companies, notably Cutter Pharmaceuticals. Cutter is highlighted as central to the tale, though the lesson is not taught to doctors. The vaccine’s growth is difficult, so Salk proposes using a primate culture near humans, specifically African green monkey kidney cells, to produce the vaccine. The first test subject for Salk’s vaccine is Dr. Ochsner of the Ochsner Medical Foundation in New Orleans, a renowned surgeon and former head of Tulane’s medical school. Ochsner, who had a storied career and a controversial reputation in New Orleans medical circles, brings the vaccine into the surgical amphitheater in 1951, where he injects his grandson and granddaughter. The grandson dies within seven days of polio; the granddaughter develops polio in her leg but does not die. The narrator notes that younger doctors in New Orleans are not taught this story, as Ochsner had died earlier but his son lived, and the narrator later trained at Ochsner Medical Foundation. The narrator recounts being in New Orleans during JFK’s era, with Oliver Stone filming in the basement of Charity Hospital, and the narrator meeting Virginia Garrison (daughter of Jim Garrison, the DA who prosecuted Clay Shaw in the JFK case). Virginia warns the narrator about Alton Ochsner, suggesting he was a nefarious figure, contrasting public perception with the stories she knew from her father’s dealings. Ochsner allegedly advocates slowing the vaccine development and recommends transferring the science to a doctor at the NIH, Bernice Eddy. Eddy investigates from 1951 to 1953/1954 and discovers that all of Salk’s original polio vaccines were tainted with SV40 (Simian Virus 40), no one knowing this because DNA had not yet been discovered. Eddy tells the NIH and FDA about the contamination, but the industrial–military complex reportedly pushes forward, distributing the vaccine to about 300 million people and contributing to a cancer epidemic. Eddy reportedly faced cancellation for revealing these findings, including a 1955 New York Academy of Sciences talk where she disclosed SV40 contamination. As a result, Eddy’s lab is defunded and she is marginalized, and historians note there is little trace of the Cutter incident on FDA/NIH sites from 1951–1957. The narrator later digs through medical school archives and talks with Ochsner’s son, a cardiothoracic surgeon, to learn more. In a later exchange with JO (Ochsner’s son), the narrator learns more about the family’s involvement, ultimately culminating in a question about why a nuclear device exists in the basement of a community hospital.

The speaker, a quality auditor at Pfizer, shares their concerns about the company's COVID-19 vaccine. They discovered that the vaccine vials were glowing and raised the issue with corporate, but received an unsatisfactory response. They also found documents in the company's database that mentioned the use of aborted fetal cell lines in the vaccine's development and the possibility of graphene oxide being present. The speaker noticed unusual security measures and a lack of proper quality control procedures. They also stumbled upon documents referencing depopulation and Satanism. Additionally, they discovered a Pfizer research and development lab in Wuhan with the address 666. The speaker believes that Pfizer, along with other organizations like the FDA and CDC, are aware of these issues. They express their distrust in vaccines and pharmaceutical companies in general.

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 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.

The speakers discuss the vaccination landscape around human papillomavirus (HPV) vaccines, focusing on a controversial issue they claim has been known and disseminated since early on: contamination with DNA (DNA residuals) from Deinococcus or related genetic material in vaccines and the implications of aluminum adjuvants used in Gardasil/Gardasil 9. - They begin by asserting that HPV vaccines, including Gardasil/Sil, have been the subject of remarkable legal actions worldwide, including four major lawsuits in Japan. They note that historically, in Japan, many young women and girls stood as plaintiffs, and that the core problem they highlight is the DNA contamination issue (referred to as “ディー エ ヌ エー 混 入 汚 染 問 題”). - The claim is that from early on, the Japanese Ministry of Health, Labour and Welfare and others acknowledged this contamination as central. They reference a 2012 paper that reportedly made the DNA contamination problem very clear, naming pathogens such as Human Papillomavirus, HPV, and DEIN? They describe that vaccine particles (HBV? HPBL DNA fragments) were found to be directly bound to aluminum adjuvant particles in Gardasil, implying a mechanism by which residual DNA could be involved in adverse effects. - The speakers say that the 2012 study, and subsequent work, led to attention from doctors worldwide who listened to the voices of women and girls and wondered what was happening with the vaccine recipients. They claim that samples showed that residual HPV DNA fragments were consistently present and directly linked to aluminum adjuvant particles, and that “PCR” detection indicated the same DNA sequences across samples. They mention that the 2012 paper’s findings were followed by reporting that, by 2014, vaccination had been suspended in Japan earlier than many would have expected. - They recount a process in which major scientists from various countries (France, the UK, and others) were involved in investigating adenoviral or genetic components (they reference Shihan? and others) and that the Japan-based researchers, including Ishii Ken, were central figures. They describe meetings, PowerPoint presentations at a hotel, and a sequence of visits to the UK and the US (including HR-related planning with U.S. FDA and the UK authorities) that were interrupted by closures in the Obama era, leading to documentation and discussions about the safety concerns. - The speakers claim that by the 2012 report and again by 2014, all vaccine samples from multiple countries contained residual DNA, and that Japan became a hub for disseminating awareness of these issues globally. They state that the issue was present not only in the early Gardasil (Gardasil-4) but also in later forms, with references to Gardasil-9 and the idea that the DNA contamination and adjuvant interactions could contribute to immune and neurological symptoms in recipients, particularly in women and girls. - They discuss changes to WHO and FDA guidelines on residual DNA limits, noting a progression from 10 picograms to higher thresholds over time, implying corporate interests in allowing higher residual DNA quantities in vaccines. They emphasize that the shift in limits is tied to pharmaceutical companies’ needs, not human biology changes, and argue that Japan highlighted the problem of Deinance-DNA contamination during the cervical cancer vaccine era, signaling that researchers, journalists, and victims were aware long before others. - Finally, Speaker 1 adds that two points became clear a year earlier: the disruption of messenger RNA–type vaccines as a response to safety concerns, and the subsequent rise in adverse outcomes after widespread vaccination, including deaths, which they claim intensified opposition to these vaccines. Note: The summary presents the speakers' claims and sequencing of events as described in the transcript without evaluation or endorsement.

Former vice president of Pfizer, Speaker 1, shares his insights on the events of early 2020. He noticed discrepancies in statements made by colleagues, including Sir Patrick Valens, which led him to question the narrative. The simultaneous global lockdowns convinced him that this was a coordinated effort beyond the local level. Speaker 1 accuses these individuals of lying and challenges them to sue him, confident in his claims. He expresses concern over the injuries caused by the vaccines, stating that they were intentionally designed to harm and kill people.

The speaker discusses the issue of DNA contamination in mRNA COVID-19 vaccines and questions the FDA's handling of the situation. They explain that normally rigorous tests are required for genotoxicity and immunogenesis, but the FDA seemed to ignore these requirements. The speaker also mentions that Moderna's own patent acknowledges the concerns related to DNA and insertional immunogenesis. They reveal that DNA fragments, including an antibiotic resistance gene and sequences from simian virus 40, were found in the vaccines. The speaker expresses concern about the potential risks associated with DNA damage, such as cancer and birth defects. They criticize the FDA for downplaying the issue and emphasize the importance of transparency.

Speaker 1 expresses concern about the presence of SV40 sequences in vaccines, suggesting it is not accidental and could lead to cancer due to insertional mutagenesis. They argue that gene therapies were delayed due to the risk of cancer from insertional mutagenesis. The speaker believes that alternative treatments like hydroxychloroquine and ivermectin are safe and questions why the FDA redacted data on endotoxin levels for 75 years. They emphasize the unusual nature of the current situation and urge the protection of citizens by not administering experimental products to pregnant women and babies. The speaker pleads for one state to take a stand and set an example for others. No questions are asked.