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The speaker discusses a WHO meeting in December 2019 where vaccine safety was questioned. It was revealed that there is no scientific proof that vaccines are safe and effective when used together. This realization exposed a 100-year bluff, leaving many concerned about the lack of evidence for vaccine safety. The cost and affordability of vaccines were also highlighted as a significant issue for families.

The speaker, a former pharmaceutical sales rep, shares their disillusionment with the industry after discovering corruption and falsified safety data. They recount their experience with vaccines and their concerns about the lack of rigorous safety studies and the toxic additives, such as aluminum, in childhood vaccines. The speaker highlights the high rates of illness in American children compared to other developed countries and attributes it to the profit-driven nature of the pharmaceutical industry. They discuss the influence of pharmaceutical companies on the media and the lack of liability for vaccine manufacturers. The speaker emphasizes the need for more research and information before mandating vaccines, citing the potential risks involved.

The speaker believes cooperation with companies developing vaccine technology should be outlawed due to "nefarious intent" and financial incentives. They claim the pharmaceutical industry profits from vaccine-induced adverse outcomes, leading to costly medical treatments and prescriptions. Vaccines are described as an "economic loss leader" for the medical-industrial complex. Healthy, unvaccinated children don't generate revenue, while vaccines can lead to health issues like asthma, allergies, ADD/ADHD, diabetes, and cancer. The speaker compares vaccines to a free gift that lures people into purchasing more expensive products or services. They argue that "free" vaccines can cost individuals their health, citing potential side effects like Guillain-Barré syndrome, transverse myelitis, encephalitis, and neurological issues, as well as turbo cancers, respiratory problems, and myocarditis. A forthcoming study will allegedly reveal a significant number of deaths from chronic renal disease linked to vaccines. The speaker concludes that the pharmaceutical industry fiercely defends the vaccine schedule because it drives their profits, especially with the advent of mRNA technology.

According to the speaker, most vaccines have never been tested in a randomized, placebo-controlled trial to evaluate their safety. The speaker claims that vaccines contain aluminum compounds because many dead vaccines don't mount an immune response without them. The speaker alleges that in a Gardasil vaccine study, the placebo group received an aluminum adjuvant instead of a true placebo, resulting in similar side effect profiles between the active vaccine and placebo groups. The speaker asserts that Merck used a novel aluminum compound and that data suggests aluminum in vaccines is profoundly toxic. The speaker states that the only true randomized controlled trial involving a vaccine was conducted on sheep with blue tongue disease. The results allegedly showed that the aluminum in the vaccine was toxic, causing the sheep to become sick, unsociable, and, in some cases, die. The speaker concludes that the assumption that aluminum adjuvants in vaccines are safe is unfounded and has never been tested.

Speaker 0 frames the issue as 'the corruption of science' and the 'capture of the agencies' by pharmaceutical industries, stating the goal is to restore integrity and credibility to science. Speaker 1 cites a CDC internal study: 'black boys who got the vaccine on time had a two hundred and sixty percent greater chance of getting an autism diagnosis than children who waited.' He adds that 'The chief chief scientist on that, Doctor. William Thompson, the senior said vaccine safety science at CDC, was ordered to destroy that data. And then they published it without that fact.' Finally, he asserts, 'So, you know that story. And you know of hundreds of stories like that. It happens all the time. We are being lied to by these agencies, and we're gonna change that right now.'

The discussion centers on the credibility of vaccine safety claims made by various health organizations and the FDA. One speaker argues that vaccines undergo rigorous testing, while the other contends that no vaccine has ever completed a long-term placebo-controlled trial before being licensed. They express distrust in the FDA, citing past issues with drugs like Vioxx and opioids, suggesting that the FDA misled doctors and the public about their safety. The speaker believes that pharmaceutical companies influence these agencies, leading to misinformation about vaccine safety. The goal is to address and rectify this perceived corruption.

A lawsuit against Merck alleges mishandling of Gardasil safety tests. Internal emails reveal Merck knew the vaccine was contaminated with HPV DNA fragments, which can trigger harmful immune responses when bound to the vaccine's aluminum adjuvant. Pathologist Dr. Soo Han Lee discovered high levels of HPV DNA in vaccines in 2011. These DNA fragments can activate the immune system, potentially leading to autoimmune disorders like POTS, and in rare cases, death. Internal emails allegedly show Merck downplayed the risks and tried to convince regulators not to test for HPV DNA. Merck's chief medical officer admitted they never looked for HPV DNA in their vaccine, instead using flawed testing methods. The lawsuit raises questions about regulatory oversight and Dr. Lee is set to testify in February. The speaker advocates for transparency, thorough safety studies, and informed consent regarding vaccines.

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 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.

- In order to make a vaccine, so you first have to extract disease from an animal or a human. - Because you can't just inject live measles into a person. - You first have to do what they call attenuating it, which is to make it less virulent. - There's a myriad of monkey kidney cells that are still used today, they've been used for a very long time. - There have been monkey viruses that were finally, after thirty years, acknowledged to have been causing tumors in human beings, been associated, heavily associated with tumors in human beings. - In addition to that, there are various unknowns that can't be picked up during testing because if you don't know something is in a vaccine, you can't test for it. - Viruses, stray viruses have been found by third parties in vaccines.

The speaker states that they believed Pfizer had two legal definitions for their jab for nefarious reasons, suspecting one would be used for FDA approval while the other, containing SV40, would be released to the public. This suspicion stems from the 1950s polio vaccine contamination with SV40. The speaker recounts how Dr. Ochsner tested the polio vaccine on his grandchildren, resulting in one death and one case of polio. Ochsner then alerted the "industrial military complex" to the problem. Dr. Bernice Eddy at the NIH discovered SV40 contamination in the polio vaccines but was silenced after revealing it. The speaker distrusted the COVID response due to this history and suspected Pfizer's use of the SV40 promoter. Kevin McKernan later tested expired vials and found SV40, suggesting a deliberate scheme to harm people who received the jab.

A speaker played a recording of a conversation where another person recalled a discussion about removing aluminum from vaccines. According to the speaker, vaccine companies were once very close to removing aluminum. The speaker claims that all the big vaccine companies were at the same table because they had the same interest to defend. The speaker suggests that banning aluminum would deeply trouble vaccine companies, completely changing manufacturing, clinical studies, and everything else. The speaker recalls that the companies argued that removing aluminum would cause a tremendous deficiency in vaccine supply, leading to the deaths of children in Africa. The speaker states that the WHO was also very much involved.

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.

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.

The speaker states they searched for years for a pre-licensing safety trial of the 72 vaccine doses effectively mandated for American children. They claim that every other medication requires a safety trial comparing health outcomes in a placebo group versus a vaccine group before FDA licensing. The speaker assumed this was also done for vaccines. They state they found out that vaccines were exempt from this requirement.

The speaker questions the safety of Thimerosal, a mercury-based preservative in vaccines, asserting it hasn't been adequately tested since 1929 when Lilly tested it on 27 meningitis patients, all of whom died. Despite this, the speaker claims Thimerosal has been used since the 1930s. The speaker challenges the witness to definitively state that the amount of mercury injected into babies is harmless. The witness admits it's impossible to make such a categorical statement with 100% certainty. The speaker then asks if it's possible that even trace amounts of mercury could neurologically damage a child. The witness says they don't think it has that capacity, but concedes they don't have evidence for every child and dose. The speaker expresses frustration at the difficulty in addressing the issue.

There is a discussion about how public trust in vaccination has changed since the pandemic. The speaker notes that years ago there were “five people in the world who were prepared to talk about the thorny issue of vaccination.” Post COVID, however, “half the adult population of the world are now saying, hold on, we don't trust you. You lied to us. It's not what you told us, safe and effective.” This skepticism extends to vaccines given to children, with the question, “Does this apply to all the other vaccines you're putting into my kids?” The speaker then asserts that “safety studies haven't been done,” suggesting that important research behind vaccines is incomplete or lacking. This leads to the claim that “they've created this mess for themselves.” Despite the frustration, the speaker emphasizes the moral weight of deception, stating, “it's really tough to lie. I mean, lying gets you into real trouble.”

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.

According to the speaker, vaccines have never been tested in a randomized, placebo-controlled trial to evaluate their safety. The speaker claims that vaccines contain aluminum compounds because many dead vaccines don't mount an immune response without them. The speaker alleges that in a Gardasil vaccine study, the placebo group received an aluminum adjuvant instead of a true placebo, so the side effect profiles of the active vaccine and placebo groups were the same. The speaker asserts that Merck used a novel aluminum compound and that data shows aluminum in vaccines is toxic. The speaker states that the only completely randomized controlled trial was on sheep using a vaccine for blue tongue disease. The speaker claims the aluminum was toxic, the sheep became sick, their behavior changed, and many died compared to the placebo group. The speaker concludes that the presumption that aluminum as an adjuvant is safe is unfounded and has never been tested.

Speaker 1 states that no vaccines, including the COVID vaccine, have been properly tested. They claim that no childhood vaccine has undergone a placebo-controlled clinical trial of sufficient duration and power to assess its safety before being injected into millions of children in America. Speaker 1 asserts this is not an opinion, but can be verified by anyone reviewing package inserts and clinical trial documents on the FDA website.

Billions of people have received contaminated products, which should not have happened. If meat at the grocery store is found to have toxins, it is immediately recalled. However, vaccines with known contamination are being administered to billions of people worldwide. This was revealed through our reporting. It is concerning that these contaminated products are still available in the consumer marketplace. When a crib causes the death of two children or a tire leads to multiple accidents, they are taken off the market. Yet, intentionally adulterated vaccines with undisclosed gene sequences are still being sold.

The speaker is questioned about his stance on childhood vaccines, with many scientific and medical organizations disagreeing with him. The audience asks how they can help him align with science. The speaker clarifies that he is not anti-vaccine, but believes vaccines should undergo safety testing like other medicines. He criticizes the lack of prelicensing placebo-controlled trials for vaccines and cites examples of potential risks and lack of long-term studies. The other speaker argues that there is evidence of vaccines preventing diseases and highlights the importance of distinguishing between association and causation. The speaker emphasizes the need for good science and questions the trustworthiness of pharmaceutical companies. The conversation ends with a discussion about the speaker's family not supporting his views on vaccines.

Speaker 0 questions Speaker 1 about the lack of clinical trial data for the MMR vaccine. Speaker 1 insists that the vaccine was extensively tested before being licensed and that millions of doses have been used. Speaker 0 asks for proof of pre-licensure clinical trials, but Speaker 1 only refers to a book and mentions studies done in the 1960s. Speaker 0 argues that the data provided is not sufficient and questions the absence of a placebo group. Speaker 1 admits uncertainty about the inclusion of control groups but maintains that safety assessments were conducted. Speaker 0 concludes that no randomized placebo-controlled study exists for the MMR vaccine. Speaker 1 agrees to provide additional information after the deposition.

The speaker believes COVID vaccine programs should be stopped. They are astounded by the number of papers critical of the vaccine or showing negative effects. The speaker claims a group of researchers funded by Pfizer and the NIH bullies editors to retract papers with negative findings about the vaccine. They assert the number of retractions is appalling. According to the speaker, in one instance where an editor resisted, Nature Springer bought the journal and retracted the paper. The speaker states that this is what they have been dealing with.