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"Just laid out the facts and that, hey, we don't the the fact is that this vaccine does not apply to eighty percent of the people." "But if you know the status, then you don't need to get that vaccine." "But that's, like, eighty percent of the people, so that's a lot less revenue." "Merck was like, we're not really making a lot of money." "We will put this or not Congress, but the FDA was like, oh, we're gonna put this on the childhood schedule so then it more could" "get the World Health Organization," "so it went global." "Would you rather create a drug that's only used when you get sick and you need it?" "Or one for everybody to quote unquote prevent that sickness?" "Therapy is gonna apply to what? One percent, half a percent of people." "Now you have 90% of the people."

The speaker discusses the use of mRNA in food and mentions a presentation about genetically engineering mosquitoes to deliver vaccines through mosquito bites. They mention that the Gates Foundation is funding this research, although they don't have proof of its viability. The speaker clarifies that they are not suggesting that the mosquitoes are currently injecting anyone with anything, but they have evidence that efforts are being made to enable mosquito injections.

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.

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.

The White House blames a few bad actors for spreading online misinformation that is causing harm. It is important to get vaccinated not only for personal protection but also to safeguard society. A member of the European Parliament from the Netherlands recently had a viral exchange with a Pfizer executive regarding whether the vaccine was tested for stopping virus transmission before being released. The executive clarified that the vaccines were extensively tested in clinical trials, but their specific effectiveness in stopping transmission was not known prior to market entry.

A year ago, the speaker requested data from Emma, including all clinical trials done by medical companies before they requested marketing authorization for the green certificate. Regarding Pfizer, the speaker notes the company submitted a clinical trial that started on January 14, 2020. The speaker questioned a Pfizer representative about how tests for the vaccine began so soon after the December 2019 emergence of COVID-19, but the representative declined to answer. The speaker also asked the CEO of Moderna how they submitted trials since 2017, years before the virus was discovered in the winter of 2019. The speaker states that the CEO of Moderna did not answer how this was possible. The speaker says these are legitimate questions that people are asking, but unfortunately, the companies are declining to answer.

The speaker claims that in Pfizer's initial vaccine trial with 20,000 vaccinated and 20,000 unvaccinated participants, the vaccinated group had 23% more deaths from all causes than the placebo group after six months. The speaker states that the claim of 100% vaccine efficacy was based on the fact that two people in the placebo group died from COVID versus one person in the vaccine group. The speaker asserts that people believed the vaccine would prevent them from getting COVID, which they now realize is false.

The speaker states that mRNA in food is a critical issue, but also highlights the potential for transgenic mosquitoes to deliver vaccines via saliva. They reference a presentation about producing a transgenic mosquito as a "flying syringe" to deliver protective vaccines. The speaker claims the Gates Foundation is funding genetic engineering of mosquitoes with the intention of using mosquito bites for vaccination. While they don't have definitive proof of its viability, they assert that this research is underway. The speaker clarifies they are not claiming current mosquitoes are injecting people with anything. However, they state they have indisputable evidence that efforts are being made to enable mosquitoes to inject people with substances in the future.

Pfizer conducted trials using a synthetic PCR process called Process 1, which involved giving 40,000 people a precise mRNA sequence for the shots. However, for mass production, a second process was used, tested on only 252 people. This involved using a complementary DNA sequence to make the body produce the spike protein. Essentially, the trials were done using a controlled synthetic process, but the majority of the vaccines given to billions of people were made using a less tested method. This can be seen as a bait and switch.

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 0 describes the plasma-derived hepatitis B vaccine as derived from “the most dangerous starting material” and asserts the starting material was blood heavily contaminated with HIV, collected from New York heroin users during what is recognized as the world’s first AIDS outbreak. He notes the vaccine’s development began with funds from Doctor Fauci’s agency, in collaboration with Tuskegee researchers, to cross-connect arteries of tranquillised chimpanzees and comatose humans, with mixed raw blood flowing between groups of chimps and humans to train the chimps’ immune systems on human hepatitis virus. The vaccine inventors warned it might work the other way as well and claims several chimpanzees tested positive for ancestors to HIV and Kaposi’s sarcoma herpes virus, the deadly combination behind AIDS; this serial passage between species is called gain of function. He concludes this created the safest vaccine we’ve ever used. Speaker 1 adds a claim about a hidden starting point: the blood used was heavily contaminated with HIV from New York heroin users, and that the vaccine’s development involved financing from Fauci’s agency and collaboration with Tuskegee researchers to cross-link chimpanzee and human circulatory systems. He states that the serial passage of viruses between species is now called gain of function and asserts this process produced HIV and Kaposi’s sarcoma herpes virus, and suggests the vaccine’s safety is paradoxical given these origins. Speaker 2 emphasizes responsibility and risk, noting AIDS’ cause was unknown at the time but fear centered on potential contamination of the vaccine with whatever caused AIDS. HIV was “sort of hanging over this vaccine like a cloud,” though he claims HIV couldn’t survive the treatments given to the vaccine. Speaker 0 transitions to Part II, a deep dive into the vaccine timeline, aiming to quickly reach the AIDS timeline ramifications. Speaker 3 provides a timeline framework: well-documented events through May 1983 to set the stage for two fiercely contested events now resolved by a federal investigation. Speaker 2 lists milestones: - 1950s: The world’s earliest confirmed HIV-positive being is a chimpanzee used to develop hepatitis B vaccines. - 1960s: Chimpanzees and New York heroin users cross-transfuse raw blood to generate chimpanzee antigens to fight human hepatitis. - 1972: Scientists at Doctor Fauci’s agency announce chimpanzee antigens protect humans from hepatitis B; first patent filed for a human vaccine made from chimpanzee antigens. - 1973: The world’s first recognized AIDS outbreak occurs among New York heroin users, the first group injected with chimpanzee plasma. - 1974: Thirteen thousand New York gay men recruited to test the vaccines. - 1975: NYBC and Merck file three patents, citing five vaccine examples all made from pure chimpanzee antigens; a circular extraction method akin to dialysis to extract large amounts of antigens for mass production. - 1978: After years of testing, nationwide placebo-controlled trials begin on gay men with NYBC’s New York trial and CDC trials mainly in California; first HIV-positive blood samples found in gay men, all collected from the cohort, all of the never-before-seen subtype B. - 1979: September—ten months into the trial—the scientist in charge wants to abort due to an unexplainable flare-up in precisely 11 participants who received the vaccine; aborting would harm the vaccine’s reputation. CDC soon reports unexplainable Kaposi’s sarcoma cases in gay men, noting that precisely eleven had the flare-up as of September 1979; by December, 19 cases and the first death, marking the onset of the world's second AIDS outbreak affecting the second group inoculated with chimpanzee plasma-derived vaccines. - 1981: A cancer researcher suggests a new infectious agent with a 50% mortality rate may be causing Kaposi’s sarcoma cases in vaccine trial sites and claims it was transmitted in the vaccine as disease progression occurred quickly in trial participants; trial scientists confirm incubation periods differ and are longer in gay men not in the trial. In the next 15 months, another 593 cases emerge and 41% die. Merck announces Heptavax B, a third US brand for domestic market; original HBVax and NYBC B Vax offered only overseas; a compromise to get FDA approval makes the new version from human blood, but without the circular chimpanzee extraction method it’s “too expensive” for large-scale use. - 1982: CDC names the disease AIDS; CDC asserts the FDA-approved vaccine uses only human blood, distancing it from earlier vaccines; WHO warns AIDS may be caused by a virus in the vaccine’s plasma. - May 1983: French scientists identify the causal virus, enabling testing of archived blood samples; it was a chimpanzee virus, and KS lesions required co-infection with a second virus found in those chimpanzees. This discovery enables verifying the AIDS origin theory: vaccine transmission by comparing HIV rates between men randomly given the hepatitis B vaccine versus a placebo during the trials. Speaker 3 notes two pivotal events in their chimp vax preprint, now settled, and states that in June 1983 two Fauci-associated scientists claimed infection rates in the New York trial were similar between vaccine and placebo; internally, they say Fauci’s scientists spread disinformation to defend the chimpanzee vaccine invention. Speaker 2 contends that the CDC claimed no difference in rates in 1984 but that the private study remains unreleased; the analysis implies nearly all HIV infections occurred in vaccinated participants, not placebo, based on limited data and interpretation. The narrative argues the CDC private study would have shown high HIV rates among the vaccine group, but details were obscured. It alleges the CDC’s withheld study used skewed comparisons to mask vaccine-associated HIV transmission. Speaker 3 briefly references Africa’s rollout in 1984, claiming AIDS emerged there a year after a symposium and that FDA officials shifted from chimpanzee vaccines to the human-blood Heptavax, enabling continued overseas sales. It asserts chimpanzee-based vaccines were widely used in poor countries by 1986, with Africa’s initial infections concentrated in newborns and young women; the WHO suppressed findings that HIV spread via medical injections, not needles alone, to protect immunization programs. Retroactive testing allegedly shows HIV was not present in most African countries before vaccination; after vaccination began, infection rates rose in certain regions. The speaker notes a group, ChimpFacts, as a best account of probable HIV origins, but mainstream preprint servers rejected it.

For Pfizer's trials, a synthetic PCR-type process was used to create the mRNA sequence for the shots, administered to 40,000 people. This was called process one. To manufacture the shots for billions, a second process was implemented, tested on only 252 people. This involved using a complementary DNA sequence to make mRNA, which would then cause the body to produce the spike protein. The speaker claims the trials used a controlled synthetic process, but the actual rollout employed a barely tested method. The speaker characterizes this as a bait and switch.

A recent study suggests that Pfizer may have excluded known deaths in the vaccine arm of its clinical trial from its data filing with the FDA in 2020. The study also found that trial subjects vaccinated with Pfizer's COVID-19 vaccine experienced a significant increase in cardiovascular deaths compared to placebo controls. This information was not disclosed by Pfizer when the FDA was evaluating the vaccine for emergency use. Additionally, researchers identified instances where Pfizer attributed potential vaccine-associated deaths to other causes, undermining vaccine safety data. The data presented to the FDA prior to the authorization of Pfizer's vaccine did not include all the deaths that occurred during the trial. The speaker raises concerns about the prioritization of profit over lives and warns against trusting Big Pharma.

For Pfizer's trials, a synthetic PCR-type process was used to create the mRNA sequence for the shots, administered to 40,000 people. This was called process one. To manufacture the shots for billions, a second process was implemented, tested on only 252 people. This involved using a complementary DNA sequence to produce mRNA, prompting the body to create the spike protein. The claim is that the initial trials used a controlled synthetic process, but mass production shifted to a barely tested method. This second process was then administered to billions of people. It is described as a bait and switch.

The Pfizer COVID vaccine was not tested for its ability to stop the transmission of the virus before it entered the market. The speaker acknowledges that they had to work quickly to understand the situation and move at the speed of science.

Speaker 0 describes finding vaccine insert materials with no printed content and says this is disheartening and “disgusting,” then adds that it “gets better” and that “more” continues to happen. Speaker 0 claims the CDC redacted every word of a 148-page study on myocarditis after COVID vaccination, and that when they asked to have the study printed, the entire document was redacted. They question what the study could have contained that required redaction and say this is “even scarier.” Speaker 1 says they are witnessing “an active cover up” of a “colossal consumer product safety debacle” affecting the entire world. They claim that in the United States the CDC, National Institutes of Health, and FDA are actively involved, and that similar actions occur in the UK with the MHRA, in Europe with European medicine agencies, and in Australia with the Therapeutic Goods Administration. Speaker 1 states that each of these regulators requires product companies to produce ninety days of safety monitoring after a product comes out, describing this as a regulatory dossier. They say that if problems arise and are reported to a company (such as Pfizer), the company must report, compile, and produce a report that is made publicly available. Speaker 1 claims that for Pfizer, whose first vaccine was approved 12/10/2020, Pfizer did not produce a report after the ninety days. They add that when people asked what was happening, Pfizer allegedly did not disclose what occurred, leading to court proceedings. Speaker 1 states that the FDA’s lawyer allegedly said the dossier should not be released for fifty-five years, and that after pressure, the Pfizer dossier was eventually released. They then claim Pfizer recorded 1,223 deaths with their product within ninety days of release and recorded over 1,200 new adverse events. Speaker 1 also says the FDA worked to cover this up, and that FDA should have regulated Pfizer with at least monthly meetings and full disclosure about “novel vaccines,” which they describe as a “genetic transfer technology platform,” the first time human beings had been injected with foreign genetic material in world history. Speaker 1 ends by stating that two thirds of the world’s population took these.

The transcript presents a wide-ranging, critical portrait of Bill Gates, intertwining biographical claims with controversial allegations about Microsoft and the Gates Foundation, as well as broader conspiracy-like scenarios. Key biographical and career points: - The narrative asserts Gates did not rise from a garage origin but was born into wealth and privilege; both his grandfather and great-grandfather were banking moguls, and his father, William Gates Sr., was a Seattle-based lawyer and political lobbyist who taught him about law, politics, and manipulation of governing power. - Gates is introduced as chairman of Microsoft. He dropped out of college to start Microsoft and is credited with inventing the Windows operating system, though the transcript states he “played no part in the invention of Windows,” instead purchasing an existing operating system from Seattle Computer Products, having it modified, and licensing it to IBM, while taking credit. - Paul Allen is described as co-founder who, while battling cancer, was targeted by Gates in an attempt to dilute Allen’s share of the company. - Gates’s business strategies are said to have been challenged by a 1998 U.S. Department of Justice antitrust lawsuit against Microsoft; a lengthy deposition is summarized with questions about non-Microsoft browsers and Gates’s responses. - A deposition clip emphasizes tensions over Gates’s concerns about competition. Philanthropy and public image: - To counter negative press, Gates invested $100 million to establish the Bill and Melinda Gates Foundation, allegedly transforming his image from monopolistic tycoon to generous philanthropist; the rebranding allegedly led to Gates being crowned the richest man in the world as his net worth doubled. - The Foundation is described as a massive vertically integrated entity spanning a supply chain from Seattle to Africa and Asia; Gates is depicted as a top donor to WHO and the CDC, wielding immense influence over global health and medical policy. - The Foundation’s vaccine initiatives are highlighted: Gates allegedly invested billions in vaccines, with a Wall Street Journal essay claiming vaccines are “the best investment I’ve ever made” and noting a reported over 20-to-1 return on investment. Controversies and criticisms: - The Foundation is accused of causing harm through “experimental vaccine programs,” with claims that it has investments in numerous polluting companies and that some portfolio companies have been accused of evictions, child labor, patient neglect, or fraud; details are not provided. - Specific vaccine-related controversies include controversial HPV vaccination campaigns in India (2009), where tribal girls purportedly received vaccines without proper informed consent, resulting in injuries and deaths; Parliament and authorities allegedly investigated and removed the Gates Foundation from involvement. - Allegations are raised about the ethics and safety of vaccines, including claims of paralysis from the oral polio vaccine and criticism of media and political manipulation surrounding vaccination campaigns. - The transcript mentions a broader pattern of distrust: “the Gates Foundation denied that it had been clinical trials,” and it describes media manipulation and political power associated with vaccination campaigns. Other asserted initiatives and associations: - Alleged participation in controversial projects such as the Stratospheric Controlled Perturbation Experiment (to block sunlight) and Earth Now’s global surveillance program; claims of a vaccine certificate system with MIT to implant quantum dot tattoos for digital immunity proof. - The EPA’s approval of an Oxitec project to release genetically modified mosquitoes to combat malaria is mentioned, with NIH noting plans for immunization via mosquito bites. - The transcript also references a New York Times report about Gates’s connections to Jeffrey Epstein, including meetings and flights on Epstein’s plane, and a debate over why a charitable trust would partner with Epstein. Overall, the transcript compiles a narrative that casts Gates as dual: a powerful, influential benefactor and a controversial figure implicated in ethical, health, and geopolitical criticisms, culminating in questions about his motives and the breadth of his influence.

In 02/2015, Bill Gates stated the world population needs to be reduced by 10 to 15% due to global warming, and this would be achieved through vaccines. In 02/2020, Gates said 7 billion people must be vaccinated. The speaker then poses the question of why they should take a vaccine for their health that is financed and produced by someone who wants to decrease the world population.

Excitement surrounds the discussion of Pfizer's top-selling drugs as of 2019, which includes four medications and one vaccine. The clinical trials for these drugs involved long-term safety follow-ups, often lasting several years with placebo control groups to assess various health impacts. In contrast, the vaccine Prevnar had only a six-month safety review, using another vaccine as a control rather than a true placebo. This raises concerns about the thoroughness of safety evaluations for childhood vaccines, which are administered multiple times in the first six months of life. The disparity in study lengths suggests that economic interests may drive pharmaceutical companies to minimize safety testing to expedite market entry, raising questions about regulatory oversight.

Pfizer's claim of 96% efficacy for their vaccine was questioned. The study and data were not independently verified, and Pfizer wanted to keep the data hidden for 75 years. The true effectiveness of the vaccine, based on absolute risk reduction, is less than 1%. More people died and were harmed in their trials compared to the placebo group. The vaccine's safety was questionable from the start, and it is not effective. Additionally, appropriate studies were not conducted for new variants.

Speaker 0 says: Today’s discussion covers the Lyme situation and claims about vaccines. The claim is that you were injected with gelatin as a child through vaccines, which made you allergic to ticks. Ticks are said to not cause disease, just to be aware. A PubMed article is cited about the association between tick bites, allergic reactions, and gelatin-containing vaccines causing the allergic reaction. Some people insist they didn’t get vaccines with gelatin, but Speaker 0 argues childhood vaccines actually contain it. Speaker 0 claims that the vaccine intended to save you is new, yet there was a past version that resulted in many lawsuits, implying a repeated pattern. The discussion then shifts to Lyme disease: if someone has Lyme, they allegedly had a PCR test that amplified the results to tell them they had an illness to sell a treatment and induce fear of ticks. Speaker 0 lists symptoms claimed to be Lyme disease: fevers, chills, headaches, fatigue, muscle aches, swollen lymph nodes, and facial palsy. These are described as side effects of vaccines as well. Even someone who says they didn’t take any vaccines is asked about exposure to wireless technology at home (microwaving), and pesticide exposure, which are claimed to cause the same symptoms. Speaker 0 references books on related topics: Peanut Allergy Epidemic, Contagion Myth, and The Poison Needle. The overarching claim is that “almost all illnesses result from vaccines, wireless, and pesticides.” Speaker 0 offers a supposed remedy: for any bug bite, use dragon’s blood and coconut oil, saying it heals ticks bites, wasps, spiders, bees quickly. The statement is presented as an example of why people were allergic to peanuts, tying vaccine use to broader allergy development. Speaker 0 concludes by reiterating the pattern: you get vaccinated, you become allergic to ticks; you get vaccinated, you become allergic to peanuts; the same mechanism is claimed to be at play.

The speaker says things become “weird” after learning that Vanderbilt University Centre in the United States has been working on a vaccine for alpha gal syndrome since 2024. They then ask who funds Vanderbilt and state that multiple donors exist, adding that the Bill and Melinda Gates Foundation has been donating to that medical centre since 2012. The speaker links that starting date to what they describe as the period when “tick related meat allergies” began “exploding,” then connects it to a further timeline involving Bill Gates. They claim that in 2013, Bill Gates publicly started promoting synthetic grown lab meats. They further claim that in 2017, he poured almost $20,000,000 into Memphis Meats, and they state that Memphis Meats later rebranded into Upside Foods. The speaker repeatedly frames the narrative around timelines, stating that they are “literally just following timelines, funding, investments, patents, and asking questions.” They also describe the rebranding as emphasizing marketing and branding, stating that they interpret this as helping avoid looking like a “criminal” while being positioned as a “savior,” while continuing to present their points as a timeline comparison. They then assert that, during a period when tick infestations are sweeping the countryside and hundreds of thousands of people are developing alpha gal syndrome, a billionaire is heavily invested in synthetic meat. In parallel, the speaker says the billionaire is also funding a university developing a vaccine for the exact condition that, according to the speaker, pushes people away from red meat. The speaker concludes by describing a sequence they call “first create the problem, then create the solution, then create the vaccine to save everyone from the problem just to end up looking like the hero.”

A year ago, the speaker requested data from Emma, including clinical trials from medical companies before they sought marketing authorization for their products. Regarding Pfizer, the speaker notes that the company submitted a clinical trial that started on January 14, 2020. The speaker questioned a Pfizer representative about how Pfizer started testing a vaccine in January 2020, just days after the Chinese government released DNA data about the virus in December 2019, but the representative declined to answer. The speaker also mentions that Moderna submitted trials dating back to 2017. The speaker asked the CEO of Moderna how it was possible to submit vaccine tests years before the virus was discovered in December 2019. The speaker states that these are legitimate questions that people are asking, but unfortunately, the companies are declining to answer.

The conversation begins with people sending videos about ticks, and then shifts to alpha-gal and vaccines—“the part that’s left out of the message.” The transcript references “one of the epicenters,” stating it is Martha’s Vineyard, where “50% of the adult population is now affected,” described as a “devastating disease.” It claims that “You can’t eat red meat for the rest of your life,” and says, “We are looking at medication.” The next speaker says Martha’s Vineyard is being treated as an epicenter for “red meat allergies,” and then describes Martha “lining up for her 55th booster,” saying, “She’s excited to have received my dosage and look forward to more boosters.” It adds that “She actually held booster clinics at her vineyard,” and notes that someone “would say, well, I never heard about that.” The transcript then asserts that “gelatin in the vaccines causes tick allergies,” describing it as “Interesting, huh?” It then asks which vaccines contain gelatin, answering: “Oh, the ones you got as a kid. MMR, measles, mumps, rubella, chickenpox, yellow fever, rabies for all your animals, and then the flu vaccine.” It claims that “the most common ones contain that.” It further says that “alpha-gal can also cause you to be allergic to beef, pork, lamb, and dairy,” and states, “Wow. It’s almost like there’s an agenda to make you stop eating those foods.” The transcript then claims that on Reddit there are “people who came down with food allergies after they were vaccinated in 2020,” and asks, “Can I see what’s going on?” It then claims that “they built the people up with the bio lab and the Plum Island and the ticks are going to get them,” while also saying that “they’re just vaccinated people and turning them into pin cushions like Martha.” Additional connections are listed: “Peanut oil used in the vaccine, 1964. There’s your peanut allergies, egg allergies from the vaccines, latex, shellfish, also cow allergies, you know, to get people away from milk. That’s another one too.” It also claims, “last but not least Pfizer, the vaccine company owns the EpiPen.” The segment concludes by stating that “it’s all kind of interconnected,” and argues that people “need to look at that rather than the ticks.” It says there is “a great book on it,” and tells viewers to look up “how many vaccines a cow gets before you consume it.”

Speaker 0 says they found “information like this,” such as vaccine insert paper, with “nothing printed on it,” which they call disheartening and disgusting. They add that it “just keeps happening” and claim the CDC redacts “every single word” of a 148-page study on a myocarditis after COVID vaccination. Speaker 0 says they asked someone to print the study, and that the entire 148 pages are redacted. They ask what a study does if “there’s nothing there,” and they ask what might have been there that required redaction. Speaker 1 says they are “witnessing an active cover up” involving “a colossal consumer product safety debacle” affecting the entire world. They claim that in the United States, the CDC, National Institutes of Health, and FDA are actively involved in a cover up, and that similar cover ups are occurring in the UK with the MHRA, in Europe with European medicine agencies, and in Australia with the Therapeutic Goods Administration. Speaker 1 states that each company that puts out a product has an obligation to produce “ninety days of safety monitoring” after the product comes out, describing it as a regulatory dossier. They claim that if someone has a problem and reports it to a company like Pfizer, Pfizer must report, write down what happened, collate it into a report, and make it publicly available. Speaker 1 says that when the ninety days elapsed for Pfizer’s first vaccine approved on 12/10/2020, Pfizer “didn’t produce a report.” They add that people asked what was happening with the vaccine, and Pfizer allegedly would not disclose what happened, leading to a court case. Speaker 1 says the lawyer for the FDA stepped in to say they did not want to release Pfizer’s dossier for fifty-five years. Speaker 1 then says that after the plaintiff pushed, the Pfizer dossier “slowly” came out. They claim Pfizer recorded one thousand two hundred and twenty-three deaths with their product within ninety days of release, and they say people called Pfizer in desperation watching family members die after taking the vaccine. Speaker 1 also claims Pfizer recorded “over twelve hundred” new adverse events and refers to “doctor Boden” discussing problems they say they have been grappling with. They conclude by claiming the FDA worked to cover this up and should have been regulating the company with at least monthly meetings and full disclosure about novel vaccines, described by Speaker 1 as a genetic transfer technology platform and as the first time human beings were injected with foreign genetic material in world history, after which “they were getting it full on.” Speaker 1 ends by saying “Two thirds of the world’s population took”