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Speaker 0 asserts that packaged DNA fragments have been found en masse as vaccine contaminants. Once they reach the nucleus, short DNA sequences have an increased propensity to insert into chromosomal DNA. The possible consequences are unending, including disruption of the exquisitely tuned network that controls cell division and differentiation, which can lead to cancer and developmental defects. Mutations in sperm and fertilized egg cells could render altered traits inheritable. Speaker 0 further states that cost effective procedures to reliably separate mass produced RNA from plasmids do not exist, and therefore contamination of RNA vaccines with plasmid DNA must be expected to be the rule and not the exception. Whoever propagates RNA vaccines as being safe and effective, whoever claims that nothing can happen to your genome is either incredibly ignorant or endlessly evil. That person is turning his back on the horror scenario that is unfolding in front of our very eyes. Fellow citizens and physicians of the world are urged to turn away from the perpetrators of this monstrous crime against humanity. Speaker 0 concludes with admonitions to do this to save yourself, your descendants, and to rescue the name of your family or go down in history as one of the greatest criminals of all time. Speaker 1 responds: Thank you very much, professor Bhakti. You continue to be an inspiration both scientifically and ethically for all of us.

The mRNA in the jab was encapsulated in a lipid nanoparticle designed to cross the blood-brain barrier to deliver drugs to brain cancer patients. This lipid nanoparticle, designed by Acuitas and invested in by Justin Trudeau, had no market from 2011 to 2019 because it killed every lab animal it was tested on. When testing lipid nanoparticles on humans, protocols dictated it could only be administered to individuals with five months or less to live. These patients agreed to the testing, believing they were contributing to the development of a brain-specific drug delivery system. The lipid nanoparticle was never approved for healthy humans due to its toxicity.

it's modified mRNA, and it's designed not to degrade, and there are studies that show it sticks around the body. We don't know how long. The lipid nanoparticle was designed to permeate difficult to permeate barriers, like the blood brain, like placenta barrier. Did you believe when Fauci told us that the mRNA shot would stay in the arm? In rats, it biodistributed all over the body, accumulated in the adrenal glands, in the ovaries. This encapsulated lipid nanoparticle distributes all over the body, and when it attaches to a cell, it unloads its mRNA into the cell and turns the cell into a manufacturing cell of a protein that is toxic to it. They're turning cells like a heart cell into a manufacturing site for the spike protein, which is toxic, the body attacks it. The designers of the injection knew it. And Anthony Fauci knew it, and he lied. DNA contamination ... McKernan study ... 36 to 627 times. The allowed amount is ten nanograms per dose. That saves three point two million lives. No. It didn't. It's impossible. That's entirely possible.

In April 2020, BioNTech and Moderna called mRNA injections experimental gene therapy. Publicly traded pharmaceutical executives admit they deceived the public by labeling them as vaccines to increase acceptance. They suggest these injections turn people into bioweapons factories and could lead to addiction to gene editing technologies. Pseudouridine, a cancer promoter, was added to shots, potentially increasing cancer risk by 400%. The pharmaceutical industry may have a financial interest in promoting these injections. This could make people customers of an industry with a history of harming citizens since 1604.

They didn't see safety signals because they didn't want to see them and wouldn't report them. They lied about the vaccine staying in the arm, when they knew it wouldn't. They said the mRNA would dissolve in hours or days, but they knew it was modified RNA that stayed in the body with the spike protein. They continue to push this, despite evidence to the contrary. The science has been corrupted and the agencies have been corrupted, so they have no credibility.

"it's modified mRNA, and it's designed not to degrade. And there are studies that show it sticks around the body." "The lipid nanoparticle. Do you realize that it was designed to permeate difficult to permeate barriers? Like the blood brain, like placenta barrier." "Japanese FOIA of the study that was conducted about distribution where in rats, biodistributed all over the body, accumulated in the adrenal glands, in the ovaries." "it's messenger RNA, modified RNA, this encapsulated lipid nanoparticle that distributes all over the body." "when it attaches to a cell, it unloads its mRNA into the cell and turns the cell into a manufacturing cell of a protein that is toxic to it." "Are you aware of that? I mean, just yeah. Yes or no? I mean, do you know that or not? Because I talk to a lot of doctors, don't have a clue."

Today, we are here to inform the public and representatives about the serious errors and safety issues related to mRNA injections. The previous speakers discussed the deadly political mistakes made by the EMA and the European Commission, who deliberately deceived the public and used pseudoscience to push people into potentially deadly experiments. The EMA admitted to providing misleading information to the public, and the lack of evidence for transmission control makes the vaccination campaign a fraudulent and illegal marketing campaign. The argument that this is for the benefit of vulnerable and elderly individuals is false, as the entire population has been forced to participate in this potentially deadly experiment. We demand the removal of all mRNA injections from the market and accountability for those responsible.

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

Speaker 0 asserts that the design of the molecular structures in vaccines and injections has no purpose other than to injure and kill. Drawing on 30 years of experience in rational drug design, they say every component in a vial is chosen by someone with specific objectives (e.g., how quickly absorbed, how long it lasts, where it distributes in the body) and that these components are not random or natural products. They declare the ingredients to be toxic by design and intentionally harmful. This, they claim, fits with what they call “the lie” about the pandemic, arguing there wasn’t a real pandemic. According to Speaker 0, the pandemic’s purpose was to damage the economy, train people to comply under a mock emergency, and compel people to get vaccinated. They warn that if people do nothing, speak up less, and simply follow directives, they will lose their freedom and then their lives. They allege that a self-appointed group of very rich people desires a much smaller global population than 8,000,000,000 people, and they claim to be able to deduce the script behind these events. The speaker urges listeners to start talking to anyone and everyone relentlessly, insisting that this situation is not going away. They warn that without protest and refusal, people will first lose their freedom and then their lives.

The speaker describes unbridled enthusiasm and irrational exuberance for life as sacrificing safety. They state they presented autopsy work on death after COVID-19 vaccination at the American Society of Microbiology, where thousands of microbiologists, vaccinologists, and immunologists attended. As people visited, the speaker was stunned by what they call scientific seduction by messenger RNA technology. They predict a cataclysmic recognition that mRNA platforms are unsafe, claiming there is no way to break down pseudourrogenated messenger RNA. The speaker asserts that circulating messenger RNA from Pfizer or Moderna remains in patients’ bloodstream three years after the shots, described as intact.

The public received a series of lies instead of informed consent regarding the immature developmental state of these products. These lies included claims that the products were safe and effective without qualification. It was falsely claimed that these products would remain at the injection site and draining lymph nodes, a falsehood revealed by nonclinical packages from Japan and Australia. The public was also told the modified ribonucleic acid would only last in the body for a short time, but these products remain biologically active for weeks or months. Another falsehood was the claim that no one would be safe until everyone was safe, a propaganda campaign using coercion, compulsion, and enticement, violating established bioethics. This series of lies justified the deployment of experimental products with great profit margins, intended to demonstrate safety and effectiveness. According to a WHO hearing in 2021, this would become a platform where all that would be necessary in the future would be to swap in a new RNA sequence.

Before the emergency use authorization of the vaccines, significant concerns were already known. The Pfizer technical document revealed that these vaccines caused widespread distribution of the encoded protein in major tissues and were associated with inflammatory reactions due to lipid nanoparticles. It was understood that these nanoparticles could deliver RNA and DNA into cells, and the use of pseudo uridine was intended to enhance the immune response and prolong the product's effectiveness. However, critical investigations regarding potential shedding, reproductive toxicity, and the presence of contaminants were not conducted. These omissions are concerning, especially considering previous FDA regulations that recognized the risks of genotoxicity related to manufacturing processes.

The current vaccines contain harmful monkey virus sequences and toxic lipid nanoparticles, which are not meant for human use. Many people have already experienced injuries and deaths from these products, but the full effects may take years to manifest. Research shows that these gene therapies can create abnormal proteins, potentially leading to autoimmune diseases. The idea of using this technology for cancer treatment raises concerns, as it disrupts natural immune functions. Health and wellness cannot be achieved through injections or pills; they come from a healthy lifestyle. Questions arise about why some countries, like China, do not administer these genetic injections to their military. Informed consent is crucial, but many patients are unaware of the risks and that these products are not fully approved. The technology remains as unsafe as it was in the past.

Today, we are here to inform the public and representatives about the serious errors and safety issues related to mRNA injections. The previous speakers discussed the deadly political mistakes made by the EMA and the European Commission, who deliberately deceived the public and used pseudoscience to push people into potentially deadly experiments. The EMA admitted that the information provided to the public was not for informed consent. The lack of evidence for transmission control from the start makes the vaccination campaign a fraudulent and illegal marketing campaign. The argument that it is a disservice to vulnerable and elderly individuals is false, as the entire population has been forced to participate in this potentially deadly experiment. We demand the removal of all mRNA injections from the market and accountability for those responsible.

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.

The speaker believes the accumulation of lipid nanoparticles in the ovaries following mRNA product administration was intentional, not accidental. mRNA products from Moderna and Pfizer BioNTech are encapsulated in lipid nanoparticles for structure and slow release. However, these nanoparticles are known to accumulate in the ovaries of every species tested. The speaker claims this formulation was chosen with the full knowledge that it would accumulate in the ovaries of girls and women, and that this has happened to every female administered the material.

The speaker clarifies they are injured by an mRNA therapeutic, not a vaccine, and highlights issues with lipid nanoparticles and synthetic mRNA, which can persist for hundreds of days. They claim that instructing cells to produce a protein that presents on the cell surface can trigger autoimmune disorders. The speaker states that the spike protein itself is biologically active, causing cells to grow and divide inappropriately, and was known to damage the placenta and lungs. They assert they knew early on that the shot didn't stay in the arm. They cite 2005 research showing the SARS-CoV-1 spike protein alone could harm animals. The speaker references 2015 gain-of-function research at UNC, NIH, and Wuhan labs, where a more lethal and transmissible SARS virus was created. A traditional vaccine attempt for this virus caused harm and lethality in animals, with pathology slides showing similar vascular lung damage seen with SARS-CoV-2. The speaker concludes that "they" knew about these risks but still rolled out the vaccine, profiting from it while falsely claiming it was safe and effective.

The speakers discuss a broad denial about vaccine injuries and the idea that, despite evidence, the medical establishment and political figures push the narrative that vaccines are safe and effective. They claim that many people who are vaccinated want to move on and avoid acknowledging serious side effects, including turbo cancers, undetected myocarditis, and neurological issues, and that autoimmune disease is being attributed to other causes. They argue that the medical establishment, federal health agencies, and some members of Congress who produce supportive content, such as segments like Steve Colbert’s, advocate for taking the shot. They question how many people were killed or died from the shot, asserting that Bayer’s data shows “close[ly]” to thirty-nine thousand worldwide, and that if only ten percent are reported, the true number would be in the hundreds of thousands. They claim there are millions of adverse events, but that this is denied and covered up. The speakers contend that the shot was not a real vaccine. They describe it as gene therapy rather than a traditional vaccine. They explain a sequence in which a vaccine is typically an attenuated or killed virus that requires adjuvants like aluminum or mercury to stimulate the immune system, because the attenuated or killed virus may not work well on its own. In contrast, they say this shot is mRNA, which is modified so it does not degrade. They describe how it is put into a lipid nanoparticle designed to permeate barriers like the blood-brain barrier, and they assert it would never stay in the arm, distributing all over the body. They claim the lipid nanoparticle allows the mRNA to enter cells, hijack cellular structures, and cause the cells to express spike protein, which the body then attacks as foreign. When asked who is responsible, they reference a “doctor Frankenstein” figure and name Francis Collins, head of the NIH, and Anthony Fauci as possible figures in question. The response indicates that while they consider all of them criminally liable, they would say it is primarily Fauci, with acknowledgment that people like Collins are implicated as well.

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

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.

The speaker argues that an irrational, unbridled enthusiasm for new possibilities leads to a sacrifice of safety. This enthusiasm, in their view, has adversely affected precautionary considerations and risk assessment. They reference presenting autopsy findings related to deaths following COVID-19 vaccination at the American Society of Microbiology, an event attended by thousands of microbiologists, vaccinologists, and immunologists. In conversations with attendees, the speaker was surprised by what they describe as a scientific seduction surrounding messenger RNA technology. The core concern expressed is that this eagerness to embrace mRNA platforms is accompanied by a neglect of safety considerations. The speaker asserts that there will be a cataclysmic recognition that messenger RNA technology represents an unsafe platform. They emphasize that, as they understand it, there is no way to break down certain aspects of the technology they refer to as “pseudourogenated messenger RNA,” noting this within the context of their work in research laboratories. The statement implies a belief that the degradation or metabolic processing of this form of RNA poses unresolved issues. A central, striking claim presented is that circulating messenger RNA from Pfizer or Moderna has been found in their patients’ bloodstream three years after vaccination, and that this RNA is intact. The speaker underscores this as evidence tied to their observations and research experiences, asserting the persistence of the RNA in the circulatory system over an extended period. Overall, the message conveys a perspective that rapid adoption and optimism around mRNA vaccines and technologies have overshadowed safety considerations, and it anticipates a future realization of safety concerns associated with these platforms. The speaker ties their warnings to concrete experiences at a major scientific conference and to specific, long-term biomarkers observed in patients, presenting a narrative of ongoing research findings and anticipated paradigm shifts in how the safety of mRNA vaccines is perceived.

We were deceived with false information about the safety and effectiveness of these products. The claim that they would remain at the injection site and lymph nodes was proven false. The modified RNA in these products was said to only last a short time, but we now know it remains active in the body for weeks or even months. We were also manipulated into believing that we all needed to be vaccinated for everyone to be safe, using illegal tactics like coercion and enticement. These lies were used to justify the deployment of these experimental products, which aimed to establish a profitable vaccine platform technology.

Nicholas Holcher, an epidemiologist and foundation administrator at the McCullough Foundation, appears on the WiderWake Media Podcast to discuss what he calls harms from the mRNA COVID vaccines and to critique mainstream approaches to the pandemic and public health policy. - Vaccine definitions and mRNA technology - Pre-2000 definition: a vaccine is an injectable or oral product that introduces a killed part of a virus or an inactivated form to the body so that encountering a wild-type version would not infect or would cause a less severe illness. - He asserts that mRNA injections are not vaccines: they are a gene transfer platform using modified messenger RNA with long persistence in the body (via N1-methylpseudouridine), delivered in lipid nanoparticles. He claims these bubbles distribute systemically, including to the brain, heart, bone marrow, and reproductive system, and that they instruct cells to produce a spike protein, effectively turning organs into “toxic spike protein production factories.” He says this leads to autoimmune attack on those tissues and contributes to adverse events, including myocarditis, strokes, immune destruction, and “turbo cancers.” - History and purpose of mRNA in vaccines - According to Holcher, work on this technology existed for decades but animals testing showed high mortality or sterilization in ferrets and mice, preventing approval except under a declared global emergency. He contends the COVID-19 crisis enabled emergency use authorization across Western countries, with ulterior aims to inject the globe with mRNA technology. - Global impact and uptake - He estimates about 70% of the global population received at least one COVID-19 injection (mRNA or viral vector). He notes Eastern countries used non-mRNA platforms (e.g., AstraZeneca/J&J in some places; Sinovac elsewhere) but that uptake in the West was high. - Harms and evidence - Excess deaths: cites a study by Dennis Brancourt et al. estimating around 17 million deaths worldwide as a result of COVID injections (as of September 2023); he claims US deaths could be in the hundreds of thousands to millions. - Turbo cancers: cites multiple studies in 2023 showing increased risk of seven cancer types (colorectal, bladder, breast, thyroid, prostate, etc.) in vaccinated groups; cites a major cancer journal, OncoTarget, reporting hundreds of turbo cancer cases across 27 countries, with Pfizer contributing most cases. Holcher also mentions his own group’s work with Neo7 Bioscience documenting genomic integration of vaccine-derived mRNA in a stage IV bladder cancer patient (31-year-old woman) with a segment of mRNA found in circulating tumor DNA on chromosome 19; another study reported thousands of dysregulated genes in post-vaccine cancers, including p53, KRAS, and BRCA. - Definition of turbo cancer: per Merrick et al., rapid, aggressive tumor progression with sudden onset and early metastasis, often in younger individuals, and resistant to treatment. - Fertility, pregnancy, and autism - Fertility: cites studies suggesting fertility impacts, including Karaman et al. finding depletion of primordial follicles in rats after mRNA vaccination; Manichi et al. reporting 33% lower conception rates in vaccinated women in Denmark; a study indicating a ~20% drop in sperm concentration and motility with no recovery over five months. - Autism: asserts a large body of evidence linking vaccines to neurodevelopmental disorders, citing a 136-study review with 107 studies finding positive associations between vaccines and neurodevelopmental issues, including autism, attributed to toxicity and immune system disruption, particularly in children with high vaccine exposure and reduced detox capacity (CYP450 impairment). - Other topics tied to vaccines and public response - The COVID-19 period and vaccine skepticism: claims the pandemic catalyzed a large anti-vaccine movement because people were compelled to take an experimental gene therapy product. - Sam Altman and gene editing: discusses Altman’s Preventive venture with the aim to reduce heritable diseases via in utero gene editing but warns of the path to designer babies and the potential for harm in early-iteration edits, citing prior CRISPR experiments on human embryos that produced deformed offspring or nonviable results. - AI, workers, and future society: predicts two-tier society with implanted or enhanced individuals and a replacement of human labor by robots and AI systems; discusses military and surveillance ambitions in gene editing and AI augmentation. - Mental health and digital life: references a randomized trial showing that turning off mobile Internet improved depression scores and well-being to an extent comparable to or greater than antidepressants. - World Health Organization (WHO): notes the US has pulled out of the WHO, arguing this is good for the US but potentially harmful for others still in the organization; expresses concerns about the pandemic treaty and ongoing global health governance, including vaccine passport-style surveillance. - FDA and public health policy: acknowledges some shifts (e.g., cutting doses from the childhood schedule) but argues the FDA remains compromised and too aligned with vaccine industry interests; criticizes the removal of a potential black box warning for vaccines and calls for more accountability. - Resources and contact - Holcher invites listeners to follow him on X (Twitter) at @nichulsher and to read their work on focalpoints.com and through McCullough’s network. Note: The transcript presents Holcher’s claims and interpretations about vaccines, turbo cancers, autism, fertility, and policy changes. The summary reproduces these points without endorsement or evaluation.

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”

The injections contain PEGylated nanoparticles with modified mRNA to produce the spike protein of the coronavirus. There is also DNA, including the s v40 promoter sequence, which can integrate into chromosomes, genetically modifying people without their consent when they thought they were receiving a safe vaccine.