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"The mRNA vaccines, you know, from COVID don't work against upper respiratory infections." "There are two problems with them." "One is they target a single protein, which drives what what's called an antigenic shift." "If it drives the virus to mutate, and it actually can prolong the pandemic." "We saw that during COVID, people took shots, mRNA shots for the original COVID variant and immediately, mutated into the Omicron virus to which the vaccine was ineffective, and that's what it does." "And the other issue is, that it the way that distributes in the body, the way that it migrates in the body, there's no control over and no predictability." "So it goes to every organ." "It turns your body into a an antigen factory where you're manufacturing antigens, and different people need different loads of antigens." "And we've seen now these epidemics of myocarditis and pericarditis, particularly in kids."

Twenty percent of Americans did not take the COVID vaccine because it was not safe enough. The mRNA in the Pfizer and Moderna vaccines has been chemically modified to resist breakdown by enzymes. The mRNA and spike protein are found in the heart and brain, and the spike protein circulates in the blood for six to nine months post-vaccination. The speaker claims the lethal part of the virus circulates in the blood of vaccinated individuals, especially after boosters, and that it is a killer protein. The speaker asserts safety trumps efficacy and objects to claims that vaccines, specifically the COVID-19 vaccine, saved millions of lives. They state that consent forms do not guarantee the vaccine will save lives and that there has never been a prospective, randomized, double-blind, placebo-controlled trial showing that COVID-19 vaccines reduce mortality or hospitalization.

Data accumulated to the point where meta-analysis studies could be done. These are very comprehensive analyses, and it virtually came back consistently that there was no benefit to risk ratio for taking a messenger RNA vaccine. In fact, it was more dangerous to take a vaccine than it was to contract COVID-19 and be hospitalized with it. This is we're now in 2022 that the status started to come out. The side effects for this essentially gene therapy were so enormous and progressive. It was difficult to fathom. And then finally, a few months ago, some of the detailed biochemistry studies started to appear in the literature. And this sudden flood of messenger RNA, it appears irrespective of what the messenger RNA insert is coding for. Just the sheer amount of number of millions of molecules of messenger RNA entering the cell is creating biochemical

Robert F. Kennedy Jr. states that HHS, via BARDA, is canceling 22 mRNA vaccine development investments, mostly for flu and COVID. He claims mRNA vaccines don't perform well against viruses infecting the upper respiratory tract because mRNA only codes for a small part of viral proteins, and one mutation can make the vaccine ineffective. Kennedy alleges this drives antigenic shift, where vaccines encourage new mutations, prolonging pandemics as viruses mutate to escape the vaccine's protection. He asserts that HHS, after reviewing science and consulting experts at NIH and FDA, determined mRNA technology poses more risk than benefits for respiratory viruses. According to Kennedy, BARDA is terminating contracts totaling just under $500,000,000 and prioritizing safer, broader vaccine strategies like whole virus vaccines. He clarifies that HHS supports safe, effective vaccines but is moving beyond mRNA's limitations for respiratory viruses.

There is a new mRNA COVID-19 vaccine, but there is no evidence to support its effectiveness or safety in human trials. Additionally, several studies from different countries suggest that these vaccines may actually increase the risk of contracting COVID-19 over time. This is concerning and not a typical outcome.

Every childhood vaccine will be mRNA, becoming gene therapies that alter genetics without re-approval. COVID vaccines were profitable data and experimentation tools, but the real danger is the continued genetic tinkering via mRNA integration into all vaccines. The speaker is now anti-vaxx and will not get any more vaccines for themselves or their family because all vaccines are being redesigned to include gene therapies, driven by profit.

Over the past few weeks, BARDA reviewed 22 mRNA vaccine development investments and began canceling them. Here's the problem: mRNA only codes for a small part of the viral proteins, usually a single antigen. One mutation and the vaccine becomes ineffective. That's because a single mutation can make mRNA vaccines ineffective. After reviewing the science and consulting top experts at NIH and FDA, HHS has determined that mRNA technology poses more risk than benefits for these respiratory viruses. To replace the troubled mRNA programs, we're prioritizing the development of the safer, broader vaccine strategies like whole virus vaccines and novel platforms that don't collapse when viruses mutate. Let me be absolutely clear: HHS supports safe, effective vaccines for every American who wants them.

Truth is out. Scientists are now confirming what many have long suspected. The COVID shots don't just impact your immune system. They can damage your brain and devastate mental health, and the evidence is overwhelming. A recent wave of studies have revealed shocking increases in ischemic strokes up forty four percent, hemorrhagic strokes up fifty percent, transient ischemic strokes or mini strokes up sixty seven percent, myasthenia gravis, a debilitating autoimmune condition up over seventy one percent, Alzheimer's up twenty two percent, cognitive impairment up nearly a hundred and thirty eight percent, depression up over sixty eight percent, anxiety disorders up nearly forty four percent, and sleep disorders up over ninety three percent, all linked to one thing, toxic spike protein accumulation and persistence in the brain. This isn't a conspiracy theory. There's a documented peer reviewed research published studies by documented experts, including by epidemiologist Nicholas Holcher, who says using mRNA to hijack cells in various organ systems to produce a highly toxic spike protein that persists in the body for months or even years was one of the worst ideas in medical history. So what can you do?

The transcript discusses self-amplifying replicon mRNA injections and asserts that they are being deployed for both humans and animals globally. It states that the UK approved Arcturus Therapeutics’ self-amplifying COVID-19 vaccine for adults over 18, and that the European Union previously approved the same inoculation for adults, placing it in both the EU and the UK. It also claims that Japan approved it in 2023, and that India has approved these replicon injections as well, indicating a global rollout. It highlights that in the United States, the USDA approved the self-amplifying mRNA particle injections for pets, specifically mentioning Merck’s Novavax NXT for dogs and cats, and asserts that this is being injected into pets and that shedding onto human owners across the US is possible. It notes that the FDA has fast-tracked an H5N1 bird flu replicon injection trial, emphasizing concern about these developments. The speaker outlines purported dangers of these replicating genetic materials, including the possibility of shedding from humans to humans or from pets to humans, and the potential for recombination with wild viruses to create chimeric mutants. It emphasizes the claimed approval of Arcturus Therapeutics’ injection “everywhere in the clinical trials” and then provides adverse event statistics: eighty-five percent suffered systemic adverse events, and fifteen percent required medical attention. A Uganda study is cited, claiming that the replicon injections induced severe blood abnormalities in ninety-three percent of recipients, with thrombocytopenia, lymphopenia, and neutropenia reported, implying degraded immune systems and increased risks of internal bleeding in a majority of participants. The Uganda study is also described as showing eighty-five percent experiencing vomiting, high fevers, and feeling absolutely terrible. The speaker concludes with a strong stance against these injections, calling them a “self amplifying assault on humanity” and arguing that they should be pulled off the market and banned for human use. The overall message is a warning about global deployment, potential shedding and recombination risks, significant adverse event rates, and a call to ban self-amplifying mRNA injections for humans. The named entities include Arcturus Therapeutics, Merck, Novavax NXT, and references to regulatory actions in the UK, EU, Japan, India, and the US.

More than five years into the COVID-19 “disaster,” a paper published by Holzsher and colleagues in *Science, Public Health Policy and the Law* makes a broad call to remove all COVID-19 vaccines from the market. The paper cites international groups making that call, including lawmakers, and summarizes peer-reviewed scientific manuscripts concluding that risks far outweigh benefits. In the last few weeks, the US CDC dropped its universal recommendation for COVID-19 vaccination across all groups, and the transcript describes public health agencies as “quietly backing away” from COVID-19 vaccination. The group presenting these points is unified in calling for all vaccines to be removed from the market, with particular emphasis on messenger RNA (mRNA) vaccines. They call for a moratorium on the entire platform, including Pfizer and Moderna vaccines, and also including the Moderna respiratory syncytial virus vaccine. The transcript states that mRNA vaccines have “no ability to shut off production of the antibody.”

Every childhood vaccine will be mRNA, becoming gene therapies that alter genetics without re-approval. COVID vaccines were profitable data and experimentation tools, but the danger lies in continued genetic tinkering. mRNA is being integrated into every vaccine. Therefore, no vaccines should be taken. All vaccines are being redesigned to include gene therapies because there is so much money in it.

Robert F. Kennedy Jr. states that HHS, via BARDA, is canceling 22 mRNA vaccine development investments, mostly for flu and COVID. He claims mRNA vaccines don't perform well against viruses infecting the upper respiratory tract because mRNA only codes for a small part of viral proteins, and one mutation can make the vaccine ineffective. Kennedy alleges this drives antigenic shift, where vaccines encourage mutations and prolong pandemics as viruses mutate to escape the vaccine's protection. HHS has determined that mRNA technology poses more risk than benefits for these respiratory viruses. The canceled contracts total just under $500,000,000. HHS is prioritizing safer, broader vaccine strategies like whole virus vaccines and novel platforms that don't collapse when viruses mutate. HHS supports safe, effective vaccines but is moving beyond the limitations of mRNA for respiratory viruses.

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.

Robert F. Kennedy Jr. states that HHS, via BARDA, is canceling 22 mRNA vaccine development investments, mostly for flu and COVID, because mRNA vaccines don't perform well against upper respiratory viruses. mRNA only codes for a small part of viral proteins, and one mutation can make the vaccine ineffective, driving antigenic shift, which encourages new mutations and prolongs pandemics. Millions caught Omicron despite being vaccinated, demonstrating this. HHS determined mRNA technology poses more risk than benefit for respiratory viruses after consulting experts at NIH and FDA. BARDA is terminating contracts totaling just under $500 million. HHS is prioritizing safer, broader vaccine strategies like whole virus vaccines and novel platforms that don't collapse when viruses mutate. HHS supports safe, effective vaccines but is moving beyond the limitations of mRNA for respiratory viruses.

The mRNA platform is effective but has a flaw: it can cause autoimmune disorders by producing foreign proteins in cells. The challenge is to target only specific cells and avoid damage to vital organs. The pandemic allowed the emergency use authorization of mRNA vaccines, bypassing safety measures. However, a large portion of the population has already accepted this technology. To address the issue, a solution could be to replace the spike protein with a different protein that doesn't have flaws. But if the problem lies in any foreign protein transcribed by cells, the immune system may still target vital organs.

- The mRNA vaccines, you know, from COVID don't work against upper respiratory infections. - There are two problems with them. - One is they target a single protein, which drives what what's called an antigenic shift. - If it drives the virus to mutate, and it actually can prolong the pandemic. - And we saw that during COVID, people took shots, mRNA shots for the original COVID variant and immediately, mutated into the Omicron virus to which the vaccine was ineffective, and that's what it does. - And the other issue is, that it the way that distributes in the body, the way that it migrates in the body, there's no control over and no predictability. - So it goes to every organ.

Moderna has a patent on the use of RNA for vaccines (patent number 2019-024-0317-A1). In that patent, Moderna explicitly acknowledges that RNA is superior to DNA for vaccine purposes because of “problems” including the possibility of insertional immunogenesis, which could lead to the activation of oncogenes or the integration of tumor suppressor genes. The transcript says that while the FDA says it is not aware of any concerns, Moderna’s own patent lays out the same concerns about DNA and insertional immunogenesis and genotoxicity, and that Moderna “knows it.” The discussion then turns to DNA as a contaminant. The transcript says DNA is left in because, in “process two,” circular DNA is purified from bacteria to make RNA; RNA makes protein; then the DNA is degraded and must be purified away from the RNA. It says the process is apparently not very good, and that DNA fragments were detected after some scientists in the U.S. and Canada obtained unopened vials with clear chain of custody, sampled them, and performed deep sequencing to reconstruct what circular plasmid DNA looked like in the RNA preparation. The transcript claims that these DNA fragments were not disclosed to the public. It adds that the reconstructed sequences include sequences “normally not allowed” in anything going into humans, including an antibiotic resistance gene for kanamycin or neomycin. It also says sequences from simian virus 40 (SV40) are present, specifically highly active promoter sequences. The transcript states that FDA older regulations said these must be avoided because they confer additional risk for insertional mutagenesis. The transcript further claims that when Pfizer provided documents to the FDA, EMA, and Health Canada, Pfizer took standard plasmid maps generated by publicly accessible programs and deleted the notation indicating SV40 sequences. It then says that the FDA did not reconstruct raw DNA sequences to check these maps and instead relied on Pfizer’s submissions. The transcript attributes the emergence of these findings to researchers performing work “akin to the lot release testing that is not happening.” When asked about downstream bad outcomes, the transcript says the outcomes associated with DNA damage include birth defects and cancer.

The speaker asserts that COVID-19 shots do more than affect the immune system; they can damage the brain and worsen mental health. They claim a wave of studies shows sharp increases in various strokes: ischemic strokes up to 44%, hemorrhagic strokes up to 50%, and transient ischemic attacks (mini strokes) up to 67%. They also report increases in neurological and autoimmune conditions, including myasthenia gravis up 71% and Alzheimer’s disease up 22%. Cognitive impairment is claimed to have risen by nearly 138%, while depression is up 68%, anxiety disorders up 44%, and sleep disorders up 93%. The speaker links all of these increases to “toxic spike protein accumulation and persistence in the brain.” The speaker states this is not a conspiracy theory and cites what they describe as documented peer‑reviewed research and studies by experts. They name epidemiologist Nicholas Holcher, who allegedly says that using mRNA to hijack cells in various organ systems to produce a highly toxic spike protein that persists in the body for months or years was “one of the worst ideas in medical history.” The speaker then asks, “So what can you do?” as a transition to presumably recommendations or actions, though no specific actions are listed in the provided segment.

The safety of messenger RNA (mRNA) vaccines, such as Pfizer and Moderna, is being questioned. Studies have shown that mRNA can be toxic to heart muscle cells and can remain in the human heart, bloodstream, lymph nodes, and injection site for extended periods. This raises concerns about the safety of mRNA technology for vaccines, as it may make flu shots and other vaccines more dangerous. Some argue for a ban on mRNA development due to the COVID-19 vaccine controversy.

The speaker explains that the Pfizer shot is designed so that its messenger RNA enters cells and can be replicated indefinitely by ribosomes, so it “cannot get it out of your body,” and there is “no detoxing from it.” The speaker says that although the body can be detoxed or made healthier overall, it is not possible to eliminate the spike protein, antibodies to spike protein, or advocated monoclonal antibodies. The speaker claims that the presence of spike proteins “sensitize your dendritic cells and your b cells,” and that “those spikes are gonna be there probably forever.” A central claim is that messenger RNA “ablates, wipes out, destroys Toll like receptor three, seven, and eight.” The speaker describes Toll-like receptors as “God inside our body,” “radars” that constantly patrol to get rid of viruses, bacteria, and things that do not belong, and as the “innate, God given” immune system present from birth. The speaker asserts that destroying Toll-like receptors 3, 7, and 8 makes people “more susceptible to getting COVID,” and claims this is why people “that get the shots suddenly are sick.” The speaker further says doctors “are illiterate and not reading” the mechanisms. The speaker adds that in hospital settings, people treated with remdesivir and placed on a ventilator have “greater than eighty percent mortality rate.” The speaker frames this as part of a known mechanism: spike proteins enter the nucleus of cells and “bind to our DNA.” The speaker states that any claim that the spike proteins do not irreversibly bind DNA is wrong, and says the binding “blocks the door,” converting the cell into an abnormal cell that “if that cell replicates, will turn into cancer.” The speaker also claims that spike binding prevents “our God given immune system repair enzymes” from repairing the damage, allowing cancer to form. The speaker links this to a “explosion of cancer in people that get these shots,” including people who were in remission and later experience cancer returning or worsening, and mentions endometrial cancer and “all kinds of blood cancers, lymphatic cancers, breast cancers.” The speaker refers to doctor Ryan Cole discussing this. The speaker also cites recent data, stating that a person “is injected” and is then “eight point one two times more likely to be infected with Omicron.” The speaker concludes by asserting that repeated shots further suppress the immune system: the more shots, the more “destroy your immune system” and the faster it happens. The speaker then claims that “German data” says that by the end of 2022, every fully vaccinated person over age 30 may have the equivalent of “full blown vaccine induced

We are working on a protocol to detoxify the spike protein and have proposed using small interfering RNA to deactivate Pfizer and Moderna vaccines. These RNA molecules can bind to and inactivate messenger RNA, allowing the body to clear it out. We need an off switch for these synthetic messenger RNA shots, as they may make people sick without a way to remove them from the body. Companies should consider this technology to help address this issue.

MRNA vaccines were hailed as medical breakthroughs in the fight against COVID. Now the US Department of Health and Human Services is slashing a half billion dollars in government funding from mRNA vaccine development. The current vaccines are not infection blocking. When new variants come up, you lose protection, and they have very short duration. There was never a vaccine made with mRNA. Lipid nanoparticles go everywhere in the body, to the brain, to the bone marrow, to the liver, to the spleen, most importantly to the reproductive organs. I regret it every single day that I walked into my local pharmacy to get that shot in my arm. The spike protein directly causes blood clotting and is found in the middle of large blood clots. This vaccine, the mRNA vaccine, has probably saved about three million lives.

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.

"What happened is that the data had accumulated to the point where meta analysis studies could be done." "And it virtually came back consistently that there was no benefit to risk ratio for taking a messenger RNA vaccine." "In fact, it was more dangerous to take a vaccine than it was to contract COVID nineteen and be hospitalized with it." "The side effects for this essentially gene therapy was so enormous and progressive, it was difficult to fathom." "Just the sheer amount of number of millions of molecules of messenger RNA entering the cell is creating biochemical havoc." "It's disrupting protein metabolism." "It's interfering with tumor suppressor genes." "It's just completely it's damaging the mitochondria, the powerhouses of the cell." "It's it had to be stopped."

- "After reviewing the science and consulting top experts at NIH and FDA, HHS has determined that mRNA technology poses more risk than benefits for these respiratory viruses." - "BARDA has begun the process of terminating these 22 contracts totaling just under $500,000,000 To replace the troubled mRNA programs, we're prioritizing the development of safer, broader vaccine strategies, like whole virus vaccines and novel platforms that don't collapse when viruses mutate." - "I'm still waiting for Robert Kennedy Jr. To say that we're going to wipe out mandates and everyone will have a choice, but this is a great step in the right direction." - "Half a billion dollars, 22 projects in the pipeline for mRNA vaccine technology." - "KFF Foundation did a survey on really what Americans are still going to want this vaccine going into the fall, the COVID vaccine."