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Gene injections, also known as vaccines, aim to stimulate adaptive immunity and neutralizing antibodies to eliminate the virus. However, the Pfizer and Moderna vaccines have shown negative efficacy, with vaccinated individuals getting infected and reinfected. This leads to the emergence of more infectious variants. Continuing the current vaccine rollout will prolong the pandemic, as new variants will keep emerging. Vaccinating during a pandemic with high infectious pressure is a catastrophic mistake. These vaccines cannot and will not work.

"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."

The Pfizer shot contains synthetic messenger RNA that stays in the body indefinitely, unable to be detoxed. It destroys toll-like receptors 3, 7, and 8, which are crucial for our immune system's defense against viruses and bacteria. This makes vaccinated individuals more susceptible to COVID-19. The spike protein from the shot enters the cell nucleus, binds to DNA, and blocks repair enzymes, potentially leading to cancer. There is evidence of an increase in cancer cases among vaccinated individuals. Multiple shots further weaken the immune system, with German data suggesting that by the end of 2022, fully vaccinated individuals over 30 may have immune suppression similar to AIDS.

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.

"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."

mRNA vaccines code for a small part of viral proteins, usually a single antigen. A single mutation can make the vaccine ineffective. This drives antigenic shift, where the vaccine encourages new mutations, prolonging pandemics as the virus mutates to escape the vaccine's protection. Millions caught the Omicron variant despite vaccination because a single mutation can render mRNA vaccines ineffective. The same risk applies to the flu.

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.

The Pfizer vaccine uses synthetic messenger RNA that replicates indefinitely in cells, making it impossible to detoxify from it. This mRNA damages toll-like receptors 3, 7, and 8, which are crucial for the innate immune response, increasing susceptibility to infections like COVID. Consequently, vaccinated individuals are more likely to become ill and face higher hospitalization rates. The spike protein can bind to DNA, potentially leading to abnormal cell growth and cancer, which explains the rise in various cancers among vaccinated individuals. Recent data indicates that vaccinated people are significantly more likely to contract omicron, and ongoing vaccinations may lead to severe immune suppression, comparable to AIDS, particularly in those over 30.

Everything was alive from the beginning, asymptomatic people don't transmit, and kids are a break on the disease, not harbingers. Lockdowns were a farce, and masks don't work. COVID-19 vaccines destroy your immune system and distribute widely in the body. The genetically modified RNA in the vaccines can't be broken down and contains contaminants. Pfizer put an SV40 promoter in the vaccine, known to bind p53, the guardian of the genome, and cause cancers. The vaccines have design flaws, distribute to the brain, bone marrow, ovaries, and testes, and have long-term production. The vaccines are dangerous, have process-related impurities, and cause cancer, strokes, and heart attacks. There were 40% more deaths in 2021 between 18 and 64, so stay away from the vaccines.

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 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.

There are three basic vaccine technologies, none of which are safe. The three technologies are live attenuated vaccines, killed-virus/virus-fragment vaccines with adjuvants, and mRNA vaccines. Live attenuated vaccines can cause one person a tiny mild infection while another may suffer a more serious one, and they can evolve and spread; though not supposed to be contagious, they can produce contagious effects. For example, the polio vaccine, live attenuated, has created many polio cases, an intolerable downside. The killed-virus approach doesn't reliably stimulate immunity unless an adjuvant is used; adjuvants are nonspecific and can trigger widespread immune activation. The mRNA approach is unsafe because it moves haphazardly through the body, causing cells to produce foreign antigens, which the immune system may attack as virally infected, potentially deadly in the heart, and tissue destruction elsewhere. In sum, three technologies, none fundamentally safe, with severe downsides.

Robert F. Kennedy Jr., as HHS secretary, explains that BARDA is canceling 22 mRNA vaccine development investments, primarily for flu and COVID. He claims mRNA vaccines don't perform well against upper respiratory viruses because they only code for a small part of viral proteins, and a single mutation can make them ineffective. This drives antigenic shift, paradoxically encouraging new mutations and prolonging pandemics. HHS has determined that mRNA technology poses more risk than benefits for these viruses. The canceled contracts total just under $500 million. HHS will prioritize safer, broader vaccine strategies like whole virus vaccines and novel platforms that don't collapse when viruses mutate. HHS supports safe, effective vaccines and is moving beyond the limitations of mRNA for respiratory viruses.

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.

Robert F. Kennedy Jr.: Hi, it's Robert F. Kennedy Jr. here, your HHS secretary. At HHS, we have a division called the Biomedical Advanced Research and Development Authority, or BARDA. BARDA drives some of our most advanced scientific research. It funds developments of vaccines, drugs, diagnostics, and other tools to fight emerging diseases and national health threats. Over the past few weeks, BARDA reviewed 22 mRNA vaccine development investments and began canceling them. Let me explain why. Most of these shots are for flu or COVID, but as the pandemic showed us, mRNA vaccines don't perform well against viruses that infect the upper respiratory tract. 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. This dynamic drives a phenomena called antigenic shift, meaning that the vaccine paradoxically encourages new mutations and can actually prolong pandemics as the virus constantly mutates to escape the protective effects of the vaccine. Millions of people, maybe even you or someone you know, caught the omicron variant despite being vaccinated. That's because a single mutation can make mRNA vaccines ineffective. The same risk applies to flu. 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. That's why after extensive review, 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 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. That's why we're moving beyond the limitations of mRNA for respiratory viruses and investing in better solutions. Thank you. Produced by the U. S. Department of Health and Human Services.

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.

Speaker 0: I was fired after thirty one years as an emergency room physician with not one single patient complaint against me in those thirty one years. I was fired for saying that somebody who had natural immunity didn't need to be vaccinated against the disease to which they were already immune. Fortunately, I still had my medical license even though I lost a significant part, at least 50% of my income and I couldn't work as an emergency room doctor anymore, I still had my private practice. So when I discovered from the the biodistribution studies that Pfizer had hidden, that we knew that these vaccines go around your entire body, they do not just stay in your arm. Pfizer's biodistribution studies on the lipid nanoparticles show that they literally take those messenger RNA strands into every part of your body that go into your brain and your lungs and your heart and your liver and your reproductive organs and your bone marrow and everywhere, which is, by the way, why these COVID shots have caused a a greater array of side effects than any other medical treatment in history because this toxic spike protein ends up in literally every every

"Unfortunately, the mRNA platform, though it is brilliant in its conception, is fatally flawed." "the myocarditis and pericarditis that showed up as a result of COVID vaccinations are inherent to the platform, not to the messenger RNA that was delivered inside these shots." "the design of this platform is to induce your own cells to make a foreign protein which gets displayed on the surface of those cells." "there's no targeting mechanism to lead it to happen only in certain tissues, it can happen haphazardly around the body, including in places like your heart." "And what that triggers is your own immune system to see those foreign proteins and conclude the only thing they can, which is that those cells have been virally infected." "the right response, the response, the natural response of the body is to take virally infected cells and destroy them."

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 Pfizer shot contains synthetic messenger RNA that stays in the body and cannot be detoxed. It destroys toll-like receptors 3, 7, and 8, which are crucial for our immune system's defense against viruses and bacteria. This makes vaccinated individuals more susceptible to getting COVID-19. The spike protein from the shot enters the cell nucleus, binds to DNA, and can cause abnormal cell replication leading to cancer. People who have received the shot are experiencing an increase in various types of cancer. Recent data shows that those who are vaccinated are 8.12 times more likely to be infected with the Omicron variant. The more shots received, the more the immune system is suppressed, potentially leading to vaccine-induced immune suppressed AIDS. This information is based on government data from Germany.

The speaker expresses concern about the mRNA vaccines, specifically the Pfizer and Moderna ones, stating that they believe there are deliberate toxicities built into these materials. They explain how the immune system normally distinguishes between self and foreign substances, but when mRNA is used to make a piece of a foreign protein, the immune system goes into attack mode. The speaker argues that these vaccines cannot be safe for mass market use as they may cause the immune system to attack its own cells. They also claim that all four companies developing COVID-19 vaccines intentionally chose the spike protein, which they believe is biologically active and potentially toxic.

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."