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Bret Weinstein breaks down the three foundational vaccine technologies, arguing that none are fundamentally safe. Each carries a severe, inherent downside. 1. Live Attenuated Vaccines: The risk here is unpredictability and evolution. A virus weakened for one person may cause a serious infection in another. Crucially, it can revert...

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Camus

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Dr. Suzanne Humphries Confirms to Joe Rogan That—YES—Vaccines Can Cause Food Allergies “It’s very well known that the vaccines that have aluminum in them skew the immune system,” she said. Here’s how it can happen in plain English... Aluminum is added to many vaccines as an adjuvant—a substance that boosts the immune response. When aluminum is present, it puts the immune system on high alert, making it more reactive to anything in the environment at that moment. If someone eats certain foods—like peanuts or eggs—around the time of vaccination, the aluminum can cause the immune system to mistakenly tag those harmless food proteins as threats. This happens because the immune system is primed to respond strongly and may associate the food with the “danger” signal caused by the vaccine. Over time, this mistaken identity can lead to a long-term food allergy. “So that’s kind of the paradox there [with vaccines],” Humphries explained.
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Dr. Suzanne Humphries Confirms to Joe Rogan That—YES—Vaccines Can Cause Food Allergies “It’s very well known that the vaccines that have aluminum in them skew the immune system,” she said. Here’s how it can happen in plain English... Aluminum is added to many vaccines as an adjuvant—a substance that boosts the immune response. When aluminum is present, it puts the immune system on high alert, making it more reactive to anything in the environment at that moment. If someone eats certain foods—like peanuts or eggs—around the time of vaccination, the aluminum can cause the immune system to mistakenly tag those harmless food proteins as threats. This happens because the immune system is primed to respond strongly and may associate the food with the “danger” signal caused by the vaccine. Over time, this mistaken identity can lead to a long-term food allergy. “So that’s kind of the paradox there [with vaccines],” Humphries explained.

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Most people don’t truly understand how mRNA vaccines work. Unlike traditional vaccines, where a factory produces the antigen and injects it into the body, mRNA vaccines turn YOUR OWN CELLS into the factory. Here’s how it works: Inside every one of your cells, there are ribosomes—tiny protein-making machines. Normally, these ribosomes get instructions from your cell’s nucleus (the brain of the cell) to produce proteins that build muscle, fight infections, and keep your body functioning. mRNA vaccines hijack this natural process by delivering a blueprint that instructs your ribosomes to produce a specific protein—like the spike protein of a virus. Your immune system then recognizes this protein as foreign, triggering a defense response and preparing your body to fight off future infections. Why does this matter? 1️⃣ Faster production – No need for external manufacturing of viral proteins, cutting vaccine development time. 2️⃣ Adaptability – The technology can be rapidly adjusted for new viruses and mutations. 3️⃣ No live virus – Unlike traditional vaccines, mRNA vaccines don’t use weakened or dead viruses, reducing risk. But here’s the big question: Are we playing with fire, or is this the future of medicine? We’re bypassing nature’s traditional immune response by directly programming our cells to make viral proteins. Dr. Mink Chawla and I break it all down in this episode. WATCH HERE:
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Most people don’t truly understand how mRNA vaccines work. Unlike traditional vaccines, where a factory produces the antigen and injects it into the body, mRNA vaccines turn YOUR OWN CELLS into the factory. Here’s how it works: Inside every one of your cells, there are ribosomes—tiny protein-making machines. Normally, these ribosomes get instructions from your cell’s nucleus (the brain of the cell) to produce proteins that build muscle, fight infections, and keep your body functioning. mRNA vaccines hijack this natural process by delivering a blueprint that instructs your ribosomes to produce a specific protein—like the spike protein of a virus. Your immune system then recognizes this protein as foreign, triggering a defense response and preparing your body to fight off future infections. Why does this matter? 1️⃣ Faster production – No need for external manufacturing of viral proteins, cutting vaccine development time. 2️⃣ Adaptability – The technology can be rapidly adjusted for new viruses and mutations. 3️⃣ No live virus – Unlike traditional vaccines, mRNA vaccines don’t use weakened or dead viruses, reducing risk. But here’s the big question: Are we playing with fire, or is this the future of medicine? We’re bypassing nature’s traditional immune response by directly programming our cells to make viral proteins. Dr. Mink Chawla and I break it all down in this episode. WATCH HERE:

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Dr. Ryan Cole issues a stark warning on the mechanism of mRNA vaccines. He states the spike protein is the virus's toxic component, directly linked to clotting, inflammation, myocarditis, and brain fog. His grave concern: any cell instructed to produce this foreign spike becomes a target for the body's own immune system. This forces the immune system to hunt and kill its own expressed cells, evoking a systemic autoimmune reaction. A critical perspective that demands attention.
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Dr. Ryan Cole issues a stark warning on the mechanism of mRNA vaccines. He states the spike protein is the virus's toxic component, directly linked to clotting, inflammation, myocarditis, and brain fog. His grave concern: any cell instructed to produce this foreign spike becomes a target for the body's own immune system. This forces the immune system to hunt and kill its own expressed cells, evoking a systemic autoimmune reaction. A critical perspective that demands attention.

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Dr. Patrick Soon-Shiong Unveils the Mechanism of Vaccine & COVID-Induced Autoimmunity and Announces a Potential Path to Treatment A groundbreaking explanation from Dr. Patrick Soon-Shiong on how COVID-19 and its vaccines can trigger autoimmune issues, and the pioneering science being deployed to reverse the damage. 1/ The fundamental problem, as detailed by Dr. Soon-Shiong, is that current vaccines do not clear the virus. They may block initial infection, but the virus can still enter cells, leading to a persistent and hidden problem. 2/ This persistence is now scientifically proven. Research funded by Dr. Soon-Shiong at UCSF, and confirmed by Harvard, shows the SARS-CoV-2 spike protein can linger in the body's cells and even circulate in the bloodstream long after the initial infection or vaccination. 3/ This creates a perfect storm. The body recognizes this persistent spike protein—an "abnormal" antigen—as a threat and mounts a continuous immune response, creating antibodies that can mistakenly attack the body's own tissues. This is the onset of autoimmune disease. 4/ Dr. Soon-Shiong identifies a "triple whammy" that paves the way for severe long-term health issues: • Persistence of the spike protein & viral RNA. • Chronic inflammation from the constant immune response. • Loss of P53, a critical guardian protein that protects against cancer. 5/ This combination is a prelude not only to autoimmune disorders but also to cancer and neurological symptoms like brain fog. It is the core pathology behind Long COVID and post-vaccine syndrome. 6/ But there is hope. The answer, he states, is not to suppress the immune system further, but to empower it. The solution lies in upregulating the body's natural assassins—NK cells and T cells—to finally seek out and clear the body of these infected, spike-protein-producing cells. 7/ To this end, Dr. Soon-Shiong announces a major clinical trial opening within weeks. This trial will focus on treating Long COVID by targeting and eliminating the persistent viral reservoir, offering a potential cure for those suffering from post-COVID and post-vaccine autoimmune conditions. This is not just management. This is the science of clearance and restoration.
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Dr. Patrick Soon-Shiong Unveils the Mechanism of Vaccine & COVID-Induced Autoimmunity and Announces a Potential Path to Treatment A groundbreaking explanation from Dr. Patrick Soon-Shiong on how COVID-19 and its vaccines can trigger autoimmune issues, and the pioneering science being deployed to reverse the damage. 1/ The fundamental problem, as detailed by Dr. Soon-Shiong, is that current vaccines do not clear the virus. They may block initial infection, but the virus can still enter cells, leading to a persistent and hidden problem. 2/ This persistence is now scientifically proven. Research funded by Dr. Soon-Shiong at UCSF, and confirmed by Harvard, shows the SARS-CoV-2 spike protein can linger in the body's cells and even circulate in the bloodstream long after the initial infection or vaccination. 3/ This creates a perfect storm. The body recognizes this persistent spike protein—an "abnormal" antigen—as a threat and mounts a continuous immune response, creating antibodies that can mistakenly attack the body's own tissues. This is the onset of autoimmune disease. 4/ Dr. Soon-Shiong identifies a "triple whammy" that paves the way for severe long-term health issues: • Persistence of the spike protein & viral RNA. • Chronic inflammation from the constant immune response. • Loss of P53, a critical guardian protein that protects against cancer. 5/ This combination is a prelude not only to autoimmune disorders but also to cancer and neurological symptoms like brain fog. It is the core pathology behind Long COVID and post-vaccine syndrome. 6/ But there is hope. The answer, he states, is not to suppress the immune system further, but to empower it. The solution lies in upregulating the body's natural assassins—NK cells and T cells—to finally seek out and clear the body of these infected, spike-protein-producing cells. 7/ To this end, Dr. Soon-Shiong announces a major clinical trial opening within weeks. This trial will focus on treating Long COVID by targeting and eliminating the persistent viral reservoir, offering a potential cure for those suffering from post-COVID and post-vaccine autoimmune conditions. This is not just management. This is the science of clearance and restoration.

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We've been told the COVID vaccines are a marvel of modern science. But what if the platform itself—the mRNA technology—is inherently dangerous, and the pandemic was used to normalize it before its flaws were solved? As Bret Weinstein explains, while the spike protein is problematic, the greater danger is the mRNA platform. "Anything you loaded onto that platform would produce many of these pathologies, because the platform itself is deeply flawed." The pandemic provided the perfect excuse to deploy this technology on billions with minimal testing, making its flaws "disappear" in the name of urgency. This normalized a platform that can be quickly reformulated for any new pathogen, creating a lifetime of repatentable products. But what is the core flaw? It's the lipid nanoparticle (LNP) delivery system. The mRNA message is wrapped in tiny fat bubbles. The critical failure: they don't stay in the deltoid muscle. They circulate throughout your entire body. Here’s why that’s catastrophic: Your cells are covered in a fatty layer. These lipid nanoparticles, being fat-based, are absorbed by any cells they encounter—your heart, liver, brain, ovaries, testes. Once inside, the cell is hijacked. It reads the mRNA instructions and begins mass-producing a foreign protein (like the spike protein). This triggers a devastating immune response. Your immune system is designed to recognize and DESTROY any of your own cells that start producing a protein they shouldn't. It treats them like cancer or a viral infection. So, the shot turns your body's cells into targets. As Weinstein states: "Their mRNA shots are a pseudovirus. They infect cells, cause those cells to make this protein, and then the immune system... destroys them." If this cellular destruction happens in an organ you can spare, like the liver, you might be okay. But if it happens in your heart? It creates a microscopic wound. Under stress, this can lead to a catastrophic event like a burst blood vessel. The platform has no targeting mechanism. It cannot control which of your vital organs becomes a battleground. The result is an unpredictable, Russian roulette of auto-immune destruction. The takeaway is stark: The problem isn't just what's in the shot, but how the shot works. Until this fundamental delivery flaw is solved—if it ever can be—any future mRNA product deployed must be met with extreme skepticism and a resounding NO. This is not anti-vax. This is pro-science. It is a demand for safe, effective, and honestly tested medical technology.
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We've been told the COVID vaccines are a marvel of modern science. But what if the platform itself—the mRNA technology—is inherently dangerous, and the pandemic was used to normalize it before its flaws were solved? As Bret Weinstein explains, while the spike protein is problematic, the greater danger is the mRNA platform. "Anything you loaded onto that platform would produce many of these pathologies, because the platform itself is deeply flawed." The pandemic provided the perfect excuse to deploy this technology on billions with minimal testing, making its flaws "disappear" in the name of urgency. This normalized a platform that can be quickly reformulated for any new pathogen, creating a lifetime of repatentable products. But what is the core flaw? It's the lipid nanoparticle (LNP) delivery system. The mRNA message is wrapped in tiny fat bubbles. The critical failure: they don't stay in the deltoid muscle. They circulate throughout your entire body. Here’s why that’s catastrophic: Your cells are covered in a fatty layer. These lipid nanoparticles, being fat-based, are absorbed by any cells they encounter—your heart, liver, brain, ovaries, testes. Once inside, the cell is hijacked. It reads the mRNA instructions and begins mass-producing a foreign protein (like the spike protein). This triggers a devastating immune response. Your immune system is designed to recognize and DESTROY any of your own cells that start producing a protein they shouldn't. It treats them like cancer or a viral infection. So, the shot turns your body's cells into targets. As Weinstein states: "Their mRNA shots are a pseudovirus. They infect cells, cause those cells to make this protein, and then the immune system... destroys them." If this cellular destruction happens in an organ you can spare, like the liver, you might be okay. But if it happens in your heart? It creates a microscopic wound. Under stress, this can lead to a catastrophic event like a burst blood vessel. The platform has no targeting mechanism. It cannot control which of your vital organs becomes a battleground. The result is an unpredictable, Russian roulette of auto-immune destruction. The takeaway is stark: The problem isn't just what's in the shot, but how the shot works. Until this fundamental delivery flaw is solved—if it ever can be—any future mRNA product deployed must be met with extreme skepticism and a resounding NO. This is not anti-vax. This is pro-science. It is a demand for safe, effective, and honestly tested medical technology.

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Top-Tier Journal Confirms Mechanism of COVID-19 Vaccine-Induced Heart Damage The conversation around vaccines is shifting, with HHS emphasizing informed consent over mandates. This new approach is having a direct market impact, with recent reports showing Pfizer and Moderna COVID-19 vaccine sales tumbling. The reason? The public is increasingly examining the science. A landmark study published in Circulation, the flagship journal of the American Heart Association and a top-tier cardiovascular publication, has delivered a critical finding. The research identifies the precise mechanism behind myocarditis and pericarditis following mRNA vaccination. Here is the breakdown in plain English: The study reveals that in certain susceptible individuals, the immune system's T cells—trained by the vaccine to attack the SARS-CoV-2 spike protein—also mistakenly attack similar-looking proteins in heart tissue. This phenomenon, known as "molecular mimicry," means the body's defenses cannot reliably distinguish the virus from the heart itself, leading to an autoimmune attack on the cardiac muscle. Crucially, the study found this specific, expanded immune response in patients with post-vaccine myopericarditis, but not in those who had developed myocarditis from a natural COVID-19 infection. The implications are profound. This is no longer a debate based on epidemiological signals or VAERS data. A leading mainstream medical journal has published a study pinpointing a direct autoimmune mechanism for vaccine-induced heart damage that is distinct from the damage caused by the virus. With this level of evidence now in the public domain, the call for a science-driven reassessment of vaccine policies has never been stronger. The argument has moved from the fringe to the forefront of established medical literature. The question now is: What will it take for health authorities to officially acknowledge these findings and adjust their recommendations accordingly?

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The Unsettling Scientific Silence on Aluminum Adjuvants A powerful point from Bret Weinstein highlights a critical failure in our public health dialogue: the refusal to properly study the systemic effects of aluminum adjuvants in vaccines. The core of his argument is not anti-vaccine; it is pro-science. He states that if injecting aluminum into muscle is safe, that is "a scientifically easy thing to establish." The fact that this foundational work remains conspicuously undone is a glaring red flag. So, what is an adjuvant? For the public, it's an additive designed to put the immune system on "high alert" so it reacts strongly to the vaccine's target antigen. But therein lies the potential danger. The alarm sounded by the aluminum is non-specific. The immune system knows it's under threat, but it doesn't know from what. This is a radical biological intervention. Weinstein, as an evolutionary biologist, posits a crucial question: Is this chronic, misdirected immune activation connected to the epidemic of modern ailments we see in younger generations? Could it be a driver of the proliferating allergies? Is it a factor in the rise of serious, sometimes fatal, autoimmune conditions like asthma? We simply do not know. These questions have not been properly investigated. The conclusion is inescapable: even if a vaccine is beneficial for the specific disease it targets, the net impact on a person's lifelong health could very well be negative. We are making a massive, population-scale bet without the necessary data. This isn't a conspiracy theory. It's a demand for rigorous, transparent science to answer a question that has been ignored for far too long.
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The Unsettling Scientific Silence on Aluminum Adjuvants A powerful point from Bret Weinstein highlights a critical failure in our public health dialogue: the refusal to properly study the systemic effects of aluminum adjuvants in vaccines. The core of his argument is not anti-vaccine; it is pro-science. He states that if injecting aluminum into muscle is safe, that is "a scientifically easy thing to establish." The fact that this foundational work remains conspicuously undone is a glaring red flag. So, what is an adjuvant? For the public, it's an additive designed to put the immune system on "high alert" so it reacts strongly to the vaccine's target antigen. But therein lies the potential danger. The alarm sounded by the aluminum is non-specific. The immune system knows it's under threat, but it doesn't know from what. This is a radical biological intervention. Weinstein, as an evolutionary biologist, posits a crucial question: Is this chronic, misdirected immune activation connected to the epidemic of modern ailments we see in younger generations? Could it be a driver of the proliferating allergies? Is it a factor in the rise of serious, sometimes fatal, autoimmune conditions like asthma? We simply do not know. These questions have not been properly investigated. The conclusion is inescapable: even if a vaccine is beneficial for the specific disease it targets, the net impact on a person's lifelong health could very well be negative. We are making a massive, population-scale bet without the necessary data. This isn't a conspiracy theory. It's a demand for rigorous, transparent science to answer a question that has been ignored for far too long.

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Bret Weinstein just delivered a truly chilling warning on Joe Rogan. MAHA needs to hear this: Myocarditis is only the “tip of the iceberg” with Covid-19 vaccine injuries. “mRNA is a haphazard, tissue-destroying technology.” “It’s like rolling the dice on destroying cells.” “If you take a bunch of boosters, each time you take one, you’re rolling the dice on losing a bunch of cells that you may or may not be able to afford losing.” “That includes things in the nervous system.” “It’s completely haphazard.” Bret Weinstein Joe Rogan
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Bret Weinstein just delivered a truly chilling warning on Joe Rogan. MAHA needs to hear this: Myocarditis is only the “tip of the iceberg” with Covid-19 vaccine injuries. “mRNA is a haphazard, tissue-destroying technology.” “It’s like rolling the dice on destroying cells.” “If you take a bunch of boosters, each time you take one, you’re rolling the dice on losing a bunch of cells that you may or may not be able to afford losing.” “That includes things in the nervous system.” “It’s completely haphazard.” Bret Weinstein Joe Rogan

Holden Culotta

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Bret Weinstein Reveals the Hidden Danger of mRNA Vaccines: "It’s Worse Than You Think" The mRNA platform was designed to make your cells produce a foreign protein—the spike—displaying it on their surface. But here’s the terrifying part: there’s no precision in where this happens. Your heart. Your brain. Your vital organs. Any cell can be hijacked to become a spike protein factory. And when your immune system sees these cells, it does what it’s programmed to do—attack them as if they’re infected by a virus. Myocarditis isn’t just a "side effect." It’s a symptom of your body literally destroying its own heart cells because they’ve been turned into targets. The inflammation? That’s collateral damage from an immune system forced to wage war on itself. This isn’t immunity. This is autoimmunity by design. And the worst part? No one knows the long-term consequences. —Bret Weinstein
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Bret Weinstein Reveals the Hidden Danger of mRNA Vaccines: "It’s Worse Than You Think" The mRNA platform was designed to make your cells produce a foreign protein—the spike—displaying it on their surface. But here’s the terrifying part: there’s no precision in where this happens. Your heart. Your brain. Your vital organs. Any cell can be hijacked to become a spike protein factory. And when your immune system sees these cells, it does what it’s programmed to do—attack them as if they’re infected by a virus. Myocarditis isn’t just a "side effect." It’s a symptom of your body literally destroying its own heart cells because they’ve been turned into targets. The inflammation? That’s collateral damage from an immune system forced to wage war on itself. This isn’t immunity. This is autoimmunity by design. And the worst part? No one knows the long-term consequences. —Bret Weinstein

Camus

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Professor Emeritus Yasufumi Murakami of Tokyo University of Science: "It is almost certain that vaccines are contaminated with DNA. mRNA vaccines containing the DNA causes turbo cancers." Professor Murakami explains the mechanism of turbo cancers: The covid vaccines are expected to contain only mRNA. However, it has been proven that the vaccines contain considerable amounts of DNA and other substances that should not be present. There is no doubt about it now. DNA can enter human cells very easily, regardless of length, and can get into cells everywhere. When DNA gets in the center of an important gene, the important gene will stop functioning. One problem is that the mRNA vaccine of Pfizer contains a promoter sequence of the cancer virus called SV40. This sequence could enter the human genome, and awakens and activates dormant carcinogenic genes. As a result, the risk of developing cancer increases. mRNA vaccines increase the risk of developing cancer while suppressing the immunity. Vaccination increases the risk of developing cancer dramatically compared to the unvaccinated state. The more people get vaccinated, the more people will probably get cancer. Vaccines appear to increase the risk of all types of cancers. There is credible information that the number of leukemia cases is on the rise. Vaccination causes the promoter sequence of the cancer virus to enter white blood cells and attach to red blood cells everywhere. As a result, more and more leukemia cases are reported. A lot of spikes of mRNA are produced. The spikes would be most protected from destruction. Possibly, long spike genes remain intact. So, if the long spike genes remain there, gene expression will continue to take place all the time. That is, spikes are generated forever. Once the DNA gets into the stem cells, the DNA will keep creating more and more spikes. As a result, IgG4 antibodies are induced. The number of spike-producing cells will not decrease, and it becomes impossible to get rid of spike-producing cells. As a results, It becomes normal for spikes to be present in cells. The produced spikes then flow into the bloodstream and cause a variety of health problems. So, any vaccine that induces IgG4 is deemed as a defective vaccine, and should no longer be produced. Normally, cancer cells are born and grow slowly. However, the vaccine suppresses the immunity, which makes it easier for cancer cells to grow. The vaccines cause turbo cancers. Suppression of the immunity is a major factor of turbo cancers. The increase in IgG4 antibodies results in suppression of cancer immunity. The more DNA the vaccine contains, the more intense the inflammation caused by the vaccine becomes. DNA is a foreign substance to the cells. So, DNA causes a severe reaction and kills the immune system of the cells. The more DNA the vaccine contains, the more severe the side effects caused by the vaccine become. Vaccines could contain many different impurities, but one possibility could be DNA. In the first place, DNA is something that should not be put into cells of your body.
6:34

Professor Emeritus Yasufumi Murakami of Tokyo University of Science: "It is almost certain that vaccines are contaminated with DNA. mRNA vaccines containing the DNA causes turbo cancers." Professor Murakami explains the mechanism of turbo cancers: The covid vaccines are expected to contain only mRNA. However, it has been proven that the vaccines contain considerable amounts of DNA and other substances that should not be present. There is no doubt about it now. DNA can enter human cells very easily, regardless of length, and can get into cells everywhere. When DNA gets in the center of an important gene, the important gene will stop functioning. One problem is that the mRNA vaccine of Pfizer contains a promoter sequence of the cancer virus called SV40. This sequence could enter the human genome, and awakens and activates dormant carcinogenic genes. As a result, the risk of developing cancer increases. mRNA vaccines increase the risk of developing cancer while suppressing the immunity. Vaccination increases the risk of developing cancer dramatically compared to the unvaccinated state. The more people get vaccinated, the more people will probably get cancer. Vaccines appear to increase the risk of all types of cancers. There is credible information that the number of leukemia cases is on the rise. Vaccination causes the promoter sequence of the cancer virus to enter white blood cells and attach to red blood cells everywhere. As a result, more and more leukemia cases are reported. A lot of spikes of mRNA are produced. The spikes would be most protected from destruction. Possibly, long spike genes remain intact. So, if the long spike genes remain there, gene expression will continue to take place all the time. That is, spikes are generated forever. Once the DNA gets into the stem cells, the DNA will keep creating more and more spikes. As a result, IgG4 antibodies are induced. The number of spike-producing cells will not decrease, and it becomes impossible to get rid of spike-producing cells. As a results, It becomes normal for spikes to be present in cells. The produced spikes then flow into the bloodstream and cause a variety of health problems. So, any vaccine that induces IgG4 is deemed as a defective vaccine, and should no longer be produced. Normally, cancer cells are born and grow slowly. However, the vaccine suppresses the immunity, which makes it easier for cancer cells to grow. The vaccines cause turbo cancers. Suppression of the immunity is a major factor of turbo cancers. The increase in IgG4 antibodies results in suppression of cancer immunity. The more DNA the vaccine contains, the more intense the inflammation caused by the vaccine becomes. DNA is a foreign substance to the cells. So, DNA causes a severe reaction and kills the immune system of the cells. The more DNA the vaccine contains, the more severe the side effects caused by the vaccine become. Vaccines could contain many different impurities, but one possibility could be DNA. In the first place, DNA is something that should not be put into cells of your body.

You

574,563 Aufrufe • vor 2 Jahren

Dr. Ryan Cole Issues Grave Warning: Mechanistic Link Between mRNA Vaccines and Cancer Formation Explained The alarming rise in aggressive cancers post-pandemic is no longer a mere statistical anomaly. It is a phenomenon with a plausible biological explanation, rooted in the fundamental mechanics of the immune system and the unique properties of mRNA COVID-19 vaccines. According to renowned clinical pathologist and immunologist, Dr. Ryan Cole, the issue is not one of simple coincidence but of direct mechanistic interference. The body’s sophisticated defense network is being suppressed and reprogrammed, creating a permissive environment for the initiation and proliferation of cancerous cells. Here is a breakdown of the mechanisms at play, as explained by Dr. Cole: 1. The Suppression of the Body’s "Marines" At any given moment, the human body circulates approximately 30 billion T-cells. This army includes "killer" cells whose sole purpose is to identify and destroy pathogenic invaders and, critically, atypical or cancerous cells. These cells, along with macrophages and dendritic cells, act as a constant surveillance unit, patrolling the body to clear threats. Dr. Cole states that post-vaccination, there is a significant suppression of these critical immune cell lines. The very technology designed to evoke an immune response initially suppresses it, crippling the front-line defenses that would normally identify and eliminate pre-cancerous cells before they can form tumors. 2. The Stealth Technology: Pseudouridine and Immune Evasion The core of the issue lies in the synthetic design of the mRNA shot. Natural mRNA is quickly recognized and broken down by the body. To circumvent this, vaccine manufacturers modified the RNA code by incorporating pseudouridine. "This is not natural," Dr. Cole emphasizes. "This synthetic sequence is packaged in a lipid nanoparticle and deliberately engineered to evade the immune system. Your body doesn't immediately recognize it as a threat, which is a form of initial immune suppression." This evasion allows the synthetic mRNA to hijack the body's own cells, turning them into factories that mass-produce the SARS-CoV-2 spike protein. 3. Persistent Antigen Production and Circulating Spike Unlike natural mRNA, which degrades in minutes to hours, peer-reviewed research from institutions like Stanford University (Dr. Röltgen et al.) has demonstrated that the synthetic mRNA from vaccines persists in lymph nodes for at least 60 days. The duration beyond that is unknown, as studies stopped there. This means the body is forced to continuously produce the spike protein for an extended, unnatural period. Furthermore, the spike protein does not remain localized; it cleaves off from the cells and enters systemic circulation, creating a constant state of inflammatory stress and immune activation. 4. The Critical Downregulation of Toll-like Receptors (TLRs) Perhaps one of the most concerning mechanisms is the impact on the body's signaling system. Toll-like Receptors (TLRs) are like the "toll roads" of the immune system—they are pattern recognition receptors that alert the body to different types of threats and orchestrate the appropriate defensive response. Citing a pivotal study from the Netherlands by Dr. Fassa, Dr. Cole highlights that the mRNA vaccine leads to the downregulation of key TLRs, specifically numbers 3, 4, 7, and 8. "This is devastating," he explains. "TLRs 7 and 8 are crucial for antiviral defense. But the suppression of TLRs 3 and 4 is directly associated with cancer pathogenesis. When you see a dropout of these receptors, you see a loss of immune surveillance against tumors." Aggressive breast cancers, prostate cancers, and leukemias are frequently found to have downregulated these specific Toll-like receptors. The vaccine appears to be inducing a biological state that mimics the immunosuppressed environment seen in these cancers. 5. Additional Pathways to Mutagenesis The cascade of dysfunction does not end there. The pseudouridine modification has also been shown to disrupt vital cellular communication pathways, including: - Protein Kinase Pathways: Essential for regulating cell growth, division, and survival. - Retinoic Acid Receptor Pathways: Critical for cell differentiation and apoptosis (programmed cell death). Disruption in these pathways can lead to uncontrolled cell proliferation and impaired ability to clear damaged cells—hallmarks of cancer initiation. Conclusion: A Perfect Storm for Oncogenesis Dr. Ryan Cole concludes that we are witnessing a "perfect storm" created by these interventions. The synthetic mRNA and lipid nanoparticles trigger a multi-faceted assault on immune competence: - Suppression of killer T-cells and natural killer cells. - Persistent production of an inflammatory antigen (spike protein). - Downregulation of critical cancer-fighting Toll-like Receptors. - Disruption of core cellular signaling and regulatory pathways. The result is a body less capable of performing its constant, natural duty of cancer surveillance and destruction. This is not speculation; it is a mechanistic explanation based on emerging science for the troubling oncological trends being observed globally. The claim demands urgent, independent investigation free from political or commercial influence.
4:43

Dr. Ryan Cole Issues Grave Warning: Mechanistic Link Between mRNA Vaccines and Cancer Formation Explained The alarming rise in aggressive cancers post-pandemic is no longer a mere statistical anomaly. It is a phenomenon with a plausible biological explanation, rooted in the fundamental mechanics of the immune system and the unique properties of mRNA COVID-19 vaccines. According to renowned clinical pathologist and immunologist, Dr. Ryan Cole, the issue is not one of simple coincidence but of direct mechanistic interference. The body’s sophisticated defense network is being suppressed and reprogrammed, creating a permissive environment for the initiation and proliferation of cancerous cells. Here is a breakdown of the mechanisms at play, as explained by Dr. Cole: 1. The Suppression of the Body’s "Marines" At any given moment, the human body circulates approximately 30 billion T-cells. This army includes "killer" cells whose sole purpose is to identify and destroy pathogenic invaders and, critically, atypical or cancerous cells. These cells, along with macrophages and dendritic cells, act as a constant surveillance unit, patrolling the body to clear threats. Dr. Cole states that post-vaccination, there is a significant suppression of these critical immune cell lines. The very technology designed to evoke an immune response initially suppresses it, crippling the front-line defenses that would normally identify and eliminate pre-cancerous cells before they can form tumors. 2. The Stealth Technology: Pseudouridine and Immune Evasion The core of the issue lies in the synthetic design of the mRNA shot. Natural mRNA is quickly recognized and broken down by the body. To circumvent this, vaccine manufacturers modified the RNA code by incorporating pseudouridine. "This is not natural," Dr. Cole emphasizes. "This synthetic sequence is packaged in a lipid nanoparticle and deliberately engineered to evade the immune system. Your body doesn't immediately recognize it as a threat, which is a form of initial immune suppression." This evasion allows the synthetic mRNA to hijack the body's own cells, turning them into factories that mass-produce the SARS-CoV-2 spike protein. 3. Persistent Antigen Production and Circulating Spike Unlike natural mRNA, which degrades in minutes to hours, peer-reviewed research from institutions like Stanford University (Dr. Röltgen et al.) has demonstrated that the synthetic mRNA from vaccines persists in lymph nodes for at least 60 days. The duration beyond that is unknown, as studies stopped there. This means the body is forced to continuously produce the spike protein for an extended, unnatural period. Furthermore, the spike protein does not remain localized; it cleaves off from the cells and enters systemic circulation, creating a constant state of inflammatory stress and immune activation. 4. The Critical Downregulation of Toll-like Receptors (TLRs) Perhaps one of the most concerning mechanisms is the impact on the body's signaling system. Toll-like Receptors (TLRs) are like the "toll roads" of the immune system—they are pattern recognition receptors that alert the body to different types of threats and orchestrate the appropriate defensive response. Citing a pivotal study from the Netherlands by Dr. Fassa, Dr. Cole highlights that the mRNA vaccine leads to the downregulation of key TLRs, specifically numbers 3, 4, 7, and 8. "This is devastating," he explains. "TLRs 7 and 8 are crucial for antiviral defense. But the suppression of TLRs 3 and 4 is directly associated with cancer pathogenesis. When you see a dropout of these receptors, you see a loss of immune surveillance against tumors." Aggressive breast cancers, prostate cancers, and leukemias are frequently found to have downregulated these specific Toll-like receptors. The vaccine appears to be inducing a biological state that mimics the immunosuppressed environment seen in these cancers. 5. Additional Pathways to Mutagenesis The cascade of dysfunction does not end there. The pseudouridine modification has also been shown to disrupt vital cellular communication pathways, including: - Protein Kinase Pathways: Essential for regulating cell growth, division, and survival. - Retinoic Acid Receptor Pathways: Critical for cell differentiation and apoptosis (programmed cell death). Disruption in these pathways can lead to uncontrolled cell proliferation and impaired ability to clear damaged cells—hallmarks of cancer initiation. Conclusion: A Perfect Storm for Oncogenesis Dr. Ryan Cole concludes that we are witnessing a "perfect storm" created by these interventions. The synthetic mRNA and lipid nanoparticles trigger a multi-faceted assault on immune competence: - Suppression of killer T-cells and natural killer cells. - Persistent production of an inflammatory antigen (spike protein). - Downregulation of critical cancer-fighting Toll-like Receptors. - Disruption of core cellular signaling and regulatory pathways. The result is a body less capable of performing its constant, natural duty of cancer surveillance and destruction. This is not speculation; it is a mechanistic explanation based on emerging science for the troubling oncological trends being observed globally. The claim demands urgent, independent investigation free from political or commercial influence.

Camus

67,994 Aufrufe • vor 10 Monaten

According to evolutionary biologist Brett Weinstein, the common narrative is dangerously misguided. The prediction that another serious pandemic is inevitable is not a fact of nature, but a probable consequence of our actions. Weinstein argues that the risk of a future pandemic requiring a radical, global response is "tightly correlated with our cryptic bioweapons research," often disguised in the U.S. as "dual-use research of concern." Were this research halted, the likelihood of a naturally occurring virus necessitating a rapid vaccine deployment is "surprisingly low." He dismantles the historical precedent often used to justify pandemic preparedness, citing the 1918 flu. Many deaths, he notes, were due to bacterial pneumonia (now treatable with antibiotics) and fatal overdoses of the then-new "wonder drug," aspirin. A similar event today would not have the same catastrophic outcome. Furthermore, Weinstein issues a stark warning on the mRNA vaccine platform itself. While it solves the problem of rapid deployment, it carries a fundamental flaw: it presents a very narrow antigenic target. Unlike natural immunity, which recognizes the entire virus, this narrow focus gives the virus an "easy problem to solve evolutionarily." This means that rather than ending a pandemic, a narrowly targeted vaccine can actively drive viral evolution, potentially prolonging the crisis it was meant to solve. The conclusion is chilling: The greatest pandemic risk may be anthropogenic. And the very technology hailed as our salvation may be inherently flawed, creating a dangerous evolutionary arms race against the virus. The question is no longer if we are prepared for the next pandemic, but whether our current path is making it more likely—and more dangerous.
3:26

According to evolutionary biologist Brett Weinstein, the common narrative is dangerously misguided. The prediction that another serious pandemic is inevitable is not a fact of nature, but a probable consequence of our actions. Weinstein argues that the risk of a future pandemic requiring a radical, global response is "tightly correlated with our cryptic bioweapons research," often disguised in the U.S. as "dual-use research of concern." Were this research halted, the likelihood of a naturally occurring virus necessitating a rapid vaccine deployment is "surprisingly low." He dismantles the historical precedent often used to justify pandemic preparedness, citing the 1918 flu. Many deaths, he notes, were due to bacterial pneumonia (now treatable with antibiotics) and fatal overdoses of the then-new "wonder drug," aspirin. A similar event today would not have the same catastrophic outcome. Furthermore, Weinstein issues a stark warning on the mRNA vaccine platform itself. While it solves the problem of rapid deployment, it carries a fundamental flaw: it presents a very narrow antigenic target. Unlike natural immunity, which recognizes the entire virus, this narrow focus gives the virus an "easy problem to solve evolutionarily." This means that rather than ending a pandemic, a narrowly targeted vaccine can actively drive viral evolution, potentially prolonging the crisis it was meant to solve. The conclusion is chilling: The greatest pandemic risk may be anthropogenic. And the very technology hailed as our salvation may be inherently flawed, creating a dangerous evolutionary arms race against the virus. The question is no longer if we are prepared for the next pandemic, but whether our current path is making it more likely—and more dangerous.

Camus

21,802 Aufrufe • vor 10 Monaten

🚨 RFK Jr. reveals the Covid shots may have PROLONGED the pandemic—and reveals why HHS halted all mRNA shots for upper respiratory viruses: “The public health agencies have not been honest.” “There’s over 5,000 peer-reviewed studies that are documenting injuries or supposed injuries from the vaccine.” “This is the reason that we discontinued the platform—again, only for upper respiratory.” “It did not prove very effective during Covid.” “It targets a single protein, which means that all the virus has to do is to mutate out that protein, and then the virus is immune to the vaccine.” “That's what happened with Omicron." “It actually encourages the virus to mutate and prolongs the pandemic.” “What the mRNA vaccine does is it turns your body into an antigen factory, and … [it could] end up in organs where it’s not supposed to work and cause injury.” Secretary Kennedy
2:52

🚨 RFK Jr. reveals the Covid shots may have PROLONGED the pandemic—and reveals why HHS halted all mRNA shots for upper respiratory viruses: “The public health agencies have not been honest.” “There’s over 5,000 peer-reviewed studies that are documenting injuries or supposed injuries from the vaccine.” “This is the reason that we discontinued the platform—again, only for upper respiratory.” “It did not prove very effective during Covid.” “It targets a single protein, which means that all the virus has to do is to mutate out that protein, and then the virus is immune to the vaccine.” “That's what happened with Omicron." “It actually encourages the virus to mutate and prolongs the pandemic.” “What the mRNA vaccine does is it turns your body into an antigen factory, and … [it could] end up in organs where it’s not supposed to work and cause injury.” Secretary Kennedy

Children’s Health Defense

125,689 Aufrufe • vor 7 Monaten

A chilling warning from Brussels: The foundational flaw in mRNA technology that the public was never told. At the launch of Make Europe Healthy Again, researcher Panagis Polykretis delivered a critical message the world needs to hear. While the pharmaceutical industry rushes to expand mRNA use for its speed and profit, a fundamental immunological principle is being overlooked: Any cell that produces a foreign protein is marked for destruction by the immune system. This isn't theoretical. Clear histopathological evidence from biopsies and autopsies confirms the vaccine's genetic material does not stay at the injection site. It enters systemic circulation and spreads uncontrollably throughout the body, including to vital organs like the brain and heart. Once there, the body's own cells are forced to produce the foreign antigen, triggering an immune attack on its own tissues. This is the mechanism behind serious adverse effects, such as myocarditis—a condition Polykretis was the first to hypothesize from the mRNA vaccines. Most alarmingly, this was known. The European Medicines Agency's own assessment report (Pfizer study 185350) from Feb 19, 2021, states on page 47 that biodistribution in rats to most tissues occurred within 48 hours. They knew. Yet, millions across Europe, including pregnant women and infants, were inoculated with these products. This mass experiment was enabled by the silence of the scientific majority. The time for accountability and rigorous, long-term safety studies is now, before this technology is expanded further.
2:26

A chilling warning from Brussels: The foundational flaw in mRNA technology that the public was never told. At the launch of Make Europe Healthy Again, researcher Panagis Polykretis delivered a critical message the world needs to hear. While the pharmaceutical industry rushes to expand mRNA use for its speed and profit, a fundamental immunological principle is being overlooked: Any cell that produces a foreign protein is marked for destruction by the immune system. This isn't theoretical. Clear histopathological evidence from biopsies and autopsies confirms the vaccine's genetic material does not stay at the injection site. It enters systemic circulation and spreads uncontrollably throughout the body, including to vital organs like the brain and heart. Once there, the body's own cells are forced to produce the foreign antigen, triggering an immune attack on its own tissues. This is the mechanism behind serious adverse effects, such as myocarditis—a condition Polykretis was the first to hypothesize from the mRNA vaccines. Most alarmingly, this was known. The European Medicines Agency's own assessment report (Pfizer study 185350) from Feb 19, 2021, states on page 47 that biodistribution in rats to most tissues occurred within 48 hours. They knew. Yet, millions across Europe, including pregnant women and infants, were inoculated with these products. This mass experiment was enabled by the silence of the scientific majority. The time for accountability and rigorous, long-term safety studies is now, before this technology is expanded further.

Camus

103,305 Aufrufe • vor 8 Monaten

"It's Over". Bombshell report speaks to EXACTLY why they fought so hard to keep Pfizer's Bio Distribution data hidden, because that's the mechanism of harm. A new study done by one of the top mainstream institutions, just proved mechanistically how mRNA covid 'vaccines' induce auto immune attack "of self" and the heart, leading to vaccine induced myocarditis. Jefferey Jaxen speaks on the The HighWire with Del Bigtree: "They say post mRNA vaccine myopericarditis is driven by molecular mimicry, so the immune system cannot determine self from non self [so] It's attacking itself [in] susceptible patients" "Well what makes patients susceptible? It goes on to say in this next line, mRNA vaccine distribution, the fact that this vaccine goes everywhere, is what makes patients susceptible" "A heat seeking missile of immune response, an anti heart autoimmune response is what's happening" "This journal is not a fringe journal [it's] the No. 3 journal in the world [so] this is the big kahuna, and they're saying this. It's over ... it's over at this point"
4:55

"It's Over". Bombshell report speaks to EXACTLY why they fought so hard to keep Pfizer's Bio Distribution data hidden, because that's the mechanism of harm. A new study done by one of the top mainstream institutions, just proved mechanistically how mRNA covid 'vaccines' induce auto immune attack "of self" and the heart, leading to vaccine induced myocarditis. Jefferey Jaxen speaks on the The HighWire with Del Bigtree: "They say post mRNA vaccine myopericarditis is driven by molecular mimicry, so the immune system cannot determine self from non self [so] It's attacking itself [in] susceptible patients" "Well what makes patients susceptible? It goes on to say in this next line, mRNA vaccine distribution, the fact that this vaccine goes everywhere, is what makes patients susceptible" "A heat seeking missile of immune response, an anti heart autoimmune response is what's happening" "This journal is not a fringe journal [it's] the No. 3 journal in the world [so] this is the big kahuna, and they're saying this. It's over ... it's over at this point"

Humanspective

467,068 Aufrufe • vor 8 Monaten

Bret Weinstein Raises Alarming Questions About Vaccine Adjuvants and Immune System Risks Dr. Bret Weinstein, evolutionary biologist and outspoken thinker, recently shared a provocative perspective on the use of adjuvants in vaccines, questioning their safety and broader implications for public health. In a world where inflammation is increasingly recognized as a driver of chronic disease, Weinstein argues that the deliberate use of adjuvants—substances like aluminum designed to hyperactivate the immune system—raises serious concerns that demand scrutiny. “When I first learned what an adjuvant was, I was stunned,” Weinstein said. “We’re using a trick to whip the immune system into overdrive just to make vaccines work. My immediate thought was: How could this possibly be safe? We’re inciting inflammation—nonspecifically—knowing full well that inflammation is the bad guy in so many health contexts. It’s like setting a controlled fire in a forest and hoping it doesn’t spread.” Weinstein’s critique centers on aluminum, the most commonly used adjuvant in vaccines. Aluminum is added to vaccines to provoke a stronger immune response to antigens that might otherwise be ignored by the body. But this deliberate immune provocation, Weinstein warns, comes with risks that are poorly understood and rarely discussed. “If you’re injecting aluminum to hyperactivate someone’s immune system, you’re rolling the dice on what else that system might start reacting to,” he said. “What’s stopping it from targeting harmless substances—like pollen, peanuts, or ragweed—and triggering lifelong allergies or autoimmune conditions?” The lack of clear guidance for patients receiving vaccines with adjuvants is a particular point of concern for Weinstein. “If we’re going to use a substance as potent as aluminum, there should be a detailed protocol,” he insisted. “Instructions like: Avoid certain foods for two weeks. Don’t get this shot during allergy season. Monitor for signs of immune dysregulation. Something! Yet, we hand out these shots like candy, with no cautionary roadmap to minimize the risk of the immune system going haywire.” Weinstein’s questions strike at the heart of a growing public health puzzle: the dramatic rise in allergies and autoimmune disorders. Could the nonspecific immune activation caused by adjuvants be a missing piece in this mystery? “We’re scratching our heads over why allergies are skyrocketing, yet we’re systematically provoking the immune system in ways that could plausibly misfire,” he said. “It’s not a conspiracy—it’s a failure to ask obvious questions.” Calling for greater transparency and research, Weinstein urges the scientific community to confront these issues head-on. “We need to study the long-term effects of adjuvants rigorously,” he said. “If we’re going to play with the immune system’s fire, we’d better understand how to keep it from burning the house down.”
1:27

Bret Weinstein Raises Alarming Questions About Vaccine Adjuvants and Immune System Risks Dr. Bret Weinstein, evolutionary biologist and outspoken thinker, recently shared a provocative perspective on the use of adjuvants in vaccines, questioning their safety and broader implications for public health. In a world where inflammation is increasingly recognized as a driver of chronic disease, Weinstein argues that the deliberate use of adjuvants—substances like aluminum designed to hyperactivate the immune system—raises serious concerns that demand scrutiny. “When I first learned what an adjuvant was, I was stunned,” Weinstein said. “We’re using a trick to whip the immune system into overdrive just to make vaccines work. My immediate thought was: How could this possibly be safe? We’re inciting inflammation—nonspecifically—knowing full well that inflammation is the bad guy in so many health contexts. It’s like setting a controlled fire in a forest and hoping it doesn’t spread.” Weinstein’s critique centers on aluminum, the most commonly used adjuvant in vaccines. Aluminum is added to vaccines to provoke a stronger immune response to antigens that might otherwise be ignored by the body. But this deliberate immune provocation, Weinstein warns, comes with risks that are poorly understood and rarely discussed. “If you’re injecting aluminum to hyperactivate someone’s immune system, you’re rolling the dice on what else that system might start reacting to,” he said. “What’s stopping it from targeting harmless substances—like pollen, peanuts, or ragweed—and triggering lifelong allergies or autoimmune conditions?” The lack of clear guidance for patients receiving vaccines with adjuvants is a particular point of concern for Weinstein. “If we’re going to use a substance as potent as aluminum, there should be a detailed protocol,” he insisted. “Instructions like: Avoid certain foods for two weeks. Don’t get this shot during allergy season. Monitor for signs of immune dysregulation. Something! Yet, we hand out these shots like candy, with no cautionary roadmap to minimize the risk of the immune system going haywire.” Weinstein’s questions strike at the heart of a growing public health puzzle: the dramatic rise in allergies and autoimmune disorders. Could the nonspecific immune activation caused by adjuvants be a missing piece in this mystery? “We’re scratching our heads over why allergies are skyrocketing, yet we’re systematically provoking the immune system in ways that could plausibly misfire,” he said. “It’s not a conspiracy—it’s a failure to ask obvious questions.” Calling for greater transparency and research, Weinstein urges the scientific community to confront these issues head-on. “We need to study the long-term effects of adjuvants rigorously,” he said. “If we’re going to play with the immune system’s fire, we’d better understand how to keep it from burning the house down.”

Camus

50,259 Aufrufe • vor 1 Jahr

Del Bigtree on the Autoimmune Crisis: The Vaccine Factor? Del Bigtree warns we're on the brink of losing our species to an immune system in chaos. No other mammal suffers like us—autoimmune diseases are skyrocketing, where our own immune systems attack our bodies, especially our children’s. It's not the fluoride or pesticides—this is about the 72 injections that repeatedly trick our immune system into thinking it’s battling disease. Imagine being injected 72 times with proteins and aluminum, which act as false enemies, confusing the immune system. Aluminum’s role? It stokes the immune response—telling the body, "Every protein you see is the enemy." Now, combine that with everyday foods—eggs, peanuts, cheese—suddenly the body is attacking those too, creating severe allergies and a surge in immune confusion. Allergies are getting worse because of this constant immune provocation and harmful vaccine ingredients. This is not just a theory; it’s an urgent signal we can no longer ignore. The time to rethink injecting aluminum-laden vaccines is now—before the immune system’s confusion claims more lives. Del Bigtree’s call echoes with urgency: It's time to stop this immune attack cycle and protect future generations from this escalating crisis. The truth about vaccines and autoimmune disease demands our attention—because what we’re seeing is a species under siege.
2:00

Del Bigtree on the Autoimmune Crisis: The Vaccine Factor? Del Bigtree warns we're on the brink of losing our species to an immune system in chaos. No other mammal suffers like us—autoimmune diseases are skyrocketing, where our own immune systems attack our bodies, especially our children’s. It's not the fluoride or pesticides—this is about the 72 injections that repeatedly trick our immune system into thinking it’s battling disease. Imagine being injected 72 times with proteins and aluminum, which act as false enemies, confusing the immune system. Aluminum’s role? It stokes the immune response—telling the body, "Every protein you see is the enemy." Now, combine that with everyday foods—eggs, peanuts, cheese—suddenly the body is attacking those too, creating severe allergies and a surge in immune confusion. Allergies are getting worse because of this constant immune provocation and harmful vaccine ingredients. This is not just a theory; it’s an urgent signal we can no longer ignore. The time to rethink injecting aluminum-laden vaccines is now—before the immune system’s confusion claims more lives. Del Bigtree’s call echoes with urgency: It's time to stop this immune attack cycle and protect future generations from this escalating crisis. The truth about vaccines and autoimmune disease demands our attention—because what we’re seeing is a species under siege.

Camus

30,746 Aufrufe • vor 8 Monaten

The REAL reason why "the mRNA platform is so dangerous" - Bret Weinstein explains. "So, why do you get myocarditis from an mRNA shot? It doesn't have anything to do with spike. Spike, maybe making the problem worse, but the fact that your heart cells are producing a foreign protein means that your your immune system will spot them as virally infected and it will destroy them and myocarditis is not the problem... myocarditis is a symptom." Watch the full "What Jessica Rose Knows" Inside Rail episode on DarkHorse available on all popular podcast platforms, Youtube, Locals, and Rumble.
3:00

The REAL reason why "the mRNA platform is so dangerous" - Bret Weinstein explains. "So, why do you get myocarditis from an mRNA shot? It doesn't have anything to do with spike. Spike, maybe making the problem worse, but the fact that your heart cells are producing a foreign protein means that your your immune system will spot them as virally infected and it will destroy them and myocarditis is not the problem... myocarditis is a symptom." Watch the full "What Jessica Rose Knows" Inside Rail episode on DarkHorse available on all popular podcast platforms, Youtube, Locals, and Rumble.

The DarkHorse Podcast

389,385 Aufrufe • vor 1 Jahr