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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...

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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.
1:23

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.

Camus

20,160 görüntüleme • 10 ay önce

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.
2:34

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.

Camus

41,604 görüntüleme • 10 ay önce

Dr. Patrick Soon-Shiong presents a fundamental paradigm shift in the war on cancer: we must stop destroying the immune system to save the body, and start supercharging it to achieve a permanent cure. The critical flaw of conventional chemotherapy and radiation is their inadvertent destruction of the very immune cells—the lymphocytes—designed to protect us. This often wins a battle but loses the war, leading to metastasis. The solution lies within us. Dr. Soon-Shiong’s work harnesses "God's design": the power of Natural Killer (NK) cells and T-cells. The breakthrough is two-fold: 1. The Activation Key: For the first time, we can effectively activate these cells using a sustained-release form of IL-15, a natural protein. A single injection can create a tenfold increase in the body's innate cancer-killing army. 2. The Army Expansion: We can now draw a patient's blood, grow billions of targeted NK cells in a lab, and reinfuse them, creating a supercharged, augmented immune response. This is not an incremental improvement. It is a move away from the failed strategy of attacking cancer from the inside-out—blocking internal pathways that cancer easily bypasses—to shattering it from the outside-in. The result is data that speaks to a potential cure: patients with metastatic pancreatic cancer alive and disease-free after five years; bladder cancer patients thriving with their organs intact a decade after treatment; long-term remission in aggressive Merkel cell carcinoma. This approach teaches the immune system "T-cell memory," creating a permanent, living surveillance system that stands guard against recurrence. This is the path to long-term survival with quality of life.
5:44

Dr. Patrick Soon-Shiong presents a fundamental paradigm shift in the war on cancer: we must stop destroying the immune system to save the body, and start supercharging it to achieve a permanent cure. The critical flaw of conventional chemotherapy and radiation is their inadvertent destruction of the very immune cells—the lymphocytes—designed to protect us. This often wins a battle but loses the war, leading to metastasis. The solution lies within us. Dr. Soon-Shiong’s work harnesses "God's design": the power of Natural Killer (NK) cells and T-cells. The breakthrough is two-fold: 1. The Activation Key: For the first time, we can effectively activate these cells using a sustained-release form of IL-15, a natural protein. A single injection can create a tenfold increase in the body's innate cancer-killing army. 2. The Army Expansion: We can now draw a patient's blood, grow billions of targeted NK cells in a lab, and reinfuse them, creating a supercharged, augmented immune response. This is not an incremental improvement. It is a move away from the failed strategy of attacking cancer from the inside-out—blocking internal pathways that cancer easily bypasses—to shattering it from the outside-in. The result is data that speaks to a potential cure: patients with metastatic pancreatic cancer alive and disease-free after five years; bladder cancer patients thriving with their organs intact a decade after treatment; long-term remission in aggressive Merkel cell carcinoma. This approach teaches the immune system "T-cell memory," creating a permanent, living surveillance system that stands guard against recurrence. This is the path to long-term survival with quality of life.

Camus

103,022 görüntüleme • 9 ay önce

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 görüntüleme • 2 yıl önce

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.
4:16

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.

Camus

104,361 görüntüleme • 10 ay önce

It’s embarrassing to watch the TGA tie itself up in knots and contradict itself over the safety of the vaccine. The mRNA vaccine is designed to attack your own cells because the antigen sits on the cell membrane. The T-cell which responds to the vaccine antigen can’t separate your cell from the spike protein. It kills both and the TGA has already admitted as much in the past conceding myocarditis is an autoimmune response. The spike proteins are not rapidly degraded as numerous studies have shown they last in the body for up to 60 days. But more importantly the mRNA is designed to last much longer and produce more proteins. This means the body produces a much larger concentration of the toxic spike protein than what the virus would have delivered. And I quote from one study: “Later studies documented similar effects for 5-methylcytidine and 2-thiouridine and observed that modified mRNAs produced 10- to 100-fold more protein compared with unmodified mRNAs. Recently, N1-methylpseudouridine (m1Ψ), the modification used in the current mRNA SARS-CoV-2 vaccines, was found to possess superior characteristics to Ψ; m1Ψ elicited less immunogenicity and increased protein production by more than an order of magnitude relative to Ψ.” And another on the Poly-A tail increases the duration. “Whether for the mRNA vaccine from Pfizer/BioNtech® laboratories or that of Moderna®, the two mRNA sequences end in a Poly(A) tail. The purpose of this addition is to increase the stability of the mRNA in biological medium and also to allow the recruitment of the ribosome, in order to initiate an efficient translation. After translation, the mRNA can be reused several times, but when this happens, it also loses part of the Adenines of its Poly(A) tail, as enzymatic degradation begins there, which only ensures a transient protection against this degradation. When this tail is too degraded, the mRNA is no longer functional and is destroyed. The poly(A) tail stabilizes mRNA and boosts protein translation, and the length of the poly(A) tail is proportional to translation efficiency. It is a critical factor in determining the longevity of mRNA molecules.” Long story short - the TGA continues to lie. Quotes from: #auspol
2:19

It’s embarrassing to watch the TGA tie itself up in knots and contradict itself over the safety of the vaccine. The mRNA vaccine is designed to attack your own cells because the antigen sits on the cell membrane. The T-cell which responds to the vaccine antigen can’t separate your cell from the spike protein. It kills both and the TGA has already admitted as much in the past conceding myocarditis is an autoimmune response. The spike proteins are not rapidly degraded as numerous studies have shown they last in the body for up to 60 days. But more importantly the mRNA is designed to last much longer and produce more proteins. This means the body produces a much larger concentration of the toxic spike protein than what the virus would have delivered. And I quote from one study: “Later studies documented similar effects for 5-methylcytidine and 2-thiouridine and observed that modified mRNAs produced 10- to 100-fold more protein compared with unmodified mRNAs. Recently, N1-methylpseudouridine (m1Ψ), the modification used in the current mRNA SARS-CoV-2 vaccines, was found to possess superior characteristics to Ψ; m1Ψ elicited less immunogenicity and increased protein production by more than an order of magnitude relative to Ψ.” And another on the Poly-A tail increases the duration. “Whether for the mRNA vaccine from Pfizer/BioNtech® laboratories or that of Moderna®, the two mRNA sequences end in a Poly(A) tail. The purpose of this addition is to increase the stability of the mRNA in biological medium and also to allow the recruitment of the ribosome, in order to initiate an efficient translation. After translation, the mRNA can be reused several times, but when this happens, it also loses part of the Adenines of its Poly(A) tail, as enzymatic degradation begins there, which only ensures a transient protection against this degradation. When this tail is too degraded, the mRNA is no longer functional and is destroyed. The poly(A) tail stabilizes mRNA and boosts protein translation, and the length of the poly(A) tail is proportional to translation efficiency. It is a critical factor in determining the longevity of mRNA molecules.” Long story short - the TGA continues to lie. Quotes from: #auspol

Gerard Rennick

62,522 görüntüleme • 1 yıl önce

Chemotherapy kills the very cells the body uses to fight cancer. A surgeon and cancer researcher just said it out loud to a national audience, and the science backing him up is growing fast. Jefferey Jaxen opens with Dr. Patrick Soon-Shiong, who told Tucker Carlson that 99.9% of oncologists pay no attention to lymphocytes, the natural killer cells and T cells that are the immune system's actual weapon against cancer, and that chemotherapy's brief response is followed by metastasis because the treatment eliminates the body's protection. The research community is beginning to build in a different direction. Researchers at Trinity College Dublin have demonstrated that interferon gamma, a naturally occurring signaling protein that activates T cells and macrophages, can be used to train immune cells before they encounter a pathogen, thereby enhancing the killing of drug-resistant tuberculosis and MRSA staph infections in both healthy and genetically vulnerable individuals. The implications reach beyond antibiotic resistance: the same principle suggests that targeted immune training for immunosuppressed individuals could replace the current practice of blanket vaccination of entire populations to protect a few. Also reported last month, a UCLA study and subsequent meta-analysis found that honeybee venom and its primary protein, melittin, induced massive cell death in triple-negative and HER2-enriched breast cancer cell lines within 60 minutes of treatment, disrupting receptor pathways that aggressive breast cancers depend on. Melittin is globally available, cost-effective, and accessible in remote regions. None of these treatments are available off the shelf yet, but the direction of the research, working with the immune system and drawing from natural environments rather than suppressing the body's own defenses, represents a genuine paradigm shift that would have been unlikely to receive funding a decade ago.
11:52

Chemotherapy kills the very cells the body uses to fight cancer. A surgeon and cancer researcher just said it out loud to a national audience, and the science backing him up is growing fast. Jefferey Jaxen opens with Dr. Patrick Soon-Shiong, who told Tucker Carlson that 99.9% of oncologists pay no attention to lymphocytes, the natural killer cells and T cells that are the immune system's actual weapon against cancer, and that chemotherapy's brief response is followed by metastasis because the treatment eliminates the body's protection. The research community is beginning to build in a different direction. Researchers at Trinity College Dublin have demonstrated that interferon gamma, a naturally occurring signaling protein that activates T cells and macrophages, can be used to train immune cells before they encounter a pathogen, thereby enhancing the killing of drug-resistant tuberculosis and MRSA staph infections in both healthy and genetically vulnerable individuals. The implications reach beyond antibiotic resistance: the same principle suggests that targeted immune training for immunosuppressed individuals could replace the current practice of blanket vaccination of entire populations to protect a few. Also reported last month, a UCLA study and subsequent meta-analysis found that honeybee venom and its primary protein, melittin, induced massive cell death in triple-negative and HER2-enriched breast cancer cell lines within 60 minutes of treatment, disrupting receptor pathways that aggressive breast cancers depend on. Melittin is globally available, cost-effective, and accessible in remote regions. None of these treatments are available off the shelf yet, but the direction of the research, working with the immune system and drawing from natural environments rather than suppressing the body's own defenses, represents a genuine paradigm shift that would have been unlikely to receive funding a decade ago.

The HighWire

11,762 görüntüleme • 1 ay önce

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:
0:48

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:

Gary Brecka

51,737 görüntüleme • 1 yıl önce

Cancer Doctor Issues Urgent Warning The mRNA COVID-19 shots “should be completely banned! If they’re going to be used for anything, it has to be what they are, gene therapies.” Prof. Angus Dalgleish says there is a “fundamental flaw” with COVID-19 shots, and the flaw is that “it carries on for an indeterminate period of time.” What that means is the modified mRNA containing N1-methyl-pseudouridine (m1Ψ) allows the mRNA in the COVID shots to last in the body for an indefinite period of time, leading to an uncontrolled amount of spike protein production. The bottom line: There is a great likelihood that the shots are causing cancer. • Spike protein inhibits the activity of tumor suppressor genes. • Spike protein interferes with BRCA, which keeps ovarian and breast cancer in check. • The N1-methyl-pseudouridine (m1Ψ) in itself leads to immune suppression. Without the immune system working in full force, it creates conditions conducive to rapid cancer growth—or what some people refer to as “turbo cancer.” As such, Prof. Dalgleish says: “You should never use them [mRNA shots] in the general population as vaccines because they’re not.” “They [COVID shots] should be completely banned!”
2:46

Cancer Doctor Issues Urgent Warning The mRNA COVID-19 shots “should be completely banned! If they’re going to be used for anything, it has to be what they are, gene therapies.” Prof. Angus Dalgleish says there is a “fundamental flaw” with COVID-19 shots, and the flaw is that “it carries on for an indeterminate period of time.” What that means is the modified mRNA containing N1-methyl-pseudouridine (m1Ψ) allows the mRNA in the COVID shots to last in the body for an indefinite period of time, leading to an uncontrolled amount of spike protein production. The bottom line: There is a great likelihood that the shots are causing cancer. • Spike protein inhibits the activity of tumor suppressor genes. • Spike protein interferes with BRCA, which keeps ovarian and breast cancer in check. • The N1-methyl-pseudouridine (m1Ψ) in itself leads to immune suppression. Without the immune system working in full force, it creates conditions conducive to rapid cancer growth—or what some people refer to as “turbo cancer.” As such, Prof. Dalgleish says: “You should never use them [mRNA shots] in the general population as vaccines because they’re not.” “They [COVID shots] should be completely banned!”

The Vigilant Fox 🦊

717,008 görüntüleme • 2 yıl önce

"It Was Clear From The Beginning, The Illness Of COVID Was Actually All About The Vaccine...A Needle Into Every Arm." Dr Peter McCullough, MD The Vaccine Did Not Save Millions Of Lives...The Shots Contain A Killer Protein That Cannot Be Turned Off...It Was Not Safe By Design. The predominant COVID-19 vaccine platforms include messenger RNA (mRNA) Pfizer, Moderna, AstraZeneca, Johnson & Johnson, Novavax & Zifi Vax – mRNA & viral vector vaccines involve the bodily synthesis of the SARS-CoV-2 Spike protein as the foundation of the immune response. Regardless of the vaccine platform used, circulating SARS-CoV-2 Spike protein is the detrimental agent through which COVID-19 vaccines cause biological harm. Here Is The 'How & Why' Of The Spike Protein Mechanism That Leads To Harm & Death: Spike protein initiates the breakdown & internalization of ACE2 receptors, which disrupts the renin–angiotensin system (RAS) & lead to increased inflammation, vasoconstriction & thrombosis. Further, Spike protein stimulates platelets & inflicts damage to the endothelium, which leads to arterial & venous thrombosis. Immune cells that have absorbed the lipid nanoparticles (LNPs) subsequently reintroduce them into the bloodstream with a higher number of exosomes carrying microRNAs & Spike protein, resulting in drastic inflammation. Long term immune surveillance is compromised by mRNA COVID-19 vaccines due to IRF7, IRF9, p53 & BRCA suppression. There is a causal link between COVID-19 mRNA vaccination & myocarditis, neurodegenerative disease, immune thrombocytopenia, Bell's palsy, liver disease, impaired adaptive immunity, impeded DNA damage response and tumorigenesis. Moreover, a recent study found that repeated COVID-19 vaccination with mRNA-based vaccines leads to the production of abnormally high concentrations of IgG4 antibodies. These antibodies fail to neutralize Spike protein, which has been shown to circulate for at least 28 days, cause immune suppression & promote the development of autoimmune diseases including myocarditis. 👇Fatal COVID-19 Vaccine-Induced Myocarditis👇 👇Cardiac Arrest After COVID-19 Vaccination👇 👇DNA Fragments In Pfizer & Moderna Vaccines👇 Speaker: Peter A. McCullough, MD, MPH® McCullough Foundation
1:28

"It Was Clear From The Beginning, The Illness Of COVID Was Actually All About The Vaccine...A Needle Into Every Arm." Dr Peter McCullough, MD The Vaccine Did Not Save Millions Of Lives...The Shots Contain A Killer Protein That Cannot Be Turned Off...It Was Not Safe By Design. The predominant COVID-19 vaccine platforms include messenger RNA (mRNA) Pfizer, Moderna, AstraZeneca, Johnson & Johnson, Novavax & Zifi Vax – mRNA & viral vector vaccines involve the bodily synthesis of the SARS-CoV-2 Spike protein as the foundation of the immune response. Regardless of the vaccine platform used, circulating SARS-CoV-2 Spike protein is the detrimental agent through which COVID-19 vaccines cause biological harm. Here Is The 'How & Why' Of The Spike Protein Mechanism That Leads To Harm & Death: Spike protein initiates the breakdown & internalization of ACE2 receptors, which disrupts the renin–angiotensin system (RAS) & lead to increased inflammation, vasoconstriction & thrombosis. Further, Spike protein stimulates platelets & inflicts damage to the endothelium, which leads to arterial & venous thrombosis. Immune cells that have absorbed the lipid nanoparticles (LNPs) subsequently reintroduce them into the bloodstream with a higher number of exosomes carrying microRNAs & Spike protein, resulting in drastic inflammation. Long term immune surveillance is compromised by mRNA COVID-19 vaccines due to IRF7, IRF9, p53 & BRCA suppression. There is a causal link between COVID-19 mRNA vaccination & myocarditis, neurodegenerative disease, immune thrombocytopenia, Bell's palsy, liver disease, impaired adaptive immunity, impeded DNA damage response and tumorigenesis. Moreover, a recent study found that repeated COVID-19 vaccination with mRNA-based vaccines leads to the production of abnormally high concentrations of IgG4 antibodies. These antibodies fail to neutralize Spike protein, which has been shown to circulate for at least 28 days, cause immune suppression & promote the development of autoimmune diseases including myocarditis. 👇Fatal COVID-19 Vaccine-Induced Myocarditis👇 👇Cardiac Arrest After COVID-19 Vaccination👇 👇DNA Fragments In Pfizer & Moderna Vaccines👇 Speaker: Peter A. McCullough, MD, MPH® McCullough Foundation

Valerie Anne Smith

67,928 görüntüleme • 1 yıl önce

Dr. Patrick Soon-Shiong on the Cancer-Fighting Immune Breakthrough: Awakening the 450 Million-Year-Old Natural Killer Cell After decades of pioneering work since discovering the natural killer cell in the 1990s—a remarkable immune cell created by God and preserved through 450 million years—Dr. Patrick Soon-Shiong reveals an extraordinary breakthrough. This cell, unknown to many until the 1970s, serves as the body's first line of defense, designed to destroy cancer cells, infections like COVID, sepsis, bacteria, and fungus. Dr. Soon-Shiong emphasizes that this is not an invention, but an enlightenment: activating the body’s own natural killer cells to combat disease naturally, shifting away from toxic chemotherapy and radiation. With a single jab, they have unlocked the secret to empowering this primal cellular protector. This is evolution’s own weapon against illness, a game-changer that taps into ancient biology to revolutionize modern medicine. This insight reframes how we think about health and cancer treatment by harnessing the immune system's innate power, moving beyond harsh treatments, and embracing nature’s original disease-fighter from within. The discovery is a call to awaken the body’s own god-given defense system for a future of empowered healing.
1:58

Dr. Patrick Soon-Shiong on the Cancer-Fighting Immune Breakthrough: Awakening the 450 Million-Year-Old Natural Killer Cell After decades of pioneering work since discovering the natural killer cell in the 1990s—a remarkable immune cell created by God and preserved through 450 million years—Dr. Patrick Soon-Shiong reveals an extraordinary breakthrough. This cell, unknown to many until the 1970s, serves as the body's first line of defense, designed to destroy cancer cells, infections like COVID, sepsis, bacteria, and fungus. Dr. Soon-Shiong emphasizes that this is not an invention, but an enlightenment: activating the body’s own natural killer cells to combat disease naturally, shifting away from toxic chemotherapy and radiation. With a single jab, they have unlocked the secret to empowering this primal cellular protector. This is evolution’s own weapon against illness, a game-changer that taps into ancient biology to revolutionize modern medicine. This insight reframes how we think about health and cancer treatment by harnessing the immune system's innate power, moving beyond harsh treatments, and embracing nature’s original disease-fighter from within. The discovery is a call to awaken the body’s own god-given defense system for a future of empowered healing.

Camus

33,407 görüntüleme • 8 ay önce

Dr. Ryan Cole on COVID mRNA Injections: A Legacy of "Turbo Cancers," Autoimmune Chaos, and Shattered Fertility In a stark and sobering assessment, Dr. Ryan Cole outlines the devastating health crisis unfolding in the wake of the COVID-19 mRNA injections. What was sold as a "vaccine" has proven to be an experimental genetic experiment with consequences that will reverberate for a generation. The core of the crisis, according to Dr. Cole, lies in the fundamental flaws of the technology itself. These injections were not the clean, precise tools they were advertised to be. A Genetic Catastrophe: The shots were contaminated with DNA plasmids, and the synthetic RNA did not simply produce the intended spike protein. Instead, it led to the creation of "Frankenstein proteins"—aberrant molecules the human body was never designed to process. When the immune system is forced to confront these unnatural and unknown proteins, it loses its ability to self-regulate. The result? A ticking time bomb for chronic autoimmune disease, where the body begins to attack its own healthy tissues. The Human Cost: The data and clinical evidence, as Dr. Cole has meticulously tracked, reveal a harrowing trajectory: • "Turbo Cancers": Aggressive and rare cancers are appearing at unprecedented rates in young, otherwise healthy individuals. These are not typical progressions; they are runaway pathologies. • Excess Mortality: The stark rise in "sudden death" and death from all causes is an undeniable signal that something has gone terribly wrong on a global scale. • Fertility Collapse: Already plummeting fertility rates in many nations point to a direct assault on reproductive health, a silent crisis for the future of populations. The lesson is as clear as it is urgent. We must never again, as a global population, allow the widespread use of experimental synthetic RNA and genetic injections. The price of this failed experiment is being paid for in autoimmune suffering, turbo-cancer diagnoses, and a compromised future. The evidence is no longer anecdotal; it is epidemiological. The time for accountability is now.
1:23

Dr. Ryan Cole on COVID mRNA Injections: A Legacy of "Turbo Cancers," Autoimmune Chaos, and Shattered Fertility In a stark and sobering assessment, Dr. Ryan Cole outlines the devastating health crisis unfolding in the wake of the COVID-19 mRNA injections. What was sold as a "vaccine" has proven to be an experimental genetic experiment with consequences that will reverberate for a generation. The core of the crisis, according to Dr. Cole, lies in the fundamental flaws of the technology itself. These injections were not the clean, precise tools they were advertised to be. A Genetic Catastrophe: The shots were contaminated with DNA plasmids, and the synthetic RNA did not simply produce the intended spike protein. Instead, it led to the creation of "Frankenstein proteins"—aberrant molecules the human body was never designed to process. When the immune system is forced to confront these unnatural and unknown proteins, it loses its ability to self-regulate. The result? A ticking time bomb for chronic autoimmune disease, where the body begins to attack its own healthy tissues. The Human Cost: The data and clinical evidence, as Dr. Cole has meticulously tracked, reveal a harrowing trajectory: • "Turbo Cancers": Aggressive and rare cancers are appearing at unprecedented rates in young, otherwise healthy individuals. These are not typical progressions; they are runaway pathologies. • Excess Mortality: The stark rise in "sudden death" and death from all causes is an undeniable signal that something has gone terribly wrong on a global scale. • Fertility Collapse: Already plummeting fertility rates in many nations point to a direct assault on reproductive health, a silent crisis for the future of populations. The lesson is as clear as it is urgent. We must never again, as a global population, allow the widespread use of experimental synthetic RNA and genetic injections. The price of this failed experiment is being paid for in autoimmune suffering, turbo-cancer diagnoses, and a compromised future. The evidence is no longer anecdotal; it is epidemiological. The time for accountability is now.

Camus

18,349 görüntüleme • 8 ay önce

'mRNA COVID Vaccines Caused 74% Of Sudden Deaths Within 7 Days Of Vaccination & Many Within The 1st 72 Hours.' It Is The Largest Autopsy Series In The World. People Who Dropped Dead After The COVID-19 Vaccine, It Was Determined That 73.9% Of Individuals Died FROM The Vaccines. Causality in each case was determined by three independent reviewers with cardiac pathology experience & expertise. The number of days from last COVID-19 vaccination until death was 6.2 & 3 days, respectively. Most of the deaths occurred within a week from the last injection. The deaths were causally linked to COVID-19 vaccination by independent adjudication. The predominant COVID-19 vaccine platforms include messenger RNA (mRNA) Pfizer, Moderna, AstraZeneca, Johnson & Johnson, Novavax & Zifi Vax – mRNA & viral vector vaccines involve the bodily synthesis of the SARS-CoV-2 Spike protein as the foundation of the immune response. Regardless of the vaccine platform used, circulating SARS-CoV-2 Spike protein is the detrimental agent through which COVID-19 vaccines cause biological harm. Here Is The 'How & Why' Of The Spike Protein Mechanism That Leads To Harm & Death: Spike protein initiates the breakdown & internalization of ACE2 receptors, which disrupts the renin–angiotensin system (RAS) & lead to increased inflammation, vasoconstriction & thrombosis. Further, Spike protein stimulates platelets & inflicts damage to the endothelium, which leads to arterial & venous thrombosis. Immune cells that have absorbed the lipid nanoparticles (LNPs) subsequently reintroduce them into the bloodstream with a higher number of exosomes carrying microRNAs & Spike protein, resulting in drastic inflammation. Long term immune surveillance is compromised by mRNA COVID-19 vaccines due to IRF7, IRF9, p53 & BRCA suppression. There is a causal link between COVID-19 mRNA vaccination & myocarditis, neurodegenerative disease, immune thrombocytopenia, Bell's palsy, liver disease, impaired adaptive immunity, impeded DNA damage response and tumorigenesis. Moreover, a recent study found that repeated COVID-19 vaccination with mRNA-based vaccines leads to the production of abnormally high concentrations of IgG4 antibodies. These antibodies fail to neutralize Spike protein, which has been shown to circulate for at least 28 days, cause immune suppression & promote the development of autoimmune diseases including myocarditis. 👇Fatal COVID-19 Vaccine-Induced Myocarditis👇 👇Cardiac Arrest After COVID-19 Vaccination👇 Speaker: Dr William Makis Video: @the_barefoot_truther
1:18

'mRNA COVID Vaccines Caused 74% Of Sudden Deaths Within 7 Days Of Vaccination & Many Within The 1st 72 Hours.' It Is The Largest Autopsy Series In The World. People Who Dropped Dead After The COVID-19 Vaccine, It Was Determined That 73.9% Of Individuals Died FROM The Vaccines. Causality in each case was determined by three independent reviewers with cardiac pathology experience & expertise. The number of days from last COVID-19 vaccination until death was 6.2 & 3 days, respectively. Most of the deaths occurred within a week from the last injection. The deaths were causally linked to COVID-19 vaccination by independent adjudication. The predominant COVID-19 vaccine platforms include messenger RNA (mRNA) Pfizer, Moderna, AstraZeneca, Johnson & Johnson, Novavax & Zifi Vax – mRNA & viral vector vaccines involve the bodily synthesis of the SARS-CoV-2 Spike protein as the foundation of the immune response. Regardless of the vaccine platform used, circulating SARS-CoV-2 Spike protein is the detrimental agent through which COVID-19 vaccines cause biological harm. Here Is The 'How & Why' Of The Spike Protein Mechanism That Leads To Harm & Death: Spike protein initiates the breakdown & internalization of ACE2 receptors, which disrupts the renin–angiotensin system (RAS) & lead to increased inflammation, vasoconstriction & thrombosis. Further, Spike protein stimulates platelets & inflicts damage to the endothelium, which leads to arterial & venous thrombosis. Immune cells that have absorbed the lipid nanoparticles (LNPs) subsequently reintroduce them into the bloodstream with a higher number of exosomes carrying microRNAs & Spike protein, resulting in drastic inflammation. Long term immune surveillance is compromised by mRNA COVID-19 vaccines due to IRF7, IRF9, p53 & BRCA suppression. There is a causal link between COVID-19 mRNA vaccination & myocarditis, neurodegenerative disease, immune thrombocytopenia, Bell's palsy, liver disease, impaired adaptive immunity, impeded DNA damage response and tumorigenesis. Moreover, a recent study found that repeated COVID-19 vaccination with mRNA-based vaccines leads to the production of abnormally high concentrations of IgG4 antibodies. These antibodies fail to neutralize Spike protein, which has been shown to circulate for at least 28 days, cause immune suppression & promote the development of autoimmune diseases including myocarditis. 👇Fatal COVID-19 Vaccine-Induced Myocarditis👇 👇Cardiac Arrest After COVID-19 Vaccination👇 Speaker: Dr William Makis Video: @the_barefoot_truther

Valerie Anne Smith

17,753 görüntüleme • 1 yıl önce

"The WHO Intends For ALL Vaccines On Earth To Be mRNA & Must Be Forbidden." Dr Sucharit Bhakdi "Every mRNA Injection Will Severely Change Your Brain, Damage Your Entire Body & Weaken Your Heart." The WHO Is A Private Club Financed By Germany & Bill Gates. They Must Be Stopped. mRNA Vaccines Do Not Save Lives...The Shots Contain A Killer Protein That Cannot Be Turned Off...It Is Not Safe By Design. The predominant vaccine platforms including messenger RNA (mRNA) are Pfizer, Moderna, AstraZeneca, Johnson & Johnson, Novavax & Zifi Vax – mRNA & viral vector vaccines involve the bodily synthesis of the S2 protein as the foundation of the immune response. Regardless of the vaccine platform used, circulating S2 protein is the detrimental agent through which mRNA vaccines cause biological harm. Here Is The 'How & Why' Of The S2 Protein Mechanism That Leads To Harm & Death: S2 protein initiates the breakdown & internalization of ACE2 receptors, which disrupts the renin–angiotensin system (RAS) & leads to increased inflammation, vasoconstriction & thrombosis. Further, S2 protein stimulates platelets & inflicts damage to the endothelium, which leads to arterial & venous thrombosis. Immune cells that have absorbed the lipid nanoparticles (LNPs) subsequently reintroduce them into the bloodstream with a higher number of exosomes carrying microRNAs & S2 protein, resulting in drastic inflammation. Long term immune surveillance is compromised by mRNA vaccines due to IRF7, IRF9, p53 & BRCA suppression. There is a causal link between mRNA vaccination & myocarditis, neurodegenerative disease, immune thrombocytopenia, Bell's palsy, liver disease, impaired adaptive immunity, impeded DNA damage response & tumorigenesis. Moreover, a recent study found that repeated vaccination with mRNA-based vaccines leads to the production of abnormally high concentrations of IgG4 antibodies. These antibodies fail to neutralize S2 protein, which has been shown to circulate for at least 700 days, causing immune suppression & promoting the development of autoimmune diseases including myocarditis. 👇Fatal mRNA Vaccine-Induced Myocarditis👇 👇Cardiac Arrest After mRNA Vaccination👇 👇DNA Fragments In mRNA Vaccines👇 Speaker: Dr Sucharit Bhakdi, Microbiologist Video: @freedom_knocks
2:19

"The WHO Intends For ALL Vaccines On Earth To Be mRNA & Must Be Forbidden." Dr Sucharit Bhakdi "Every mRNA Injection Will Severely Change Your Brain, Damage Your Entire Body & Weaken Your Heart." The WHO Is A Private Club Financed By Germany & Bill Gates. They Must Be Stopped. mRNA Vaccines Do Not Save Lives...The Shots Contain A Killer Protein That Cannot Be Turned Off...It Is Not Safe By Design. The predominant vaccine platforms including messenger RNA (mRNA) are Pfizer, Moderna, AstraZeneca, Johnson & Johnson, Novavax & Zifi Vax – mRNA & viral vector vaccines involve the bodily synthesis of the S2 protein as the foundation of the immune response. Regardless of the vaccine platform used, circulating S2 protein is the detrimental agent through which mRNA vaccines cause biological harm. Here Is The 'How & Why' Of The S2 Protein Mechanism That Leads To Harm & Death: S2 protein initiates the breakdown & internalization of ACE2 receptors, which disrupts the renin–angiotensin system (RAS) & leads to increased inflammation, vasoconstriction & thrombosis. Further, S2 protein stimulates platelets & inflicts damage to the endothelium, which leads to arterial & venous thrombosis. Immune cells that have absorbed the lipid nanoparticles (LNPs) subsequently reintroduce them into the bloodstream with a higher number of exosomes carrying microRNAs & S2 protein, resulting in drastic inflammation. Long term immune surveillance is compromised by mRNA vaccines due to IRF7, IRF9, p53 & BRCA suppression. There is a causal link between mRNA vaccination & myocarditis, neurodegenerative disease, immune thrombocytopenia, Bell's palsy, liver disease, impaired adaptive immunity, impeded DNA damage response & tumorigenesis. Moreover, a recent study found that repeated vaccination with mRNA-based vaccines leads to the production of abnormally high concentrations of IgG4 antibodies. These antibodies fail to neutralize S2 protein, which has been shown to circulate for at least 700 days, causing immune suppression & promoting the development of autoimmune diseases including myocarditis. 👇Fatal mRNA Vaccine-Induced Myocarditis👇 👇Cardiac Arrest After mRNA Vaccination👇 👇DNA Fragments In mRNA Vaccines👇 Speaker: Dr Sucharit Bhakdi, Microbiologist Video: @freedom_knocks

Valerie Anne Smith

16,998 görüntüleme • 1 yıl önce

Incidences of cancer have skyrocketed since the Covid mRNA vaccine rollout in 2021, especially in young adults, which is very uncommon. There is now direct evidence the spike protein binds to p53, a tumor suppressor gene. With inability to suppress tumor growths, cancers can grow unhindered by immune system checks and balances, even when the immune system is otherwise strong. This is extremely alarming. Ryan Cole
7:41

Incidences of cancer have skyrocketed since the Covid mRNA vaccine rollout in 2021, especially in young adults, which is very uncommon. There is now direct evidence the spike protein binds to p53, a tumor suppressor gene. With inability to suppress tumor growths, cancers can grow unhindered by immune system checks and balances, even when the immune system is otherwise strong. This is extremely alarming. Ryan Cole

Dr Dave Cartland BMedSc MBChB Ex-MRCGP

146,990 görüntüleme • 1 yıl önce

New Research Deep Dive: The "Shedding" Conversation Just Got More Serious A new in-vitro study (using human cells in a lab) on the Pfizer mRNA vaccine has revealed critical findings that can no longer be ignored. Let's break it down. The researchers confirmed two major things: 1️⃣ Spike Protein Production: The cells successfully took up the mRNA and began producing the SARS-CoV-2 spike protein, displaying it on their surface. This was expected. 2️⃣ Spike Protein "Shedding" via Exosomes: Here's the crucial part. The cells didn't just keep the spike protein to themselves. They packaged it into exosomes—tiny extracellular vesicles cells use to communicate—and excreted them into the environment. Why does this matter? This provides a potential mechanistic blueprint for how spike protein could travel systemically throughout the body after vaccination. These spike-laden exosomes can enter the bloodstream and, theoretically, deliver their cargo to distant organs and other cells. But the most alarming part? The authors note a profound lack of safety data. They explicitly state: We have no scientific studies to determine if this exosome-mediated spread of spike protein is toxic to other human cells. Even more concerning, they observed "pathological changes" and toxicity within the cells producing the spike. And these weren't weak cells—they were robust, immortalized embryonic kidney cells, chosen for their resilience. If these cells showed adverse effects, what is the impact on our more delicate primary cells? The authors themselves caution that proper toxicology studies on normal human cell lines are urgently needed... and are currently unavailable. This isn't conspiracy theory. This is cell biology. The conversation must evolve from if spike protein can travel, to what are the systemic consequences when it does. The call for rigorous, independent safety science has never been louder.
2:20

New Research Deep Dive: The "Shedding" Conversation Just Got More Serious A new in-vitro study (using human cells in a lab) on the Pfizer mRNA vaccine has revealed critical findings that can no longer be ignored. Let's break it down. The researchers confirmed two major things: 1️⃣ Spike Protein Production: The cells successfully took up the mRNA and began producing the SARS-CoV-2 spike protein, displaying it on their surface. This was expected. 2️⃣ Spike Protein "Shedding" via Exosomes: Here's the crucial part. The cells didn't just keep the spike protein to themselves. They packaged it into exosomes—tiny extracellular vesicles cells use to communicate—and excreted them into the environment. Why does this matter? This provides a potential mechanistic blueprint for how spike protein could travel systemically throughout the body after vaccination. These spike-laden exosomes can enter the bloodstream and, theoretically, deliver their cargo to distant organs and other cells. But the most alarming part? The authors note a profound lack of safety data. They explicitly state: We have no scientific studies to determine if this exosome-mediated spread of spike protein is toxic to other human cells. Even more concerning, they observed "pathological changes" and toxicity within the cells producing the spike. And these weren't weak cells—they were robust, immortalized embryonic kidney cells, chosen for their resilience. If these cells showed adverse effects, what is the impact on our more delicate primary cells? The authors themselves caution that proper toxicology studies on normal human cell lines are urgently needed... and are currently unavailable. This isn't conspiracy theory. This is cell biology. The conversation must evolve from if spike protein can travel, to what are the systemic consequences when it does. The call for rigorous, independent safety science has never been louder.

Camus

48,219 görüntüleme • 7 ay önce

Of all the casualties in the war on cancer, the most critical have been the most ignored: your NK and T cells. As Dr. Patrick Soon-Shiong explains, while oncology has long treated the anemia and neutropenia caused by chemotherapy, it has overlooked the destruction of the very immune cells that fight cancer. For 35 years, there was no treatment for this catastrophic side effect. That era is over. Dr. Soon-Shiong announces ANKTIVA, the first FDA-approved therapy proven to activate NK cells, T cells, and memory T cells. The result? Documented complete responses in bladder cancer patients, free of disease for over nine years. This breakthrough shatters a long-standing medical blind spot. Whether from chemo, radiation, or a severe viral infection, the body's primary defense is often wiped out. ANKTIVA represents a paradigm shift—from solely attacking disease to actively re-arming the patient's own immune system. The future of medicine is not just fighting the enemy, but empowering the army within.
3:35

Of all the casualties in the war on cancer, the most critical have been the most ignored: your NK and T cells. As Dr. Patrick Soon-Shiong explains, while oncology has long treated the anemia and neutropenia caused by chemotherapy, it has overlooked the destruction of the very immune cells that fight cancer. For 35 years, there was no treatment for this catastrophic side effect. That era is over. Dr. Soon-Shiong announces ANKTIVA, the first FDA-approved therapy proven to activate NK cells, T cells, and memory T cells. The result? Documented complete responses in bladder cancer patients, free of disease for over nine years. This breakthrough shatters a long-standing medical blind spot. Whether from chemo, radiation, or a severe viral infection, the body's primary defense is often wiped out. ANKTIVA represents a paradigm shift—from solely attacking disease to actively re-arming the patient's own immune system. The future of medicine is not just fighting the enemy, but empowering the army within.

Camus

55,260 görüntüleme • 8 ay önce

Dr. Michael Nehls on Tucker Carlson: The mRNA spike protein shuts down new brain cell growth in the hippocampus — leading to depression, anxiety, and Alzheimer’s. NEHLS: “The spike protein produced by the mRNA that is injected… is doing just the opposite. The spike protein activates neuroinflammation in the brain… they shut down the hippocampus, they shut down the production of new nerve cells in the hippocampus.” “If it’s chronic… the consequences are depression, anxiety, and in the long run is Alzheimer’s.” “So they actually identified after the mRNA injections after a few months that the Alzheimer rate went up in a study published in South Korea… And I predicted this already in my book, the Indoctrinated Brain.” “Being human in my opinion means that you are able to produce these cells… if you shut down the production of new nerve cells in the hippocampus people lose essentially the ability to be human. They lose themselves. And the ultimate losing of oneself is having Alzheimer’s.”
5:17

Dr. Michael Nehls on Tucker Carlson: The mRNA spike protein shuts down new brain cell growth in the hippocampus — leading to depression, anxiety, and Alzheimer’s. NEHLS: “The spike protein produced by the mRNA that is injected… is doing just the opposite. The spike protein activates neuroinflammation in the brain… they shut down the hippocampus, they shut down the production of new nerve cells in the hippocampus.” “If it’s chronic… the consequences are depression, anxiety, and in the long run is Alzheimer’s.” “So they actually identified after the mRNA injections after a few months that the Alzheimer rate went up in a study published in South Korea… And I predicted this already in my book, the Indoctrinated Brain.” “Being human in my opinion means that you are able to produce these cells… if you shut down the production of new nerve cells in the hippocampus people lose essentially the ability to be human. They lose themselves. And the ultimate losing of oneself is having Alzheimer’s.”

Defiant Ghost

129,798 görüntüleme • 11 gün önce

More Bad News for the COVID Vaccinated Countless warnings about the shots have been labeled “conspiracy theories” only to be later confirmed. The latest example comes from a comprehensive review by an international consortium of scientists who raised concerns that a specific vaccine ingredient, N1-methyl-pseudouridine (m1Ψ), may play a role in immune suppression and cancer proliferation. The review stresses that incorporating N1-methyl-pseudouridine (m1Ψ) in mRNA vaccines significantly compromises critical immune responses, severely hindering the body’s initial interferon signaling. Interferon is vital for the immune system’s ability to fend off infections and combat diseases like cancer. The researchers wrote: “Based on this compelling evidence, we suggest that future clinical trials for cancers or infectious diseases should not use mRNA vaccines with a 100 % m1Ψ (N1-methyl-pseudouridine) modification, but rather ones with the lower percentage of m1Ψ modification to avoid immune suppression.” Given the extensive “immune suppression” observed, it’s not a stretch to say the COVID shots are largely responsible for the alarming rise in cancer cases among young people. However, corporate media outlets like The Wall Street Journal continue to run cover for Big Pharma. One of their recent headlines reads: “Cancer Is Striking More Young People, and Doctors Are Alarmed and Baffled.” They might be “baffled,” but we aren’t.
4:59

More Bad News for the COVID Vaccinated Countless warnings about the shots have been labeled “conspiracy theories” only to be later confirmed. The latest example comes from a comprehensive review by an international consortium of scientists who raised concerns that a specific vaccine ingredient, N1-methyl-pseudouridine (m1Ψ), may play a role in immune suppression and cancer proliferation. The review stresses that incorporating N1-methyl-pseudouridine (m1Ψ) in mRNA vaccines significantly compromises critical immune responses, severely hindering the body’s initial interferon signaling. Interferon is vital for the immune system’s ability to fend off infections and combat diseases like cancer. The researchers wrote: “Based on this compelling evidence, we suggest that future clinical trials for cancers or infectious diseases should not use mRNA vaccines with a 100 % m1Ψ (N1-methyl-pseudouridine) modification, but rather ones with the lower percentage of m1Ψ modification to avoid immune suppression.” Given the extensive “immune suppression” observed, it’s not a stretch to say the COVID shots are largely responsible for the alarming rise in cancer cases among young people. However, corporate media outlets like The Wall Street Journal continue to run cover for Big Pharma. One of their recent headlines reads: “Cancer Is Striking More Young People, and Doctors Are Alarmed and Baffled.” They might be “baffled,” but we aren’t.

The Vigilant Fox 🦊

1,600,584 görüntüleme • 2 yıl önce