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BREAKING STUDY: SPIKE PROTEIN TRIGGERS PRION-LIKE PROTEIN MISFOLDING, AMYLOID FORMATION, AND MULTI-ORGAN DAMAGE We found that both COVID “vaccine” spike protein and lab-made SARS-CoV-2 spike protein are potent prion-like drivers of proteostatic collapse, pathological cross-seeding, transcriptional instability, and progressive tissue dysfunction across multiple organ systems. Spike protein contains intrinsic...

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Nicolas Hulscher, MPH

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Dr. McCullough Shares Good News for Vaccine Regretters “Look at these cardiac arrests, major blood clots, people going down. It’s because the spike protein is not being cleared out of the body,” says Dr. McCullough. He urges taking action with three natural substances: 1.) Nattokinase - degrades the spike protein. 2.) Bromelain - accelerates the clearance of spike proteins. 3.) Curcumin - reduces inflammation and spike protein damage. Dr. Peter A. McCullough, MD, MPH® mentioned that this is a base therapy, and other things can be added to it. He also stressed: “People ought to get going on this because these syndromes, as we’re finding out, are bad ... People can take control of their own bodies and get after this.”
1:13

Dr. McCullough Shares Good News for Vaccine Regretters “Look at these cardiac arrests, major blood clots, people going down. It’s because the spike protein is not being cleared out of the body,” says Dr. McCullough. He urges taking action with three natural substances: 1.) Nattokinase - degrades the spike protein. 2.) Bromelain - accelerates the clearance of spike proteins. 3.) Curcumin - reduces inflammation and spike protein damage. Dr. Peter A. McCullough, MD, MPH® mentioned that this is a base therapy, and other things can be added to it. He also stressed: “People ought to get going on this because these syndromes, as we’re finding out, are bad ... People can take control of their own bodies and get after this.”

The Vigilant Fox 🦊

1,498,879 görüntüleme • 2 yıl önce

New findings from Dr. Peter McCullough and a German research lab confirm that Pfizer and Moderna mRNA vaccines leave behind synthetic spike protein in the body for at least 3.2 years post-injection. These proteins circulate in the bloodstream and embed in tissues, with no known human enzymes capable of breaking them down. Key Revelations: - Pseudouridinated mRNA does not degrade naturally, leading to prolonged spike protein production. - Cancer trends shifting—2023 data shows rising breast and prostate cancers, while overall rates remain stable. - 2021 global mortality was among the worst in history, raising urgent questions about long-term vaccine effects. Potential Solutions? Natural enzymes like nattokinase, bromelain, serrapeptase, and lumbrokinase show promise in breaking down spike protein—but public awareness is critical. Why This Matters: If mRNA and spike protein persist for years, the long-term health consequences could be devastating. The medical establishment must address this—before it’s too late.
1:21

New findings from Dr. Peter McCullough and a German research lab confirm that Pfizer and Moderna mRNA vaccines leave behind synthetic spike protein in the body for at least 3.2 years post-injection. These proteins circulate in the bloodstream and embed in tissues, with no known human enzymes capable of breaking them down. Key Revelations: - Pseudouridinated mRNA does not degrade naturally, leading to prolonged spike protein production. - Cancer trends shifting—2023 data shows rising breast and prostate cancers, while overall rates remain stable. - 2021 global mortality was among the worst in history, raising urgent questions about long-term vaccine effects. Potential Solutions? Natural enzymes like nattokinase, bromelain, serrapeptase, and lumbrokinase show promise in breaking down spike protein—but public awareness is critical. Why This Matters: If mRNA and spike protein persist for years, the long-term health consequences could be devastating. The medical establishment must address this—before it’s too late.

Camus

77,549 görüntüleme • 1 yıl önce

Degrade Deadly Spike Proteins: Here’s How in 96 Seconds, Per Dr. Peter McCullough “We infer that people who have taken the vaccine have gotten a lot more of the deadly spike protein in their body than people who have gotten the infection,” Dr. Peter A. McCullough, MD, MPH® denoted to Dr. Naomi Wolf. 8 NYT Bestsellers. DPhil, Poetry.. “And the big news now is that we have products that can 𝗱𝗲𝗴𝗿𝗮𝗱𝗲 the spike protein.” Here’s what Dr. McCullough recommends: 1. Nattokinase - Multiple preclinical studies suggest it degrades spike proteins. 2. Bromelain - Works separately from nattokinase to target spike. 3. Circumin - Has randomized trials of people who have taken the vaccine showing benefit. ------------------------------ Share with a friend in need. And follow (The Vigilant Fox 🦊) for more informative and newsworthy clips.
1:36

Degrade Deadly Spike Proteins: Here’s How in 96 Seconds, Per Dr. Peter McCullough “We infer that people who have taken the vaccine have gotten a lot more of the deadly spike protein in their body than people who have gotten the infection,” Dr. Peter A. McCullough, MD, MPH® denoted to Dr. Naomi Wolf. 8 NYT Bestsellers. DPhil, Poetry.. “And the big news now is that we have products that can 𝗱𝗲𝗴𝗿𝗮𝗱𝗲 the spike protein.” Here’s what Dr. McCullough recommends: 1. Nattokinase - Multiple preclinical studies suggest it degrades spike proteins. 2. Bromelain - Works separately from nattokinase to target spike. 3. Circumin - Has randomized trials of people who have taken the vaccine showing benefit. ------------------------------ Share with a friend in need. And follow (The Vigilant Fox 🦊) for more informative and newsworthy clips.

The Vigilant Fox 🦊

1,058,504 görüntüleme • 3 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

REPORT: A new study confirms that COVID-19 mRNA injections spread to vital organs and trigger systemic, toxic spike protein production. This “conspiracy theory” just became a reality. The new study, published in Nature Biotechnology, reveals alarming details about the biodistribution of lipid nanoparticles (LNPs) carrying SARS-CoV-2 spike mRNA. The study demonstrated that even at extremely low doses (0.0005 mg/kg), these LNPs deliver mRNA to cells in vital organs, leading to the production of toxic spike protein. According to the researchers, this protein triggers immune activation and causes damage to blood vessels. Meanwhile, autopsy findings now confirm the systemic presence of spike protein in tissues and organs, raising serious questions about the safety of these so-called vaccines. Epidemiologist Nicolas Hulscher, MPH didn’t hold back in his response to the news of this study, stating: “Biodistribution studies should have been performed BEFORE mass ‘vaccination’ of the entire world’s population. These invasive gene therapy injections must be pulled from global markets immediately.”
3:39

REPORT: A new study confirms that COVID-19 mRNA injections spread to vital organs and trigger systemic, toxic spike protein production. This “conspiracy theory” just became a reality. The new study, published in Nature Biotechnology, reveals alarming details about the biodistribution of lipid nanoparticles (LNPs) carrying SARS-CoV-2 spike mRNA. The study demonstrated that even at extremely low doses (0.0005 mg/kg), these LNPs deliver mRNA to cells in vital organs, leading to the production of toxic spike protein. According to the researchers, this protein triggers immune activation and causes damage to blood vessels. Meanwhile, autopsy findings now confirm the systemic presence of spike protein in tissues and organs, raising serious questions about the safety of these so-called vaccines. Epidemiologist Nicolas Hulscher, MPH didn’t hold back in his response to the news of this study, stating: “Biodistribution studies should have been performed BEFORE mass ‘vaccination’ of the entire world’s population. These invasive gene therapy injections must be pulled from global markets immediately.”

The Vigilant Fox 🦊

396,969 görüntüleme • 1 yıl önce

REPORT: Up to 15 MILLION Americans may be suffering from the devastating effects of the COVID shots, says Alabama-based physician Dr. Jordan Vaughn. In his clinic, he now sees teenagers who can’t stand and previously healthy adults suffering strokes with no identifiable cause. Dr. Vaughn explained that the S1 subunit of the spike protein is not a benign protein. It “triggers inflammation, it disrupts endothelial barriers, it induces fibrin resistant to breakdown, and it promotes a lot of amyloid aggregates.” These effects impair oxygen delivery, damage blood vessels, and fuel a tidal wave of symptoms: racing heart, brain fog, shortness of breath, and post-exertional crashes. Using immunofluorescent microscopy, Vaughn detects these abnormalities firsthand: clear signs of spike-induced damage in patients who were once thriving. He warned that the mRNA injections led to uncontrolled spike protein production, which didn’t stay localized. It spread throughout the body, reaching the heart, brain, ovaries, and testes. Regulators claimed the vaccine stayed in the arm. That was a lie. A Yale study now shows some people are still producing spike protein more than 700 days after injection. We didn’t just inject people. We turned them into spike protein factories. What have we done?
2:02

REPORT: Up to 15 MILLION Americans may be suffering from the devastating effects of the COVID shots, says Alabama-based physician Dr. Jordan Vaughn. In his clinic, he now sees teenagers who can’t stand and previously healthy adults suffering strokes with no identifiable cause. Dr. Vaughn explained that the S1 subunit of the spike protein is not a benign protein. It “triggers inflammation, it disrupts endothelial barriers, it induces fibrin resistant to breakdown, and it promotes a lot of amyloid aggregates.” These effects impair oxygen delivery, damage blood vessels, and fuel a tidal wave of symptoms: racing heart, brain fog, shortness of breath, and post-exertional crashes. Using immunofluorescent microscopy, Vaughn detects these abnormalities firsthand: clear signs of spike-induced damage in patients who were once thriving. He warned that the mRNA injections led to uncontrolled spike protein production, which didn’t stay localized. It spread throughout the body, reaching the heart, brain, ovaries, and testes. Regulators claimed the vaccine stayed in the arm. That was a lie. A Yale study now shows some people are still producing spike protein more than 700 days after injection. We didn’t just inject people. We turned them into spike protein factories. What have we done?

The Vigilant Fox 🦊

392,384 görüntüleme • 1 yıl önce

We talk a lot about the COVID jabs causing cancer, blood clots, myocarditis, etc. But don't forget about (spreadable) prion diseases! "As a scientist, I'm having to listen very carefully to the eugenicists and those people who dream of a far lower number of human beings...." Dr. Kevin McCairn, PhD (Kevin W. McCairn PhD), a retired Principal Investigator at the Korea Brain Research Institute Systems Neuroscience and Movement Disorders Laboratory, describes during a discussion posted by Health Alliance Australia how the spike protein of both SARS-CoV-2 and the spike coded by the mRNA COVID injections is an engineered prion. (For reference, a prion is a misfolded protein that causes other proteins in the brain to misfold, leading to fatal brain diseases.) Health Alliance Australia notes in its description of this interview that these "weaponized prions" have "grave implications for humanity because [they] are far more dangerous than viruses." Health Alliance Australia adds in its description that "The most commonly known prion disease is CJD or Creutzfeldt-Jakob disease, which is a spongiform encephalopathy where the brain becomes spongy, wastes away, and ultimately leads to a horrible death. Alzheimer’s and Parkinson’s are other neurodegenerative diseases associated with prions." Considering the deployment of these "weaponized prions," McCairn says that "as a scientist, I'm having to listen very carefully to the eugenicists and those people who dream of a far lower number of human beings on this planet." The scientist adds, "if you wanted a method to do that, well, you're going to struggle through normal viral or bioweapon means... whereas the spread of prion within a population would be very, very difficult to detect unless you are specifically looking for these misfolded proteins." ---------------Partial transcription of clip-------------- "So SARS CoV-2 spike amyloid fibrils specifically and selectively accelerates amyloid fibril formation of, and this is the critical part, human prion protein and the amyloid beta peptide. And this means that we have to take a very, very long hard look at what this means with respect to biowarfare strategies and techniques because prions have been a subject of biowarfare research for a long time. "The problem was that you could aerosolize prion, the protein, and it's lethal in that respect. But the spreading is limited. And but as I mentioned earlier, as they focused on the weaponization and contraction, honing down the peptide sequences to their most essential disease causing elements, I think that they've been focusing on how to find a way to get prion to spread person to person, not directly with even though we consider prion disorder, what's called TSEs, transmissible spongiform encephalopathies. Meaning, we know that if you come into contact with them, ingest them, there's a high chance that you'll develop the prion disease and you'll have a bad outcome, meaning invariably death. Horrible death at that. A horrible death. It's not pretty. "So, I'm just gonna read out the part that I've got highlighted here. So they say, we here provide evidence of significant spike amyloid fibril seeded acceleration of amyloid formation of CJD associated human prion protein using an in vitro conversion assay. So what that means is that just it's not in cell test systems yet. It's just they're doing the molecular biochemistry in a manner in which they can detect change over time. Right? And so you basically take this epitope sequence. And so they say, we showed that the amyloid fibril formation of, in this case, Alzheimer associated amyloid beta-142 was accelerated by spike amyloid fibrils of 7 different 20 amino acid long peptides, spike 532 to 551 meaning just this 20 amino acid long sequence, was the most efficient at seeding human prion protein, whilst another segment, 601 to 620, was most effective at seeding amyloid beta. "Now if you just look at the data from their experiment, the fastest reaction that they have is with the conversion to the human prion, the scrapy form, meaning the diseased form of the prion protein in the data set, which is just this cluster down here, Spike532 seed. And so when we see a signal like this on top of all the other data points that we've seen over the last 4 years, it's incumbent upon us to think, have these people through malfeasance, perhaps perhaps it was just a research project, gone [wrong] or at this stage. It's it's difficult to say for certain it's these groups. "But, I think, as a scientist, I'm having to listen very carefully to the eugenicists and those people who dream of a far lower number of human beings on this planet. And if you wanted a method to do that, well, you're going to struggle through normal viral or bioweapon means, right? So you could go for the bacterial route, but there's likely we'd develop countermeasures in that respect. We can deal with them and the onset of sickness, etcetera, has very typical presentations, whereas the spread of prion within a population would be very, very difficult to detect unless you are specifically looking for these misfolded proteins. "And then remember, we're in an we're in an area where the it's more complex than just like for like conversion. We now have to operate in a world of what's called cross-seeding amyloidogenic peptide seeds, meaning these small, small epitopes."
5:25

We talk a lot about the COVID jabs causing cancer, blood clots, myocarditis, etc. But don't forget about (spreadable) prion diseases! "As a scientist, I'm having to listen very carefully to the eugenicists and those people who dream of a far lower number of human beings...." Dr. Kevin McCairn, PhD (Kevin W. McCairn PhD), a retired Principal Investigator at the Korea Brain Research Institute Systems Neuroscience and Movement Disorders Laboratory, describes during a discussion posted by Health Alliance Australia how the spike protein of both SARS-CoV-2 and the spike coded by the mRNA COVID injections is an engineered prion. (For reference, a prion is a misfolded protein that causes other proteins in the brain to misfold, leading to fatal brain diseases.) Health Alliance Australia notes in its description of this interview that these "weaponized prions" have "grave implications for humanity because [they] are far more dangerous than viruses." Health Alliance Australia adds in its description that "The most commonly known prion disease is CJD or Creutzfeldt-Jakob disease, which is a spongiform encephalopathy where the brain becomes spongy, wastes away, and ultimately leads to a horrible death. Alzheimer’s and Parkinson’s are other neurodegenerative diseases associated with prions." Considering the deployment of these "weaponized prions," McCairn says that "as a scientist, I'm having to listen very carefully to the eugenicists and those people who dream of a far lower number of human beings on this planet." The scientist adds, "if you wanted a method to do that, well, you're going to struggle through normal viral or bioweapon means... whereas the spread of prion within a population would be very, very difficult to detect unless you are specifically looking for these misfolded proteins." ---------------Partial transcription of clip-------------- "So SARS CoV-2 spike amyloid fibrils specifically and selectively accelerates amyloid fibril formation of, and this is the critical part, human prion protein and the amyloid beta peptide. And this means that we have to take a very, very long hard look at what this means with respect to biowarfare strategies and techniques because prions have been a subject of biowarfare research for a long time. "The problem was that you could aerosolize prion, the protein, and it's lethal in that respect. But the spreading is limited. And but as I mentioned earlier, as they focused on the weaponization and contraction, honing down the peptide sequences to their most essential disease causing elements, I think that they've been focusing on how to find a way to get prion to spread person to person, not directly with even though we consider prion disorder, what's called TSEs, transmissible spongiform encephalopathies. Meaning, we know that if you come into contact with them, ingest them, there's a high chance that you'll develop the prion disease and you'll have a bad outcome, meaning invariably death. Horrible death at that. A horrible death. It's not pretty. "So, I'm just gonna read out the part that I've got highlighted here. So they say, we here provide evidence of significant spike amyloid fibril seeded acceleration of amyloid formation of CJD associated human prion protein using an in vitro conversion assay. So what that means is that just it's not in cell test systems yet. It's just they're doing the molecular biochemistry in a manner in which they can detect change over time. Right? And so you basically take this epitope sequence. And so they say, we showed that the amyloid fibril formation of, in this case, Alzheimer associated amyloid beta-142 was accelerated by spike amyloid fibrils of 7 different 20 amino acid long peptides, spike 532 to 551 meaning just this 20 amino acid long sequence, was the most efficient at seeding human prion protein, whilst another segment, 601 to 620, was most effective at seeding amyloid beta. "Now if you just look at the data from their experiment, the fastest reaction that they have is with the conversion to the human prion, the scrapy form, meaning the diseased form of the prion protein in the data set, which is just this cluster down here, Spike532 seed. And so when we see a signal like this on top of all the other data points that we've seen over the last 4 years, it's incumbent upon us to think, have these people through malfeasance, perhaps perhaps it was just a research project, gone [wrong] or at this stage. It's it's difficult to say for certain it's these groups. "But, I think, as a scientist, I'm having to listen very carefully to the eugenicists and those people who dream of a far lower number of human beings on this planet. And if you wanted a method to do that, well, you're going to struggle through normal viral or bioweapon means, right? So you could go for the bacterial route, but there's likely we'd develop countermeasures in that respect. We can deal with them and the onset of sickness, etcetera, has very typical presentations, whereas the spread of prion within a population would be very, very difficult to detect unless you are specifically looking for these misfolded proteins. "And then remember, we're in an we're in an area where the it's more complex than just like for like conversion. We now have to operate in a world of what's called cross-seeding amyloidogenic peptide seeds, meaning these small, small epitopes."

Sense Receptor

23,288 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 • 9 ay önce

Colon Cancer in 8-Year-Olds. Pancreatic Cancer in 13-Year-Olds. Dr. Soon-Shiong's Chilling Explanation: The Spike Protein. A stark and urgent warning from Dr. Patrick Soon-Shiong: The medical establishment's singular focus on the SARS-CoV-2 spike protein, both in vaccine design and viral understanding, may have catastrophic long-term consequences, including a looming cancer crisis in younger populations. In a revealing discussion, Dr. Soon-Shiong articulates a critical question that has been largely ignored: Why did we develop vaccines that do not clear the virus and that are based solely on the virus's most pathogenic component—the spike protein? He introduces the concept of "spikeopathy"—the pathological damage caused by the spike protein itself, whether from the virus or from mRNA vaccines. The central, terrifying hypothesis is that the spike protein may not be inert. If it can persist and replicate within the body, it could potentially suppress crucial tumor-suppressor proteins like P53. This is not mere speculation for Dr. Soon-Shiong. He directly links this mechanism to the alarming and unprecedented rise in early-age cancers he is witnessing clinically. He asks the question the entire world should be asking: Is the spike protein a ticking time bomb, acting similarly to known oncoviruses like HPV and Hepatitis? Could this be the explanation for the inexplicable: 8-year-olds with colon cancer? 13-year-olds with metastatic pancreatic cancer? Dr. Soon-Shiong believes these are not anomalies but potential harbingers of a future wave of spike-driven oncogenesis. This is no longer just a debate about vaccine efficacy vs. COVID-19. This is a warning about a potential iatrogenic contribution to a future pandemic of cancer. The questions he raises are among the most important of our time. The scientific and medical community must address them with transparency and urgency. The health of a generation may depend on it.
1:31

Colon Cancer in 8-Year-Olds. Pancreatic Cancer in 13-Year-Olds. Dr. Soon-Shiong's Chilling Explanation: The Spike Protein. A stark and urgent warning from Dr. Patrick Soon-Shiong: The medical establishment's singular focus on the SARS-CoV-2 spike protein, both in vaccine design and viral understanding, may have catastrophic long-term consequences, including a looming cancer crisis in younger populations. In a revealing discussion, Dr. Soon-Shiong articulates a critical question that has been largely ignored: Why did we develop vaccines that do not clear the virus and that are based solely on the virus's most pathogenic component—the spike protein? He introduces the concept of "spikeopathy"—the pathological damage caused by the spike protein itself, whether from the virus or from mRNA vaccines. The central, terrifying hypothesis is that the spike protein may not be inert. If it can persist and replicate within the body, it could potentially suppress crucial tumor-suppressor proteins like P53. This is not mere speculation for Dr. Soon-Shiong. He directly links this mechanism to the alarming and unprecedented rise in early-age cancers he is witnessing clinically. He asks the question the entire world should be asking: Is the spike protein a ticking time bomb, acting similarly to known oncoviruses like HPV and Hepatitis? Could this be the explanation for the inexplicable: 8-year-olds with colon cancer? 13-year-olds with metastatic pancreatic cancer? Dr. Soon-Shiong believes these are not anomalies but potential harbingers of a future wave of spike-driven oncogenesis. This is no longer just a debate about vaccine efficacy vs. COVID-19. This is a warning about a potential iatrogenic contribution to a future pandemic of cancer. The questions he raises are among the most important of our time. The scientific and medical community must address them with transparency and urgency. The health of a generation may depend on it.

Camus

207,307 görüntüleme • 10 ay önce

Are COVID injections causing a new form of rapid-onset dementia? This isn't just a theory—it's a clinical reality being witnessed by frontline doctors. In a stunning discussion, Dr. Pierre Kory and Dr. Jordan Vaughn, alongside clinician Scott Marsland, revealed groundbreaking and alarming findings. They point to the late Dr. Luc Montagnier, a Nobel Prize-winning virologist, whose final research paper highlighted a terrifying link: the original spike protein contains amino acids that code for PRION DISEASE. This prion-like mechanism is implicated in causing: 🔹 Protein deformations 🔹 Amyloid plaque formation in the brain 🔹 A "reservoir" of spike protein in the brain that evades normal treatments The result? Patients are presenting with rapid, atypical neurological decline that conventional doctors misdiagnose as standard dementia, Parkinson's, or ALS. But the cases don't fit the classic patterns. Here's the HOPE that the medical establishment isn't offering: Marsland shares an incredible anecdote of a patient he had referred to palliative care. As a last resort, they tried N-Acetylcysteine (NAC) to cross the blood-brain barrier and clear the spike. In just 3 WEEKS, she regained the ability to walk, feed herself, and even returned to gardening. Dr. Kory confirms this, stating that when you treat the root pathology—the spike protein and its microvascular damage—instead of just the symptoms, over 50% of these "hopeless" patients see significant recovery. The takeaway is urgent: The system is failing these patients by forcing them into a diagnostic box with no hope. A new paradigm of treatment, focused on the true mechanism of injury, is not just possible—it's saving lives. This is the conversation they don't want you to have.
4:10

Are COVID injections causing a new form of rapid-onset dementia? This isn't just a theory—it's a clinical reality being witnessed by frontline doctors. In a stunning discussion, Dr. Pierre Kory and Dr. Jordan Vaughn, alongside clinician Scott Marsland, revealed groundbreaking and alarming findings. They point to the late Dr. Luc Montagnier, a Nobel Prize-winning virologist, whose final research paper highlighted a terrifying link: the original spike protein contains amino acids that code for PRION DISEASE. This prion-like mechanism is implicated in causing: 🔹 Protein deformations 🔹 Amyloid plaque formation in the brain 🔹 A "reservoir" of spike protein in the brain that evades normal treatments The result? Patients are presenting with rapid, atypical neurological decline that conventional doctors misdiagnose as standard dementia, Parkinson's, or ALS. But the cases don't fit the classic patterns. Here's the HOPE that the medical establishment isn't offering: Marsland shares an incredible anecdote of a patient he had referred to palliative care. As a last resort, they tried N-Acetylcysteine (NAC) to cross the blood-brain barrier and clear the spike. In just 3 WEEKS, she regained the ability to walk, feed herself, and even returned to gardening. Dr. Kory confirms this, stating that when you treat the root pathology—the spike protein and its microvascular damage—instead of just the symptoms, over 50% of these "hopeless" patients see significant recovery. The takeaway is urgent: The system is failing these patients by forcing them into a diagnostic box with no hope. A new paradigm of treatment, focused on the true mechanism of injury, is not just possible—it's saving lives. This is the conversation they don't want you to have.

Camus

53,205 görüntüleme • 9 ay önce

In a phone interview, Del Bigtree, a fierce advocate for medical freedom, left a New York Times reporter speechless by dismantling the claim that “the vaccine is safer than catching the virus.” His logic was unassailable. The reporter argued myocarditis and pericarditis are more common from a live COVID infection than the vaccine. Bigtree met her on her terms, zeroing in on the spike protein—the key culprit in both. “Can we agree the spike protein causes the blood issues, myocarditis, and pericarditis?” he asked. She conceded: Yes. Bigtree pressed: “If the spike protein in the virus and vaccine is the same, don’t they carry equal risk?” He hinted at evidence the vaccine’s spike protein might persist longer but set that aside for fairness. Assuming identical spike proteins, he delivered the knockout: “The vaccine guarantees you get the spike protein, injected directly into your body. Catching the virus? That’s random—you might never encounter it.” This is seismic. Vaccination ensures exposure to the harmful spike protein, bypassing natural barriers like the respiratory system. With the virus, chance plays a role—you might dodge it. “Mandating vaccines forces everyone to take that risk, increasing myocarditis and pericarditis cases compared to randomized viral exposure,” Bigtree argued. The reporter’s response? “Oh my god.” For once, she was stunned, grappling with his clarity. He wasn’t done: “You’re bypassing the immune system’s first line of defense—our natural barriers. Why ignore the body’s design?” This exchange is a clarion call: question narratives. Demand logic. The vaccine vs. virus debate deserves scrutiny.
2:13

In a phone interview, Del Bigtree, a fierce advocate for medical freedom, left a New York Times reporter speechless by dismantling the claim that “the vaccine is safer than catching the virus.” His logic was unassailable. The reporter argued myocarditis and pericarditis are more common from a live COVID infection than the vaccine. Bigtree met her on her terms, zeroing in on the spike protein—the key culprit in both. “Can we agree the spike protein causes the blood issues, myocarditis, and pericarditis?” he asked. She conceded: Yes. Bigtree pressed: “If the spike protein in the virus and vaccine is the same, don’t they carry equal risk?” He hinted at evidence the vaccine’s spike protein might persist longer but set that aside for fairness. Assuming identical spike proteins, he delivered the knockout: “The vaccine guarantees you get the spike protein, injected directly into your body. Catching the virus? That’s random—you might never encounter it.” This is seismic. Vaccination ensures exposure to the harmful spike protein, bypassing natural barriers like the respiratory system. With the virus, chance plays a role—you might dodge it. “Mandating vaccines forces everyone to take that risk, increasing myocarditis and pericarditis cases compared to randomized viral exposure,” Bigtree argued. The reporter’s response? “Oh my god.” For once, she was stunned, grappling with his clarity. He wasn’t done: “You’re bypassing the immune system’s first line of defense—our natural barriers. Why ignore the body’s design?” This exchange is a clarion call: question narratives. Demand logic. The vaccine vs. virus debate deserves scrutiny.

Camus

58,898 görüntüleme • 1 yıl önce

Dr. Peter McCullough Breaks Down How the COVID Vaccines Injure and KiII Cardiovascular Disease • "We've seen cardiac arrest now two years after these shots." • Myocarditis (heart inflammation) • Acceleration of atherosclerotic cardiovascular disease • Heart attacks • Posterior orthostatic tachycardia syndrome (POTS) • Aortic dissection • Atrial fibrillation • Cardiac arrest in the absence of myocarditis Neurologic Disease • Stroke (both ischemic and hemorrhagic) • Guillain–Barré syndrome (can cause ascending paralysis leading to death) • Small fiber neuropathy (numbness and tingling) Blood Clots • "The spike protein is the most thrombogenic protein we've ever seen in human medicine." • Unusually large and resistant blood clots • Blood clots that are not dissolving with conventional treatments Immunologic Abnormalities • Vaccine-induced thrombotic thrombocytopenia • Multisystem inflammatory disorder Peter A. McCullough, MD, MPH®
3:24

Dr. Peter McCullough Breaks Down How the COVID Vaccines Injure and KiII Cardiovascular Disease • "We've seen cardiac arrest now two years after these shots." • Myocarditis (heart inflammation) • Acceleration of atherosclerotic cardiovascular disease • Heart attacks • Posterior orthostatic tachycardia syndrome (POTS) • Aortic dissection • Atrial fibrillation • Cardiac arrest in the absence of myocarditis Neurologic Disease • Stroke (both ischemic and hemorrhagic) • Guillain–Barré syndrome (can cause ascending paralysis leading to death) • Small fiber neuropathy (numbness and tingling) Blood Clots • "The spike protein is the most thrombogenic protein we've ever seen in human medicine." • Unusually large and resistant blood clots • Blood clots that are not dissolving with conventional treatments Immunologic Abnormalities • Vaccine-induced thrombotic thrombocytopenia • Multisystem inflammatory disorder Peter A. McCullough, MD, MPH®

The Vigilant Fox 🦊

1,541,384 görüntüleme • 2 yıl önce

Every Vax-Injured Person Needs to See This: Recovery Insights from Dr. Peter McCullough “If we don’t address the spike protein, it’s not going to get better.” Dr. McCullough recommends three key substances for those seeking recovery after the shots. 1.) Nattokinase. Why? It degrades spike proteins, as suggested by preclinical studies. • Take 2000 units twice a day. 2.) Bromelain. Why? Similar to nattokinase, it also breaks down spike proteins. • Take 500 milligrams once a day 3.) Curcumin. Why? Reduces inflammation and spike protein damage. • Take 500 milligrams twice a day and combine with 5 or 10 mg of piperine to enhance its absorption. That summarizes Peter A. McCullough, MD, MPH®’s “Base Spike Detoxification” protocol. ADDITIONAL TREATMENTS Hydroxychloroquine: Added if there are signs of autoimmunity. Ivermectin: Included if there are signs of persistent infection. Colchicine: Used if there are significant signs of pleuropericardial problems (involving the membrane around the heart and lungs). Nicotine Patch or Oral Aciclovir: These are considered if there are neurological symptoms like brain fog. Low-dose Naltrexone: Used to enhance the body’s natural painkilling response and reduce inflammation. Please bookmark this post and share it with every vax-injured person you know.
2:17

Every Vax-Injured Person Needs to See This: Recovery Insights from Dr. Peter McCullough “If we don’t address the spike protein, it’s not going to get better.” Dr. McCullough recommends three key substances for those seeking recovery after the shots. 1.) Nattokinase. Why? It degrades spike proteins, as suggested by preclinical studies. • Take 2000 units twice a day. 2.) Bromelain. Why? Similar to nattokinase, it also breaks down spike proteins. • Take 500 milligrams once a day 3.) Curcumin. Why? Reduces inflammation and spike protein damage. • Take 500 milligrams twice a day and combine with 5 or 10 mg of piperine to enhance its absorption. That summarizes Peter A. McCullough, MD, MPH®’s “Base Spike Detoxification” protocol. ADDITIONAL TREATMENTS Hydroxychloroquine: Added if there are signs of autoimmunity. Ivermectin: Included if there are signs of persistent infection. Colchicine: Used if there are significant signs of pleuropericardial problems (involving the membrane around the heart and lungs). Nicotine Patch or Oral Aciclovir: These are considered if there are neurological symptoms like brain fog. Low-dose Naltrexone: Used to enhance the body’s natural painkilling response and reduce inflammation. Please bookmark this post and share it with every vax-injured person you know.

The Vigilant Fox 🦊

1,417,282 görüntüleme • 2 yıl önce

Dr. McCullough: The COVID Vaccines Are Causing the ‘Largest Blood Clots We’ve Ever Seen’ “My experience with these blood clots are they’re enormously resistant to blood thinners,” disclosed Dr. Peter A. McCullough, MD, MPH®. “Wuhan spike protein is inside the blood clots, and it’s folding, forming what’s called amyloid structures.” “They [researchers] found astronomical rates of blood clots in the retinal arteries and retinal veins in those vaccinated compared to the unvaccinated. And that was only with two shots back in 2021,” he detailed. “Two years later ... the risk is there. So, what I’m telling you is these vaccines have a very long effect in the human body. And when we see blood clots in the arteries, small arteries, and veins of the eyes, they’re reflecting what’s going on in the body.”
2:21

Dr. McCullough: The COVID Vaccines Are Causing the ‘Largest Blood Clots We’ve Ever Seen’ “My experience with these blood clots are they’re enormously resistant to blood thinners,” disclosed Dr. Peter A. McCullough, MD, MPH®. “Wuhan spike protein is inside the blood clots, and it’s folding, forming what’s called amyloid structures.” “They [researchers] found astronomical rates of blood clots in the retinal arteries and retinal veins in those vaccinated compared to the unvaccinated. And that was only with two shots back in 2021,” he detailed. “Two years later ... the risk is there. So, what I’m telling you is these vaccines have a very long effect in the human body. And when we see blood clots in the arteries, small arteries, and veins of the eyes, they’re reflecting what’s going on in the body.”

The Vigilant Fox 🦊

2,032,305 görüntüleme • 3 yıl önce