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As Bret Weinstein, Ryan Cole MD predicted, mRNA tech is FUNDAMENTALLY flawed. Dr Cole: "The platform isn't proven or safe, [it's] not about the spike protein [it's] about ANY sequence" NEW study from Stanford University on "How covid vaccines can cause Heart Damage" just raised this very issue, mentioning...

26,427 просмотров • 8 месяцев назад •via X (Twitter)

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"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

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67,928 просмотров • 1 год назад

"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 просмотров • 1 год назад

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

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104,361 просмотров • 11 месяцев назад