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The REAL reason why "the mRNA platform is so dangerous" - Bret Weinstein explains. "So, why do you get myocarditis from an mRNA shot? It doesn't have anything to do with spike. Spike, maybe making the problem worse, but the fact that your heart cells are producing a foreign...

389,385 次观看 • 1 年前 •via X (Twitter)

10 条评论

Clayton J Baker MD 的头像
Clayton J Baker MD1 年前

@BretWeinstein The entire mRNA platform is ill conceived. It’s potential to spark autoimmune disease alone makes it fundamentally toxic.

Noah Kau 的头像
Noah Kau1 年前

@BretWeinstein Bret Weinstein makes a crucial point. The real danger of mRNA technology is the immune system attacking heart cells as if they’re infected. This is a side effect that deserves much more scrutiny.

Patriotic 🇺🇸Suzanne⭐️⭐️⭐️ 的头像
Patriotic 🇺🇸Suzanne⭐️⭐️⭐️1 年前

@Steph93065 @BretWeinstein Every one of those that pushed for these vaccines knowing what they really were belongs in prison.

ferrelrobot 的头像
ferrelrobot1 年前

@BretWeinstein The sad thing is in the poker game of humanity. All 7 other players including the dealer were actively playing against the Freedom loving Patriots. All the media, governments and religions have conspired. Now it's time for Team Humanity to enact Nuremberg 2.0

fly over country 的头像
fly over country1 年前

@BretWeinstein It is the very definition of an autoimmune disorder. I have 3 already. I told my GP no thanks for the covid shot. She couldn't understand my reasoning. That's when I knew I needed a different GP. Most GP's have zero intellectual curiosity.

Censorship Sucks 的头像
Censorship Sucks1 年前

@BretWeinstein They are still injecting newborns.

EchoesOfFuture 的头像
EchoesOfFuture1 年前

@BretWeinstein Unpacking mRNA-induced myocarditis is crucial for broader understanding.

Marc Girardot 的头像
Marc Girardot1 年前

@BretWeinstein I remember a time, 4 years ago, when I was the only one talking about T-cells, and people looked at me in disbelief. Remember Jessica? So, yeah, T-cells are a part of the issue. But this isn't exactly what is happening: ------------------------------------------ (1) Myocarditis often happens several days or weeks after the T-cell attacks. Typically 2 weeks. T-cells attack within 5 days after injection. So it's not the T-cells on myocytes creating inflammation. ------------------------------------------ (2) There's very little evidence that LNPs actually penetrate the tissue (they'd have to pass the endothelial barrier in the heart first!). And transfection in tissue is very ineffective anyhow as shown by how much material escapes the arm. ------------------------------------------ (3) There's much more evidence of endothelial damage. It's the arteries (coronaries), arterioles and capillaries that get transfected and attacked by T-cells! ------------------------------------------ (4) Myocarditis has been demonstrated to be caused by leaky capillaries of the heart. So it's the leak into the cardiac tissue letting in metabolic waste that creates inflammation. ------------------------------------------ (5) How does a leak happen? By simple destruction of the endothelial wall in the capillaries (all endothelial cells are destroyed, and can't be replaced quickly). This explains not only myopericarditis, but all neurodegenerative diseases (leaky BBB), all hyper secretion hormonal diseases, leaky gut, tinnitus, eczema, endometriosis, etc... ------------------------------------------ (6) How can transfection happen in a concentrated fashion? Only via a bolus of particles carpet-bombing the area as observed with white-clots. ------------------------------------------ (7) How does a bolus occur? By direct IV injection of part of the dose. #BolusTheory ------------------------------------------ Read "The Needle's Secret" by @GirardotMarc. All the answers are there.

Julia Zaja, PharmD 的头像
Julia Zaja, PharmD1 年前

@SurfsBri @BretWeinstein Jesus Christ This explains so much… My SLE was out of control after my 2nd jab to the extent my rheumatologist had me file a VAERS report for it

John 🇺🇸 Nightvision 的头像
John 🇺🇸 Nightvision1 年前

@BretWeinstein Check out her SubStack "Unacceptable Jessica".

相关视频

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 次观看 • 10 个月前

"The makers of this immunotoxic vaccine knew [it would kill people]...You can't make something this damaging to humanity without doing it on purpose...It would not be so able to hijack your immune system to kill you slowly or quickly if it was not done purposefully." This is a clip of testimony given by Dr. Chris Shoemaker (Chris Shoemaker, MD), a comprehensive physician in Canada, during a recent session of the National Citizens Inquiry (National Citizens Inquiry (NCI | CeNC)). The National Citizens Inquiry (NCI) is a citizen-led and citizen-funded public inquiry into the Covid-19 health-protection measures taken by all levels of government in Canada. ---------------Partial transcription of clip--------------- "We all understand transplants. We understand if someone's kidney is put into you or someone's heart is put into you, your own natural immune system would attack the heck out of that transplanted kidney or attack the heck out of that transplanted heart if the surgeons and the internists didn't give a great degree of immune suppression, very heavy drugs that that would make your immune system basically go to sleep so that that new heart or that new kidney could settle into your body. "Here's the problem with spike protein. When spike protein goes into your body, you got 30,000 sorry, 30,000 billion cells in your body. You've got 40,000 billion mRNAs; enough to go into every cell of your body. So they're all going in and they're all creating a flag. They are all creating the fact that your body recognizes your heart is no longer your heart. It's a transplanted heart. Your kidney is no longer your kidney. It's a transplanted kidney...and that's why the body goes after it. And that's why the attacks are so varied. That's why one person could be suffering massively from a hepatitic or a kidney ailment, and another person will have a dissection in their aorta because their aorta is being inflamed by the attack or the heart. "The typical one is myocarditis in children, young adolescents, male and female, getting pain and troponin elevations and all the features of myocarditis. And it's because your immune system—it's not the spike itself—that's harming you. It's your immune system going after the spike that has changed the genetic image of your heart. And your body thinks it's not your heart, and that's why it attacks the heck out of it. "This is basic immunologic science. The makers of this immunotoxic vaccine knew this. They knew this for a purpose. You can't make something this damaging to humanity without doing it on purpose. And that is actually my major message of my talk today is I accuse someone—and I can't name them right now—but I accuse some entity of highly purposefully making things in the fashion that they did because it would not be as toxic as it is. It would not be so able to hijack your immune system to kill you slowly or quickly if it was not done purposefully. It has been done purposefully."

Sense Receptor

25,280 次观看 • 1 年前

"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 次观看 • 1 年前

"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 次观看 • 1 年前

mRNA injections as the "Trojan Horse"? Neil Oliver listens to Bret Weinstein think through a hypothetical military and biodefence perspective which the mRNA injections could function as, in the art of war. Stunningly, Bret points out that the IgG4 class switching could essentially be, what Neil Oliver refers to, as a Trojan Horse. Bret Weinstein: "I don’t know if we’ve talked about this before [but] the fact that somebody who’s gotten two of these mRNA injections produces IgG4 in response to the spike protein means that, at least, we have a novel solution to an age-old problem in bioweapons." "A weapons manufacturer has to figure out how to build a weapon that the enemy will suffer from that his own army will not." "The production of IgG4 by multiple mRNA injections, specifically in response to spike protein, opens up the reverse play [because] you can make a population vulnerable if you can get them to take the vaccine". Neil Oliver: "So, the thing that you’re calling, in that gameplay, the thing that you’re calling and offering to people as a vaccine—and we’ve all learned to question what’s exactly meant anymore by that word—it functions as a Trojan horse. Because you get people to take what they think is going to protect them when, in fact, it’s releasing into them all the little soldiers that are going to make them susceptible to the disease that’s coming anyway." Remember....China, Iran and Russia largely didn't use mRNA technology

Humanspective

69,306 次观看 • 1 年前