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“We were completely lied to…” Nicolas Hulscher, MPH joined “The HighWire” and shared some information from an upcoming study. A 51-year-old man developed multi-system complications after mRNA vaccination, including: 🛑Myocarditis 🛑Pulmonary embolism 🛑Neurological disturbances 🛑Persistent skin disease 3.6 years after his last shot, investigators detected: ➡️Circulating mRNA from the...

19,702 görüntüleme • 6 ay önce •via X (Twitter)

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'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

"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

A stunning testimony before the Massachusetts Legislature demands our full attention. Dr. Janci Chunn Lindsay, a PhD molecular biologist and toxicologist, delivered a methodical and devastating critique of the COVID-19 mRNA injections, asserting that the public was built upon a foundation of falsehoods. According to Dr. Lindsay, the very platform was "sold with a bunch of lies." She systematically listed the key promises made to the public that, in her professional assessment, have proven untrue: ▪️ The Nature of the Product: We were assured it was not a gene therapy. ▪️ Localized Effect: We were told the injection would remain localized in the arm. ▪ mRNA Stability: We were told the modified mRNA would break down rapidly. ▪️ Cellular Mechanism: We were told the spike protein could not enter the cell nucleus. ▪️ Genomic Impact: We were told reverse transcription and integration into human DNA was impossible. ▪️ Vaccine Purity: We were told there was no risk of DNA contamination altering our genetics. ▪️ Protein Specificity: We were told the shots would only produce the intended spike protein. ▪️ Treatment Alternatives: We were told no other safe and effective treatments existed. ▪️ Efficacy: We were told the shots were effective at preventing severe disease and death. ▪️ Transmission: We were told the products could not be shed to others. Her conclusion is stark: "All of these were lies." This testimony from a credentialed expert challenges the core narrative of the global pandemic response. It raises profound questions about institutional trust, scientific transparency, and informed consent. This is not a fringe theory; it is a formal allegation from a scientist with the background to make it. The conversation can no longer be avoided.

Camus

158,182 görüntüleme • 10 ay önce

Dr. Byram Bridle, a virologist, has sounded a critical alarm about the systemic biodistribution of COVID-19 mRNA vaccines and their alarming presence in breast milk. Years ago, Bridle warned that lipid nanoparticles in these shots could spread to organs like the bladder, intestines, and skin, raising concerns about vaccine shedding through urine, feces, sweat, and skin oils. Now, peer-reviewed science confirms his fears: fragments of synthetic mRNA from the vaccines are definitively present in the breast milk of vaccinated mothers. Bridle explains the mechanism: after injection, the vaccine migrates from the shoulder—contrary to claims it remains localized—through the lymphatic system and blood vessels to breast tissue. There, lipid nanoparticles fuse with mammary gland cells, which produce spike protein and release exosomes—tiny fat bubbles containing synthetic mRNA fragments—into breast milk. This means breastfeeding infants, including those under six months for whom the vaccines are not approved, are unknowingly ingesting these components orally, a route never authorized. Even more disturbing, Health Canada’s own vaccine monographs for Pfizer and Moderna shots admit there are no safety data for pregnant or breastfeeding women and no assurance that vaccine components won’t reach breast milk or harm infants. Despite this, the shots continue to be pushed on breastfeeding mothers without full disclosure, undermining informed consent. Bridle’s revelations demand urgent action. Why are infants being exposed to unapproved vaccine components? Why are breastfeeding women not informed of the risks?

Camus

45,284 görüntüleme • 1 yıl önce

THE PFIZER COVID MRNA PRODUCT TRAVELS TO ALL THESE BODY SYSTEMS...AND NZ DRUG REGULATORS KNEW BEFORE THEY AUTHORISED THE PRODUCT.... NZ OIA confirms that NZ drug regulators received this information BEFORE they approved the Pfizer mRNA Covid injection in NZ. (OIA Ref: H2024046787) They received this chart and the document at the link (see link in comments) They KNEW the contents of the Pfizer mRNA travels freely throughout the body. They KNEW this when they approved this product, and New Zealanders were repeatedly told "it stays in the muscle of the arm". This chart shows the biodistribution of the Lipid Nano Particles (LNPs) used in the Pfizer mrna Covid injection. In March 2023 the Australian TGA released information under a Freedom of Information request, pertaining to the movement of the Mrna carrying LNPs through the body, post injection. From the very start Government's around the world (including Australia and NZ) have categorically assured us that the injected LNP/mRNA combination stays ONLY in the deltoid muscle where it is injected, with a small amount possibly reaching the local lymph node. This assurance was KEY in calming the fears of the people. We were (are still) told repeatedly that ONLY the Deltoid muscle cells produced the spike protein, in response to the mRNA that made it's way into muscle cells, carried by the LNPs. The chart below demonstrates the TRUE pathways throughout the entire body. Of note: *within 15 minutes of injection, the LNPs (and their mRNA payload) have been taken up by both whole blood and blood plasma. e.g. within 15 minutes the vaccine is circulating around your body in the bloodstream. *8 hours post injection the concentrations in the blood have dropped significantly BUT at the same time concentrations in various organs continue to rise rapidly. *The liver, spleen and adrenal glands have the highest concentration of accumulated LNPs *Notice that the study was arbitrarily discontinued at the 48 hours post injection mark DESPITE the still increasing levels of accumulation in various organs. *Almost every organ was still showing INCREASING bioaccumulation at the point of study discontinuation. *Between the 24 and 48 hrs post injection measures, the LNP accumulation in the OVARIES more than doubled. We have NO idea how much more accumulation happened after the 48 hour point. This study is a massive red flag for safety, and we still have no idea of the long term implications of spike mRNA production in almost every organ of the body. (link in comments) Video: Chief vaccine advisory committee in USA (ACIP) discusses BIODISTRIBUTION of mRNA Covid injectables

NZ and the MRNA

22,877 görüntüleme • 10 gün 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

Valerie Anne Smith

16,998 görüntüleme • 1 yıl önce

"There's absolutely no question that this was not an accident...the fact that we have one-third DNA product and two-thirds RNA product [in the C19 jabs] is, for whatever reason, the ratio that the makers wanted it to be. They have lied to us in the extreme." Canadian Comprehensive Physician Dr. Chris Shoemaker (@CShoemakerMD) describes for the RAIR Foundation (RAIR Foundation USA) how the DNA contamination of the COVID injections "was not an accident." Shoemaker notes that "They have lied to us in the extreme" and "We are in danger in the extreme, not just in the short term." "There's absolutely no question that this was not an accident. There's absolutely no question that it was carefully and scientifically accomplished," Shoemaker says. "And the fact that we have one-third DNA product and two-thirds RNA product is, for whatever reason, the ratio that the makers wanted it to be." "What's the difference [if there is] DNA is in [the jabs] instead of just mRNA? The difference is that...the DNA, functionally, once in the nucleus, can influence the nucleus, [and] can produce mRNA near the nucleus and have that mRNA migrate out into the cytoplasm of the cell," Shoemaker says. "And once that's done, what should be, at worst, an 8-month process inside your body is, in fact, an 8- to 10-year process inside your body because of the nefarious decision to allow DNA in these shots." Partial transcription of clip: "There's absolutely no question that this was not an accident. There's absolutely no question that it was carefully and scientifically accomplished. And the fact that we have one-third DNA product and two-thirds RNA product is, for whatever reason, the ratio that the makers wanted it to be. They have lied to us in the extreme. "We are in danger in the extreme, not just in the short term. We know the 2 percent, 3 percent of people who passed away suddenly and surprisingly and that's way more than should happen. But the long term effect on the ability to fight cancer or for a cancer to perhaps be a turbo cancer, all these are being influenced by both DNA and RNA that is within us. "The key thing is that it makes the whole process last longer. If it was only mRNA, it would probably be 8 to 12 months only that mRNA would seed out into your body and be repeatedly creating spike, repeatedly creating spike. Remember, the end-product is the most dangerous part of this human engineered genome. The spike protein is the thing that congeals blood cells against each other. The spike protein is the thing that, if it's in your liver, is waving a flag saying, Hey, I'm not your liver. I'm not a human liver. I've got this strange created spike protein. You can identify that I'm not your liver, and you can attack it, and you can make hepatitis for this person because it's not even their liver. "This is what mRNA does is create a flag so that you're attacking through your healthy immune system. Your healthy immune system is going after it in organ after organ after organ. For some people, it's just a specific organ that was already a bit weak to begin with. And for other people, it's a different organ. But either way, mRNA produces a spike flag, which your immune system attacks. "To return to your question about DNA, what's the difference that DNA is in there instead of just mRNA? The difference is that the DNA can, for years, not just 8 to 12 months. The DNA, functionally, once in the nucleus, can influence the nucleus, can produce mRNA near the nucleus and have that mRNA migrate out into the cytoplasm of the cell. And once that's done, what should be, at worst, an 8-month process inside your body is, in fact, an 8 to 10 year process inside your body because of the nefarious decision to allow DNA in these shots."

Sense Receptor

95,273 görüntüleme • 1 yıl 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

Gerard Rennick

62,522 görüntüleme • 1 yıl önce