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Dr. Mercola explains Dr. Bridle’s revelations regarding Spike Proteins in mRNA Vaccines


June 22, 2021: Osteopathic Physician Dr. Joseph Mercola offers a detailed review of recent landmark research conducted and published by Dr. Byram Bridle. Provided immediately below is an audio link to the most recent Dr. Bridle interview followed by a detailed review of Dr. Bridle's mRNA Vaccine Spike Protein research by Dr. Mercola. The risks associated with biologically active and cytotoxic spike proteins in mRNA vaccines is of crucial importance to note.


Audio Link: Dr. Byram Bridle on Spike Protein based mRNA Vaccines



Dr. Joseph Mercola's Review of Dr. Bridle's Spike Protein Research (June 14, 2021)


Story At-a-Glance


Canadian immunologist and vaccine researcher Byram Bridle, Ph.D., has gained access to Pfizer’s biodistribution study from the Japanese regulatory agency. The research, previously unseen, demonstrates a huge problem with all COVID-19 vaccines:


- The assumption that vaccine developers have been working with is that the mRNA in the vaccines would primarily remain in and around the vaccination site. Pfizer’s data, however, show the mRNA and subsequent spike protein are widely distributed in the body within hours.


- This is a serious problem, as the spike protein is a toxin shown to cause cardiovascular and neurological damage. It also has reproductive toxicity, and Pfizer’s biodistribution data show it accumulates in women’s ovaries.


- Once in your blood circulation, the spike protein binds to platelet receptors and the cells that line your blood vessels. When that happens, it can cause platelets to clump together, resulting in blood clots, and/or cause abnormal bleeding.


- Pfizer documents submitted to the European Medicines Agency also show the company failed to follow industry-standard quality management practices during preclinical toxicology studies and that key studies did not meet good laboratory practice standards.


- The more we learn about the COVID-19 vaccines, the worse they look. In a recent interview1 with Alex Pierson (above), Canadian immunologist and vaccine researcher Byram Bridle, Ph.D., dropped a shocking truth bomb that immediately went viral, despite being censored by Google.


It also was featured in a “fact” check by The Poynter Institute’s Politifact, which pronounced Bridle’s findings as “false” after interviewing Dr. Drew Weissman,3 a UPenn scientist who is credited with helping to create the technology that enables the COVID mRNA vaccines to work. But, as you can see below, unlike Bridle, Politifact neglected to go beyond interviewing someone with such a huge stake in the vaccine’s success.


In 2020, Bridle was awarded a $230,000 government grant for research on COVID vaccine development. As part of that research, he and a team of international scientists requested a Freedom of Information Act (FOIA) access to Pfizer’s biodistribution study from the Japanese regulatory agency. The research, previously unseen, demonstrates a huge problem with all COVID-19 vaccines.


“We made a big mistake,” Bridle says. “We thought the spike protein was a great target antigen; we never knew the spike protein itself was a toxin and was a pathogenic protein. So, by vaccinating people we are inadvertently inoculating them with a toxin.”


This toxin, Bridle notes, can cause cardiovascular damage and infertility — a claim echoed by researchers such as Stephanie Seneff, Ph.D., and Judy Mikovits, Ph.D., whom I’ve interviewed about these issues.


Pfizer Omitted Industry-Standard Safety Studies


What’s more, TrialSite News reports that Pfizer documents submitted to the European Medicines Agency [EMA] reveal the company “did not follow industry-standard quality management practices during preclinical toxicology studies … as key studies did not meet good laboratory practice (GLP).”


Neither reproductive toxicity nor genotoxicity (DNA mutation) studies were performed, both of which are considered critical when developing a new drug or vaccine for human use. The problems now surfacing matter greatly, as they significantly alter the risk-benefit analysis underlying the vaccines’ emergency use authorization. As reported by TrialSite News:


“Recently, there has been speculation regarding potential safety signals associated with COVID-19 mRNA vaccines. Many different unusual, prolonged, or delayed reactions have been reported, and often these are more pronounced after the second shot.


Women have reported changes in menstruation after taking mRNA vaccines. Problems with blood clotting (coagulation) — which are also common during COVID-19 disease — are also reported. In the case of the Pfizer COVID mRNA vaccine, these newly revealed documents raise additional questions about both the genotoxicity and reproductive toxicity risks of this product.


Standard studies designed to assess these risks were not performed in compliance with accepted empirical research standards. Furthermore, in key studies designed to test whether the vaccine remains near the injection site or travels throughout the body, Pfizer did not even use the commercial vaccine (BNT162b2) but instead relied on a ‘surrogate’ mRNA producing the luciferase protein.


These new disclosures seem to indicate that the U.S. and other governments are conducting a massive vaccination program with an incompletely characterized experimental vaccine.


It is certainly understandable why the vaccine was rushed into use as an experimental product under emergency use authority, but these new findings suggest that routine quality testing issues were overlooked in the rush to authorize use.


People are now receiving injections with an mRNA gene therapy-based vaccine, which produces the SARS-CoV-2 spike protein in their cells, and the vaccine may be also delivering the mRNA and producing spike protein in unintended organs and tissues (which may include ovaries).”


Toxic Spike Protein Enters Blood Circulation


The assumption that vaccine developers have been working with is that the mRNA in the vaccines (or DNA in the case of Johnson & Johnson and AstraZeneca’s vaccines) would primarily remain in and around the vaccination site, i.e., your deltoid muscle, with a small amount draining into local lymph nodes.8


Pfizer’s data, however, show this isn’t the case at all. Using mRNA programmed to produce luciferase protein, as well as mRNA tagged with a radioactive label, Pfizer showed that the majority of the mRNA initially remain near the injection site, but within hours become widely distributed within the body.9


We have known for a long time that the spike protein is a pathogenic protein. It is a toxin. It can cause damage in our body if it gets into circulation. ~ Dr. Byram Bridle


The mRNA enters your bloodstream and accumulates in a variety of organs, primarily your spleen, bone marrow, liver, adrenal glands and, in women, the ovaries. The spike protein also travel to your heart, brain and lungs, where bleeding and or blood clots can occur as a result, and is expelled in breast milk.


This is a problem, because rather than instructing your muscle cells to produce the spike protein (the antigen that triggers antibody production), spike protein is actually being produced inside your blood vessel walls and various organs, where it can do a great deal of damage.


“It’s the first time ever scientists have been privy to seeing where these messenger RNA [mRNA] vaccines go after vaccination,” Bridle told Pierson.


“Is it a safe assumption that it stays in the shoulder muscle? The short answer is: absolutely not. It’s very disconcerting … We have known for a long time that the spike protein is a pathogenic protein.


It is a toxin. It can cause damage in our body if it gets into circulation … The spike protein on its own is almost entirely responsible for the damage to the cardiovascular system, if it gets into circulation.”


The Spike Protein Is the Problem


Indeed, for many months, we’ve known that the worst symptoms of severe COVID-19, blood clotting problems in particular, are caused by the spike protein of the virus. As such, it seemed really risky to instruct the body’s cells to produce the very thing that causes severe problems.


Bridle cites research showing that laboratory animals injected with purified spike protein from SARS-CoV-2 straight into their bloodstream developed cardiovascular problems and brain damage.


Assuming that the spike protein would not enter into the circulatory system was a “grave mistake,” according to Bridle, who calls the Japanese data “clear-cut evidence” that the vaccine, and the spike protein produced by it, enters your bloodstream and accumulates in vital organs. Bridle also cites recent research showing the spike protein remained in the bloodstream of humans for 29 days.


Once in your blood circulation, the spike protein binds to platelet receptors and the cells that line your blood vessels. As explained by Bridle, when that happens, one of several things can occur:


It can cause platelets to clump together — Platelets, aka thrombocytes, are specialized cells in your blood that stop bleeding. When there’s blood vessel damage, they clump together to form a blood clot. This is why we’ve been seeing clotting disorders associated with both COVID-19 and the vaccines:


- It can cause abnormal bleeding

- In your heart, it can cause heart problems

- In your brain, it can cause neurological damage


Importantly, people who have been vaccinated against COVID-19 absolutely should not donate blood, seeing how the vaccine and the spike protein are both transferred. In fragile patients receiving the blood, the damage could be lethal.


Breastfeeding women also need to know that both the vaccine and the spike protein are being expelled in breast milk, and this could be lethal for their babies. You are not transferring antibodies. You are transferring the vaccine itself, as well as the spike protein, which could result in bleeding and/or blood clots in your child. All of this also suggests that for individuals who are at low risk for COVID-19, children and teens in particular, the risks of these vaccines far outweigh the benefits.


The Spike Protein and Blood Clotting


In related news, Dr. Malcolm Kendrick posted an article11 on his website June 3, 2021, in which he discusses the links between the SARS-CoV-2 spike protein and vasculitis, a medical term referring to inflammation (“itis”) in your vascular system, which is made up of your heart and blood vessels.


There are many different types of vasculitis, including Kawasaki’s disease, antiphospholipid syndrome, rheumatoid arthritis, scleroderma and Sjogren’s disease. According to Kendrick, all of them have two things in common:


1. Your body for some reason starts to attack the lining of your blood vessels, thereby causing damage and inflammation — The “why” can differ from one case to another, but in all cases, your immune system identifies something foreign in the lining of the blood vessel, causing it to attack. The attack causes damage to the lining, which results in inflammation.


Blood clots are a common result, and can occur either because the platelets clump together in response to the vessel wall damage, or because your anticlotting mechanism has been compromised. Your most powerful anticlotting system is your glycocalyx, the protective layer of glycoproteins that lines your blood vessels.


Among many other things, the glycocalyx contains a wide variety of anticoagul