The biodistribution studies were done independently. This prevents researchers and regulatory agencies from being able to determine if a product is actually safe or effective.Īs mentioned, the pharmaceutical companies did not conduct studies to see how the injected biologicals were distributed in the body or how long the immune stimulation would continue-which is absolutely vital as regard to safety and the risk of long-term side effects. You should be aware that the so-called “studies” by these makers of the vaccines were badly flawed, in that placebos and blinding of the studies were abandoned before adequate studies were completed. Meetings by the regulatory agencies were unable to come to a firm conclusion on the length of the studies needed, so EUA proceeded despite the inherent dangers to the public. In this case, these companies were studying these vaccines for only two months before they were released, despite the recommendation by the FDA they be studied a minimum of 2 years before approval. The vaccine approval process for an experimental vaccine normally requires a period as long as ten years of intensive study before a vaccine is approved. In order to allow the population to use these entirely experimental biologicals the government had to declare this “pandemic” a medical emergency and utilize Emergency Use Authorization (EUA)-which emphasizes that the agents are not approved and are entirely experimental. Most important, one should understand these are experimental vaccines and do not have the approval of the regulatory agencies, such as the Food and Drug Administration (FDA). In such a location as the brain, the spike protein will act as a continuous source of inflammation and excitotoxicity (immunoexcitotoxicity), known to be a central mechanism of several neurodegenerative diseases, such as Alzheimer’s dementia, Parkinson’s disease and ALS, among others. This means that the mRNA from the vaccine is producing large amounts of the spike protein directly into your brain for what could be a prolonged period. It is also important to appreciate that biodistribution studies have shown that the mRNA injected into a person’s body has been found to deposit a small amount of the mRNA into several tissues, most importantly into the brain. Moderna and Johnson & Johnson have never made a vaccine before this. Since no studies have been done on what happens to the spike proteins once they have been injected and most important, how long the mRNA will keep producing the spike proteins, we have no idea concerning the safety of these vaccines.
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Blaylock’s Informed Consent Brochures available at Citizens For Free Speech. The two main sites it invades with the spike protein are the liver and the spleen-both major immune regulating sites.ĭr. Once in the body this spike protein can enter all tissues-including the heart, the brain, the lungs, the kidneys, the eyes, and the liver. In essence, you have a man-made virus, and mRNA biological that does exactly what the COVID-19 virus does to you-it exposes you to massive amounts of spike protein. You should know that the spike protein is the pathological part of the COVID-19 virus. This man-made virus literally infects the person with a spike protein-containing virus.
The latter two biologicals, from Johnson & Johnson and AstraZeneca, utilize a single vaccine technology involving the use of an altered, attenuated virus (Adeno26) to generate antibodies to the spike protein. This prolongs the survival of the mRNA, allowing it to continuously produce the spike protein in your body. The mRNA biologicals encase spike protein producing mRNA within a nanoparticle capsule–LNP to protect the mRNA from enzymatic destruction by the vaccinated person’s cells. Two (Pfizer and Moderna) use a technology never before approved or used “vaccine” called a messenger RNA (mRNA) biological. There are four major companies offering the COVID-19 “vaccines” (biological bioengineered agents) Pfizer, Moderna, Johnson & Johnson and AstraZeneca.
Blaylock wrote this especially for this purpose. Prior to taking any unapproved drug, you have the right to receive a broad and complete spectrum of information about the potential effects of those drugs on your body, in order for you to give “informed consent” or to refuse.
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