COVID-19 Vaccines Aren’t Real Vaccines
Info and excerpts from an interview with Judy Mikovits
“Judy Mikovits is Among Her Generation’s Most Accomplished Scientists.” —Robert F. Kennedy, Jr. Dr. Mikovits joined NIH in 1980 as a Postdoctoral Scholar in Molecular Virology at the National Cancer Institute and began a 20-year collaboration with Frank Ruscetti, a pioneer in the field of human retro virology. More on Dr. Mikovits here:
The COVID-19 vaccine really isn’t a vaccine in the medical definition of a vaccine. It does not improve your immune response to the infection, nor does not limit you from getting the infection. It’s really an experimental gene therapy that could prematurely kill large amounts of the population and disable exponentially more.
“I’m just beside myself with anger over this synthetic gene therapy, this chemical poison, and what they’re doing worldwide,” Mikovits says. “We’re already seeing deaths from this shot. It’s illegal. It shouldn’t be done. It should be stopped right now. It should have never been allowed to happen, yet we see it being forced on the most vulnerable populations.”
Indeed, news and social media reports suggest recipients are starting to drop like flies. Many die of unknown causes within days, sometimes hours of getting the first or second shot.
Baseball legend Hank Aaron passed away two weeks after receiving the vaccine, yet this was not ever mentioned in his New York Times obituary. Surely, had he tested positive for SARS-CoV-2, he would have been declared a COVID-19 fatality, whether the virus actually had anything to do with it or not.
But when it comes to the vaccine, even eyebrow-raising timing is dismissed as coincidental and irrelevant. Now all of a sudden, old people dying shortly after vaccination are shrugged off with the excuse that they’re old and could have died any day anyway. Old people dying with SARS-CoV-2, however, must be stopped at any cost. Funny how that works.
The Problem With Synthetic RNA
The messenger RNA (mRNA) used in many COVID-19 vaccines are not natural. They’re synthetic. Since naturally produced mRNA rapidly degrades, it must be complexed with lipids or polymers to prevent this from happening. COVID-19 vaccines use PEGylated lipid nanoparticles, and PEG is known to cause anaphylaxis.2 Lipid nanoparticles may also cause other problems.
In 2017, Stat News discussed Moderna’s challenges in developing an mRNA-based drug for Crigler-Najjar, a condition that can lead to jaundice, muscle degeneration and brain damage.
“In order to protect mRNA molecules from the body’s natural defenses, drug developers must wrap them in a protective casing. For Moderna, that meant putting its Crigler-Najjar therapy in nanoparticles made of lipids.
And for its chemists, those nanoparticles created a daunting challenge: Dose too little, and you don’t get enough enzyme to affect the disease; dose too much, and the drug is too toxic for patients.
From the start, Moderna’s scientists knew that using mRNA to spur protein production would be a tough task, so they scoured the medical literature for diseases that might be treated with just small amounts of additional protein.
‘And that list of diseases is very, very short,’ said the former employee … Crigler-Najjar was the lowest-hanging fruit. Yet Moderna could not make its therapy work … The safe dose was too weak, and repeat injections of a dose strong enough to be effective had troubling effects on the liver in animal studies.”
However, if they call their drugs vaccines, they can bypass the safety studies. All of a sudden, they expect us to believe that all of these safety issues have been resolved? Another problem is related to how long the mRNA remains stable in your system. It’s encased in nanolipid to prevent it from degrading too rapidly, but what happens if the mRNA degrades too slowly, or not at all?
The idea behind mRNA vaccines is that by tricking your body into creating the SARS-CoV-2 spike protein, your immune system will produce antibodies in response. But what happens when you turn your body into a viral protein factory, thus keeping antibody production activated on a continual basis with no ability to shut down?
In addition, your body sees these synthetic particles as non-self and much of the perpetual antibody response will be autoantibodies attacking your own tissues.
“Now you’ve got PEG, PEGylated and polyethylene glycol, and a lipid nanoparticle that will allow it to enter every cell of the body and change the regulation of our own genes with this synthetic RNA, part of which actually is the message for the gene syncytin …
Syncytin is the endogenous gammaretrovirus envelope that’s encoded in the human genome … We know that if syncytin … is expressed aberrantly in the body, for instance in the brain, which these lipid nanoparticles will go into, then you’ve got multiple sclerosis.
The expression of that gene alone enrages microglia, literally inflames and dysregulates the communication between the brain microglia, which are critical for clearing toxins and pathogens in the brain and the communication with astrocytes.
It dysregulates not only the immune system, but also the endocannabinoid system, which is the dimmer switch on inflammation. We’ve already seen multiple sclerosis as an adverse event in the clinical trials, and we’re being lied to: ‘Oh, those people had that [already].’ No, they didn’t.
We also see myalgic encephalomyelitis. Inflammation of the brain and the spinal cord, which is [associated with] exogenous gammaretroviruses, the XMRVs.”
These High-Risk Groups Should Avoid COVID-19 Vaccine
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