The mRNA is synthetic, which the body sees as “non-self.” This can trigger the production of autoantibodies to attack your own tissues as doctor Judy Mikovits, explains in her book Ending Plague.

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The long term higher rates of the following diseases will be seen in the general population : migraines, Parkinson’s disease, microvascular disorders, cancer, fibromyalgia and arthritis, bladder problems, kidney disease, psychosis, neurodegenerative diseases such as Lou Gehrig’s disease (ALS) and sleep disorders, including narcolepsy.

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.

In 2017, Stat News discussed Moderna’s challenges in developing an mRNA-based drug for Crigler-Najjar,

“To protect mRNA molecules from the body’s natural defenses, drug developers 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 challenge: Dose too little, and it will be ineffective;

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.

‘not many diseases qualified,’ according to a former employer; Crigler-Najjar was the lowest-hanging fruit. Yet Moderna could not make its therapy work. The safe dose was too weak, and injections of a strong enough dose had debilitating effects on the liver (animal studies)

However, if they call their drugs vaccines, they can bypass the safety studies. 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 ?

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?

The synthetic RNA in COVID-19 vaccines may escape degradation for months or even years. Previous attempts to create a coronavirus vaccine, failed due to the vaccines causing paradoxical immune reactions, or antibody-dependent immune enhancement. Animals used during the testing had antibodies against the virus, but still died after exposure to wild coronavirus. As a result of these vaccine qualities in the long term higher rates of the following disease will be seen in the general population : migraines, Parkinson’s disease, microvascular disorders, cancer, fibromyalgia and arthritis, bladder problems, kidney disease, psychosis, neurodegenerative diseases such as Lou Gehrig’s disease (ALS) and sleep disorders, including narcolepsy.

Flu Vaccines weaken the most vulnerable, following that up with a Covid shot can be fatal

Others who are at high risk from these COVID-19 gene therapies include those who have gotten seasonal influenza vaccines, Blacks and Hispanics. Blacks and Hispanics are particularly at risk for antibody-dependent immune enhancement, due to genetics.

If you already have a neural inflammatory disease, why wouldn’t you object to receiving a neural inflammatory toxin?

Infertility will also become more commonplace as syncytin (the gammaretrovirus envelope encoded in the human genome the expression of which can be dysregulated by the synthetic syncytin RNA in the vaccine) is required for proper fusion of the placenta in the uterus and implantation of the egg. That is why even the WHO is warning pregnant women to not get the Moderna or Pfizer vaccines. Normally, messenger RNA is not free in your body because it’s a danger signal.

“As a molecular biologist, the central dogma of molecular biology is that our genetic code, DNA, is transcribed, written, into the messenger RNA. That messenger RNA is translated into protein, or used in a regulatory capacity … to regulate gene expression in cells.

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.

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 (that they already had it).

myalgic encephalomyelitis. Inflammation of the brain and the spinal cord, which is associated with exogenous gammaretroviruses, the XMRVs.”