The interviews below are not the faint hearted, it is a deep dive into the science of the mRNA Vaccine and what physical reaction, effects, symptoms and disease may follow in years to come.
In the first interview, Stephanie Seneff, Ph.D., and Judy Mikovits, Ph.D., a dream-team in terms of deep insights into the scientific details, explain the problems they see with gene-based COVID-19 vaccines. There is a load of highly useful technical information that you can use to defend your opposition to these dangerous vaccines.
The second interview Stephanie Seneff, Ph.D. talks about her latests published research of the mRNA vaccines and what those who got vaccinated can expect.
Is the Spike Protein a Bioweapon?
According to Mikovits and many others including Pfizer , the worst symptoms of COVID-19 are created by the SARS-CoV-2 spike protein. The same spike protein the gene therapy developed and produced my moderna and Pfizer is instructing the body to abundantly manufacture. If this was not bad enough the spike protein the mRNA instructing the body to create has been genetically modified, making it far more toxic.
“The SARS-CoV-2 infection never was what they said it was… the spike protein is clearly [causing] the disease.” Mikovits says. “So, you just injected the envelope of HIV … a syncytin gammaretrovirus envelope, and a SARS S2 receptor binding domain. That’s not a vaccine. It is the disease-causing agent. It’s a bioweapon. So now your cells are all producing that bioweapon and you’re going to take out the innate immunity, NK [natural killer] cells and dendritic cells … You’re going to disrupt your white blood cells, your immune response. You’re going to turn on an anti-inflammatory cytokine signature in every cell of your body. It exhausts your NK cells’ ability to determine infected cells. It’s the nightmare we predicted.”
mRNA Spike Protein Produced by the Body – Highly Unnatural
In her paper, “Worse Than The Disease: Reviewing Some Possible Unintended Consequences of mRNA Vaccines Against COVID-19,” published in the International Journal of Vaccine Theory, Practice and Research in collaboration with Dr. Greg Nigh,2 Seneff explains that a significant part of the problem is that while the natural spike protein is bad, the spike protein your body produces in response to the vaccine is even worse.
“Normally, enzymes that are in your system would just break down that RNA. RNA is very fragile, but they’ve made it sturdy by putting in PEG [polyethylene glycol], by adding this lipid membrane, and the lipid is positively charged, which causes the cell to be very upset when that goes into the membrane of the cell.
But I think maybe the most disturbing thing is they actually modified the [RNA] code so that it doesn’t produce a normal version of the spike protein. It produces a version that has a couple of prolines in it, side by side at the critical place where this spike protein normally would fuse with the cell that it’s infecting.
So, the spike protein binds to the ACE2 receptor once it’s produced by the human cell … but it’s a modified version of the spike protein. It has these two prolines that make it very stiff so that it can’t reshape. Normally it would bind to the ACE2 receptor and then it would reshape and go straight into the membrane like a spear.
Because of this redesign, it can’t do that, so it sits there on the ACE receptor, exposed … That allows the immune cells to produce antibodies specific to that place where it should be fusing with the cell, the fusion domain. It messes up the fusion domain, keeps the protein open, and prevents the protein from getting in, which means the protein will just stick there on the ACE2 receptor, disabling it.
When you disable ACE2 receptors in the heart, you get heart failure. When you disable them in the lungs, you get pulmonary hypertension. When you do it in the brain, you get stroke. Lots of nasty things happen when you disable ACE2 receptors …
The other thing they’ve done with the RNA is they’ve stuck in a lot of extra Gs (guanine) and Cs (cytosine), which makes it much better at making proteins. It’s turned up the gain on the natural virus 1,000-fold, making the RNA much more willing to make a protein. So, it’ll make a lot more spike protein than you would’ve had from a natural RNA virus.”
Dormant Viruses May Flare up after COVID jab
Seneff and Mikovits’ findings points out that many problems we’re seeing in the vaccinated with this gene-therapies develop herpes and shingles infection.
“Basically, you’ve got these latent viruses that are not bothering you at all until your immune system gets completely distracted by this crazy thing going on in the spleen with all this messenger RNA and all these spike proteins,” Seneff says.
“Immune cells are distracted from their other job of keeping these viruses in check. So, you get these other conditions showing up, and there are several. There’s Bell’s palsy (facial palsy), for example. There are over 1,200 cases of Bell’s palsy reported after the vaccine in the Vaccine Adverse Event Reporting System (VAERS).
And when you look at the research of what causes that, they really point to the herpes virus and the varicella virus as being the source of Bell’s palsy. The Type I interferon system is what you need to keep these guys in check, and so those viruses are getting enabled and they’re causing symptoms.
That is actually a very bad sign. If a woman who’s pregnant has a herpes flare-up during pregnancy, she has a twofold increased risk of producing an autistic son.
Also, in a study on 200 Parkinson’s patients, compared to 200 age- and gender-matched controls, six of those Parkinson’s patients had at least one episode of Bell’s palsy in the past, whereas none of the controls had. So, it looks to me like the Bell’s palsy is an indicator of a future risk of Parkinson’s disease.”
Was SARS-CoV-2 Spike Protein Engineered With HIV?
Mikovits claims there’s evidence showing the SARS-CoV-2 spike protein was engineered by integrating HIV and XMRV proteins. XMRV stands for xenotropic murine leukemia virus-related virus, a human retrovirus that is very similar to endogenous retroviruses also found in other mammals.
“Our endogenous gammaretrovirus is called human endogenous retrovirus-W (HERV-W). HERVW is all the way back in genesis in our original endogenous genome. It’s a gammaretrovirus that expresses only the envelope, because in retroviruses, the envelope alone is enough to cause the disease. That envelope protein is called syncytin. They’re [now] calling it ‘spike protein’ just to throw us all off,” Mikovits says.
Mikovits suggests, that the SARS-CoV-2 virus was created by introducing a mutation into a molecular clone. Vero E6 monkey tissues are known to be infected with SIV and other gammaretroviruses, and the SARS-CoV-2 virus has markers suggesting it was grown in a Vero E6 cell line, she says.
“So syncytin is the gammaretrovirus; it cross-reacts with the mouse and monkey gammaretroviruses. Monkeys, mice all have syncytin. Endogenous viruses express, especially during hormonal cycles. When it’s expressed in the wrong place, like in the brain or the spinal cord, it’s long been associated with the inflammatory disease and the destruction of the myelin sheet in multiple sclerosis (MS).
So, syncytin expressed it in the wrong place gives you the paralytics diseases. We know Parkinson’s is associated with Type I interferon responses. We’re now starting to appreciate that there is low-level expression of our endogenous virome all the time, and that in our innate immune response it’s trying to shape and educate our Type I interferon pathways …
The final and biggest problem is these exosomes, because your body’s exosomes are like your cells’ response to express its regulatory RNAs, small inhibitory RNAs, long-chain non-coding RNA — which Ritchie Shoemaker has long associated with chronic Lyme and ME/CFS — and the TGF-beta I pathway.
TGF-beta I, that’s the master switch to turn on which Type I interferon, which [is needed for] myelopoiesis. But these exosomes are packaging not only RNA that you’re making, but now you’ve dysregulated the methylation so you’ve woken up your endogenous virome, and then syncytin is going to be expressed.”
Can mRNA Alter our DNA?
Seneff describes in her paper, how mRNA can alter our DNA, essentially integrating the instructions to make spike proteins into our genome. Usually, mRNA could not be integrated directly into our genes because it need reverse transcriptase.
Reverse transcriptase converts RNA back into DNA (reverse transcription). Given that there’s a wide variety of reverse transcriptase systems already embedded in our DNA, it is possible. Mikovits has studied this for decades, here is what she says:
“When you activate latent and defective viruses, you turn on reverse transcriptase; you turn on the virome. But you also need an integrase gene. So how are retroviruses silenced? [Through] DNA methylation. [When] you throw in a lot of GC-rich regions — you’ve got that synthetic viral particle [i.e., the vaccine-induced spike protein RNA] — now you’ve woken up your herpes viruses.
[Latent viruses] are silenced [through] DNA methylation, but as our soil is depleted in minerals, we have people with methylation defects. This is why I said the first people who are going to die are people with inflammatory conditions and cancer.”
Could SARS-CoV-2 Spike Protein Be a Prion?
Seneff also discusses in her paper evidence that SARS-CoV-2 spike protein may be a prion:
“I’m now thinking that may be the worst aspect of these mRNA vaccines, because they’re producing this abnormal spike protein that doesn’t want to go into the membrane. Prion proteins are known to be membrane proteins. They’re alpha-helices in the membrane and then they misfold, becoming beta-sheets in the cytoplasm, and that’s what leads to the prion problem.
They form a crystal that draws in other proteins and makes this big mess and builds fibrils and Alzheimer’s plaque. The main prion protein is PrP, which is in Creutzfeldt-Jakob disease, the human form of mad cow disease. It’s a sort of protein-source infection. It’s quite wild because there’s no DNA involved, no RNA involved, just protein.
But the thing is, when you have produced a version of mRNA that knows how to spew out tons of a prion protein, the prion proteins become problematic when there’s too many of them and the concentration is too high in the cytoplasm.
And the spike proteins that these mRNA vaccines are producing … isn’t able to go into the membrane, which I think is going to encourage it to become a problematic prion protein. Then, when you have inflammation, it upregulates alpha-synuclein [a neuronal protein that regulates synaptic traffic and neurotransmitter release].
So, you’re going to get alpha-synuclein drawn into misfolded spike proteins, turning into a mess inside the dendritic cells in the germinal centers in the spleen. And they’re going to package up all this crud into exosomes and release them. They’re then going to travel along the vagus nerve to the brainstem and cause things like Parkinson’s disease.
So, I think this is a complete setup for Parkinson’s disease. What may happen is that because they got this vaccine, they get Parkinson’s disease five years earlier than they would have gotten it otherwise. It’s going to push forward the date at which someone who has a propensity towards Parkinson’s is going to get it.
And it’s probably going to cause people to get Parkinson’s who never would have gotten it in the first place — especially if they keep getting the vaccine every year. Every year you do a booster, you bring the date that you’re going to get Parkinson’s ever closer.”
The discussion continue to explore more questions: Are Viral Vector Vaccines Better or Worse? Can COVID Vaccines ‘Shed’ or Transmit Infection? Which Vaccine Is Most Dangerous? What Can We Expect to See More Of?
Are there any solutions?
Mikovits suggests the following remedies could help with disease that might develop post-vaccination:
- Hydroxychloroquine and ivermectin treatments
- Low-dose antiretroviral therapy to reeducate your immune system
- Low-dose interferons such as Paximune, developed by interferon researcher Dr. Joe Cummins, to stimulate your immune system
- Peptide T (an HIV entry inhibitor derived from the HIV envelope protein gp120; it blocks binding and infection of viruses that use the CCR5 receptor to infect cells)
- Cannabis, to strengthen Type I interferon pathways
- Dimethylglycine or betaine (trimethylglycine) to enhance methylation, thereby suppressing latent viruses
- Silymarin or milk thistle to help cleanse your liver
Dr Mecola believes the best thing you can do is to build your innate immune system. To do that, you need to become metabolically flexible and optimize your diet. You’ll also want to make sure your vitamin D level is optimized to between 60 ng/mL and 80 ng/mL (100 nmol/L to 150 nmol/L), ideally through sensible sun exposure. Sunlight also has other benefits besides making vitamin D.
Use time-restricted eating and eat all your meals for the day within a six- to eight-hour window. Avoid all vegetable oils and processed foods. Focus on certified-organic foods to minimize your glyphosate exposure, and include plenty of sulfur-rich foods to keep your mitochondria and lysosomes healthy. Both are important for the clearing of cellular debris, including these spike proteins. You can also boost your sulfate by taking Epsom salt baths.
To combat the toxicity of the spike protein, Seneff suggests optimizing autophagy, which may help digest and remove the spike proteins. Time-restricted eating will upregulate autophagy, while sauna therapy, which upregulates heat shock proteins, will help refold misfolded proteins. They also tag damaged proteins and target them for removal.
It is important that your sauna is hot enough (around 170 degrees Fahrenheit) and does not have high magnetic or electric fields. Last but not least, Mikovits recommends never getting another vaccination.
“We knew the flu shot would drive the disease,” she says. “It’s the combinations. That’s a ticking time bomb sitting there in every cell. So never get another vaccine and be very careful about drugs that compromise your immune system.
The answer is, don’t hyper-immune activate. Don’t eat GMO. Don’t ingest it and don’t inject it. And don’t put it on your skin. Don’t use toxins on your hair. Use essential oils, use antimicrobials … ozonated balms and creams break apart the lipid particles, cannabis balms and creams normalize skin, [which is part of] your immune system …
Remember, immune dysfunction accelerates every time you add an immune activation event. So, if the entire world never again took another shot, even the most susceptible populations, they could stay well … We really have to say no more shots because they’re the single biggest toxin to anyone, and an immune dysregulator.”
SARS-CoV2 / CoViD-19
I could remember in the early days everyone and the MSM was calling the disease “CoViD 19” from the SARS-CoV2. Then the fear porn wasn’t working enough by them, so they ramped it up a few weeks later, in part, by switching the name from CoViD 19 to “CoViD.”
CoViD is the generalisation for just Corona Virus Disease.This was to scare people on anything Corona Virus related whether it was just the Corona Virus responsible for the Common Cold, CoViD 19(SARS-CoV2), or any other kind.
Now we see that after the “CoViD” narrative mindcontrol stuck in much of the general population, we also see most of the Conservative Media followed lockstep by the influence of the MSM Syndrome. Many doctors and nurses which should know better are doing it, too.
People it is NOT CoViD that came out of the 2019 Plandemic, but is CoviD 19 as per the SARS-CoV2. There is a huge distinction, and we need people to know this, so that they’re not in fear of everything corona virus related; they’re not all the same!
The public needs to know the correct label, just as if you were writing an itemised bill, or a science article, or an announcement to the public.
Dr Martin | The CoViD 19 (modified) mRNA Gene-Code(Editing) Serum is an inoculum, NOT A VACCINE. I refer to it as an mRNA injection.
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