Can the COVID-19 vaccines cause irreparable harm? Should we be anticipating massive numbers of neurological diseases, reproductive harm, and other problems? Stephanie Seneff, Ph.D., and Judy Mikovits, Ph.D., believe it’s possible. Seneff has published a paper on the potential of neurological disease resulting from the COVID-19 vaccines, and Mikovits has warned that fertility rates may drop due to the SARS-CoV-2 spike protein creating antibodies that attack syncytium. Scientists and doctors are now beginning to see this.
Despite this, the CDC recommends that pregnant women and children as young as 12 get the “jab.”
The spike protein is the bioweapon
According to Mikovits, the worst symptoms of COVID-19 are produced by the SARS-CoV-2 spike protein. The gene-based vaccines instruct your body to produce the spike protein in a genetically modified form that makes it more toxic.
“The SARS-CoV-2 infection never was what they said it was,” Mikovits says. “There was no infection asymptomatically. It’s a monkey virus coming out of a monkey cell line and that’s the problem, but the spike protein is clearly causing the disease.
“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.”
The spike protein produced in your body is 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, Seneff states that the natural spike protein is bad, but the spike protein your body generates after the vaccine is much worse than the natural version.
This is due to the fact that the synthetic RNA has been manipulated to create a very unnatural spike protein that results in it not collapsing on itself into the cell once it attaches to the ACE2 receptor. This would be the normal reaction. Instead it stays open and attached to the ACE2 receptor, disabling it and causing problems with the heart, lung, and immune system.
As explained by Seneff:
“They modified the RNA to make it really sturdy so the enzymes can’t break it down … 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 a 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.”
Reactions may be worse than expected
With more information flowing in from people who have reactions to the vaccine, Mikovits believes that the vaccine may be far worse than she initially expected. She believes the lipid nanoparticle is dangerous. And the genetically modified mRNA is more capable at avoiding its natural breakdown.
Free RNA acts as a red alert signal for your body while the RNA remains viable. The manipulated RNA has the spike protein RNA sequence that looks part bacteria, part virus, and part human concurrently.
She states:
“We use poly(I:C) [a toll-like receptor 3 agonist] to signal the cell to turn on the type I interferon pathway,” Mikovits explains, “and because this is an unnatural synthetic envelope, you’re not seeing poly(I:C), and you’re not [activating] the Type I interferon pathway.
You’ve bypassed the plasmacytoid dendritic cell, which combined with IL-10, by talking to the regulatory B cells, decides what subclasses of antibodies to put out. So, you’ve bypassed the communication between the innate and adaptive immune responses. You now miss the signaling of the endocannabinoid receptors …
A large part of Dr. [Francis] Ruscetti’s and my work over the last 30 years has been to show you don’t need an infectious transmissible virus — just pieces and parts of these viruses are worse because they also turn on danger signals. They act like danger signals and pathogen-associated molecular patterns.
So, it synergistically leaves that inflammatory cytokine signature on that spins your innate immune response out of control. It just cannot keep up with the myelopoiesis [the production of cells in your bone marrow]. Hence you see a skew-away from the mesenchymal stem cell towards TGF-beta regulated hematopoietic stem cells.
This means you could see bleeding disorders on both ends. You can’t make enough firetrucks to send to the fire. Your innate immune response can’t get there, and then you’ve just got a total train wreck of your immune system.”
The COVID vaccines have pieces of the virus that are worse than the whole virus. The manufacturing process leaves fragmented genetically modified RNA in the vaccine. Many experts assume these pieces are harmless, while other scientists disagree and believe the vaccine is dangerous.
Scientists now see latent viruses flaring after the jab
Scientists following vaccine reactions are seeing an increase in herpes and shingles after a person receives the jab. This is typical in people who have a disabled interferon pathway. Scientists suspect that the messenger RNA and spike proteins act as distractions in the immune cells, which allows latent viruses to flare. There are over 1,200 cases of Bell’s palsy reported after the vaccine in the Vaccine Adverse Event Reporting System (VAERS). Research points to the varicella virus and herpes virus as the cause of Bell’s Palsy. The Type I interferon system keeps these viruses in check. This is a huge red flag that must be considered. If a pregnant woman has a herpes flare-up during pregnancy, her child has a twofold increased risk of autism.
Another study of 200 Parkinson’s patients showed indications that Bell’s palsy may be an indicator of future risk of Parkinson’s disease.
So, pregnant women who get the jab are at increased risk of miscarriage, future infertility, and having an autistic child. It’s mind-boggling that the CDC continues to recommend the COVID-19 vaccine for pregnant women.
The importance of type I interferon
Innate immune interferon is your entire frontline defense. Patients with HIV/AIDS have dysregulated Type I interferon. This enables parasites to thrive. Antiparasitic drugs like hydroxychloroquine and ivermectin have been shown to be effective against COVID-19, both prophylactically and in treatment.
COVID-19 vaccines can cause considerable damage, especially since they can cause dysregulation of your innate and adaptive immune systems and enable viruses to thrive. Studies show that the herpes virus is implicated as a cause of AIDS. And human herpesvirus 6 has been implicated in chronic fatigue syndrome and myalgic encephalomyelitis.
SARS-CoV-2 spike protein may be a prion
Seneff suggests that the SARS-CoV-2 spike protein may be a prion. She states:
“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.”
Can COVID vaccines ‘shed’ or transmit infection?
Google the topic, and you will find a broad range of “facts” that seem to contradict themselves. There is growing evidence that the COVID-19 vaccines may also cause problems for people who choose not to receive the vaccine. This comes from being in close proximity to those who received the vaccine. While it is not viral shedding, there appears to be a transmission of the spike protein.
A series of papers by Yuichiro Suzuki, et al, argue that the spike protein can cause a signaling response in the vasculature with serious results. The researchers observed that severe cases of COVID-19, SARS-CoV-2 caused significant morphological changes to the pulmonary vasculature. Follow-up papers showed that the spike protein S1 subunit suppresses ACE2, causing a condition resembling pulmonary arterial hypertension (PAH), a severe lung disease with very high mortality.
The researchers also demonstrated that the S1 component in low concentrations activated the MEK/ERK/MAPK signaling pathway to promote cell growth. This could lead to heart vasculature leading to coronary artery disease and stroke.
In addition, they suggested that the mRNA vaccines may cause a similar response, which would lead to potential long-term consequences in adults and children who have been vaccinated.
What other problems could happen?
While scientists can’t accurately predict every disease that may result from the vaccine, some general predictions can be made. We may see an increase in cancer, Huntington’s disease, Parkinson’s disease, neurodegenerative disorders, and autoimmune diseases.
Mikovits suspects many will die rapidly. “We have evidence in the HTLV-1 associated myelopathy that these things go from long latency periods to [putting] you in a wheelchair in six months,” she says. “So, with all these other toxins combined hitting you, it’s not going to be ‘live and suffer forever.’ It’s going to be suffer five years and die.”
She worries that the COVID-19 vaccines will act as a “kill switch” for those with previous vaccine injuries. She notes that 6% of the American population are asymptomatically infected with XMRVs and gammaretroviruses from contaminated vaccines. The COVID shot will effectively accelerate their death by crippling their immune function. “The kids that are highly vaccinated, they’re ticking time bombs,” she says.