STORY AT-A-GLANCE
- COVID-19 vaccines are capable of causing damage in a number of different ways. Disturbingly, all these different mechanisms of harm have synergistic effects when it comes to dysregulating your innate and adaptive immune systems and activating latent viruses
- The worst symptoms of COVID-19 are created by the SARS-CoV-2 spike protein, and that is the very thing gene-based COVID vaccines are instructing your body to make
- While the natural spike protein is bad, the spike protein your body produces in response to the vaccine is even worse, as the synthetic RNA has been manipulated in such a way as to create a very robust and unnatural spike protein
- The spike protein is toxic in and of itself, and has the ability to induce vascular, heart and neurological damage
- The COVID-19 vaccine disables the Type I interferon pathway, which explains why vaccinated patients are reporting herpes and shingles infection following COVID-19 vaccination
In this 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.
However, unless you have deeply studied molecular biology and genetics, it would be wise to view the video two or three times, as with each review, you will learn more and understand just how dangerous these vaccines are. I recently interviewed Seneff about the excellent paper1 she published on this topic. That interview was featured in âCOVID Vaccines May Bring Avalanche of Neurological Disease.â
In May 2020, I also interviewed Mikovits about the possibility of these vaccines causing reproductive harm and other health problems. At the time, Mikovits warned that fertility rates may drop thanks to the SARS-CoV-2 spike protein creating antibodies that attack syncytium, and indeed, weâre now starting to see that.
Still, the U.S. Centers for Disease Control and Prevention are recommending pregnant women get these vaccines, as well as children as young as 12, which is unconscionable, considering the potential lifelong risks and impairment of fertility.
As noted by Mikovits, we now know that the worst symptoms of COVID-19 are created by the SARS-CoV-2 spike protein, and that is the very thing these gene-based vaccines are instructing your body to make. But itâs far worse, as the vaccines do not cause your body to make the same spike protein as SARS-CoV-2 but one that has been genetically modified, making it far more toxic. So, itâs no wonder things are going wrong.
âThe SARS-CoV-2 infection never was what they said it was,â Mikovits says. âThere was no infection asymptomatically. Itâs a monkey virus coming out of a monkey cell line and thatâs 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. Thatâs not a vaccine. It is the disease-causing agent. Itâs a bioweapon. So now your cells are all producing that bioweapon and youâre going to take out the innate immunity, NK [natural killer] cells and dendritic cells âŠ
Youâre going to disrupt your white blood cells, your immune response. Youâre going to turn on an anti-inflammatory cytokine signature in every cell of your body. It exhausts your NK cellsâ ability to determine infected cells. Itâs the nightmare we predicted.â
The Spike Protein Produced in Your Body Is Highly Unnatural
In her paper, âWorse Than The Disease: Reviewing Some Possible Unintended Consequences of mRNA Vaccines Against COVID-19,â 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.
The reason for this is because the synthetic RNA has been manipulated in such a way as to create a very unnatural spike protein that result in it not collapsing on itself into the cell once it attaches to the ACE2 receptor, as it normally does. Instead it stays open and attached to the ACE2 receptor, disabling it and causing a host of problems leading to heart, lung, and immune impairment. As explained by Seneff:
âThey modified the RNA to make it really sturdy so the enzymes canât break it down ⊠Normally, enzymes that are in your system would just break down that RNA. RNA is very fragile, but theyâve 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 doesnât 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 itâs infecting.
So, the spike protein binds to the ACE2 receptor once itâs produced by the human cell ⊠but itâs a modified version of the spike protein. It has these two prolines that make it very stiff so that it canât 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 canât 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 âŠ
The other thing theyâve done with the RNA is theyâve stuck in a lot of extra Gs (guanine) and Cs (cytosine), which makes it much better at making proteins. Itâs turned up the gain on the natural virus 1,000-fold, making the RNA much more willing to make a protein. So, itâll make a lot more spike protein than you wouldâve had from a natural RNA virus.â
Reality Is Exponentially Worse Than Predicted
With the added information provided by Seneff, Mikovits now believes the reality of these vaccines may be exponentially worse than she initially predicted a year ago. Not only is the lipid nanoparticle a serious hazard, as weâve seen with Gardasil and some of the newer hepatitis B vaccines, but we now also have the added issue of unnatural mRNA, made more robust so as to evade its natural breakdown.
As explained by Mikovits, free RNA acts as a danger signal inside your body, so now your system is on red alert for however long the RNA remains viable. Now, by manipulating the RNA code to be enriched in G and C, and configured as if itâs a human messenger RNA molecule ready to make protein by adding a polyA tail, the spike proteinâs RNA sequence in the vaccine looks as if it is part bacteria,3 part human4 and part viral at the same time.
âWe use poly(I:C) [a toll-like receptor 3 agonist] to signal the cell to turn on the type I interferon pathway,â Mikovits explains, âand because this is an unnatural synthetic envelope, youâre not seeing poly(I:C), and youâre not [activating] the Type I interferon pathway.
Youâve 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, youâve bypassed the communication between the innate and adaptive immune response. You now miss the signaling of the endocannabinoid receptors âŠ
A large part of Dr. [Francis] Ruscettiâs and my work over the last 30 years has been to show you donât need an infectious transmissible virus â 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 canât make enough firetrucks to send to the fire. Your innate immune response canât get there, and then youâve just got a total train wreck of your immune system.â
With respect to Mikovitsâ comment that pieces and parts of the virus are actually worse than the whole virus, that is precisely what we have with the COVID vaccines. In last weekâs interview with Seneff, she explained how the manufacturing process leaves fragmented genetically modified RNA in the vaccine. They are not filtered out and assumed to be harmless, but as Mikovits states, this is not the case. This is being completely missed as one reason why this vaccine is so dangerous.
Latent Viruses May Flare if You Receive the COVID Vaccine
As noted by Seneff, her and Mikovitsâ findings mesh well to explain many of the problems weâre now seeing from these gene-therapies. For example, vaccinated patients are reporting herpes and shingles infection following COVID-19 vaccination, which youâd expect if your Type I interferon pathway is disabled.
âBasically, youâve 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,â Seneff says.
âImmune 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. Thereâs Bellâs palsy (facial palsy), for example. There are over 1,200 cases of Bellâs 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 Bellâs palsy. The Type I interferon system is what you need to keep these guys in check, and so those viruses are getting enabled and theyâre causing symptoms.
That is actually a very bad sign. If a woman whoâs 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 Parkinsonâs patients, compared to 200 age- and gender-matched controls, six of those Parkinsonâs patients had at least one episode of Bellâs palsy in the past, whereas none of the controls had. So, it looks to me like the Bellâs palsy is an indicator of a future risk of Parkinsonâs disease.â
To summarize, it looks as though pregnant women who are getting the COVID-19 vaccine are at increased risk not only for miscarriage but also for future infertility and having an autistic child. So, please, be careful out there and spread the word.
The best way to treat any disease is to prevent it. These vaccines simply are not decreasing COVID-19 but radically decreasing the health of those who receive it, especially pregnant women that the CDC merely a month ago encouraged to get vaccinated without a shred of safety evidence.
The Importance of Type I Interferon
Mikovits has done a great deal of research on interferon for the last 40 years. Innate immune interferon makes up your entire frontline defense. People with HIV/AIDS have dysregulated Type I interferon, which allows parasites to gain a solid foothold. Interestingly enough, antiparasitic drugs such as hydroxychloroquine and ivermectin have been shown to be effective against COVID-19, both prophylactically and in treatment.
COVID-19 vaccines are capable of causing damage in a number of different ways. Disturbingly, all these different mechanisms of harm have synergistic effects when it comes to dysregulating your innate and adaptive immune systems and activating latent viruses.
Mikovits cites a research paper5 titled âWar and Peace Between Microbes,â which details how HIV-1 interacts with coinfecting viruses, thereby accelerating the disease. Herpes viruses in particular have been implicated as a cause of AIDS. Human herpesvirus 6 (HHVS-6) has also been implicated in myalgic encephalomyelitis or chronic fatigue syndrome (ME-CFS).
In short, these diseases, AIDS and ME-CFS, donât appear until viruses from different families partner up and retroviruses take out the Type 1 interferon pathway.
In short, the COVID-19 vaccines are capable of causing damage in a number of different ways. Disturbingly, all these different mechanisms of harm have synergistic effects when it comes to dysregulating your innate and adaptive immune systems and activating latent viruses. âItâs just an explosion of a nightmare of crippling every area of your immune response,â Mikovits says.
SARS-CoV-2 Spike Protein Engineered With HIV
According to Mikovits, thereâs 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.
XMRV has been linked to ME-CFS. HIV, which can cause AIDS, is another human retrovirus (although as mentioned earlier, HIV does not appear to trigger AIDS all by itself. It needs a coinfection.)
âOur endogenous gammaretrovirus is called human endogenous retrovirus-W (HERV-W). HERVW is all the way back in genesis in our original endogenous genome. Itâs 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. Theyâre [now] calling it âspike proteinâ just to throw us all off,â Mikovits says.
According to Mikovits, 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.
âSo 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 itâs expressed in the wrong place, like in the brain or the spinal cord, itâs 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 Parkinsonâs is associated with Type I interferon responses. Weâre now starting to appreciate that there is low-level expression of our endogenous virome all the time, and that in our innate immune response itâs trying to shape and educate our Type I interferon pathways âŠ
The final and biggest problem is these exosomes, because your bodyâs exosomes are like your cellsâ response to express its regulatory RNAs, small inhibitory RNAs, long-chain non-coding RNA â which Ritchie Shoemaker has long associated with chronic Lyme and ME/CFS â and the TGF-beta I pathway.
TGF-beta I, thatâs the master switch to turn on which Type I interferon, which [is needed for] myelopoiesis. But these exosomes are packaging not only RNA that youâre making, but now youâve dysregulated the methylation so youâve woken up your endogenous virome, and then syncytin is going to be expressed.â
How mRNA Can Alter Your DNA
In her paper, Seneff also describes how mRNA can, in fact, alter your DNA, essentially integrating the instructions to make spike proteins into your genome. Typically, mRNA cannot be integrated directly into your genes because you need reverse transcriptase.
Reverse transcriptase converts RNA back into DNA (reverse transcription). However, thereâs a wide variety of reverse transcriptase systems already embedded in our DNA, which makes this possible. This is an area that Mikovits has studied for decades, so, commenting on Seneffâs findings, she says:
âWhen 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 â youâve got that synthetic viral particle [i.e., the vaccine-induced spike protein RNA] â now youâve 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.â
SARS-CoV-2 Spike Protein May Be a Prion
In her paper, Seneff also discusses evidence suggesting the SARS-CoV-2 spike protein may be a prion, which is yet another piece of really bad news. âItâs absolutely terrifying to me,â she says, adding:
âIâm now thinking that may be the worst aspect of these mRNA vaccines, because theyâre producing this abnormal spike protein that doesnât want to go into the membrane. Prion proteins are known to be membrane proteins. Theyâre alpha-helices in the membrane and then they misfold, becoming beta-sheets in the cytoplasm, and thatâs what leads to the prion problem.
They form a crystal that draws in other proteins and makes this big mess and builds fibrils and Alzheimerâs plaque. The main prion protein is PrP, which is in Creutzfeldt-Jakob disease, the human form of mad cow disease. Itâs a sort of protein-source infection. Itâs quite wild because thereâs 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 thereâs too many of them and the concentration is too high in the cytoplasm.
And the spike proteins that these mRNA vaccines are producing ⊠isnât 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, youâre 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 theyâre going to package up all this crud into exosomes and release them. Theyâre then going to travel along the vagus nerve to the brainstem and cause things like Parkinsonâs disease.
So, I think this is a complete setup for Parkinsonâs disease. What may happen is that because they got this vaccine, they get Parkinsonâs disease five years earlier than they would have gotten it otherwise. Itâs going to push forward the date at which someone who has a propensity towards Parkinsonâs is going to get it.
And itâs probably going to cause people to get Parkinsonâs who never would have gotten it in the first place â especially if they keep getting the vaccine every year. Every year you do a booster, you bring the date that youâre going to get Parkinsonâs ever closer.â
Are Viral Vector Vaccines Better or Worse?
Two of the four COVID-19 vaccines on the market in Europe and the U.S., AstraZeneca and Johnson & Johnson, are using viral vectors and DNA rather than using nanolipid-coated mRNA. Unfortunately, while potentially slightly less dangerous than Modernaâs and Pfizerâs mRNA versions, they can still cause significant problems through mechanisms of their own. As explained by Mikovits:
âAs mentioned, itâs an adenovirus vector expressing the protein. So, the HIV, the XMRV envelope, the syncytin, the HERV-W envelope and the ACE2 are already being expressed in the vector.
With respect to the RNA component, itâs less dangerous because youâre not going to see much of the mechanisms weâve been talking about. But these adenovirus vector protein-producing vaccines are grown in an aborted fetal tissue cell line, so now youâve got human syncytin [in there]. Youâve got 8% of the human genome of another human.
So, again, looking at the communication that has to regulate your Type I interferon response, itâs going to give you autoimmunity. In immunocompromised people, itâs going to continue to express and that will give you a live infection, and you already have your firetrucks fighting another [infection]. You canât fight a war on three fronts.
I say, âYou only need one shot because itâs the most toxic.â Itâs the most toxic in that sense. We have many mechanisms to degrade RNA, and we can restore methylation machinery. Itâs a nightmare, but I believe our immune system can break it [the synthetic vaccine mRNA) down.â
Can COVID Vaccines âShedâ or Transmit Infection?
Disturbingly, it appears the COVID-19 vaccines may also cause trouble for those who decide not to get the shots but spend time in close proximity to people who did. While it cannot be viral shedding, as none of the vaccines use live or even attenuated virus, there appears to be some sort of spike protein transmission going on.
âIn a series of papers, Yuichiro Suzuki in collaboration with other authors presented a strong argument that the spike protein by itself can cause a signaling response in the vasculature with potentially widespread consequences.
These authors observed that, in severe cases of COVID-19, SARS-CoV-2 causes significant morphological changes to the pulmonary vasculature ⊠Furthermore, they showed that exposure of cultured human pulmonary artery smooth muscle cells to the SARS-CoV-2 spike protein S1 subunit was sufficient to promote cell signaling without the rest of the virus components.
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 âŠ
Suzuki et al. (2021) went on to demonstrate experimentally that the S1 component of the SARS-CoV-2 virus, at a low concentration ⊠activated the MEK/ERK/MAPK signaling pathway to promote cell growth. They speculated that these effects would not be restricted to the lung vasculature.
The signaling cascade triggered in the heart vasculature would cause coronary artery disease, and activation in the brain could lead to stroke. Systemic hypertension would also be predicted. They hypothesized that this ability of the spike protein to promote pulmonary arterial hypertension could predispose patients who recover from SARS-CoV-2 to later develop right ventricular heart failure.
Furthermore, they suggested that a similar effect could happen in response to the mRNA vaccines, and they warned of potential long-term consequences to both children and adults who received COVID-19 vaccines based on the spike protein.
An interesting study by Lei et. al. (2021) found that pseudovirus â spheres decorated with the SARS-CoV-2 S1 protein but lacking any viral DNA in their core â caused inflammation and damage in both the arteries and lungs of mice exposed intratracheally.
They then exposed healthy human endothelial cells to the same pseudovirus particles. Binding of these particles to endothelial ACE2 receptors led to mitochondrial damage and fragmentation in those endothelial cells, leading to the characteristic pathological changes in the associated tissue.
This study makes it clear that spike protein alone, unassociated with the rest of the viral genome, is sufficient to cause the endothelial damage associated with COVID-19. The implications for vaccines intended to cause cells to manufacture the spike protein are clear and are an obvious cause for concern.â
As explained by Mikovits, the transmission that appears to be occurring from vaccinated individuals to unvaccinated ones is the transmission of exosomes, basically, the spike protein. The problem is these exosomes look like a virus to your immune system, and âIf that synthetic nanoparticle is a virus-like particle and theyâre literally self-assembling, then youâve got yourself a synthetic nightmare,â she says.
Which Vaccine Is Most Dangerous?
As for which vaccine might be the most dangerous, Mikovits believes the vector-based DNA vaccines (AstraZeneca and Johnson & Johnson) are the most dangerous for those with chronic Lyme disease or any inflammatory disease associated with an abnormal host immune response, such as shingles, viral infections or cancer, women who have already received the Gardasil vaccine (as this may predispose them to problems with the lipid nanoparticle), and those with Parkinsonâs or Huntington-like diseases.
Seneff, meanwhile, worries that children may be susceptible to either type of COVID vaccine, simply because theyâve already received so many different vaccines. Mikovits agrees, but believes the mRNA vaccines may be more harmful in this age group:
âThe most dangerous to the children are the mRNA vaccines because their immune systems are growing, growing, growing, growing. You introduce or you turn on a fire, what happens? All the stem cells that are important for growing that say, âOK, all is calm in the immune system, go build bone, go build brain cells, go do the pruning with the macrophages.â You canât have your macrophages clearing all the viruses.
And yes, reverse transcriptase is âon,â itâs expressed in telomeres. Youâre growing. Thatâs the whole idea of everything. All the brakes are off. Same thing in pregnancy. Thatâs why we donât do anything in pregnancy because youâve got to stay unmethylated in order to respond to your environment, that endogenous genome of the virome. Thatâs your Type I interferon responses.
You donât want myelopoiesis, you want embryonic development. Weâre going to see things like Down syndrome ⊠Rett syndrome. Rett syndrome, thatâs inappropriate DNA methylation in little girls. So, for the kids, the worst thing in the world is the RNA vaccines.â
What Can We Expect to See More Of?
While the variety of diseases we may see a rise in as a result of this vaccination campaign are myriad, some general predictions can be made. Seneff believes weâll see a significant rise in cancer, accelerated Parkinsonâs-like diseases, Huntingtonâs disease, and all types of autoimmune diseases and neurodegenerative disorders.
Mikovits suspects many will die rather rapidly. âWe 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,â she says. âSo, with all these other toxins combined hitting you, itâs not going to be âlive and suffer forever.â Itâs going to be suffer five years and die.â
She likens the COVID-19 vaccines to a âkill switchâ for all who have been previously injured by vaccines, whether they actually realize it or not. As noted by Mikovits, itâs been shown 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. âThe kids that are highly vaccinated, theyâre ticking time bombs,â she says.
What Are the Solutions?
While all of this is highly problematic, there is help. As noted by Mikovits, remedies to the maladies that might develop post-vaccination include:
- 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
From my perspective, I believe 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. Youâll 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.
âWe knew the flu shot would drive the disease,â she says. âItâs the combinations. Thatâs 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, donât hyper-immune activate. Donât eat GMO. Donât ingest it and donât inject it. And donât put it on your skin. Donât 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 âŠ
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 theyâre the single biggest toxin to anyone, and an immune dysregulator.â
The National Vaccine Information Center (NVIC) recently posted more than 50 video presentations from the pay-for-view Fifth International Public Conference on Vaccination held online October 16 to 18, 2020, and made them available to everyone for free.
The conferenceâs theme was âProtecting Health and Autonomy in the 21st Centuryâ and it featured physicians, scientists and other health professionals, human rights activists, faith community leaders, constitutional and civil rights attorneys, authors and parents of vaccine injured children talking about vaccine science, policy, law and ethics and infectious diseases, including coronavirus and COVID-19 vaccines.
In December 2020, a U.K. company published false and misleading information about NVIC and its conference, which prompted NVIC to open up the whole conference for free viewing. The conference has everything you need to educate yourself and protect your personal freedoms and liberties with respect to your health.