Dr. Mercola Interviews the Experts
This article is part of a weekly series in which Dr. Mercola interrogations many experts on a variety of health publications. To interpret more expert interrogations, click here.
In this interview, Stephanie Seneff, Ph.D ., and Judy Mikovits, Ph.D ., a dream-team in terms of deep insights into the technical details, explain the problems they realize with gene-based COVID-1 9 inoculations. There is a laded of highly helpful technical information that you can use to defend your opposition to these dangerous vaccines.
However, unless you have seriously studied molecular biology and genetics, it would be wise to view the video two or three times, as with each evaluate, you will learn more and understand just how dangerous these inoculations are. I recently interviewed Seneff about the excellent paper1 she published on this topic. That interrogation was featured in “COVID Vaccines May Bring Avalanche of Neurological Disease.”
In May 2020, I too interviewed Mikovits regarding the possibility of these vaccines generating reproductive harm and other health problems. At the time, Mikovits warned that fertility rates may stop thanks to the SARS-CoV-2 spike protein creating antibodies that affect syncytium, and undoubtedly, we’re now starting to see that.
Still, the U.S. Center for Disease Control and Prevention are recommending pregnant women get these inoculations, as well as children as young as 12, which is unfair, considering the potential lifelong probabilities and disorder of fertility.
The Spike Protein Is the Bioweapon
As noted by Mikovits, we now know that the worst evidences of COVID-1 9 are created by the SARS-CoV-2 spike protein, and that is the very thing these gene-based inoculations are instructing your body to stimulate. But it’s far worse, as the vaccines do not cause your torso to originate the same spike protein as SARS-CoV-2 but one that has been genetically modified, moving it far more toxic. So, it’s no wonder things are going wrong.
“The SARS-CoV-2 infection never was what they said it was, ” Mikovits says. “There was no infection asymptomatically. It’s a ape virus coming out of a monkey cadre strand and that’s the problem, but the spike protein is clearly[ stimulating] the disease.
So, you time injected the envelope of HIV … a syncytin gammaretrovirus envelope, and a SARS S2 receptor covering subject. That’s not a vaccine. It is the disease-causing agent. It’s a bioweapon. So now your cadres are all causing that bioweapon and you’re going to take out the innate exemption, NK[ natural killer] cadres and dendritic cadres …
You’re going to stop your grey blood cells, your immune response. You’re going to turn on an anti-inflammatory cytokine signature in every cadre of your form. It exhausts your NK cells’ ability to determine fouled 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 Upshot of mRNA Vaccines Against COVID-1 9, ” 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 person causes in response to the vaccine is even worse.
The reason for this is because the synthetic RNA has been influenced 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 stands open and attached to the ACE2 receptor, disabling it and motiving a multitude of difficulties leading to heart, lung, and immune disorder. As illustrated by Seneff 😛 TAGEND
“They modified the RNA to make it actually sturdy so the enzymes can’t break it down … Normally, enzymes that exist in your plan would just break down that RNA. RNA is very fragile, but they’ve stirred it sturdy by position in PEG[ polyethylene glycol ], by adding this lipid layer, 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 conclude maybe the most disturbing thing is they actually revised the[ RNA] code so that it doesn’t produce a regular edition of the spike protein. It develops 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 cadre that it’s infecting.
So, the spike protein fastens to the ACE2 receptor once it’s produced by the human cell … but it’s a modified edition 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, uncovered … That allows the immune cells to produce antibodies specific to that home where it should be fusing with the cell, the fusion province. It messes up the fusion discipline, keeps the protein open, and frustrates the protein from get in, which wants the protein will exactly stick there on the ACE2 receptor, incapacitating it.
When you disable ACE2 receptors in the heart, you get coronary failure. When you disable them in the lungs, you get pulmonary hypertension. When you do it in the ability, you get movement. Parcels of horrible 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 Grams( guanine) and Cs( cytosine ), which attains it considerably better at offsetting proteins. It’s turned up the gain on the natural virus 1,000 -fold, starting 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.”
Reality Is Exponentially Worse Than Predicted
With the included information provided by Seneff, Mikovits now accepts the reality of these inoculations may be exponentially worse than she first foresaw a year ago. Not only is the lipid nanoparticle a serious hazard, as we’ve seen with Gardasil and some of the newer hepatitis B inoculations, but we now too have the supplemented issue of inhuman mRNA, offset more robust so as to evade its natural breakdown.
As explained by Mikovits, free RNA acts as a danger signal inside your torso, so now your organization is on red alerting for nonetheless long the RNA remains feasible. Now, by manipulating the RNA code to be enriched in G and C, and configured as if it’s a human messenger RNA molecule ready to conclude protein by adding a polyA tail, the spike protein’s RNA sequence in the inoculation seems as if it is part bacteria, 3 portion human4 and fraction viral at the same time.
“We use poly( I: C)[ a toll-like receptor 3 agonist] to signal the cell to turn on the different types I interferon pathway, ” Mikovits shows, “and because this is an inhuman synthetic envelope, you’re not determining poly( I: C ), and you’re not[ triggering] the Type I interferon pathway.
You’ve bypassed the plasmacytoid dendritic cadre, which combined with IL-1 0, 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 response. You now miss the signaling of the endocannabinoid receptors …
A vast part of Dr.[ Francis] Ruscetti’s and my work over the last 30 times has been to show you don’t need an virulent transmissible virus — really articles and parts of these viruses are worse, because they likewise turn on danger signals. They act like danger signals and pathogen-associated molecular patterns.
So, it synergistically leaves that inflammatory cytokine signature on that gyrations your innate immune response out of control. It precisely cannot keep working with the myelopoiesis[ the production of cells in your bone marrow ]. Hence you picture a skew-away from the mesenchymal stem cell towards TGF-beta modulated hematopoietic stem cells.
This means you could see bleeding agitations on both missions. You can’t utter 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.”
With respect to Mikovits’ comment that sections and parts of the virus are actually worse than the whole virus, that is precisely what we have with the COVID vaccines. In last week’s interview with Seneff, she explained how the manufacturing process leaves scrapped genetically modified RNA in the vaccine. They are not filtered out and assumed to be harmless, but as Mikovits positions, 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 Mikovits’ sees mesh well to explain many of the problems we’re now witnessing from these gene-therapies. For pattern, vaccinated patients are reporting herpes and shingles infection following COVID-1 9 vaccination, which you’d expect if your Type I interferon pathway is disabled.
“Basically, you’ve got these latent viruses that are not inconveniencing you at all until your immune organization gets absolutely disconcerted by this crazy thing going on in the spleen with all this messenger RNA and all these spike proteins, ” Seneff says.
“Immune cells are confused from their other activity of continuing these viruses in check. So, you get these other conditions registering 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 inoculation 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 arrangement is what you need to keep these people 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 research studies on 200 Parkinson’s cases, comparison with 200 age- and gender-matched assures, six of those Parkinson’s patients had at least one occurrence of Bell’s palsy in the past, whereas nothing of the holds had. So, it inspects to me like the Bell’s palsy is an indicator of a future peril of Parkinson’s disease.”
To summarize, it appears as though pregnant women who are getting the COVID-1 9 vaccine are at increased risk not only for mishap but too for future infertility and having an autistic child. So, delight, be careful out there and spread the word.
The best space to treat any malady is to prevent it. These vaccines simply are not decreasing COVID-1 9 but radically abridging the health of those who receive it, extremely pregnant women that the CDC simply a month ago encouraged to get inoculated without a shred of security 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 clears up your entire frontline justification. People with HIV/ AIDS have dysregulated Type I interferon, which gives parasites to gain a solid foothold. Interestingly fairly, antiparasitic dopes such as hydroxychloroquine and ivermectin have been shown to be effective against COVID-1 9, both prophylactically and in treatment.
COVID-1 9 inoculations are capable of causing damage in a number of different ways. Disturbingly, all these different mechanisms of harm have synergistic results when it is necessary to dysregulating your innate and adaptive immune systems and activating latent viruses.
Mikovits quotes a research paper5 designation “War and Peace Between Microbes, ” which items how HIV-1 interacts with coinfecting viruses, thereby accelerating the disease. Herpes viruses in particular have been implicated as a crusade of AIDS. Human herpesvirus 6( HHVS-6) has also been implicated in myalgic encephalomyelitis or chronic myalgic encephalomyelitis( ME-CFS ).
In short-lived, these infections, AIDS and ME-CFS, don’t appear until viruses from various kinfolks spouse up and retroviruses take out the Type 1 interferon pathway.
In short-lived, the COVID-1 9 inoculations are capable of causing damage in a number of different ways. Disturbingly, all these different mechanisms of harm have synergistic impacts when it is necessary to dysregulating your innate and adaptive immune systems and activating latent viruses. “It’s exactly an outburst of a nightmare of crippling every expanse of your immune response, ” Mikovits says.
SARS-CoV-2 Spike Protein Engineered With HIV
According to Mikovits, there’s evidence testify 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 too 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 .)
“Our endogenous gammaretrovirus is called human endogenous retrovirus-W( HERV-W ). HERVW is all the highway back in genesis in our original endogenous genome. It’s a gammaretrovirus that shows simply the envelope, because in retroviruses, the envelope alone is enough to cause the disease. That envelope protein is called syncytin. They’re[ now] announcing it’ spike protein’ time to propel us all off, ” Mikovits says.
According to Mikovits, the SARS-CoV-2 virus was created by introducing a mutation into a molecular clone. Vero E6 ape 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. Apes, mouse all have syncytin. Endogenous viruses carry, especially during hormonal cycles/seconds. When it’s expressed in the wrong place, like in the mentality or the spinal cord, it’s long been associated with the inflammatory illness and the shattering of the myelin membrane in multiple sclerosis( MS ).
So, syncytin uttered 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 showing of our endogenous virome all the time, and that in our innate immune response it’s trying to shape and inform 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 necessary to] myelopoiesis. But these exosomes are packing not only RNA that you’re becoming, but now you’ve dysregulated the methylation so you’ve woken up your endogenous virome, and then syncytin is going to be expressed.”
How mRNA Can Alter Your DNA
In her article, Seneff likewise describes how mRNA can, in fact, vary your DNA, essentially integrating the instructions to acquire spike proteins into your genome. Frequently, mRNA cannot had been incorporated immediately into your genes because you need reverse transcriptase.
Reverse transcriptase alters RNA back into DNA( turn transcription ). However, there’s a wide variety of reverse transcriptase structures already embedded in our DNA, which concludes this possible. This is an area that Mikovits has studied for decades, so, commenting on Seneff’s results, she says 😛 TAGEND
“When you activate latent and defective viruses, you turn on overrule 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 parts — you’ve went that synthetic viral corpuscle[ i.e ., the vaccine-induced spike protein RNA] — now you’ve woken up your herpes viruses.
[ Latent viruses] are stillness[ through] DNA methylation, but as our grunge is sapped in minerals, we have beings with methylation flaws. This is why I said the first people who are going to die are beings with inflammatory predicaments and cancer.”
SARS-CoV-2 Spike Protein May Be a Prion
In her article, Seneff too discusses exhibit advocating the SARS-CoV-2 spike protein may be a prion, which is yet another piece of really bad news. “It’s absolutely scaring to me, ” she says, lending 😛 TAGEND
“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 tissue and then they misfold, becoming beta-sheets in the cytoplasm, and that’s what leads to the prion problem.
They form a crystal that selects in other proteins and acquires this big mess and builds fibrils and Alzheimer’s plaque. The primary prion protein is PrP, which is in Creutzfeldt-Jakob disease, the human form of mad moo-cow canker. It’s a sort of protein-source infection. It’s relatively wild because there’s no DNA involved , no RNA involved, just protein.
But the thing is, when “youve had” induced a form of mRNA that knows how to spew out tons of a prion protein, the prion proteins become questionable when there’s too many of them and the concentration are excessive in the cytoplasm.
And the spike proteins that these mRNA vaccines are rendering … 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 settles synaptic congestion and neurotransmitter handout ].
So, you’re going to get alpha-synuclein drawn into misfolded spike proteins, been transformed into a mess within the dendritic cells in the germinal middles in the spleen. And they’re going to package up all this crud into exosomes and liberate them. They’re then going to travel along the vagus nerve to the brainstem and effect things like Parkinson’s disease.
So, I think this is a complete setup for Parkinson’s disease. What may happen is that because they go this vaccine, they get Parkinson’s disease 5 year earlier than they would have gotten it otherwise. It’s going to push forward the time 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 remain getting the inoculation every year. Every year you do a booster, you raising the time that you’re going to get Parkinson’s ever closer.”
Are Viral Vector Vaccines Better or Worse?
Two of the four COVID-1 9 vaccines on the market in Europe and the U.S ., AstraZeneca and Johnson& Johnson, are using viral vectors and DNA rather than employ nanolipid-coated mRNA. Unfortunately, while potentially slightly less dangerous than Moderna’s and Pfizer’s mRNA editions, they can still cause significant problems through mechanisms of their own. As illustrated by Mikovits 😛 TAGEND
“As mentioned, it’s an adenovirus vector carry 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, it’s less dangerous because you’re not go to much of the mechanisms we’ve been talking about. But these adenovirus vector protein-producing vaccines are growing in an aborted fetal tissue cadre indication, so now you’ve went human syncytin[ in there ]. You’ve got 8% of the human genome of another human.
So, again, looking at the communication that has to regulate your Type I interferon response, it’s going to give you autoimmunity. In immunocompromised parties, it’s going to continue to express and that will give you a live infection, and you already have your firetrucks defending another[ infection ]. You can’t campaigned a campaign on three breasts.
I say,’ You exclusively need one shot because it’s the most toxic.’ It’s the most toxic in that sense. We have many mechanisms to cheapen RNA, and we can reinstate methylation equipment. It’s a ordeal, but I imagine our immune structure can break it[ the synthetic vaccine mRNA) down.”
Can COVID Vaccines’ Shed’ or Transmit Infection?
Disturbingly, it seems the COVID-1 9 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 molt, as nothing of the inoculations use live or even attenuated virus, there appears to be some sort of spike protein transmission going on.
While the spike protein cannot replicate or multiply like a virus, it is toxic in and of itself. In her article, Seneff items how the spike protein acts as a metabolic poison, capable of triggering compulsive mar leading to lung damage and heart and brain sickness: 6
“In a series of papers, Yuichiro Suzuki in collaboration with other scribes acquainted a strong argument that the spike protein by itself can cause a signaling response in the vasculature with potentially widespread consequences.
These scribes observed that, in severe cases of COVID-1 9, SARS-CoV-2 reasons significant morphological modification of the pulmonary vasculature … Furthermore, they showed that exposure of cultured human pulmonary vein smooth muscle cadres to the SARS-CoV-2 spike protein S1 subunit was sufficient to promote cell signaling without the rest of the virus components.
Follow-up articles showed that the spike protein S1 subunit curbs ACE2, starting a condition resembling pulmonary arterial hypertension( PAH ), a severe lung disease with very high mortality …
Suzuki et al.( 2021) went on to demonstrate experimentally that the S1 component of the SARS-CoV-2 virus, at a low-grade concentration … triggered 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 motive coronary artery sicknes, and activating in the mentality could have contributed 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 same accomplish could happen in response to the mRNA vaccines, and they warned of potential long-term consequences to both children and adults who received COVID-1 9 vaccines on the basis of the spike protein.
An interesting study by Lei et. al.( 2021) found that pseudovirus — orbits decorated with the SARS-CoV-2 S1 protein but shortcoming any viral DNA in their core — caused inflammation and impair in both the routes and lungs of mouse exposed intratracheally.
They then disclosed healthful human endothelial cells to the same pseudovirus molecules. Bind of these specks to endothelial ACE2 receptors contributed significantly to mitochondrial shatter 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-1 9. The ramifications for inoculations intended to cause cells to create the spike protein are clear and are an self-evident cause for concern.”
As explained by Mikovits, the transmission that appears to be occurring from inoculated characters to unvaccinated ones is the transmission of exosomes, basically, the spike protein. The problem is these exosomes look like a virus to your immune organisation, and “If that synthetic nanoparticle is a virus-like particle and they’re literally self-assembling, then you’ve got yourself a synthetic ordeal, ” she says.
Which Vaccine Is Most Dangerous?
As for which vaccine might be the most dangerous, Mikovits guesses the vector-based DNA vaccines( AstraZeneca and Johnson& Johnson) are the most dangerous for those with chronic Lyme disease or any inflammatory malady are connected with an abnormal legion immune response, such as shingles, viral infections or cancer, women who have already received the Gardasil vaccine( as this may predispose them to problems linked to the lipid nanoparticle ), and those with Parkinson’s or Huntington-like diseases.
Seneff, meanwhile, worries that children may be susceptible to either type of COVID vaccine, simply because they’ve already received so many different inoculations. Mikovits agrees, but believes the mRNA vaccines may be more harmful in this age group 😛 TAGEND
“The most dangerous to the children are the mRNA vaccines because their immune organisations are growing, ripening, proliferating, flourishing. You establish or you turn on a volley, what happens? All the stem cells that are important for proliferating that say,’ OK, all is calm in the immune structure, move improved bone, disappear build ability cadres, depart do the snipping with the macrophages.’ You can’t have your macrophages clearing all the viruses.
And yes, overturn transcriptase is’ on, ’ it’s expressed in telomeres. You’re stretching. That’s the whole idea of everything. All the restraints are off. Same thing in gestation. That’s why we don’t do anything in pregnancy because you’ve got to stay unmethylated in order to respond to your environment, that endogenous genome of the virome. That’s your Type I interferon responses.
You don’t want myelopoiesis, you demand embryonic growing. We’re going to see things like Down syndrome … Rett syndrome. Rett syndrome, that’s unwarranted DNA methylation in little girls. So, for the kids, the most difficult thing in the world is the RNA vaccines.”
What Can We Expect to See More Of?
While the variety of ailments we may see a rise in as a result of this vaccination safarus are myriad, a few general prophecies can be made. Seneff believes we’ll realise a significant rise in cancer, intensified Parkinson’s-like cancers, Huntington’s disease, and all types of autoimmune diseases and neurodegenerative disorders.
Mikovits supposes numerous will die very rapidly. “We have prove in the HTLV-1 accompanied myelopathy that these things run from long latency seasons to[ putting] you in a wheelchair in six months, ” she says. “So, with all these other virus compounded touching you, it’s not “re going to be”‘ live and suffer forever.’ It’s going to be suffer 5 year and die.”
She likens the COVID-1 9 inoculations to a “kill switch” for all who have been previously disabled by vaccines, whether they actually realize it or not. As noted by Mikovits, it’s been shown that 6% of the American population are asymptomatically infected with XMRVs and gammaretroviruses from infected vaccines. The COVID shot will effectively accelerate their death by crippling their immune purpose. “The boys that are highly vaccinated, they’re ticking time bombs, ” she says.
What Are the Solutions?
While all of this is highly problematic, there is help. As noted by Mikovits, alleviates to the maladies that might develop post-vaccination include 😛 TAGEND
Hydroxychloroquine and ivermectin treatments
Low-dose antiretroviral care 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 gp1 20; it blocks attaching and illnes of viruses that use the CCR5 receptor to pollute cadres)
Cannabis, to strengthen Type I interferon pathways
Dimethylglycine or betaine( trimethylglycine) to enhance methylation, thereby smothering latent viruses
Silymarin or milk thistle to help cleanse your liver
From my perspective, I belief the best thing you can do is to build your innate immune arrangement. To do that, you need to become metabolically resilient and optimize your diet. You’ll likewise want to make sure your vitamin D tier is optimized to between 60 ng/ mL and 80 ng/ mL( 100 nmol/ L to 150 nmol/ L ), ideally through sensible sunshine show. Sunlight also has other benefits besides determining vitamin D.
Use time-restricted eating and eat all your banquets 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 batch of sulfur-rich meat to keep your mitochondria and lysosomes health. Both are important for the clearing of cellular junks, including these spike proteins. You are also welcome to improved your sulfate by taking Epsom salt baths.
To combat the toxicity of the spike protein, Seneff hints optimizing autophagy, which may help digest and remove the spike proteins. Time-restricted eating will upregulate autophagy, while sauna therapy, which upregulates hot surprise proteins, will help refold misfolded proteins. They too tag injury proteins and target them for removal.
It is important that your sauna is hot fairly( around 170 magnitudes Fahrenheit) and does not have high magnetized or electric studies. Last but not least, Mikovits recommends never coming another vaccination.
“We knew the influenza shot would drive the disease, ” she says. “It’s the combinations. That’s a ticking time bomb sitting there in every cadre. So never get another vaccine and be very careful about stimulants that jeopardize 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 threw it on your surface. Don’t use toxins on your whisker. Use essential petroleums, use antimicrobials … ozonated ointments and creams break apart the lipid specks, cannabis ointments and creams normalize scalp,[ which forms part of] your immune organisation …
Remember, immune dysfunction intensifies each time you add an immune activation incident. So, if the entire world never again took another shot, even the most susceptible populations, they could stay well … We actually have to say no more shots because they’re the single biggest toxin to anyone, and an immune dysregulator.”
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