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In this interview, Stephanie Seneff, Ph.D., a senior research scientist at MIT, reviews the health impacts of glyphosate. She has just finished writing a book about glyphosate called “Toxic Legacy: How the Weedkiller Glyphosate is Destroying Our Health and the Environment,” which is expected to be published in June 2021.
For years, glyphosate was assumed safe and claims of toxicity were vehemently denied. But in recent years, studies on glyphosate have been demonstrating toxicity even at very low levels. Seneff also believes glyphosate exposure may be a key player in cases of severe COVID-19, which we’ll unravel in this interview.
The “gly” in glyphosate actually stands for the amino acid glycine. The glycine amino acid in glyphosate has a methylphosphonate group attached to its nitrogen atom, which is responsible for its effects and toxicity.
After studying the research literature on glyphosate, Seneff has reached the conclusion that your body sometimes substitutes glyphosate for the amino acid glycine when it is constructing proteins, and this can have devastating consequences in some cases. The proteins created with glyphosate instead of glycine simply don’t work because glyphosate is much larger than glycine and also negatively charged, and as a result this alters important physical characteristics.
Monsanto’s own research, dating back to the late 1980s, shows that glyphosate accumulates in various tissues, even though they claim it doesn’t.1 The Monsanto researchers proposed that it was “incorporated into” the proteins in the tissues. This is not widely appreciated, even in the natural health community.
Now, if you have a distorted analog of glycine (in the form of glyphosate), the protein constructed from it is not going to work like it’s supposed to. In her book, Seneff details the amino acids in proteins that are most susceptible to damage because of what she calls a “glyphosate susceptible motif.”
“It’s really fascinating biology and so terrifying when you think of the potential consequences, if I'm right,” she says. “It matches so well with all the diseases that are going up dramatically in our society that I really think I'm onto something huge here.”
An aromatic amino acid called EPSP synthase is a critical enzyme that almost surely gets disrupted by glyphosate through this mechanism of substituting for glycine. This gets a bit technical, but it is important. The plant version of EPSP synthase binds a phosphate group in its substrate phosphoenolpyruvate at a site where there is a highly-conserved glycine residue (highly conserved usually means that it is critical for proper function).
It has been shown experimentally that, if you change the DNA code so that the glycine is substituted by an amino acid called alanine (one extra methyl group), the enzyme becomes completely insensitive to glyphosate at any concentration. It also takes a hit on phosphate binding because of the extra methyl group, but you can tweak another amino acid nearby to fix this problem, while still keeping its insensitivity to glyphosate.
Researchers from Dow-Dupont did exactly this to a maize version of EPSP synthase using CRISPR technology and were able to create synthetically a version of the maize’s own EPSP synthase that was completely resistant to glyphosate. The title of this paper is: “Desensitizing Plant EPSP Synthase to Glyphosate: Optimized Global Sequence Context Accommodates a Glycine-to-Alanine Change in the Active Site.”2
The shikimate pathway is the pathway that produces aromatic amino acids, which are essential to humans as we cannot create these amino acids in our body. The argument is we're not susceptible to glyphosate because our cells don't have EPSP synthase — in fact, they don’t have the entire shikimate pathway.
However, our gut microbes do have that pathway, and they use it to make essential amino acids for the host. So, our gut microbes are indeed affected by glyphosate, and when they’re damaged, our health can suffer in any number of ways.
But what might be an even more devastating problem with glyphosate is the way it probably messes up a large number of proteins that bind phosphate at a site where there is at least one, and often three, highly conserved glycine residues. Glyphosate slips its methylphosphonate group into the spot that is supposed to be where phosphate from the substrate fits snugly. Phosphate can’t bind because glyphosate is in the way.
The arguments for why glyphosate specifically disrupts proteins that depend on glycine for phosphate binding are described more fully in a paper Seneff published together with colleagues arguing that glyphosate is a major factor in kidney failure among young agricultural workers in Central America.3
Laszlo Boros is a professor of pediatrics at UCLA and an expert on deutenomics, “the science of autonomic deuterium discrimination in nature.”4 After reading one of Seneff’s papers, he contacted her, suggesting she look into deuterium.
“I was blown away, and I immediately saw the connection to glyphosate,” she says. “This was a year ago in December, and I've just been reading everything I can on deuterium since then and hooking it to glyphosate. It's just astonishing what I found, even, ultimately, [linking it] to COVID-19.
It's been quite a year for me in terms of major breakthroughs in my understanding of how metabolism works and how it's getting messed up by glyphosate, and then how that's causing us to not be able to effectively deal with COVID-19.”
In normal physiology, your cells, specifically the mitochondria, function to help deplete your body of deuterium. Deuterium is a naturally occurring isotope of hydrogen. If you didn’t already know, deuterium is also known as heavy hydrogen, because it has a neutron in addition to the proton and electron in the hydrogen atom.
Provided your cell is healthy, it has deuterium-depleting enzymes and organelles that help remove deuterium from your cells. If your mitochondria are damaged by glyphosate, they’re not going to be able to eliminate the deuterium properly.
Deuterium is like iron in the way that it’s both essential in the right amounts and toxic in excess. Hydrogen is the smallest atom and by far the most common atom in your body. Deuterium, being a heavy hydrogen, has one extra neutron, in addition to the normal proton and electron that regular hydrogen has.
Now, your cells are surrounded by structured water, which is negatively charged and contributes to your body’s energy production by supplying deuterium-depleted hydrogen to lysosomes and mitochondria. The structured water is maintained by sulfates, which makes sulfate extremely important for health. Sulfate is made dysfunctional by glyphosate, which in turn destroys structured water, resulting in impaired energy production in the cell.5
“The mitochondria have [a] membrane, which has a part inside the membrane that's really, really important,” Seneff says. “That's where you have those protons, and you really don't want it to be deuterons. This is what Laszlo brought home to me."
Endothelial NOS (eNOS) makes nitric oxide (NO), and for every molecule of NO that it makes, it produces two molecules of water, which are deuterium depleted. Stephanie believes the NO created by eNOS may act as a signal that deuterium-depleted water has been created. Interestingly enough, deuterium-depleted water is also created during the inflammatory process.
“The inflammation is there for a good reason, and the reason is to produce deuterium-depleted water,” Seneff says. “It’s all because the mitochondria are failing in their task of producing their own deuterium-depleted water, which they get in part through the structured water from the sulfate [and] through enzymes that are highly skilled at choosing hydrogen over deuterium …
NADH and NADPH are also fascinating. I've been chasing them through all the proteins. They are interesting because they are the carriers of that wonderful hydrogen that's not deuterium. When you trace what’s doing what, where, you realize that the cytoplasm is producing NADH and handing it over to the mitochondria.
The mitochondria then take that H [hydrogen atom] off and throw it into the intermembrane space. So, the whole process ends up with the intermembrane space being assured that this is H [hydrogen] and not D [deuterium].
This is crucial because then those protons, once they build up, come back through the ATPase [ATP synthase] pump. If they are deuterons, they are going to wreck the pump … You release reactive oxygen species [that] break it, and of course, then you can't make ATP.”
For clarification, the ATP synthase pump works like a mini-motor. When a hydrogen atom with one proton goes through it, it works flawlessly and generates ATP. If deuterium enters it, which has one neutron and one proton, making it twice the weight of hydrogen, it breaks that motor.
Interestingly, deuterium is everywhere, naturally, but your body has developed an intricate way to make it harmless by trapping it in the structured water, where it’s beneficial, as it actually supports the creation of structured water.
Problems arise when you cannot make enough structured water to sequester it all. Then, the deuterium gets loose, causing mitochondrial dysfunction, impairing energy production and contributing to chronic disease.
As noted by Seneff, glyphosate harms your health in a number of ways. For example, she cites a recent paper showing it causes endocrine disruption, which can lead to breast cancer, reproductive issues, obesity and thyroid problems.6
Another paper shows glyphosate sensitizes cells to be more receptive to cancer after exposure to other chemicals.7 “Glyphosate makes everything else more toxic than it would otherwise be,” Seneff says. “It disrupts your defense system against toxic chemicals.” Other research shows epigenetic and generational effects, even when no apparent problems can be found in the first generation exposed.8
Glyphosate also impairs flavoproteins — proteins that bind flavins. Many of these proteins play a crucial role in transferring hydrogen from NADH or NADPH to other molecules, essentially supporting the delivery of pure hydrogen to the mitochondria. Flavoproteins have a characteristic GxGxxG motif at the site where they bind phosphate in the flavins. The ‘G’ stands for glycine and the ‘x’ is a wildcard — any amino acid, including glycine.
This means they have at least three susceptible glycines at this critical region of the protein. Flavoproteins are molecules that facilitate the transfer of protons and electrons, and know how to avoid deuterium, by exploiting a special feature of hydrogen called proton tunneling.
All of them can be expected to be disrupted by glyphosate. A critical flavoprotein is succinate dehydrogenase, and several papers have shown it is adversely affected by glyphosate, Seneff says. It is the only enzyme that plays a role in both oxidative phosphorylation and the citric acid cycle in the mitochondria.
In addition to aromatic amino acids, the shikimate pathway is essential for riboflavin synthesis, and riboflavin, a B vitamin, is the main precursor to flavins. This means that riboflavin deficiency can be triggered from glyphosate exposure as well. Glyphosate also causes damage by:
According to Seneff, it appears deuterium-depleted water plays a central, hitherto unappreciated role in metabolism, as your body has so many ways to create it. For example, deuterium-depleted water is created through:
• Fatty acid synthesis and metabolism — The enzymes that synthesize fatty acids incorporate hydrogen that is carried by NADPH. This hydrogen atom has been carefully selected to be assured not to be deuterium. Interestingly, lipoxygenase is a protein expressed during conditions of stress, and according to Seneff, it has the greatest ability to select protons over deuterons of any protein.
It is highly upregulated in severe COVID-19 infection. It appears the virus triggers an increase in lipoxygenase because the virus captures linoleic acid (LA) in pockets in the viral membrane. However, lipoxygenase is not a flavoprotein, and it also doesn’t bind heme — this makes it resistant to damage from glyphosate. So, its activation becomes an alternative pathway to fix the mitochondrial deuterium problem.
SARS-CoV-2 picks up the omega-6 LA as it crosses the cellular membrane, and the LA then triggers the production of lipoxygenase that modifies the LA into leukotrienes — signaling molecules that bring in damaging macrophages.
But deuterium-depleted water is also produced in this process, by yanking two hydrogen atoms out of the fat and combining them with oxygen to make water. Note that this is just yet another way that excess LA damages your body, but with an ulterior motive that we often fail to appreciate.
• Sterol synthesis and metabolism — including cholesterol, vitamin D, cortisol, and sex hormones.
• Aromatic amino acid derivatives — including melatonin and neurotransmitters such as dopamine and serotonin, as well as thyroid hormone.
“All these molecules that go through these complicated steps are all focused on delivering deuterium-depleted water to the mitochondria,” Seneff says. “I mean, it's an absolute obsession that the cell has.” She goes on to review how processes that may appear to have nothing but harmful effects are actually an effort to heal the body. This, for example, seems to be the case in COVID-19:
“I believe that whatever biology is doing, it's doing it for a good reason. There may be damage, but there's a good reason why you need that damage in order to survive long term. It's trying to fix a problem that's very serious, and that's what I think is happening with [SARS-CoV-2].
Not only does it induce this lipoxygenase, which produces deuterium-depleted water, it then creates this inflammatory environment, which brings in the platelets and the macrophages, the immune cells and the stem cells. All these are having a big party in there in all this fluid that's building up inside the lungs.
Meanwhile, it also increases the production of hyaluronic acid. Hyaluronic acid is able to trap deuterium-depleted water. It makes structured water. So, you get structured water inside the alveoli of the lungs, and then you get fluid water in the interstitial spaces.
The blood vessels are leaky, the capillaries are leaky. Everything's coming out of the capillaries into this interstitial space where there's this fluid water, and you've got this lipoxygenase making deuterium-depleted water.
So, you're producing this environment of deuterium-depleted water, inviting the macrophages to come in, and the platelets release their mitochondria … the stem cells also come in and release their mitochondria, and then macrophages sweep up the mitochondria — and all this is happening in the interstitial space in the lungs where the fluid is. This is why you cannot breathe. You're drowning.
Maybe one of the most important things platelets do is hang on to mitochondria that they can deliver to the macrophages under conditions of stress. So, what happens is all these mitochondria get released in that interstitial space, and the macrophages induce this macropinocytosis, where they actually sweep up the water and everything that's in it and bring it inside the macrophage, including the mitochondria.
It's actually been shown that platelets can release mitochondria into the environment, and macrophages can take them up and use them as perfectly functioning mitochondria. It's astonishing. So, what they're doing is restoring the mitochondrial health to the immune cells.”
As explained by Seneff, your immune cells are impaired by glyphosate, so the older you are, the more likely you’ve been exposed to glyphosate for decades and therefore have poorly functioning immune cells. Interestingly, Seneff points out that the comorbidities of COVID-19 — obesity, diabetes and high blood pressure — are also diseases whose prevalence is going up dramatically over time, exactly in step with glyphosate usage on core crops.
“So, I think it's mostly about glyphosate,” she says. “If you've accumulated a lot of glyphosate in your tissues, you're not going to do well with COVID-19, and that's because [your body] is trying to repair the mitochondria in the immune cells so that the immune cells can actually clear the virus. If they can't make ATP, they can't do their job, and the virus flourishes.”
The key take-home message here is that this is yet another reason to clean up your diet to make sure you’re not exposed to glyphosate. It basically wrecks your immune cells, and the cascading damage that takes place in severe cases of COVID-19 appears to be your body’s response to salvage or repair those poorly functioning immune cells.
The answer to this problem is, first of all, to eat certified organic foods whenever possible. “We won't buy it if we can't find certified organic, and we've really seen health improvements since we've started doing that,” Seneff says. “I really swear by it, and I try to get all my friends to do the same. I think if you can eliminate glyphosate, you can really see great improvements in your health no matter what your problems are.” Other dietary recommendations include eating/drinking more:
Sulfur-containing foods such as organic eggs and seafood |
Organic grass fed milk and butter. Butter is one of the lowest deuterium foods available |
Glacier water, which is naturally low in deuterium |
Animal fats, which are also low in deuterium |
Molecular hydrogen |
Probiotics foods such as sauerkraut and apple cider vinegar |
To help “push” glyphosate out of your body and mitigate its toxicity, you can take an inexpensive glycine supplement. I take between 5 and 10 grams a day. It has a light, sweet taste, so you can actually use it as a sweetener.
“It makes sense because it's basically going to outnumber the glyphosate molecules,” Seneff says. “Remember, glyphosate’s going to compete with glycine in building the protein. If there's a lot of glycine around, then it's much less likely that glyphosate will get in there.”
Dr. Mercola Interviews the Experts
This article is part of a weekly series in which Dr. Mercola interviews various experts on a variety of health issues. To see more expert interviews, click here.
In April 2020, I interviewed Judy Mikovits, Ph.D., about the potential role played by human gammaretroviruses in COVID-19. Mikovits is a molecular biologist1 and researcher, and was the founding research director of the Whittemore Peterson Institute in Nevada.
Her book, “Plague of Corruption,” ended up being a No. 1 best seller on the lists of The New York Times, USA Today and The Wall Street Journal in 2020. Her new book, “Ending Plague: A Scholar’s Obligation in an Age of Corruption,” will hopefully do just as well. It’s available for preorder on Amazon.
She may be one of the most censored researchers on the planet at this point, thanks in no small part to her participation in the documentary “Plandemic,” which went viral in a big way (plandemicseries.com).
Case in point: YouTube suspended our account for one week as soon as we uploaded today’s interview — even though the video was UNLISTED and not available for public viewing yet. Even worse, Mikovits’ third and most recent book, “The Case Against Masks: Ten Reasons Why Mask Use Should Be Limited,” is so heavily censored, no one can buy it.
“I don't even have a copy,” she says. “I'm sitting here with two copies of the other books but I can't even buy it. What the book sellers did, like Amazon, is they bought them all up from Skyhorse, the publisher, and now they won't ship them out of the warehouse.”
Clearly, Mikovits is considered a serious threat to the technocratic status quo, and once you hear what she has to say about COVID-19 vaccines — which as you’ll see is a complete misnomer — you may start to understand why.
The COVID-19 vaccine really isn’t a vaccine in the medical definition of a vaccine. It does not improve your immune response to the infection, nor does not limit you from getting the infection. It’s really an experimental gene therapy that could prematurely kill large amounts of the population and disable exponentially more.
“I'm just beside myself with anger over this synthetic gene therapy, this chemical poison, and what they're doing worldwide,” Mikovits says. “We're already seeing deaths from this shot. It's illegal. It shouldn't be done. It should be stopped right now. It should have never been allowed to happen, yet we see it being forced on the most vulnerable populations.”
Indeed, news and social media reports suggest recipients are starting to drop like flies. Many die of unknown causes within days, sometimes hours of getting the first or second shot.
Baseball legend Hank Aaron passed away two weeks after receiving the vaccine, yet this was not ever mentioned in his New York Times obituary. Surely, had he tested positive for SARS-CoV-2, he would have been declared a COVID-19 fatality, whether the virus actually had anything to do with it or not.
But when it comes to the vaccine, even eyebrow-raising timing is dismissed as coincidental and irrelevant. Now all of a sudden, old people dying shortly after vaccination are shrugged off with the excuse that they’re old and could have died any day anyway. Old people dying with SARS-CoV-2, however, must be stopped at any cost. Funny how that works.
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.2 Lipid nanoparticles may also cause other problems.
In 2017, Stat News discussed Moderna’s challenges in developing an mRNA-based drug for Crigler-Najjar, a condition that can lead to jaundice, muscle degeneration and brain damage:3
“In order to protect mRNA molecules from the body’s natural defenses, drug developers must 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 daunting challenge: Dose too little, and you don’t get enough enzyme to affect the disease; 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.
‘And that list of diseases is very, very short,’ said the former employee … Crigler-Najjar was the lowest-hanging fruit. Yet Moderna could not make its therapy work ... The safe dose was too weak, and repeat injections of a dose strong enough to be effective had troubling effects on the liver in animal studies.”
However, if they call their drugs vaccines, they can bypass the safety studies. All of a sudden, they expect us to believe that all of these safety issues have been resolved? 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, or not at all?
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?
In addition, your body sees these synthetic particles as non-self and much of the perpetual antibody response will be autoantibodies attacking your own tissues. Mikovits explains:
“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.
So, taking a synthetic messenger RNA and making it thermostable — making it not break down — [is problematic]. We have lots of enzymes (RNAses and DNAses) that degrade free RNA and DNA because, again, those are danger signals to your immune system. They literally drive inflammatory diseases.
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 …
Syncytin is the endogenous gammaretrovirus envelope that's encoded in the human genome … We know that if syncytin … is expressed aberrantly in the body, for instance in the brain, which these lipid nanoparticles will go into, then you've got multiple sclerosis.
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: ‘Oh, those people had that [already].’ No, they didn't.
We also see myalgic encephalomyelitis. Inflammation of the brain and the spinal cord, which is [associated with] exogenous gammaretroviruses, the XMRVs.”
According to Mikovits, research shows 4% to 6% of Americans have already been infected with XMRV gammaretroviruses via contaminated vaccines and blood supply for more than three decades, which is driving a number of chronic health conditions. Now, these synthetic gene therapies (the so-called COVID-19 vaccines) will further add to the chronic disease burden by triggering myalgic encephalomyelitis.
Making matters worse, the synthetic mRNA also has an HIV envelope expressed in it, which can cause immune dysregulation. “This is a nightmare,” Mikovits says. “I'm angry, as this should never be allowed.”
As we discussed in previous interviews, SARS-CoV-2 has been engineered in the lab with gain-of-function research that included introducing the HIV envelope into the spike protein.
Mikovits’ hypothesis is that those who are most susceptible to severe neurological side effects and death from the COVID-19 vaccines are those who have previously been injected with XMRVs, borrelia, babesia, mycoplasma, through contaminated vaccines, resulting in chronic disease. (Her book, “Plague of Corruption,” details the science and history of XMRVs, which is a fascinating read.)
“Yes, absolutely,” she says. “That's one of our hypotheses. But also, anyone with an inflammatory disease like rheumatoid arthritis, Parkinson's disease, chronic Lyme disease, anybody with an acquired immune deficiency from any pathogens and environmental toxins.
Those are the people who will be killed, murdered, by this vaccine, and Anthony Fauci knows it … I can't even sleep [because of] how evil this is. This is so deadly, I can't scream it loud enough from the rooftops.”
The chart below lists 35 diseases associated with XMRV infection. If you have any of these, you may want to think long and hard before you line up for an mRNA COVID-19 vaccine, as your chances of severe side effects or death are likely far higher than someone who does not have any of these diseases.
This is not a complete list. There may be many other conditions that can put you into a high-risk category. One example is idiopathic thrombocytopenia (ITP), a deadly bleeding disorder. According to Mikovits, her work shows 30% of all ITP are associated with XMRVs.
Interestingly, one example is the 58-year-old Florida doctor who recently got the COVID-19 vaccine and died from sudden onset of ITP two weeks later. Dr. Jerry L. Spivak, an expert on blood disorders at Johns Hopkins University, told The New York Times “it is a medical certainty” that Pfizer’s COVID-19 vaccine caused the man’s death.4,5 Pfizer, of course, denies any connection.
So, just how long will the synthetic RNA in COVID-19 vaccines be maintained within your body, causing your cells to produce this aberrant protein? Mikovits believes it will escape degradation for months, years, maybe even for life in some cases.
All of this is eerily reminiscent of previous attempts to create a coronavirus vaccine, all of which failed due to the vaccines causing paradoxical immune reactions, or antibody-dependent immune enhancement. While the animals appeared to have antibodies against the virus, and should theoretically have been protected, when they were exposed to wild coronavirus, they got severely ill and most died.
Such failures may be why so many vaccine makers decided to use mRNA rather than following conventional vaccine development strategies, but the end result is likely going to be the same or worse.
“I have a 41-year-old daughter-in-law with a very aggressive colon cancer. We're seeing an explosion of chronic disease and these patients are not being discouraged from getting the vaccine. In fact, they're being scared by physicians into getting it.
How do we wake people up? Is it going to take millions of Americans and people worldwide dying? Will Hank Aaron dying help the Black community? … We know the mechanisms. We know that Blacks and Hispanics can't degrade RNA viruses as rapidly as Caucasians. We know that from studies all the way back to MMR. The MMR vaccine is associated with ITP. It says it right there on the package insert.
If you have a single nucleotide polymorphism in one of those RNases called RNase-L, you are more likely to get aggressive breast cancers, prostate cancers and other cancers from an XMRV infection (So why inject mRNA of syncytin, a gamma retrovirus envelope?).”
According to Mikovits, one solution is to use functional genomics technologies like Breakthrough Genomics, a company which uses machine learning to look at full genome sequences to determine which single nucleotide polymorphisms in ACE2 receptors, antiviral pathways like RNASEL and Interferons can make a person most susceptible to harm from these gene therapy “vaccines.”
“We have the technology to see who's susceptible to severe effects. It will be a huge part of the population,” Mikovits says.
While one size clearly doesn't fit all in any vaccine strategy, forcing a gene therapy on an entire population when it can be predicted that millions will die and develop deadly diseases like ITP is simply unconscionable. Yet anyone who dares speak about this, as Mikovits knows, risks having their careers and lives destroyed.
Many of the symptoms now being reported are suggestive of neurological damage. They have severe dyskinesia (impairment of voluntary movement), ataxia (lack of muscle control) and intermittent or chronic seizures. Many cases detailed in personal videos on social media are quite shocking.
Equally shocking is that these videos are quickly removed by the social media platforms, ostensibly for violating some term of service. It’s hard to fathom how a personal experience can be considered “false information.”
“What is causing this is the neuroinflammation,” Mikovits says. “It's the brain on fire. You're going to see tics, you're going to see Parkinsonian disease, you're going to see ALS, you're going to see things like this developing at extremely rapid rates, and it's inflammation of the brain.”
Side effects are also suggestive of a dysregulated innate immune response and a disrupted endocannabinoid system, which acts as a dimmer switch on your immune system.
“We see mast cell activation syndromes (MCAS). The clinical symptoms are going to be the inflammatory diseases. We hear everybody calling it ‘long haul COVID’ — the extreme, profound, crippling fatigue, the inability to produce energy from your mitochondria.
It's not long haul COVID. It's exactly what it always was — myalgic encephalomyelitis, inflammation of the brain and the spinal cord. What they're intentionally doing is killing off [certain] populations, which they previously injured.”
Another common side effect from the vaccine we’re seeing is allergic reactions, including anaphylactic shock. A likely culprit in this is PEG, which an estimated 70% of Americans are allergic to. “These instantaneous effects are almost certainly the PEG and that lipid nano particle, the toxic particle that's being injected,” Mikovits says.
In the longer term, she suspects we’ll see a significant uptick in migraines, tics, Parkinson’s disease, microvascular disorders, different cancers, including prostate cancer, severe pain syndromes like fibromyalgia and rheumatoid arthritis, bladder problems, kidney disease, psychosis, neurodegenerative diseases such as Lou Gehrig’s disease (ALS) and sleep disorders, including narcolepsy. In young children, autism-like symptoms are likely to develop as well, she thinks.
Aside from the chronic diseases listed earlier, 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, in particular, due to genetics. Tragically, these vaccines are given to the most susceptible under the guise of racial and social justice.
“Johns Hopkins laid out that plan a few months ago to vaccinate ethnic minorities and the mentally challenged first. If your brain is already on fire, if you already have a neural inflammatory disease, why in the world would you inject this neural inflammatory toxin? You're killing the people who are the most susceptible.”
Women of childbearing age may also be at risk for infertility, 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. Indeed, the World Health Organization is now saying pregnant women should not get the Moderna or Pfizer vaccines due to reports of late-term miscarriages.6
The primary reason why I wanted to interview Mikovits was to find out her recommendations for those who chose to get the vaccine and now regret it. Interestingly, what I learned is you use the same strategies that you would use to treat the actual SARS-CoV-2 infection.
I’ve written many articles over the past year detailing simple strategies to improve your immune system, and with a healthy immune system, you’ll get through it without incident even if you end up getting sick. Below, I’ll summarize some of the strategies you can use both to prevent COVID-19 and address any side effects you may encounter from the vaccine.
First of all, you’ll want to eat a “clean,” ideally organic diet. Avoid processed foods of all kinds, as they are loaded with damaging omega-6 linoleic acid that wrecks your mitochondrial function. Also consider nutritional ketosis and time-restricted eating, both of which will help you optimize your metabolic machinery and mitochondrial function. As noted by Mikovits:
“We have to think about detoxing metal, we have to think about glyphosate … We have to prevent inflammation in all tissue sites and we have to keep our immune system healthy ... You're going to want to be burning ketones instead [of sugar] for the neuroinflammation, so you're going to want to get into ketosis and take the stress off the mTOR pathway.”
With regard to glyphosate, a simple way to block glyphosate uptake is to take glycine. Approximately 3 grams, about half a teaspoon, a few times a day should be sufficient, along with an organic diet, so that you’re not adding more glyphosate with each meal.
To improve detoxification, I recommend activating your natural glutathione production with molecular hydrogen tablets. All of these strategies should help improve your resilience against SARS-CoV-2, and may even help your body detoxify if you’ve made the mistake of getting this experimental gene therapy.
Another helpful strategy is to maintain a neutral pH. You want your pH to be right around 7, which you can measure with an inexpensive urine strip. The lower your pH, the more acidic you are.
A simple way to raise your pH if it’s too acidic (and most people are) is to take one-fourth teaspoon of sodium bicarbonate (baking soda) or potassium bicarbonate in water a few times a day. Improving your pH will improve the resiliency of your immune system and reduce the mineral loss from your bones, thereby reducing your risk of osteoporosis.
Nutritional supplementation can also be helpful. Among the most important are:
Vitamin D — Vitamin D supplements are readily available and one of the least expensive supplements on the market. All things considered, vitamin D optimization is likely the easiest and most beneficial strategy that anyone can do to minimize their risk of COVID-19 and other infections, and can strengthen your immune system in a matter of a few weeks. |
N-acetylcysteine (NAC) — NAC is a precursor to reduced glutathione, which appears to play a crucial role in COVID-19. According to one literature analysis,7 glutathione deficiency may actually be associated with COVID-19 severity, leading the author to conclude that NAC may be useful both for its prevention and treatment. |
Zinc — Zinc plays a very important role in your immune system’s ability to ward off viral infections. Like vitamin D, zinc helps regulate your immune function8 — and a combination of zinc with a zinc ionophore, like hydroxychloroquine or quercetin, was in 2010 shown to inhibit SARS coronavirus in vitro. In cell culture, it also blocked viral replication within minutes.9 Importantly, zinc deficiency has been shown to impair immune function.10 |
Melatonin — Boosts immune function in a variety of ways and helps quell inflammation. Melatonin may also prevent SARS-CoV-2 infection by recharging glutathione11 and enhancing vitamin D synthesis, among other things. |
Vitamin C — A number of studies have shown vitamin C can be very helpful in the treatment of viral illnesses, sepsis and ARDS,12 all of which are applicable to COVID-19. Its basic properties include anti-inflammatory, immunomodulatory, antioxidant, antithrombotic and antiviral activities. At high doses, it actually acts as an antiviral drug, actively inactivating viruses. Vitamin C also works synergistically with quercetin.13 |
Quercetin — A powerful immune booster and broad-spectrum antiviral, quercetin was initially found to provide broad-spectrum protection against SARS coronavirus in the aftermath of the 2003 SARS epidemic,14,15,16 and evidence suggests it may be useful for the prevention and treatment of SARS-CoV-2 as well. |
B vitamins — B vitamins can also influence several COVID-19-specific disease processes, including17 viral replication and invasion, cytokine storm induction, adaptive immunity and hypercoagulability. |
Mikovits also recommends Type 1 interferons.
"The type 1 [interferon] — the primary source of interferon, alpha and beta — is the plasmacytoid dendritic cell. We know that's dysregulated in people with HIV, with XMRVs, with aberrant retroviral expression. Those people can't make interferon.
Type 1 interferons can be provided in a spray that you can spray directly into your throat, your nose, and that will give you the protection you need so that the virus doesn't [replicate]. It degrades it right away … Should you feel cough or fever, headache, immediately up your Type 1 interferon. Take a couple of sprays of that per day prophylactically as well, and that will keep the viral load down.
We know [SARS-CoV-2] isn't a natural virus, we know this is lab-created, but it'll calm the expression, it'll degrade the RNA for those who can't degrade the RNA, and that's the job of Type 1 interferon — to have your macrophages be these little Pac-Men that simply degrade the viral mRNA.”
My personal choice for the treatment of COVID-19 symptoms is nebulized peroxide. It’s a home remedy I recommend everyone familiarize themselves with, as in many cases it can improve symptoms in mere hours. You can also use it as a preventive strategy if you know you’ve been exposed to someone who is ill.
Nebulizing hydrogen peroxide into your sinuses, throat and lungs is a simple, straightforward way to augment your body’s natural expression of hydrogen peroxide to combat infections and can be used both prophylactically after known exposure to COVID-19 and as a treatment for mild, moderate and even severe illness.
Dr. David Brownstein, who has successfully treated over 100 COVID-19 patients with nebulized peroxide, published a case paper18 about this treatment in the July 2020 issue of Science, Public Health Policy and The Law. He also reviews its benefits in “How Nebulized Peroxide Helps Against Respiratory Infections.”
Nebulized hydrogen peroxide is extremely safe, and all you need is a desktop nebulizer and food-grade hydrogen peroxide, which you’ll need to dilute with saline to 0.1% strength. I recommend buying these items beforehand so that you have everything you need and can begin treatment at home at the first signs of a respiratory infection.
In the video above, I go over the basics of this treatment. Be sure to buy a nebulizer that plugs into an electrical outlet, as battery-driven ones are too low-powered to be truly effective. Also make sure your nebulizer comes with a face mask, not just a mouth piece. If it doesn’t come with a face mask, you can pick one up separately. Just search Amazon for “nebulizer face mask for adults.”
Hopefully, we’ve provided enough information to make you reconsider the COVID-19 gene therapy “vaccine.” At bare minimum, do more research before you make your decision. The simple truth is you don’t need it, so it’s an unnecessary risk.
To learn more, be sure to preorder a copy of “Ending Plague: A Scholar’s Obligation in an Age of Corruption.” We’re in a crisis in far more ways than one, and getting educated — and then educating others — is absolutely crucial. The lives of millions of people are at stake. So please, take the time to digest this information, understand it, and share it with those you love.