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Feb. 14, 2021 - Jim Fetzer
01:06:47
SARS-CoV-2 mRNA Vaccines / Dr. Mercola with Dr. Judy Mikovits
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Time Text
SARS-CoV-2 immunizations or vaccinations, which is an absolute misnomer because this is not a vaccine.
This is an experimental gene therapy and it's been given now for about a month and we are seeing people die as a result of this intervention and we are going to see many, many more deaths and even worse, permanent Disabilities.
So what do we do?
How do we know how to mitigate against this?
Well, I thought I'd get one of the leading experts in the entire world, a genius at molecular
biology and virology, and one of the few people who could help us understand why this experimental
gene therapy is having such a catastrophic side effect.
I'm just actually literally beside myself with anger over this gene therapy, this synthetic
chemical poison and what they're doing worldwide.
We're already seeing the victims of the deaths from this from this shot.
It's illegal.
It shouldn't it shouldn't be done.
It should be it should be stopped right now.
It should have never been allowed to happen.
Taking a synthetic messenger RNA, making it thermostable, that is, making it not break down.
We have lots of RNAases and DNAases.
Those are enzymes that degrade free RNA and DNA, because again, those are danger signals to your immune system and they literally, you know, turn on the flame or drive inflammatory diseases.
What is causing this is the neuroinflammation.
It's the brain on fire.
As you mentioned, you're going to see the 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 rate.
It's the inflammation of the brain.
You know, Johns Hopkins laid out that plan a few months ago to vaccinate the ethnic minorities and mentally challenged first.
So if your brain's already on fire, if you already have a neuroinflammatory disease, why in the world would you inject this neuroinflammatory toxin?
You're killing the people who are the most susceptible.
Anyone with an inflammatory disease like, you know, 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 are dying and who will be killed, murdered by this vaccine.
Is it going to take millions of Americans and people worldwide dying?
How do we educate people?
How do we wake people up?
Welcome everyone, it's Dr. Mercola helping you take control of your health and today we are in for a mind-blowing, unbelievable connection, reconnection with Dr. Judy Mikevitz, who we last interviewed, believe it or not, because it just seems like it was the other day, but it was in the fall nine months ago.
And at that time, her book had just been published.
I don't think it skyrocketed, but it achieved a very rare feat of being the number one most purchased book in the entire United States.
By the, not by, was it the New York Times?
Did you get?
Okay, you got New York Times and Amazon.
And Amazon and USA Today and Wall Street Journal.
So congratulations for that.
That was an amazing feat and that was despite the mainstream media suppressing this information and basically removing you from every platform that had the opportunity to do so.
So that was an amazing achievement and a lot has happened since then and we really want to focus today on this incredible introduction of the COVID-19 vaccine and to call it a vaccine is a misjustice of the language because in no way shape or form Even comes close to the legal definition of a vaccine.
It does not improve your immune response to the infection.
It does not increase you from, limit you from getting infection.
This is a gene therapy, an experimental gene therapy that has the potential to prematurely kill large amounts of the population and disable exponentially more.
So, We are going to dive deep today to give you the information, the ammunition you need to be motivated to not only avoid this dangerous therapy for yourself, but for all of those that you know and love.
So welcome back and thank you for joining us again.
Thank you, Mike.
Dr. McCullough, it's a pleasure to be here, and thanks to Mike for setting this up.
I'm just actually literally beside myself with anger over this gene therapy, this synthetic, you know, as you mentioned, gene therapy, chemical poison, and what they're doing worldwide.
they're already, not just the potential to kill, but in fact, we're already seeing the victims
of the deaths from this shot that it's not only, it's illegal, it shouldn't be done,
it should be stopped right now, it should have never been allowed to happen.
And yet we see it being forced on school populations.
That's what I have to do is I have to go, you know, talk at school board, talk at churches, talk at meetings, do everything we can to stop the innocent victims who are being lied to.
And this fraud perpetrated even further than the fraud of SARS-CoV-2 and what really COVID-19 is.
Yeah, I think the media is going to do everything they can to suppress the truth.
And the truth is that people are starting to drop like flies.
And in those people, you're going to see celebrities and prominent people in the news media.
We have baseball legend, Hank Aaron, who passed away, no question, two weeks after getting the experimental gene therapy.
And when his obituary was published in the New York Times, not a microgram of any mention of that vaccine connection was ever made.
And then we had Larry King just died two days ago.
And it's unclear, but it appears that he may have gotten it.
So we're in the process of compiling all of this data together Or coordinator can collaborate with sites that have already done it because it's going to start piling up quickly as we're into about a month of the administration of this therapy.
So, lots of questions!
Right.
So, one of the burning questions I had, this is a messenger RNA vaccine, and you are a molecular biologist and a virologist, so there's very few people who are more qualified to give their insights and commentary on this.
And I'm wondering, it's unclear from the literature to me, but, you know, it's been a long time since I took genetics, but even if I had taken it yesterday, I don't even know if it's known how long Messenger RNA lasts in the delivery system.
And this is not regular messenger RNA.
This is messenger RNA that's encapsulated with nanoliposomes that are attached to something called PEG, polyethylene glycol, which is used to allow it to survive the transmission and the injection into the body, which in itself is probably causing a lot of the complications.
But how long does messenger RNA last in the body?
Well, and in fact, this isn't even messenger RNA from nature.
This is actually synthetic.
Normally messenger RNA is not in the body, free in the body.
Because a danger signal.
So, you know, as a molecular biologist, the central dogma of molecular biology is that our genetic code, which is DNA, is transcribed, written into RNA, the messenger RNA.
That messenger RNA is Translated into protein or used in a regulatory capacity.
Not translated into protein and used to regulate gene expression in cells.
So taking a synthetic messenger RNA, making it thermostable, that is making it not break down.
We have lots of RNAases and DNAases.
Those are enzymes that degrade free RNA and DNA because again, those are danger signals to your immune system and they literally, you know, turn on the flame or drive inflammatory diseases.
And as you just mentioned, now you've got it With PEG, pegylated, and polyethylene glycol, and an in-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 that actually is the message for, synthetically, for the gene syncytin, the HERV-W, the endogenous envelope
virus that we have, everyone has in their genome.
So now you're putting a synthetic syncytin.
We know that if syncytin, it's a gamma retrovirus envelope, and we know if it's expressed aberrantly in the body in different places in the body, for instance, In the brain, which these lipid nanoparticles will go, then you've got multiple sclerosis.
So the expression of that gene alone enrages microglia, literally inflames and dysregulates the communication between the brain microglia, the critical for clearing Toxins and pathogens in the brain and the communication with the astrocytes.
It dysregulates not only the immune system, but the endocannabinoid system, which is the dimmer switch.
So there we've already seen in the clinical trials, we've already seen multiple sclerosis as an adverse event and we're being lied to.
Those people had that.
No, they didn't.
And we also see, as we know, myalgic encephalomyelitis, inflammation of the brain and the spinal cord, which is what we associated the exogenous gamma retroviruses, the XMRVs.
So now you have the aberrant expression, the mouse viruses in In many of the vaccines including the polio vaccines which we know from the our studies at the end of the day between four and 6% of America that the so called control group were were infected with the gamma retroviruses and.
And now you're going to inject and drive, you know, myalgic encephalomyelitis.
We're seeing that already.
We're seeing you've got an envelope of HIV expressed in that synthetic gene therapy.
So you're expressing HIV GP120, which again is the surface unit that can cause immune dysregulation.
That's also, I thought it was just a spike protein, but it's also this HIV protein?
Yeah, the spike proteins of SARS-CoV-2 contained HIV and syncytin, so you've put all three.
You've put the ACE2 receptor from a coronavirus, you've put HIV, and you've expressed the gamma retrovirus envelope protein that is cross-reactive with our human syncytin.
So this is why people are testing positive as you express that gene abruptly under stress as you wear the mask and cripple your immune system and change the expression of our genes.
You know, this is a nightmare.
It's beyond, I'm angry at this point in time.
Your previous work in your last book focused on this XMRV, which you referenced, and it's a fascinating story.
And if you're interested in it, I definitely would encourage you to pick up The Plague of Corruption, which really goes into in great detail.
But is it your premise or hypothesis that Those that are most susceptible to dying or developing severe neurological side effects are those that have been previously infected with the XMRB virus?
Yeah, absolutely.
That's one of our hypotheses, but also anyone with an inflammatory disease like Um, you know, rheumatoid arthritis, um, Parkinson's disease, chronic Lyme disease, anybody with an acquired immune deficiency from, from any pathogens and environmental toxins.
Those are the people who, um, who are dying and who will be, um, you know, will be killed, murdered by this vaccine.
And Tony Fauci knows it.
I understand he was on the CBS morning news show yesterday whining because I called him a criminal.
He is a criminal and he should literally be tried for treason and murder and crimes against humanity because it is very clear.
After he destroyed my career and covered up XMRVs and the damage that they had done by a heavily contaminated blood supply for 30 years and the contaminated vaccines, what he did Um, to these families so he began immediately after 2012 when he when he stopped the the so called Lipkin replication study and in which was fraud.
That's a fascinating story and I really would encourage people to listen to our previous interview where you go in great detail on that.
But you had mentioned that those with autoimmune pre-existing autoimmune disorders should not get this vaccine and I'm so glad that the vaccine companies Pfizer and Moderna acknowledged that and put that as a severe black box warning because if you have those you should not get the vaccine.
If you have cancer, if you have rheumatoid arthritis.
That was a joke.
That was sarcasm.
It's not a black box warning.
Oh, there's nothing on there?
No!
There's no warning.
Anyone can get this vaccine.
They're mandating it.
They're killing people.
It's not governmentally mandated.
It's mandated in certain circumstances.
If you're a worker in a health care system, then in those situations, typically that's required.
But it's just crazy.
You know, it's a very clever marketing scheme, if you think about it.
And I've studied marketing.
They've introduced a scarcity model.
Don't have enough vaccine for everyone, so they make it be like this prestige, this badge of honor, if you can only get the vaccine that's going to save you.
And it's just a powerful catalyst for human behavior to obtain something, you know, when they think they can't get it.
Wow.
It's just, it's very clever, very sophisticated, and they're using these tools.
The tools in themselves are not intrinsically good or bad, but the way they're using them, clearly you can qualify it as perniciously evil.
So getting back to this messenger RNA, what's your guess on the range of the time that is maintained within the body causing your cells to produce this aberrant protein?
Well, because they changed, because it's synthetic and because it's in an adenovirus vector, and they changed the cleavage sites, that means... Okay, wait, wait.
That's a pretty important piece of the puzzle, and I don't understand what that means.
So how is it integrated?
How is the messenger RNA integrated into an adenovirus vector?
Well, it's synthetically put into the vector.
That's in molecular biology.
You put it in an expression vector and then you wrap it in this nanoparticle and you change the normal cleavage site so that those RNases and DNases can't break it up.
It's literally gene therapy.
These are the gene therapy vectors.
That's what they use for CRISPR technology.
So that adenovirus allows it to penetrate all the cells and the nanoliposome lipid envelope allows it to escape metabolism or degradation by the body's normal circumstances.
So you think it might stay in there for weeks or months?
Yeah, or forever.
Oh my gosh, that's crazy!
Yeah, and in some of the small animal models with others of these, they follow it with the luciferase gene.
Which lights it up which is so give you and you can track it and you can see it stay in the spleen and you can see that it goes to the brain.
So you've hit to the heart of your of your white blood cells of your ability to to make immune responses.
So I can see this and then those of course with chemokine and cytokine signaling the inflammatory cytokine storm you're going to get when you inject this synthetic It can traffic everywhere in the body.
For me, it's just, I can't even sleep just how evil this is.
This is just so deadly.
I can't scream it loud enough from the rooftops.
You know, it's interesting.
Previously, the largest vaccine manufacturer in the world, I believe, was Merck.
And as we're recording this, I believe the day before yesterday, The day that Larry King died or the day after, they reported that they were discontinuing their efforts for a COVID-19 vaccine.
Now, they didn't take the messenger RNA route.
They did a more traditional route, but they realized it just failed miserably.
They were unable to produce these antibodies, but certainly Pfizer and Moderna did.
Well, they're not vaccines.
I know, they're not vaccines.
I get that, but I wanted to say, going along the traditional vaccine route, the coronavirus, this is not the first coronavirus.
They've been around for a long time, and there's been more than 10 years of efforts to develop coronavirus vaccines, and all of them failed, and it was worse than failed.
They produced this paradoxical immune reaction, which essentially allowed the immunized Animals that they didn't remember.
Animal studies were not done.
They were eliminated.
They bypassed that.
And when they did the animal studies for the previous coronavirus vaccines, they were developed immunity.
But the next time they were exposed to the coronavirus, most of the animals died because of this paradoxical immune reaction.
So it's a miserable failure.
It's probably one of the reasons why they go to this route.
And it would seem it's really a pretty clever system where you can just tell your body to produce the specific proteins that's responsible for it and then shut off that signal because to have it continue for months or years is just insane!
They're turning our bodies into this protein production factory Which we have no consequence and no safety studies at all to understand what this is going to do.
Absolutely.
And again, I think there's enough studies to show over the last 20 years, as you mentioned, with SARS, with MERS, even with HIV.
They've been trying to make for other RNA viruses like HIV.
So why would you express the envelope protein in a synthetic form in every cell of the body and not expect to cause AIDS?
You know, which is what you, you know, is going to happen.
These 20, 32, I have a slide Let's see, I have a slide in the slide show I sent you last week.
The population susceptible, you know, then there are probably 35 diseases on that.
We're going to include that list in the article in a nice table, so thank you for sending that.
Yeah, and things like ITP, idiopathic thrombocytopenia.
That was the last, that was the last disease.
You know, before my career was ended, I presented work showing 30% of all idiopathic thrombocytopenia, which is a deadly bleeding disorder, which that 58 year old doctor in Florida died of after he got the vaccine, literally again, two weeks later.
So we had shown in a, in a blinded study with a world's expert that the XMRBs were associated with the development of of ITP.
So now when you're expressing syncytin and HIV envelope and the ACE2 receptor binding domain in every cell of the body, it's just beyond comprehension the damage it's going to do.
And those 32 diseases, you know, cancer patients, you know, I have a 41-year-old daughter-in-law with a very aggressive colon cancer.
I mean, these kids have cancer, neuroendocrine tumors.
We're just 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 doing that, just as they're driving their disease With the masks.
So that's the last book we wrote last year was the case against the masks.
10 reasons why masks use should be limited.
And, and, and people are wearing masks and getting these shots, which is going to drive.
And that book's so heavily censored, nobody can buy it.
I don't even have a copy.
I'm sitting here with two copies of the other books, but I can't even buy it.
So what the booksellers did, like Amazon, is just buy them all up from Skyhorse, the publisher, and now they won't ship them out of the warehouse.
So how do we educate people?
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?
I've done at least three shows and all the way back in, not even a show, December 18th, I was called along with RFK, Robert F. Kennedy Jr., Dr. Neunschwinder, Dr. James Leinsweiler, we were called by the Honorable Minister Louis Farrakhan to his Chicago office, if you will, and called to inquire as to the data that show this will be deadly for Black populations.
And we did that in a day-long meeting with those Three doctors and showed them that you know all the way back December 18th that the black community would in fact be adversely affected more than the white community and and killed and we see it in now in in in Hank Aaron and You know got that call by a sobbing Atlanta reporter who's been trying to wake up the black community and
You know, Saturday morning or whatever, two days ago.
So, we know the mechanisms.
We know that the Blacks can't degrade RNA viruses.
We know that from the studies all the way back to MMR.
The MMR vaccine is associated with ITP.
The MMR, it says it right there on the package insert.
So, people having had these vaccines and already With an inability that was, that was where the viruses were doing damage with the XMRV.
If you don't have, if you have a single nucleotide polymorphism in one of those RNases called RNase L, we knew that RNase L, you were more likely to get aggressive breast cancers and prostate cancers and other cancers.
Um, um, from an XMRV infection.
And that was, that was, you know, the data, uh, that built upon the hypothesis that we had, um, years, uh, a few years later and, and more than a decade ago.
So we absolutely know the molecular mechanisms, the people, the communities, people with defects in the type one interferon pathway in the slideshow.
I, I gave you, I showed solutions, which is what we're always trying to do and show A technology called Breakthrough Genomics, which this company used machine learning to look at, you know, full length, full genome sequences, not just proteins, but looking at introns where you can see who's going to be most susceptible in the entire type 1 interferon pathway, who's going to be most susceptible
With certain single nucleotide polymorphisms in ACE2 receptors.
So you can actually, we can, we do have the technology to see who's susceptible from severe effects.
It will be a huge part of the population.
And again, this, you know, one size clearly doesn't fit all in any vaccine strategy.
But, you know, forcing a chemotherapy and a gene therapy on an entire population where Where millions of Americans, millions of people worldwide will die and we'll get these deadly diseases like ITP.
We know this.
The scientific community knows this.
Not only is it being censored, but our careers or our lives are being destroyed if we dare talk about this.
We'll get this information out.
We'll definitely want to focus on solutions, which is the primary reason why I wanted to connect with you.
Unfortunately, this message that is going to be communicated in this interview will not be received by most of the people who need it, and it's going to be too late for them, so we need to focus on what they can do after they get it.
But let's talk now about some of the symptoms, because these videos are starting to appear from people who've gotten the vaccine and are reporting their side effects.
Some of them are neurological.
They have severe dyskinesia, ataxia, stumbling around.
It's just shocking and almost equally shocking but not surprising is that very quickly after these videos are posted they're taken down because it violates community policy.
Correct.
So, what is causing this?
I mean, you mentioned earlier the connection with MS.
This is not an MS.
It's an MS-like symptom, but it's much more acute.
So, why don't you discuss some of those and some of the other complications that we're seeing now?
Well, the neuroinflammation.
So, what is causing this?
is the neuroinflammation.
It's the brain on fire.
As you mentioned, you're going to see the ticks.
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 the inflammation of the brain.
It's the dysregulation, primarily of the innate immune response and the crippling and this again, this is what's happening with the masks.
You're crippling your antioxidant machinery, particularly glutathione with the mask.
And then you're crippling your type one interferons, because those are the interferons that are going to be at your mucosal surfaces.
So just the sheer quantity, just expressing that, those three envelope proteins, those binding domains in every cell of the body, is just going to overwhelm It's going to disrupt the endocannabinoid receptors, the communication, the dimmer switch on the immune system, which we talked about in great length.
I mean, everything we talked about in May with the epigenetics, the DNA methylation, it's literally, we've known this, we've known this for two decades, especially you and I.
Um, as we've tried to, you know, um, tried to stop this.
So it's the brain inflammation.
I show you there a 2014 paper, um, in, in that slideshow.
And, um, right in that slideshow is a paper from a review article published October, 2014.
And I've got the reference right on the slide.
Um, but it, it shows you that inflammatory cytokine storm.
So trauma, infection, toxic metabolites, nuclear and cytosolic proteins, tangling, prions, LPS, just the quantity of toxins in our world.
We already, everybody in this world already has a brain that is at least at some level on fire.
That's the inflammatory cytokine storm.
So you that immune insult, you know, systemically results in what is called pathogenic priming, you know, and we call the term now pathogenic priming of the of the M1 macrophage, you know, and you'll get it to the macrophage can't do its job.
It turns ramified.
I mean, I've been showing these slides for two decades.
You know, courtesy of Dr. Rossetti's wife, Sandy, because she had been doing research for 30 years into how these animal viruses cause disease, and it's at the level of the priming, the pathogenic priming of the glial cells.
And that turns up the flame, the TNF alpha, the IL-1 beta, the IL-18, the IL-6, you know, in all, you know, Th2 cytokines, IL-4, IL-10, that'll turn into an immune suppressive effect.
It's everything we've seen.
In vaccine injury, and I hate to say it, but then on steroids, because we just just ramped it up, you know, 100 times.
So the brain's on fire.
You've already got neural inflammation going on and.
And stress is the most powerfully immune suppressive, so the mask is causing fear, stress, everything, and so we are primed literally to have that wherever sites of tissue injury are, but it's going to be at the level of the brain, and we're seeing it, you know, literally cardiac arrest.
We've seen this in vaccine court, in influenza vaccines.
So, you know, the very people who should never be given a shot are being, and it includes healthcare workers, because the nosocomial spread, we as lab workers, as healthcare workers, people who have been making these gene therapy vectors, We knew back in 2011 that these XMRBs from mice cells and everything we worked with all the animal tissues in the lab, we knew that these were being spread in aerosols.
These were being spread, you know, exactly the way, you know, the mask is actually concentrating those things.
It's not stopping the spread.
It's actually exacerbating the spread.
We never wore a mask in a lab.
But now we know these were contagious cancers, contagious disease.
Many of my colleagues died well before 60 of cancers associated with the expression, the aberrant expression of these genes and the inability to turn off the flame.
You can't regulate the macrophage.
We see mast cell activation syndromes.
We see essentially all of this.
So the clinical symptoms are going to be the inflammatory diseases.
Everything you're talking about.
Certainly we hear everybody calling it long-haul COVID.
The extreme profound Crippling fatigue, the inability to produce energy from your mitochondria.
We already have the crippled mitochondria in most everyone who's been injected, so you're seeing that.
It's not long-haul COVID.
It's exactly what it always was that Tony Fauci's been covering up for.
You know, since HIV AIDS, you know, myalgic encephalomyelitis, inflammation of the brain and the spinal cord.
And that's what they're intentionally doing is killing off that population.
And I'm sorry you can't see it molecularly any other way.
In any other way, can you see this?
And Tony Fauci knows very well the molecular biology behind this.
And this is the kill switch.
To cover it all up, call it SARS-CoV-2, it absolutely is not the result of a natural infection.
It's a result of these injections.
And we knew Flu shots drove it, and so now this vaccine is going to kill those populations who have gotten flu shots, worn masks.
That's what we're seeing.
We saw the picture of Hank Aaron getting the flu shot, wearing the mask, so he already has a brain on fire.
He's already driven those molecular pathways.
Again, that single paper won a case in vaccine court of the vaccine causing SIDS, causing a sudden infant death in a six-month-old black baby.
We've known this.
We've known this for at least a decade.
And as you said, for two decades, we've known that it's not possible It's not possible to make vaccines against coronaviruses, against RNA viruses, retroviruses like HIV, like the XMRVs.
We know that.
We know you can't, we can't do that without causing this type of pathogenic priming.
And there's an antibody-dependent enhancement, completely other mechanisms The antibody-dependent enhancement, which in blacks, they make twice the antibodies just given their genetic background.
They have different, you know, vitamin D receptors.
Their vitamin D receptors control 300 at least immune reactions.
So, there are differences in different populations.
So, if you already make two times an antibody signal by nature, Um, then you're going to have antibody-dependent enhancement anytime you see, um, a, um, these RNA viral vaccines.
So when they're constructed in such a way, um, that you give them to the most, you know, susceptible, this is what we're seeing.
So, you know, blacks, Hispanics, they're not Not more susceptible to RNA viruses.
There's not, you know, the NIH article or that CNN talk that I put a quote of in that slideshow under the guise of racial justice.
You know, Johns Hopkins laid out that plan a few months ago to vaccinate the ethnic minorities and mentally challenged first.
So if your brain's already on fire, if you already have a neuroinflammatory disease, why in the world would you inject this neuroinflammatory toxin, this chemotherapy, gene therapy?
There's a good answer to that.
They're calling the herd.
Well, yeah, you're killing the people who are the most susceptible.
Yeah, yeah.
So you had mentioned, this is intriguing because I want to discuss this with you, the long-haul syndrome, which is a result of the SARS-CoV-2 infection.
Clearly we're seeing that, but is it your belief that the gene therapy intervention that's being promoted will also cause a long-haul syndrome?
Absolutely.
And it's not SARS-CoV-2 that's causing this.
It's the XMRV envelopes and the HIV envelopes.
We knew that.
You know, that's what happened in AIDS.
You get AIDS with the T cell abnormalities.
There's a, you know, MECFS came up in AIDS.
We know it's associated with XMRVs.
Let me stop you there because just so I'm clear on it and everyone watching this is clear.
So when you say it's the AIDS, this is most likely due to the HIV protein that was integrated, we believe, by genetic technology, which you talked about, to the initial SARS-CoV-2 that originated from Wuhan.
And this is what's causing it.
And this is the same protein that's integrated into the experimental gene therapy?
Correct, and our XMRB envelope, and syncytin, the surface unit.
What is syncytin?
Why don't you help us understand what that is, because I'm a little bit confused on it.
Okay, so syncytin is the name given to the endogenous gamma retrovirus envelope.
An envelope.
We have the viral envelope protein of the gamma retrovirus known as HERV-W.
It's not a beta retrovirus.
It's not HERV-K.
It's not what you've been lied to.
It's not how our data were corrupted back in 2011.
And Tony Fauci himself said, oh, it's just endogenous retrovirus.
No, you don't dysregulate the expression of your gamma retrovirus HERV-W.
Syncytin is a viral envelope.
That's encoded in the human genome.
So again, everybody's going to test positive in the PCR test, because not only is HIV constructed into this SARS-CoV-2, which is not just the coronavirus, it's a weapon.
You've now got syncytin being expressed in this gene therapy, and it is in the SARS-CoV-2 viral strains, and it's in your human genome.
So when you express a synthetic or another animal gamma retrovirus, like the mouse, like the monkey, like the cow, all the way to lizards have syncytin.
You know, it's encoded in the genome.
It's in the human genome.
So if you activate syncytin, the protein, In biology, in virology, syncytia are the fusion.
So what these envelope proteins do is fuse your cells together.
And it is syncytin that allows us to have, you know, a placenta.
In the uterus fused together.
And so that's the normal, the expression of this in a good way allows us.
I was going to ask you about that.
I thought it was more highly expressed in the placenta.
So that, does that also contribute to the projected or observed effects on fertility?
It will.
Yeah.
Cause that allows implantation.
So if you can't implant, cause what you're going to do when you're injected with a synthetic one, And when you're, we know this from being injected with the animal ones.
This was the monkeys, the mouse retroviruses, the families, Malonium Murine Leukemia viruses, those were all those things we found in people with ME CFS, with cancers, with CLL, with multiple myeloma.
So when you express these aberrantly in the body and in the wrong place, You literally destroy autoimmune reaction against, because that's not self, that's non-self, so you attack your own syncytin.
And the microglia, as I mentioned, the macrophages, you'll get inflammation-induced destruction of those cytokine storms of reactive oxygen species.
That's exactly a model that was That was in our original, all the way back in 2007, Dr. Dennis Taub, who is the author of the paper I showed in that slideshow, from 2004 in Nature, when we realized that when you express aberrantly this viral envelope that's in everybody's genome, encoded in the genome, in the brain, in the wrong place, that it's strongly associated with the development of multiple sclerosis.
And so we knew this, that was the proposal that we wrote.
It was all the way back in 2007, the first one that was awarded between Dennis Taub, Brian Cresetti at the Institute of Aging and at the National Cancer Institute.
Now, one of the other side effects of this gene therapy intervention is our Allergic reactions even up to anaphylactic reactions and it's interesting that I think one of the very first nurses to get this was on a national broadcast.
She literally passed out from a sinkable episode.
So and so many more reports from that and what do you believe is the trigger for this?
Allergic reaction.
Is it the PEG, the polyethylene glycol?
It's almost certainly the PEG.
Almost 70% of America will have such an allergic reaction, and it can be severe to the point of death from the polyethylene glycol.
We know this.
I mean, my colleagues in the field are looking at this saying, what do you mean you're putting that in there?
That's just like Well, and you know, and this is what we saw.
This is again another virus-like particle or lipid nanoparticle is used in the Gardasil vaccine.
And we see the same thing in Gardasil injury.
So that young woman almost certainly got the Gardasil vaccine.
So she's got a pathogenic priming event.
Um, and, and now young women, you know, these nurses, we saw that severe case of the CNA, the, the nurses certified nursing assistant who just had the Korea like, um, uh, couldn't stop the movements of her body anywhere.
as Dr. Neunschwinder discussed the neurology behind it on the high wire a few weeks ago with Dale Bigtree.
So we're seeing all of these things, and I believe the PEG is causing a lot of it,
along with the expression of other things, but these instantaneous effects are almost certainly
the PEG in that lipid nanoparticle, the toxic particle that's being injected.
That makes sense.
So, what is your projection for some of the other symptoms that will develop as a result of administration of this therapy, experimental therapy?
It's never been proven.
To be effective.
And it's never, ever been shown or even suggested that it prevents infection with SARS-CoV-2.
It doesn't, which is kind of a moot issue anyway, but it doesn't prevent infection.
So it's just kind of shocking that they could justify this type of intervention.
Well, they don't need to justify it because you're simply, you know, there's, there's no science behind any of it.
There wasn't any, there's no justification for shutting down the country.
There's no scientific basis for wearing the mask.
There's no basis for killing the millions you've already killed with the mask.
So it's like, hey, full steam ahead.
Nobody's listening to us.
Nobody cares about us.
They just censor us and and they're murdering millions of Americans.
So, yeah, it's bad.
Yeah, it's it's definitely a challenge.
So what is your projection for the onset of some of the new symptoms that will develop over
time.
Because we know that with traditional vaccines, I mean, you have the acute reactions, but
then you have the longer term ones, which should be weeks, months down the road, maybe
even years.
So what is your projection that we should anticipate?
So this neuroinflammation symptoms get worse as it builds up with time?
I think we're going to see severe, severe headaches, migraines, I think tics, the tics
and the shaking, the Parkinsonian shakes.
I see the microvascular disorders because that's what, you know, the angiogenesis, the problems in microvascular disorders, which the expression of the envelope alone, syncytia, can cause, can drive, you know, prostate cancers.
I think we're going to see tumor development, a lot of it, and An expansion of those with tumors.
I can't even fathom, as I said, sitting down here that, you know, a doctor, an oncologist is encouraging cancer patients to get this, just like they sat cancer patients in a mask.
Have they not heard of hypoxia inducible factor one alpha, which, you know, is like throwing a blowtorch on a cancer.
So, Again, you're going to see the symptomatology, the pain, severe pain syndromes like fibromyalgia, like rheumatoid arthritis.
I think we're going to see that severe, severe pain.
We're going to see the kinds of things we've seen in vaccine injury with Gardasil.
We're going to see bladder problems.
You know, these kids with Gardasil injury are in diapers.
And I don't mean kids, I mean 21-year-olds and young adults.
So we're going to see kidney disease.
We're gonna see kidney cancer, bladder cancer.
We're gonna see, again, just the inflammatory diseases.
Do you don't think it'll progress to like symptoms with those on the autism spectrum disorder?
So it won't go to that level.
Oh, I think it will.
And you see, that's what we see in that particular slide I was discussing earlier.
That's what you see in the psychosis.
No, it's psychosis.
So in adults, You know, it's going to be the rage, the anger, the psychosis, the, you know, inability, you know, just to sleep, the sleep disorders.
I think you're going to see narcolepsy as we see in, you know, in Gardasil.
I think we are going to see neurodegenerative diseases.
I mean, we have kids, lots and lots of kids with Lou Gehrig's disease.
I think you're going to see it in the athletes.
I think we're already seeing in the athletes, the injuries on the football field, because that's trauma.
You know, we're going to, again, the cancers, those are acquired immune dysfunction, deficiency.
And we're seeing all of that now.
And those will be the first to die.
But now we'll see that accelerated in younger and younger people.
And again, we out in the field of doing these cases in vaccine court, we're going to see all of that.
We're going to see these pain syndrome to the severity that we see in the movie Bats.
We're going to see the kids dying as we saw In fact, to where it's going to be it's going to look just like that.
Now they say this shot isn't going to be given this chemotherapy isn't going to be given to people under 16.
But again, they're giving nine year olds Gardasil.
And those commercials haven't stopped on TV.
Nobody's saying, oh, wait a minute, you know, you've seen some of the cancer chemotherapies, some of them targeted chemotherapies, and it says, oh, well, don't get this, you know, ozempic or whatever, la la la, for your pain.
You're going to see the skin lesions, you know, the dermatitis that everybody's got, or not everybody, all the heavily vaccinated populations.
I think we're just, we're going to see all of the things that we've been seeing in vaccine court.
Speaking of vaccine court, your publisher and person who wrote the forward to the corruption, Robert Kennedy Jr., I don't know if he understood it at the time, but he certainly understood it within the last year.
He has severe dysphonia, as anyone who's listened to him knows, and he realized as he was preparing a case for a vaccine court, or Maybe it wasn't vaccine court specifically, but it was for some vaccine litigation that he was involved with, realized that he himself had the flu vaccine shortly before he developed his dysphonia.
So he's pretty convinced that's what caused it.
Right.
And we see that quite a bit.
You're absolutely right.
And we'll see polyps on vocal cords.
We see a lot of cystic Um, polycystic ovary disease.
So as, as you know, we mentioned, you know, the sterilization, these are the things we're seeing severe ovarian dysfunction, a huge increase in ovarian cancers, again, in younger and younger people.
So yeah, those are flu vaccines.
So what have we done this year in particular is, oh, this year more than ever get that flu shot.
Yeah, this year more than ever help us out folks.
It's so much easier if you kill yourself.
then we don't have to kill you. It's just, it's tough. So we, hopefully we provided enough,
more than enough information to make any serious objective person be concerned about
ever getting this experimental gene therapy.
Don't get it.
That's the best single strategy and we, you know, I've written a lot about it, done many, many videos on different things that you can do to build up your immunoresilience so that you don't get the SARS-CoV-2 infection or any other viral infection and radically lower your risk for almost every chronic degenerative disease.
But what I'd like to focus on now, because it's an unusual niche and I don't think there's anyone more qualified in the world than you to answer this question, is say someone has failed to understand this and they've gotten this experimental gene therapy and they're coming down with symptoms.
Is it the same set of strategies that we would implement to prevent SARS-CoV-2?
Or is there something different or additional that needs to be implemented?
Yeah, I think it's the same set of things.
And we have to think about detoxing metals.
I think everything that Stephanie Seneff has said over the years, we have to think about glyphosate.
We really have to think about all the pathogen-associated molecular patterns and all the disease-associated molecular patterns.
And prevent, you know, so again, SARS-CoV-2 is not the disease.
COVID-19 is the disease, so we have to prevent the inflammation.
In all tissue sites, we have to keep our immune system healthy.
We have to particularly, and as I mentioned earlier, the breakthrough genomics technology, we have the technologies, you know, to know in the individual what is their single nucleotide polymorphism?
What are their sites of tissue injury?
What are their biggest single issues?
We can really get this down to personalized medicine.
And so, yes, you're gonna want things like quercetin, berberine.
You're gonna wanna be burning ketones instead of for the neuroinflammation.
So you're gonna wanna get into ketosis and take the stress off the mTOR pathway.
We're going to have to look at, you know, it's literally everything we've all been doing for decades for these patient populations.
Those are great recommendations, Judy.
And I just wanted to add something to that, because I recently interviewed Dr. Seneff, and she's going to be on after our review, because this was a little higher priority.
And we discussed that very issue about the use of glycine.
And you'd mentioned that glycine is certainly glutathione, but it's in very small amounts.
You're talking milligram amounts.
So, and you need much larger levels of glycine if you're going to use that as an effective Inhibitory blocker of glyphosate because glyphosate, of course, the central molecule in glyphosate is glycine.
That's where the gly comes from.
And if you take it in larger amounts, like three grams, you know, like a half a teaspoon a few times a day, that should be sufficient.
Now, ideally, the best thing is to avoid all non-organic food because it potentially could be contaminated with glyphosate.
That's the number one thing.
But it would be wise to take glycine as a supplement.
Uh, then two other things.
Once you mentioned the pH diet, uh, that certainly is good.
Uh, you can go plant-based or you can go carnivore, but I think, and I'm a more of a fan of carnivore, but the, uh, I think optimizing the pH is really crucial and it's very simple and easy to understand how to do that and, and assess it for yourself individually.
And the way you do that is you get some litmus paper.
You can get it easily on Amazon or anywhere else.
It's inexpensive.
and you dip it in your urine, and it should be about seven.
Now, if you're not doing anything specific to address your pH, I can almost guarantee you
it's gonna be six or five or even four.
The lower it is, the more acidic you are.
You don't really wanna go much above seven, you wanna be eight, nine, or 10.
So somewhere between seven and eight.
And then if you're at that level, then your pH is optimized because your body's pH is about 7.4.
And the easiest, simplest way to do this, it was with bicarbonate.
And you can do it one of two ways.
The inexpensive, cheap way is baking soda, which is sodium bicarbonate.
And you and it tastes pretty terrible but you know if you put a quarter of a teaspoon you don't need large amounts of a quarter to a half a teaspoon a few times a day and figure out what dose you use to turn your urine pH.
You can test it yourself and you can see if you're taking too much or not enough and you just find the right dose for you.
Now once you've found the right dose you typically don't have to retest your urine because it's going to be about the same but that's a simple easy way to improve it and will not only improve Your pH, your resiliency for your immune system, but also protects your bones from mineral loss.
Because when your pH is acidic, you have to extract minerals like calcium, magnesium from your bones to nullify or neutralize those acids.
So it helps you retain the Minerals in your bones and it decreases your risk of osteoporosis.
So simple thing.
You could also use potassium bicarb, maybe alternate between the two is another option.
And then finally, with respect to increasing glutathione, I couldn't agree more, but I'm not a big fan of supplements because I believe the body's intuitive wisdom is best.
That's why I like to activate a specific pathway called NRF2.
NRF2 is a A gene system that activates as a transcription factor, when it's activated by knocking off the KEEP1 or KEEP2 protein, it goes to the ARE, which is the antioxidant response elements in your DNA, in your nucleus, and causes them to make not only glutathione, but catalase and superoxide dismutase, in a wide variety, I think dozens if not hundreds of other antioxidants that help improve
Your ability to reduce oxidative stress and and decrease that so that and so that if you don't have this oxidative assault then you won't be making more of glutathione because you know making providing your body with something that's good that you don't need it's not a good strategy so rather than take glutathione I like to activate it my favorite activator is molecular hydrogen. So that is just absolutely terrific.
I take it every day.
It's in look at my previous videos with Tyler, the Baron, who is the expert in the U.S. and probably
the world on this topic. And you don't it's not something you want to drink all day long.
You want to take it in a high, but cyclical boost or burst.
And the way you do that is just by taking two, three, four, sometimes once a day, and that's all you have to do it.
And rather than drinking it all day long.
So those are great strategies that should hopefully not only improve your resilience against SARS-CoV-2, but should you have made the mistake of getting this experimental gene therapy, then it will help your body detoxify.
With respect to ketosis, I mean, most people, 90% of the population is not going to be able to do that.
So it's a long, slow strategy.
You could use things like MCT oils or caprylic acid, C8.
You could even use ketone esters.
Do you think that there's a benefit?
See, ketone esters, I'm not sure if you're familiar with it, but they get into the system and they will raise your serum ketones rapidly.
And they're expensive.
You know, it could be $10, $20, $30, $40 a dose.
Do you think that there's a benefit to raising those high levels of ketones as a potent neuro anti-inflammatory?
Would that be valuable in someone who's acutely symptomatic?
Well, yes, maybe, but I actually like, I don't like to do that.
I like to use some of the formulations of quercetin and cinnamon bar and therapeutics that we've made in the laboratory over the last decades.
What about gamma interferon?
I mean, you had recommended that for SARS-CoV-2.
Well, I recommend Alpha Interferon.
Well, I'm sorry, Alpha Interferon.
Yeah, absolutely.
Absolutely, the Gamma Interferons are very important because many of those pathway defects, when we've looked at some of the most severely with COVID-19, again, it's not SARS-CoV-2 causing this, and so Within COVID-19, we've looked at the most severe, so we've used quercetin, berberine, we've used this type 1 interferon.
It's a spray that you can spray directly into your nasal passages, your throat, your nose, and that will give you the protection you need so that The virus doesn't ever make a particle.
It degrades it right away.
So one of the big problems in this... Is it also good for the gene therapy?
Because we know it's good for the virus.
Okay.
Yeah, because what we're going to do is we're going to activate the dormant viromes.
You're going to see CMV just like you saw with HIV-AIDS.
So everything we've learned in HIV-AIDS is going to help.
Peptide tea, calm the interaction between the macrophage.
You know, I see a new industry, you know, peptide tea never made it for therapy, but we've talked to Dr. Mike Ruff, Candice Peart, the late Candice Peart's Along those lines, would it make sense for nebulized hydrogen peroxide therapy?
Oh, absolutely.
There's a... Wow!
That is so great!
Oh, absolutely.
Should you feel the cough or the fever or the headaches, so you immediately up your type 1 interferon, take a couple of sprays of that a day, prophylactically as well, and that will keep the viral load down.
We know this isn't a virus.
We know this is synthetic, but it's the same thing.
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-Man that simply degrades the RNA. And then your
dendritic cells, the plasma cytoid dendritic cells, usually make 97 to 98% of all the type 1
interferon in your body. I'd just say alpha and beta, because now we're seeing epsilons and a lot of
different ones. Let's just say the type 1, the primary source of interferon alpha and beta, is the
plasma cytoid dendritic cell.
Well, we know that's dysregulated in people with HIV, with XMRVs, with aberrant retroviral expression.
Those people can't make interferon.
That's just what I was looking for.
Precisely what I was looking for and you know what's on your plate now for the upcoming near future?
Do you have just going to continue to spread the message at events throughout the country or writing a new book?
It's called Ending Plague, A Scholar's Obligation in an Age of Corruption.
I show the cover there.
I did see it.
So when is that going to be out?
That should be out in late spring.
So we're almost finished with that.
I'd say another month or so.
That's the lead author on that will be Dr. Rossetti and then Ken Tech and Lively and I are right there.
Send me a copy and we'll get you on again.
Oh great, yeah, as soon as I get one.
Just send me the draft, electronic, this way I can read it.
Oh sure, I don't have it yet, but when we're finished I absolutely will get it to you.
Thanks so much.
Because it's called a scholar's obligation in an age of corruption.
So what do we do, you know, other than just get angry and throw pillows at people?
Yeah, be positive.
We have to be positive.
We have to.
And since we have the solution, since, you know, I think the good news of this is the ability.
We can network.
We are networking.
We have the solution.
So you, Joe, are going to be very, very busy because you've had the solutions for decades.
And so now all I'm going to be doing is going around doing everything I can to stop everyone from Wearing the mask and taking any shot ever again because that otherwise... That's my new passion now is to educate people about this because it's such an acute challenge and we just there are millions of lives on the line now not only from acute death but permanent disability so
We just have to, I mean, this is an emergency.
This is an absolute emergency catastrophe that we have to address.
So, you know, everyone watching this should understand that, digest this, learn it, understand it, and share the information with those you love so that we don't have to have those people injured.
Because it's shocking, absolutely shocking, how many smart people Have succumbed to the propaganda and are rushing to get immunized.
Not immunized, getting experimental gene therapy.
Yeah, yeah, rushing to get shot.
You know, I used to say, don't let anybody shoot you.
It's really not a good idea.
Well, I can't thank you enough.
If you were here virtually, but if you were here physically, I would just embrace you with a giant hug because you deserve it.
You're an angel.
You're just a gift to everyone.
I just can't Thank you and appreciate you for everything you've done and will continue to do.
You're just amazing.
Well, thanks so much.
I appreciate that.
I really need that big hug now because I'm really discouraged.
Well, we're going to hang in there.
We're going to do it because, you know, and we can't reach everyone, but we can reach an important number of people and those will be the ones that need to be reached.
And you're doing a great job of helping us understand why this is.
You came through like a champ.
I knew there was only one person that could explain this at a level that makes sense.
Because this is so, I mean, this is all experimental stuff and, you know, you've got to be a molecular biologist to figure this thing out.
I mean, regular science PhDs just don't understand it.
So you did it.
You knocked it out of the park and, you know, you provided us with the explanation we needed.
So again, you are amazing.
Thanks.
Thank you.
You are as well.
Thank you.
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