COVID “vaccine” spike protein and lab-made SARS-CoV-2 spike protein are prion-like drivers of proteostatic collapse, pathological cross-seeding, transcriptional instability, and tissue dysfunction.
Nic, congrats on your new paper highlighting the amyloidogenic nature of the spike protein (from both the Covid virus and the Covid mRNA vaccines). This phenomenon really is wrecking havoc with the human body, especially the vascular system of those affected.
I will be attending the "CHD in DC" conference next month in Washington D.C. to speak with Senators Ron Johnson and Rand Paul. It's time for Senator Johnson to have a hearing on the WHITE FIBROUS CLOTS and MICRO-CLOTTING that we know is affecting a large portion of the population.
I hope to see you, Dr. McCullough, and John Leake at the conference next month so that we can have a nice discussion like we did at the last CHD conference in Austin.
Absolutely, Senator Johnson needs to hold a hearing covering the white fibrous clots. Time is of the essence because those clots can be and have been removed at a cath lab or in surgery. Since people can be saved from dying from the white frbrous clots, it's imperative Johnson hold that hearing in order to help get the word out to more people. I hope lots of us Will send this article to Senator Johnson And Senator Paul and request. such a hearing be held.
Had that stopped the mRNA shots? No! People can still get their ConVid booster and now their mRNA flu shot. I know many people who line up for their next vax
Your complaining that the hearings are useless is useless. You simply don't need to write to Senator Johnson. Others believe differently so they will write him.
So better not to publicise this information and leave everybody in the dark? Some will take note and refuse the next plandemic round... the more the better! Don't be so negative!
Not being negative just realistic. CONgress only has hearings to make it appear that they are doing something The MSM will not report most of this. A new “crisis” will emerge to give them cover to move on from the last one.
Case in point what became of the Fast and Furious hearings in 2012 other than top department heads being forced to resign or reassigned. Eric Holder was held in contempt of Congress and still has a law license in good standing, Obama called “executive privilege”
After the hearings and findings have they removed the ConVid shots? No, they just approved another mRNA flu vax
THEY ARE PLAYING RUSSIAN ROULETTE WITH LIFE ITSELF and NOBODY IS SAYING STOP!
So, you create a chimeric GOF and then you try to play God and create a antidote!
The core warning came from Ralph Baric at UNC, one of the pioneers of this exact technique. In his own 2015 paper he wrote:
"The potential to prepare for and mitigate future outbreaks must be weighed against the risk of creating more dangerous pathogens... Scientific review panels may deem similar studies building chimeric viruses based on circulating strains too risky to pursue."
That's a researcher admitting — in print — that the work he was doing carried a genuine risk of creating something more dangerous than what exists in nature.
The warning has several distinct parts:
1. You're building viruses nature never made
Chimeras don't exist in the wild. They're synthetic combinations whose properties are unknowable in advance. As MIT Technology Review put it, there was "no way of knowing whether the final chimeras would be stronger or weaker."
2. The safety level was inadequate
Baric explicitly said he "would never argue that WIV1 or SHC014 should be studied at BSL-2" because they could grow in primary human cells. Yet that's exactly the containment level some of this work was conducted under.
3. The "luck runs out" problem
Baric's bluntest warning:
"If you study a hundred different bat viruses, your luck may run out."
This is the statistical reality — the more dangerous pathogens you deliberately engineer, the higher the odds one of them escapes, or one of them turns out to be pandemic-capable in a way the lab didn't predict.
4. The dual-use dilemma
The same technology that prepares us for outbreaks is the same technology that could cause one. The line between "defensive research" and "accidental bioweapon" is essentially nonexistent when the work involves making viruses more transmissible.
🏛️ What Happened to the Warning
The warning was not heeded — it was funded past.
The NIH funded chimeric coronavirus work at the Wuhan Institute of Virology despite Baric's own caution
The WIV went on to make chimeras from eight different bat coronaviruses, some replicating well in human cells
Institutions repeatedly insisted this "wasn't gain-of-function" by narrowing the definition until the work fell outside it
When concerns arose, the establishment response was to deny, redefine, and defund critics — not to pause the work
The crucial point: this wasn't a fringe warning from outsiders. It was the lead researcher in the field publicly flagging that his own technique was dangerous, and the funding apparatus ignored him and scaled it up anyway. That's the textbook pattern — the people closest to the risk sound the alarm, and the institutions with the money and prestige bury it.
The lesson isn't that virology is evil. It's that gain-of-function and chimeric-virus research concentrates catastrophic risk in a handful of labs, with oversight provided by the same institutions that benefit from the funding — which is no oversight at all.
This study gives even more weight to Stephanie Seneff and Greg Nigh’s May 2021 paper. Appreciate very much your inclusion of countermeasures. Difficult to find protocols to help the many, many people who took the shot.
Spot on. While most reader inveigh against the villains, real and presumed, those who were damaged by the mRNA injections continue to look for ways to regain their health and vigor. Vengeance may be sweet, but renewed health is the best prize of all.
Thankyou Nicolas for your research and resulting paper digging into the problems with MRNA technology. I agree with your last statement that those responsible need to be held accountable. So was this a medical research mistake or was the deep state pursuing some other agenda? Is this a case of trying to depopulate, break the population so they will accept one world government or making more business for the medical business?
about the question whether covid was an agenda it might be enlightening to listen for some four minutes of the conversation between Dr. Philip McMillain and Dr. Shankara Chetty.
Letter Encouraging Senator Johnson to hold White Clot Hearing
Senator Johnson, thank you and God bless you for all of the work you have done to publicize the harms caused by the covid mRNA shots. I feel TIME is of the essence for you to hold a hearing about the white amyloid clots that are a result in some people of the covid shots. People can be SAVED from death if they have these clots, but they need to learn about the available, cutting edge treatments and therapies in time. See the work of Dr Kevin McCairn in removing these clots in Japan and see the work reported and even video taped by some cath lab workers of removing the white clots in the lab. I know in more than one case the white clots have been removed in surgery. Since the Moderna mRNA flu shot will be out for this flu season, it is even more imperative that this information get to more people than it already has. You can help publicize these clots and the available therapies, including Nattokinase to eliminate spike protein, through holding a senate hearing about them. See Nicholas Huelscher's Substack article today about the new paper covering the spike protein and amyloid clots, which was just released by The McCullough Foundatiion. I recommend the hearing include Tom Haviland, Dr McCairn, Dr. McCullough, Nicholas Huelscher, and Richard Hirschman and one or two other embalmers who have reported on removing the white clots. I'm sure that Tom Haviland would know how to get you in touch with those who have been effectively treating or removing the white clots and anyone else he would recommend attend the hearing.
Why do you not mention the groundbreaking work of Kevin McCairn in Japan? Not only did he perform most of the experimental work but he is successfully treating patients at the Edogawa Hospital with Dual Filtration Plasma Apheresis.
Credit where it is due please.
DFPA (Dual Filtration Plasma Apheresis / immunoadsorption hybrid) combines filtration with affinity adsorption; ligand columns such as tryptophan bind autoantibodies and immune complexes; the mechanism is chemical binding, not size exclusion; this allows more of the normal plasma proteome to be preserved;
DFPA removes what specifically binds; If the pathology is driven by functional species such as autoantibodies or amyloidogenic complexes, size alone is a blunt tool; affinity capture gives you targeted removal.
Dr. Kevin McCairn and patient Ken Evans joined me to discuss a promising intervention for severe COVID-19 vaccine injuries. Conducted from Japan, where McCairn and colleagues treat patients, the conversation highlights the debilitating effects of vaccine-induced amyloid formation and a novel therapeutic approach offering dramatic recoveries.
McCairn, who has treated approximately 25 patients, describes vaccine injuries linked to abnormal amyloid and mis-folded proteins, often triggered by spike protein. These cause widespread microclots, autoimmune responses, brain fog, extreme fatigue, heart irregularities, neuropathy, and organ damage.
The Japan protocol involves jugular-vein dual filtration apheresis using specialized canisters to remove autoantibodies, amyloids, and misfolded proteins directly from cerebral outflow, combined with stem cell growth factors (SGF) derived from dental pulp to promote regeneration and inhibit further clotting. Unlike peripheral vein methods, this targets neurovascular injury.
All we need to know is that the whole SARS-CoV-2 virus was created and patented by Ralph S. Baric et al. and the University of North Carolina Chapel Hill, designed to become contagious to humans (proudly announced in a press release by UNC Chapel Hill in March 2016) that it war ready to go for the Plandemic being prepared to offer a global experiment for the mRNA "vaccine" that had been in the works for more than 20 years (NO -- it was NOT Warp Speed! Trump was lied to by the Doctor of Death).
Everyone should by now know everything that the medical-pharmaceutical industrial complex, including all the government agencies knew from the get-go. They lied to us. Will we ever believe anything any pharma company or medical doctors tells us ever again? NO! I didn't believe them from the start when I downloaded the patents for the SARS virus in 2020 and shared it widely with my family, friends and anyone who would accept my e-mails! This will never happen again!
The proliferation of poison in the Covid injectables (so called, 'vaccines') continues even though It has not prevented injuries or deaths. Injecting toxic substances into the human bloodstream used to be called murder.. People were put on trial and imprisoned for actions like this.
If I'm understanding correctly among other horrific consequences related to COVID injections resultant misfolded proteins are inducing misfolding in normal proteins. In other words the proteins themselves are pathogenic.
I've also heard that injection mRNA had poor mRNA integrity resulting in synthesis of proteins other than spike protein. Could that also be producing pathogenic misfolded proteins?
Then why in the world with all that is mentioned as bad outcomes l, WHY is this vac not totally banned??!! Any doctor worth his/her salt must know this…bu it appears most still have their heads in the sand…playing politics with their patients!
Well done, Nicolas, and thanks to you and Dr. McCullough for seeing this through. The issue of PROTEIN MISFOLDING IS THE DISASTER, going forward, that must be handled. I know that DMSO is a known protein folding chaperone. Perhaps you may engineer a protocol to head off this catastrophic result of Covid 19 "vaccinations", using DMSO along with the proteolysing enzymes you already have identified, and which you also provide for use by those in need. However, ATTENTION MUST BE GIVEN also to addressing the metals in the vaccines. They cause the red blood cells to clot together by eliminating the natural negative electrical charge, but also, that same loss of negative charge causes sedimentation in the vessels. The aluminum in the "vaccines" is contributing to the fibrous clots by interacting/reacting with self and spike protein. THIS IS A DISASTER FOR HUMANS. I hope you are able to engineer a solution for the misfolding soon. Millions of lives are at stake.
I conducted research on DMSO regarding the protein misfolding a few years back, unfortunately it is not the magic bullet. TUDCA may hold some promise, but no research has been conducted to explore it fully.
And aluminum is found everywhere. It leaches significantly into cans of soda. Iron is another contributor, and other heavy metals, to the loss of zeta potential you mention.
No mention of the driving force of this seriously flawed platform, of DARPA/DOJ’s intention of being able to respond quickly to alleged threats, at the expense of the general populace. Sigh, like unbridled despots from years gone by, they keep pushing their bioweapon insanity.
Nic, congrats on your new paper highlighting the amyloidogenic nature of the spike protein (from both the Covid virus and the Covid mRNA vaccines). This phenomenon really is wrecking havoc with the human body, especially the vascular system of those affected.
I will be attending the "CHD in DC" conference next month in Washington D.C. to speak with Senators Ron Johnson and Rand Paul. It's time for Senator Johnson to have a hearing on the WHITE FIBROUS CLOTS and MICRO-CLOTTING that we know is affecting a large portion of the population.
I hope to see you, Dr. McCullough, and John Leake at the conference next month so that we can have a nice discussion like we did at the last CHD conference in Austin.
Absolutely, Senator Johnson needs to hold a hearing covering the white fibrous clots. Time is of the essence because those clots can be and have been removed at a cath lab or in surgery. Since people can be saved from dying from the white frbrous clots, it's imperative Johnson hold that hearing in order to help get the word out to more people. I hope lots of us Will send this article to Senator Johnson And Senator Paul and request. such a hearing be held.
Sure more “hearings” that is what we need. As if any of the hearing since ConVid which happened in 2020 have gone anywhere. What year is it 2026! LOL
Useless government hearings that go NOWHERE. CONgress that does nothing but lie and line their pockets.
If you think any CONgressional member will do anything you are sadly barking up the wrong tree.
They are all captured including Paul and Johnson
His hearings have helped publicize harms from the clot shots because they can be watched on CSPAN and have been discussed by some news outlets.
Had that stopped the mRNA shots? No! People can still get their ConVid booster and now their mRNA flu shot. I know many people who line up for their next vax
Your complaining that the hearings are useless is useless. You simply don't need to write to Senator Johnson. Others believe differently so they will write him.
So better not to publicise this information and leave everybody in the dark? Some will take note and refuse the next plandemic round... the more the better! Don't be so negative!
Not being negative just realistic. CONgress only has hearings to make it appear that they are doing something The MSM will not report most of this. A new “crisis” will emerge to give them cover to move on from the last one.
Case in point what became of the Fast and Furious hearings in 2012 other than top department heads being forced to resign or reassigned. Eric Holder was held in contempt of Congress and still has a law license in good standing, Obama called “executive privilege”
After the hearings and findings have they removed the ConVid shots? No, they just approved another mRNA flu vax
Thank you, Sandy, for your faithful support!
I mean, god damn it! There’s nothing that can make this right.
No doubt. The more I read about it, the more pissed I get that it is still not acknowledged by too many and nothing ever gets done about it anyways.
THEY ARE PLAYING RUSSIAN ROULETTE WITH LIFE ITSELF and NOBODY IS SAYING STOP!
So, you create a chimeric GOF and then you try to play God and create a antidote!
The core warning came from Ralph Baric at UNC, one of the pioneers of this exact technique. In his own 2015 paper he wrote:
"The potential to prepare for and mitigate future outbreaks must be weighed against the risk of creating more dangerous pathogens... Scientific review panels may deem similar studies building chimeric viruses based on circulating strains too risky to pursue."
That's a researcher admitting — in print — that the work he was doing carried a genuine risk of creating something more dangerous than what exists in nature.
The warning has several distinct parts:
1. You're building viruses nature never made
Chimeras don't exist in the wild. They're synthetic combinations whose properties are unknowable in advance. As MIT Technology Review put it, there was "no way of knowing whether the final chimeras would be stronger or weaker."
2. The safety level was inadequate
Baric explicitly said he "would never argue that WIV1 or SHC014 should be studied at BSL-2" because they could grow in primary human cells. Yet that's exactly the containment level some of this work was conducted under.
3. The "luck runs out" problem
Baric's bluntest warning:
"If you study a hundred different bat viruses, your luck may run out."
This is the statistical reality — the more dangerous pathogens you deliberately engineer, the higher the odds one of them escapes, or one of them turns out to be pandemic-capable in a way the lab didn't predict.
4. The dual-use dilemma
The same technology that prepares us for outbreaks is the same technology that could cause one. The line between "defensive research" and "accidental bioweapon" is essentially nonexistent when the work involves making viruses more transmissible.
🏛️ What Happened to the Warning
The warning was not heeded — it was funded past.
The NIH funded chimeric coronavirus work at the Wuhan Institute of Virology despite Baric's own caution
The WIV went on to make chimeras from eight different bat coronaviruses, some replicating well in human cells
Institutions repeatedly insisted this "wasn't gain-of-function" by narrowing the definition until the work fell outside it
When concerns arose, the establishment response was to deny, redefine, and defund critics — not to pause the work
The crucial point: this wasn't a fringe warning from outsiders. It was the lead researcher in the field publicly flagging that his own technique was dangerous, and the funding apparatus ignored him and scaled it up anyway. That's the textbook pattern — the people closest to the risk sound the alarm, and the institutions with the money and prestige bury it.
The lesson isn't that virology is evil. It's that gain-of-function and chimeric-virus research concentrates catastrophic risk in a handful of labs, with oversight provided by the same institutions that benefit from the funding — which is no oversight at all.
Oh my goodness this is beautifully clarifying, concise and succinct. Well said, sir, well said.
This study gives even more weight to Stephanie Seneff and Greg Nigh’s May 2021 paper. Appreciate very much your inclusion of countermeasures. Difficult to find protocols to help the many, many people who took the shot.
Spot on. While most reader inveigh against the villains, real and presumed, those who were damaged by the mRNA injections continue to look for ways to regain their health and vigor. Vengeance may be sweet, but renewed health is the best prize of all.
Thank u for keeping the narrative going . The side effects are not going away and way for the next round of mRNA jabs .😡
Thankyou Nicolas for your research and resulting paper digging into the problems with MRNA technology. I agree with your last statement that those responsible need to be held accountable. So was this a medical research mistake or was the deep state pursuing some other agenda? Is this a case of trying to depopulate, break the population so they will accept one world government or making more business for the medical business?
hello Fred,
about the question whether covid was an agenda it might be enlightening to listen for some four minutes of the conversation between Dr. Philip McMillain and Dr. Shankara Chetty.
This is the link to it: https://philipmcmillan.substack.com/p/if-this-was-gain-of-function-what
The time point to start is at 26:44 minutes. The connection for unknown reasons freezes twice when McMillian puts up a central question.
I do not give it away which is the direction of Chetty's answer to this question.
To me it is a joy to listen to this man because he is so clear in mind.
Yes.
Letter Encouraging Senator Johnson to hold White Clot Hearing
Senator Johnson, thank you and God bless you for all of the work you have done to publicize the harms caused by the covid mRNA shots. I feel TIME is of the essence for you to hold a hearing about the white amyloid clots that are a result in some people of the covid shots. People can be SAVED from death if they have these clots, but they need to learn about the available, cutting edge treatments and therapies in time. See the work of Dr Kevin McCairn in removing these clots in Japan and see the work reported and even video taped by some cath lab workers of removing the white clots in the lab. I know in more than one case the white clots have been removed in surgery. Since the Moderna mRNA flu shot will be out for this flu season, it is even more imperative that this information get to more people than it already has. You can help publicize these clots and the available therapies, including Nattokinase to eliminate spike protein, through holding a senate hearing about them. See Nicholas Huelscher's Substack article today about the new paper covering the spike protein and amyloid clots, which was just released by The McCullough Foundatiion. I recommend the hearing include Tom Haviland, Dr McCairn, Dr. McCullough, Nicholas Huelscher, and Richard Hirschman and one or two other embalmers who have reported on removing the white clots. I'm sure that Tom Haviland would know how to get you in touch with those who have been effectively treating or removing the white clots and anyone else he would recommend attend the hearing.
TIME is of the essence for saving lives
Sincerely,
Sandy
In his final paper with Perez, Montagnier tried to warn us! https://vimeo.com/user192601857/review/1021313092/2e32d43335
They crucified Luc for speaking the truth!
Why do you not mention the groundbreaking work of Kevin McCairn in Japan? Not only did he perform most of the experimental work but he is successfully treating patients at the Edogawa Hospital with Dual Filtration Plasma Apheresis.
Credit where it is due please.
DFPA (Dual Filtration Plasma Apheresis / immunoadsorption hybrid) combines filtration with affinity adsorption; ligand columns such as tryptophan bind autoantibodies and immune complexes; the mechanism is chemical binding, not size exclusion; this allows more of the normal plasma proteome to be preserved;
DFPA removes what specifically binds; If the pathology is driven by functional species such as autoantibodies or amyloidogenic complexes, size alone is a blunt tool; affinity capture gives you targeted removal.
https://synapteklabs.com/
McCairn says nattokinase and bromelain are ineffective at dealing with these amyloids.
His treatment works. People arrive in wheelchairs and leave walking.
RFK jr and the president have been informed of this treatment- crickets. You are on your own in the USA.
Mary Talley Bowden is trying to bring this treatment to the US.
https://x.com/MaryBowdenMD/status/2044236425026031655
A Patient’s Redemption: Breakthrough Treatment for COVID Vaccine Injuries
https://drbowden.substack.com/p/a-patients-redemption-breakthrough
Dr. Kevin McCairn and patient Ken Evans joined me to discuss a promising intervention for severe COVID-19 vaccine injuries. Conducted from Japan, where McCairn and colleagues treat patients, the conversation highlights the debilitating effects of vaccine-induced amyloid formation and a novel therapeutic approach offering dramatic recoveries.
McCairn, who has treated approximately 25 patients, describes vaccine injuries linked to abnormal amyloid and mis-folded proteins, often triggered by spike protein. These cause widespread microclots, autoimmune responses, brain fog, extreme fatigue, heart irregularities, neuropathy, and organ damage.
The Japan protocol involves jugular-vein dual filtration apheresis using specialized canisters to remove autoantibodies, amyloids, and misfolded proteins directly from cerebral outflow, combined with stem cell growth factors (SGF) derived from dental pulp to promote regeneration and inhibit further clotting. Unlike peripheral vein methods, this targets neurovascular injury.
In a hearing about the white fibrous clots, Senator Paul should have McCairn go over his work and success in treating the clots.
AI generated comment. Think and express for yourself please. I do not want to discuss with a machine.
All we need to know is that the whole SARS-CoV-2 virus was created and patented by Ralph S. Baric et al. and the University of North Carolina Chapel Hill, designed to become contagious to humans (proudly announced in a press release by UNC Chapel Hill in March 2016) that it war ready to go for the Plandemic being prepared to offer a global experiment for the mRNA "vaccine" that had been in the works for more than 20 years (NO -- it was NOT Warp Speed! Trump was lied to by the Doctor of Death).
Everyone should by now know everything that the medical-pharmaceutical industrial complex, including all the government agencies knew from the get-go. They lied to us. Will we ever believe anything any pharma company or medical doctors tells us ever again? NO! I didn't believe them from the start when I downloaded the patents for the SARS virus in 2020 and shared it widely with my family, friends and anyone who would accept my e-mails! This will never happen again!
The proliferation of poison in the Covid injectables (so called, 'vaccines') continues even though It has not prevented injuries or deaths. Injecting toxic substances into the human bloodstream used to be called murder.. People were put on trial and imprisoned for actions like this.
If I'm understanding correctly among other horrific consequences related to COVID injections resultant misfolded proteins are inducing misfolding in normal proteins. In other words the proteins themselves are pathogenic.
I've also heard that injection mRNA had poor mRNA integrity resulting in synthesis of proteins other than spike protein. Could that also be producing pathogenic misfolded proteins?
Then why in the world with all that is mentioned as bad outcomes l, WHY is this vac not totally banned??!! Any doctor worth his/her salt must know this…bu it appears most still have their heads in the sand…playing politics with their patients!
Well done, Nicolas, and thanks to you and Dr. McCullough for seeing this through. The issue of PROTEIN MISFOLDING IS THE DISASTER, going forward, that must be handled. I know that DMSO is a known protein folding chaperone. Perhaps you may engineer a protocol to head off this catastrophic result of Covid 19 "vaccinations", using DMSO along with the proteolysing enzymes you already have identified, and which you also provide for use by those in need. However, ATTENTION MUST BE GIVEN also to addressing the metals in the vaccines. They cause the red blood cells to clot together by eliminating the natural negative electrical charge, but also, that same loss of negative charge causes sedimentation in the vessels. The aluminum in the "vaccines" is contributing to the fibrous clots by interacting/reacting with self and spike protein. THIS IS A DISASTER FOR HUMANS. I hope you are able to engineer a solution for the misfolding soon. Millions of lives are at stake.
I conducted research on DMSO regarding the protein misfolding a few years back, unfortunately it is not the magic bullet. TUDCA may hold some promise, but no research has been conducted to explore it fully.
https://factsdontcare.substack.com/p/can-tudca-dmso-or-methylene-blue?r=4x1ar&utm_campaign=post-expanded-share&utm_medium=web
And aluminum is found everywhere. It leaches significantly into cans of soda. Iron is another contributor, and other heavy metals, to the loss of zeta potential you mention.
They must, indeed.
No mention of the driving force of this seriously flawed platform, of DARPA/DOJ’s intention of being able to respond quickly to alleged threats, at the expense of the general populace. Sigh, like unbridled despots from years gone by, they keep pushing their bioweapon insanity.