Repeated injections of IntraVenous Immunoglobulin-g (IVIg) with no spike to bind to will naturally lead to anti-IVIg antibodies, which, by design, cross-react with spike-antigen tests. QED.
“A notable finding was that markedly elevated levels of full-length spike protein (33.9±22.4 pg/mL), unbound by antibodies, were detected in the plasma of individuals with postvaccine myocarditis, whereas no free spike was detected in asymptomatic vaccinated control subjects (unpaired t test; P<0.0001).”
“First, S-protein expression kinetics were determined in the serum of mice dosed with 1 × 109 vp of Ad26.COV2.S (Figure A4). S-protein levels were detected at Day 1 (26.7 pg/mL), remained detectable until Day 6, and decreased to background levels by Day 10 after dosing.”
My fibrinogen has been tested (not elevated) and well, I wouldn’t know, but since IMD Berlin is a accredited laboratory, I have no reason to question their findings..
Thank you, so do I.
I’m awaiting the results from a clinical genetic test but as far as my non-geneticist eyes can see, my genome does seem to be somewhat challenged
That's a BS article that compared at different times. They took myocarditid pagient a day4 and healthy vaccinated at day 10 (if my memory served mz well)
In Ogata et al, the average is 63pg/ml and the max is 150pg/mL.
I feel far better today than i did the first 4+ months, but like many injured, I still suffer from a long list of mostly unspecific symptoms, with intensities that varies from day to day.
Yes endothelial damage is undoubtedly part of it - I’ve had all sorts of vascular spasms throughout this - still have. But I’m also fairly confident that immunogenetics play a fundamental role. Apart from it making good sense, I got hold of the data files, generated by the lab during my genetic analysis, and it seems that, unless I’m hyper-methylated, there’s many and large structural changes present.
You’re most likely right - I just did a quick search in order to get an idea of the levels typically found (only to find out that I’m unable to upload the screenshots on Substack :-S ).
Either way, considering my last vaccine was 2 years ago it’s at least an interesting amount.
Those aren't very high numbers, but they are significant enough to indicate something.
Are you sick in any way?
There are 3 possibilities:
(1) your body is actually producing its own fibrinolytic (Plasmin) and it's dissolving white clots. That would be very good news bc it would mean your endothelium is repairing itself and you are healing.
(2) the ELISA test is cross-reacting with something else and giving you a false-positive.
(3) you are still producing spike protein in significant quantities. that would mean stem cells have been contaminated and that you would have a very high risk of cancer.
My apologies if you took my message wrongly. I am here to help.
I have sacrificed 4,5 years of my life and my family to help the vaccine-injured.
It's your choice to read my work or not, but coming on my Substack with the fallacies you have been sold and not even taking the time to read my work is a bit hard for me.
Respectfully, I am fed up with a lot of the BS the freedom doctors have been stating for nearly 4 years now.
If you talk about immunology while breaking the most sacred laws of immunology (you're not the only one most freedom fighter and biologists doctors shamefully break basic Laws of immunology), and you hope to contribute to helping vaccine-injured, respectfully, you are part of the problem.
Antibodies bind. T-cells destroy contaminated cells. Circulating spike protein theory breaks those 2 fundamental laws and many other autopsy observations!
Let me repeat:
(1) Spike protein is the antigen. That is the mechanism of action of the vaccine by design. Everybody gets it, not everybody is harmed. So circulating spike protein is not specific...it is thus not the cause.
(3) Circulating spike proteins are "nothing burgers" like with all foreign proteins. When given time, the body deals fine with proteins (Amyloids, spike...), ANTIBODIES deal with it. Read "Circulating SARS-CoV-2 Vaccine Antigen Detected in the Plasma of mRNA-1273 Vaccine Recipients" by Ogata et al. You will see that circulating spike proteins are not detectable post Day 9 Jab 1, first they are neutralized. After Jab2 , they simply are hardly produced simply because T-cells do their job and destroy the contaminated cell very quickly (which explains IgG4 switching bc there are no spike proteins!).
Natural and specific antibodies would mitigate the harm even if you had spike protein post-vax.
(4) More importantly, despite not having Spike, all transfecting vaccines produce the same adverse reactions. Think about it: many people have had the same thing you are suffering from despite never being injected with mRNA or spike.
(5) Taking IVIg is just stupid because there are no spike proteins, and so the body needs to create anti-anti-spike antibodies. These will react to spike tests by design. But the IVig will do nothing to help, nothing to help reduce the fibrin blocking the arteries and the capillaries, mend the holes poked in the vascular system, and repair the necrosed organs, ...
My research has already helped a few people suffering for 3 years. I have nothing to gain. I don't sell therapies, I don't sell consulting, I help probono. But I don't accept on my Substack fallacious theories that harm the very people I am trying to help. I hope you will understand.
also i know the vax injured you’re speaking of and there’s more systems involved that’s causing a majority of issues - you have to look at the whole complex pic- the ones of us who survived with severe injuries are still making spike/ i’ve proven with my panels - all 3 monocyte lines transferred with vax spike- we cleared the lines and now it’s back in one monocyte line- also my t cells cd3,cd4,cd8 are tanked and i’m negative for hiv so i have the vaids- also my spike ab test 8 months after moderna was 2,000 then 4 months later my pfizer put me into cytokine storm- which in still in- NIH disclosed from their own mouths to bri dresden and the other trial participants who were injured that the spike protein causes an immune mediated response- once we cleared my lines i started to progress functionally to 60% then after we stopped my protocol - i started to decline back to 30% functioning 6 months later and that’s when we retested it and saw it came back in the lines-
my other point is - why do you think they stopped testing in the trials for spike production after what 60-90 days i can’t remember? bc we are still producing it 3-4 years later hence the failing one by one of our systems- now it’s affecting my adrenals and hormones- i’m trying to save my ovaries and myself bc it’s pushing me into early menopause- tanked my hormones and cortisol-
my dna results will be back this coming week - stay tuned
"Many vaccine-injured people have testified that they keep producing spike proteins three years after vaccination, or so their tests say…"
My SARS COV 2 AB, TOTAL SPIKE SEMI QN was < 0.4, 1 week after injection. It increased 8 months later and again at 22 months before reaching a max at 24 months. I've had it tested 3x since the max and each time it is lower. Based on the trend line, I will retest at 42 months post vax. The max was at 2 years and the slope shows it should be approaching 0 at 1.5 years from the max. So a total of 3.5 years. But my main concern is inflammation from lipid nanoparticles, which ties into the next part where Dr. Cole discusses them associated with turbo cancer.
"As I have explained in the chapter on Cancer, stem cell transfection should trigger many replications and cancer, and I have yet to hear anyone talking about spike production simultaneously with cancer."
He talks about the spike protein & lipid nanoparticles being an issue with turbo cancer in the interview. Dr. Ryan Cole says one of the very big problems with the CV19 vax is it destroys the immune system and stops your ability to fight cancer. The truth-telling medical community is calling these new aggressive fast-spreading cancers turbo cancer.
Antibodies against spike aren't the same thing as spike. What you are describing is normal.
Dr. Cole hasn't fully grasp the mechanics of cancer genesis with the vaccines in general. It is not tied to spike, it is tied to Stem cell contamination.
Turbo cancer are tied to the seniority of the stem cells contaminated (they are less differentiated and have a much greater scale. ex: triple negative breast acncer).
You need to read my other articles on the bolus theory.
I suggest my letter to Steve Kirsch or my September of 2022 article on the Bolus Theory.
If your spike antibodies go up after vaccination and then return to ~0, you still may have spike persist in the body? Am I understanding correctly? Thanks.
Thanks Marc. I will read read your other articles on bolus theory. In regards to issues people are having years after vaccination, do you think is it only from vaccine directly injected intravascularly wreaking havoc on the body, or is there also remaining spike / vaccine excipients that persist in the body?
Spike theory is a hoax. Our bodies deal very well with (1) mitigating harm, (2) neutralizing and processing foreign proteins...imagine all the food you eat and the metabolic waste it creates...if things accumulated somewhere you'd die pretty soon. We get it out.
Accumulations occur when your immune system is down or is senescent (age).
MHC-carrying cells are all destroyed, whatever happens to spike.
The only scenario in which a spike protein could penetrate a nucleus is when a stem cell is contaminated and starts producing spike.
That is a possibility because stem cells replicate often and then the nucleus dissolves to let the chromatids separate into 2 sets of chromosomes. During that phase, it's a possibility, and no I doubt the body knows how to deal with that.
If you read my book, you will discover that stem cell contamination is the likely cause of cancers and genetic disorders.
Certain gut and colon bacteria are creating a supportive environment for replication of the S1 protein.
IVM and antibiotics appear to be effective in clearing this. Rebuilding the gut biome with certain probiotics will be the challenge, ie establishing if the S1 supportive environment is being rebuilt or not.
Possible Clue: Fresh hamburger meat was found to support activation of the S1 protein.
s1 s2 and s1 mutant and s2 mutant found by patterson in monocytes too- i definitely don’t agree with the statement our bodies can handle foreign proteins- bc i’m living the hell of it- i wake up poisoned everyday and there’s no stopping it now
Respectfully, if one wants to cure and feel better, one needs to do real science.
I have done the root cause, proposed solution to heal.
I understand you are suffering, but I can guarantee not from circulating spike.
You are allowed to disagree. But if 3 years down the road you are still suffering maybe you diagnostic is wrong?
Patterson proves nothing. What hypothesis does Patterson respond to? Peptides sequences are routinely used by the immune system to train itself. Do you know that all the sequences of past viruses are stored in immune cell DNA? How do you think the immune system knows what to fight?
Read my book if you want a true root-cause analysis. Fear-mongering and BS science only scare people and won't help anybody. People who take IVIg
will produce antibodies to clean up the IvIg that are equivalent to spike. IVIg won't help at all.
I falsified the circulating spike theory in 14 ways...1 in science is sufficient.
Here I have 14 different demonstrations "Circulating spike theory" is hoax, and has nothing to do with the endothelial damage that is caused by a direct reaction to vaccine transfection. Conversely the Bolus Theory is consistent wth autopsies, biopsies.
Already some of my readers are feeling better with the implementation of HBOT...I hope you get a chance to investigate it with your integrative medicine doctor
"No reason to believe antibodies would work for other foreign proteins but not for this Covid-vaccine-induced one."
Early on there was a researcher at Harvard (boo) I believe that stated she found five different cloaking (from the immune system) aspects of -19. Hypothesis being, that is what allowed it to replicate in some with near immunity from attack until other issues were caused, pneumonia etc. I don't know what became of her research if anything.
We have lots of data, real world data, where spike treatment HCQ, IVM, etc. is helping people who at least appear to be producing spike. I stated as such in my white paper on the scam of flu vax from 1976 forward. The irony would be (this was six months after the vax began) those that got a "good" dose, not necessarily a Bolus you were just running this up the flagpole if I recall June 2021 time frame, would need HCQ or IVM their entire life.
As I read more on this and am taking a class in virology something has come to mind. Yes, way beyond the accepted "science" but my case study of one now turning to two seems to be working.
Issue: Over the course of a lifetime, you are exposed and get untold number of viruses. Most go "dormant" and many you never have any symptoms because the immune system handles them because your family tree, as it were, has had them for millennium.
Hypothesis
What does dormant really mean? You probably can help here but I am not sure I believe the accepted science here. By that I mean, almost like a program running in the background they are always there to some extent, and you just show symptoms/immune response when they are no longer "dormant" Like shingles or any of the herpes viruses. Or said another way, your body is always producing some kind of immune response we are not detecting. I realize the answer would be anti-bodies but what if they are there at such low levels or modified in a way we don't detect them. Crazy, yes, but that would be me. LOL
Proof per se.
1. HCQ, IVM are a) binding to spike b) they have unknown benefits we are still learning about i.e. cancer treatment and the like, possibly helping with those "dormant" viruses to reduce immune system load and impact of endothelial lining and the rest.
My personal "trial". 2. I have been taking Z-Stack for three months, loaded if you will two a day the first month and now one a day. I can see a marked changed in how I feel and the, I don't even know what it is breakout/shingle/pyrosis on my lower legs as well, in the past three years, but it is helping there. The last one was 1/10 the size and time. The Dr. gave me steroid cream for not knowing what it was.
I eat as good as anyone in the west save those that live on a farm. And take other supplements to help fill in the gaps. Time will tell but my second "subject" is two weeks in and I will let you know here outcome.
P.S. Like with Bolus two things can be true at one, IMHO.
(1) Dormant probably means it's stored somewhere in a cell with a high alkaline level and sits inside a cell until that cell's pH level changes (stress , fatigue, sun...) in which case its content is spilled in the cell and the cell starts producing virions again.
(2) HCQ, IVM don't bind to spike proteins that' s not how the antiviral works.
(3) Antibodies aren't so important against viruses, Tcells and fever are. T cells destroy the contaminated cells and the fever destroy the virions in the blood stream with heat and blood acidification.
(4) Z-stack probably boosts your stem cells and those go on to repair your body and trigger T cells production that would keep shingles under control.
You know I am new to the biology/virology side of the equation, and I appreciate the wisdom. The more you learn the more there is to know.
What is a good to fight against pH rise?
What is HCQ doing then. The way I heard it was it binds, probably bad term to the spike so it can be disposed of i.e. helping the immune system.
So, when they say after vax to prove they "work" You produce anti-bodies they are really saying T Cell production?
Still looking forward to you coming back on. We started and new County paper and we are in the middle of election season, so I am swamped. If WW III is not upon us before the end of the year. I will get my notes together for another chat. Godspeed my friend, you are doing the Lord's work.
Actually, there ARE doctors talking about spike proteins as they relate to cancer; namely, Dr William Makis and Dr Peter McCullough have cited how the spike proteins inhibit the P-53 DNA repair gene which they speculate accounts for a surge in cancers.
Interestingly, I have people around me (friends) who’ve been manifesting increasing symptoms of mRNA side effects… now years after their initial injections. In several cases, I’ve managed to convince them to get D-dimer blood tests…and all three have come back with elevated dimers beyond the normal range. I’ve speculated that they’re still producing spike proteins which have gradually accumulated into significant levels to cause symptoms. All three began with unexplained pain in their calves/legs, shortness of breath and low endurance or weakness.
Spike proteins don't cause D-dimers; they are mitigated by natural abs and neutralized by specific abs. T cells attacking your endothelium do.
D-dimers are created by fibrin decomposition. They likely have white clots from the vaccines that are slowly decomposing. The literature suggests going on a high dose of fibrinolytic like Nattokinase.
Presumably then, spike proteins circulating within the vascular system and binding to endothelial cells are causing the immune response by T-cells to destroy the ‘bound cells’ which results in D-dimers.
Marc, can you tell me what a high dose range (might be)using Nattokinase to dissolve the clots?
The recommended.dose in the article I share in *The Needle's Secret" is I believe 10,800FU/day of Nattokinase and reduces plaque by up to 95% in one year.
I’m waiting for my book delivery (expected August 10-15)and believe I’ll learn a lot from reading it. I’ve convinced several friends to get D-diner tests, who’ve all tested with elevated D-dimers above the normal range….each having significant symptoms…such as unexplained leg pains, brain fog/headaches, low energy/endurance and breathlessness walking upstairs or uphill. Do you happen to know if the level of D-dimers would ordinarily have a linear relationship to the seriousness of symptoms?
Please catch the ones who forced the whole world that they had to take the vacc or eles. All those in top gov positions must be made to take a test to prove that their DNA has the Spike proline or not. We need to know please. They HAVE TO PAY FOR WHAT THEY HAVE DONR.
I bought it just after a watched an Iv with you..probably about a month after the book was launched.Its showing as a kindle in Amazon.com as well right now..Of course I enjoyed it....
I can’t speak for others nor their tests, but my circulating spike protein has quadrupled since February (yes it’s free spike (ELISA) - not AB).
I have never had an IVIg treatment or been able to tolerate any of the detox protocols.
Not very high?
“A notable finding was that markedly elevated levels of full-length spike protein (33.9±22.4 pg/mL), unbound by antibodies, were detected in the plasma of individuals with postvaccine myocarditis, whereas no free spike was detected in asymptomatic vaccinated control subjects (unpaired t test; P<0.0001).”
https://www.ahajournals.org/doi/10.1161/CIRCULATIONAHA.122.061025
“First, S-protein expression kinetics were determined in the serum of mice dosed with 1 × 109 vp of Ad26.COV2.S (Figure A4). S-protein levels were detected at Day 1 (26.7 pg/mL), remained detectable until Day 6, and decreased to background levels by Day 10 after dosing.”
https://www.mdpi.com/2076-393X/12/
My fibrinogen has been tested (not elevated) and well, I wouldn’t know, but since IMD Berlin is a accredited laboratory, I have no reason to question their findings..
Thank you, so do I.
I’m awaiting the results from a clinical genetic test but as far as my non-geneticist eyes can see, my genome does seem to be somewhat challenged
That's a BS article that compared at different times. They took myocarditid pagient a day4 and healthy vaccinated at day 10 (if my memory served mz well)
In Ogata et al, the average is 63pg/ml and the max is 150pg/mL.
Thank you for asking :-)
I feel far better today than i did the first 4+ months, but like many injured, I still suffer from a long list of mostly unspecific symptoms, with intensities that varies from day to day.
Yes endothelial damage is undoubtedly part of it - I’ve had all sorts of vascular spasms throughout this - still have. But I’m also fairly confident that immunogenetics play a fundamental role. Apart from it making good sense, I got hold of the data files, generated by the lab during my genetic analysis, and it seems that, unless I’m hyper-methylated, there’s many and large structural changes present.
You’re most likely right - I just did a quick search in order to get an idea of the levels typically found (only to find out that I’m unable to upload the screenshots on Substack :-S ).
Either way, considering my last vaccine was 2 years ago it’s at least an interesting amount.
How are you feeling? The damage is mostly endothelial-related.
Interesting. Are you taking Nattokinase or an equivalent?
No can’t tolerate
Additional info:
3x Pfizer, latest one October 2022.
1 x Covid January 2022.
Serum free spike protein February 2024 (6.9 pg/ml) + September 2024 (25.4 pg/ml)
Those aren't very high numbers, but they are significant enough to indicate something.
Are you sick in any way?
There are 3 possibilities:
(1) your body is actually producing its own fibrinolytic (Plasmin) and it's dissolving white clots. That would be very good news bc it would mean your endothelium is repairing itself and you are healing.
(2) the ELISA test is cross-reacting with something else and giving you a false-positive.
(3) you are still producing spike protein in significant quantities. that would mean stem cells have been contaminated and that you would have a very high risk of cancer.
I sincerely hope for you it's (1) or (2).
Best, Marc
no i’d say the spike is affecting IVIG and was contaminated with spike- a lot of of our IVIG peeps had to switch to SQ bc of this
Have you read any of my work?
I have the only theory today that hasn't been falsified.
Not sure who your immunologists are, but they need to go back to school.
Respectfully, you are being gaslit.
i don’t have one - i’m speaking of what we see in the community- you know hard based evidence from the evidence- no need to be rude
and dr cole has found spike on autopsy- disproves you any further
Dear Lyndsey,
My apologies if you took my message wrongly. I am here to help.
I have sacrificed 4,5 years of my life and my family to help the vaccine-injured.
It's your choice to read my work or not, but coming on my Substack with the fallacies you have been sold and not even taking the time to read my work is a bit hard for me.
Respectfully, I am fed up with a lot of the BS the freedom doctors have been stating for nearly 4 years now.
If you talk about immunology while breaking the most sacred laws of immunology (you're not the only one most freedom fighter and biologists doctors shamefully break basic Laws of immunology), and you hope to contribute to helping vaccine-injured, respectfully, you are part of the problem.
Antibodies bind. T-cells destroy contaminated cells. Circulating spike protein theory breaks those 2 fundamental laws and many other autopsy observations!
Let me repeat:
(1) Spike protein is the antigen. That is the mechanism of action of the vaccine by design. Everybody gets it, not everybody is harmed. So circulating spike protein is not specific...it is thus not the cause.
(2) T-cells kill MHC-carrying cells that present spike peptides (spike fragments). Here's the Pfizer graphic https://substackcdn.com/image/fetch/f_auto,q_auto:good,fl_progressive:steep/https%3A%2F%2Fsubstack-post-media.s3.amazonaws.com%2Fpublic%2Fimages%2Ffdc5a63b-7665-489a-9307-f77fad8467d9_1140x675.jpeg
(3) Circulating spike proteins are "nothing burgers" like with all foreign proteins. When given time, the body deals fine with proteins (Amyloids, spike...), ANTIBODIES deal with it. Read "Circulating SARS-CoV-2 Vaccine Antigen Detected in the Plasma of mRNA-1273 Vaccine Recipients" by Ogata et al. You will see that circulating spike proteins are not detectable post Day 9 Jab 1, first they are neutralized. After Jab2 , they simply are hardly produced simply because T-cells do their job and destroy the contaminated cell very quickly (which explains IgG4 switching bc there are no spike proteins!).
Natural and specific antibodies would mitigate the harm even if you had spike protein post-vax.
(4) More importantly, despite not having Spike, all transfecting vaccines produce the same adverse reactions. Think about it: many people have had the same thing you are suffering from despite never being injected with mRNA or spike.
(5) Taking IVIg is just stupid because there are no spike proteins, and so the body needs to create anti-anti-spike antibodies. These will react to spike tests by design. But the IVig will do nothing to help, nothing to help reduce the fibrin blocking the arteries and the capillaries, mend the holes poked in the vascular system, and repair the necrosed organs, ...
My research has already helped a few people suffering for 3 years. I have nothing to gain. I don't sell therapies, I don't sell consulting, I help probono. But I don't accept on my Substack fallacious theories that harm the very people I am trying to help. I hope you will understand.
also i know the vax injured you’re speaking of and there’s more systems involved that’s causing a majority of issues - you have to look at the whole complex pic- the ones of us who survived with severe injuries are still making spike/ i’ve proven with my panels - all 3 monocyte lines transferred with vax spike- we cleared the lines and now it’s back in one monocyte line- also my t cells cd3,cd4,cd8 are tanked and i’m negative for hiv so i have the vaids- also my spike ab test 8 months after moderna was 2,000 then 4 months later my pfizer put me into cytokine storm- which in still in- NIH disclosed from their own mouths to bri dresden and the other trial participants who were injured that the spike protein causes an immune mediated response- once we cleared my lines i started to progress functionally to 60% then after we stopped my protocol - i started to decline back to 30% functioning 6 months later and that’s when we retested it and saw it came back in the lines-
my other point is - why do you think they stopped testing in the trials for spike production after what 60-90 days i can’t remember? bc we are still producing it 3-4 years later hence the failing one by one of our systems- now it’s affecting my adrenals and hormones- i’m trying to save my ovaries and myself bc it’s pushing me into early menopause- tanked my hormones and cortisol-
my dna results will be back this coming week - stay tuned
"Many vaccine-injured people have testified that they keep producing spike proteins three years after vaccination, or so their tests say…"
My SARS COV 2 AB, TOTAL SPIKE SEMI QN was < 0.4, 1 week after injection. It increased 8 months later and again at 22 months before reaching a max at 24 months. I've had it tested 3x since the max and each time it is lower. Based on the trend line, I will retest at 42 months post vax. The max was at 2 years and the slope shows it should be approaching 0 at 1.5 years from the max. So a total of 3.5 years. But my main concern is inflammation from lipid nanoparticles, which ties into the next part where Dr. Cole discusses them associated with turbo cancer.
"As I have explained in the chapter on Cancer, stem cell transfection should trigger many replications and cancer, and I have yet to hear anyone talking about spike production simultaneously with cancer."
He talks about the spike protein & lipid nanoparticles being an issue with turbo cancer in the interview. Dr. Ryan Cole says one of the very big problems with the CV19 vax is it destroys the immune system and stops your ability to fight cancer. The truth-telling medical community is calling these new aggressive fast-spreading cancers turbo cancer.
https://rumble.com/v3og3mw-cv19-vax-causes-turbo-cancer-dr.-ryan-cole.html
What's your view of harm from lipid nanoparticles with the vaccine? FYI, I have never heard of IVIg or tried it.
Antibodies against spike aren't the same thing as spike. What you are describing is normal.
Dr. Cole hasn't fully grasp the mechanics of cancer genesis with the vaccines in general. It is not tied to spike, it is tied to Stem cell contamination.
Turbo cancer are tied to the seniority of the stem cells contaminated (they are less differentiated and have a much greater scale. ex: triple negative breast acncer).
You need to read my other articles on the bolus theory.
I suggest my letter to Steve Kirsch or my September of 2022 article on the Bolus Theory.
I have also 2 papers on cancer. Best.
If your spike antibodies go up after vaccination and then return to ~0, you still may have spike persist in the body? Am I understanding correctly? Thanks.
Thanks Marc. I will read read your other articles on bolus theory. In regards to issues people are having years after vaccination, do you think is it only from vaccine directly injected intravascularly wreaking havoc on the body, or is there also remaining spike / vaccine excipients that persist in the body?
Spike theory is a hoax. Our bodies deal very well with (1) mitigating harm, (2) neutralizing and processing foreign proteins...imagine all the food you eat and the metabolic waste it creates...if things accumulated somewhere you'd die pretty soon. We get it out.
Accumulations occur when your immune system is down or is senescent (age).
Just curious: can the body also clear the spike proteins that get inside the nucleus of cells?
MHC-carrying cells are all destroyed, whatever happens to spike.
The only scenario in which a spike protein could penetrate a nucleus is when a stem cell is contaminated and starts producing spike.
That is a possibility because stem cells replicate often and then the nucleus dissolves to let the chromatids separate into 2 sets of chromosomes. During that phase, it's a possibility, and no I doubt the body knows how to deal with that.
If you read my book, you will discover that stem cell contamination is the likely cause of cancers and genetic disorders.
You make some excellent arguments Marc!!
Hope your book sells big time!!
From my perspective, its one of the finest books in the Vaccination genre!!
Unfortunately, it's pretty much stalled right now. Need to build awareness, but it's a journey.
Perhaps another piece to the puzzle:
Certain gut and colon bacteria are creating a supportive environment for replication of the S1 protein.
IVM and antibiotics appear to be effective in clearing this. Rebuilding the gut biome with certain probiotics will be the challenge, ie establishing if the S1 supportive environment is being rebuilt or not.
Possible Clue: Fresh hamburger meat was found to support activation of the S1 protein.
Respectfully, this is all more scaremongering.
The body can deal with all this.
Biome can indeed be damaged when a leaky gut problem occurs.
This brand-ization of spike and S1 is part of a messaging technique to scare people and get more budget for their bio-lab research.
Our bodies can deal with foreign proteins.
s1 s2 and s1 mutant and s2 mutant found by patterson in monocytes too- i definitely don’t agree with the statement our bodies can handle foreign proteins- bc i’m living the hell of it- i wake up poisoned everyday and there’s no stopping it now
Dear Lindsey,
Respectfully, if one wants to cure and feel better, one needs to do real science.
I have done the root cause, proposed solution to heal.
I understand you are suffering, but I can guarantee not from circulating spike.
You are allowed to disagree. But if 3 years down the road you are still suffering maybe you diagnostic is wrong?
Patterson proves nothing. What hypothesis does Patterson respond to? Peptides sequences are routinely used by the immune system to train itself. Do you know that all the sequences of past viruses are stored in immune cell DNA? How do you think the immune system knows what to fight?
Read my book if you want a true root-cause analysis. Fear-mongering and BS science only scare people and won't help anybody. People who take IVIg
will produce antibodies to clean up the IvIg that are equivalent to spike. IVIg won't help at all.
I falsified the circulating spike theory in 14 ways...1 in science is sufficient.
Here I have 14 different demonstrations "Circulating spike theory" is hoax, and has nothing to do with the endothelial damage that is caused by a direct reaction to vaccine transfection. Conversely the Bolus Theory is consistent wth autopsies, biopsies.
Already some of my readers are feeling better with the implementation of HBOT...I hope you get a chance to investigate it with your integrative medicine doctor
Best, Marc
respectfully he proves evidence based science- with the injured- respectfully i think your full of 💩 and i will not be reading your book
i can prove your theory wrong with my labs sir! try again
Yes. As planned.
Love the way you think Marc!
"No reason to believe antibodies would work for other foreign proteins but not for this Covid-vaccine-induced one."
Early on there was a researcher at Harvard (boo) I believe that stated she found five different cloaking (from the immune system) aspects of -19. Hypothesis being, that is what allowed it to replicate in some with near immunity from attack until other issues were caused, pneumonia etc. I don't know what became of her research if anything.
We have lots of data, real world data, where spike treatment HCQ, IVM, etc. is helping people who at least appear to be producing spike. I stated as such in my white paper on the scam of flu vax from 1976 forward. The irony would be (this was six months after the vax began) those that got a "good" dose, not necessarily a Bolus you were just running this up the flagpole if I recall June 2021 time frame, would need HCQ or IVM their entire life.
As I read more on this and am taking a class in virology something has come to mind. Yes, way beyond the accepted "science" but my case study of one now turning to two seems to be working.
Issue: Over the course of a lifetime, you are exposed and get untold number of viruses. Most go "dormant" and many you never have any symptoms because the immune system handles them because your family tree, as it were, has had them for millennium.
Hypothesis
What does dormant really mean? You probably can help here but I am not sure I believe the accepted science here. By that I mean, almost like a program running in the background they are always there to some extent, and you just show symptoms/immune response when they are no longer "dormant" Like shingles or any of the herpes viruses. Or said another way, your body is always producing some kind of immune response we are not detecting. I realize the answer would be anti-bodies but what if they are there at such low levels or modified in a way we don't detect them. Crazy, yes, but that would be me. LOL
Proof per se.
1. HCQ, IVM are a) binding to spike b) they have unknown benefits we are still learning about i.e. cancer treatment and the like, possibly helping with those "dormant" viruses to reduce immune system load and impact of endothelial lining and the rest.
My personal "trial". 2. I have been taking Z-Stack for three months, loaded if you will two a day the first month and now one a day. I can see a marked changed in how I feel and the, I don't even know what it is breakout/shingle/pyrosis on my lower legs as well, in the past three years, but it is helping there. The last one was 1/10 the size and time. The Dr. gave me steroid cream for not knowing what it was.
I eat as good as anyone in the west save those that live on a farm. And take other supplements to help fill in the gaps. Time will tell but my second "subject" is two weeks in and I will let you know here outcome.
P.S. Like with Bolus two things can be true at one, IMHO.
Hi my friend,
(1) Dormant probably means it's stored somewhere in a cell with a high alkaline level and sits inside a cell until that cell's pH level changes (stress , fatigue, sun...) in which case its content is spilled in the cell and the cell starts producing virions again.
(2) HCQ, IVM don't bind to spike proteins that' s not how the antiviral works.
(3) Antibodies aren't so important against viruses, Tcells and fever are. T cells destroy the contaminated cells and the fever destroy the virions in the blood stream with heat and blood acidification.
(4) Z-stack probably boosts your stem cells and those go on to repair your body and trigger T cells production that would keep shingles under control.
my two cents.
Best,
Marc
Thanks my friend,
You know I am new to the biology/virology side of the equation, and I appreciate the wisdom. The more you learn the more there is to know.
What is a good to fight against pH rise?
What is HCQ doing then. The way I heard it was it binds, probably bad term to the spike so it can be disposed of i.e. helping the immune system.
So, when they say after vax to prove they "work" You produce anti-bodies they are really saying T Cell production?
Still looking forward to you coming back on. We started and new County paper and we are in the middle of election season, so I am swamped. If WW III is not upon us before the end of the year. I will get my notes together for another chat. Godspeed my friend, you are doing the Lord's work.
I think HCQ and IVM either slow the contamination or activate the T cells. Possibly both.
Interesting, I wonder if there is some information on the mechanism in the Malaria trials?
Don't know much about Malaria...I must admit.
I haven't looked into it yet.
Actually, there ARE doctors talking about spike proteins as they relate to cancer; namely, Dr William Makis and Dr Peter McCullough have cited how the spike proteins inhibit the P-53 DNA repair gene which they speculate accounts for a surge in cancers.
This is not what I am talking about.
Anyhow p53 is always inhibited in stem cells.
I am talking zbout people having high level of spike proteins and cancer.
Oh, I understand.
Interestingly, I have people around me (friends) who’ve been manifesting increasing symptoms of mRNA side effects… now years after their initial injections. In several cases, I’ve managed to convince them to get D-dimer blood tests…and all three have come back with elevated dimers beyond the normal range. I’ve speculated that they’re still producing spike proteins which have gradually accumulated into significant levels to cause symptoms. All three began with unexplained pain in their calves/legs, shortness of breath and low endurance or weakness.
Spike proteins don't cause D-dimers; they are mitigated by natural abs and neutralized by specific abs. T cells attacking your endothelium do.
D-dimers are created by fibrin decomposition. They likely have white clots from the vaccines that are slowly decomposing. The literature suggests going on a high dose of fibrinolytic like Nattokinase.
Presumably then, spike proteins circulating within the vascular system and binding to endothelial cells are causing the immune response by T-cells to destroy the ‘bound cells’ which results in D-dimers.
Marc, can you tell me what a high dose range (might be)using Nattokinase to dissolve the clots?
Thank you so much Marc! You’re turning me into a believer.
The recommended.dose in the article I share in *The Needle's Secret" is I believe 10,800FU/day of Nattokinase and reduces plaque by up to 95% in one year.
Hi Marc,
I’m waiting for my book delivery (expected August 10-15)and believe I’ll learn a lot from reading it. I’ve convinced several friends to get D-diner tests, who’ve all tested with elevated D-dimers above the normal range….each having significant symptoms…such as unexplained leg pains, brain fog/headaches, low energy/endurance and breathlessness walking upstairs or uphill. Do you happen to know if the level of D-dimers would ordinarily have a linear relationship to the seriousness of symptoms?
Thanks!
Your new convert,
Tom
Please catch the ones who forced the whole world that they had to take the vacc or eles. All those in top gov positions must be made to take a test to prove that their DNA has the Spike proline or not. We need to know please. They HAVE TO PAY FOR WHAT THEY HAVE DONR.
It's a pity that “The Needle’s Secret” cannot be bought at Kobo´s online shop.
It looks like the digital form is censored on Amazon as well. Only the physical book is purchaseable. I apologize. I do what I can...
Its still available to amazon.com.au for Australians in hard copy and kindle.I have a kindle version!!!
Thanks, Mike.
When did you buy it?
If you bought it, they can't censor it. But they seem to make it impossible to buy now...
Hope you enjoy it, and are sharing the word. :-)
info - Bought it Kindle on Amazon Canada in April. Still shows as available there.
I bought it just after a watched an Iv with you..probably about a month after the book was launched.Its showing as a kindle in Amazon.com as well right now..Of course I enjoyed it....
Any chance you could self publish the electronic format?
Get the physical book, Marius, it's worth the trouble!
Of course. But a self published ebook is practically impossible to censor and it doesn't require shipping (can be bought from anywhere).
Unfortunately, o have a contract with Amazon.
I’d like to buy the book, but I’m in Thailand. If it’s censored, that’s a good sign that it’s valuable
just join Australia in amazon.
https://www.amazon.com.au/NEEDLES-SECRET-UNRAVELING-MYSTERY-REVOLUTION-ebook/dp/B0CZTTSCW2/
Thank Mike!, I checked your link and can order the paperback but not the Kindle version. For me in Thailand, it’s cheaper to order from the US
Am sure Amazon can deliver in Thailand, Tom.
Maybe you buy it on Amazon Japan or Australia.
Thanks for your trust.
Okay! I’ll check it out now.