This isn’t the only crime they have committed, however this is the crime, the crime of all crimes, that if thoroughly prosecuted with all evidence available and forthcoming, would result, if justice prevailed, in a full Nuremberg 2.0. This crime against humanity deserves nothing less than the death penalty, for many. They know this, and will sacrifice every other crime for this one. They also know that their best protection is a populace that doesn’t want to know. That is better than the best legal defense team can provide. It will always be cultivated.
This is a new research area and researchers are all too eager to be the first to publish about it. Fortunate that we have the ability now to demonstrate the actual cause of harm in the case of PACVS. It is possible now to lift the fingerprint of the criminal.
I wonder what antibody families predominate in the post-vaccine syndrome patients.
Due to the chronic presence of spike protein in those whose cells produce it for a long time, for months, IgG4 antibodies, which are tolerance-antibodies, not interference antibodies, come to predominate.
It seems that autoimmune problems and spike-opathy are both factors, but where is the funding to ask these questions that the DoD, big pharma and the federal government don't want answered?
They use Ig4 backbones in chimeric antibodies. They become pathogenic in high amounts and are related to diseases like Bulbous Pemphigoid, which is a reported side effect.
Hi Liz, I don't know if this would help you any, but I live in the US and got mine done from a lab that does labwork that an individual can pay for and get done and they do all of the labwork a doctor would order for a patient. My doctor did order mine for me, I had to tell her about it, she had not heard of it.
When you inject foreign proteins into the body, or the message to make them, we need to keep in mind that T-cells, the immune cells that can recognize foreign proteins, can NOT detect those proteins AFTER they are released from the cells that made them. T-cells can detect and destroy cells that are making foreign proteins BEFORE they get released, but they’re not going to get all of them. So, foreign proteins do get made and released. APCs (antigen presenting cells), specifically dendritic cells and macrophages, can and will detect those free-floating proteins, take them inside, chop them up, and present smaller pieces of them to the T-cells. This presentation happens on special sites called MHC type 2 sites. T-cells have been trained in the thymus gland to recognize patterns on these protein parts that are like self-proteins, and that protects us from making antibodies against self. The protection against autoimmunity is a very complicated communication between the T-cells and B-cells, the immune cells that make the antibodies. The danger is this: B-cells CAN detect the free-floating proteins once they have been released from the cells that made them. If there is an overabundance of proteins being made and released from cells, B-cells can autoactivate and start cranking out dangerous antibodies that can attach to self-proteins. This can happen with all mRNA platform shots regardless of the proteins they code for. It’s dangerous and should be prohibited in humans and animals.
After COVID At night my hand felt like it was on fire and 2 fingers went numb for a few months. I pity anyone with these symptoms and God damn the creators of this thing and the profiteers who ran this project to where we are today. I always assumed that my memory loss and brain fog during the last couple of years was just a part of being 67. I'll never know. I would love to find out that it might be something that can heal if that's what it is.
Hi Alio, please check out The Wellness Company. You can join or just contact a telehealth doctor who could help you with your questions and suggest possible help. They are very helpful.
Very good work Nicholas. I am curious about the iron metabolism impairment aspect in particular. I believe that protein misfolding is a consequence of the jabs...and is also the root cause of Hereditary Hemochromatosis. Amyloid plaques are the result of the aggregation of misfolded protein...clots and fibroids causing death and senility/cognitive impairments occur in both etiologies. EDTA CHELATION presents some promise here for treatment for both concurrently. EDTA appears to quickly undo the jab-induced rouleaux formations in red blood cells additionally, providing better oxygen delivery. (Mihalcea,2024).
Amazing -- please keep sharing these articles and your insights. I agree that it seems far more likely that "long Covid" is mostly vaccine syndrome or nocebo. Do you have any peer-reviewed and published data on the success of the spike detox regimen you've advocated?
The article specifies that this study proves that the autoantibodies arise AFTER vaccination. Also, do note that they make zero effort to explain the connections between antibodies, but would like to sell you detox.
Here's the list and their optogenetics connections in 'G' proteins:
ACE2
Cell entry.
MAS1
Gene Ontology (GO) annotations related to this gene include G protein-coupled receptor activity and peptide hormone binding.
ATR1
Gene Ontology (GO) annotations related to this gene include G protein-coupled receptor activity and angiotensin type II receptor activity.
STAB1
ene Ontology (GO) annotations related to this gene include calcium ion binding and protein-disulfide reductase activity.
ADRA2A
Gene Ontology (GO) annotations related to this gene include G protein-coupled receptor activity and protein heterodimerization activity.
Here's an NIH search page for 'G' coupled receptors and optogenetics:
Two immediate thoughts, one serious and one cheeky.
First, this type of study is EXACTLY why the gold standard for any new medication is five years of human trials and the platinum standard is ten years. We got the pewter standard.
Second, would we say even the risk of developing such symptoms is worse than catching covid/flu especially if doctors actually treated with antivirals and antibiotics? Oh, gee, I wonder.
This is an excellent paper... still can't figure out why we are doing next to nothing while a democide continues to be carried out.
This isn’t the only crime they have committed, however this is the crime, the crime of all crimes, that if thoroughly prosecuted with all evidence available and forthcoming, would result, if justice prevailed, in a full Nuremberg 2.0. This crime against humanity deserves nothing less than the death penalty, for many. They know this, and will sacrifice every other crime for this one. They also know that their best protection is a populace that doesn’t want to know. That is better than the best legal defense team can provide. It will always be cultivated.
This is a new research area and researchers are all too eager to be the first to publish about it. Fortunate that we have the ability now to demonstrate the actual cause of harm in the case of PACVS. It is possible now to lift the fingerprint of the criminal.
They are putting the MRNA vax in your food you need to
do this right now....... https://t.co/KXjORB2xR3
"The purpose of a thing is what it does", as the saying goes...
;-(
Where can one run the mentioned autoantibody panels (ACE2, MAS1, ATR1, STAB1, ADRA2A)?
I wonder what antibody families predominate in the post-vaccine syndrome patients.
Due to the chronic presence of spike protein in those whose cells produce it for a long time, for months, IgG4 antibodies, which are tolerance-antibodies, not interference antibodies, come to predominate.
It seems that autoimmune problems and spike-opathy are both factors, but where is the funding to ask these questions that the DoD, big pharma and the federal government don't want answered?
They use Ig4 backbones in chimeric antibodies. They become pathogenic in high amounts and are related to diseases like Bulbous Pemphigoid, which is a reported side effect.
Does the Wellness Company have mail out tests for this AB's?
Hi,
Great article.
I’m from Australia and am wondering where I would go to get a spike protein test? Is this something that an Australian doctor would be aware of?
Hi Liz, I don't know if this would help you any, but I live in the US and got mine done from a lab that does labwork that an individual can pay for and get done and they do all of the labwork a doctor would order for a patient. My doctor did order mine for me, I had to tell her about it, she had not heard of it.
When you inject foreign proteins into the body, or the message to make them, we need to keep in mind that T-cells, the immune cells that can recognize foreign proteins, can NOT detect those proteins AFTER they are released from the cells that made them. T-cells can detect and destroy cells that are making foreign proteins BEFORE they get released, but they’re not going to get all of them. So, foreign proteins do get made and released. APCs (antigen presenting cells), specifically dendritic cells and macrophages, can and will detect those free-floating proteins, take them inside, chop them up, and present smaller pieces of them to the T-cells. This presentation happens on special sites called MHC type 2 sites. T-cells have been trained in the thymus gland to recognize patterns on these protein parts that are like self-proteins, and that protects us from making antibodies against self. The protection against autoimmunity is a very complicated communication between the T-cells and B-cells, the immune cells that make the antibodies. The danger is this: B-cells CAN detect the free-floating proteins once they have been released from the cells that made them. If there is an overabundance of proteins being made and released from cells, B-cells can autoactivate and start cranking out dangerous antibodies that can attach to self-proteins. This can happen with all mRNA platform shots regardless of the proteins they code for. It’s dangerous and should be prohibited in humans and animals.
Thank you for all of the information!
After COVID At night my hand felt like it was on fire and 2 fingers went numb for a few months. I pity anyone with these symptoms and God damn the creators of this thing and the profiteers who ran this project to where we are today. I always assumed that my memory loss and brain fog during the last couple of years was just a part of being 67. I'll never know. I would love to find out that it might be something that can heal if that's what it is.
Hi Alio, please check out The Wellness Company. You can join or just contact a telehealth doctor who could help you with your questions and suggest possible help. They are very helpful.
They are putting the MRNA vax in your food you need to
do this right now....... https://t.co/KXjORB2xR3
Very good work Nicholas. I am curious about the iron metabolism impairment aspect in particular. I believe that protein misfolding is a consequence of the jabs...and is also the root cause of Hereditary Hemochromatosis. Amyloid plaques are the result of the aggregation of misfolded protein...clots and fibroids causing death and senility/cognitive impairments occur in both etiologies. EDTA CHELATION presents some promise here for treatment for both concurrently. EDTA appears to quickly undo the jab-induced rouleaux formations in red blood cells additionally, providing better oxygen delivery. (Mihalcea,2024).
I don't have a clue what that means but I am truly grateful to you and the ones who do.
Amazing -- please keep sharing these articles and your insights. I agree that it seems far more likely that "long Covid" is mostly vaccine syndrome or nocebo. Do you have any peer-reviewed and published data on the success of the spike detox regimen you've advocated?
- AT THE MIDDLE OF A FIGHT ONE MUST OFTEN
F I N D UNKNOWN RESOURCES (INSIDE OF
H I M /GOD) , ET.AL., … OTHERS , TO HELP WITH AN OVERCOMING SITUATION … •••
— “ W I N N E R S “ -
“THERE IS HONOR IN —
W O R K …!!!! “
“THE BEST FRIENDSHIPS ARE EARNED …”
— A M E N … !!!!! A M E N … ‼️‼️‼️‼️‼️‼️‼️‼️‼️‼️🚸🚸🚸🚸🚸🚸🚸🚸🚸🚸🚸🔆🔆🔆🔆🔆🔆🔆🔆🔆🔆🔆
Elon Musk: Google "Polygraph test of Ella Gareeva"
If they're biomarkers related to optogenetics, one must ask why they're being removed.
The article specifies that this study proves that the autoantibodies arise AFTER vaccination. Also, do note that they make zero effort to explain the connections between antibodies, but would like to sell you detox.
Here's the list and their optogenetics connections in 'G' proteins:
ACE2
Cell entry.
MAS1
Gene Ontology (GO) annotations related to this gene include G protein-coupled receptor activity and peptide hormone binding.
ATR1
Gene Ontology (GO) annotations related to this gene include G protein-coupled receptor activity and angiotensin type II receptor activity.
STAB1
ene Ontology (GO) annotations related to this gene include calcium ion binding and protein-disulfide reductase activity.
ADRA2A
Gene Ontology (GO) annotations related to this gene include G protein-coupled receptor activity and protein heterodimerization activity.
Here's an NIH search page for 'G' coupled receptors and optogenetics:
https://www.ncbi.nlm.nih.gov/pmc/?term=G+protein-coupled+receptor+optogenetics
Biomarkers related to optogenetics from covid vaccines? That is extremely serious if the report is true. Also points the finger at colleges.
It is wise for people to get familiar with optogenetics and how they can be used.
.
My favorite parts of Covid:
#16
That the vaccine injured are allergic to themselves.
.
Two immediate thoughts, one serious and one cheeky.
First, this type of study is EXACTLY why the gold standard for any new medication is five years of human trials and the platinum standard is ten years. We got the pewter standard.
Second, would we say even the risk of developing such symptoms is worse than catching covid/flu especially if doctors actually treated with antivirals and antibiotics? Oh, gee, I wonder.