SPIKE PROTEIN INDUCED CYTOKINES AND B-CELL DYSREGULATION: ARE B CELLS OVERPRODUCING MONOCLONAL ANTIBODIES CAUSING AMYLOIDOSIS, AUTOIMMUNITY AND THE REPORTED BLOOD HYPERVISCOSITY?
SPIKE PROTEIN INDUCED CYTOKINES AND B-CELL DYSREGULATION: ARE B CELLS OVERPRODUCING MONOCLONAL ANTIBODIES CAUSING AMYLOIDOSIS, AUTOIMMUNITY AND THE REPORTED BLOOD HYPERVISCOSITY?
Thanks Walter. Great work again. I fear the end game fast approaches. MSM is allowing this to be viewed and read. Why? They want uproar, rebellion. They want martial law. Whatever happens now, thank you for all your hard work dedication. Hope to see people on the other side, whatever that looks like. Chaos is coming, take care, thanks
Once again another excellent article! Complex for those of us who are not as skilled and trained in this particular area. However, what would we do without you Walter delivering such brilliant research! I have a “normal” chest infection and am utterly terrified l may have to enter the “kill zone” at my local hospital to receive treatment. I have noticed that all software in the UK has also been re-written to read what “they” require it to ..
Software used in vital measurements of “vitals” has been re-written to give falsified readings which fall within “guidelines for discharge” people are being discharged home who still required hospital treatment. CRP (Inflammatory markers) for men now readings of <5 ok for women <10 if you x this by the “discharge figure” of <100 you are sending some pretty sick folks home. Example: l was inadvertently “sprayed” with pesticides 10 years ago - my CRP Markers read >200 l was almost dead - killed my dogs almost instantly - l was given Pipercillan Tazobactum by IV Magnesium also by IV - Oxygen. Was in hospital 3 months .. long epistle as to where my research took me and how l ended up here today speaking with you from my lowly but ever intrigued and fascinated level.
Wow very interesting. I was hospitalized in January for SVT&Cov. My CRP was 1.0 and the test limit was 0.3 mg/dL. Also elevated D-Dimer, ferritin, lactate dehydrogenase, troponin. They gave me "belly shots" of a blood thinner. I'm having the blood work redone to look for improvement, but I will be sure to check the limits.
I am really pleased that you “survived” the ordeal .. It’s extremely interesting that your CRP was 1.0 against the test limits .. hmm .. l too received the enforced shots of blood thinner - however l now have blood clots in both legs - supremely fit women until “the event” .. Are you being treated privately? You may well be working “from a different system” then .. NHS intolerant of “questioning” and seemingly producing PILS - l was not offered a Patient Information Leaflet (PIL) for the “anti-clot-shot” Make sure you really do check the limits my friend! I am new to this site but have a few great photos and evidence to offer - not sure how to produce photos on here - have AZ phial packet it’s shocking - what wouid you expect? Take care! Stay in touch!
Thanks! I am in the US, so different limit-setting rules. Many labs set their own limits. Just for curiosity, I am going to make a list of the measurement limits in my blood work since 2015, same lab. I'll comment if I find any significant changes. And no, I was not given any disclosures in hospital.
Walter have you seen Steve Kirsch's offer for funding? He's offering to fund replication analysis of what's in the vax. In it he's saying the analysis was the same as Kevin's in so far as PEG but- no phosphorus. If Steve is not connected to Kevin, and this isn't Kevin's work, I hope you can broker that bridge as it would be a replication. Even though this is a US based offer of funding, I bet he'd fund Kevin's research. https://stevekirsch.substack.com/p/want-to-know-whats-inside-the-vaccine
I'm curious also. In fact, I wish to know what blood parameters describe thickening of the blood?
I was hospitalized early January for severe SVT with covid. Among other things, elevated D-Dimer, Ferritin, Lactate Dehydrogenase, Troponin... Now wondering what I should get tested to see if my blood has recovered.
Walter great interview with GifaohmBiological. This is the Greet interview referenced in the comments which is very interesting end to end (prediction @ 19is min) https://www.youtube.com/watch?v=sqp4jUDhJRI. You have a real gift compared to other technical writers. You don't waste words. You get right to the essential and your pith description is easily accessible. You speak as you write. Well done. I'm sorry that you are experiencing Noah-Cassandra. It shouldn't be this way. Thank you. You ARE making a difference.
We are dealing with TWO types of IgG abs: normal (Sars-Cov-2 coded with Uracil) and isomeric (cmRNA vaccines coded with Pseudouridine). Severe cases of Sars-Cov-2 were caused by two lethal antibodies, REGN10987 and B38. But now, because of the vaccination campaign, we have to deal with isomeric abs (including the isomeric version of the lethal abs which have been described above), which are awaiting an activation. Isomeric abs were discovered in 1994. Pseudouridine (Pseudouracil) is an ISOMER.
Better make it sooner, because Russia entered Ukraine exactly after Nato had vaccinated its troops with the cmRNA genetic code.
The immune system will fabricate both kinds of abs, here is the mechanism. Upon injection, the immune system will create a huge number of binding isomeric abs and a smaller than normal quantity of normal abs (whether binding or neutralizing). The severe cases of Covid-19 were caused by two lethal abs: REGN10987 and B38. Hence, since the volume of normal abs (including the two lethal ones described above) is smaller than usual, they can claim that "you get vaccinated, you will get a mild form of Covid-19". However, now, thanks to the vaccination campaign, the immune systems were forced to create isomeric abs, including the isomeric lethal version, and these isomeric abs can become neurotoxic/misfolded in a fraction of a second, given the right sufficient conditions. Had the vaccines been coded with mRNA, ALL OF THE VACCINEES would have contracted immediately very severe cases of Covid-19, since the immune system would have been forced to produce huge quantities of normal abs, including the lethal versions. No medical doctor, with a degree in epidemiology or virusology, HAS ANY IDEA of the issues involved here. They have no knowledge of the existence of isomeric abs, of the fact that Uracil was replaced 100% with an isomer (Pseudouracil/Pseudouridine), or that in fact the vaccines are cmRNA and not mRNA.
The spike proteins produced by the immune system in response to the cmRNA vaccines have nothing to do with Sars-Cov-2: they are isomeric proteins, coded with Pseudouridine. That is why they cannot stop transmission or anything else.
Trigger: an isomeric Sars-Cov-2 (or Mers-Cov-2/Omicron), a series of volcanic eruptions (volcanic ash/dust) which in turn will cause great fevers (misfolding as an effect of the change in temperature), a period of great stress (perhaps famine).
Please Excuse my ignorance as a mere non-Scientist/MD/Phd, but I Could Care Less about "Research"
At this point Who Cares? Perhaps the 5 or 6 dead doctors within 1 week in Canada after getting their 4th Jab would care. I Don't. Never "trust" Gov Pharma ever again. I never did, No VaXXXes Covid or Flu.
Wondrous Walter, HUGE thanks for summarizing and sharing all of your brilliant research. " In conclusion, based on these data it could be hypothesized that the presence of a monoclonal spike during the inflammatory phase could reflect the degree of immune hyperactivation in patients with severe COVID-19."
Also, apologies if you discussed this PREPRINT posted on July 29th.
SARS-CoV-2 infection is associated with anti-desmoglein 2 autoantibody detection
" Our results reveal the potential for DSG2 protein and autoimmunity to DSG2 to contribute to unexpected pathologies associated with COVID-19 infection."
Thanks Walter. Great work again. I fear the end game fast approaches. MSM is allowing this to be viewed and read. Why? They want uproar, rebellion. They want martial law. Whatever happens now, thank you for all your hard work dedication. Hope to see people on the other side, whatever that looks like. Chaos is coming, take care, thanks
https://genervter-substack-com.translate.goog/p/ein-fass-ohne-boden-uber-toll-like?_x_tr_sl=de&_x_tr_tl=en&_x_tr_hl=de&_x_tr_pto=wapp
Oh dear Walter... It is so awful and there is a reason we are all discussing the same issues.
I would be honored if you would take the time to read my last part. I don't think you will need the crash course I mention at the beginning.
Best regards twittermitated 2Genervter (Annoyed Citizen) and now 3 Annoyed.
I'm afraid I'll need the crash course and some more, but I find it really interesting!
Many Thanks.
Once again another excellent article! Complex for those of us who are not as skilled and trained in this particular area. However, what would we do without you Walter delivering such brilliant research! I have a “normal” chest infection and am utterly terrified l may have to enter the “kill zone” at my local hospital to receive treatment. I have noticed that all software in the UK has also been re-written to read what “they” require it to ..
Curious about your software comment (as an obsolete software engineer...), can you elaborate?
Software used in vital measurements of “vitals” has been re-written to give falsified readings which fall within “guidelines for discharge” people are being discharged home who still required hospital treatment. CRP (Inflammatory markers) for men now readings of <5 ok for women <10 if you x this by the “discharge figure” of <100 you are sending some pretty sick folks home. Example: l was inadvertently “sprayed” with pesticides 10 years ago - my CRP Markers read >200 l was almost dead - killed my dogs almost instantly - l was given Pipercillan Tazobactum by IV Magnesium also by IV - Oxygen. Was in hospital 3 months .. long epistle as to where my research took me and how l ended up here today speaking with you from my lowly but ever intrigued and fascinated level.
Wow very interesting. I was hospitalized in January for SVT&Cov. My CRP was 1.0 and the test limit was 0.3 mg/dL. Also elevated D-Dimer, ferritin, lactate dehydrogenase, troponin. They gave me "belly shots" of a blood thinner. I'm having the blood work redone to look for improvement, but I will be sure to check the limits.
I am really pleased that you “survived” the ordeal .. It’s extremely interesting that your CRP was 1.0 against the test limits .. hmm .. l too received the enforced shots of blood thinner - however l now have blood clots in both legs - supremely fit women until “the event” .. Are you being treated privately? You may well be working “from a different system” then .. NHS intolerant of “questioning” and seemingly producing PILS - l was not offered a Patient Information Leaflet (PIL) for the “anti-clot-shot” Make sure you really do check the limits my friend! I am new to this site but have a few great photos and evidence to offer - not sure how to produce photos on here - have AZ phial packet it’s shocking - what wouid you expect? Take care! Stay in touch!
Thanks! I am in the US, so different limit-setting rules. Many labs set their own limits. Just for curiosity, I am going to make a list of the measurement limits in my blood work since 2015, same lab. I'll comment if I find any significant changes. And no, I was not given any disclosures in hospital.
Walter have you seen Steve Kirsch's offer for funding? He's offering to fund replication analysis of what's in the vax. In it he's saying the analysis was the same as Kevin's in so far as PEG but- no phosphorus. If Steve is not connected to Kevin, and this isn't Kevin's work, I hope you can broker that bridge as it would be a replication. Even though this is a US based offer of funding, I bet he'd fund Kevin's research. https://stevekirsch.substack.com/p/want-to-know-whats-inside-the-vaccine
Has the thickening of the blood been shown to return to normal at some point in any patients?
I'm curious also. In fact, I wish to know what blood parameters describe thickening of the blood?
I was hospitalized early January for severe SVT with covid. Among other things, elevated D-Dimer, Ferritin, Lactate Dehydrogenase, Troponin... Now wondering what I should get tested to see if my blood has recovered.
Walter great interview with GifaohmBiological. This is the Greet interview referenced in the comments which is very interesting end to end (prediction @ 19is min) https://www.youtube.com/watch?v=sqp4jUDhJRI. You have a real gift compared to other technical writers. You don't waste words. You get right to the essential and your pith description is easily accessible. You speak as you write. Well done. I'm sorry that you are experiencing Noah-Cassandra. It shouldn't be this way. Thank you. You ARE making a difference.
We are dealing with TWO types of IgG abs: normal (Sars-Cov-2 coded with Uracil) and isomeric (cmRNA vaccines coded with Pseudouridine). Severe cases of Sars-Cov-2 were caused by two lethal antibodies, REGN10987 and B38. But now, because of the vaccination campaign, we have to deal with isomeric abs (including the isomeric version of the lethal abs which have been described above), which are awaiting an activation. Isomeric abs were discovered in 1994. Pseudouridine (Pseudouracil) is an ISOMER.
https://pubmed.ncbi.nlm.nih.gov/9217014/
Conformational isomerism of IgG antibodies
https://www.researchgate.net/figure/The-schematic-layout-of-the-IgG-subclasses-and-isomers-thereof-A-The-IgG-subclasses_fig2_267814149
I believe that even if harmful, isomeric antibodies from the V's will be cleared from the body sooner or later.
Maybe the problem is that the V's trained the immune system to make these isomeric antibodies instead of the regular ones, on every reinfection?
Better make it sooner, because Russia entered Ukraine exactly after Nato had vaccinated its troops with the cmRNA genetic code.
The immune system will fabricate both kinds of abs, here is the mechanism. Upon injection, the immune system will create a huge number of binding isomeric abs and a smaller than normal quantity of normal abs (whether binding or neutralizing). The severe cases of Covid-19 were caused by two lethal abs: REGN10987 and B38. Hence, since the volume of normal abs (including the two lethal ones described above) is smaller than usual, they can claim that "you get vaccinated, you will get a mild form of Covid-19". However, now, thanks to the vaccination campaign, the immune systems were forced to create isomeric abs, including the isomeric lethal version, and these isomeric abs can become neurotoxic/misfolded in a fraction of a second, given the right sufficient conditions. Had the vaccines been coded with mRNA, ALL OF THE VACCINEES would have contracted immediately very severe cases of Covid-19, since the immune system would have been forced to produce huge quantities of normal abs, including the lethal versions. No medical doctor, with a degree in epidemiology or virusology, HAS ANY IDEA of the issues involved here. They have no knowledge of the existence of isomeric abs, of the fact that Uracil was replaced 100% with an isomer (Pseudouracil/Pseudouridine), or that in fact the vaccines are cmRNA and not mRNA.
What's the trigger for neurotoxicity/misfolding?
Reinfection with another variant?
Another virus to come?
Something else?
The spike proteins produced by the immune system in response to the cmRNA vaccines have nothing to do with Sars-Cov-2: they are isomeric proteins, coded with Pseudouridine. That is why they cannot stop transmission or anything else.
Trigger: an isomeric Sars-Cov-2 (or Mers-Cov-2/Omicron), a series of volcanic eruptions (volcanic ash/dust) which in turn will cause great fevers (misfolding as an effect of the change in temperature), a period of great stress (perhaps famine).
Dear Walter , gratitude for all your research . I think this will fit into your picture https://twitter.com/3Annoyed/status/1553894226265612288/photo/1 https://www.researchgate.net/publication/45096890_B-Cell_Depletion_In_Vitro_and_In_Vivo_with_an_Afucosylated_Anti-CD19_Antibody .
Thanks and best of Luck for whats coming
you can go on and on - WHERE IS YOUR "PRESCRIPTION"?
Consult Dr Fauci......
Systrom's Keynote Address Kicks off IACFS/ME ME/CFS and Long-COVID Conference
https://www.healthrising.org/blog/2022/07/29/systrom-keynote-iacfs-me-conference-long-covid/
A lot of interesting information and a mention of amyloidosis.
Please Excuse my ignorance as a mere non-Scientist/MD/Phd, but I Could Care Less about "Research"
At this point Who Cares? Perhaps the 5 or 6 dead doctors within 1 week in Canada after getting their 4th Jab would care. I Don't. Never "trust" Gov Pharma ever again. I never did, No VaXXXes Covid or Flu.
Wondrous Walter, HUGE thanks for summarizing and sharing all of your brilliant research. " In conclusion, based on these data it could be hypothesized that the presence of a monoclonal spike during the inflammatory phase could reflect the degree of immune hyperactivation in patients with severe COVID-19."
Also, apologies if you discussed this PREPRINT posted on July 29th.
https://www.medrxiv.org/content/10.1101/2022.07.26.22278002v1
SARS-CoV-2 infection is associated with anti-desmoglein 2 autoantibody detection
" Our results reveal the potential for DSG2 protein and autoimmunity to DSG2 to contribute to unexpected pathologies associated with COVID-19 infection."