Keep in mind that this experiment (covid) was conducted on a population that is widely vitamin D deficient. Against that backdrop, the final common path of covid and covid vax injuries is harmful inflammation exacerbated by dysfunctional vitamin D deficient immune systems. It’s nice to know how the spike protein is killing us but more important to know how to prevent it…take your vitamin D.
Ironic you say that, I have been a proponent of Vitamin D for... well, since the start and a new paper (I will cover it tomorrow) will cement that once and for all.
Vitamin D will most certainly help with recovery, regardless where the initial damage came from.
Does this suggest a need to add some dysbiosis mitigation supps to the stack? Probiotics, tryptophan, colustrum right when infected or after jabbed to prevent escalation?
I can say i personally had nasty reaction to omicron despite getting delta a few months prior. NAC and rest of stack wasnt helping it but big dose of colustrum had me 100% in less than a day. I don't think it was coincidence.
Interesting. My DH is just getting over omicron having never been vaxxed or had previous covid. He has some intestinal issues - irritable bowel - and did get more GI problems then anyone else I know that has had Covid. I made him Chinese Turkey porridge which has seaweed in it and he started to feel better shortly afterward - especially the GI effects. Possibly just anecdotal, but seaweed has pre-biotics so possibly helpful. His elderly mother has it now - also has some irritable bowel problems and is having significant GI problems. I sent her some porridge but she hasn't had any yet. Tomorrow I will make sure she eats some!
Wow! What amazing research and journalism. We all need to understand what is happening here. The vaccine is designed to immunize us by entering the cell and getting our ribosomes to produce spike protein that provoke an antigenic response. But the spike is itself an antigen that provoked inflammation and thrombosis. Wow! Scary! Set aside the bacteriophage, dysbiosis and reverse transcription. WTF! Monstrous and targeted to the elderly and immune senescence, but hangs around for years, like shingles, waiting to strike. No wonder Xi has zero-Covid policy.
Hello John Paul... This may or may not be something...
I consider this conference abstract from late 2021 to be a critical data point in building a big picture view of what's going on with these jabs. Although other commentators have started to use other data to suggest that everyone getting these shots is sustaining at least some low level of sub-clinical heart damage, the data in this abstract very clearly showed this, and the most elevated signal of all (in the suite of heart attack predictive blood tests called PULS) was Hepatocyte Growth Factor, or HGF. This paper followed the PULS results for 566 patients in a cardiology practice, baselining them before and testing again after double jabbing. The results were astounding, as imputed (i.e. algorithmically determined by the nine or so underlying PULS-specified blood tests) 5-year projected heart attack risk went from a mean of 11% --> 25% post jabs!!! HGF is associated with, i.e. plays a directing role in, T-cell infusion into heart tissue
Anyway, since HGF was among the most elevated of the component tests, I have been researching it over time. It is known to be stimulated by antigens in heart tissue... so it may be as straightforward as spike protein in the heart endothelium... but then I found this;
"To identify physiologic sites of T cell priming in the presence of HGF, we analyzed and compared the production of HGF mRNA by a number of murine tissues, including liver and heart, both in steady-state conditions and 24 hr after the injection of 100 μg LPS. As shown in Figures 3A–3C, in addition to the liver, heart parenchyma was found to express HGF mRNA, particularly in inflammatory settings provoked by endotoxin. Immunohistochemical analysis confirmed that this cytokine is constitutively present in low amounts in cardiac tissue, and it is upregulated by inflammatory stimuli induced by LPS (Figure 3C). In addition, mRNA transcripts for the chemokine CXCL10, but not CCL4 or CCR4 ligands, were found induced in inflamed cardiac tissue (Figure 3D)."
If the wonderful, immune-evading, pseudo-uridine protected spike is transporting LPS... that may be another means by which the heart tissue inflammation cycle kicks off.
Remarkable finding. I took the liberty to screenshot and share this, with your name in the screenshot, giving you proper credits.
For a possible byproduct of engineering the Spike Protein, this is ending up being one of the biggest backfires in human history. Imagine creating a protein for whatever reason and a unforseen result is your protein binding to the most toxic endotoxin know to man.
Thank you for the attribution on Twitter John Paul.. I may actually join now that it's in better hands. Regarding this hypothesis, I am now wondering whether the seeming usefulness of antibiotics in many of the early treatment protocols could be acting to kind of starve the beast, limiting the LPS available for the spike to grab onto? Anecdotally, when one of the Omicrons ripped through my totally unvax'ed household in June of this year, my 12 year old daughter had a smoking fever, up to 103. Maybe it was just her young, reactive immune system doing it's thing... but my wife and I, who got sick in the next week, each used full Zelenko +, i.e. Z-pack. I had literally no fever, my wife very mild.
Phages as new human viral pathogens a la the Tetz researchers?
"Here, for the first time, we presented the concept of bacteriophages as human pathogens, implying phages as previously overlooked factors that might be associated with human diseases. This concept adds phages and phagobiota to the growing list of factors associated with human health, and moreover suggests that bacteriophages and the alteration of their abundances may be a target for therapeutic intervention. Substantial additional experimental work is required to distinguish which bacteriophages contribute to the development of human diseases and to evaluate the roles of human’s genetic and microbiota susceptibilities therein."
By the way, from March, There is the study, Hijacking time: How Ophiocordyceps fungi could be using ant host clocks to manipulate behavior. https://pubmed.ncbi.nlm.nih.gov/35103986/
This was a great comment, thank you, this is in line with what I will try to conveil in Part II, but yes, I do agree that the Spike and virus enter and interact with bacteria, it has been a observation of mine since 2020 (you can find the screenshots around here... somewhere lol).
Interesting you share that Ophiocordyceps paper, I shared one about how a fungal infection manipulate the behavior of ants (by using kynurenine and its metabolites) to create a zombie-like state.
Immunological Mechanisms Explaining the Role of Vaccines, IgE, Mast Cells, Histamine, Elevating Ferritin, IL-6, D-dimer, VEGF Levels in COVID-19 and Dengue, Potential Treatments Such as Mast Cell Stabilizers, Antihistamines: Predictions and Confirmations
This is insanity, from my next review - researchers actually used LPS to deliberately induce brain injury:
Wang X, Yu JY, Sun Y, Wang H, Shan H, Wang S. Baicalin protects LPS-induced blood-brain barrier damage and activates Nrf2-mediated antioxidant stress pathway. Int Immunopharmacol. 2021 Jul;96:107725. doi: 10.1016/j.intimp.2021.107725. Epub 2021 May 28. PMID: 34162131.
LPS is one of the common lab tools that are used to provoke immune response or cell injury / death, and then see what happens to whatever it is that your research question is testing. For instance, protective benefit of X rescued Y% of cells (in the presence of LPS).
Another place that LPS pops up is the history of vaccine research, investigating its potential as an adjuvant to provoke an immune response. Vaccines are optimized to induce a strong immune response with the idea of achieving lasting immune memory, and also to avoid issues that were there in the past when the antigen was too weak, thus requiring multiple doses (good we solved that).
In one of the Kanduc articles that DoorlessCarp's entry on autoimmune motifs referenced, Kanduc found quite a few classic immunogenic peptides hidden in Spike. Classic, being things that have again been used for decades in lab work or vaccine research because, like LPS, the body recognizes these Pathogen-Associated Molecular Patterns and has an innate strong immune response to them. These triggers are added to something when you want to train the body to attack it: for instance tetanus-toxin paired with HCG or other reproductive sequences in the case of anti-fertility vaccines, which Kanduc also found in the Spike.
I wonder if LPS or a derivative played a role in the development of Spike or in the vaccines, or if it's something random like size and charge that lets it get stuck in there.
John Paul observes that Spike seems to have some bacterial properties. Maybe this comes from incorporation of bacterial sequences that the body responds to, akin to PAMPs like LPS? It's my understanding that at this point in time, we're not as advanced in being able to create elegant polysaccharide / glycan etc. structures the way that we can cut-and-paste peptides. So using antigenic peptide motifs could be a practical way to get around that set-back?
"The 29 pentapeptides common to SARS-CoV-2 spike gp and tumor-suppressor proteins ...are not only present in immunoreactive epitopes ...but, in addition, almost all of them (24 out of 29) are also present in microbial organisms such as Bordetella pertussis , C. diphtheriae , C. tetani , H. influenzae , and N. meningitides ( Table 3 )."
JC Couey thinks that one of the reasons the new bivalent Deathvax ™️ includes the extinct Wuhan variant is to generate an immune response as Omicron evolved away from some of these, as all that matters for the talking heads is antibodies, antibodies and yet more (non neutralizing) antibodies...
That the immunogens are worse than the disease is just collateral damage.
Do you have ties to a lab where you can test some of your ideas?
Far-ahead / novel thinkers are basically stuck with that frustration and it won't change, wherever you apply your mind. Managing that potential is hard.
Is that a joke ? I have said time and time again I am just a dude, a nobody. But that was written based on scientific evidence available at the time, not a opinion, so there is that too.
I have covered the HIV sequences, but the malaria germ is... crazy talk I guess. The HIV sequences are small parts of HIV that DO in fact have functional roles.
Whats the lowdown on HIV and RSV - were they engineered too? I think I saw a guy on MccairnDojo say they both came from 1970s gainnof function of monkey viruses or such. But i may have that wrong.
In Leonard Horowitz's 1996 book _Emerging Viruses: AIDS & Ebola_, he explores the history and lab-creation of the HIV bioweapon. In Chapter 1, we read how the US's Deputy Director of the Department of Defence, per the Congressional Appropriations Hearings in 1969 on the development of immune-system destroying agents for biological warfare, opined that at a total cost of $10 million, within 10 years they could likely produce what was desired -- "a new infective microorganism" that "might be refractory to the immunological and therapeutic processes upon which we depend to maintain our relative freedom from infectious disease." That transcript was classified but later obtained via FOI request.
According to the 1988 Strecker Memorandum, "[t]he United States Defence Department requested and got $10 million to make the AIDS virus in labs as a political/ethnic weapon to be used mainly against Blacks. The feasibility program and labs were to have been completed by 1974-1975; the virus between 1974-1979. The World Health Organization started to inject AIDS-laced smallpox vaccine into over 100 million Africans (population reduction) in 1977. And over 2000 young white male homosexuals (Trojan horse) in 1978 with the hepatitis B vaccine through the Centers for Disease Control/New York Blood Center."
Dr Isaac Elias researches modified citrus pectin to lower galectin-3. A search of his name will bring up many interviews he has done on subject. His company EcoNugenics sell his version of modified citrus pectin called Pectasol. Just had my galectin levels drawn curious to see what they are had Covid in April.
There are other ways to modulate Galectin-3, synergestic and "cheaper", I will cover them on my Galectin substack, well, just explain they do that, but I already covered it before in some ways, they are part of my "stack".
I’ll look forward to it. I’ve also seen some preliminary data indicating that folic acid disrupts attachment of the spike protein to the furin binding site. So that could be additive to your discussion of natto.
I’m probably way off, but could any of this explain the “extremely unusual” autopsy findings in the congressman’s daughter’s (SADS victim) blood culture? Clostridium sordellii and septicum? Even if they didn’t consider it to be a contributing factor?
Keep in mind that this experiment (covid) was conducted on a population that is widely vitamin D deficient. Against that backdrop, the final common path of covid and covid vax injuries is harmful inflammation exacerbated by dysfunctional vitamin D deficient immune systems. It’s nice to know how the spike protein is killing us but more important to know how to prevent it…take your vitamin D.
Ironic you say that, I have been a proponent of Vitamin D for... well, since the start and a new paper (I will cover it tomorrow) will cement that once and for all.
Vitamin D will most certainly help with recovery, regardless where the initial damage came from.
Does this suggest a need to add some dysbiosis mitigation supps to the stack? Probiotics, tryptophan, colustrum right when infected or after jabbed to prevent escalation?
I can say i personally had nasty reaction to omicron despite getting delta a few months prior. NAC and rest of stack wasnt helping it but big dose of colustrum had me 100% in less than a day. I don't think it was coincidence.
Interesting. My DH is just getting over omicron having never been vaxxed or had previous covid. He has some intestinal issues - irritable bowel - and did get more GI problems then anyone else I know that has had Covid. I made him Chinese Turkey porridge which has seaweed in it and he started to feel better shortly afterward - especially the GI effects. Possibly just anecdotal, but seaweed has pre-biotics so possibly helpful. His elderly mother has it now - also has some irritable bowel problems and is having significant GI problems. I sent her some porridge but she hasn't had any yet. Tomorrow I will make sure she eats some!
3x shorter flu with it vs flu vax so makes sense to work here too
Yes. It does, Omicron has a lesser degree of this, but given how fast it replicates, it indeed will cause this to some level.
Wow! What amazing research and journalism. We all need to understand what is happening here. The vaccine is designed to immunize us by entering the cell and getting our ribosomes to produce spike protein that provoke an antigenic response. But the spike is itself an antigen that provoked inflammation and thrombosis. Wow! Scary! Set aside the bacteriophage, dysbiosis and reverse transcription. WTF! Monstrous and targeted to the elderly and immune senescence, but hangs around for years, like shingles, waiting to strike. No wonder Xi has zero-Covid policy.
Hello John Paul... This may or may not be something...
I consider this conference abstract from late 2021 to be a critical data point in building a big picture view of what's going on with these jabs. Although other commentators have started to use other data to suggest that everyone getting these shots is sustaining at least some low level of sub-clinical heart damage, the data in this abstract very clearly showed this, and the most elevated signal of all (in the suite of heart attack predictive blood tests called PULS) was Hepatocyte Growth Factor, or HGF. This paper followed the PULS results for 566 patients in a cardiology practice, baselining them before and testing again after double jabbing. The results were astounding, as imputed (i.e. algorithmically determined by the nine or so underlying PULS-specified blood tests) 5-year projected heart attack risk went from a mean of 11% --> 25% post jabs!!! HGF is associated with, i.e. plays a directing role in, T-cell infusion into heart tissue
https://www.ahajournals.org/doi/abs/10.1161/circ.144.suppl_1.10712
Anyway, since HGF was among the most elevated of the component tests, I have been researching it over time. It is known to be stimulated by antigens in heart tissue... so it may be as straightforward as spike protein in the heart endothelium... but then I found this;
https://www.cell.com/immunity/fulltext/S1074-7613(15)00212-5
"To identify physiologic sites of T cell priming in the presence of HGF, we analyzed and compared the production of HGF mRNA by a number of murine tissues, including liver and heart, both in steady-state conditions and 24 hr after the injection of 100 μg LPS. As shown in Figures 3A–3C, in addition to the liver, heart parenchyma was found to express HGF mRNA, particularly in inflammatory settings provoked by endotoxin. Immunohistochemical analysis confirmed that this cytokine is constitutively present in low amounts in cardiac tissue, and it is upregulated by inflammatory stimuli induced by LPS (Figure 3C). In addition, mRNA transcripts for the chemokine CXCL10, but not CCL4 or CCR4 ligands, were found induced in inflamed cardiac tissue (Figure 3D)."
If the wonderful, immune-evading, pseudo-uridine protected spike is transporting LPS... that may be another means by which the heart tissue inflammation cycle kicks off.
Remarkable finding. I took the liberty to screenshot and share this, with your name in the screenshot, giving you proper credits.
For a possible byproduct of engineering the Spike Protein, this is ending up being one of the biggest backfires in human history. Imagine creating a protein for whatever reason and a unforseen result is your protein binding to the most toxic endotoxin know to man.
Thank you for the attribution on Twitter John Paul.. I may actually join now that it's in better hands. Regarding this hypothesis, I am now wondering whether the seeming usefulness of antibiotics in many of the early treatment protocols could be acting to kind of starve the beast, limiting the LPS available for the spike to grab onto? Anecdotally, when one of the Omicrons ripped through my totally unvax'ed household in June of this year, my 12 year old daughter had a smoking fever, up to 103. Maybe it was just her young, reactive immune system doing it's thing... but my wife and I, who got sick in the next week, each used full Zelenko +, i.e. Z-pack. I had literally no fever, my wife very mild.
Thank you so much for the primer (more hard science for dumbo me, YIKES! )
Really, another great post!!!
Pursuant to your assertion that the spike could interact with, inter alia, bacteria.....
All I could think of was the Tetz researchers:
https://www.mdpi.com/2076-2607/6/2/54/htm
Spike enters bacteria?
Phages as new human viral pathogens a la the Tetz researchers?
"Here, for the first time, we presented the concept of bacteriophages as human pathogens, implying phages as previously overlooked factors that might be associated with human diseases. This concept adds phages and phagobiota to the growing list of factors associated with human health, and moreover suggests that bacteriophages and the alteration of their abundances may be a target for therapeutic intervention. Substantial additional experimental work is required to distinguish which bacteriophages contribute to the development of human diseases and to evaluate the roles of human’s genetic and microbiota susceptibilities therein."
Plus, this"https://lightonlight.education/ italian-researchers-vaccines-will-not-work-because-sars-cov-2-is-also-entering-bacteria
By the way, from March, There is the study, Hijacking time: How Ophiocordyceps fungi could be using ant host clocks to manipulate behavior. https://pubmed.ncbi.nlm.nih.gov/35103986/
This was a great comment, thank you, this is in line with what I will try to conveil in Part II, but yes, I do agree that the Spike and virus enter and interact with bacteria, it has been a observation of mine since 2020 (you can find the screenshots around here... somewhere lol).
Interesting you share that Ophiocordyceps paper, I shared one about how a fungal infection manipulate the behavior of ants (by using kynurenine and its metabolites) to create a zombie-like state.
Immunological Mechanisms Explaining the Role of Vaccines, IgE, Mast Cells, Histamine, Elevating Ferritin, IL-6, D-dimer, VEGF Levels in COVID-19 and Dengue, Potential Treatments Such as Mast Cell Stabilizers, Antihistamines: Predictions and Confirmations
https://europepmc.org/article/PPR/PPR241819
The mRNA vaccines are contaminated with endotoxins.
https://vinuarumugham.substack.com/p/leaked-eu-pfizer-agreement-reveals
This is insanity, from my next review - researchers actually used LPS to deliberately induce brain injury:
Wang X, Yu JY, Sun Y, Wang H, Shan H, Wang S. Baicalin protects LPS-induced blood-brain barrier damage and activates Nrf2-mediated antioxidant stress pathway. Int Immunopharmacol. 2021 Jul;96:107725. doi: 10.1016/j.intimp.2021.107725. Epub 2021 May 28. PMID: 34162131.
https://www.sciencedirect.com/science/article/pii/S1567576921003611
LPS is one of the common lab tools that are used to provoke immune response or cell injury / death, and then see what happens to whatever it is that your research question is testing. For instance, protective benefit of X rescued Y% of cells (in the presence of LPS).
Another place that LPS pops up is the history of vaccine research, investigating its potential as an adjuvant to provoke an immune response. Vaccines are optimized to induce a strong immune response with the idea of achieving lasting immune memory, and also to avoid issues that were there in the past when the antigen was too weak, thus requiring multiple doses (good we solved that).
In one of the Kanduc articles that DoorlessCarp's entry on autoimmune motifs referenced, Kanduc found quite a few classic immunogenic peptides hidden in Spike. Classic, being things that have again been used for decades in lab work or vaccine research because, like LPS, the body recognizes these Pathogen-Associated Molecular Patterns and has an innate strong immune response to them. These triggers are added to something when you want to train the body to attack it: for instance tetanus-toxin paired with HCG or other reproductive sequences in the case of anti-fertility vaccines, which Kanduc also found in the Spike.
I wonder if LPS or a derivative played a role in the development of Spike or in the vaccines, or if it's something random like size and charge that lets it get stuck in there.
John Paul observes that Spike seems to have some bacterial properties. Maybe this comes from incorporation of bacterial sequences that the body responds to, akin to PAMPs like LPS? It's my understanding that at this point in time, we're not as advanced in being able to create elegant polysaccharide / glycan etc. structures the way that we can cut-and-paste peptides. So using antigenic peptide motifs could be a practical way to get around that set-back?
Potentially antigenic sequences found in Spike are listed in Table 3 by Kanduc (2021, doi: 10.1055/s-0041-1735590) on DoorlessCarp's entry (https://doorlesscarp953.substack.com/p/autoimmune-disorders-covid-19-spike),
"The 29 pentapeptides common to SARS-CoV-2 spike gp and tumor-suppressor proteins ...are not only present in immunoreactive epitopes ...but, in addition, almost all of them (24 out of 29) are also present in microbial organisms such as Bordetella pertussis , C. diphtheriae , C. tetani , H. influenzae , and N. meningitides ( Table 3 )."
JC Couey thinks that one of the reasons the new bivalent Deathvax ™️ includes the extinct Wuhan variant is to generate an immune response as Omicron evolved away from some of these, as all that matters for the talking heads is antibodies, antibodies and yet more (non neutralizing) antibodies...
That the immunogens are worse than the disease is just collateral damage.
I literally wrote why, and how months ago =(.
Do you have ties to a lab where you can test some of your ideas?
Far-ahead / novel thinkers are basically stuck with that frustration and it won't change, wherever you apply your mind. Managing that potential is hard.
Is that a joke ? I have said time and time again I am just a dude, a nobody. But that was written based on scientific evidence available at the time, not a opinion, so there is that too.
:)
Well, when you spent so long creating a masterpiece, would be a shame for it to fade away.
Luc Montagnier said spike contains HIV sequences and a "malaria germ" and I keep wondering what that means...
I have covered the HIV sequences, but the malaria germ is... crazy talk I guess. The HIV sequences are small parts of HIV that DO in fact have functional roles.
Whats the lowdown on HIV and RSV - were they engineered too? I think I saw a guy on MccairnDojo say they both came from 1970s gainnof function of monkey viruses or such. But i may have that wrong.
In Leonard Horowitz's 1996 book _Emerging Viruses: AIDS & Ebola_, he explores the history and lab-creation of the HIV bioweapon. In Chapter 1, we read how the US's Deputy Director of the Department of Defence, per the Congressional Appropriations Hearings in 1969 on the development of immune-system destroying agents for biological warfare, opined that at a total cost of $10 million, within 10 years they could likely produce what was desired -- "a new infective microorganism" that "might be refractory to the immunological and therapeutic processes upon which we depend to maintain our relative freedom from infectious disease." That transcript was classified but later obtained via FOI request.
According to the 1988 Strecker Memorandum, "[t]he United States Defence Department requested and got $10 million to make the AIDS virus in labs as a political/ethnic weapon to be used mainly against Blacks. The feasibility program and labs were to have been completed by 1974-1975; the virus between 1974-1979. The World Health Organization started to inject AIDS-laced smallpox vaccine into over 100 million Africans (population reduction) in 1977. And over 2000 young white male homosexuals (Trojan horse) in 1978 with the hepatitis B vaccine through the Centers for Disease Control/New York Blood Center."
Read the book here: https://archive.org/details/emergingvirusesa00horo
Also, see: https://larouchepub.com/eiw/public/1997/eirv24n44-19971031/eirv24n44-19971031_018-origins_of_the_aids_virus_accide.pdf
Nick Petosky does a fantastic 30 min presentation on this subject if reading books is too hard. 😁https://rumble.com/v24j3qs-medical-anthropology-presentation-003.html
Dr Isaac Elias researches modified citrus pectin to lower galectin-3. A search of his name will bring up many interviews he has done on subject. His company EcoNugenics sell his version of modified citrus pectin called Pectasol. Just had my galectin levels drawn curious to see what they are had Covid in April.
There are other ways to modulate Galectin-3, synergestic and "cheaper", I will cover them on my Galectin substack, well, just explain they do that, but I already covered it before in some ways, they are part of my "stack".
Would be curious too.
I’ll look forward to it. I’ve also seen some preliminary data indicating that folic acid disrupts attachment of the spike protein to the furin binding site. So that could be additive to your discussion of natto.
I’m probably way off, but could any of this explain the “extremely unusual” autopsy findings in the congressman’s daughter’s (SADS victim) blood culture? Clostridium sordellii and septicum? Even if they didn’t consider it to be a contributing factor?
Recall Toxic Shock Syndrome....
https://pechse.com/what-disease-does-clostridium-sordellii-cause/
"It’s typically connected with tampon usage in girls"