Wow! This is great reporting and cutting edge stuff, but you do not draw the spiders web together into a coherent pathology. The connecting tissue, I believe is franktalkine released from monocytes that cause permanent remodelling of endothelium and microvasculature via NFKb inflammasome and tau pathologies. Also, platelets have ACE-2 receptors on them and are generated from the lungs. Activation of platelets leads to massive histamine release.
Further unification of spike protein microvascular disease and tauopathy: TLR-2. I believe I can now fully explain why Tauopathies are occurring in association with SARS-CoV-2 and its Spike Protein. Radiation PERMANENTLY alters NF-kB expression and reprograms endothelial cells resulting in vascular disease. The very same activation also increases the effects of ALL risk factors associated with Alzheimer's Disease. (What's a better way to collapse a medical system than with incurable brain disease.) Of course, SARS-CoV-2 is NOT radiation. However the Spike Protein MIMICKS THE EFFECTS OF RADIATION EXACTLY including activation of NF-kB via TLR-2. This also explains why the elderly are far more at risk of IMMEDIATE severe disease and death. Young mice have virtually NO NF-kB levels in their Hypothalamus! With links to studies. Treatment in the comments. NAC dissolves blood clots but also amyloid plaque. https://wmcresearch.substack.com/p/further-unification-of-spike-protein?utm_source=email
"Dr Hervé Seligmann said that, in his opinion, the transfer of spike protein/accompanying substances from vaccinated to unvaccinated can occur through all fluids excreted by the vaccinated: mucus (cough or even normal breathing), sexual intercourse, breast milk ..."
Wow! This is great reporting and cutting edge stuff, but you do not draw the spiders web together into a coherent pathology. The connecting tissue, I believe is franktalkine released from monocytes that cause permanent remodelling of endothelium and microvasculature via NFKb inflammasome and tau pathologies. Also, platelets have ACE-2 receptors on them and are generated from the lungs. Activation of platelets leads to massive histamine release.
Did you read Dr Chestnut's post on tau?
Further unification of spike protein microvascular disease and tauopathy: TLR-2. I believe I can now fully explain why Tauopathies are occurring in association with SARS-CoV-2 and its Spike Protein. Radiation PERMANENTLY alters NF-kB expression and reprograms endothelial cells resulting in vascular disease. The very same activation also increases the effects of ALL risk factors associated with Alzheimer's Disease. (What's a better way to collapse a medical system than with incurable brain disease.) Of course, SARS-CoV-2 is NOT radiation. However the Spike Protein MIMICKS THE EFFECTS OF RADIATION EXACTLY including activation of NF-kB via TLR-2. This also explains why the elderly are far more at risk of IMMEDIATE severe disease and death. Young mice have virtually NO NF-kB levels in their Hypothalamus! With links to studies. Treatment in the comments. NAC dissolves blood clots but also amyloid plaque. https://wmcresearch.substack.com/p/further-unification-of-spike-protein?utm_source=email
Yes, I did read it. L-Lysine Acetyl Salicylate-Glycine inhibits inflammasome remodelling. Also try NRF2 by Pure.
Yes, and cyproheotadine.
Is that why anti histamines are useful as a treatment?
Thank you!
Do you feel that EXOSOMES may be play here?
http://www.nakim.org/israel-forums/viewtopic.php?t=270992
"Dr Hervé Seligmann said that, in his opinion, the transfer of spike protein/accompanying substances from vaccinated to unvaccinated can occur through all fluids excreted by the vaccinated: mucus (cough or even normal breathing), sexual intercourse, breast milk ..."
Thankyou for your research. The masses need to read this!
Feel free to share the link with a bit of description with it. I find a description is helpful to busy people to give them a reason to read the link.
Thank you. This is valuable information that needs to be spread far and wide.