DEPLETED BH4 can cause the cell to make superoxide, a damaging molecule, and in turn, peroxynitrite about which I have posted earlier in reference to ‘itis’ conditions (caused by peroxynitrite) and reduced by DMSO. Note that there is no evidence of a thing called SARS COV2 in a human body. The mechanisms of whatever is making people sick with ‘long haul COVID’ symptoms like ferroptosis (also referenced in a previous post) can be sleuthed out using functional genomics.
Forwarded from Heather Rae, Functional Health Practitioner
Parking this nugget here for future reference. What is LONG HAUL COVID and how to treat? It looks to be a combination of MAST CELL ACTIVATION SYNDROME, MACROPHAGE ACTIVATION SYNDROME (excess macrophages) and ANTI-PHOSPHOLIPID SYNDROME (lipid peroxidation, disruption of phospholipids which looks a lot like LUPUS/AUTOIMMUNITY), excess intravascular iron (FERROPTOSIS) which causes excess GLUTAMATE and blocks CYSTEINE which damages the cell (lipid peroxidation)... Use vitamin E (for ferroptosis, selenium for GPX4. Nrf2 support, NAC/cysteine .. lactoferrin, skullcap.
“Insufficient BH4 leads to the uncoupling of the inducible Nitric Oxide Synthase (iNOS) and thereby initiates self-perpetuating oxidative stress with excess superoxide and peroxynitrite.”
“Insufficient BH4 impedes and may even prevent the downregulation of this hyperinflammatory oxidative stress and the return to oxidative homeostasis.”
Aluminum blocks the making of BH4 (tetrahydrobiopterin). It is in chemtrails, personal care products, cookware, pharmaceuticals and canned food. The flu shot contains aluminum. In functional genomics, we look at genes (enzymes) associated with BH4 (DHFR,QDPR, MTHFR, SUCLA1, SPR, PTS, and GCH1) ... and NOS.
Forwarded from Heather Rae, Functional Health Practitioner
Nitric Oxide Indicator Strips | HumanN
https://shop.humann.com/products/nitric-oxide-indicator-strips?subscription=1&variant=19861378072687
https://shop.humann.com/products/nitric-oxide-indicator-strips?subscription=1&variant=19861378072687
FUNGUS (CITRININ. MEVINOLIN), STATINS &
THE CHOLESTEROL MYTH ... connecting the dots.
One of the several experiences that brought me to functional health was the death of my cocker spaniel as a result of “auto-immune hemolytic anemia” that was caused by a vaccine containing penicillin (lepto). It was contraindicated for Buford but the vet gave it to him just the same. It took me three years to talk about his death without immense grief. I had killed my dog by following medical advice.
Years later, in a course on integrative medicine, I learned that penicillin drugs can cause the same disease in people. I sat frozen and stunned. “They know!”
About then, my father began to lose his balance. He had been robust but was faltering. I began to research the blood medications he was taking ... “the trif***ta”. I learned about depletion of magnesium and quinones and cholesterol (brain and neuro food) and the source of statins.
Statins (HMG CoA reductase inhibitors, an enzyme blocker), like lepto and many other pharma drugs derive from mycotoxins (fungi, molds). Statins were originally isolated from Penicilllium citrinum in 1976 by a Japanese researcher named Endo who worked in pharma. Merck set out to find its own statins and in February 1979 isolated a mold very similar to citrinin in chemical structure, called mevinolin, from the fungus Aspergillus terreus.
In a graphic above, we can see how citrinin blocks the anti-inflammatory cytokine, IL10.
In Barbara O’Neill’s presentation on vascular disease, we see what causes damage to the arteries and why cholesterol is not the problem.
In short, organized medicine prescribes a toxic fungus to block the body from making a lipid necessary for neurological health, a lipid that does not cause vascular disease (the cholesterol myth).
Barbara ONeill explains what does cause damage to the arteries and cholesterol’s role in healing that damage. You will see why she has been disgraced on Wikipedia ;)
THE CHOLESTEROL MYTH ... connecting the dots.
One of the several experiences that brought me to functional health was the death of my cocker spaniel as a result of “auto-immune hemolytic anemia” that was caused by a vaccine containing penicillin (lepto). It was contraindicated for Buford but the vet gave it to him just the same. It took me three years to talk about his death without immense grief. I had killed my dog by following medical advice.
Years later, in a course on integrative medicine, I learned that penicillin drugs can cause the same disease in people. I sat frozen and stunned. “They know!”
About then, my father began to lose his balance. He had been robust but was faltering. I began to research the blood medications he was taking ... “the trif***ta”. I learned about depletion of magnesium and quinones and cholesterol (brain and neuro food) and the source of statins.
Statins (HMG CoA reductase inhibitors, an enzyme blocker), like lepto and many other pharma drugs derive from mycotoxins (fungi, molds). Statins were originally isolated from Penicilllium citrinum in 1976 by a Japanese researcher named Endo who worked in pharma. Merck set out to find its own statins and in February 1979 isolated a mold very similar to citrinin in chemical structure, called mevinolin, from the fungus Aspergillus terreus.
In a graphic above, we can see how citrinin blocks the anti-inflammatory cytokine, IL10.
In Barbara O’Neill’s presentation on vascular disease, we see what causes damage to the arteries and why cholesterol is not the problem.
In short, organized medicine prescribes a toxic fungus to block the body from making a lipid necessary for neurological health, a lipid that does not cause vascular disease (the cholesterol myth).
Barbara ONeill explains what does cause damage to the arteries and cholesterol’s role in healing that damage. You will see why she has been disgraced on Wikipedia ;)
Forwarded from Christiane Northrup M.D (Christiane Northrup)
Paul Ehrlich’s Side-Chain Antibody Theory (1900) Part 1 – ViroLIEgy
https://viroliegy.com/2022/05/01/paul-ehrlichs-side-chain-antibody-theory-1900-part-1/
https://viroliegy.com/2022/05/01/paul-ehrlichs-side-chain-antibody-theory-1900-part-1/
FROM EHRLICH TO PATTERSON: HYPOTHETICAL THEORIES ALL. https://www.healthrising.org/blog/2021/07/21/patterson-cracked-long-covid/
Health Rising
Has Bruce Patterson Cracked Long COVID? - Health Rising
Bruce Patterson believes that not only does he know what causes long COVID but that he knows how to treat it as well. He plans next to move to chronic fatigue syndrome, fibromyalgia and Lyme Disease.
BY WHAT CRITERIA 'COVID'? And by what evidence of a 'virus'? The lack of intellectual integrity spins the mind!
"a COVID patient with a poor T-cell response was still shedding the virus 90 days after becoming infected" "Infected"? "infected' by what, exactly, since SARS COV2, an in silico computer generated fabrication, has never been found in a human body? Exposure to myriad kinds of toxins would elicit the same biochemical responses. The body does not reserve a specific cytokine response unique to a 'virus' or other toxins/poisons or stressor (like citrinim). IOW, toxins/stressors elicit the same biochemical inflammatory and detoxification responses and there is no evidence that a 'virus' is the cause.
When you see SARS COV2 or "coronavirus protein" or 'COVID-19" in these papers, replace the words with 'spike protein' and note that (*that*) is what was presumably injected into people, aong with toxic adjuvants.
"a COVID patient with a poor T-cell response was still shedding the virus 90 days after becoming infected" "Infected"? "infected' by what, exactly, since SARS COV2, an in silico computer generated fabrication, has never been found in a human body? Exposure to myriad kinds of toxins would elicit the same biochemical responses. The body does not reserve a specific cytokine response unique to a 'virus' or other toxins/poisons or stressor (like citrinim). IOW, toxins/stressors elicit the same biochemical inflammatory and detoxification responses and there is no evidence that a 'virus' is the cause.
When you see SARS COV2 or "coronavirus protein" or 'COVID-19" in these papers, replace the words with 'spike protein' and note that (*that*) is what was presumably injected into people, aong with toxic adjuvants.
LYME, ME/CFS, 'LONG HAUL COVID' ... and their overlapping inflammation markers: CCL5/RANTES, IL-2, IL-4, CCL3, IL-6, IL-10, IFN-γ, and VEGF. Is 'COVID' a novel.disease, or like AIDS, a new name for existing illnesses, repackaged and caused by a phantom 'virus'? All I can hear is kaching for IntellDX and statin pushers.
TRANSHUMANISM BEGINS with INJECTION OF MAN-MADE TOXINS (VIRUSES) and treating people as if we are computers ... just soulless bits and bytes, 0s and 1s, machines with built-in obsolescence, in constant need of genetic updates.