Looks like you can buy RANTES for $225 USD from STEMCELL Technologies ... https://www.stemcell.com/products/human-recombinant-rantes-ccl5.html
Stemcell
Human RANTES | STEMCELL Technologies
RANTES recruits a variety of leukocytes into inflammatory sites, including T cells, macrophages, eosinophils, and basophils.
The functional genomic analysis gives us deep insight into inflammation from toxins like molds (citrinin for example), glyphosate and other pesticides, plastics, EMFs, and aluminum and other metals ... to name some of the toxins shown in those diagrams above. In functional health coaching, we find ways to reduce those stressors, improve nutrients to dampen inflammation and support weaknesses in genes (enzymes) involved in detoxification. The aim is to rebalance immune responses that may be in a negative feedback loop of perpetual inflammation.
For anyone suffering from ‘long haul COVID’ or post-injection sickness and vaccine injury, we will look at these enzymes very closely: TNF, SIRT1, HMOX, NRF2, KEAP1, NOX (NADPH oxidase), NOS and BH4 (folate), IL6, SOD/CAT, FADS, KIT as well as histamine receptor and clearance genes (HNMT, DAO, MOA).
I posted a while back a paper showing that people with up-regulating variants in IL6 and ACE would respond badly to spike proteins (glycoproteins) which are said to be in the mRNA shots. We still do not know what individuals are receiving in the injections, and we still do not have a truthful test for these glycoproteins in a person.
If you have had the “vaccine(s)” we will first look at the genes (enzymes), nutrients and exacerbating toxins associated with RANTES (see above posts on RANTES).
Medications for so-called ‘blood diseases’ (ACE inhibitors, statins) and shots for the flu and other non-sense are toxins that deplete nutrients like magnesium and cholesterol and/or contain toxic adjuvants like aluminum which blocks the making of BH4 (not good, see post below); these ‘medications’ will be factored in the analysis as toxins. The mRNA genetic code for the spike protein is said to be wrapped in a glycol called PEG. Glycol is a precursor to acrolein, another toxin about which I posted above.
I posted a while back a paper showing that people with up-regulating variants in IL6 and ACE would respond badly to spike proteins (glycoproteins) which are said to be in the mRNA shots. We still do not know what individuals are receiving in the injections, and we still do not have a truthful test for these glycoproteins in a person.
If you have had the “vaccine(s)” we will first look at the genes (enzymes), nutrients and exacerbating toxins associated with RANTES (see above posts on RANTES).
Medications for so-called ‘blood diseases’ (ACE inhibitors, statins) and shots for the flu and other non-sense are toxins that deplete nutrients like magnesium and cholesterol and/or contain toxic adjuvants like aluminum which blocks the making of BH4 (not good, see post below); these ‘medications’ will be factored in the analysis as toxins. The mRNA genetic code for the spike protein is said to be wrapped in a glycol called PEG. Glycol is a precursor to acrolein, another toxin about which I posted above.
Heather Rae, Functional Health Practitioner pinned «For anyone suffering from ‘long haul COVID’ or post-injection sickness and vaccine injury, we will look at these enzymes very closely: TNF, SIRT1, HMOX, NRF2, KEAP1, NOX (NADPH oxidase), NOS and BH4 (folate), IL6, SOD/CAT, FADS, KIT as well as histamine receptor…»
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/