Heather Rae, Functional Health Practitioner
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TERRAIN MODEL health coach based in Jalisco Mexico
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I was just banned from Steve Kirsch’s telegram account which was created to address ‘Twitter censorship’. My comment was about being banned from Telegram channels. Oh, the sad irony. 😏
HAIR LOSS ... THE HORMONE PERSPECTIVE
The main idea is to support the production of carbon dioxide through the mitochondria as shown [above] (i.e., oxidative metabolism).” ~ Danny Roddy
THE CDC & ARTICLE 3 JUDGES ... DOES ANY JUDGE HAVE JURISDICTION TO MANDATE “PUBLIC HEALTH” POLICIES FOR CITIZENS OF THE (NON-CORPORATE) UNITED STATES?
“The real issue is whether the CDC had legal authority to issue such an edict in the first place – and if so, did it issue the rule as prescribed by law. The answer to both questions is: no.”
But here is another question: does Judge Kathryn Mizelle have jurisdiction in this case ... is she an Article 3 judge who would therefore have legal authority outside DC and US territories? The answer is: no. She is acting under color of law but has no judicial authority over you, me or quite likely, the CDC which definitely has no authority over anybody.
https://townhall.com/columnists/philipholloway/2022/04/25/the-cdcs-mask-mandate-is-dead-and-wont-be-back-heres-why-n2606292
ACROLEIN & ALDH ENZYME VARIANTS
"Toxicokinetics
Following inhalation exposure, acrolein can be deposited in the nasal cavity and respiratory tract, where the majority is retained irreversibly due to its high tissue reactivity. Eventually, some traces can be absorbed into the blood and be distributed throughout the body. The uptake of acrolein in the nasal cavity is influenced by its solubility and inspiratory flow rate. Glutathione conjugation is the dominant detoxification
pathway for acrolein.
Further metabolism takes place in the liver resulting in glycidaldehyde and a number of metabolites that can be excreted in the urine as well as some unchanged acrolein. Most of the free acrolein is excreted in the exhaled breath."
Forwarded from The Solari Report
Solari Report: The War on Food



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Catherine will be discussing the state of the global food supply and the war on food with Del Bigtree on Highwire on April 28th 11am pst/ 2pm est.


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The Frugal Garden, our side-alley vegetable garden, is sprouting seeds and we eagerly await a compost tube and worms!
RANTES & INFLAMMATION .... The graphics below illustrate how enzymes (genes) participate in conditions such as Lyme, mycotoxins, Mast Cell Activation Syndrome (histamine), and ‘COVID’ related blood disorders.
RANTES (CCL5) which stands for Regulated upon Activation, Normal T cell and Expressed and Secreted is a chemokine secreted by platelets, so it has everything to do with blood (think clotting). It is a protein that is part of interleukin 8 cytokine family. It modulates and signals release of inflammatory immune cells from the bloodstream into tissues. You’ll need it to heal a cut, but in excess, driven by toxins and unregulated by variants in certain enzymes (genes) and nutrient deficiencies, too much of a good thing can go terribly wrong (like atherosclerosis, strokes and liver disease).
RANTES looks a lot like a country on the west coast of the African continent, and ‘omicron’ looked like the African continent itself. Go figure.
REAL FOOD CHANGES EVERYTHING
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.
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…»