FOR CLARITY: those “vaccine” trials aimed to demonstrate reduction in the cold-like symptoms of a made up disease called ‘COVID’. Never did the trials aim to reduce ‘infection’ or ‘transmission’ of the purported cause of these symptoms (a ‘virus’ called SARS COV2). It is logical that these ‘vaccines’ have failed to reduce ‘infection’ or the numbers of COVID ‘cases’ -- measured via inaccurate PCR and rapid antigen ‘tests’ — as there was no virus, no variants of virus of a thing called SARS COV2, ever verified to be present in a human being. It was an invented idea, its genetic sequence contrived in a computer. Further, the ‘spike protein’ (the genetic code, purportedly of mRNA) does not equate to SARS COV2. That is a bait/switch done in nearly all PubMed papers on ‘COVID’. The spike protein is a glycoprotein (sugar/protein), as are antibodies, all theoretical. (See posts above about the history and theory behind those antibodies - against life — especially David Crowe’s papers). Virology is a fiction, like a Harry Potter series, spun out of imagination, a lucrative story of war against humanity that only ends when people, behaving like children, stop buying it. Only then, can we get on with real work of re(gaining) ownership of our mind, body, health.

DETOXIFICATION & SULFUR
(CYSTEINE/NAC, GLUTATHIONE, MSM, DMSO)
“.... we care about sulfur is because three of the liver’s Phase II Detoxification processes (rendering a toxic molecule less harmful) require sulfur. These are sulfation, glucoronidation, and glutathione-S-transferase.”
A functional genomic analysis looks at the enzymes (genes) involved in these three detoxification pathways, and other enzymes involved in detoxification, like CYP450 (Phase I), PON, NQO1.

The cause of a “sulfur sensitivity” may actually be poor enzyme (gene) activity in sulfation, excess ammonia, and a toxic burden from heavy metals.

A “Know Your DNA” and organic acids test — with professional analysis of findings — goes a long way to understanding your unique makeup and whether or not you are best served by taking supplements like NAC (cysteine) and glutathione. Because you are unique and bioindividual and protocols that work for someone else may backfire for you!

You can support sulfation and liver function through myriad simple home-based therapies like Epsom Salt (magnesium sulfate) soaks, castor oil packs, and enemas using coffee and other compounds. Home-based testing strips for sulfate, pH and nitrites are basic and useful guides.

https://www.drlaurendeville.com/ARTICLES/SULFUR-INTOLERANCE/

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.

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."

Acrolein - an overview | ScienceDirect Topics
https://www.sciencedirect.com/topics/medicine-and-dentistry/acrolein

NAC & ACROLEIN. ... this little diagram illustrates how NAC blocks death of a cell (apoptosis) when exposed to acrolein. Acrolein is a byproduct of the PEG (glycol) found in these so-called ‘vaccines’ (and vapes, btw). Perhaps this illustrates why some MDs, I am hearing, prescribe NAC for ‘COVID’ and why pharma is making moves to control NAC.

VIRUS? NO VIRUS? YOU DON’T KNOW WHAT YOU KNOW
Coppolino archived COVID’s chronology of propaganda overwhelm, perpetual contradictions, obfuscations, disembodied chaos, snow-jobbing ringer scientists creating dualistic conflict, and discrediting public statements hiding internal correspondence.
The evidence falls to the “no virus” conclusion. No isolation/purification. No test to prove existence of a ‘virus’. Just one giant shit storm.
The window to maintain credibility for the ‘virus-pushing clot-shot opponents’ is closing rapidly.
We can now get on with understanding and addressing the actual roots of chronic health conditions ... toxins, nutrient deficiencies, genetic variants, poor pH/voltage, trauma, vagus nerve disruption ....
https://drsambailey.com/videos/the-covid-chronology-with-eric-coppolino/

In the late 90s, Lois Gibbs’ nonprofit in DC assisted a citizens group I had created to fight a nuclear facility, and the public agencies which supported it for decades, as it uncontrollably released radioactive cobalt into our rural neighborhood.

“One editorial note: in my comments, the word "covid" is usually placed in quotations because its meaning is unclear. It is a byword, used and defined many ways, with its meaning evolving — usually pertaining to "whatever one was sick from or died with starting some time in November 2019." It has no distinct or remarkable symptomology or etiology (disease progression). It may be "diagnosed" with or without a diagnostic test or symptoms.” ~ Eric Coppolino

THE “COVID” CHRONOLOGY incorporates activity in the global markets https://audio.pwfm.tech/documents/covid-chronology-4.9.7.pdf

Oh cool

Plant-Derived Exosomes as Cross-Species Messengers and Beacons of Epigenetics https://besovereign.com/o/greenmedinfo/community/plant-derived-exosomes-as-cross-species-messengers-and-beacons-of-epigenetics "Cross-talk between plant and animal cells may be accomplished via microRNA-carrying exosomes, gene-regulating elements contained in plants which reinforce that food is information and suggests an inextricable co-evolutionary relationship between these two disparate kingdoms."