VACCINE INJURY & YOUR GENETICS (a close up) In the past few years, I've participated in genomic analysis of over 100 case studies of people struggling with complex chronic health conditions. Then came "COVID" I knew the 'SARS COV2 'virus' had never been found in a human being, so it wasn't clear, not at all, what "COVID" meant. When my mentor said, "COVID" or "virus" my brain exploded a little, and I made mental holding place for 'whatever that is." Then came the "COVID injections" and spike proteins, I got really deep into the inflammation (genes/enzymes) of spike proteins and those angiotensin enzymes that kick up histamine and mast cells and RANTES. Now these genomic analyses have shifted to looking at inflammatory NF-kB and TNF (mentioned a couple posts above). "COVID" so goes the narrative, activates inflammatory NF-kB and TNF-a. The ovals in the diagram above are genes/enyzmes. In the next post, I'll list the names of the natural compounds and pharma drugs that suppress TNF-a.

NATURAL SUPPRESSION OF TNF-a black cumin seed oil, milk thistle, boswellia, nicotinamide, ECGC, licorice, luteolin, andrographis, fisetin, resveratrol

PHARMA SUPPRESSION OF TNF-a ivermectin, rapamycin, cannabis/THC, statins/red rice yeast, low dose naltrexone

The thing about "COVID" (whatever that is) is this: if you have other toxins on board, they too will activate these inflammatory compounds, TNF-a and NF-kB. We're talking glyphosate, myotoxins, and excess iron and excess oxalates and glutamate and EMFs. We're talking damaged cells and bacteria coming in to clean up. We're talking about toxins in an injection, toxins which have yet to be fully disclosed to the public. A 'virus' is a convenient cover story for Fauci and Fraudsters, but believing in unicorns simply keeps people from figuring out what's really causing them to be ill and taking the proper steps to right their ships, to find homeostasis and equilibrium in mind and body.

"DMSO reduces the secretion of 13 cytokines important in inflammatory response" including both TNF-a and NF-kB. https://www.researchgate.net/publication/320995707_Dimethyl_Sulfoxide_DMSO_Decreases_Cell_Proliferation_and_TNF-a_IFN-g_and_IL-2_Cytokines_Production_in_Cultures_of_Peripheral_Blood_Lymphocytes "Dimethyl Sulfoxide (DMSO) Decreases Cell Proliferation and TNF-α, IFN-γ, and IL-2 Cytokines Production in Cultures of Peripheral Blood Lymphocytes"

LONG HAUL COVID INFLAMMATION TEST (you do not need a practitioner to order this test) https://www.innovativebioanalysis.com/

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), FERROPTOSIS (excess intravascular iron) which causes excess GLUTAMATE and blocks CYSTEINE which damages the cell (lipid peroxidation)
A few suggestions .... vitamin E (for ferroptosis), selenium for GPX4. Nrf2 support, NAC/cysteine .. lactoferrin, skullcap.

Watch for varicose/spider veins ... indication of blood dysregulation from the 'vaccine'

FERROPTOSIS "Ferroptosis is a type of programmed cell death dependent on iron and characterized by the accumulation of lipid peroxides, and is genetically and biochemically distinct from other forms of regulated cell death such as apoptosis." https://pubmed.ncbi.nlm.nih.gov/33454595/ The role of iron in the pathogenesis of COVID-19 and possible treatment with lactoferrin and other iron chelators

MARCH 2022 PAPER ON CENTRAL NERVOUS SYSTEM DISORDERS ... just last month, a paper was released describing in detail inflammation and genes (enzymes) associated with neurological disorders. It describes neuro damage occurring in “COVID vaccine” injury and “long haul COVID” ... without stating it. It is the activation of the things I wrote about above: NF-kB, TNF-a, NLRP3, Nrf2, as well as MindMap inflammation markers also above. In a genomic analysis, we can see how well an individual’s enzymes (genes) are designed to manage toxins like injections and identify specific nutritional supports to bring the inflammation to resolution.
https://www.researchgate.net/publication/359568061_Targeting_NLRP3_Inflammasome_With_Nrf2_Inducers_in_Central_Nervous_System_Disorders

NRF2/KEAP1 ... KEAP1 controls the master signaling molecule called Nrf2; when you have variants in KEAP1, you will hold on to Nrf2. Nrf2 signals the body to use glutathione, a master anti-oxidant. When you have variants in both KEAP1 *and* Nrf2, you will have double difficulty releasing the Nrf2 signal to make glutathione. If you have variants in the genes that make and recycle glutathione (like GSR) you should not take glutathione straight up. Nitric oxide and vitamin and toxins also play a role. In short, you will need to be smarter about nutritional support, know your DNA, else you can make yourself worse off.

SULPHUR (CYSTEINE) & HEALING NEURODEGENERATION (from March 2022 paper above.) “SFN, an organosulfur compound abundantly found in cruciferous vegetables like broccoli and cabbage, is a strong electrophile
modifying cysteine 151 on KEAP1. Due to SFN’s
cytoprotective features, such as anti-inflammation and anti-
oxidation, it is applied in a wide range of disorders in vitro
and in vivo (196). SFN is being clinically tested for various CNS-
related disorders, including PD, schizophrenia, autism spectrum
disorder, and depression. Furthermore, Sulforadex, an SFN-
derived active compound, has been administered to patients
with subarachnoid hemorrhage (197). Likewise, electrophilic
polyphenolic compounds, curcumin extracted from turmeric
(Curcuma longa), and resveratrol derived from nuts and
berries are the most clinically tested compounds after SFN.
Because of their anti-oxidative and anti-inflammatory
properties, as well as their ability to react with KEAP1 via its
cysteine 151 residue, they could serve as potent Nrf2 modulators
(11,185). They have been clinically tested in commonly
occurring neurodegenerative diseases such as AD, Mild
Cognitive Impairment, ALS, Huntington’sdisease,
neuropsychiatric disorders such as schizophrenia, depression, MS and Friedreich’s Ataxia.”

While You Were Distracted by Will Smith, the International Elitists Met at The World Government Summit

"What goes unsaid in the panel description is that making the government “invisible” will actually lead to a world of no accountability for government and politicians. In reality, the Technocrats imagine a world where the tyrannical technological systems are invisible and the average person has zero recourse for preventing exclusion or punishment based on their social credit score."

https://www.thelastamericanvagabond.com/while-you-were-distracted-by-will-smith-the-international-elite-met-at-the-world-government-summit/