GOAL OF MRNA: DECEIVE THE BODY THAT THE GMO-SPIKE PROTEIN IS A PROTEIN FAMILIAR TO THE HUMAN BODY ... WHAT COULD POSSIBLY GO WRONG? "Unmodified mRNA induces an immune response that leads to high serum levels of interferon­α (IF­ α), which is considered an undesirable response. However, researchers have found that replacing all of the uridines in the mRNA with N-­methyl­pseudouridine enhances stability of the molecule while reducing its immunogenicity" "The genetically modified version of the spike protein produced by the human host cell following instructions from the vaccine mRNA [might linger] in the plasma membrane bound to ACE2 receptors." "The two emergency ­approved vaccines only contain mRNA code for spike protein (without E or M), and there must have been a good reason for this decision, despite its observed poor performance." "Both mRNA vaccines currently deployed against COVID­19 utilize lipid­based nanoparticles as delivery vehicles. The mRNA cargo is placed inside a shell composed of synthetic lipids and cholesterol, along with PEG to stabilize the mRNA molecule against degradation." "Human spike protein monoclonal antibodies were found to produce high levels of cross­reactive antibodies against endogenous human proteins." "26 heptapeptides [are] found in humans and in the spike protein." "They discovered that there was a high level of binding not only with the SARS­CoV­2 spike protein, but against a wide range of endogenous proteins. '[W]e found that the strongest reactions were with transglutaminase 3 (tTG3) and transglutaminase 2 (tTG2) [celiac disease], ENA, myelin basic protein (MBP) [multiple sclerosis], mitochondria, nuclear antigen (NA), α­myosin, thyroid peroxidase (TPO) [Hashimoto's thyroiditis], collagen, claudin 5+6, and S100B.'” (Vojdani and Kharrazian, 2020)." "SARS­CoV­2 membrane protein antibody reacted with 18 out of the 55 tested antigens.” These 18 endogenous antigens encompass reactivity to tissue in liver, mitochondria, the nervous and digestive system, the pancreas, and elsewhere in the body." “[O]ne of the potential side effects of giving a mass vaccine could be an emergence [sic] of autoimmune diseases especially in individuals who are genetically prone for autoimmunity [associated with autoantibodies to cardiolipins and phospholipids, hepatocytes, gastric cells, cerebral spinal fluid] " The mRNA vaccines may be suppressing the innate immune response. There is cross­talk between TNF­ α and type I interferon in autoimmune disease, wherein each suppresses the other. TNF­ α is sharply upregulated in an inflammatory response, which is induced by the lipid nanoparticles in the vaccine." "Spike protein alone, unassociated with the rest of the viral genome, is sufficient to cause the endothelial damage associated with COVID­19. The implications for vaccines intended to cause cells to manufacture the spike protein are clear and are an obvious cause for concern." "In an in vitro study of the blood­brain barrier, the S1 component of the spike protein promoted loss of barrier integrity, suggesting that the spike protein acting alone triggers a pro­inflammatory response in brain endothelial cells, which could explain the neurological consequences of the disease The implications of this observation are disturbing because the mRNA vaccines induce synthesis of the spike protein, which could theoretically act in a similar way to harm the brain."

https://undercurrents723949620.wordpress.com/2021/05/30/long-term-damage-from-covid-vaccination/ "Lots of nasty things happen when you disable ACE2 receptors."

DISRUPTION OF THE LIPIDS IN THE MEMBRANE OF THE CELL, THE BRAIN OF THE CELL, CREATES DISEASE. The lipid membranes of the cell and of the mitochondria need to be fluid and flexible. The injection for COVID 19 stiffens the membrane, inhibiting it from functioning.

AUTOPHAGY & SPIKE PROTEINS "Autophagy is surely critical in the clearance of spike protein produced by immune cells programmed to produce it through the mRNA vaccines." Support autophagy via Nrf2/KEAP1

SIRT3 is an NAD+-dependent deacetylase enzyme responsible for the regulation of mitochondrial function, resistance to oxidative stress, and metabolism. SIRT3 appears to activate AMPK, and subsequently autophagy. Research suggests several polymorphisms may have the potential to decrease SIRT3 expression.

Nrf2 supports the production, recycling, and the expression of glutathione, SOD, and catalase. It is like a sprinkler system in a building, as it expresses the antioxidants when there is oxidative stress. Nrf2 also regulates iron sequestration, NADPH production, the enzymes that reduce Hydrogen Peroxide, and has influence of the critical process of AUTOPHAGY (the cleaning of cellular debris).

ESSENTIAL OILS TO SUPPORT NRF2/AUTOPHAGY Rosemarinus officinalis (Rosemary) , Pogostemon cablin (Patchouli) , Lavandula
spica (Spike Lavender) , Lavandula angustifolia (Fine Lavender)

COMPOUNDS TO SUPPORT NRF2/AUTOPHAGY
Bioflavonoid Complex (Lemon (Citrus lemon - 90% Bioflavonoids)
Ellagic Extract 90%
Grape (Vitis vinifera) Seed Extract (95% Proanthocyanidins)(France)
Green Tea (Camellia sinensis) Leaf Extract (50% EGCG)
Milk Thistle (Silybum marianum) Seed extract (80% Silymarin)
ParActin® (Andrographis paniculata)
Pterostilbene
Resveratrol (Polygonum cuspidatum) Root Extract
Selenium (as L-Selenomethionine)
TrueBroc® SGS Broccoli Seed Extract (13% Glucoraphanin)
Turmeric Extract (Curcuma longa) C3

GENETIC PREDISPOSITION TO DAMAGE FROM COVID INJECTIONS ... Nrf2/KEAP1, TP53, BRCA; also take a look at your variants in IL6, ACE

GENETICS & COVID ... a study on polymorphisms in the renin, angiotensin-aldosterone (blood pressure, mast cell/histamine/cytokine pathways). https://bmcmedicine.biomedcentral.com/articles/10.1186/s12916-020-01673-z

KNOW YOUR DNA ... genome-wide studies of enzymes like ACE2 are interesting, but who cares? What matters is you, your unique divinely-designed genetics. The above screenshots show variants in genes associated with the spike protein in the COVID injections.