Got Spike?

Potential Solutions for Spike Protein Poisoning

Old Mr. Spike Protein: a bioweapon, many contend, on its own without a coronavirus attached. Where did it come from?

Most Snarky Answer: ‘who cares?’, a bunch of asshole scientists are trying to kill us, ALWAYS and FOREVER.

Short Answer: It was patented at the University of North Carolina, Chapel Hill.

Longer Answer: Viral immunologists, microbiologists, zoologists and geneticists worked for our governments to create a bioweapon for the last fifty years, all compounding the disgusting work on the shoulders of militarily-subverted geniuses.

The real question is: what do we do about this specific toxin created to destroy us all? Please find below some information on the spike protein and how it attacks us on a cellular (and even on the nuclear scale), followed by some real-world health solutions.

Well, first off, we are discovering the toxic effects of the spike protein literally daily. This is not some run-of-the-mill-poison, it is an elegant and extremely varied group of systems and subsystems that corrupt our human body on hundreds of different levels.

Worse, it was designed to mutate and utilize various sick humans to create the next ‘variant’. It was designed with weak polyvalent bonds (on a molecular level) so it will specifically morph and change to suit the hosts’ current inflammation. It attacks every one of us differently as each one of us has separate and latent infections and inflammation (and microbiome); this has been designed to weaken our systems and go towards inflammation to attack.

The spike protein is categorized as a DREADD - ‘Designer Receptor Exclusively Activated by Designer Drugs. Pioneered by Bryan L. Roth (also at University of North Carolina Chapel Hill…), DREADDs are chemogenetic (macromolecule engineering) engineered-proteins that allow scientists to control nerve cell activity. DREADDs can be activated by other drugs or a various multitude of other methods (electromagnetic waves is one way), and are designed to go where the scientists WANT them to go.

“Nobody understood what this would possibly be useful for,” Dr. Bryan Roth laughs. “It’s nice to see that it has turned out to be a useful technology.” - Ughhh… fistfight, anyone?

In the case of the spike protein, they were specifically designed to go to anywhere the body is producing inflammation and specifically ACE2 receptors. But that is only one portion of what the spike protein DREADD does.

Anatomy of a Bioweapon

In the above patent for “Methods and compositions for chimeric coronavirus spike protein”, the inventors (Ralph ‘Fuckface’ Baric - UNC Chapel Hill) list two specific bat coronaviruses that they combined with MERs to make this chimeric (a single organism composed of cells with more than one distinct genotype) toxin.

The Chimera

The three heads of this chimera are: Receptor Binding Domain (RBD), Furin Cleavage (PRRA amino acid insert) and Glycoprotein-120 (GP-120). Find a more detailed explanation link here.

Let us delve into the basics of this chimeric devil and understand how to increase our cellular health to stop new infection, get rid of existing infections, and potentially undo some of the post-infection damage to other systems that this man-made-death-toxin has caused.

Receptor Binding Domain (RBD) - (patent here - also UNC Chapel Hill - seeing it yet?)

What does it ‘do’?

• binds to our cells and disrupts cellular communication and processes

• direct effects:

  • regulates control of vasoconstriction and an increase in blood pressure

  • acts as Na+/H+ exchanger to stimulate Na+ reabsorption and H+ excretion which is coupled to bicarbonate reabsorption

  • regulates Adipic systems (fat mass expansion)

  • regulates cardiovascular direction of vasoconstrictors

  • regulates prothrombotic adhesion and aggregation of platelets

  • acts on the adrenal cortex causing a release of aldosterone - causing kidneys to lose potassium and retain salt

• indirect effects on humans

  • Thrombocytopenia - leading to cardiac cell growth through protein ‘kinase c’ ie. Myocarditis & Pericarditis

  • Kidney malfunction

  • Hemochromatosis - iron overload in cells

  • Sperm motility

  • Sleep Disorder

  • Cellular apoptosis (programmed cell death)

Furin Cleavage Site (patent here)

What does it ‘do’?

• increases infectivity

• direct effects:

  • disrupts microRNA processing and error checking - miRNA, Dicer & Drosha (detailed post here)

  • disrupts encoding of type 1 membrane bound protease that is expressed in many tissues (MAKES THE CELL MORE INFECTABLE)

  • regulates trans-Golgi network communication through endosomes (disrupts cellular-nuclear communications)

  • substrates affected by RBD include

    • proparathyroid hormone, transforming growth factor beta 1 precursor proalbumin (REGULATES CANCER TUMOURS)

    • pro-beta-secretase (enzyme that regulates Alzheimer’s & neurocognition)

    • membrane type-1 matrix metalloproteinase (finds and disrupts malignant tumors)

    • beta subunit of pro-nerve growth factor (altered pain receptors)

• indirect effects on humans

  • Alheimer’s and other Central Nervous System conditions

  • Tumor Growth aided

  • More genetic cellular mutations (miRNA system disruption)

  • Cellular apoptosis (programmed cell death)

Glycoprotein-120 (GP-120)

What does it ‘do’?

• attaches to cells and creates a low-electron required transfer point for RNA instructions

• direct effects:

  • induced cytotoxicity - caused DNA strand breakage

  • involved in virion entry through binding to CD4

  • gp-120 can interact with the membranes of all types of endothelial cells, not just with CD4

  • disrupts cellular cytotoxicity-mediating antibodies

  • induce apoptosis (cellular death) in those cells it interacts with

  • changes in lymphocyte homing (adhesion of the circulating lymphocytes in blood to specialized endothelial cells)

  • access the brain through damaged endothelium membrane

• indirect effects on humans

  • Central Nervous System conditions

  • brain death - binds neuron cell membrane coreceptors (CCR3, CCR5, and CXCR4) and elicits apoptosis

  • destruction of the helper lymphocyte (from B & T cells)

  • promotes Pneumocystis (SARs by itself)

  • delayed ‘hypersensitivity’ - response to organisms such as mycobacteria - unable to mount an effective specific humoral antibody response

  • infect monocytes and some non-immune system cells in the central nervous system

  • Cellular apoptosis (programmed cell death)

Solutions

We need to make our cells healthier. Stop eating simple sugars is step 1. Get your diet up to snuff with the proper nutrient and micronutrient understanding. Obviously vitamin C, D, B and A are a great place to start and along with zinc, help your cells manage their own, healthy nuclear communication and cell substrate.

Regulate and change Circadian Cycle

Lack of sunshine, being forced to work all day and night in your home, lack of play and fun… leads to low melatonin and vitamin D. Emotional or physical stress can create formaldehyde within us which may also be in smog, smoke, or off noxious-gases from plastic items. To change our circadian cycle, it easily starts by cutting down or removing all things that disrupt our circadian rhythms, which include EMF waves and even reading your phone/computer before bed. “Early to bed makes us healthy, wealthy and wise”, says the idiom.

• Dark sleep with EMF devices TURNED off at night

• Vitamin D and melatonin - plus potentially NAC+ or flush-Niacin to get our Na+/H+ cell substrate in order

Increase microbiome health

The microbiome is the collection of all microbes, such as bacteria, fungi, viruses, and their genes, that naturally live on our bodies and inside us. Because the microbiome is a key interface between the body and the environment, these microbes can affect health in many ways and can even affect how we respond to certain environmental substances. Some microbes alter environmental substances in ways that make them more toxic, while others act as a buffer and make environmental substances less harmful.

• Pine needle tea - yes, collect new/young pine needles, put in tea. Pine needles contain Suramin (reagent to inhibit the activation of heterotrimeric G proteins - glycoprotein-120 ‘be-gone’)

• Get out into the forest, dig in the dirt, walk barefoot in the sand, get sun on your skin.

• Ferment some food - make some sauerkraut etc.

  • fermented foods provide many health benefits such as anti-oxidant, anti-microbial, anti-fungal, anti-inflammatory, anti-diabetic and anti-atherosclerotic activity.

  • Various vegetables, when fermented, make butyrate which can signal the niacin receptor & help immune function and remove inflammation.

Mitochondrial Support & Detox

• Nrf2 promoters support mitochondrial function and increase our own production of glutathione, which is needed in the Citric Acid Cycle - the multi-step chemical pathway in which a molecule of glucose is broken down for the release of the energy stored in the double bonds of the carbon ring. Nrf2 (nuclear factor erythroid 2-related factor 2 gene) has been reported as one of the prognosis markers for various diseases, including cancer.

  • eg. Fulvic Acids, humic substances, GABA

• Methyl donors, folate and hydroxy or methyl cobalamin and choline protect mitochondrial DNA from genetic changes

• Magnesium is needed in significant amounts within mitochondria to protect against oxidative stress damage

• Manganese -2.3 mg / 5 mg - essential enzyme used in the Citric Acid Cycle

• Niacin, flush type, nicotinic acid, activates the GP109 receptor which increases removal of inflammation as heat. It can cause an 'uncoupling' of the Citric Acid Cycle from ATP production and release the energy as heat instead - the same type of event occurs in brown adipose tissue, which helps keep us warm in cold weather. Gradually increasing from 250 mg, or 25 mg if severely inflammed to 1000 mg twice a day with meals can increase inflammation and toxin removal.

• All of the B vitamins are needed though, & in balance: thiamine (B1) is needed in greater amounts during severe infection or inflammation (300 mg), riboflavin (B2), pantothenic acid (B5), and possibly extra methyl donors, folate, hydroxy cobalamin, and choline would be needed.

• CoQ10 - 30-100 mg / 60–1200 mg. CoQ10 may be low for people taking statin medications, or anyone exposed to glyphosate residue (which is most people).

• Alpha Lipoic Acid - 200 mg / 600-1800 mg

• NAC, N-acetylcysteine - an amino acid derivative commonly found in any protein food. 600 mg / x 4 - 2400 mg

• Carnitine, Acetyl-L-Carnitine - 1 to 6 gr/day

• Manganese Superoxide dismutase (MnSOD) - we need Nrf2 promoting foods & phytonutrients in our diet to help us make MnSOD, & Manganese

Phytonutrients

• Vitamin C and zinc

• Quercetin - onions, pear & other fruit peels, figs, greens. 500 mg once or more a day, produce rich diet may provide that.

• EGCG - 2-3 cups green tea, 200 mg, pomegranate peel, 1/4 teaspoon inner peel dried, once or more a day.

• Artemisinin - 200 mg 1 -2 x day

• Sweet Wormwood tea, teaspoon in one mug of water, steep for a few minutes

• Berberine - Goldenseal root and other herbs.

• Black Walnut Extract - may prevent protein misfolding/prion risk.

• Black Seed Oil, Olive Leaf Extract, Oregano Oil

• Resveratrol - grape skins, red wine (2-6 oz/day may be beneficial)

• NAC, Garlic, Nicotine, Caffeine, chocolate, red wine

Receptor function restoration

• Beta-glucan helps activate dectin-1 receptors, involved in defense against fungal infection. Mushrooms, 1/3 cup, or Nutritional Yeast Flakes, 2 tsp. once or a few times.

• ACE2 receptors are protected by EGCG in pomegranate peel and also other phytonutrient antioxidant. Goji berries, red raspberries (a little), green tea. nAChR receptors are activated, protecting function, by nicotine.

• Ferroportin (porphyrin) overactivity may need to be blocked by removing spike with detox aids: Bentonite clay, Activated Charcoal, Zeolite, bromelain or nattokinase, or NAC; cope with the excess iron with iron chelators, which might also help remove graphene oxide (GO); support with varied antioxidants & vitamin C being cautious of pro-oxidant risk if GO may be present.

• EDTA Chelation - For over 50 years EDTA chelation therapy has improved blood flow and benefited every cell in the body. It now serves as a highly effective and safe treatment (intravenous or Detoxamin suppository) for the elimination of toxic heavy metals and improvement of circulation and health. EDTA Chelation Therapy is used worldwide for arteriosclerosis, heavy metal toxicity, memory problems, heart disease, fatigue, circulation problems and more.