![440px-B_anthracis_diagram_en.png](https://images.hive.blog/DQmSwhAbqQYi86MgWAxhKTatM3qVU1pzh2oXHPaH8d9j7ZU/440px-B_anthracis_diagram_en.png)

the Plastid in Anthrax.. is linked to formation of Prion.

my suspension is the Circular DNA of Prion & Protist Plastid is a direct link.

meaning Prion/Virus are non-living organism (dormant) until inside a very specific part of the correct kind of mitochondria.

meaning Malaria & Anthrax should have similar chemical reactions, just at different rates of biological degeneration.

im just so frustrated with "pathways" without any conclusion, when they all match this ancient extremophile algae inside all of them, with different names, all doing exactly the same thing.

Anthrax, acting like Malaria, because its the same kind of critter, one living inside a protozoa, the other living in a bacteria, but the same thing.

take the critter from Anthrax, put it into Mycoplasma.

the Plasmid/Plastid is a natural biological algae mitochondria transfer, then weaponized.

the parasite makes deposits of the things it dosnt like, like Potassium & Iron, kicks them out of the cell, and makes toxic acids to protect themselves.

it seems to be following Glyphosate acidic toxin pathways (round-up), and making Prion (spikes) from inside the cell mitochondria, that self assembles into Amyloid Plaque.

B1 is the only B vitamin with the 5-carbon like Fenbendazole, plus the Nitrogen & Sulfur.

thinks its called a Pyrrole, and is responsible for Heme, which keeps iron inside the cell.

guess the critter gets upset when the iron & potassium are inside the cell, where its supposed to be.

the same benefits from B1 are identical to Radish (high in B1), and Fenbendazole tastes like Radish.

im going to try B1, because i wonder if not only does it heal the toxic damage of mitochondria or even stem cells, but the critter itself may be effected, i just need to see how it makes me feel overall.

the original idea was to potassium citrate zwitterions to pry apart toxic acid biofilm like glyphosate, from inside cell mitochondria, except DNA parasites push all the iron & potassium out of the cell, B1 brings potassium puts back intercellular, pushing out sodium & recharges enzymatic activity.

spike protein is a prion, prion follow glyphosate pathways, glyphosate is gmo round-up, prion is similar to bacteria plastid, plastid is similar to protist plasmid, plasmid is malaria, and the only medications that treat this kind of critter is pyrrole-pyrimidine-thiazole, which is fenbendazole & B1 thiamine derivative.

tasting B1 is the same bitter flavor as enzime supplements, not so much horseradish.

im convinced a Prion is a variant of Plasmid/Plastid that can hyjack mitochondria & bacteria, as a form of endosymbiont algae/yeast like lifeform, that can go dormant for 20 plus years, depending upon the environment conditions.

this lifeform is mislabeled a virus, that can infect bacteria carboxysome, an icosahedral microcompartment of bacteria, and appear as a virus.

in a non-hospitable environment it goes dormant, requiring the perfect environment of mitochondria to reproduce in exosome.

is suspect carboxysome is being used to transmit & manufacture prion, self assembling amyloid plaques.

the icosahedron shape is perfect for self assembling of biomass.

the way virus have spore-like extentions out of the icosahedron corners, and some virus coil like tobacco virus, its a protist phage.

this is why antimalarial drugs can cure it to some degree, until the infection goes into the bone marrow, then goes dormant, to a degree, and becomes chronic wasting disease, or chromosome malfunctioning, genetic disease.

i am very disappointed with pathways science, it seems like they can only see the pathways, and not the connection between microbes, how they can interact with biological processes.

more specifically weaponized variants, such as Herpesviridae evolution from aquatic algae.

how viruses are living things that require very specific environments to break hybridization, much like plant seeds, of fungus spores.

dormancy spores, that target mitochondria & bone marrow, mislabeled as a non-living virus.

anyway, im my own imagery friend, and make up nonsense as a religious experience.

Herpesviridae corral reef alga protist plastid, transversed as bacteria plasmid phage into amyloid prion plaque, an algae bloom from inside the mitochondria.

B1 Thiamine was originally discovered from a dye manufacturing method.

Congo Red & Methylene Blue are used as stains for Prion testing, and the paper says a very close derivative traps it somehow.

Thienyl Pyrimidine Compounds Traps Prion Infectivity

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taking this combination right now

B1: 2000mg
Magnesium 800mg
Vitamin C 2000mg

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cant understand why extremophile plasmids are required to enhance a virus, and when the circular dna is so similar to a plastid, virus "life cycle", just makes me think mitochondria parasites & misfolding.

my only point is, nobody has an explanation that makes sense to me, only Garth Nicolson has a pinch of anything i can relate to, and even that is not complete in my mind, viruses seem to be alive, yet only inside the mitochondria, otherwise goes dormant & called not alive.

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my left hand, the pinkie finger knuckle was in pain last week, now its fine, the pain moved to the middle finger knuckle.

same hand has been struggling with weakness for a few years, for some reason B1 is making my knuckles sore, right where the arthritis was forming.

my neck has multiple fractures from childhood head traumas, so my neck is always kinked, hurting & popping, the B1 also went to that injury spot, i think it is fighting the Osteoporosis & Arthritis?

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low dose dosnt seem to do the trick, but high dose may not be good for long periods?

i dont think high dose should be permanent, might do something not helpful.

i would recommend at looking at it as a medicine, and take for a few weeks high, then go back to low dose.

2000mg was taken once in the morning & again in the afternoon, making 4000mg, it was too much, didnt feel very good today, that must be the limit.

i have a medium high tolerance for random supplemental experimentation, and i recommend 4000mg is definitely too much.