C19 mRNA injections of spike venom – some background notes on efficacy of Chlorine Dioxide and Methylene Blue on snake venom
Here’s a few links for context:
“Dr Ardis video here from last year providing the logic behind a clip called “Antidote” in which he explains how the make0ip of boom slang, krait and king cobra venom is identical to the spike protein (hence why I call the experimental C19 mRNA injections spike venom”).
He also explains that melatonin naturally protects children and how nicotine is non-addictive, nicotine receptor cells exist in every cell in the body and how nicotine is ten times more effective than even ivermectin inn blocking the effects of the spike venom.”
Here’s a flashback to the mind numbingly obtuse Pfizer “expert” explaining how great it was to develop infections of the spike venom into people because Pfizer had the technology I August 2021.
And here’s a link to the excellent Maria Gutschi detailing the quality issues in the modified mRNA injections all the way back in November 2022:
Maria Gutschi - Review of Quality Issues with mRNA Injections 5 Nov 2022 (bitchute.com)
Which turned out to be features as well as bugs! Note Maria discovered adulteration more than the contamination found by Kevin McKernan – both of which are product fails in the norma, course of events, but were “de facto” approved by regulatory agencies.
Kay, re-armed with those three links to set the scene, I thought about methylene blue and Chlorine dioxide and their potential to inhibit snake and C19 spike venom.
I could not find much of anything on research for ClO2, except maybe this:
If There is Snake Venom in That So-Called ‘Virus’ WHAT is The Treatment? (plasmaenergysolution.com)
“Chlorine dioxide is a ‘slicer’ for the snake venom molecules. If you are using city water for drinking water, the chlorine dioxide treatment can be followed by water filtration. Chlorine Dioxide is able to help halt the blood clotting caused by mRNA that causes the body’s cells to produce pro-clotting factors—ie, proteins and snake venom peptides.”
There is this interesting general paper on the treatment of snake venom here:
Snake bite? Chemists figure out how to easily and cheaply halt venom's spread | ScienceDaily
I think the above article was derived from this paper in 2016.
“Using directed synthetic evolution to optimize a nanoparticle (NP) formulation capable of sequestering and neutralizing venomous phospholipase A2 (PLA2), we demonstrate that broad-spectrum neutralization and sequestration of venomous biomacromolecules is possible via a single optimized NP formulation.
Furthermore, this optimized NP showed selectivity for venomous PLA2 over abundant serum proteins, was not cytotoxic, and showed substantially long dissociation rates from PLA2. These findings suggest that it may show efficacy as an in vivo venom sequestrant and may serve as a generalized lipid-mediated toxin sequestrant.”
Lots of now familiar terms in that paper! – not viewed as significant enough for federal funds of course – modified mRNA or nothing, right!
There’s probably some PLA2 in the C19 modified mRNA doses? I will avid that rabbit hole for now!
There is this article that says you can use snake venom to treat some symptoms of C19 from September 2021!!!
Ok, here’s a study UV “sensitized” methylene blue:
No doubt, sentences like this will mean something to experts, but its way outside my wheelhouse!
“Agkistrodon piscivorus venom was irradiated by exposure to UV light (mercury vapour quartz, 250 uW/cm ) from a distance of 10 cm for 1 h. and 3 h. The irradiated venom sample exhibited 3-4 fold increase in LD50 value. The loss of toxicity parallels the loss of enzymes, which include phospholipase A2, protease, and phosphodiesterase.
The effect of irradiation on phospholipase A2 has been shown to be particularly sensitive by the time required for complete inactivation of the enzyme, paralleling the loss of venom toxicity (8).
The mechanism of photodynamic action of the sensitizer MB on protein molecules by incident radiation involves the formation of photoperoxides (SO2) and photooxidised forms of protein (PO2) by reaction of long-lived excited species of MB with molecular oxygen. S and P in a complex form generate long-lived excited species of SP (sensitizer protein) and in water environment generate reduced substates of S and photooxidised form of P molecules (PO) with the liberation of hydrogen peroxide in the presence of molecular oxygen (7).”
Defintionn of some of the letters in the above:
“… phosphate buffer (B), methylene blue (S), venom protein (P) was exposed to UVR (ultra violet radiation) for 2 hours at 37°C. Stable excited species (S) were generated by photodynamic action. These in B environment produced reduced substates SH2 and photooxidised products PO.”
From here: Effect of methylene blue on the toxicity of cobra venom - PubMed (nih.gov) to here:
Methylene Blue: Miracle Antidote for Poisonings and Overdoses - ENDALLDISEASE
“In this article, you’ll learn how and why methylene blue can be used as an antidote for all types of chemical poisonings or drug overdoses. Also included is the exact dose used by hospital as an antidote to chemical poisoning.”
Dr Ana Mihalcea and Dr Tess Lawrie have been signing the praises of methylene blue:
(100) Methylene Blue: A molecule made for this time? (substack.com)
One can only wonder why clinical trials are not underway, or maybe they are for both ClO2 and methylene blue.
Onwards!!
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wonder whether the body eventually clears the venom or if, in fact, the body now makes it and keeps making it.