Will Zionist Vaxpass Killers use EMFs to compromise Jab-Recipients’ DNA?
Swiss Scientists from the ETH Zurich University claim to be capable of controlling human DNA with Electricity.
I previously wrote an article showcasing an interview with Karen Kingston, warning how the next PLANdemic could be orchestrated using Electromagnetic Frequencies in conjunction with both the Lipid Nanoparticle Hydrogel (LNP) and the Spike Protein already injected into “CVD” jab recipients.
Electromagnetic Programmable Lipid Nanoparticles (LNPs) & Bio-Synthetic Life Forms (Spike Glycol-Proteins) - Karen Kingston & Dr. Ana Maria Mihalcea (here)
Now it seems that there is another Moderna patent to be concerned about that shows the potential to compromise jab recipients’ DNA.
The lipid nanoparticles have a size of between 80nm and 100nm and contain a modified mRNA encoding a polypeptide. It includes a cationic lipid, a neutral lipid, a cholesterol, and a PEG lipid. “Lipids” host a positive electro-magnetic field. There is no lipid in nature that does that; they are using the word lipid instead of nanotechnology.
Modified Polynucleotides for the Production of Secreted Proteins
An Electro Genetic Interface directly controlling DNA (here)
The devil is absolutely in the details as far as LNPs are concerned.
Without these lipid shells, there would be no mRNA vaccines for “Covid-19” (here)
A Model of Nanoparticles as the Primary Agent of COVID-19 Vaccine Injury (here)
Master patent for mRNA vaxsins
Fully programmable self-assembling nanoparticles
US 10,703,789, B2
Modified polynucleotides for the production of secreted proteins (here)
Marc Girardot has researched COVID-19 Vaccine side effects and believes the lipid nanoparticles to be the primary suspect for most of the dangerous cardiovascular damage in recipients experiencing severe adverse reactions
Marc is brilliant at explaining what goes on post-injection. I prefer to view our cells as “self-cleansing protective cells and leave the “immune system” language out, i.e, no viruses proven, in fact, the opposite. Naming everything under the “self-cleansing, protective cells” lens makes everything he says changes slightly, the magic “virus” is a poison (toxin). Injected non-self shit increases all cause death “data”, fullstop.
RTE Discussions #8 (Take Two): Evidence of Lipid Nanoparticle Harm With Marc Girardot (here)I don’t think it’s fair to take the “No Virus” Challengers seriously. Dr. Tom Cowan puts forward remarkable information.
The "No Virus" Challengers are laughing at the "science" that the "Health Freedom Movement" supports
Controls that disprove Polio “virus” and all other alleged “viruses” (here)For more on the toxic LNPs
Let's cause more disease and endlessly profit (here)
It’s been put forward that N-Acetylcysteine (NAC) helps remove the LNP hydrogel from the body. Kingston put forward that one of the 4 layers of the hydrogel is comprised of graphene oxide (benzene). This would potentially facilitate the amplification of EMFs within the jab recipient’s body. It is also understood that 5G amplifies the body’s absorption of toxicity and that Glyphosate decreases the body’s ability to absorb vitamin D. Vitamin D, after two days, turns into vitamin D hormone which then powers the ATP of the mitochondria of one’s cells i.e. this helps the body function/detox effectively. Should Dr. Bryan Ardis be right regarding the venomous “spike protein’s” ability to reduce Zinc, which is synergistic to vitamin D functionality, then the “CVD” narrative could be a perpetual problem i.e. use of fraudulant “virus testing” combined with people’s health endlessly being compromised with EMFs combined with toxic exposure (incl. vaxsins). This DNA problem is compounded by the notion that the “spike protein” could shape-shift (after EMF pulses) into another toxin.
Electromagnetic Frequencies + Toxification = "COVID-19" (prove me wrong) (here)
How can one detox the mRNA bioweapons? (work in progress) (here)
NAC and Selenium create a protective effect against Traumatic Brain Injury-induced oxidative brain injury and interleukin production by inhibiting free radical production, regulating cytokine-dependent processes, and supporting the antioxidant redox system.
Telomeres play a central role in cell fate and aging by adjusting the cellular response to stress and growth stimulation on the basis of previous cell divisions and DNA damage. At least a few hundred nucleotides of telomere repeats must "cap" each chromosome end to avoid activation of DNA repair pathways.
Chronic treatment with N-acetylcysteine delays cellular senescence in endothelial cells isolated from a subgroup of atherosclerotic patients (here)
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