There have been so many decoys, distractions and diversions in the Covid-19 journey, that the secret camera confessions of ‘Pfizer guy’ to Project Veritas yesterday seemed to be leading us up yet another blind alley. But actually at least half of what he had to say (in a giggling, slighting inept way) was true. Here’s why.
Siegfried Herrmann (see yesterday’s article) stated that foreign protein injected in to the body, primed an immune response, creating fever that seemed to cure any diseases present. Those could be animal protein or denatured human protein.
Denatured protein is protein that has been broken up in to small peptides for recycling or elimination and through oxidative damage.
We discovered recently that the Spike Protein contained a continuous chain of equally small peptides that were present in a wide range of HUMAN proteins. Proteins which we know are affected by ARSENIC contamination: Zinc finger motifs, enzymes, phosphate containing proteins etc.
Arsenic sticks to, breaks up, rejoins and misfolds proteins so they LOOK foreign.
Virologists take tissue from ‘infected’ areas of the human body, find foreign-looking proteins that they then call VIRUS X, Y or Z. They then culture these proteins in different combinations. These are tested in the laboratory to see if they create a HEAT SHOCK RESPONSE (fever) in the test animal - which is the whole aim. The final product, in the case of Covid-19, is the spike protein.
The spike protein used in the vaccines is, therefore, indeed NOVEL, because we believe it was constructed to be completely different from any other previously designed ‘foreign’ protein. It also most likely was made from protein chains of reorganised human peptides.
Each peptide may act as a tiny tag, reminding the immune system where it needs to look to find similar faulty proteins that need removing, whilst the overall protein structure primes the heat shock response.
Different VARIANTS are probably an excuse for the vaccine manufacturer to slightly change the protein construction. WHY?
If the same protein is used again after the recipient has had a heat shock response, CD4+ cells will remember it well. This could create an autoimmune reaction upon second exposure, and potentially a life threatening allergic one. Read more about that here.
Reshuffling and tweaking the constructed protein might avoid the CD4+ response, instead triggering Natural Killer Cell (CD8+) and heat shock responses again.
Hopefully.
This may be why the vaccines were out of date so quickly - so they could not be used again.
Reshuffled and tweaked proteins sound a lot like the directed evolution ‘Pfizer guy’ was getting all animated about. In order to keep the immune system mounting the right type of attack, the spike protein must be MUTATED (changed) each time.
IMPORTANT NOTE: Healthy cells cannot use foreign proteins OR replicate foreign mRNA proteins. Arsenic contaminated cells are very unlikely to reproduce proteins from anything masquerading as a foreign mRNA consistently. See this article again.
What the body CAN do is copy HUMAN mRNA and it can also use ready-made proteins.
Heat shock proteins promote cell death, detoxification and healing as well as increasing white blood cells and other toxin fighting compounds. Fever producing proteins are governed by HEAT SHOCK FACTOR PROTEIN 1. So when an article on Astra Zeneca popped up, the last piece of the puzzle fell in to place.
The Astra Zeneca vaccine contained, according to the authors, heat shock proteins. They didn’t say exactly which ones, but it will surely be written down somewhere. All the vaccines analysed contained at least 50% protein of human origin.
So in effect there is a VACCINE BLUEPRINT of a constructed protein, that is ‘mutated’ over time to prevent an autoimmune reaction. That protein is likely chaperoned by ‘heat shock proteins’ (either made outside or inside a healthy cell), which in turn encourage the immune system to develop fever.
Key takeaways are:
There IS a ‘foreign’ protein masquerading as a Covid-19 spike protein, but it is very likely laboratory made from human peptides
The foreign protein won’t be mRNA
Pfizer is probably producing their own ‘VARIANT’ foreign proteins so they can be used interchangeably or combined with other brands of vaccines.
All foreign proteins will need to be reconfigured regularly to prevent autoimmunity (in advance).
Astra Zeneca and Pfizer vaccines likely contain one or more Human heat shock proteins
Clean cells can make heat shock proteins from mRNA, or could use ready made proteins delivered by the vaccines
The vaccines do not need to contain arsenic to induce fever (bonus point)
The vaccine is exactly what they have said it is except…
…‘VIRUS’ = chopped up, arsenic-contaminated and denatured human protein which probably bears little resemblance to the ‘Spike Protein’ in the vaccine
The Whistleblowers were both right and wrong. Pfizer guy has shown us exactly why!
thanks for sharing your thoughts. it makes sense a lot in line everything else I've learned so far.
One question I have with regards to this part, you wrote: "Heat shock proteins promote cell death, detoxification and healing as well as increasing white blood cells and other toxin fighting compounds."
Is this driven by oxidative cellular processes or by antioxidant pathways?
There's so much confusing sales talk about (mostly plant) antioxidants these days but I can't wrap my head around how one would be able to accomplish apoptosis or promote other types of cell death and detox/healing with down-regulating oxidation?
Interesting theory. My theory is it's deliberate nonsense to keep the virus narrative going. I don't think autoimmunity is a thing, I don't think the body gets confused nor attacks itself.
It's also interesting that people with autistic symptoms experience a noticeable improvement in behaviour and social interactions when they are febrile. Thought to be due to heat shock proteins. 'widespread anecdotal reports have suggested that fever can dramatically but temporarily ameliorate the disturbed behavior of many autistic patients (21). Notably, the degree of improvement (mostly in stereotypic behavior and inappropriate speech) was unrelated to the severity of fever or of autism (21). This study explicitly suggested that elucidation of the fever response might provide insight into the mechanisms of ASD and point to new therapeutic approaches (21, 22). Fever up-regulates heat-shock proteins and related mechanisms central to multiple cellular processes in the CNS, including synaptic transmission (23, 24), and may improve long-range cerebral cortical connectivity that is depressed in ASD (25). Sulforaphane also up-regulates expression of the heat-shock response (26)' https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4217462/
they found that supplementation with sulphoraphane from brocolli sprouts significantly improved ASD scores.
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