Working theory, "Show replies" at the end for all.
Is SARS-CoV-2 a lab-created chimera?
A Frankenstein virus created from the genetic material of other lethal organisms, creating similar pathophysiological mechanisms in the body?
Gene sequences say YES >
The SC2 spike protein contains gene sequences that are homologous to those found in HIV, SEB, animal venoms, herpes, malaria, rabies and more.
The sequences from these organisms could release toxic peptides and pathophysiological mechanisms in the body similar to those found >
in the original lethal organisms.
Mechanisms are chemical recipes, like baking recipes.
A list of instructions from the genes that, when followed, produce a unique product like micro clots or a cytokine storm.
Just as a recipe for 🎃 pie produces 🎃 and not 🍎 pie. >
It is interesting to see the similarities between the mechanisms produced by SARS-CoV-2 and the original lethal organisms it shares gene sequences with. Several scientists have sequenced the the genome of the spike protein >
The Laboratory of Molecular Biology and Immunology, The U of Patras, @ konstantinospo7 identified a toxin-like sequence, similar to 🐍 venom in the genome of the spike protein > pubmed.ncbi.nlm.nih.gov/32823591/
The Craniomed group of carlobrogna1 identified 🐍🐌 toxin-like peptides produced in COVID patients > pubmed.ncbi.nlm.nih.gov/35106136/
Prashant Pradhan and teams from Kusuma School of Biological Sciences, Indian Inst. of Technology, U of New Delhi and SUNY Stonybrook found gene inserts similar to HIV in the spike. #PradhanWasRight > biorxiv.org/content/10.110…
Luc Montagnier, Pasteur Inst. and Jean Claude Perez, IBM European Research Center on AI, found gene sequences similar to HIV in the spike. > osf.io/d9e5g/
These genes, and the toxic peptides they produce, could make SARS-CoV-2 (SC2) and its spike protein (SP) an aerosolized bioweapon.
A coronavirus that causes the severe endothelial damage, clots and immune disorder of COVID.
A lethal cold.
How might this manifest? >
Covid is a bi-phasic disease.
The 1st phase is a cold-like respiratory virus.
One which most immune systems can destroy without 💊.
Or it can be overcome with early treatments like the Zelenko and FLCCC protocols. >
The 2nd phase is Acute COVID (AC)
Here the pathology of the bioweapon commences,
the patient becomes severely hypoxic, losing 02 at a cellular level as the virus destroys the cells of the endothelium and the mitochondria and causes micro clots.
The lethal phase of COVID. >
SC2 causes a specific amyloid clotting cascade, and inflammo-thrombotic-response (see Doctor_I_am_The) /cytokine feedforward loop. This mechanism is quite similar to the one produced in the envenomed prey of Cobra and Krait snakes and Cone snails. >
Amyloid clots are made of disordered, fibrous misfolded proteins, during AC and envenomation they are produced rapidly. > en.wikipedia.org/wiki/Amyloid
The viral SP infects the cells of the endothelium. It permeablizes membranes and is expressed on the outside of cells.
The endothelium is the largest vital organ in the body. It lines, protects and regulates every 🩸 vessel, lymph node and organ. > study.com/academy/lesson…
When the SP is expressed on endothelial cells it signals the start of a feed forward loop. The immune system is hyperactivated, a "cytokine storm" occurs.
It attacks the cells expressing foreign spike protein, and damages the endothelium. >
The spike and the immune system begin to destroy the membranes, vasculature, and all organs.
Organelles like mitochondria responsible for cellular respiration, and delicate cells/tissues like erythrocytes, alveoli, and capillaries are shredded.
This results in ferroptosis >
vessel leakage, bleeding.
O2 is lost in cells in many areas of the endothelium simultaneously.
Repair mechanisms begin amyloid clot formation to repair damaged vessels. This causes fibrosis and stiffening of the vessels and organs. Sepsis, lymphocytopenia and dysregulation >
of the autonomic nervous system also occur.
Shock, respiratory failure, pulmonary embolism, cardiac failure, or stroke cause death. > ccforum.biomedcentral.com/articles/10.11…
The pathophysiology caused by the genetic sequences in COVID is similar to the pathophysiology caused by the similar sequences found in the original lethal organisms.
SARS-CoV-2 could be a lab created chimera.
A corona virus with a toxic spike protein, an aerosolized bioweapon.
Several researchers sequenced the genome of SC2.
They detected gene sequences similar to sequences found in other lethal organisms. >
spliced together in the spike protein. (HIV, SEB, Hepatitus, Herpes, Malaria, Rabies, Venoms).
These genes code for toxic peptides which are produced in the body, like a recipe.
The peptides produce mechanisms and symptoms similar to those found in the original organisms. >
Text👇 is a quote, I forgot to put quotation marks.
Descripton of the amyloid micro clotting mechanism seen in COVID. This is similar to the mechanism in envenomed prey of 🐍. The clots are ssimilar, the symptoms are ssimilar, the deaths are ssimilar. >
It's simple, the DoD has been funding gain of function venoms research and coronavirus research for years in the U.S. and CCP bioweapons labs.
They recently reinstated the funding.
No one is hiding it. 🙄 #ItCameFromALab
They are 💀 because of the disastrous pandemic response directed by Fauci.
Fauci gave conflicting medical advice and censored
life-saving early 💊s in order to shield DoD bi0weapons programs from scrutiny and enable a novel warp speed mRNA 💉 >
Grok explains the potential for oncogenesis from the C0VID 💉s based on lab results of bacterial DNA impurities and other published data. @ScottAdamsSays
Millions around the 🌎 are 💀 from a pandemic panic caused by a chimeric 🦠 created in a ☣️🧪 by
🇨🇳 👩🔬🧑🔬 conducting Gain of Function research
with 🇺🇸 data and 💰 directed by
Dr. Anthony Fauci.
SARS‑CoV‑2 enters through the ACE2 receptor,
which is abundantly expressed in cardiac pericytes, endothelial cells, and cardiomyocytes.
Studies demonstrate that infection of pericytes compromises capillary perfusion, producing micro‑ischemia.
Autopsies confirmed viral RNA and protein in about 40% of🫀s.
This evidence shows that SARS2 reaches the myocardium directly, setting the stage for injury. >
Once inside the vasculature, the 🦠 damages the endothelium — the inner cellular lining of 🩸vessels.
There is complement deposition and fibrin micro clots in small cardiac vessels consistent with inflammatory endotheliitis.
This process decreases nitric‑oxide signaling and damages pericytes, producing local edema and hypoperfusion.
This causes patches of perfusion defects and troponin elevations seen in COVID‑19 cardiomyopathy. >
Using research of: Arne Burkhardt, Sucharit Bhakdi, Kevin McCairn, Kevin McKernan, Bruce Patterson,
Ram Yogendra, Ethical Skeptic, Lyndsey House,
James Thorpe, Janiesaysyay, Jessica Rose,
John Beaudoin Sr, Marc Girardot, Mary Talley Bowden, Nicolas Hulscher, Peter McCullough, Robert Malone, Resia Pretorius, Akiko Iwasaki, Lynn Fynn, Ryan Cole, Sabine Hazan, William Makis, and others.
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Here we look at how the injection goes wrong from the start, this is Girardot's #BolusTheory
The deltoid muscle is full of tiny 🩸 vessels, so even a careful 💉 can hit one, sending LNPs straight into the 🩸 like an EpiPen.
They hitch a ride on proteins like ApoE and head to organs hungry for lipids, like the adrenals.
In 🤰 hormones make everything leakier, helping LNPs slip through the placenta via receptor uptake and membrane fusion.