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 π pie produces π and not π 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 π venom in the genome of the spike protein > pubmed.ncbi.nlm.nih.gov/32823591/
The Craniomed group of carlobrogna1 identified ππ 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/10.110β¦
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 π.
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
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/10.11β¦
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. >
Textπ 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 π. 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. π #ItCameFromALab
What turns cancer into hyperprogressive or #TurboCancer?
One factor might be an abundance of lipids.
"...lipid metabolism may be a causal factor of tumor malignant progression and metastatic behavior." π§΅
For tumors to grow, they need "biomass" components. Excess lipids provide the needed biomass for growth.
More lipids = more efficient tumor growth. >
The Covid π contains lipids.
The Covid π¦ &π contain the SARS2 spike protein.
The spike protein is efficient at entering and permeabilizing the cellular membrane.
The cell membrane is primarily composed of lipids. Upon permeabilization the lipids can leak out. >
Snake Cathelicidin is valued for its highly stable nature and for its membrane destroying properties.
It is in development as an antimicrobial theraputic in medicine. >
Venom cathelicidins work by destroying the cell membrane of bacteria and assisting in healing wounds. >
2021, a Japanese Pfπzr biodistribution study showed the lipid nanoparticles of the COVID π did not stay πͺ in the injection site but were distributed systemically in the body with large accumulation in certain organs, especially the liver. Now >
another study confirms systematic LNP distribution.
This distribution threatens the entire mRNA gene therapy platform because it shows that if the LNPs go everywhere, including the π§ &π«, then the mRNA payload goes everywhere too.
LNPs and mRNA have been shown to be toxic >
to cells, as has the spike protein.
Cells forced to express ANY foreign protein would activate the immune system to target them for destruction.
Resulting in >