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Here is why holding the people accountable for the coverup of the lab origin of SARS-CoV-2 is vital. Years ago several of us said the SARS2 spike protein was a chimera with HIV-like gene analog inserts. (Pradhan et al., Montagnier et al.) We said these inserts caused SARS2 to generate similar pathologies in the body as HIV does, that C0VID was a form of aerosolized immune deficiency. The following link is a very important interview to understand the extent of the bio🔫 crime against humanity which Fauci, Collins, Morens and the #ProximalOrigins group covered up. The problem of spikeopathy, the spike protein from SARS-CoV-2 persisting in the body and causing immune deficiency, is accelerating. Joachim Gerlach and the German group are the only one I know of testing 🩸 for circulating SAR2 spike protein from either (🦠💉) and analyzing the results. What they are finding is troubling. Remember the spike alone, with or without the 🦠 can cause amyloid fibrin micro clots (Pretorius & Kell: “sui generis”.) #TeamClots #MicroClots are associated with Long C0VID, AIDS, thrombosis, autoimmune disease, cancer and dementia. Per Wafik El Deiry, former director of the Brown U. Legoretta Cancer Center, the SARS2 spike (🦠💉) binds the p53 gene the “Guardian of the Genome,” tumor suppressor gene. Spike inactivates the body’s major cancer protection. Per Sabine Hazan, founder of Progena Biome, the SARS2 spike (🦠💉) wipes out the good bifidobacteria in the gut. This bacteria is a prime factor in our immune system, once it's gone, leaky gut and disease follow. What does all of this mean? There is growing evidence of increasing amounts of a toxic protein in the population. A protein which is amyloidogenic, oncogenic and causes immune deficiency. A protein which was created from research by Ralph Baric and the WIV, and covered up by leaders at the NIH and the W.H.O. >