The document weaves a step-by-step narrative, in which each step builds on a real-world source to take the story a little further:

Step 1 — The scientific seed. In June 2020, Changeux, Amoura, Rey, and Miyara (Institut Pasteur/Collège de France) published a hypothesis: SARS-CoV-2 might interact with nicotinic acetylcholine receptors (nAChR). They noted that a loop in the spike protein shares a short sequence similarity with snake neurotoxins (cobratoxin, bungarotoxin), and that nicotine might compete with the virus.

Step 2 — Extrapolation. The document transforms this partial similarity into an identity: the virus is a snake neurotoxin. COVID = snakebite.

Step 3 — The toxin factory (Brogna). SARS-CoV-2 is said to be a bacteriophage: it infects gut bacteria, which then produce conotoxins, phospholipase A2, and metalloproteinases—explaining thrombosis, bronchoconstriction, cytokine storms, and fecal transmission.

Step 4 — Vaccines as a Second Envenomation (Ardis). mRNA injections are said to contain venom genes in DNA plasmids. The key argument: an experiment in which two plasmids, each containing half of a cobratxin, killed mice when combined—drawn as a parallel to the two vaccine doses. The company “Cobra Biologics” (an actual manufacturer of plasmids) serves as a “signature.”

Step 5 — Artificial origin. The furin cleavage site (2025 White House report, 2018 Bonnin thesis) would prove a gain of function: the virus possesses “a characteristic that does not exist in nature.”

Step 6 — Long COVID as a sequela of envenomation. The persistent symptoms (anosmia, fatigue, neuropathies) are reportedly identical to the documented sequelae of snake bites.

Conclusion of the narrative: the virus and the vaccine are two versions of the same poison; long COVID is untreated snakebite poisoning; scientific authorities have deliberately covered it up.

Promoted by Dr. Nacima Mdhafar-Bouzeroura and her team of independent physicians.

Translated with DeepL.com (free version)

Translated with DeepL.com (free version)