People have already started appearing in various chronic illness forums around the world with what sounds very much like ME/CFS after having caught Sars2. The official diagnosis takes at least 6 months of having the symptoms and its notoriously badly diagnosed throughout the world due to the incredibly flawed PACE study that painted it as a physchological disease.

Doctors need to be quickly educated on the known blood bio marker combination (igG, lymocytes 2% and antibody complexes all abnormal) until the Stanford nano needle salt stress test is developed and released. They need to ensure patients are put onto a pacing regime which will slow the rate at which they get worse.

Many epidemics have caused ME/CFS "outbreaks" and it has no treatment and almost no research has even been done. 5% of people recover but some also die, most are broken for life. Doctors often think its diabetes as it presents with similar systemic issues but the insulin tests usually come up fine. Its critical they do immune system and full thyroid tests and get the diagnosis and the treatment correct early as each over exertion will permenantly degrade their patients energy levels.