This is heartbreaking enough for those who became chronically ill during covid. But LC is (almost certainly) a subset of myalgic encephalomyelitus (ME/CFS or ME,) an illness that has reduced a great many formerly active people to mere shadows of our former selves. People can live for DECADES feeling like shit, hardly able to get out of bed. Doctors have dismissed us and told us our suffering is all in our minds.
As covid-19 began, we ME/CFS folks knew what would happen. We were going to be joined by a huge new cohort of this sad club that nobody wants to join. As terrible as the prospect was, the silver lining was that it offered a hope that our illness would finally be taken seriously. With so many newly disabled people, surely research money would flow! We dared to hope that at least we might all benefit from the medical breakthroughs that could result. But no. Once again heartless, unscrupulous people would rather let millions rot than allow government and science to help us.