Thanks again Mayo Clinic for this outstanding flyer summarizing #MyalgicEncephalomyelitis and urging physicians to take the CME. I just sent it to administrators at UW Medicine which, again, has no M.E. specialist nor any physician who's current on M.E. research: #PwME

President Biden We need a clear plan to address #longcovid. I hope that happens next week.

Is there anything worse for the cause than a *checks notes* person with ME?

The impact of ME/CFS versus funding Illnesses listed on the bottom if you can't see it Sickle Cell Disease, Brain Cancer, Parkinson's, Multiple Sclerosis, HIV/AIDS, ME/CFS. From Jeffrey Tran's video (warning: a bit noisy) tiktok.com/@poisedleft/vi… #MEcfs #CFS #PwME

ME is the only illness where they have to research a cure for the doctors before they can move on to the patients.

A short piece in Brabants Dagblad today, about my part in Stichting Long COVID's documentary on Long Covid, which premieres tomorrow Nederlands Film Festival, and my basic view on the matter. Thanks to Pieter van Klinken for the interview.

I no longer giving grace to people calling Long Covid a mysterious new disease with lots of symptoms to chase. It’s not. It’s got subgroups. The predominate one causing chronic disability is ME/CFS. PEM is a unifying construct. There’s the approach in a tweet. Go discover stuff.

Totally fine to not reply with “you’ll get better if you believe x” etc. here btw.

Hey vitalik.eth, have you heard about this? A potential mechanism of ME/CFS and LongCOVID has been found by Mitodicure and they want to start clinical trials but are still in search of financing.

Hi Twitter hive mind - I'm looking for the most reliable statistics on the economic impact of LC in the UK. Any recommendations or trusted sources you can point me to? Thanks in advance!

Nature: “For [ME/CFS], the ratio of burden to funding is 0.04. For HIV/AIDS, the ratio is 15.6.” nature.com/immersive/d415… Turns out the world’s top doctors and scientists miss a lot when they don’t even look.