I occasionally try to explain and comment on ME research, or even contribute to it. And I advocate for more and better research.

Living with ME/CFS since 1983. An advocate since my diagnosis in 1988.

https://simondelfavero.com

Disabled by very Severe Post-COVID ME/CFS. Not always able to use phone. Bedridden. Unable to Speak. I care. Ⓐ💚, (FR/DE/EN, but posts in english) Clinging