https://simondelfavero.com

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

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

Surviving MyalgicE aka ME/CFS & AAG to tell the story, pwME & advocate w/ a JD. Into MEdical, Social, Climate Justice & Arts. ME-dical apolide, Human Neutrino,

News and information about interventional trials for Long Covid, ME/CFS, POTS, and other post-viral illnesses. Message or tag me if you’re in a trial or otherwi

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

Es gibt immer noch eine große Lücke zwischen dem, was die Öffentlichkeit über COVID-19 weiß, und dem, was sie wissen sollte. Deshalb hier Infos über COVID-19.

Living with Long Covid. Doing my bit to support UK healthcare workers with Long Covid. Chair of Supporting Healthcare Heroes UK. Associate Member Long Cov

Life long repro advocate. Here for social Justice, science, and pet picts. Officially tired. **Wear a mask- everywhere.** LC, EDS. Love a good debate, but won’t

Currently out of order due to Long Covid and ME/CFS Graphic design student she/her