https://simondelfavero.com

begrudgingly online for chronic illness research & disability justice community. living meaningfully & unapologetically as a hermit against my will.

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

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

God first! | #mecfs | Oecotrophologin | Redakteurin

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 MS and ADHD in the best way I can. Open University student. Interested in HSD, EDS, ME/CFS, Long Covid, neurodiversity, and neuroplasticity. Everyth

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.

non-practicing intellectual on war & tech NL/EN

Cat lady, neulootikko, psykologi ja sosiaalipsykologian väitöskirjatutkija.

ME secondary to Covid vaccination. pro vax/vax injured. Zero tolerance for personal abuse. Do unto others as you would have others do unto you.