(They) Digital & narrative trainings. Host of Graphic Policy Radio: a podcast on genre media & movements for social change. 🤘🏻 🏳️‍🌈 🖖🏻 Public Health, uni

https://simondelfavero.com

Geocaching, Pfadfinder, Wetter, Klima, Musik, Fotografie

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

Lisa Smith. Writer, narrator, migraine advocate, connector of dots, Masshole. Sarcasm free of charge. She/her. (I block lots of ppl for tons of reasons, rarely

95% of posts on #MyalgicEncephalomyelitis, #LongCovid or #chronicillness. With ME/CFS 37 years, severe ME 32 years. @IrishMECFSAssoc trustee 29 years 26 publ

Old straight white aspie male 1. Buy British, eg 70% PRUK 30% GILS 2. HODL 3. Profit! (maybe 50/50 just now) One party for the 5% (aristocracy, oligarchs, el

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,

#DemandDemocracy I have dreamed a dream but now that dream is gone from me (former?) grand-masters #runner Please support #LongCovid research #LongCovidAthl

Skeets und Gedanken über Recht, Leben, Lieben, Leidenschaft ✈️ + was sonst noch so anfällt. Nicht immer das, was man hören will xD ME is not a joke. AuDHD is

Post little, here to learn. Long Covid (mild fortunately) - still try to run, ex cyclist & karateka. Recently became a Snorthern when I moved to Sheffield from

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

Passionate swimmer housebound due to LongCovid. Interested in biology, biochemistry, systems theory, exercise science and LongCovid/MECFS

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.

Climate lawyer on pause with ME/CFS and LC

Hypatia of Seattle (high-PAY-she-uh; they/she). Bi transbian, hopepunk cheerleader, white intersectional feminist, social justice bard. Dying & salty about it.

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

Independent historical researcher (involuntarily self-taught), writing at a frustratingly slow 🐌 pace due to severe chronic illness.

ME after covid infection Feb'22. Bedbound. 🛌 #ThereForME #GreatestMEdicalScandal #PEM 🇬🇧🇲🇫🇪🇦🇧🇪

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

www.omf.ngo

Previously: Researcher and PhD candidate @ RWTH Aachen University, now probably disabled by Long COVID. Physics simulation, mathematics, software and science

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

reader🌙🔮📚she/her