https://simondelfavero.com

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

NZ museums and heritage aficionado, shoe fancier, curator baiter, demure chocoholic, and all-round-caffeine fiend. Personal views; Not those of my employer.

ME. Spouse w LC, ME. Writer, bread baker, daydreamer. Still waiting on fair funding and apology from HHS. Masking like someone’s life depends on it.

Chaotic mix of politics and ME/CFS

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

Mutter des großen (K1) und des kleinen Chaos (K2)

Was: Facilitation & organisational culture nerd for do-gooders; climate & sustainability. Healthy, athletic; MTB, ski, mountaineering, outdoors. Everything on p

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

non-practicing intellectual on war & tech NL/EN

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.

New main account of @violetta.bsky.social #PwME #MEcfs #PoTS #CPTSD #MCAS #SFN #FQtoxicity #TalkCollapse #CR41W Wishlists: https://paths.to/VioletsWishl

God first! | #mecfs | Oecotrophologin | Redakteurin

reader🌙🔮📚she/her

#PwME #Music #Crochet #PersonalGrowth #MECFS #DignityRespectCivility

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