Philosophy graduate | former science event organiser | former performance artist | ‘former’ and ‘ex’ at most of everything due to #MEcfs

MWF 55+. Autistic. She/Her. Gen X. Caretaker of chronically ill spawn. I like audiobooks, animals, nature, science, spooky quantum stuff. Everyone deserves fo

Part time artist, full time sick person

Science, history, nonsense, and even more | BUGAPSE

#MECFS

Clarinettist. Conductor. Caregiver. 4 cats, 2 kids, 1 husband.

Anthropologist in the margin

Love crafts, history, stories, natural world & spending time with husband, children, family & friends. When M.E /CFS & POTS doesn't stop me - which is most of t

Nicht mehr ganz neu hier; inzwischen gern hier. Auch bei #DieLinke. (pronomen: maskuline = okay, "they" aber ggf. ebenso) #MaskeAuf.😷 Njezažny dźiwnuch. #t

Horizontal advocate for #pwME. 🇳🇱 in 🏴󠁧󠁢󠁳󠁣󠁴󠁿. Ally. Cis. PwME/LC. Volunteer with @meactionscotland.bsky.social. He/Him. #SaveSavannah #BIPOCLivesMatte

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

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

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

Irish Myalgic Encephalomyelitis/Chronic Fatigue Syndrome Association-for Information, Support & Research NB: Posts ≠ advice. Registered Charity RCN 20100254.