Fact, history, opinion, and sarcasm, with an occasional side dose of sass. Primary function of being occasionally useful in between shitposting and ranting abou

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

⚒️Aotearoa Uppity disabled poor person Political commentator Knowledgeable but always learning AuDHD #StillCoviding #landback Human made only Consider supporti

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

🚫No DM’s. Raging lefty. ME warrior (every second of every day, yawn). Wrong kind of Jew for Zionists. 🚫no DM’s🚫 no porn🚫 No DM’s🚫

Not a doctor; not even a dog. Autistic and unhinged. Wannabe Mad Scientist. Aspire to be a demigod. 𒃲𒌋𒅗𒆪𒁉 This is my 𒅎𒄘𒇲(slate library)

Housebound by MECFS, mostly bed/ Sofa since 2022 Bildschirm triggert PEM, deshalb selten hier & Energiebudget reicht nur für liken und weiter verbreiten Lebe in

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.