Vegetarian, book lover📚 Living with ME/CFS since 1990 ♿️ She/Her ME/CFS = myalgic encephalomyelitis / chronic fatigue syndrome Please use #AltText on images/GIFs/videos ❤️ Avatar photo: Old photo of my cat, tabby with white chest & paws. Banner photo: A grove of leafy green trees in a park. My posts, no boosts = https://justmytoots.com/@ahimsa_pdx@disabled.social?public_only=true #MEcfs #PwME
Soul of a goth in cowboy duds. Weirdly American. Religious but not spiritual. #Writer of What A Charming House. Deuteronopically colorblind and neurodivergent as hell. #LongCOVID caregiver. Cat dad. I post a lot about #books. #Sober desperado. #Accessibility. 📍 Grays Harbor, Washington #Bookstodon #BelieveInFilm #WhatACharmingHouse Alt text for pic: Drawing of person in glasses with respirator mask.
95% of posts on #MyalgicEncephalomyelitis, #LongCovid or #chronicillness. With ME/CFS 37 years, severely affected 31 years. Health has deteriorated post Covid (March 2022). Irish ME/CFS Association* trustee 29 years. 26 publications in peer-reviewed journals. MEpedia entry which has links to my social media accounts (among other things): https://me-pedia.org/wiki/Tom_Kindlon #ChronicFatigueSyndrome #MECFS #PwME #fedi22 *IrishMECFSAssociation@mastodon.ie
📺 https://peer.adalta.social/w/kqRH8K2ZTgjShFoaNHUR1g 🔗 🇩🇪🇺🇸🇫🇷 🔗 ℹ️
La publication d'un plan de soins spécialisé marque un tournant dans la prise en charge de ces pathologies invalidantes.
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