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
Ahimsa
@ahimsa_pdx@disabled.social
disabled.social
From #MEAction for Severe ME Day (Aug. 8)
"Honoring Severe ME Day & Sharing our Severe ME Artists Project 2026"
https://www.meaction.net/post/honoring-severe-me-day-sharing-our-severe-me-artists-project-2026
"#MEAction is proud to share the Severe ME Artists Project 2026!
... over 100 of you submitted photos, drawings, writing, and videos of your work! We debuted this project in 2021 and five years later we continue to be humbled and honored to bring you the work of the Severe ME community"
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@mecfs@fedigroups.social
#MEcfs #SevereME #SevereMEcfs #PwME #Art #Disability
Tom Kindlon
@tomkindlon@disabled.social
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
disabled.social
Proposed Framework for Personalized Severity Assessment in ME/CFS to Capture Variation in ME/CFS Severity and Life Impairment across Patients and Time (2024)
https://www.frontiersin.org/journals/immunology/articles/10.3389/fimmu.2024.1369295/full
#MEcfs #CFS #PwME #SevereME #SevereMECFS
#SevereCFS #VerySevereME @mecfs@fedigroups.social
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