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tomkindlon
@tomkindlon@disabled.social95% of posts on #MyalgicEncephalomyelitis, #LongCovid or #chronicillness.
With ME/CFS 35 years, severely affected 29 years. Health has deteriorated post Covid (March 2022).
Irish ME/CFS Association* trustee 26 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
ahimsa_pdx
@ahimsa_pdx@disabled.socialVegetarian, book lover📚 Living with ME/CFS and Dysautonomia since 1990 ♿️ She/Her
Please use #AltText on images/GIFs❤️
Yes, I'd love to see a photo of your cat😻
Avatar photo: Old photo of my cat, tabby with white chest & paws. Banner photo: Trees in a park with green leaves.
Just my posts, no boosts = https://justmytoots.com/@ahimsa_pdx?public_only=true
#MEcfs #PwME #Dysautonomia #POTS #LongCovid #Disability #Accessibility
zaivala
@zaivala@hostux.socialLinux user since 2002, never a sys admin or IT guy. Podcaster on mintCast, Distrohoppers' Digest, and Full Circle Weekly News podcasts. Chief Bard of Triad Bardic College. Filker. Avid reader. Pagan priest and multi-ordained minister. Substitute teacher. Wrong as much as right, and always left. Southeastern US.
et_alia
@et_alia@strangeobject.spaceavi description: a piece of digital art of a smiling, femme-presenting, bald, pale-skinned, blue eyed person. wearing a strappy pink coloured top, jeans, glasses, and sat in a wheelchair. art by @Cosmix
we are a mentally and physically disabled unemployable trans plural system
im my next life i intend to be born either as a sentient slime or a rock with googly eyes
halcionandon
@halcionandon@aus.socialAnother T*****r immigrant. It’s nice here. Better profile pending. See intro: https://aus.social/@halcionandon/109312394494110821 Please be mindful that I’m energy limited & it takes a lot of effort to reply to posts, boost, ie I’m putting a lot of effort into our interactions. Feel special! I’ll likely forget to reply or take a while (weeks/months) if having a bad time. #Science #Writing #MMT #Auspol #MedicalResearch #Healthcare #NDIS #ChronicIllness #pwME #MECFS #LongCovid #Disabled #NEISVoid #Melbourne, #Australia
yesterzine
@yesterzine@topspicy.socialPlayer : Doomed Colonist : https://www.twitch.tv/totally_unoriginal_hde
Member : Big Red Arrow Club : https://www.youtube.com/@BigRedArrowClub
Editor : Yesterzine : https://tiny.cc/yesterzine
Rest of the links : https://linktr.ee/yesterzine
ImmedicableME
@ImmedicableME@mastodon.onlineFormer medical librarian now #Disabled by #MECFS, #Dysautonomia/#hyperPOTS, #MCAS, nonepileptic #Seizures, #HEDS, and more. Really, really overeducated for my current career as a couch surfer and bed hopper (just trying to make “bedridden” and “housebound” sound more exciting). Late-diagnosed #ActuallyAutistic. Social awkwardness is my copilot. A “really nice guy, for a girl.” Never knowingly unkind—it’s ok to let me know if something I post is problematic. #Lesbian. She/her. United States.
imstilljeremy
@imstilljeremy@babka.socialtentatively back from hiatus (sorta):
Tylko trochę Polsce.
קצת עברית.
Largely limited to: #Jewdiverse #Mazeldon #Politics #USPolitics #BlackLivesMatter #Disabilities #WheelOfTime #WoT #Pluralism #SFF #Michigan
IrishMECFSAssociation
@IrishMECFSAssociation@mastodon.ieThe Irish Myalgic Encephalomyelitis/Chronic Fatigue Syndrome Association – for Information, Support & Research. NB: Posts should not be considered advice. Registered Charity Number: 20100254 CHY 22039
#MEcfs #PwME Currently also sharing some items relating to #LongCovid given various research studies have found a significant percentage satisfy ME/CFS criteria
