ahimsa @disabled.social Vegetarian, 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\[email protected]?public\_only=true
\#MEcfs #PwME #Dysautonomia #POTS #LongCovid #Disability #Accessibility
@[email protected]
"I think a government shouldn’t be overly concerned about follower counts and interactions, but rather about providing free, autonomous communication that is independent of third-party companies."
Agreed!
Plus if they post on X then anyone who does not have an X account cannot see threads/replies, only the first post.
And even then it's kind of wonky! Sometimes when I look at an X profile (not logged in since I have no account) I see old posts and not the latest ones.
From (https://disabled.social/tags/MEAction):
From #MEAction:
(please any send questions to them!)
"#MEAction is thrilled, once again, to partner with Shannon Williams-Bramburger of Nourish Therapeutic Yoga to provide a 30 minute, virtual, very modified movement class on Thursday, Feb 8th at 11 am PT / 2 pm ET / 7 pm BST that has been crafted specifically for people with ME.
The whole class will be lying down and can be done from bed"
Details here:
https://www.meaction.net/event/meaction-is-offering-a-very-modified-movement-class/
The Massachusetts ME/CFS and FM Association has posted a recording of their November 19 webinar:
The Massachusetts ME/CFS and FM Association has posted a recording of their November 19 webinar:
"What Sociology and the Illness Narratives Can Teach Us About Living with Chronic Illness"
https://www.youtube.com/watch?v=WoX2nN\_1EF8
\#MEcfs #CFS #PwME #MyalgicEncephalomyelitis #ChronicIllness #Sociology #MassME