My Mom was disabled by ME, but I didn’t understand until I developed Long COVID. I wrote an apology letter to her. - The Sick Times (thesicktimes.org)

submitted 3 weeks ago by FundMECFSResearch@lemmy.blahaj.zone to c/myalgicencephalomyelitis@lemmy.blahaj.zone

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[-] Alexstarfire@lemmy.world 6 points 3 weeks ago

The title would really benefit from not using the abbreviation ME (myalgic encephalomyelitis).

[-] FundMECFSResearch@lemmy.blahaj.zone 3 points 3 weeks ago

Fair. But I shared it to a community for patients and caregivers.

[-] Alexstarfire@lemmy.world 2 points 3 weeks ago

Also fair. But it's gonna show up for plenty outside the community as well. Don't know if this is app specific but mine basically functions as /r/all on Reddit. Just pulls posts from everywhere.

[-] FundMECFSResearch@lemmy.blahaj.zone 2 points 3 weeks ago

On most apps you can see “all” but also have a feed for your subscribed communities.

this post was submitted on 10 Dec 2024

13 points (93.3% liked)

ME/CFS

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A community for people with Myalgic Encephalomyelitis (ME), sometimes called Chronic Fatigue Syndrome (CFS).

No quackery or denialism. Empathy first, is a must to participate. No unsolicited advice.

founded 3 months ago

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