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 months ago by FundMECFSResearch to c/myalgicencephalomyelitis

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

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

[-] FundMECFSResearch 3 points 3 months ago

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

[-] Alexstarfire@lemmy.world 2 points 3 months 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 2 points 3 months 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

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ME/CFS

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

Since Lemmy is small, this community also serves as a hub for common comorbidities of ME/CFS. Long COVID (Post COVID), POTS (Postural Orthostatic Tachycardia Syndrome), OI (orthostatic intolerance), MCAS (mast cell activation syndrome), and more!

For those who want an even more general community, check out !chronicillness@lemmy.world

Also please DM me I need to add some mods!

Rules: Instance Rules, No Ableism + No quackery or denialism. Empathy first, is a must to participate. No unsolicited advice.

founded 6 months ago

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