cross-posted from: https://lemmit.online/post/5623716
This is an automated archive made by the Lemmit Bot.
The original was posted on /r/cfs by /u/Johannes_Keppler on 2025-04-11 08:11:54+00:00.
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.
I wish I knew about pacing sooner. I was under therapy for CFS/ME through telephone sessions and they really helped me especially with pacing. I still have fatigue but I've been better at being able to manage it and realise my limits.