this post was submitted on 05 Jul 2026
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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.
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Reminds me of my disability evaluation where my ability to lift my arm over my head once translated to them that I'd be able to wash myself.
Not faking it would mean that my wife wouldn't even let them see me because their mere presence could be too much for me.
These crazy hoops we jump through, just to meet the needs of public perception...
I felt utterly humiliated at times, altho it's what the situation called for, essentially.