ME/CFS
Outcome unclearNeeds ongoing treatment
Chronic pain with ME/CFS, some routines help but managing it is a full-time job
- Condition
- ME/CFS
- At worst
- Not stated
- Ill for
- Not stated
- Last post
- May 2026
In their words
- Condition: ME/CFS
r/chronicfatigue
In context ↗
Read from 1 of their posts and comments; links to the one this page draws on
Summary
They described living with chronic pain that needs constant management: stretching routines, sleep adjustments, activity pacing and avoiding flare-ups. Some of it helps, they said, but the upkeep feels like a full-time routine just to stay functional, and the mental exhaustion of managing it all can be as draining as the pain itself. No onset, duration or treatment outcomes were given.
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What they tried
Also tried
Their words about each treatment
- stretching routines · Not said
Stretching routines, sleep adjustments, activity pacing, recovery work, avoiding flare-ups, changing how you sit or move.
In context ↗
Symptoms mentioned
Their words about their symptoms
- Pain & fibromyalgia
I think one of the hardest parts of chronic pain is how much mental energy goes into managing it.
In context ↗