ME/CFS
Outcome unclear
ME/CFS, with pacing mattering most; no clear picture of how they are now
- Condition
- ME/CFS
- At worst
- Not stated
- Ill for
- Not stated
- Last post
- Dec 2025
Read from 1 of their posts and comments; links to the one this page draws on
Summary
Writing in December 2025 on an ME/CFS forum, this person said that something of theirs had improved slowly over time, and that pacing mattered more than anything. They gave no other details of their illness course, treatments or how they are now.
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What they tried
Also tried
Their words about each treatment
- Pacing · Helped
Yes, mine improved slowly over time. Pacing mattered more than anything.
In context ↗
Symptoms mentioned
Their words about their symptoms
- POTS & dysautonomia
Yes, mine improved slowly over time.
In context ↗