ME/CFS
Outcome unclear
ME/CFS with no specialist support, online pacing resources got them through rough patches
- Condition
- ME/CFS
- At worst
- Not stated
- Ill for
- Not stated
- Last post
- Oct 2026
In their words
- Condition: ME/CFS
navigating a health system that's not even your own while dealing with cfs
In context ↗
Read from 1 of their posts and comments; links to the one this page draws on
Summary
A Reddit user with ME/CFS wrote about coping with no specialist support. They said the Workwell Foundation's online pacing resources got them through some rough patches when they had zero specialist support. They gave no onset, severity, symptoms or current state of their own, and mentioned naltrexone as something others get off-label, not as their own treatment, cost or outcome.
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What they tried
Their words about each treatment
- the stuff from the workwell foundation · Helped
the stuff from the workwell foundation got me through some rough patches when i had zero specialist support
In context ↗