ME/CFS
Outcome unclear
ME/CFS diagnosis sought for university support; no treatment, pain clinics no help
- Condition
- ME/CFS
- At worst
- Not stated
- Ill for
- Not stated
- Last post
- Jan 2020
Read from 1 of their posts and comments; links to the one this page draws on
Summary
They want a diagnosis so they can get the support they need at university, while knowing there is no treatment and that pain clinics are no help either; doctors they have met seem to follow an “if I can’t see it, it doesn’t exist” policy.
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What they tried
Also tried
Their words about each treatment
- pain clinics · No change
I know from pain clinics that that’s no help either
In context ↗