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ME/CFS Outcome unclear

ME/CFS: NHS pacing treatment not worth the wait, nothing beyond online

Condition
ME/CFS
At worst
Not stated
Ill for
Not stated
Last post
Nov 2024
Read from 1 of their posts and comments; links to the one this page draws on

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Summary

A Reddit user with ME/CFS who attended NHS treatment for it. They said the treatment was not worth the wait, that it offered nothing they could not find online, and that it focused on pacing. They did not say when their illness began, how severe it was or how they are now, so their outcome is unknown.

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What they tried

Their words about each treatment
  • NHS treatment · No changeI personally did not find the NHS treatment worth the wait. Wasn't anything you can't find online and was focussed on pacing. In context ↗

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