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ME/CFS Outcome unclear

ME/CFS: what they tried made symptoms 10x worse, so they cap trials at three months

Condition
ME/CFS
At worst
Not stated
Ill for
Not stated
Last post
Sep 2023
Read from 1 of their posts and comments; links to the one this page draws on

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Summary

A Reddit user in r/cfs said that what they were trying made them feel "10x worse" and that there was no option to vote for "made my symptoms incredibly worse". They said they would not try anything for more than three months when it was making them feel that way.

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What they tried

Also tried

Their words about each treatment
  • LDN · Much worseNo option to vote for "made my symptoms incredibly worse" ... it is literally making me feel 10x worse In context ↗

Adverse events

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