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ME/CFS Outcome unclear

ME/CFS pain, with swimming two or three times a week dulling it

Condition
ME/CFS
At worst
Not stated
Ill for
Not stated
Last post
Nov 2021
Read from 1 of their posts and comments; links to the one this page draws on

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Summary

Crest 17685, posting in r/cfs in November 2021, said that a few years earlier they had a membership and swam two or three times a week with their roommate, floating or doing exercises in the water. They said the swimming made a difference in dulling their pain, and that they missed it a lot. They gave no details on how the illness began, how ill they were, or how they were doing when they wrote the post.

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What they tried

Also tried

Their words about each treatment
  • swimming · HelpedIt definitely made a difference in dulling my pain and I miss it a lot. In context ↗

Their path

They say too little about how ill they were at each step to draw it on the severity scale, so the steps are listed as they describe them. Dates are when they posted.

WhenWhat happened
a few years before November 2021swam and floated in the water two or three times a week; pain dulledIt definitely made a difference in dulling my pain In context ↗
2021-11-09no longer swimming; misses the pain relief it gaveI miss it a lot In context ↗

Symptoms mentioned

Their words about their symptoms

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