ME/CFS
Mild → no benefit
Struggling with life and work while seeking ME/CFS assessment, no improvement
- Condition
- ME/CFS
- At worst
- Mild (working or studying, with limits)
- Ill for
- Not stated
- Last post
- Apr 2023
In their words
- Condition: ME/CFS
was wanting some pointers about broaching the topic of CFS
In context ↗ - At worst: Mild
I am still struggling with life and work
In context ↗ - Now: No benefit
I am still struggling with life and work
In context ↗
Read from 1 of their posts and comments; links to the one this page draws on
Summary
They posted in April 2023 while seeking a CFS assessment, saying they still struggled with life and work. Most other causes had been ruled out, their B12 was stable, and CPAP had reduced their sleep apnoea index from 61 to 1, but their overall functioning remained limited. They did not report a CFS treatment or any change over time.
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What they tried
Also tried
Their words about each treatment
- cpap · No change
my OSA since starting cpap has dropped from 61 to 1, but I am still struggling with life and work
In context ↗