ME/CFS
Outcome unclear
Brain fog with ME/CFS; wheelchair helped a lot but OT questioned it
- Condition
- ME/CFS
- At worst
- Moderate (mostly housebound)
- Ill for
- Not stated
- Last post
- Jun 2024
In their words
- At worst: Moderate
if i could choose between losing my leg strength and getting less brain fog vs walking more and having more brain fog
In context ↗
Read from 1 of their posts and comments; links to the one this page draws on
Summary
Living with brain fog, they had recently tried a wheelchair and got a lot out of it. At a local chronic pain clinic their occupational therapist questioned the wheelchair, while their psychologist had been enthusiastic about it. They said they would rather lose leg strength than walk more with more brain fog, and were annoyed by the OT's response.
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What they tried
Also tried
Their words about each treatment
- wheelchair · Helped
I mentioned trying a wheelchair and getting a lot out of it a week or so ago
In context ↗
Symptoms mentioned
Their words about their symptoms
- Brain fog
getting less brain fog vs walking more and having more brain fog
In context ↗