ME/CFS
Outcome unclear
Mild ME/CFS with brain fog, trying therapy with no change reported
- Condition
- ME/CFS
- At worst
- Mild (working or studying, with limits)
- Ill for
- Not stated
- Last post
- Aug 2026
In their words
- Condition: ME/CFS
I'm undiagnosed but suspect mild cfs
In context ↗ - At worst: Mild
I think I'd be able to work in this state, I just won't be the most exceptional employee in the world.
In context ↗
Read from 1 of their posts and comments; links to the one this page draws on
Summary
An undiagnosed Reddit user who suspected mild ME/CFS described brain fog that made it hard to think on their feet and trouble expressing themselves in therapy. They were preparing for a cafe job interview while hoping to keep living with their parents, who were threatening a group home. They thought they could work in that state, and said that if working pushed them from mild to moderate it would confirm the diagnosis. They mentioned trying therapy; no change in their condition was reported.
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What they tried
Also tried
Their words about each treatment
- therapy · Not said
I've been trying therapy and have found it's super hard to express myself.
In context ↗
Symptoms mentioned
Their words about their symptoms
- Brain fog
How to do well at a job interview with brain fog?
In context ↗ - Brain fog
I have trouble thinking on my feet if they ask me something I haven't memorized
In context ↗