ME/CFS
Moderate → no benefit
ME/CFS for decades, worse after COVID, with no improvement
- Condition
- ME/CFS
- At worst
- Moderate (mostly housebound)
- Ill for
- decades
- Last post
- May 2026
In their words
- Condition: ME/CFS
I've had it for decades as well.
In context ↗ - At worst: Moderate
Power chair. It's much easier to put into a car etc, and has a smaller footprint
In context ↗ - Now: No benefit
Though my symptoms did get worse and my flares more frequent after covid.
In context ↗
Summary
A Reddit user who had ME/CFS for decades said their symptoms worsened and their flares became more frequent after COVID. They did not mention treatment or recovery and gave no concrete level of function. In May 2026 they mentioned a power chair as easier to put into a car and with a smaller footprint.
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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.
| When | What happened |
|---|---|
| — | ME/CFS for decadesI've had it for decades as well.In context ↗ |
| after covid | symptoms worsened and flares became more frequent after COVIDThough my symptoms did get worse and my flares more frequent after covid.In context ↗ |
| 2026-05-24 | still ill; uses a power chairPower chair. It's much easier to put into a car etc, and has a smaller footprintIn context ↗ |