ME/CFS
Outcome unclear
ME/CFS: two weeks of oxaloacetate, no difference in energy, pain or brain fog
- Condition
- ME/CFS
- At worst
- Not stated
- Ill for
- Not stated
- Last post
- Apr 2025
In their words
- Condition: ME/CFS
other cfs folks
In context ↗
Read from 1 of their posts and comments; links to the one this page draws on
Summary
A person with ME/CFS took oxaloacetate for two weeks and reported no difference in energy levels, pain levels or brain fog. They called it very expensive and said they could not imagine continuing unless there were clear benefits, but worried about stopping too early in case it took longer to work.
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What they tried
Also tried
Their words about each treatment
- oxaloacetate · No change
I've been on it for 2 weeks and haven't noticed any difference in my energy levels, pain levels, or brain fog.
In context ↗
Symptoms mentioned
Their words about their symptoms
- Brain fog
haven't noticed any difference in my energy levels, pain levels, or brain fog
In context ↗