ME/CFS
Outcome unclearNeeds ongoing treatment
ME/CFS and CPTSD with brain fog and no quality rest; tried MCAS treatment and famotidine
- Condition
- ME/CFS
- At worst
- Not stated
- Ill for
- Not stated
- Last post
- Sep 2026
In their words
- Condition: ME/CFS
Wow, I could have written most of this post myself. I also have CPTSD and a bunch of other diagnoses.
In context ↗
Read from 1 of their posts and comments; links to the one this page draws on
Summary
They have CPTSD, brain fog and couldn't get quality rest, and had tried everything they could to cope. Getting their MCAS treated helped a lot: fexofenadine twice a day eased brain fog, but famotidine was the key, calming their body from the first dose and letting yoga nidra work. When they miss a famotidine dose now they see the difference.
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What they tried
Their words about each treatment
- fexofenadine · Helped
It does help a lot with my brain fog, but the real key for my whole system to take things down a notch and for the yoga nidra to work, was famotidine.
In context ↗ - famotidine · Helped a lot
When I miss a dose now I see the difference.
In context ↗ - yoga nidra · Not said
the real key for my whole system to take things down a notch and for the yoga nidra to work, was famotidine
In context ↗
Symptoms mentioned
Their words about their symptoms
- Brain fog
It does help a lot with my brain fog
In context ↗ - Mast cell (MCAS) & allergies
I got my MCAS treated
In context ↗ - Sleep problems
I still couldn’t get quality rest
In context ↗