ME/CFS
Outcome unclear
ME/CFS, unsure if symptoms are muscular, trying magnesium with B6 with no clear change
- Condition
- ME/CFS
- At worst
- Mild (working or studying, with limits)
- Ill for
- Not stated
- Last post
- Aug 2025
In their words
- Condition: ME/CFS
/r/chronicfatigue/
In context ↗ - At worst: Mild
I try to stay active as much as possible
In context ↗
Read from 1 of their posts and comments; links to the one this page draws on
Summary
They said their protein is okay and they try to stay as active as possible, but they can't really tell if it's muscular. They are taking magnesium chelate with B6 and have been for a few days without seeing a huge difference; they asked whether magnesium level was checked before taking it and whether magnesium makes an instant difference. No cause, duration or overall outcome was given.
Ask Miruvor AI
What they tried
Also tried
Their words about each treatment
- magnesium chelate B6 · No change
Iam taking magnesium chelate B6 too. ... Cause I've been taking it for a few days now and don't really see a huge difference
In context ↗