r/mecfs is a subreddit with 10k members. The most common kinds of discussions are advice requests and solution requests, and the community frequently discusses me/cfs, struggling, support, tired, and long covid.
For discussion about research, treatment and recovery from Myalgic Encephalomyelitis / Chronic Fatigue Syndrome (ME/CFS). Recovery is possible, and attacking recovered patients or denying their illness will not be tolerated.
Popular Themes in r/mecfs
#1
Advice Requests
: "My girlfriend who has moderate ME/CFS wants to move to a Reform part of the country in the UK to be closer to her family, but I really don't want to. Am I being unreasonable/irrational?"
11 posts
#2
Solution Requests
: "Healthhack: make a tests and imaging binder"
3 posts
#3
Pain & Anger
: "Mini rant about moderate ME"
3 posts
Popular Topics in r/mecfs
#1
Me/cfs
6 posts
#2
Struggling
4 posts
#3
Support
3 posts
#4
Tired
3 posts
#5
Long Covid
2 posts
#6
Doctor
2 posts
#7
Pem
2 posts
#8
Workplace
1 post
#9
Misconceptions
1 post
#10
Watch
1 post
Flair Used in r/mecfs
#1
vent
: "Mini rant about moderate ME"
2 posts
#2
Research
: "Low Dose Naltrexone for Post-COVID Fatigue Syndrome: A Randomized Controlled Trial"
1 post
Member Growth in r/mecfs
Yearly
+6k members(138.8%)
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About
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Last updated: October 27, 2026