// SUBREDDIT_PROFILE
r/mecfs
› 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.
// MEMBERS
9,801
› subscribers
// POSTS_INDEXED
304
› analyzed records
// COMMUNITY_AGE
4y
› since 2022-06-20
// STATUS
[ok] active
› feed indexed
// QUICK_ACTIONS
// RELATED_COMMUNITIES
[ 12 communities · comparable size ]
r/palmpals
› 9,850 members · 125 posts indexed
r/RotatorCuff
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// FAQ [ 3 entries ]
01 › What is r/mecfs about? [ expand ↓ ] [ collapse ↑ ]
r/mecfs is a Reddit community with 9,801 members. 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.
02 › How active is r/mecfs? [ expand ↓ ] [ collapse ↑ ]
r/mecfs has 9,801 subscribers and 304 posts in our index. It was created on 2022-06-20, 4 years ago.
03 › Which subreddits are similar to r/mecfs? [ expand ↓ ] [ collapse ↑ ]
Communities of a comparable size include r/palmpals (9,850 members), r/RotatorCuff (9,844 members), r/AskBulgaria (9,839 members), r/Cochlearimplants (9,837 members). Each is listed with its own subscriber and post counts in the related communities section above.