r/mecfs
For discussion about research, treatment and recovery from Myalgic Encephalomyelitis / Chronic Fatigue Syndrome (ME/CFS).
r/mecfs Subreddit Stats & Analytics
r/mecfs is a Medical Advice subreddit in the World category with 8,337 members. Use this page to track r/mecfs stats, subscriber growth trends, daily and weekly analytics, and similar subreddits with related audiences.
Recent r/mecfs growth: +27 members today (+0.32%) and +108 members this week (+1.31%).
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Similar subreddits to r/mecfs include r/cfs, r/chronicfatigue, r/MyastheniaGravis, r/SyringomyeliaSupport, r/CRPS.
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Similar Subreddits to r/mecfs
For research, treatments, and personal stories regarding Myalgic Encephalomyelitis (ME)/Chronic Fatigue Syndrome (CFS). ME/CFS is a multi-systemic neurological disease, distinct from chronic fatigue as a symptom. For more information, please see our FAQ.
Chronic fatigue is a symptom of many conditions, while Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS) is a complex multi system illness. ME/CFS often occurs after infections but the pathogenesis is not certain. The syndrome "Long COVID" may be a subset of ME/CFS or a distinct condition. An array of symptoms is required for ME/CFS diagnosis, with the most distinctive symptom being post-exertional malaise (PEM). ME/CFS cannot be improved by exercise or psychiatric treatment.
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