r/mecfsSD↗
Welcome to the official subreddit of ME/CFS San Diego, a 501(c)(3) non-profit dedicated to raising awareness of, educating about and advocating for Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS). This space is for reposting vital information, research updates, and advocacy efforts to support the ME/CFS community. Our goal is to connect and share resources to improve care, awareness, and quality of life for those affected by ME/CFS and related conditions. EIN: 87-0963019
39 subscribers22 posts / mo in Sep 20261 authors / mosince 2025
r/mecfsSD has 39 members. It gets about 22 posts a month from 1 people.
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How r/mecfsSD has grown
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Who posts on r/mecfsSD
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Posts and activity for Sep 2026. Members from Reddit's subscriber counts. Read from the same data the app runs on. Our research





