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/r/guillainbarre is a small, welcoming community for those who have survived or are currently battling Guillain Barre Syndrome or Chronic Inflammatory Demyelinating Polyneuropathy, the family/friends of patients and survivors, and for those curious about the disease. We welcome anything related to GBS/CIDP: questions, insightful articles or news, stories about experiences or just general ranting (because, let's be honest, sometimes it sucks!). Feel free to grab a flair and share (or vent!) away.

Notice: This subreddit is not actively monitored, so the posts here are only a small subset of what exists on reddit.

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