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r/rareEhlersDanlos

@rareEhlersDanlos

This subreddit is designed for users who have a confirmed diagnosis of a rare Ehlers Danlos subtype. (mEDS, clEDS, spEDS, kEDS, BCS…

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There is not enough data yet

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Online

There is not enough data yet

  • 1D
  • 1W
  • 1M
  • All time

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r/ehlersdanlos

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