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EDS documentary

November 9, 2011

A short trailer of a documentary by Lara Bloom (who also suffers with POTS and EDS). Filmed to raise awareness of Ehlers-Danlos syndrome. When I say to someone that I’m in constant pain, it doesn’t sound believable, but this short trailer explains it much better than I ever could…

I hope to have some time over the weekend to post an update about my trip to the Lake District last week.

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2 Comments
  1. Thank you for this, Liam, is the documentary out yet? This looks wonderful for informing the public of both POTS and EDS! I found out about your blog from Simon Waller in London, and it is fantastic, thank you!

    • Thank you Stacy.

      I spoke with another of my EDS/Pots friends today and they said its not out yet, and there is no release date at the moment. But I will let you know as soon as i know anymore.

      I’m looking forward to seeing the finished documentary – like you say, it should be good to help raise awareness!

      All the best, Liam.

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