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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.

  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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