EDS Documentary

Here is a short EDS documentary centered on a young woman (around my age) who has EDS. Her name is also Sarah (she has an H though) and she has a similar story to mine. She is in Canada, so some of the aspects of the healthcare system are different for her than me. The documentary is only about 12 minutes long, but it is a wonderful video that portrays many of the realities and struggles of living with EDS. You can watch the documentary, entitled "Still Talking" over at https://vimeo.com/125161284. Sarah also has a Facebook page that chronicles her journey with EDS and other conditions, as well as raises awareness for these conditions, called "Sarah's Shout: Fighting and Raising Awareness for EDS and More". If you would like to follow her for more updates on her journey her page can be found here: https://www.facebook.com/sarahsshout/?fref=ts

Thanks as always for helping to raise awareness and understanding for EDS and related conditions!