EDS Austin is a group for people with Ehlers-Danlos Syndrome, and those who are pursuing a diagnosis. I hope this group will become a resource for information and support. I have EDS hypermobility type diagnosed last year.
I've recently taken over this group and hope to schedule some meetings very soon. Some ideas include a meet and greet, group fitness meet ups (an easy walk, class with an instructor sensitive to EDS/joint hypermobility/chronic pain, etc.), support group/information exchange, and doctor Q&A.