Katybug Posted November 26, 2012 Report Share Posted November 26, 2012 Hey folks! I got the official EDS Type 3 diagnosis last week from the geneticist. She wants me to find a physical therapist that does myofascial release to gain control of my pain. Do you have any EDS forums that you belong to that I can join to see if others in the Baltimore area can help me find a PT? Quote Link to comment Share on other sites More sharing options...
DoozlyGirl Posted November 26, 2012 Report Share Posted November 26, 2012 Hi Katie,I'm so glad you are connecting more dots. Congratulations for this milestone. I hope this can bring you relief. EDNF Forumhttp://www.inspire.com/groups/ehlers-danlos-national-foundation/EDS Organization - great resource http://www.ednf.org/Take Care,Lyn Quote Link to comment Share on other sites More sharing options...
lumpchp Posted November 26, 2012 Report Share Posted November 26, 2012 Like doozlygirl said, the folks at EDNF are great :-) Quote Link to comment Share on other sites More sharing options...
Katybug Posted November 27, 2012 Author Report Share Posted November 27, 2012 Having good success at Inspire/EDNF. Thanks ladies! Quote Link to comment Share on other sites More sharing options...
Recommended Posts
Join the conversation
You can post now and register later. If you have an account, sign in now to post with your account.