r/ehlersdanlos•
lapatrona8

Any EDS groups local to Pittsburgh, PA?

General

Hi there -- just relocated to Pittsburgh/western PA and am looking for any local groups specific to our region. I've checked FB and Google and not seeing anything but holding hope that it might ring a bell for someone in here.

It's been a bummer reestablishing care in new city -- feel like I'm starting the cycle all over again with no one believing in or having basic knowledge of hypermobile connective tissue disorders -- and want to find recs for PTs and the like for ongoing care (not diagnosis, already have it).

Posted May 12, 2026, 2:46 PM UTC

22
Loading comments…