Wirelessly posted (droid)
You would think so. I have a hunch what it is. Testing is around $900 and will not affect treatment. Most doctors don't want to deal with it. I've heard that it's hard for Ehlers-Danlos syndrome patients to find doctors who will treat them, too. Unfortunately, it's all about $$$ in the U.S. Doctors want to see l a lot of patients in the smallest time intervals possible. A GP told me that it doesn't matter because I can't do anything about it, and this is a person that I know socially.
