Does anyone ever doubt themselves still even after a diagnosis? I was diagnosed in 2018 with EDS but realized that I still struggle to accept my illness (and therefore properly treat myself). I think it comes from several experiences with primary care givers and family members too. I find myself writing off my pain a lot as not as bad as others or rereading what qualifies as hypermobile EDS/wishing for the genetic test. I guess I wonder how you cope with these feelings if they come up for you?
Posted by heart7119 at 2022-10-04 01:54:28 UTC