Frustrated and Confused...?

We did some research in class and I came across EDS and it sounds a lot like me (only my joints don’t dislocate). I’ve been sorta chronically ill my entire life and deal with a lot of things that I thought were normal so when I read those article and realized it wasn’t I was kinda scared. So I went to my mom to talk to her about it and she didn’t seem to care... she said we’d mention it to my primary care physician when I have my next appointment in July. I don’t know... am I being over dramatic... the symptoms all seem like me and I don’t know. I’m sorta scared. We always go to the doctor when it’s a diagnosis she think I have but when I bring one up it seems irrelevant and that my symptoms are normal. Am I just like thinking I have this?? Is that a thing...? I don’t know.

EDIT: talked to my mom and she gets it. She was talking to a friend in health care and she totally thought I could have this. So we’re getting into the doctor soon.