Anyone else feel like their EDS progresses?
Okay so, I just wanna see if anyone else has had their EDS symptoms progress throughout life? Like, for me, I just started rolling my ankles in grade school, and getting finger dislocations and stuff, as I've gotten older, more and more joints have joined the hypermobile gang. First, my right knee cap started getting more and more hypermobile to the point where it one day fully dislocated, today this joint is *probably* my most hypermobile? Bc this bitch goes out of place with the touch of a finger.
Anyways, next my Jaw joined, at least the left side of it. It dislocated and I couldn't close my mouth for almost three days, also obviously couldn't eat solid foods during this time.
Now, since I've been using forearm crutches bc of my kneecap, my right elbow is starting to get hypermobile, and this is somewhat scary to me, because I thought forearm crutches would help but they are just making my elbow hypermobile now.
Am I going crazy? Or are my joints *actually* getting looser??? Has anyone experienced anything like this?