I’m a uni student and am currently undergoing testing for the more severe types of Ehlers Danlos Syndrome after being confirmed to meet the criteria for the hypermobile type of EDS.
I often have to use crutches to get around because my joint from the hips down can be very painful and unreliable, but recently my upper joints are getting worse, which can make the use of crutches hurt more.
What other options do I have, and where or how do I go about getting that help?