I wish that hEDS was more widely known, so people could get diagnosed in a timely manner. I wish this for all rare conditions, not just mine. I also wish doctors were better educated about the entire hypermobility spectrum and would take hypermobility spectrum disorder (#HSD) as seriously as hEDS, since they are indistinguishable for many people and it’s even harder to find someone qualified to diagnose hEDS. 

@ehlers.danlos

#hEDS

#EDS

#invisibleillness

#invisibledisability

#edsawareness

#ehlersdanlossyndrome

#ehlersdanlos

#hypermobilityspectrumdisorders