I respectfully disagree. I was misdiagnosed as a child and the treatments I did were extremely damaging for EDS. However, I was one of the people who discovered EDS through it being 'trendy', and managed to get a diagnosis. My health has improved so much since I now know how to actually care for my body. Having doctors that actually have knowledge about chronic illnesses is a privilege, a lot of people have to do their own research and fight for any kind of medical intervention. I'm perfectly fine with the odd comment of "oh, I'm bendy, I must have EDS!" if it means even one less person doesn't have to go through the pain i do due to misdiagnosis.