Hello! I'm Piper. I've been diagnosed with Elhers-Danlos Syndrome. Anyone else have this diagnosis? I'm currently looking for recommendations for a nice shoulder brace because my shoulder just won't stay the heck in, tips on living with EDS, info about EDS.... And why yes, I'd also love some sympathy. haha.
Ah, another zebra!
Oooh! 3 zebras! We almost have a herd!
@PiperMckenna not formally diagnosed as I could not do the genetic testing. But yup! I am a zebra!
Hello I am also a zebra. I have Ehlers-danlos and dislocate basically whatever can dislocate.
I cannot recommend any shoulder supports but I do know of some good Facebook pages that offer great community and advice
Ah, you know the snaps and pains and stretchiness! I'd love to join those FB pages. I'm just now "coming out" about having EDS. I don't know why, but I've been ashamed of it for years. I always felt like it wasn't a real diagnosis. And doctors being clueless didn't help. I finally found a doc that did test and was supportive and I don't feel crazy! Yay!! So yup. I'm okay with being a zebra now.
@PiperMckenna there are a lot of stigmas and misinformation even with doctors that really hinders EDS progress and knowledge. That is for sure.
It wasn't until last year that I'd even heard of it. I was always called a hypochondriac, klutz, attention seeking faker, etc but now I feel justified and vindicated with my diagnosis and the knowledge I have gained of just how powerful this disorder really is.
It most certainly isn't shameful at all, nor is it just crazy in your head. And you definitely aren't alone.
@LadyAlyxandrea This has been my experience too! I'm really happy that my family and 2 new doctors believe me and are sympathetic. It's really changed how I look at myself and treat myself! There were so many things about me I knew weren't normal, but I didn't know were symptoms of EDS. Now it makes so much more sense!