Help make research possible and raise awareness

I finally got a name for the multiple strange, vague, and seemingly unassociated signs and symptoms on December 6, 2013. That name was life changing and explained almost everything I had experienced for many years. When I told all my doctors my diagnosis, they had heard of it but weren't familiar with it. Being a nurse and someone with Ehlers-Danlos, and because of learning all I could, I help others advocate for themselves to get the care they need, friends and strangers alike, that message me on social media desperate for answers.

Help fund research for those living with Ehlers-Danlos so they can be believed by their providers and get the care they need, and raise awareness.