Support Research for Ehlers-Danlos Syndrome

Reasons for signing

See why other supporters are signing, why this petition is important to them, and share your reason for signing (this will mean a lot to the starter of the petition).

Thanks for adding your voice.

Savvy Throckmartin
3 years ago
I have EDS

Thanks for adding your voice.

Alisha Hayles
3 years ago
I relate your story, my surgeon didn't know it existed when i was a child it took 17 years for me also to be diagnosed.

Thanks for adding your voice.

Jeff Rineer
3 years ago
EDS - Hypermobile type NEEDS more research and researchers need financial support to continue and advance their research. Cancer and other illnesses have ample support and are well known. Lesser known conditions, like EDS, need all the supportive research it can get.

Thanks for adding your voice.

Donna Barber
4 years ago
Donna l Barber

Thanks for adding your voice.

louise bell
4 years ago
I know several people who have suffered with this. One is 28 & may not live many more years because of this disease.

Thanks for adding your voice.

Gloria Willis
4 years ago
I also have EDS

Thanks for adding your voice.

Jake Amendola
4 years ago
Of a friend