Heather Harmon

Heather Harmon's Fundraiser

We can educate the US doctors, and medical staff about EDS. Many people with EDS take years to be diagnosed. image

We can educate the US doctors, and medical staff about EDS. Many people with EDS take years to be diagnosed.

We can educate the public about "invisible" syndromes/diseases.

We are no longer accepting donations on this campaign, but there are other ways for you to support us today!
Share:

$0 towards $200

Please help us raise awareness of this "Invisible" Syndrome. Many times people with Ehlers-Danlos syndrome go undiagnosed for years. This genetic syndrome effects most parts of the body. Our medical community needs to become educated about it. In honor of my daughter and niece, who both have EDS with hypermobility, please give generously. Also, please research EDS. Our Zebras need your help!! The Zebra is the mascot because the medical community rules out everything else before getting to the rare. Z is the end of the line. Thank you for your help!!

Just a small donation will go a long way to helping me meet my goal for The Ehlers-Danlos Society