Sarah Cadman's Fundraiser
Support everyone with EDS going through the same daily struggles as myself
Together we can find a CURE!!!
We are no longer accepting donations on this campaign, but there are other ways for you to support us today!
Lynn Cadman
"Supporting daughter who fights EDS with such grace and selfishness. She is an amazing person. I am so proud and blessed with such a gift. "
$50
I have joined the May Awareness Month Challenge to spread awareness and raise funds to support The Ehlers-Danlos Society by participating in this you help give us a fighting chance to change medince for the better. Please support me by donating to my fundraising page. Together, even a small amount can make a huge difference!
The Ehlers-Danlos syndromes (EDS) are a group of heritable connective tissue disorders that produce a spectrum of complex problems across multiple systems of the body. Symptoms that are often seen across all types are hypermobile joints, (that can move farther than normal), stretchy skin, & fragile tissues. Each case is unique and severity may range dramatically, even within families.
The Ehlers-Danlos Society is a global community dedicated to saving & improving the lives of those affected by the Ehlers-Danlos syndromes, hypermobility spectrum disorders, & related conditions. Our goal is world-wide awareness and better quality of life for all who suffer from these conditions, regardless.