Katie Carty

Katie Carty's Fundraiser

Support #myEDSchallenge and help raise awareness for Ehlers danlos for us to open the door for more knowledge for doctors. image

Support #myEDSchallenge and help raise awareness for Ehlers danlos for us to open the door for more knowledge for doctors.

Together we can improve the lives of all with EDS, world wide!

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I have joined the May Awareness Month Challenge to spread awareness and raise funds to support The Ehlers-Danlos Society by participating in the #myedschallenge. Please support me by donating to my fundraising page. Together, even a small amount can make a huge difference!

I was misdiagnosed in 2011, there has always been something wrong that noone could pin point. 26 years later, we know what that issue was. Eds can change your life in a blink of an eye. I would love to be apart of something special to gain awareness.

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 of geography.

Please support me as I overcome my challenges with EDS to participate in the #myedschallenge by donating. Thank you!