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

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!