Support #myEDSchallenge and help me reach my goal!

I have joined the May 2019 Awareness Month Challenge to spread awareness and raise funds to support The Ehlers-Danlos Society in finding a cure for myself and others with Ehlers-Danlos Syndrome. Please support me by donating to my fundraising page. I need just 4 donors! We can reach the EDS goal of $40 together!

My Ehlers-Danlos is beyond just stretchy skin and flexible joints. I have have multiple, debilitating comorbidities, including benign increased intracranial pressure (pressure on the brain), autonomic dysfunction, postural orthostatic tachycardia syndrome, and osteopenia - all at the young age of 35! Not to mention, they are not done diagnosing me yet!

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 2019 EDS Awareness Challenge by donating. Thank you!