Abigail Ham's Fundraiser
Help support EDS research worldwide!
Those who hope in the LORD will renew their strength. They will soar on wings like eagles; they will run and not grow weary, they will walk and not be faint. -Isaiah 40:31
#wingslikeeagles
I am raising awareness and funds for The Ehlers-Danlos Society. I was diagnosed with EDS a year ago, and my symptoms include hyper-mobility, joint instability, numbness, and chronic pain. Although my symptoms do impact how I live, I am grateful for how much I am able to do and want to do whatever I can to support those who are no longer able to participate in their passions. Together, even a small amount can make a huge difference!
The Ehlers-Danlos syndromes (EDS) are a group of 14 heritable connective tissue disorders that produce a spectrum of complex problems across multiple systems of the body. Hallmark symptoms across all types are hypermobile joints, skin hyperextensibility, & tissue fragility. 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, and together we will overcome!