Peggy Markham's Fundraiser
Help Us Spread the Word About Connective Tissue Disorders
Help me give to the foundation that gives HOPE to all those whose lives are affected by Ehlers-Danlos syndromes. Teaching people about these rare disorders helps us grow a more compassionate world.
$150 towards $500
Zebra Strong for The Ehlers-Danlos Society
I am raising awareness and funds for The Ehlers-Danlos Society because I have a family member with this rare disorder. 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!