Samantha Gibson

Samantha Gibson's Fundraiser

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Help Us Raise Awareness

Overcoming EDS Challenges

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$215 towards $1,000

Zebra Strong for The Ehlers-Danlos Society

I am raising awareness and funds for The Ehlers-Danlos Society. 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.

I was diagnosed with Ehler's Danlos Type III in late 2019. I have suffered from symptoms my entire life but in recent times they have worsened. There are so many people just like me looking for answers. There is no cure for EDS and so far no concrete treatment (other than managing the many symptoms). This disorder affects even the smallest parts of your body making everyday life more challenging.


Please support me, and together we will overcome!