EDS Awareness

Zebras Exist! · 1 May 2022
Hi! Thanks for visiting 😊
Getting diagnosed with Ehlers Danlos changed my life. It provided answers and understanding to a world of symptoms and pain that wasn't initially being taken seriously. However, so few physicians and medical professionals have awareness of EDS to the extent patients really need. Like many chronic conditions, EDS patients benefit when there's a whole team of doctors on the same page, dedicated to working and fully understanding our sometimes obscure symptoms, pain levels, sensitivities, and all else that EDS comes with. The Ehlers Danlos Society is starting to help make this happen globally! They just need more help from our community to not only raise money, but awareness as well.
I appreciate you taking the time to visit this fundraising page!
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