#ehlersdanossyndrome
September 5, 2026 at 10:58 PM
Ok this is ridiculous right?! 🧏🏻‍♀️Or is it just me 🙋🏻‍♀️🤷🏻‍♀️🤦🏻‍♀️I have to spend $400 to get 🧬 tests to prove the type of #EhlersDanosSyndrome
I have?! What if you don’t have $400? You live on SSI. That’s insulting. #julydisabilitypridemonth
I have #cv-EDS and been denied 🙅🏻‍♀️ care my entire life!
July 11, 2025 at 8:46 PM