I got the email from The Ehlers-Danlos Support UK to sign a petition for funding EDS Research, with an awesome way to create our own EDS personalized story graphic to share on social media. This is great! I live in the US and I'd like to see something like that here, does anyone know of a similar initiative? There is zero funding here for EDS research as well 😪

Posted by Trustinbeing at 2023-05-23 23:36:51 UTC