Ehlers Danlos & I

Hello! My name is Laura, and I have a rare genetic connective tissue disorder called Hypermobile Ehlers Danlos Syndrome (hEDS). It is my goal to create quick and concise educational videos about hEDS to help other people who may have this disorder or want to share easy to understand videos with their friends and family about their condition. I'll also be sharing with you tips and tricks on navigating life with hEDS and reviewing products that help (or don't help) me. Thanks for watching!