Disclaimer: Individuals undertake their chosen activities at their own risk. My name is Jack Orman, I am 24 years old and currently living in Colorado. I was diagnosed with hypermobile Ehlers-Danlos syndrome (hEDS) in December of 2016 at the age of 19. I wanted to share my story because there is a lot of fear View page
Hello! My name is Teena Amador and I am Ms. Pennsylvania US United 2021 and my platform that I plan to promote during my reign is chronic and invisible illness awareness. I have hypermobile EDS (hEDS) formally known as EDS type 3, Chiari malformation, and polycystic ovary syndrome (PCOS). My hope to inspire someone with View page
My name is Alexander VanHouten. I have Ehlers-Danlos syndrome, and though living with pain and constant threat of injury every day is no walk in the park, I am thankful for the trajectory my life has taken because of this disease. When I was a child I was, like most young boys, a hyperactive, rambunctious View page
