My name is Elizabeth Vota. I am 15 years old and heading into my sophomore year in high school. For as long as I can remember, I have been actively involved in sports and physical fitness. That all changed at my tenth birthday party when I fell on my knees while skating. For the next three years I visited numerous doctors to try and determine why my knee never healed properly but never received a viable diagnosis. I was finally diagnosed with Ehlers Danlos Syndrome (EDS) by a terrific doctor. He taught me that EDS is a connective tissue disorder which makes my joints flexible and hypermobile, allowing my joints to easily dislocate in my body. He introduced me to a great physical therapist and great team of doctors. EDS effects my entire body which results in chronic pain everyday. I also have Postural Orthostatic Tachycardia Syndrome (POTS) which causes me to have a rapid heart rate and low blood pressure, causing me to have frequently dizzy and fainting spells.