My daughters journey with Dysautonomia started 5 years ago but it wasn't until Oct 28 2016 that she was "officially" diagnosed. She's a fun loving 16 year old girl who has been robbed by this ugly diease. She's lucky if she can make a week of school without missing a day or getting sent home because she's dizzy or the headaches are so bad she can't stay a full day. She's just started her first job and has already had to call out sick twice. She has been told on several occasions "there is nothing wrong with you, you look fine". But how can you fake a disease that is so hard to live with. This disease is not well know even to some doctor's that don't specialize in it. I'm asking for your help to donate what ever you can to the research of Dysautonomia to help find a cure.