Going bald in memory and for FAST

Nicole M Young is organizing this fundraiser.

Donation protected

We need your help!! Angelman Syndrome (AS) is a severe neurological disorder. Children and Adults with Angelman Syndrome suffer from developmental delays, problems with motor coordination, balance, sleep disorder and epilepsy. They do not develop functional speech.Individuals with AS tend to have a happy demeanor characterizered by frequent laughing, smiling and excitability. People with AS also require life long care, intense therapies to help develop functional skills and quality of life. THERE IS HOPE!!! We know what is wrong in Angelman Syndrome. We just need funding for Scientific research!! My goal is to raise money for F.A.S.T and for my beautiful daughter Emma who has Angelman Syndrome. Lets raise some money for me to SHAVE MY HEAD!! On June 1st 2014, with a goal of $5,000 I will shave my head. I will post a video of my head being shaved for the world to see. I will be brave for her cause she is brave everyday!! Thank you for you $1, $5, $10, $20+ donation. TOGETHER WE CAN MAKE A DIFFERENCE!!!!!!! To learn more about Angelman Syndrome or to donate Directly to Fast please go to www.cureangelman.org