As most of you know our daughter Ashlynne was born with a rare disease called Prader Willi Syndrome. No matter how much she eats, she is constantly hungry! Because of people like you there have been huge strides made in research in the last 12 years! When she was born the doctors gave us some some papers they printed from the internet and said they honestly didn't know much about it and we should just google for more information. Today there are 3 phase 3 clinical trials for a cure, one of which Ashlynne gets to be a part of!
Funds raised will be used to advance PWS research through the Foundation for Prader-Willi Research. You can learn more about PWS and the research that is underway at http://www.fpwr.org.
Please join me and donate now!