2nd Annual Long Island Walk for PWS Fundraising Page
Thank you for visiting our fundraising page!
Our son, Peter, was diagnosed with Prader- Willi Syndrome (PWS) at one month old. PWS is a complex and rare genetic disorder affecting appetite, growth, metabolism, cognitive function and behavior.
Last year, we started the Annual Long Island Walk for PWS to raise money for research. Donating to our walk will benefit the Prader-Willi Syndrome Association (USA) to help improve the lives of those affected and fund research to find a cure.
On May 17th at 10am, we will host the 2nd Annual Long Island Walk for Prader- Willi Syndrome at Wantagh Park, Wantagh, NY. Last year, we raised almost $7500 thanks to many of you. We hope to make the walk bigger and better this year and we need your help! With your participation and donations, you can help us acheive our goal.
Please help us make a difference.
We thank you for your support and ask that you forward our page to anyone you think may be interested in donating too.
For more information on Prader-Willi Syndrome, please visit www.pwsausa.org.
Donating through this website is simple, fast and totally secure.
Many thanks for your support!
Nancy, Chris & Peter