When Noelle was first born 16 years ago, there were so many uncertainties about her future. Her diagnosis with Prader-Willi Syndrome only intensified our doubts and worries. The supports and information provided by PWANY (and PWSAUSA) have been invaluable to our family as we have attempted to navigate the complexities of life with PWS. Education, advocacy, medical information, research in regard to treatments, connections with resources in times of crisis... all of this is available to families and providers of those with PWS, but is dependent on the donations of supporters like you!
In honor of Noelle’s 16th birthday, would you consider being a part of accomplishing the Prader-Willi Alliance of New York’s mission of Support, Advocacy and Hope?