Foundation for Prader-Willi Research

The mission of Foundation for Prader-Willi Research (FPWR) is to eliminate the challenges of Prader-Willi syndrome through the advancement of research. High-quality research will lead to more effective treatments and an eventual cure for this disorder. By working together, we intend to free our loved ones from the burdens of PWS, allowing them to lead full and independent lives. Prader-Willi syndrome (PWS) is a genetic disorder that occurs in approximately one out of every 15,000 births. PWS affects males and females with equal frequency and affects all races and ethnicities. PWS is recognized as the most common genetic cause of life-threatening childhood obesity.


Charity Navigator Ratings

Overall Rating

(4/4)|91.49 Score

Financial

(3/4)|88.66 Score

Accountability & Transparency

(4/4)|96 Score

EIN

31-1763110


Headquarter Address

340 South Lemon Avenue
Suite 3620
Walnut, CA 91789