Thank you for supporting FPWR
Prader-Willi syndrome (PWS) is a genetic disorder that occurs in approximately one out of every 15,000 births. It is recognized as the most common genetic cause of life-threatening childhood obesity.
FPWR is working to eliminate the challenges of Prader-Willi syndrome through the advancement of research. By working together, we intend to free our loved ones from the burdens of PWS, allowing them to lead full and independent lives.
Please fill out the form at right to make your donation.
To donate offline, please send your check to:
Foundation for Prader-Willi Research
DEPT LA 23216
Pasadena, CA 91185-3216