PWSA (USA) is an organization of families and professionals working together to promote and fund research, provide education, and offer support to enhance the quality of life of those affected by Prader-Willi syndrome.

Get Involved

• Membership
  • Become a member
  • Register your child with PWS with us
• Events
  • Current Events
  • Schedule an event
  • Suggested Fundraising ideas
• Volunteer
• Join a State Chapter
• Join an eSupport Group

Spread Awareness

• Educational Efforts
• Fundraising
• Advocacy
• Media
• Wrist Band Sale
• Posters and Magnets
• Awareness Items
• Other Awareness Ideas
• Contact Your Local Chapter
• Tools You Can Use
• Wear a T-Shirt "Still Hungry for a Cure"