News Welcome to the new PWCF website. Check out our new and improved resources area.
Newly diagnosed?
Receive clear guidance, practical resources, and compassionate support to help you understand Prader-Willi syndrome and confidently take your next steps.
Connect with a real person
Personalized support is just a click away and PWCF is here to help. Call or email us.
Choose your path
Our Mission
PWCF provides individuals with PWS, their families, and professionals with a network of education, advocacy, and support services throughout California.
1979
Founded
850
Active Members
Education
Support
Advocacy
Awareness
Research
What is Prader-Willi syndrome?
A concise overview of this rare complex genetic disorder, with foundational information for people who are just beginning to learn about PWS.
Latest News
Walking for PWS 2025
Celebrate 25 years of the Walking for PWS events at a city near you! This event series happens once a year during National PWS Awareness […]
A PWS Athlete’s Story
The PWCF Walks are now behind us, and from what I have heard they were once again amazing. This year, however, for first time in […]
A Chance Encounter
“Nobody is promised tomorrow, stay strong and savor the moment.” – Nichole Broussard Prader-Willi syndrome appears in about every 1 out of 15,000 live births. […]
Upcoming Events
Featured event
Further information including speakers, registration and more to be revealed soon.
Become a Member
PWCF serves family and professional members throughout California, offering programs and services across our five program areas: education, support, advocacy, awareness, and research.
