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.
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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
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. […]
Walking for PWS 2024
Register for the San Francisco Walk Register for the Fullerton Walk Register for the San Diego Walk Ready, Set, GLOW! The 24th annual Walking for […]
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.
