Stride Towards a Full Life Without Limits

When Emile was diagnosed with PWS at age 3 1/2 one of my first phone calls was to PWCF. I immediately felt less alone and supported. When the school needed to hear the details of this rare genetic syndrome from an expert, PWCF was there to offer training to staff. When Emile transitioned to middle school and high school they offered more training and support. Larry and I took classes and attended annual conferences. When we had a million questions about how to help Emile with the intense struggles and how to get people to listen, we called PWCF. We expect to be leaning on PWCF in the near future when she ages out of the school program. This organization is the ONLY one in California that exclusively serves the PWS community.

AND now I'm a member of the board of directors! So, I'm excited to be attending the walk scheduled for April 30th in Rancho Bernardo as a parent and a board member!

Your donation helps to provide these ongoing services:

• Support of all newly diagnosed families in California
• Funding of PWS Multidisciplinary Medical Clinics
• Maintaining a 24-hour PWS Medical Crisis line
• Providing the only medically specialized camp in California that exclusively serves persons with PWS
• Producing educational articles, brochures, webinars, and a monthly eNews
• Providing advocacy and support services to families and care providers
• Educating and supporting teachers, physicians, and allied health professionals
• Weekly chats and activities on Zoom for people with PWS
• Support groups for parents and caregivers of people with PWS
• And so much more!

Donating via this web page is what's best, but if you prefer to donate by check:

• Make the check payable to: Prader-Willi California Foundation
• Be sure to include your fundraiser's name on the envelope.
• Mail the check to:

Prader-Willi California Foundation
Attention: Your Fundraiser's Name
1855 First Avenue, Suite 201
San Diego CA 92101.

Thank you for your support!

The Beers!