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A full life

without limits.

The success of people with Prader-Willi syndrome depends greatly upon the knowledge and support of the community around them.

Prader-Willi California Foundation is committed to being an integral part of your support community.

Who we are
Why we’re here

Our Mission

Individuals with Prader-Willi syndrome should have the opportunity to pursue their hopes and dreams to the full extent of their talents and capabilities. The success of people with Prader-Willi syndrome depends greatly upon the knowledge and support of the community around them. The Prader-Willi California Foundation provides individuals with PWS, their families and professionals with a state network of information, advocacy and support services.

What we strive for

Our Vision

A full life without limits.

Services we provide

How we help

Prader-Willi California Foundation provides the following comprehensive range of services:

How we help

Prader-Willi California Foundation provides the following comprehensive range of services:

Programs benefit children, parents, physicians, health care professionals, teachers, Regional Center personnel, and vocational and residential service providers.

Children with PWS and their siblings, parents, and community members gain valuable knowledge and support.

Financial assistance helps children attend an exclusive PWS camp (the only one in California) at a specialized, medically monitored mountain facility.

In-service trainings help those contributing to a child’s IEP (Individual Educational Plan) access important PWS information, production of a DVD titled Understanding the Student with Prader-Willi Syndrome, Strategies for Success, which is distributed locally, nationally, and internationally. Without these informative materials, children with PWS are simply not able to secure the appropriate medical, therapeutic, and educational services they need.

PWCF funds healthcare specialists within clinic and hospital settings who provide state-of-the-art treatment to children with PWS.

Teaching provides individualized training, technical assistance, and workshops to improve the lives of children and adults with PWS.

Group meetings, on-line support services, parent mentors, and 24 hour a day crisis phone lines are provided.

1:1 assistance helps families obtain Regional Center services and various medical, therapeutic, educational, and vocational services necessary to improve the health and welfare of a child with PWS.

Community education is provided through PWCF’s website, quarterly newsletters, public service announcements, press releases, radio interviews, awareness booths and Jumbotron messaging at sporting events, and walk-a-thon/picnics. PWCF writes and produces brochures, articles, and educational DVDs.

Interest free loans and grants are provided to residential facilities and vocational work sites that support persons with PWS. Exercise equipment and furniture grants have been given to group homes serving those with PWS. Production of a Residential Services Staff Training DVD and study guide to assist residential facilities and families.

PWCF supports state and national research by working with local universities, teaching hospitals, researchers, and scientists to help recruit research subjects and disseminate research materials to families.

Services we provide

How we help

Prader-Willi California Foundation provides the following comprehensive range of services:

Programs benefit children, parents, physicians, health care professionals, teachers, Regional Center personnel, and vocational and residential service providers.

Children with PWS and their siblings, parents, and community members gain valuable knowledge and support.

Financial assistance helps children attend an exclusive PWS camp (the only one in California) at a specialized, medically monitored mountain facility.

In-service trainings help those contributing to a child’s IEP (Individual Educational Plan) access important PWS information, production of a DVD titled Understanding the Student with Prader-Willi Syndrome, Strategies for Success, which is distributed locally, nationally, and internationally. Without these informative materials, children with PWS are simply not able to secure the appropriate medical, therapeutic, and educational services they need.

PWCF funds healthcare specialists within clinic and hospital settings who provide state-of-the-art treatment to children with PWS.

Teaching provides individualized training, technical assistance, and workshops to improve the lives of children and adults with PWS.

Group meetings, on-line support services, parent mentors, and 24 hour a day crisis phone lines are provided.

1:1 assistance helps families obtain Regional Center services and various medical, therapeutic, educational, and vocational services necessary to improve the health and welfare of a child with PWS.

Community education is provided through PWCF’s website, quarterly newsletters, public service announcements, press releases, radio interviews, awareness booths and Jumbotron messaging at sporting events, and walk-a-thon/picnics. PWCF writes and produces brochures, articles, and educational DVDs.

Interest free loans and grants are provided to residential facilities and vocational work sites that support persons with PWS. Exercise equipment and furniture grants have been given to group homes serving those with PWS. Production of a Residential Services Staff Training DVD and study guide to assist residential facilities and families.

PWCF supports state and national research by working with local universities, teaching hospitals, researchers, and scientists to help recruit research subjects and disseminate research materials to families.

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 our family’s history we were not able

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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. It is the rare genetic syndrome that

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