Resources, information and community for people affected by
Fetal Alcohol  Spectrum Disorder

What Are You Looking For?

Our Vision

Our vision is that every person in Southern California who is affected by prenatal alcohol exposure has the resources and the opportunity to achieve his or her fullest potential in all aspects of life.

Our Mission

Our mission is to enhance the quality of life — through information, advocacy and service — for children, adolescents and adults in Southern California affected by prenatal alcohol exposure, and to empower those who care for or serve them.

The FASD Network of Southern California (formerly known as the Southern California FASD Information & Support Network) is an information and support resource for parents, caregivers, advocates, educators and treatment professionals of persons who have been diagnosed with Fetal Alcohol Spectrum Disorder (FASD) or anyone who is suspected of being affected by FASD. It is also useful for students or professionals who are interested in the challenges faced by families affected by these conditions.

In 2014, the United States Internal Revenue Service (IRS) granted the FASD Network of Southern California status as a 501(c)(3) tax-exempt nonprofit charitable organization.

Special Issues

Persons with FASD face unique challenges in everyday living at every stage of life. Here are  resources and insights for dealing with those challenges. 

Tips and Tactics

Learn "what works" for persons with FASD. These tips and tactics come from families with a loved one affected by FASD, or from others who know someone affected by prenatal alcohol exposure. 

Commonly-asked questions about FASD, and our Network are answered. If you've searched this site and cannot find what you're looking for, please email us with your questions and recommendations..

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