Connect With Us

Mailing Address:
FASD Network of Southern California
PO Box 595
Manhattan Beach, CA 90267-0595


The Network lacks a physical office. The Network connects with others virtually, and in person at events, trainings, and meetings. 

These are the FASD Network of Southern California contacts for each county within our network. He or she can help you best in identifying resources in your county.

Imperial County

T.L. “Tom” Wentz, PhD.
Organization: Private Practice
Phone: (760) 217-8283

Tom currently lives and works in Texas. Contact him by email for more information about FASD resources in Imperial County.

Kern County

Barbara Fowler
Phone: (661) 345-2864

Certified CDC/Arc FASD Trainer

Eveyln Mora

Organization: Parents 4 Kids Support Group
Phone: (661) 565-2960

Comments:Adoptive mother of three children with FAS
Note: Parents 4 Kids meets every third Tuesday of the month in Bakersfield, from 10:00 am till 12:00 pm. For information contact Evelyn at (661) 565-2960 or Dee at (661) 862-0783

Los Angeles County

Annette Kunzman
Organization: FASD Network of Southern California
Phone: (310) 717-9763

Comments: Annette is the current President of the Network’s Board of Directors. She has two adult children with FASD, and she coordinates Network support meetings in Los Angeles County.

Tyla Sawyer

Organization: Bill Dubofsky FASD Memorial Lending Library
Phone: (310) 210-4237

Comments:Adoptive parent of two children with FASD. Extremely knowledgeable.

Orange County

Michelle Carey
Organization: Southern California FASD Information & Support Network
Phone: (714) 283-3400

Comments:Adoptive parent of FAS-affected child

Riverside County

Eva Carner
Office: (951) 677-0578
Cell: (951) 805-6551
Fax: (951) 677-1540

Comments:Adoptive parent of adult son with FAS. Very knowledgeable and helpful.

San Bernardino County

Julia Bogany 
Organization: Keepers of Indigenous Ways
Phone: (909) 264-0309

Comments:Training and education specialist

San Diego County

Peggy Combs-Way
Organization:Birth Mother Network/Circle of Hope and NOFAS So Cal
Phone: (619) 865-4991

Comments:Birth parent of daughter born with FAS who is now an adult. As a leader and mentor of Circle of Hopenetwork for birth mothers of persons with FASD, Peggy assists women who drank alcohol and/or used drugs while pregnant, who need to know that they are not alone. Peggy also is a Founder of the NOFAS affiliate chapter in Southern California

San Luis Obispo County


Santa Barbara County

Shelley Reed Cole
Organization: FASD Network of Southern California
Phone: 805-687-0543

Comments:Adoptive parent of young adult daughter with prenatal alcohol exposure

Ventura County

Joeli Gutfleisch
Organization: FASD Network of Southern California
Phone: (805) 495-4887

Comments:Adoptive parent of  school-age child with FAS. Leader of local Ventura County FAS parents’ support group.

Danielle Onstot Shaw, M.D.

Organization: FASD Network of Southern California
Phone: (805) 479-7905

Comments:Adoptive parent of young adult woman with FASD. Practicing pediatrician, who completed a post-graduate training program in psychiatry in 2018 at Emory University in Georgia.

The FASD Network of Southern California email listis a way to share information about living with the issues and challenges of FASD and to find effective resources for diagnosis and treating people affected by FASD in Southern California. Participants in the email list also vent frustration and share triumphs as well ask for information or share resources.  

This email discussion group is designed for persons who live or work in San Diego, Imperial, Orange, Riverside, San Bernardino, Los Angeles, Ventura, Santa Barbara and/or Kern Counties. Anyone whose FASD-affected client, student, patient, congregant, romantic partner, coworker, customer, classmate, neighbor, friend, or family member lives or works in Southern California may also participate in the discussion group.

How do I sign up?

Use the following method to join the discussion group:

  1. Create an email message to
  2. In the Subject line, enter Subscribe
  3. In the Message, enter Subscribe youremail. For example, Subscribe
  4. Click Send.

How do I unsubscribe?

If you need to leave the discussion group, use the following method:

  1. Create an email message to
  2. In the Subject line, enter Unsubscribe
  3. In the Message, enter Unsubscribe youremail. For example, Unsubscribe
  4. ClickSend.


Members of our discussion group also attend network meetingsin order to share experiences, network ideas and resources, learn about current issues, and explore strategies to help FASD-affected individuals succeed.

The Network began in 2011 as informal lunch get-togethers attended by a small group of parents of teens and young adults who had either been diagnosed with FASD or who were suspected of being affected by it. We originally connected via one of a number of email lists for parents to discuss FASD.

These meetings became the cornerstone of the Network.

The camaraderie, experience and referrals to resources throughout Southern California for our children was helpful. The face-to-face contact made a special difference. It helped to ease the sense of isolation many of us felt. The attendees “got” FASD. We understood what it takes, and how it feels to care for and advocate on behalf of an individual with FASD.

Over time, we formalized these gatherings into regularly-scheduled meetings that combined the emotional support and an educational component.


The Network is committed to providing you, your organization, and your community, with relevant and current information about FASD.


At these events, respected experts on FASD from across the U.S. delivered training on understanding the physical, emotional and psychological characteristics of FASD, and taught participants ways to assist our loved ones or clients living with the condition.

Today the Network intends to present at least one professional-level training program every year. We pride ourselves on sponsoring training programs that attract both professional who serve individuals with FASD or their families and family members who struggle to provide both a loving home and the structure that many persons with FASD need.

When parents and other loved ones of persons with FASD and the clinicians and other professionals we rely on for help meet together to learn more about FASD, we improve our ability to understand each other’s challenges and priorities, and we improve our ability to work together on behalf of Southern Californians living with FASD.

To find an upcoming Network-sponsored meeting, training, or event, CLICK HERE.