Our History
The Brighterside of Down Syndrome was founded in 2006 by Jean Wiltz and Carrie Norris, proud moms of children with Down Syndrome. These two moms had first hand experience with the joys and the hardships of raising a child with individual, special needs. These friends knew the joy of celebrating each other’s victories, and the security of having support during inevitable challenges, making the journey with their child so much richer. Jean and Carrie saw a need in the central valley for an organization to connect and serve families living with Down syndrome.They understood the importance of connecting with other families on this adventure. TBODS was formed to provide support and connection for families in all of San Joaquin County, and at that time no other group in the area was dedicated to advocate specifically for persons with Down syndrome. Within months, TBODS applied for and received its non-profit number from the state. A constitution and bylaws were developed, and in 2009 TBODS was finally incorporated.
Our Founders
Jean Wiltz - Mom to Aaron
In 2006, another parent and I co-founded TBODS. My son, Aaron, was born in 1976 and was diagnosed with Down syndrome. So, I have years of first-hand knowledge and experiences to share with other parents. In 2009, I retired after 33 years of teaching. Almost 30 of those years were enjoyed as an Infant Development Specialist working with families who has an infant birth to three years of age with a special needs diagnosis. Currently, I have a private practice and am a vendored IDS for our local Regional Center. My vision is for TBODS to provide a comfortable and relaxed environment for parents to share, brag, learn, encourage, develop friendships and gain information from each other.
I truly believe my family has been blessed by having Aaron. He definitely changed who I was becoming, and has made huge impacts on his father, two brothers and all other close friends and relatives. Aaron is God's gift to our family!