I have had a 21-year personal relationship with those who have special needs [because of our son, adopted at birth]. I do not know what my husband and I, both eggheads, would have done without the practical and research-based wisdom of the VKC. Nicholas’s first VKC program was TRIAD, a place where we all learned how to live with structure, what to attend to, what to let go. We also learned that we were not alone and that the professionals at VKC were actively working to make my family’s and other families’ lives better. That matters when your child is nothing like any other child you know. But my child could do more….The VKC has showed us how another way is possible. That our children can and will have another way.

Robbie Pinter - Parent

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[The VKC] is an absolutely amazing place to work, but more importantly, people here truly help to change lives for the better. I’ve worked here in some capacity since I graduated from the Master’s of Special Education program in 2007, and I cannot think of a better place to refer families who have a loved one with a disability. In my own work, we are helping high school students with autism and their families prepare for the transition from high school, and we are also helping faith communities as they support people with disabilities to find and hold employment.

Jenny Gustafson - Special Education Alumna and VKC Disability Professional

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My father was a psychiatrist, and as a young child, I spent Saturdays at his clinic and so was accustomed to being with people with disabilities. Later, we lived on the grounds of a state mental health hospital, where I had many friends with different types of developmental and psychiatric difficulties. I wanted to better understand their lives and stories. At the Yale Child Study Center, my experiences with children with fragile X syndrome started me on the path of looking at other genetic syndromes, since they offer unique windows for understanding the connections among genes, brain, and behavior, as well as specific ways to optimize interventions with individuals and families. My husband and I moved to Vanderbilt because we wanted to be part of a community of researchers and others dedicated to understanding people with developmental disabilities on a number of different levels—genetics, brain science, treatments, supporting families, public policy, and advocacy. The VKC embodied all of that in one place.

Elisabeth Dykens, Ph.D. - Psychology, Psychiatry, and Pediatrics

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I am the proud parent of four young children, one of whom has Down syndrome. Besides benefiting from their vast array of supports and services, I am currently receiving valuable research experience as a doctoral student in special education and receiving specialized disability-specific training through the VKC.

Thomas Boehm - Parent, Doctoral Student in Special Education, and VKC UCEDD Trainee

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