Reflections

As part of the Vanderbilt Kennedy Center's 50th anniversary celebration, families, researchers, staff, trainees, and others shared their reflections. View a sample below, and select "more" to view additional comments.

A reflection from a family
Becky and Chris Link - Parents

The Kennedy Center has been so important to our family. Our son Seth who is now 25 was born with Williams syndrome, which presents both physical and cognitive challenges. The programs at the Vanderbilt Kennedy Center have focused on Seth’s abilities and highlighted his talents. Seth has participated for the past 9 years in a music camp for individuals with Williams syndrome, which takes place in Nashville at the Kennedy Center with the campers writing and performing a song at the Grand Ole Opry and participating in research during the week. It has been transformative for Seth and he has made life-long friends through these amazing opportunities.

Becky and Chris Link - Parents

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A reflection from a trainee

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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A reflection from a researcher
Elisabeth Dykens, Ph.D. - Psychology, Psychiatry, and Pediatrics

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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A reflection from a professional

I was introduced to the Kennedy Center in 1975 when I was an undergraduate at Peabody College, now Vanderbilt University. It changed my life, and set me on my career path. I left as a graduate, and I came back for graduate studies. And I work in disability and I still count on the Kennedy Center every day.

Carol Westlake - Tennessee Disability Public Policy Advocate

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