Families/caregivers of children with ASD experience problems and disparities in healthcare and service delivery first hand. As a result, they can provide valuable input in the development of a system that best meets the needs of these children. Results from an informal, open response survey completed by participants of the 2011 Autism Speaks Walk in Little Rock most commonly identified the need for better quality educational/interventional services and the need to develop or transform community assets to be more knowledgeable and supportive of individuals with autism as major gaps in the system of care for their children.
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