Founded in 1970 by a group of parents who were concerned about the lack of diagnostic and treatment services for their children, the Autism Society of North Carolina has grown to become an organization that provides a variety of services for people with autism spectrum disorder and their families.

The primary focus of the organization has and continues to be advocacy for individuals and families and ongoing education of the public about the needs of the autism community. Since autism spectrum disorder is a lifelong disorder, the organization works with families, professionals, providers, and policy makers to ensure that needed services and options are available throughout the life-span of people on the spectrum.

With regional community services and advocacy offices throughout the state the Society has grown tremendously since its beginning. Governed by a Board of Directors, the Autism Society of North Carolina continues to seek input and feedback from individuals on the autism spectrum and their families as we work together to increase options and opportunities for people on the autism spectrum.