SHAWN LAPIN ...continued

“In 1969 when the Lanterman Act was passed, autism was not included because it was not considered a developmental disability. It was considered a mental illness. When Shawn was diagnosed in 1970, there were no services available. It wasn’t until 1975 that a law was passed that said children with autism had to be educated.” The Lapins have been longtime advocates for children and adults with autism. They stress the importance of parents becoming informed and getting involved by joining support groups and getting to know their legislators.

Today at 39-years-old, Shawn Lapin resides in his own home with the assistance of support staff in a supported living setting. He also has been self-employed, selling hot dogs, and running a messenger service.

“Children and adults with autism want what everybody else wants, and this is what you must think about. What do you want? You want friends, relationships, and you want to be happy. People with disabilities want the same thing. They want to live in their own place, they want to have choices including who they live with, and they want to have friends and relationships,” says Connie.

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<< PHOTO: Shawn with his aide, Louie, left, and mother Connie.