The law must allow relatives to open group homes for the severely autistic

Public comment to the IACC: “This system breaks families apart.”

Now that they are men with the intellect of young children, they need adequate housing and support, beyond our home.” But “there is a severe shortage of Res Hab homes for the profound population.”

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By Sara Polito

Our boys were diagnosed with profound ASD at 18 months. They are now grown men. Our hopes of finding a 'cure' or adequate community supports are long gone. The agencies designed to 'help' have almost a decade waitlist. We waited 8 years for any type of help. Now that they are men with the intellect of young children, they need adequate housing and support, beyond our home. There is a severe shortage of Res Hab homes for the profound population. By mandating that only non-family individuals, Not-for- Profit organizations, and corporations, be allowed to start and operate a group home is wholly inadequate. Parents or blood relatives cannot form group homes. This leaves parents at the mercy of whoever wants to open a home - good or bad. Depending on the level of services needed, the only 'bed' open may be across the state (away from the family home). This makes staying close, and visiting, almost impossible. This system breaks families apart. Families or blood relatives need to be able to form their own group homes, so this won't happen. The ones who care the most about these kids/ adults are the families. Not corporations running a home to make a profit off their disability.

This statement was submitted to the IACC as a public comment.

Disclaimer: Blogposts on the NCSA blog represent the opinions of the individual authors and not necessarily the views or positions of the NCSA or its board of directors.

Jill Escher, President

Jill Escher is president of the National Council on Severe Autism and the mother of two children with nonverbal forms of autism. Through the Escher Fund for Autism she promotes and funds research on the genetic toxicology of autism and related neurodevelopmental conditions, and she has served on the governing council of the Environmental Mutagenesis and Genomics Society, where she co-chairs its Germ Cell and Heritable Effects special interest group. She was president of Autism Society San Francisco Bay Area from 2013 to 2019 and, through her family business, Claradon Properties, provides housing to adults with developmental disabilities in the Bay Area. See more of her work at jillescher.com.

https://www.jillescher.com/
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"The IACC needs to hold a session on inpatient and outpatient care options for the severely autistic who can no longer live safely at home"