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Reports, school meetings and news stories use words that can be confusing at first. This page explains the terms you will meet most often — and why the words people choose matter to many autistic people.

Based on NIMH · CDC · NICHD · NIDCD · Autistic Self Advocacy Network · AAP / HealthyChildren.org · All sources · Checked November 3, 2026
Both forms are used, and families will hear both. Person-first language (“child with autism”) puts the word person first; CDC’s public materials use it. Identity-first language (“autistic child”) treats autism as part of who the person is. The Autistic Self Advocacy Network explains that many autistic self-advocates prefer identity-first language because they understand autism as an inherent part of identity that cannot be separated from the person — in the same way one says “Jewish” or “athletic” — and because “person with autism” can suggest the person would be better off without it. ASAN also acknowledges that many parents and professionals prefer person-first language to emphasize the person’s humanity, and urges respectful discussion between the two views.
The American Academy of Pediatrics notes that preferences in the autistic community vary and that HealthyChildren.org is moving to identity-first language to align with neuro-affirming practice. Autism Family uses both forms, and the best guide is always the individual: ask the autistic person — or their family — which they prefer.
ASAN notes that both self-advocates and many parents object to phrases such as “suffers from autism.” Describing a person by their diagnosis alone (“the autistic”) is also widely seen as disrespectful. Autism is not a disease, and there is no “cure”; talking about support, access and acceptance reflects how public health agencies and autistic-led organizations describe it today.
Adapted from the National Institute of Mental Health, “Autism Spectrum Disorder,” revised 2025. Our website’s presentation does not imply NIMH endorsement.
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