The following is a personal essay that reflects the opinions and experiences of its author.June 12, 2025In the weeks since officials from the U.S.
Department of Health and Human Services (HHS) first announced plans to create an autism registry — then subsequently dubbed its efforts a national “data platform” to “uncover the root causes of autism” — providers like myself have witnessed a notable effect on patients seeking care.As a clinical psychologist, I specialize in diagnosing and supporting neurodivergent adults.
But my clients tell me that they’re cancelling their kids’ pending evaluations for autism, ADHD, or other conditions in other clinics, citing HHS database fears.
I’ve also received emails asking whether it’s safe to seek or obtain a diagnosis given the current political climate.A colleague who diagnoses autism and ADHD in adults reports that people on the practice’s waitlist have been cancelling their appointments, and that no-shows have increased since news of the HHS registry first broke.
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