Health Secretary Robert F. Kennedy set the tone back in April when he announced the Trump administration’s plan to find the cause of autism. He declared that “autism destroys families.” He described children “who will never hold a job, they’ll never play baseball, they’ll never write a poem, they’ll never go out on a date.”
President Donald Trump carried that message forward, calling autism a “horrible, horrible crisis” and suggesting — without evidence — that Tylenol could be the cause and that leucovorin, a type of folic acid, might be a treatment. Food and Drug Administration Commissioner Marty Makary added, “if you’ve seen a kid with autism, with severe autism, it’s hard to watch.”
Their words left many in the autism community stunned. They’d come expecting answers and action. Instead they were offered suspect causes and unproven cures. They were reminded of a past filled with blame and judgment.
The depictions left many of them feeling hurt and dehumanized, reflecting a fundamental misunderstanding of their lived experience. And ultimately they worry there will be a broad backslide in public attitudes about autism.
“What will come out is unfortunately more confusion, more headlines, more misinformation that will just add to the burden of people like me,” says Russell Lehmann, a disability awareness and inclusion specialist at UCLA, who is autistic.
The suggestion that autism was somehow preventable — and the underlying message that the world would be better off without it — was particularly gut-wrenching. “Hearing them say that their goal is to end autism? That’s deeply alarming in our community,” says Colin Killick, executive director of the Autistic Self Advocacy Network. “What we know — and when I think any expert will tell you — is that autism is not a disease you can eradicate because it’s a fundamental part of neurodiversity. Autistic people have always existed.”
Even in parts of the autism community where the messaging didn’t necessarily offend, and in fact, helped some families feel seen for the first time, there was still recognition that portraying it in such a one-dimensional way was problematic. Judith Ursitti, cofounder of the Profound Autism Alliance, said she appreciated the overdue “candid awareness about the realities that we face.” But Ursitti also was deeply worried about the language being used and how it could harm many autistic self-advocates who are dear to her.
Where everyone in the community agrees though, is that sham solutions and false promises won’t help anyone. And they are particularly galling when, at the same time, the administration is making deep cuts to the research and services that actually make a difference.
This spring, scores of grants that supported studies seeking to understand which environmental exposures might contribute to autism were canceled. A Reuters analysis found that spending by the National Institutes of Health on autism fell by about $31 million between January and April of this year.
The Trump administration has instead touted a new $50 million autism data science initiative, centered on pinpointing the causes of autism. Yet while the 13 new grants announced last week went to reputable institutions, none of it directly addresses what experts and autistic individuals say is most urgently needed: studies that identify which supports and interventions work best for different groups of children, or clinical trials of potential treatments.
But this misguided shift in the research agenda also overshadows a more immediate concern: the Trump administration’s steep cuts to Medicaid which will inflict direct harm on autistic children and adults with intellectual or developmental disabilities.
If there is any silver lining, it’s that the president’s disastrous plan has galvanized a deeply divided community. Different factions have long held polarized views on the causes, treatment and even how to describe autism. Now, for the first time, they are uniting in opposition, Lehmann says. “Hopefully this will be the impetus to stir up our community to speak up louder and stronger and more authentically.”
Let us hope so — and that eventually, someone in the administration begins listening to autistic individuals and acting on what they so urgently need and want. An easy place to start would be treating them with the respect and fundamental humanity they deserve.
Lisa Jarvis is a Bloomberg Opinion columnist covering biotech, health care and the pharmaceutical industry.
https://www.orlandosentinel.com/2025/10/02/commentary-autism-needs-support-not-blame-and-judgment/
