Treatment for Autism? We Want Understanding and Help
The following is a personal essay, and reflects the opinion of its author.
September 30, 2025
The Trump administration continued its attack on autism last week, this time by linking Tylenol (acetaminophen) use in pregnancy to autism and strongly discouraging its use. (“Fight like hell not to take it” and “tough it out,” Trump told expectant moms.)
White House Press Secretary Karolina Levitt said, “The Trump administration does not believe popping more pills is always the answer for better health.”
Hold on: I am healthy. So are my autistic friends — and if they aren’t, their health problems aren’t ASD.
Trump isn’t offering a cure for autism. Instead, he and RFK, Jr., are contributing to the burden of stigma that autistic people deal with every day. Autism is not a disease or a mental health condition. It’s both a disability and a kind of neurodivergence.
“Curing Autism” Is Ableist
First off, blaming autism on pregnant people taking Tylenol isn’t just wrong — it’s potentially dangerous. Since ibuprofen and aspirin are known to harm developing fetuses, acetaminophen remains the only painkiller available and safe for pregnant people, as backed by the American College of Obstetricians and Gynecologists, the Society for Maternal-Fetal Medicine, the Autism Science Foundation, and the American Academy of Pediatrics.
During each of my three pregnancies, round ligament pain left me nearly unable to walk. If I had not been allowed to take Tylenol, I would have been bedridden, which can cause deep vein thrombosis, a loss of bone mass, and injury to the heart and lungs.
It’s true that many parents and children would benefit from a better understanding of autism, as well as improved therapies that emphasize accommodation and communication strategies.
Manifestations of autism, to be sure, can cause difficulty and frustration. Challenges with social communication and interaction, as well as “restrictive and repetitive behaviors,” can lead to friction. And autism is a spectrum condition — some people can “mask” their autism and pass for neurotypical. Others may have difficulty communicating their basic needs. For some parents, the difficulties inherent in caring for so-called “low-functioning” autistic children can be enormous. (Though it’s important to recognize that terms such as “low-functioning” are also inherently ableist; autistic people all function differently.)
Those parents need both support and improved interventions. But their children’s brain differences don’t need to be “cured.” We don’t want a “cure.” We want accommodation and understanding.
Claiming that autistic people need to be cured to fit into everyday society implies that neurodivergent people are a burden. “These are kids who… will never pay taxes,” RFK, Jr. said. “They’ll never hold a job, they’ll never play baseball, they’ll never write a poem, they’ll never go out on a date. Many of them will never use a toilet unassisted… and we need to put an end to it.”
As a published poet, I can only assure you that autistic people do indeed write poetry. Beyond that, this language and framing of autism are terrifying — echoing rhetoric that has fueled some of the darkest moments in human history. (That people are linking this administration’s language and policies to eugenics is not an overblown reaction.)
We Don’t Want a Cure for Autism
The vast majority of autistic people don’t want a cure. The idea of curing us pathologizes the way we think, feel, and interact with the world. Instead of a cure, we need help and accommodations from a society structured to favor neurotypical people.
“This administration seems to care a lot about autism as a supposed epidemic,” said Colin Killick, the executive director of the Autistic Self Advocacy Network. “It does not seem to care much at all about autistic people.”
If this government cared, it would enact comprehensive disability legislation (currently being gutted), fund special education for autistic children (also on the chopping block), and provide adequate workplace accommodations and protections for autistic adults (harder to do with the DEI rollback). Instead, our existence is being called “a family tragedy.”
This rhetoric belies the administration’s claims to care about autistic people. Instead, it tells us that priorities lay with eradicating and demonizing people it misidentifies as a societal burden. But we’re far from a burden. Autistic people have the same rights as any other American: the right to joy, the right to self-determination, and the right to make medical decisions without government interference.
We don’t want a cure. We want our value to be acknowledged.
Understanding Autism: Next Steps
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