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Home»Opinions»Opinion | Dealing with the Realities of Extreme Autism
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Opinion | Dealing with the Realities of Extreme Autism

DaneBy DaneMay 11, 2025Updated:May 11, 2025No Comments5 Mins Read
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Opinion | Dealing with the Realities of Extreme Autism
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To the Editor:

Re “Kennedy Described My Daughter’s Actuality,” by Emily Might (Opinion visitor essay, April 27):

Ms. Might mentioned what too many people mother and father of autistic youngsters have been compelled to bury. Profound autism isn’t an thought. It’s not an identification slogan. It’s a actuality that steals language, security and futures — and pretending in any other case helps nobody.

Just like the creator, I’ve spent years refusing the script that calls for both silence or celebration. Naming our youngsters’s ache isn’t betrayal. It’s love, safety, survival.

Ms. Might’s voice doesn’t stand alone. It joins a rising motion — mother and father who’re finished asking permission to inform the reality. We’re constructing new alliances, pushing for actual analysis and refusing to let our youngsters’s struggling be edited out for political consolation.

The outdated establishments failed us as a result of they concern actuality greater than they love our children. We’re writing one thing new, not as a result of we needed this struggle, however as a result of our youngsters deserve it.

Thanks, Ms. Might, to your braveness.

Sarah Kernion
Westfield, N.J.
The author is a mom of two youngsters with nonspeaking autism and the founding father of Saturday’s Story, a neurodiversity advocacy agency.

To the Editor:

Thanks for publishing Emily Might’s cry from the guts about her daughter who has profound autism. I want you’d additionally publish a succinct piece about how determined the necessity is for “a separate diagnostic class for such youngsters — to assist tailor analysis, coverage and providers extra successfully,” as Ms. Might writes.

Neurodiversity is usually a present, and I strongly help the efforts to acknowledge this. I’ve mates in the neighborhood of high-functioning autistic individuals, and I’ve obtained a analysis of consideration deficit hyperactivity dysfunction. We’ve been helped by attitudes that see us as completely different, not disabled. However individuals like Ms. Might’s daughter are being harmed by being grouped with all autistic individuals below one umbrella. Please make a clarion name for this mandatory change.

Nancy Wirsig McClure
Portland, Ore.

To the Editor:

I appreciated Emily Might’s trustworthy and candid reflections on her 6-year-old autistic daughter. Her account helped spotlight the most important disservice in Robert F. Kennedy Jr.’s feedback: his declare that autistic youngsters will “by no means” be capable of do issues like write a poem, go on a date or have a job.

One lesson from my 5 many years supporting autistic individuals and their households is that for autistic individuals, as with all individuals, growth continues throughout the life span. I’ve recognized many youngsters matching Ms. Might’s description at 6 and even older who grew into adults with full and purposeful lives.

Current developments are giving many nonspeaking individuals on the spectrum the instruments to speak successfully. What many share is how tough and damaging it has been to undergo life deeply misunderstood and underestimated. Whereas we shouldn’t low cost the challenges many autistic individuals face, expertise has taught me by no means to say by no means.

Barry Prizant
Cranston, R.I.
The author is a professor on the College of Rhode Island, the creator of “Uniquely Human: A Totally different Approach of Seeing Autism” and a co-host of “Uniquely Human: The Podcast.”

To the Editor:

I’ve an older brother with autism and twin 30-year-old sons, each with profound developmental disabilities. I’ve lengthy been conscious that the incapacity neighborhood suffers from having enabled its personal setting of exclusion.

Inclusion means every voice is elevated so people might be supported collaboratively in response to want. It’s a fundamental aspiration for us all and a civil proper. Sadly Robert F. Kennedy Jr. overtly generalizes the expertise of 1 group along with his personal restricted model of predictive destructive outcomes.

No individuals with disabilities ought to should defend their legitimacy. We have now made strides lately in constructing dignity, irrespective of how critical the challenges. What’s wanted is extra help for households to construct entire lives for all. Interval. All the things else is distraction.

Amy Brenner Mitz
Sugar Hill, N.H.

To the Editor:

I need to attain out to Emily Might. I’ve a 48-year-old son who was nearly precisely like her daughter at that age. I perceive her weariness and despair at occasions. I hope my son’s story will assist.

For my son, studying to speak took years, however he did study. I keep in mind my elation the primary time he requested a “why” query. He was 13. He has had jobs, performs sports activities, loves music and is a superb prepare dinner. He’s additionally the kindest individual I do know.

Is that this everybody’s story? No, however it describes many extra individuals than she might imagine proper now. If I have been to provide her one piece of recommendation, it will be to achieve out to different particular wants households for help. We’re a vibrant neighborhood, higher in a position to perceive her than most professionals, irrespective of how properly which means. We routinely share useful ideas and tales with each other. We care.

Stephanie Niedringhaus
Haddonfield, N.J.

To the Editor:

We not too long ago took my 21-year-old nonverbal autistic son to the dentist for a tooth cleansing. The process requires sedation, however since we’re unable to speak with him to elucidate what lay forward, we needed to depend on his compliance. As he entered the workplace, there was anticipated agitation and a glance of resigned betrayal.

As soon as the process was completed and we have been secure at residence, the look modified to begrudging forgiveness. I’d wish to say this sort of expertise is a uncommon incidence, however it’s simply considered one of our “regular” days.

Decompressing afterward, I discovered the present of this text. I’ve few hopes for my son, and plenty of fears. I like him fiercely, however I’m damaged. I’m unable to specific what I really feel, however your phrases, for a second, broke down my very own nonverbal barrier. Thanks.

Brian Pakkala
Kenmore, Wash.

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