It's finally autistic people's turn to get a "I want an refund for my shitty kid" NYT OP-Ed.
It's finally autistic people's turn to get a "I want an refund for my shitty kid" NYT OP-Ed.
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I fucking hate these people so much.
It's finally autistic people's turn to get a "I want an refund for my shitty kid" NYT OP-Ed.
archive.is
I fucking hate these people so much.
the reality and pain of a subset of parents of children with autism who feel left out of much of the conversation around the condition.
If anything they are always dominating the conversation despite being in the minority of autism cases. I understand it's hard for them, but it's not all about you and you're talking over autistic adults who should be heard more.
They’re always talking over their children. Makes sense to ignore everyone who has lived experience with autism in favor of parents getting over the narcissistic wounding that came with having a kid that didn’t fit their fantasy.
If anything they are always dominating the conversation despite being in the minority of autism cases. I understand it's hard for them, but it's not all about you and you're talking over autistic adults who should be heard more.
we had a nonverbal kid on the school bus one year and it was really cool of his parents and the school system to abuse that kid and by extension everyone else on the bus route on top of school starting too damn early in the morning. I'm not even sure if low-support adults are able to be effective advocates for the kids who have it the worst.
"Finally" our turn? I thought we were one of the first...
It's Journalism's Sacred Duty To Endanger The Lives Of As Many Trans Autistic People As Possible.
Disgusting article
We have moved from viewing disability through a purely medical lens — as something broken to be fixed — to a social lens that puts the onus on society to accommodate it.
Ah yes, viewing disability as a problem to be fixed is very medical and rational and totally not based entirely on how your society is structured. I am very smart. It's not like someone with disabilities could ever be anything but a burden no matter how much society accommodates them, right? Stephen Hawking? Who's that?
I consider myself squarely left of center.
And yet, I think his remarks echo the reality and pain of a subset of parents of children with autism who feel left out of much of the conversation around the condition. Many advocacy groups focus so much on acceptance, inclusion and celebrating neurodiversity that it can feel as if they are avoiding uncomfortable truths about children like mine.
Once again we see how poisoning political definitions has created a reality where people believe they can call themselves left while believing textbook harmful right-wing ideology.
A Harvard-affiliated research center halted a panel on autism awareness in 2022, after students claimed that the panel’s language about treating autism was “toxic.” A student petition circulated on Change.org said that autism “is not an illness or disease and, most importantly, it is not inherently negative.”
"I, a NYT writer, know more about Autism than the people who fucking research it for a living. I am very smart and believe in science."
I understand why Mr. Kennedy is such a polarizing figure. I did not support his cabinet appointment, and I don’t believe his platform will materially help families like mine. I think his policies are likely to harm. I don’t think he was the right person to make those comments. But I was struck by his willingness to speak frankly about the painful parts of my child’s life. I don’t care if my child ever pays taxes — but I do care that she may never have the opportunity to work or live independently. She did not destroy my family, but I live in constant fear for her safety. I care deeply about her quality of life, and the limited options ahead. I appreciated his acknowledgment, because most of the time, families like mine are invisible.
The "center-leftist" siding with a literal Nazi and not realising the only reason he's acknowledging them is to dehumanise them.
My daughter turns 7 next month. I’ve long accepted that I may never hear her call me mom. I have grieved a million tiny deaths of the things I once assumed would be.
And there we have it, it's not about her child, it's about her. She became a parent because she wanted a "normal child" and now selfishly feels entitled to a "normal child" so she can fit in with societal expectations. The child is a mark of social progression to her, like a car or a home. When you have a child you shouldn't assume they will be anything you expected, they are an independent life that you are devoting yourself to ensuring their best life, not a pet.
Ah yes, viewing disability as a problem to be fixed is very medical and rational and totally not based entirely on how your society is structured.
That last paragraph you wrote reminded of that page from Flowers for Algernon, where the father defends his son Charlie from his mother.
Matt - the father - loved his son and accepted him regardless of his disabilities.
We should all be grateful we are not divorced from love, even if just as a concept of it, as Emily May is.
We have moved from viewing disability through a purely medical lens — as something broken to be fixed — to a social lens that puts the onus on society to accommodate it.
Neurotypical fascist whining about having to put up with the uppity autistics, example 99472772874.
The worst part is this isn’t some fascist hardliner anomaly view, but the opinion of the average neurotypical. I could count the number of neurotypicals I’ve met who wouldn’t put the neurodiverse “burdens” on flights to El Salvador on one hand. When Trump starts doing just that, I’ll expect nothing short of celebration from the average person, whether or not they openly do so. Sick and diseased society
I don’t care if my child ever pays taxes — but I do care that she may never have the opportunity to work or live independently. She did not destroy my family, but I live in constant fear for her safety. I care deeply about her quality of life, and the limited options ahead.
”Does the society we live in have a role in this? No, it's my child who is wrong.”
So many parents view having a "normal" child as their right. "Oh but I spent so long fantasizing about this, how could it not come true?".
The NYT really loves letting the worst people have op-eds dont they
They've been known to request them.
When Robert F. Kennedy Jr. said in a recent press briefing that autistic children will “never pay taxes,” “never hold a job,”
How terrible that must be
yeah i love not being able to participate in society
Robert Kennedy is more concerned with how much a worker can be exploited
Didn't take much for the "left of centrist" to side with fascist shit.
There isn’t a vat of boiling acid hot enough to drown this person in
I have no interest in defending Mr. Kennedy, whose shaky science and conspiracy theories will do nothing to benefit those with autism and their families.
And yet...
If I had such parent I wouldn't speak either
oh yeah it's consent manufacturing time
Yeah I only made it through the first few paragraphs before it became clear this was antivax propaganda.
"I asked why she regressed, doctor says it's common"
"RFK Jr says..."
"I got her vaccinated"
Just right in a row.
So gross.
Whenever a ghoul proposes doing the most evil thing possible the NYT will be there to publish an article about how it's good actually
I live in terror of the day she outgrows cute, and I worry constantly that as she grows bigger, her world grows
What the fuck
When she isn't cute I don't want her anymore
My general disgust towards parents who seem to think the most important thing their kids could do is have grandkids
Jesus fucking Christ it’s always the Godamn parents
Someone wanna fill me in on what else the Kennedy ghoul said that must be so controversial it's not included in this article?
[ redacted ]
parents of children with autism who feel left out of much of the conversation around the condition.
Oh yea, totally. The parents of autistic children are hardly ever heard from 🙄
We have moved from viewing disability through a purely medical lens — as something broken to be fixed
YOU CAN'T FIX IT!! god, why do people think if you invest enough tech points in an issue anything is possible? Just completely treat it as magic. I hate this attitude and it is so pervasive. You see people calling for conversion therapy with language like this too. Lots of disabilities are just- not fixable.
There’s a resistance to parents who wish their children were less disabled
I- I think everyone wishes your child was less disabled.
ugh, ew
i wish these people would question why the inability to hold a job and pay taxes is what makes someone considered worthless
Yet another example of how the logic of capitalism leads inexorably to fascism.
Parents are encouraged not to use words like “severe,” “profound,” or even “Level 3” to describe our child’s autism
yeah, i wonder why. what a fucking nightmare this person is, i feel bad for her daughter. i like pokemon, i'm not literally a pokemon. when we say this shit has levels to it, i don't think ranking and numbering them is what anyone meant.
Maybe, just maybe, laypeople shouldn’t use the same clinical and/or medicalized language used by professionals who know what the hell they’re talking about to describe their own children.
Same energy as the parents I was talking to a few months ago saying they have a “male son.” Oh okay, I thought this was a parent-teacher conference, but apparently I’m speaking to a couple zoologists.