Why does RFK Jr want to put my family on an ‘autism registry’? | Deborah Bloom

TruthLens AI Suggested Headline:

"Concerns Raised Over RFK Jr.'s Comments on Autism and Neurodiversity"

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TruthLens AI Summary

The author reflects on her upbringing with neurodivergent parents, both of whom exhibit traits associated with autism. Her mother, a former mathematician, and her father, a computer programmer, have faced challenges due to their unique cognitive profiles. While the author initially felt embarrassed by their differences, she has come to appreciate their qualities as integral to their identities. The narrative highlights a shift in societal understanding of neurodivergence, framing it not as a flaw but as a variation of human experience that can enrich relationships and foster empathy. The author expresses concern over comments made by RFK Jr., who has labeled autism as a 'preventable disease' and referred to the increasing prevalence of autism spectrum disorder (ASD) as a 'cataclysm.' This rhetoric evokes fear about the implications for individuals on the spectrum, suggesting a stigma that could undermine the progress made in recognizing and accepting neurodiversity.

The article further critiques the potential consequences of RFK Jr.'s statements and the federal government's approach to autism. While the government aims to allocate resources toward understanding ASD, it simultaneously threatens to cut funding for crucial support services for autistic individuals. The author emphasizes that autism is a complex neurodevelopmental disorder, not merely a condition needing eradication. The piece highlights the need for greater societal understanding and acceptance of neurodivergent individuals, advocating for more inclusive policies and support systems. The author concludes by reflecting on her parents' experiences, positing that their lives—and her own—could have been significantly improved in a society that embraced neurodiversity rather than stigmatizing it. This commentary calls for a reassessment of how autism is perceived and supported within communities, ultimately arguing for a more empathetic approach to neurodivergence.

TruthLens AI Analysis

The article provides a personal narrative that reveals the author's perspective on neurodivergence within her family, specifically relating to her parents' experiences with autism and how societal perceptions have evolved over time. The mention of RFK Jr. and his controversial statements regarding autism suggests a deeper critique of public discourse surrounding the condition.

Exploring Personal Experiences with Neurodivergence

The author begins by sharing her family's unique characteristics and challenges associated with neurodivergence. By illustrating her parents' intelligence and struggles, she humanizes the conversation around autism, making it relatable to a broader audience. This personal touch aims to foster empathy and understanding regarding the complexities of neurodiversity. The author’s journey from embarrassment to acceptance of her parents’ differences serves to challenge stigmas associated with autism.

Critique of Public Discourse

The author's fear of RFK Jr.'s remarks about an "autism epidemic" highlights the potential for harmful narratives that can arise in political discourse. By labeling autism as an epidemic, it can inadvertently contribute to negative stereotypes and fear among the public. This criticism aims to raise awareness about the impact of language and framing in discussions about autism, suggesting that mischaracterizations can have tangible effects on the lives of neurodiverse individuals and their families.

Manipulation and Public Perception

The article subtly suggests that political figures may manipulate public perception regarding autism for various agendas. By framing autism in a catastrophic light, RFK Jr. may be attempting to garner support for his initiatives, potentially at the expense of those affected by the condition. This raises questions about the motivations behind such statements and whether they serve to advance societal understanding or perpetuate fear.

Impact on Society and Community

The narrative encourages readers to consider the broader implications of how autism is discussed and perceived in society. By promoting a more nuanced understanding of neurodiversity, the article suggests that greater acceptance and integration can lead to more supportive communities. It also implies that public figures should be cautious about the language they use, as it can influence public attitudes and policies that affect the autistic community.

Comparative Context

When compared to other narratives surrounding autism, this article stands out for its personal approach. It emphasizes individual experiences over generalized statements often found in political rhetoric. This personal storytelling can resonate more deeply with the audience, fostering a connection that statistics and political rhetoric often fail to achieve.

Potential Societal Outcomes

The ideas presented could influence societal attitudes towards autism, potentially leading to increased advocacy for neurodiverse individuals and more inclusive policies. Conversely, if fear-driven narratives dominate, it may result in further stigma and isolation for those on the autism spectrum. The article serves as a reminder of the power of language in shaping perceptions and policies.

Supportive Communities

The narrative appears to resonate more with communities advocating for neurodiversity, inclusion, and acceptance. It speaks to those who may have personal connections to autism, whether through family or friends, and seeks to empower them to share their stories and perspectives.

Economic and Political Implications

While the article does not directly address economic impacts, it suggests that public discourse on autism can influence healthcare policies and funding. If negative perceptions prevail, it could affect resource allocation for autism research and support services.

Considering the content and the emotional undertones, the reliability of the article is strong. It combines personal experience with a critical view of public narratives, advocating for a more compassionate understanding of autism.

Unanalyzed Article Content

I always knew my parents operated on a different wavelength than most.

For one, they are both exceptionally smart. My mother is a former mathematician, who studied the various levels of infinity as part of her master’s thesis. My father is a computer programmer who, at 17 years old, was one of the youngest people to ever be able to communicate with ships in morse code. They met at a party for members of Mensa, a club for the highly intelligent.

But their gifts have come with challenges. My dad struggles with eye contact and can become easily overwhelmed in social settings, where emotion and nuance can short-circuit his systems. My mother has difficulty with executive function, and finds it tough to stay neat and organized. Regulating their emotions and reading social cues don’t come easily to either of them.

My father was first diagnosed with what was then known as Asperger’s syndrome in his 20s. My mother has never been officially diagnosed as autistic, but identifies as such. When I was a child desperately wanting to fit in with others, I found their neurodivergence to be embarrassing. I wanted what I thought other kids had: parents who got them to school on time, who didn’t have unpredictable, emotional flare-ups or constantly messy homes.

Now as an adult, living in a time when neurodivergence is more openly discussed and understood, I’ve come to see their quirks not as flaws but as unique features of who they are. I’ll call my mom when I’m struggling across a tricky math problem, knowing she’ll light up with excitement at the opportunity to assist me with her expertise. I love watching my dad pour himself into his ham radio community, where friendships are forged without the pressure of eye contact.

That’s why, when I first heardRFK Jrvow to the Trump administration to find the cause behind the so-called “autism epidemic”, describing it as a “cataclysm”, I got scared. Was the person in charge of the federal government’s healthcare apparatus really describing my parents as victims of an illness that we, as a society, have let get out of control?

Later that week, he doubled down, callingautismspectrum disorder a “preventable disease” that “tears families part”, citing thegrowing ratesof ASD among children: one in 31 kids in 2022, compared with one in 36 kids in 2020. “These are kids who will never pay taxes. 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.”

Autism is, in fact, being diagnosed more than ever before, but scientists largely attribute this to increased awareness and a broader diagnostic criteria for the disorder. “When I started in this field in the late 60s, autism was a last resort diagnosis,” says Dr Catherine Lord, a clinical psychologist whose primary focus is ASD. “It was primarily given to kids with intellectual disabilities.”

It’s also true that people in my generation have more autism diagnoses than our parents. But there are plenty of us out there who suspect our parents may have been on the spectrum, even though they were never formally evaluated. “It’s rare for a parent first to be diagnosed with autism, and then a child realizes they are also autistic,” Lord says. “It’s much more common for a parent to realize they’re on the spectrum after their kid’s been diagnosed.”

RFK Jr’s blanket description of 2% of the population fails to take into account the wide spectrum of symptoms that people with autism experience. Some have higher needs than others. Many are able to mask their symptoms. Some are non-verbal – about 30%, according to the National Institutes of Health. All deserve to live in a society where they are understood, recognized and supported – not categorized, as RFK Jr describes, as a “tragic” aberration that needs to be snuffed out.

The federal government says it’s committing resources to finding the cause behind ASD (a condition that has been studied since the 1940s and is overwhelmingly attributed by scientists to genetics) and that it isstarting an autism databaseto track the private medical information of numerous Americans. At the same time, it is also poised to cut funding for autism research and support.Slashes to theDepartment of EducationandNational Science Foundationmean less money for special needs kids and intervention programs.Reduced funding to the Substance Abuse and Mental Health Services Administrationmeans autistic people, who are particularly vulnerable to mental illness, will have less access to mental health services. Meanwhile, there areconcerns that Congress will cut Medicaid coverage, which would lead to less behavioral support for autistic people, especially children and low-income families. “It just seems so contradictory,” Lord says.

By saying autism is a “preventable disease,” rather than a complex neurodevelopmental disorder, RFK further stigmatizes an already vulnerable population and threatens to set back a decades-long effort to bring ASD into public awareness and acceptance. Schools already struggle with how to incorporate autistic children into everyday learning, and few programs exist (let alone are publicly funded) specifically for neurodivergent kids. An infinitesimal percentage of workplaces recognize the unique needs of their neurodivergent employees, making it difficult for people with ASD to find and keep employment.

Neither set of my grandparents understood their children were autistic, and so the support my parents received was limited. My mom’s parents shrugged their shoulders and categorized her as weirdly obstinate. My dad’s parents treated him like a prodigy, which, although a kinder approach, fostered a superiority complex and a host of anti-social behaviors, making it tough for him to find friends. As adults, both my parents struggled to hold down full-time employment at office jobs, presumably in part because their workplaces probably adhered to a rigid social compact and failed to recognize their unique needs.

These days, my parents have learned to mask their autism to varying degrees. My father eventually taught himself how to sustain eye contact with others, and can now hold a conversation with minimal downward glances. They both, to a degree, have become more socially aware and work for themselves.

So, no, autism did not ruin my family, as RFK Jr claims. If anything, their conditions have made me a more empathetic, understanding adult, which I believe makes me a better journalist, friend and daughter. But, I sometimes wonder: what would my parents’ lives have been like if society had made more room for them and others like them? I suspect that in a less ableist world, they would have led happier childhoods. And, I think, so too would I.

Deborah Bloom is a text and video journalist who covers breaking news and human interest stories about gender, culture, mental health and the environment

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Source: The Guardian