Let’s Talk about this Coming “Avalanche” of Autistic Adults

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It is autism “awareness” month, that time of year when autistic people are told that they are costly and burdensome, that they ruin families, and even worse, that they’re growing in numbers (oh, the horror.) A petition has even circulated since Donald Trump took over the White House that claims autism must be declared a public health emergency.

While these ideas remain disturbingly common, some parents are changing their tune, albeit not in ways that actually diverge from “awareness” unfortunately. Nowadays, parents and professionals are increasingly alarmed at the incoming “avalanche” of autistic adults ill-prepared for the lack of services and support they’ll have access to after high school. It is true that autistic adults face a world that scarcely cares to accommodate their support needs, yet at the same time can no longer just “disappear” them into institutions like they used to. We have the disability rights movement to thank for winning important reforms over the last several decades mandating access to the same education available to non-disabled people. Basic civil rights like non-discrimination in public and private institutions and services, in hiring, in residential facilities, etc., had to be demanded before what should be considered routine accommodations were mandated by law. But many autistic adults require access to–and deserve–quality services and support to guarantee their basic needs are met, allowing for full inclusion into their communities. This simply does not exist in most communities. And yet being fully aware of this problem does not justify using the bigoted language of “awareness” to scare everyone into action.

I have a question. It is a question seldom asked by the “autism community” of non-autistic parents and “experts.” Why do we have this scarcity of services and support for adults? I’m not exaggerating. This simple question is never adequately addressed if it is asked at all. When it is asked by some parents and professionals, it is erroneously framed as being based around an assumption, that this state of affairs was always going to exist because the world has yet to catch up with the reality of the “epidemic” at their doorsteps.

On the contrary, this is what I see: there is no incoming “avalanche” of autistic adults. There is simply autistic adults that would have always been born, that would have always existed whether or not services and support were available to them.

This is what I see: an “autism industrial complex” that has emerged in recent decades, its purpose being the development of “treatments” and locating the source of autism to possibly cure it.

This is what I see: in childhood, an overwhelming focus on Early Intervention, extending as far back as two years of age or earlier, with therapies that are justified on the basis of teaching “skills” but which frequently exhibit the curious properties of behavioral modification, compliance-training, and normalization.  

This is what I see: a tunnel-visioned focus on autism as a childhood disorder that erases any notion that these children will grow up into autistic adults, with decidedly adult needs.

This is what I do not see: any ability on the part of the “autism community” to connect the dots, so to speak. While this community of non-autistic parents and professionals stumbles to come up with answers to the oncoming “crisis” of autistic adults, autistic adults are already here and have a lot to say about it. Perhaps we ought to start with the obvious question: why is it that you continually separate the way autistic children are treated and the way autistic adults are treated? These are not separable issues. Autistic children are treated as “fixable” or amenable to “recovery” with intensive Early Intervention as early as age two. The “autism community” says that they should be subjected to hours upon hours of therapy to reduce “problem behaviors” and learn “skills.” This community believes that the only hope for autistic people is through experimental social engineering therapy that seeks an unmistakable goal of autistic erasure. How can the needs of autistic people across their lifespan ever be properly addressed when so much money and energy goes into erasing their neurology before they ever reach adulthood? Meeting the needs of autistic people across the duration of their lives is incompatible with seeing them grudgingly as human beings after they’ve been through years of therapy and behavior modification and–shocker!–came out autistic in the end anyway.

So is there really an “avalanche” of autistic adults coming? Parent of an adult autistic daughter Cindy Godwin believes so, and she doesn’t hold back on the insulting, pathologizing, and fearmongering language that usually accompanies “awareness” either:

“As the number of autistic children grows, so does the number of autistic adults. Their needs remain much the same as they age, yet the support they once received fades. Though families like mine are feeling it most acutely, this is an issue for everyone to consider. The tsunami of adults with autism is coming.”

We’ve now graduated from an avalanche to an even scarier and more devastating “tsunami.” She prefaces her piece by reminding her audience that “autistic children never really grow up.” So what do we do with these children in adult bodies?

She describes the “scene” found at her daughter’s townhome, because boundaries like privacy need not be observed when it comes to your autistic kids. She may be near thirty years old, but no matter, she’s too feeble-minded to have any concept of privacy, like not having her parents describe what her executive functioning disabilities look like at home as though she’s a human zoo exhibit displaying the autistic adult in its natural environment for millions of people to read.

“She’s sitting on the sofa playing video games. Dirty dishes are everywhere in the kitchen, pizza boxes and empty soda bottles cover the countertops, the trash is overflowing and stinks, the patio is littered with cigarette butts, laundry needing to be done is stuffed into black garbage bags. The notice of a certified letter, announcing that she has been dropped from her therapeutic art program for non-attendance, sits on top of a stack of unopened mail and unread handouts from her counselor.

This was the scene I walked in on recently. “She” is my 29-year-old daughter.”

This mom, who states she “suffers combat level stress daily,” along with hundreds of thousands of other parents, evidently equates executive functioning disabilities with immaturity. Remember, “autistic children never really grow up.” As an autistic adult with similar executive functioning disabilities, this is beyond insulting, but standard fare coming from the “awareness” community.

To be fair, not all parents are fixated on the standard impending crisis and tragedy narrative. Father of an autistic son Raquel Regalado published a recent short piece entitled Time for Autism Awareness to Grow Up.

“As the parent of an autistic teen I can attest to the old axiom, “little kids, little problems, big kids, big problems.” And while we appreciate the social and developmental gains our children have made, the older they get the harder it becomes to find services, programing and opportunities for them because funding and public opinion is fixated on early signs and intervention.”

He is absolutely correct when he says “funding and public opinion is fixated on early signs and intervention.” Let me be clear: this must be the starting point for the divided autistic community and autism community to find common ground in discussing the needs of autistic adults.

But there is an alternative to seeing this as an “avalanche,” and there is certainly no justification for using dehumanizing and pathologizing language to describe a problem that no autistic adult had any part in creating. Autistic adults do face a severe lack of services and support. But they also regularly face an “avalanche” of bigotry from non-autistic parents and experts and even the President of the United States, anti-vaccine cure cultists, Early Intervention and ABA social engineering conversion therapists, and a highly influential international organization that makes a lot of money but has little intention of using it to address the most important needs of autistic people and their families. 

But let us say that there is an avalanche of autistic adults. I welcome it. Because autistic adults are adults, not children in adult bodies, and the failure to meet their needs as adults creates a space for them to begin advocating for the services and support they need. And more than advocating, but demanding it. Unlike so many other parents, I don’t see myself as the “voice” of my own autistic son. When he grows up, he grows up into an autistic adult, and no matter his communication challenges (he is non-verbal now, but he’s also three years old), he can learn to advocate for himself along with other autistic adults. Autistic adults are only a “crisis” when autism itself is understood as a crisis. There is only an “avalanche” of autistic adults when autistic children are understood as an “epidemic.” Accepting autistic people as autistic people, and allowing them the same self-determination that every other person has a right to regardless of their support needs, will turn this bogus avalanche into a simple issue of human rights. Never again should any person, based on their different neurology and disability, be described in this way. Accept autistic children as autistic children and there will not be an avalanche, only a need to make certain that autistic children grow up to be autistic adults with their adult needs met and fully accommodated.

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8 thoughts on “Let’s Talk about this Coming “Avalanche” of Autistic Adults

  1. Pingback: Let’s Talk about this Coming “Avalanche” of Autistic Adults | dawumps

  2. Why is it always the talk about the Adult Autistic people that are coming?
    What about those of us who were not diagnosed, or misdiagnosed, had no early intervention and still managed to become adults?
    There are Many of us. We are adults, Ranging in ages from 18 to, Well, my mother is 69, and she was diagnosed LAST Year.
    I’m 47, I was also diagnosed last year.
    We’re already here, Autistic Avalanche phobics.
    Thank you for writing this.

    Liked by 2 people

  3. Brilliant.
    Thank you for writing this.
    It goes a long way to explaining why studies that show that the prevalence rate is the same for kids and adults seem to be ignored by parent-focused groups.

    Liked by 2 people

  4. There have always been autistic adults. There will always be autistic adults.
    I’m in my thirties and got diagnosed last year. My mother is in her seventies and she’s looking for a diagnosis, as is her elder brother thanks to that diagnosis. From what she’s told me about other family members, including her aunt (my great-aunt), there’s a decent chance they were on the spectrum. Reaching out to second cousins, there’s autism diagnoses there as well.
    Honestly, these has helped immeasurably. It’s explained a lot and it’s given us a new measure of understanding on things which have created friction (sometimes for years).

    Liked by 2 people

  5. There have always been autistic adults. My husbands family is loaded with them in the past, present and future. Many times they were not so diagnosed. Considered cognitively disabled (and some may have been in addition to being autistic) or mentally ill (again, that may well have been in addition to the autism), they were lumped into those groups and treated as those who had those diagnoses and could not support selves. Mental institutions, schools and homes for such people, nursing homes, and sadly prisons for those who were found dangerous and convicted of crimes. Those families who could, often kept autistic family members within the family folds. What family does not have someone who was not able to support self? For those who could be taught behavior modification to keep them relatively safe, not attract attention from bullies, outside jobs and self sufficiency could and did happen. They might meet a significant other who would accept and delight in them, and help get through life together.
    These days with the information out there for all on autism, and that it has become a lucrative field in working with children with the same, autistic adults should be given preferential treatment in getting positions working with autistic children and adults. Who better to deal with the issues? Parents involved in these programs should insist that they are staffed with autistic adults thereby possibly ensuring jobs for their children in the future. Why should only “normals” get this funding, get the money , the ear, the work that is out there? There is more opportunity out there today for autistic children which should translate to more opportunities for autistic adults.
    Though I am specifying autism here, I think the same should be for all disabilities. Shane on the Down Syndrome camp with no counselors and employees with Down syndrome. We are seeing some progress made in this direction in schools where those serving mostly minorities are now making more of an effort to staff with minorities. Still a ways to go. But the same effort is not there for disabled children and adults. There should be an effort and priority that disabled employees are hired to do this work.

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  6. I don’t understand how you can point out there’s a lot of autistic adults out there who aren’t getting services b/c autism is perceived as a childhood illness, and we need to pay attention, but when Cindy Godwin points out the exact same thing in the first paragraph you quoted, with no inflammatory language, she’s being pathological. What’s the difference, except that she’s a parent of an autistic child, and …that makes her opinion wrong somehow?

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    • I’m a parent of an autistic child too. He is considered “low-functioning” because he doesn’t speak and has developmental disabilities. So I’ll just get the “real” autism card out of the way that I have to play in order to be taken seriously by “autism parents,” since being autistic yourself doesn’t always count for much. These same parents have invented and perpetuated misleading narratives about those who advocate within the neurodiversity paradigm, that we all ignore or dismiss the challenges involved. To address your main point: yes, Cindy is concerned about what autistic children face when they reach adulthood, and it is indeed a real problem I am equally concerned about. And yet we understand autism very differently and necessarily reach very different conclusions despite this brief moment of agreement. Individuals, like myself or Cindy or you, cannot be or “act” pathological, either in our actions or our words. The pathology paradigm exists whether we see it or not, whether you’re aware of it or not. This means that some people will not recognize the consequences of the language they use. They will not be aware of the harm it can cause nor the bigotry it conveys. This is because the pathology paradigm is so omnipresent that its body of ideas and the language that flows from it are considered part of normal everyday autism discourse. It is entirely possible to talk about the problems facing autistic adults and autistic children without ever referencing an “epidemic” or an “avalanche,” the latter being the logical conclusion that flows directly from seeing autism as an epidemic. This is not Cindy Godwin “being pathological.” This is Cindy Godwin talking through the prism of pathology, where all her erroneous ideas, shared by many other parents like her, were informed and shaped. There is another prism with which to see autistic people, and it doesn’t ever require stigmatizing language. If you cannot see the problem here than I highly suggest you read more from the autistic community. We can acknowledge the problems faced by our children, and the problems we ourselves face, and discuss these problems with others, and ask for help from others who were autistic children once or parents who’ve learned a lot from their children over time, and all without ever needing to ring alarm bells with a demeaning narrative and bigoted language.

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