Tweak

InsaneJournal

Tweak says, "I want meat buns."

Username: 
Password:    
Remember Me
  • Create Account
  • IJ Login
  • OpenID Login
Search by: 
  • View
    • Create Account
    • IJ Login
    • OpenID Login
  • Journal
    • Post
    • Edit Entries
    • Customize Journal
    • Comment Settings
    • Recent Comments
    • Manage Tags
  • Account
    • Manage Account
    • Viewing Options
    • Manage Profile
    • Manage Notifications
    • Manage Pictures
    • Manage Schools
    • Account Status
  • Friends
    • Edit Friends
    • Edit Custom Groups
    • Friends Filter
    • Nudge Friends
    • Invite
    • Create RSS Feed
  • Asylums
    • Post
    • Asylum Invitations
    • Manage Asylums
    • Create Asylum
  • Site
    • Support
    • Upgrade Account
    • FAQs
    • Search By Location
    • Search By Interest
    • Search Randomly

dkmnow ([info]dkmnow) wrote,
@ 2008-04-01 10:22:00

Previous Entry  Add to memories!  Tell a Friend!  Next Entry
Autism Awareness: "Wait -- you're saying that YOUR prejudice is a 'symptom' of MY autism?"
[crossposted from my WordPress blog]

So, the dreaded "Autism Awareness Month" has arrived, and thus, the seasonal deluge of parental angst and professional avarice shall soon be upon us.

For my own part, I will indeed be attempting to participate in the "Blogging for Autism Awareness" project. Here, have a button:



As words are often in short supply for me (well, coherent ones, at least), I expect I'll mostly just be linking back to various classics in autistic self-advocacy and disability rights genres. But for this stab, I'm going to indulge in a bit of self-quotation, plus links.

In a recent e-mail, the intrepid Ari Ne'eman of ASAN asked if I might have any talking points to contribute for future discussions with Dr. Harold S. Koplewicz, pertaining to any future "awareness" campaigns to be embarked upon by his Child Study Center at NYU. Sometimes, my random replies to random e-mails take on a life of their own, and I end up expounding endlessly on things I should be saying to the world at large. When I sit down in hopes of doing a bit of formal blogging, however, words flee from me like frightened mice.

So, rather than risk never getting around to saying these things at all, below is the bulk of my reply to Ari, with minor edits and links added.

------

I still think one of the most important points to drive home, and one of the most difficult to convey with any clarity, is this:

1) The continual day-to-day effects of widespread social prejudice are, almost without exception, far more genuinely debilitating, both in the immediate sense, and throughout the life-span, than anything that is truly intrinsic to autism itself. And in the case of intrinsically debilitating mental illnesses, that social prejudice is an enormous part of the "vicious-cycle" that very reliably erodes self-confidence and functional competence, thus making the debilitating symptoms progressively far worse than they would otherwise become in an accepting and supportive society. But the prejudice of society is not a "symptom" of autism, nor of any genuine mental illness -- it is an independently operating cause of needless psychological harm and distress. To trivialize or ignore the role of social prejudice as an independent cause is to leave that cause free to do its worst -- to continue destroying lives.

As you well know, such a great many of us have said this countless times, in countless different ways. The first sentence in the above has become nearly "echolalic" for me. I wish I could find a way to say it that is more accessible to a wider audience, but I've had no luck with that. For those of us who live it, it scarcely needs to be said. But for those with no insight into the matter -- just as is the case with "white privilege" and such -- how can it be put into terms and concepts that will convey anything useful or meaningful to those who have not experienced it? For most people, it just doesn't translate at all.

Getting back to Koplewicz, that message clearly hasn't gotten through to him with any real impact, if at all. As you may recall, his reply to me on this point was both evasive and self-contradictory. Similarly, NIMH director and IACC chair, Dr. Thomas Insel, has apparently managed to sidestep it as well, despite enormous effort on the part of so many. Kathleen Seidel's letter to him, three years ago, and her subsequent reply to his reply, were both polite and extraordinarily lucid. And yet, as I gather, he persists in the worst sort of inflammatory rhetoric ("wipe autism off the map"? Did he really say that?). But, of course, anything we say is dismissed as a "personal attack." How to break through that kind of entrenched bias and cavalier disregard? For Koplewicz in particular, the point must be made -- or rather, the answer to his evasion -- whether he can stomach it or not:

2) The clinical community IS at the very forefront of sustaining social prejudice -- by virtue of the very language and imagery they use in describing human difference -- and no outpouring of "good intentions" can absolve them of responsibility for what they say about us.

Now, personally, I see little hope of getting through to Koplewicz and those like him (and Insel appears to have been cut from that very same cloth). That's why I feel it's necessary to take our arguments to them, and their replies to us, and make it all readily available to the public, along with our analysis and criticism. If using such means to bring public pressure to bear upon them is the only way to motivate them to govern their own behavior, if not reform their views, then so be it. Obviously, they won't like it. But they are presuming to tell the world what to think about us -- it's hardly reasonable of them to expect us to stay silent.

I have yet to read Koplewicz's book(s), and I want to do so before launching any more specific arguments against what he advocates. But, from what I have seen thus far, I think I have a pretty good feel for his rationale, and his "ethics." As he seems to lack the benefit of a sociological perspective, I honestly don't think him capable of grasping the enormity of what social prejudice can do. Now, his main premise, "it's nobody's fault," is something I might agree wholeheartedly with, but in a very different sense than how he uses it. Deconstructing the "blame game" and coming to terms with a realistic grasp of personal responsibility -- if we are to approach it with any honesty -- is damned hard work, and takes most people a lifetime. There is no miracle pill, literal or otherwise, that can spare us the arduous soul-searching and self-reform that admirable figures throughout history have had to face in leading the way to the wholesome and ethical life. For those of us who wish to follow, there are no substitutes, no surrogates, no "magic bullets."

But with his nearly exclusive focus on "brain-disease" medicalization of human difference, Koplewicz actively trivializes and marginalizes any sincere acknowledgment of the brutal realities of real mental illness as experienced by the actual victim, and most consequentially, he trivializes and obfuscates the bulk of its real causes. By consistently pretending that there is no connection between "mental illness" (by his definitions) and the preponderance of psychological abuse that continues to pervade our society, he is being no more ethical than those who claim that victims of rape "asked for it" or "got what they deserved." Koplewicz may not be explicitly blaming the victims, but he is quite irresponsibly diverting attention from the primary cause, thereby further enabling abusers of all stripes.

Added to that are his many vested career interests -- among other things, his childlike devotion to the psych-med industry is the stuff of legend. From where I stand, Koplewicz seeks to create a "feel-good" movement for parents and professionals, where, instead of the hard work of honestly facing and coming to terms with their own possible roles in harming children, he warmly invites them to shift all responsibility onto some abstract construct under the conveniently amorphous heading of "medical issues." This diversion is not remotely helpful in understanding or addressing any genuine form of mental illness, but it is extremely compelling for those who unconsciously seek absolution, and it is very profitable for those who seek to pander to the angst of outright abusers, and of those parents who are just plain confused. It sweeps the primary cause of mental illness under the rug in order to sustain and inflate the market for whatever "services" the mental health industries wish to sell. Deliberate or not, that is the effect, and that effect is part of what drives the process. Round and round. Meanwhile, children continue to suffer abuse and exploitation in the name of "love" and "treatment," and as they become adults, the cycle begins all over again ...

And Koplewicz, Insel, "Autism Speaks," Big Pharma, et al, are all uniquely positioned to profit from this cycle. On the flip-side of the hype-machine, we have Kirby, Wakefield, Geier and Geier, well-heeled anti-vax lawyers and countless others, likewise poised to make a killing from whatever misinformation and fear they can peddle.

And there we are, right in the middle -- those of us who must actually live the crumbs of life they leave us with; we who both camps of exploiters insist they only want to help, though by their own rhetoric and posturing, they make of us their mutual arch-enemy -- our voices drowned out by reactionary shouting from both sides. Some of them really are True Believers in their various causes, but it makes no difference how sincere their "good intentions" may be. The effect is the same. They lavishly pave the road, and fully expect us to ride it straight to Hell, thanking them all the way.

I recognize the merits of trying to work with them, to some extent, but I find it hard to avoid a sense of futility in that regard. Most days, I feel that the only possible progress can come from exposing what they do. But to do that effectively, of course, is not only very complicated, it also places at risk many aspects of cooperation that might, despite my cynicism, truly lead to reform. In the face of such ambivalence, my philosophical roots chime in to suggest the proverbial "middle way." Maybe that's really the hardest part of it all: finding the right balance between defiance and cooperation -- or harder still by far, finding the balance within ourselves to walk a straight line amid conflict.

Hmmm ...

(Post a new comment)


[info]bibliotech
2008-04-03 05:25 am UTC (link)
OH GOD THIS IS WHY EVERYONE'S POSTING GODAWFUL ARTICLES. If I see one more post on iReports about how their poor baby has autism and is therefore completely ruined for life as we know it, I'll scream.

(Reply to this) (Thread)


[info]dkmnow
2008-04-03 06:10 am UTC (link)
Yeah, that's pretty much the size of it. Today was "World Autism Day," which, between you and me, is not one of the things I'm most grateful to the UN for. But I expect the very worst of it will taper off in a few days. Meanwhile, a lot of us are lavishly administering antidotes to the poison. Ari is out there kicking ass and taking names, among others. And Alex Plank, of WrongPlanet.net, got off a brilliant preemptive strike against Autism Weeps yesterday:
http://www.wrongplanet.net/article366.html

(Reply to this) (Parent) (Thread)


[info]bibliotech
2008-04-03 06:31 am UTC (link)
Also, I'm tired of people assuming "autistic" = "child". When someone says "oh, autism is such a terrible thing" and someone else pipes up with "I know, the poor children". First of all, screw you. Second of all, I don't personally know anyone autistic under the age of 21, and I don't think any of them want to be known as children, including me.

Also, thank you for the link, I get the feeling I might spend a lot of time wandering around there.

(Reply to this) (Parent) (Thread)


[info]dkmnow
2008-04-03 08:33 am UTC (link)
The Autistic Adults Picture Project was started several years ago as rebuttal to the near-exclusive focus on children. I had the privilege of pitching in my two cents on its creation, back when I was active in the AutAdvo Group, but I never submitted my own pictures. The more I have thought about it over the years, the less I want pictures of me anywhere on the web. Having sparred with the likes of "synthetikmisery" and Anthony "Robin Artisson," I'm sure you understand...
And there are even worse characters in the anti-autistic cults (i.e., John Best). But that's irrelevant now, since my digital camera smoked itself.

The myth/prejudice persists, of course, and is actively sustained by the biggest charities. When you set out to use an entire class of people to prove your own "nobility" to the world while raking in the bucks, you want those people to be cute and mute. You can't have them speaking for themselves. By this model, kids stop being "autistic" when they stop being cute -- most especially, when they grow up and start communicating their own opinions. Since they almost never say what parents and professional want to hear, the easiest way to fix the problem is just to erase them from society's Big Picture.

Many of the best self-advocacy blogs are linked to from the Autism Hub page/feed. Some of the parents' stuff can get a bit tedious, but for the most part, it's all very pro-autistic. One in particular that you don't want to miss is Whose Planet Is It Anyway?, by "afbh" (that stands for "Autistic Bitch From Hell"). Actually, I'd be surprised if you hadn't already found that one. :-) But if you haven't followed it, you'll at least want to check out what she has to say about "Autism Speaks."

While at WrongPlanet, be sure to check out the testimony that was given at the last IACC meeting by Ari, Alex and Katie. Should all be accessible from the home page, or under Articles.

(Reply to this) (Parent)


[info]dkmnow
2008-04-03 10:10 am UTC (link)
Excerpt from speech delivered today -- er, yesterday, that is -- by Ari Ne'eman of ASAN, to the Florida Autism Task Force:

"There remains a shocking lack of awareness for the needs – and even the very existence – of autistic adults. In many circles, it is assumed that autism is something relevant only to children and as a result legislation and policymaking has been focused mostly on early childhood. However, there is a large population of adults and adolescents on the spectrum with needs that are not being met. In areas like employment accommodations and other aspects of disability service-delivery, adults on the spectrum are frequently unable to access the supports that are currently available, due to a lack of knowledge of our particular needs. Many of us, as is the case for others with less obvious, "invisible" disabilities, face pervasive employment discrimination as a result of communication difficulties. Vocational Rehabilitation agencies in many states are unaware of how to address these issues, due to the fact that while many of us have the skills for competitive employment, difficulties with transportation, the interview process and the social aspects of the workplace can often interfere with holding a job. It is important not only to educate the general public about autism, but also disability service-delivery professionals who are too often unfamiliar with our population."

Full text at:
http://www.autisticadvocacy.org/modules/smartsection/item.php?itemid=27

(Reply to this) (Parent)



Home | Site Map | Manage Account | TOS | Privacy | Support | FAQs