To clarify…
I ranted about Michael Savage yesterday. I think I’ve since calmed down, with “think” being the key word.
Several autism advocacy organizations have combined their energies and submitted a letter to Savage’s sponsors. I keep mulling over his follow-up show, how he treated his guests, how he decided which experts to pick for the discussion. It all reminded me of how much I loathe politicians and political discourse. I suppose that, being entrenched in the study of feminist rhetorical practices (among other things), it’d be fairly ridiculous for me to coin myself apolitical. I also suppose that apolitical is a sort of paradoxical parlance, especially since refusing politics is, in and of itself, its own political alignment.
I’m entirely gullible, I’ve realized. Or perhaps “indecisive” is the better word. That, and I rely too much on other’s perceptions, reactions, and ideas about social propriety since I tend to lack awareness of what is socially appropriate and acceptable. I’m never quick enough to realize when I should be saying “stupid flaming liberals” or “stupid staunch conservatives.” I’ve also come to realize that saying the wrong phrase in the wrong venue has the potential to result in personal injury. More often than not, I opt to say nothing at all, if only because I can’t process nuance fast enough.
Back to Savage. I’m often hesitant to label Asperger’s as a disability, if only because I don’t see my cognitive perceptions as negative constructs, as something horribly, terribly wrong with me. I prefer to think of Asperger’s as a difference, and some of the accommodations that I need aren’t fixes for my supposedly “wretched medical problems” — just alternative methods for me, as a particular individual, to get by. Moreover, so much of Asperger’s is wrapped up in social matters that I’d be committing a form of self-suicide to merely think that every failed situation is the fault of my “miswired” brain: social issues are social issues, issues wrapped up in a one-size-fits-all, more-often-than-not universally designed (or desired) society, a society obsessed with bell curves and misplaced chitchat about the weather. (Yes, I can see the sun, read the temperature on the bank’s LCD display, and feel the humidity against my skin. But thanks for bringing the current environmental condition to my attention.)
After listening to Savage and his claims that the autism spectrum is a bogus way for drug companies and doctors to reap in extra purse change, I feel as though any attempts I have at rebuttal are compromised. On the one hand, I defend my diagnosis of Asperger’s fervently: based on current scientific evidence, academic and medical communities at large define Asperger’s as high-functioning autism. I am autistic. And defensively so. I have a disability.
On the other hand, I’m not disabled in Savage’s sense of the word — there’s a huge linguistic gap emerging here. Sure, I have “problems,” and sure, I need “accommodations” sometimes, and sure, I have trouble “functioning socially” on many an occasion. I do not, however, need pity, and I am not tragic — neither tragically sad nor tragically cool nor tragically trendy nor tragically misdiagnosed. Tragic and I only fit in the same semantic unit when referring to my fashion sense, which is sadly and grossly lacking. According to Savage, “true autism is devastating.” Devastating for who? Devastating for what? His ratings?
Generally, I assume that when parents learn that their child has autism, they rarely jump for joy. Their lives change considerably, and often they lack the support services that they and their child truly need. But these challenges do not mean that their child is necessarily suffering in perpetuity, that their child is somehow lacking as a human being. Savage’s first guest, Wendy Fournier, president of the National Autism Association, unfortunately bolstered this idea, even though she claimed to be defending the interests of autistic children and their families. We have, she claimed, “a generation of impaired children.” Fournier also believes that vaccinations and heavy metal toxicity are in part responsible for autism, which made her seem all the less credible. Despite my many points of contention with Fournier’s beliefs, I was glad to find a letter she wrote in response to her spot on Savage’s show. When I listened to the show, it often seemed as though she was agreeing with a lot of Savage’s claims concerning overdiagnosis and misdiagnosis. As it turns out, she was placed on MUTE for much of the show, in order for Savage to soliloquize. She further maintains that she disbelieves Savage’s out-of-context/pharma defense, especially since most families do not receive governmental support, cannot sue anybody for causing their child’s autism, and are often placed on years-long waiting lists for necessary support services.
Rhetorically and editorially, this is all very interesting. The more I read about the Savage debacle, the more I realize why pathos is so de-legitimized (and demonized) as a persuasion tool within academic circles.
