Song in the Dentist's Chair

End of summer. Birds sing shorter notes. Dying requires only the smallest arias, eh Puccini?

NB: of Puccini and birds all I know for sure is the maestro loved duck hunting—the joke is, he ate every duck in Italy.

For a poignant theme, remember all songs are time sensitive. Meantime:

let us praise our maker, sing a little air—these fake teeth will outlast me—like love we don’t know where. 

Tähän päättyy kesä (This concludes the summer)

—contemporary Finnish folktale

 

The northern wind is (unaccountably) making my grandfather silly—though he’s in his grave—though he was (unaccountably) Lutheran—though he redacted joy during his sojourn on earth. 

He gets in touch. “Pine turps and baby coffins,” he says, via Morse, with a branch and a window. Then, for a long time, he’s silent, drinking in the marl-ish ichor of eternity. Then, tap tap tap: 

“Winter wind. Stop. Bells ringing in underworld. Stop. 

The dead laugh, throw spoons in snow.”

 

  

Disability Studies and the Flaming Pie

 

 

Disability Studies came to me on a flaming pie as Paul McCartney would say. The pie flew in the window while I was half asleep. The year was probably 1985 or ’86—somewhere in there, Reagan was sawing the nation in half and I was fresh out of graduate school in creative writing, home after two years of study in Europe, feeling discomfort with the way disability was used as metaphor both in literature and in public. I read and re-read Susan Sontag’s Illness as Metaphor and began studying blindness and figurative language. I spent considerable time in the archives at The American Foundation for the Blind. I envisioned writing a book with the working title: “The Cyclops and the Seer: Blindness in Literature and Film” or something along those lines. The sharp dichotomy of vision loss as symbol either spelled abjection, monstrosity, blankness, or death—or it spelled compensatory powers of divination, intuition, spiritual grace—none of which has anything to do with real blindness. I began writing turbid, abstruse prose about reification, valorization, disambiguation, and god knows what else and then it dawned on me that I’m essentially a creative writer and I should write something in the manner of Joan Didion, nonfiction as story—the term “creative nonfiction” didn’t yet exist—but I knew what I wanted: lyric prose, prose like poetry, steeped in scholarship, rich with personal detail, and which, if properly composed would take non-disabled readers on a journey through blindness—a strange, rich journey, for though blindness is not what the metaphors say it is, its more interesting than able bodied people customarily allow. This approach eventually lead me to complete my first book, a memoir entitled Planet of the Blind. 

 

I didn’t know at the time there were others in my generation—that we’d become “wave one” of disability studies—Simi Linton, Kenny Fries, Brenda Brueggemann, Rosemarie Garland-Thomson, Lenny Davis—and so many many more. All of us were coming of age and entering the public square at the very same moment. As I say, I didn’t know there were others because my blindness in the 1980’s and early ’90’s was still a mountain—less figurative than might be supposed—for I couldn’t navigate on my own and spent my time in the smallest neighborhoods where I knew the streets. And while provincial life and poor navigation kept me isolated I also lost my adjunct teaching job at Hobart and William Smith Colleges—a loss that lead me to sue the school. They settled with me out of court and all I can say about the matter is it was disability related and ugly. I was in serious distress. I called the New York State Commission for the Blind, hoping they would help me find a new job. 

 

 

**

 

I felt like a bald man in a barber shop: people stopped talking when they saw me. Colleagues who I’d once thought friendly shied away. I’d lost my job in the summer and then it was autumn and with legally blind eyes I saw the trees flare into gold and I walked with a bent white cane and a cd player and listened to Viennese love songs, songs like cream puffs, and I decided it was time to get married. I would marry a dog. I’d been reading about guide dogs in the public library. I figured I’d marry a dog though all I owned was a suitcase tied with a rope. 

 

 

Of course I owned more than a suitcase. I had hundreds of poetry books and opera records. And I owned the streets with their long shadows. When you’re legally blind you can see a little but the window of my sight was growing smaller owing to mid-life cataracts. I went to a famous eye surgeon who said that removing the cataracts would destroy my retinas. He said it was better to go entirely blind. I went home and played Verdi’s La Traviata on my stereo and wept. It wasn’t the blindness that bothered me, it was the prospect of nothing. And the poetry books whispered you can surely count on nothing. I remembered Wallace Stevens’ closing lines from his poem “The Snowman”–The nothing that is not there/and the nothing that is. 

 

Then I was visited by a man from the agency for the blind. He was very nice—affable, with a voice you might hear on the radio. He wanted to help me find a new job. We spent long minutes talking about my resume: graduate school for poetry writing; eight years of part-time college teaching with administrative experience thrown in. As I say, he was very nice, which meant he couldn’t lie. “I don’t think you’ll ever find another job,” he said. And the poetry books agreed. What instruments we have all agree/the day of his death was a dark cold day.

 

Leaves flew past the windows. Some struck the glass and I thought of them as little counsels. As the agency man talked I thought of some lines of poetry by Christina Rossetti who was imagining the advantages of being dead: 

 

I shall not see the shadows,

  I shall not feel the rain;

I shall not hear the nightingale

  Sing on, as if in pain;

And dreaming through the twilight

  That doth not rise or set,

Haply I may remember,

  And haply may forget.

 

  

 

Meanwhile, as I was thinking about dying, the agency man added there was a local manufacturing company that made plastic lemons–the ones you see in the grocery store with the lemon juice inside. He said that they occasionally hired blind people. I might be able to sort the plastic lemons. I lit a cigarette then, and inhaled deeply. I’d give up smoking later that year but for the moment smoking was repressed laughter for I saw myself among thousands of plastic lemons in a cramped shed. I was wearing a suit made of moonlight. I could see myself juggling the lemons like a metaphysician. I was half in love with the idea. I had secret aspirations that I’d never be able to share. 

 

When the agency man left I grabbed the telephone and called the guide dog school. In the white tent of my mind I had a future. 

 

**

 

To this day the only diploma I’ve framed is from the guide dog school, as in March of 1994 I became an independent traveler for the first time. While others in the disability studies movement were gathering at the Modern Language Association, starting the arduous work turning academic attention to disability and social constructions of embodiment, I was walking with a guide dog around New York City, learning how to go places.  

 

We rode the subway to Fort Tryon Park in northern Manhattan to see “The Cloisters”—the Metropolitan Museum’s replica of a medieval monastery. We took the A Train to 190th St.—a trip that would have been unimaginable just a month before. People on the train loved the sight of my guide dog Corky. An old man said: “That dog looks strong as a tree!” And she did look strong. I could feel Corky’s strength in large and small ways—through her harness, and when she was simply lying at my feet on a rocking train.

At 190th St we took the M4 bus about a block. Poof!  We were in the middle ages.

 

We were visiting the unicorn tapestries, man and dog. We were in a quest. Corky was pulling hard, happy with the day. The tapestries depicted a hunt for the unicorn, a creature all school children know. We were early at the Cloisters and a guard offered to describe things. With a dog and a kindly stranger I entered the world of a unicorn hunt.In the last panel a unicorn, half goat, half narwhal, glowing like Jupiter, sat under a pomegranate tree, radiating magic against a backdrop of stars. 

 

**

 

Although I’m part of disability studies, I’m provisional within the field, my own choice perhaps, but maybe not. I distrust essentialism. I’m weary of the balkanization of alterities—suspicious of identity flags. Perhaps this has to do with my physical location which is always precarious and risky. Maybe I’m sufficiently Marxian to feel uncomfortable at the crossroads of neoliberalism and postmodernism. I’m fond of the book Marxism Against Postmodernism in Educational Theory, edited by Dave Hill, Peter McLaren, Mike Cole, and Glenn Rikowski. To whit: 

 

“Following tectonic shifts in the geopolitical landscapes of the 1980s and 1990s, postmodern social and political theory—with its preening emphasis on language, culture, and identity—has become the de rigeur conceptual attire among social scientists attempting to make sense of contemporary social life within late capitalism. Mining the terrain of identity politics, consumer fetishism and privatopia has become a central academic activity and is now considered theoretical chic. In contrast, Marxism has been mummified along with Lenin’s corpse, and its scholarly exercise has been likened to tampering with historical relics.

 

The joint ambition of uncovering the hidden ideologies secreted within Western representations of the ‘other’ and refashioning the antifoundational self, has disposed postmodern theorists to dampen their euphoria surrounding social transformation at the level of relations of production and to heighten their regard for reforming and decentering dominant discourses and institutional practices at the level of cultural transactions. According to Sam J. Noumoff, postmodern politics attempts (a) to separate culture from ideology, (b) to employ culture as a construct that diminishes the centrality of class, (c) to insert a neoliberal political system of intelligibility and policy agenda, (d) to perpetuate the belief in the ultimate futility of the[…]”

 

Excerpt From: Dave Hill. “Marxism Against Postmodernism in Educational Theory.” iBooks. https://itun.es/us/ylrtE.l

 

 

I just can’t be convinced that sexual politics, gender oppression, racial discrimination and disability abjection are remediated by performativity or deconstruction, for these activities are all privileged by the circuits of an economic system that relies precisely on privatopia and its variegated forms of consumer fetishism. 

 

I was late to the disability studies party because I was learning how to walk. I’m still late to the party because I don’t believe decentering dominant discourses of normative rhetoric does enough to protect the most vulnerable among us. I started with “Flaming Pie” and will end with an apology to Paul Simon—“Still Provisional After all These Years…”

 

 


Solo

 IMG 0431 

I am writing a poem in mist

Deer eating the fallen apples—later it will snow.

As a child I talked to my hands 

Blind and alone—later it would snow. 

Later night was quiet 

Like a dream of dreaming— 

Boyhood was that way, 

I could look down

See myself asleep at our piano.

When I say I love my life 

I’m playing there, that dream instrument—snow at the window.


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On Running Away Without My Teeth

Last night my teeth fell out. I mean my real teeth. Well, not really, but a temporary “bridge” popped into my pumpkin bread during a ceremonial dinner honoring Chancellor Nancy Cantor of Syracuse University who is leaving us. I am one of the hundreds of faculty who love her. I’m sorry she’s departing. And I sat there at Table 18 with my mangled bridge and thought, “how hard it is to be human, fully fully human, comprehensive, engaged in community, caring about those who do not have our advantages.” That’s what I thought while holding my teeth. And then I quietly left. 

 

  

After Walking Alone in New York with a Guide Dog for the First Time, We Rode Home

Corky and I rode home on the train, headed for Syracuse, then Ithaca. After three days in the city my dog seemed larger. She sat with her head on my knee and stared at me. Blind people know when their dogs are staring—it feels like visual cinnamon—a thing both soft and memorable. We sat a long time like that in a rocking railway car—the two of us taking in each other’s growth. We’d had a superb journey. 

 

I’d seen Art Blakey. Corky had seen three super sized rats under the fountain at the Plaza Hotel. I’d seen—no, felt, how it really was to take the subway without a human partner—she saw the lightning of underground trains and didn’t flinch. And so we really were larger, together. It’s this largeness that makes a guide dog team—invisible, rich, made all the richer by experience—like love itself. And like survival. I saw that if you survive the unknown without bitterness you grow. You grow when your name has taken on new progressive meanings. This is why tribal people have always had spirit journeys for their young people. Corky and I had gone into the woods and come had home again with stronger identities. I’d followed my dog; had stopped when she told me to; and she’d trusted me to make the right directional choices. There are two streets for guide dogs and their partners—the visible one, the one with the traffic—then there’s the hidden one, the one seen only by dog and man—the road of moonbeams and faith. “Jesus,” I thought. “No wonder we feel accomplished. We’ve just walked all over New York on a net of moonbeams.”

 

Bad Day for the Blind

Baltimore, Maryland (November 6, 2013): The National Federation of the Blind, the oldest and largest nationwide organization of blind people, today expressed severe disappointment in the Department of Transportation (DOT) for its final rule purporting to extend Air Carrier Access Act requirements to airline Web sites and automated kiosks. The long-awaited rule, released November 4 on DOT’s Web site, gives air carriers an overly generous two years to make select portions of their online services accessible to blind and otherwise disabled customers, allows three years for carriers to make their Web sites compliant, and grants carriers and airports a lavish ten years to make only a quarter of their fleet of kiosks accessible. The rule intends to update the law and improve the travel experience of disabled passengers, but it is far too weak to achieve this goal.

Dr. Marc Maurer, president of the National Federation of the Blind, said: “The Department of Transportation’s final rule on airline Web sites and kiosks falls profoundly short of its objective. Technology offers an opportunity for a mainstream, expedited experience for all travelers, but for far too long, blind people have been needlessly relegated to lengthy fare searches over the phone, higher rates for flights, and segregation in long check-in lines because airlines have failed to embrace readily available accessibility solutions for their Web sites and kiosks. After years of anticipation, we expected the rule released November 4 to be significantly stronger. Instead, the rule sets an appalling time frame of an entire decade for airlines to make only a portion of their kiosks accessible, allowing ten more years of discrimination and ten more years of missed opportunities for innovators. Access delayed is access denied, so we strongly urge the Department of Transportation to amend the rule to be consistent with the department’s original commitment to ensure equal access for disabled travelers.”

Art Blakey and the Guide Dog

 

In the 1970’s when I was in college in provincial Geneva, New York, I felt myself to be too blind to go alone to New York City. I wanted so much to visit CBGB and Max’s Kansas City—to hear Lou Reed and Patti Smith; to attend poetry readings on the lower east side at St. Mark’s Place. But in those days I didn’t know how to go. And suddenly in 1994 there we were—guide dog Corky and I just noodling along, talking with almost anyone. 

 

We went to Bradley’s, now gone, a great little jazz bar on University Place just opposite the old offices of the Village Voice. I listened to John Hicks at the piano. I shook hands with Art Blakey. I discussed the work of Larry Rivers with the bar tender. I was having spontaneous conversation. Stan Getz said:  “as far as playing jazz, no other art form, other than conversation, can give the satisfaction of spontaneous interaction.” And that was the thing: we were taking jazz steps. 

 

“What’s your guide dog’s name?” people would ask at street corners. “Jazz,” I said. 

 

 

  


Tell Your Senator You Support the Convention on the Rights of Persons with Disabilities

NATIONAL CALL-IN FOR THE CRPD

WE NEED YOUR HELP!

The opposition is flooding Senate offices with calls against the treaty!

The U.S. Senate Committee on Foreign Relations will be holding a hearing TOMORROW on the Convention on the Rights of Persons with Disabilities (CRPD). We need you to call your Senators TODAY to show your support!

The CRPD provides a vital framework for creating legislation and policies around the world that embrace the rights and dignity of all people with disabilities. The Americans with Disabilities Act (ADA) was the model for the CRPD. On December 4, 2012 the Senate considered the ratification of the CRPD but fell only 5 votes short of the super-majority vote required. 

We need you to take action with these 3 easy steps:

Call each of your Senators at (202) 224-3121 TODAY. When you are transfered to your Senator, just give your name, zip code, and say “I support the Convention on the Rights of Persons with Disabilities.” That’s it!Email your Senators by clicking here. Go to the hearing tomorrow if you can!

Our target Senators are Robert Menendez (D-NJ) and Bob Corker (R-TN), but we need EVERY U.S. Senator to be contacted and to know that the disability community is leading the movement for U.S. ratification of this international disability treaty. We particularly need you to contact your Senators BEFORE the hearing TOMORROW. 

Forward this message onto your lists of friends and colleagues so they can join us in sending a message to the Foreign Relations Committee that we support the CRPD! Thank you for your help!

To find out more, please go to http://www.disabilitytreaty.org.