Beauty Is a Verb

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Beauty Is a Verb Page 15

by Jennifer Bartlett


  hot damn, you are dead

  nuts, right on. That is the essence

  of all of this, isn’t it? So let me tell you—

  they begin as piles of bones,

  the animals in my dreams do.

  Each night, they clink & clonk

  & rise like a time lapse video

  of sky-scraper construction.

  One animal turns into a man

  & the man gives birth

  to a dead dog. In just seconds

  the other animals have rent them apart

  & then, I’m awake. Night-

  swallows knife through the morning

  fog as I stand at the window

  listening to the coyote song.

  My entire body is killing me,

  & I have witnessed my own death

  & lived—I whisper my wagers

  against disaster into the dark air.

  Other Good

  Anesthesia dumb, scalpel-paste

  Rawing my tongue, I found

  Myself star-fished in sky

  Spinning days. I stared into my eyelids’

  Bustling magic, the black

  Of my hands. Oh, how darkness

  Swaggered, dealt fluorescent-blurs

  & the choke of the sea. This is my everything—

  Bright shuddered my cheeks,

  Shadows whistled through their teeth.

  Hallways thrummed & snorted,

  The surgeons in my brain

  Pissed with no hands.

  Each day nurses wore their best

  Tin-foil skirts, buried

  Their caresses in my side

  While pillows whispered

  In spite of your scars you are tickled

  To death of life.

  I couldn’t understand this

  Always being held. Lung-machines

  Sang louder. Wavesong & useless.

  Midnights & swearing. Blue.

  Who prayed for me—my thanks

  But I can’t keep anything down.

  Who knew it had nothing to do

  With the wind by how light

  Flickered with falling knives?

  And No More May I Be

  So this is calamity: calendula-

  oiled hands cupping a mouth

  that sings through the caving

  away thunderlight as the weeks

  keep swinging by—house finches

  shivering groundward in the catgut

  blight. Black boughs absent of any

  living weights. In the rain a man

  ducks into his coat to light a smoke.

  The park bitter with echoing space.

  The park freezing. In the rain a man

  ducks into his coat like the split-

  ribbed chest of a dead horse

  swallowing a wet-cheeked boy.

  Benches slick red. Benches freezing.

  In the rain a soaked man

  watching in the rain. In the rain

  my hands pink hands numb

  in the rain. Beneath the skin

  a humming is. Geese wreathed

  in their own winter-coming

  breath. Skinhulled. Taut

  skin bustling. Bottle caps old

  buttons half-buried hard in the dirt.

  Laurie Clements Lambeth

  RESHAPING THE OUTLINE

  Having dispensed with the neurological tests and their curious implements (pizza wheel for the sole of my foot, reflex hammer, tuning fork), having ceased the comparison of MRI results over ten years, recognizing the progression of my illness, the doctor asked what I’d been writing lately. I said I’d been writing about multiple sclerosis (MS)—about MRIs, areas of damage that turn from brilliant white spots to “black holes,” irreparable. We had counted something like seven new black holes during the exam. I remember the doctor paused and lowered her head in profile, as though laboring to offer wisdom.

  “I think you’re very...intelligent, and very...creative,” she said, turning her face toward me, “but writing about your MS isn’t going to make it better.”

  How does one respond?

  “Oh, I’m perfectly aware of that. I’m under no illusions that anything at all will make me better.” I wanted to tell her that my writing and my disease have existed side by side from the moment I was diagnosed at seventeen, my new physical life giving birth to my life in words.

  Poet Gregory Orr points out that while in English “to bless” is to confer divine benevolence on someone or something, in French the verb blesser means to wound. The two are linked, he suggests, beyond logic. This coincides with my experience; the disease that wounds channels in my brain and spine, that disrupts my ability to feel through skin, that distorts my vision, that tightens some muscles while weakening others, is indeed the blessing-wound that changed my thinking and brought me to poetry.

  My first recognizable MS symptom—although there were others I didn’t yet understand—was a numb left hand, as though plastic wrap surrounded each finger. Over time it rose up my arm, then down my left thigh. The outlines between things blurred. Unable to detect the difference between my skin and fabric, my thumb and a buttonhole, my hair and the elastic I stretched to contain it, I slipped into a dimension where there was little distinction between the outside world and the inner contours of my own body. I had planned to be a cartoonist, so most of my drawing was defined by outlines. And now this shading moved in, this nuance. About six weeks later the numbness subsided, but it left its physical traces that would rise up again, and more importantly, a permanent mark on my consciousness: outlines shifted, faded.

  In the catalog to his 1809 exhibition of paintings in his brother’s sock-shop, on view two hundred years later at the Tate Gallery, William Blake stresses the importance of the outline: “How do we distinguish the oak from the beech, the horse from the ox, but by the bounding outline? How do we distinguish one face or countenance from another, but by the bounding line and its infinite inflexions and movements?” He goes on to warn, “Leave out this line and you leave out life itself; all is chaos again.” Chaos. There is indeed a chaotic quality to a disability that shifts and interrupts, leaves and reenters one’s life in new, surprising ways that at once echo earlier experience and carve new notches into the body.

  Gregory Orr observes, in his essay “Poetry and Survival,” that poetry has the power to take crises—loss, pain, illness, instability—and give them shape. To order the chaos in our lives through language: “Rather than the transcendence and abstraction counseled by philosophy and religion, the personal lyric urges the self to translate its whole being into language where it can dramatize and re-stabilize itself in the patterned language of the poem.” Poetry helped me investigate and reinforce the blur I felt between body and world, and gave me the space to insist upon the bounding line’s fluidity. In metaphor, for instance, I could bypass all that tenor and vehicle business and create images that were simultaneously literal and figurative, hovering somewhere in-between. It was this way that MS entered my poetry—not in subject, but in the ways it altered my perception of my body’s place in the world, as though the outline of what I could call “me” was a broken line, permeable and wavering, and what was inside that perimeter was a shimmering transparency, at once me and not me.

  For eight years I did not write about the disease, aside from one particularly rough poem in my senior year of high school. The subject was too expansive and tentacled, too emotionally unpredictable, too difficult to harness into free verse. Orr’s description of the lyric poem’s role as the provider of order via “patterned language” rang true for me. I needed the cage of a villanelle—so restrictive, in that very few lines can truly further the poem along, and yet so obsessive a form—to house the poem. In fact, even that high school poem was propelled by repetition, what Orr would call “the consoling power of repeated sounds.” After living with MS for eight fairly uneventful years and being woken up one night by something like a seizure, neurons misfiring, arms and le
gs flailing beyond my conscious control, I wrote about the experience in my villanelle “The Shaking.” The poem takes on two possibly melodramatic hazards for poetry: love and sickness. Either could have gone horribly out of control, but the project of formal containment allowed for necessary perspective to tinker, prune, dissect and question, long after the poem was originally published.

  As MS more fully entered my poetry, my experience of disability deepened, or vice-versa. They helped each other along. While I wouldn’t go so far as to say that poetry is therapy, it is a means for me to take something that may not be considered desirable or beautiful (dragging a leg, losing the sense of touch), investigate it, sculpt it and create something outside of my body that is vividly physical, in subject and in form. I am moved to craft different formal responses to each somatic experience. In my first book, the most obvious formal departure can be found in the prose fragments addressing memory loss, low vision, ocular pain and incontinence. These subjects are difficult to handle in poetry without risking melodrama or perceptions of shock or self-pity, so it felt deeply satisfying to tighten prose into a voice that is at once stark and lyrical, then to juxtapose those fragments against more lyrically expansive poems.

  Two poems included in this book, near companions if not for the time elapsed between each poem’s composition, address the difficulty of communicating impaired sensation: “Hypoesthesia” and “Dysaesthesia.” These narrative lyrics attempt to describe lack of sensation (numbness), or the feeling of pain without source, dysaesthesia: “wrong feeling.” In each, there is a sense of the possibility of formal connection that is not actualized. This is not how their shapes were planned; I write far more organically than that. But the feeling in each is a sense of hesitancy, a disruption in fluidity, reflective of the inability to share physical experience, even at our most intimate or domestic moments. In “Hypoesthesia” this is actualized in certain long lines and sentences disrupted mid-stream and continuing mid-line in the next stanza, as though they were dropped straight down. In “Dysaesthesia” the slanted gutter down the middle performs the same task, except this poem is addressing pain, so its language and form are more halting, frantic. Their brokenness exists far more on the surface than in “Hypoesthesia,” where the speaker finds some pleasure and gratitude in shifting her sensibilities.

  In either case, fitting form to the poem, lending it shape and order, granted me a tremendous sense of power—not to change my physical condition at all (why would I want to change?), but to relay its essence and create a thing of beauty that speaks simultaneously about the individual and a more universal sense of alienation, all of us trapped in chaotic bodies, the potential of unrest ever-present in every body, which I hope, if the poem’s shaped well and the reader willing to follow, will foster empathy, not sympathy, for the blessing-wound.

  Hypoesthesia

  Hypoesthesia: numbness, the absence of sensation. Absence often feels like something.

  —INSIDE MS

  All those years

  I made love to a man without thinking

  how little his body had to do with me

  —MARK DOTY

  For now (who knows how long now is) his touch is nothing but warmth and trace

  trailing his hand up my thigh and around my stomach. I feel a little

  something crystallize after each pass of his hand, then it’s dust.

  Whoever thought sex could be so literally senseless? The first time (my first time)

  I cried a little because I did not want it, but gave to make my boyfriend stop asking.

  That was a different kind of senselessness.

  I wanted to cry this time, too, another first since the new flare-up broke:

  feet, knee, thigh, stomach, hip, hollow of the back, neither my body nor my skin

  but a loose-fitting carapace, bubble, prosthetic even.

  Are you touching me,

  I thought to ask, but instead watched as he kissed each part and caressed

  and did what we do when I feel right. I didn’t say I can’t feel that,

  but let his hands and mouth travel.

  For the first time in my life I let go of my body a while and looked down

  with fascination at the man I love in the process of loving me—:

  the way the window’s meager light managed

  to illuminate his nails with each finger’s lengthening, how it raised

  his tendons (like spines) before his knuckles into glow. Stunning

  to see his eyebrows and lashes crush, devoted,

  with each kiss planted along my belly, to feel only the cool afterward.

  Strange that now would be the time I comprehend our otherness, these bodies

  wanting more: luminous, impossible whole.

  The Shaking

  I know I scared you last night by shaking,

  the only time you were forced to share

  a dream that shook me to waking.

  Your left hand pressed upon my aching

  thigh as it kicked and flailed; how compare

  your strength to synapse whims, wild shaking?

  You know my nervous system could be taking

  over any time; disease is unfair.

  Remember: it seems bad when you’re waking.

  Many times I’ve trembled when you’re making

  love to me, my round shoulders open, bare,

  but never have I broken into such shaking,

  when my body shows us our lives breaking

  apart. Still, you hold me. Your kind is rare,

  who know (or pretend) dreams seem worse upon waking.

  Surprising you stayed: here you are, forsaking

  quiet nights for me. Will you be there

  when it worsens, my gait palsied with shaking?

  Who could be strong enough to hold back its waking?

  Seizure, or Seduction of Persephone

  I convulsed so hard I broke

  open, broke the earth,

  erupted and pushed out

  a narcissus by the roots.

  It doesn’t matter where

  the flower broke on my body,

  through the skin, a pimple,

  my head, or the belly.

  I could not tell you.

  What I can say is this:

  my limbs flailed and seized

  in the bed. I watched, both

  inside and outside, skin

  the sheet of a Richter scale,

  delicate needles charting

  the shifting of earth’s plates,

  limbs all speaking

  unknown tongues, plotting

  maps and pathways deep

  into the body. As he held

  me still in that bed,

  how was I to discern

  if he then learned

  his way through the flesh

  into my need, or if

  he chose this blue moment

  to come out, rupture

  the field from within

  my own unruly body?

  Seduction: nothing but

  a man’s hand depressing

  and a flower jolting out.

  Some void here between my hips.

  Dysaesthesia

  When I tell Ian my hands are on fire,

  when I first pull them from the warm bed

  and release them to the air’s sting,

  begin the morning routine, measure

  dog food, twist open ridged lids of jars

  upon which I scratch my palms,

  when I lift and unscrew the milk bottle,

  fingers sparking without cause,

  when I pour coffee, rubbing the hands

  on any rough surface because they smolder,

  when I tell him I watched myself drop

  the spoon as though in a movie, not me

  that wincing, palms turned up and why,

  their inner tremble radiating holding nothing,

  I remember James Dean

  in the police department, so
angry

  he pummels a desk, and I said last week

  when we watched it again, wait for it:

  he broke his hand there in the take—that’s real pain,

  and I read my hand like his, roiling under skin

  while he clutches his wrist in close-up,

  when I hear myself gasp and can’t help it,

  just the shock, I can say spark or burn

  or electric, and Ian asks me if I mean

  the hands are hot as in temperature.

  Not hot, just on fire. Flameless, sourceless—

  how else to say it but fire, this mistake

  creeping between spine and skin? How to discern

  this pain, these hands, who operates them?

  Brian Teare

  LYING MEDITATION

  I’m not a practicing Buddhist, but the longer I live with two chronic diseases, the more often I turn and return to Buddhist theology and poetry as ways of helping me to conceptualize and accept the unpredictable. I can’t know when my body will be disabled or when my body will be able. Gouty rheumatoid arthritis means daily low-level pain in my feet and knees, but monthly there are days of significantly limited movement and yearly I experience crippling bouts of swelling that last anywhere from two to ten days. Celiac disease and a severe soy allergy mean that even a minor deviation from my increasingly narrow diet—due to poorly labeled packaging, “hidden” ingredients, cross-contamination, misinformed wait staff or my own ignorance—gives an entire day or more over to symptoms. Thus, while I wouldn’t feel comfortable claiming a “disability” in the strictest sense of the term, the epithet “temporarily able-bodied” favored by some disability activists makes a lot of sense to me. “[B]revity is natural / it makes sense,” writes Laozi in Thomas Meyer’s translation of the Dao De Jing,

 

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