Monthly Archives: September 2011

After the News

The tea bag sinks to the bottom of the cup.
I wait a few minutes; watch as the water turns dark.
I sip the tea. It works no magic.

I go outside; watch the sun set.
As it sinks into the Pacific,
Cirrus clouds—high overhead—turn pink.

In Sarajevo, Mufid’s mother
Marinated pink rose petals in large glass jars of sugar water.
She set the jars on the window sill early in the morning—
They made the most of ordinary light.

In Osaka, sakura yuki. Cherry blossom snow.
That’s what I called it.
Walking along the river in the wind and rain—
Cherry blossoms.

At Kibbutz Usha, I killed a snake
On the stoop out back behind the kitchen.
In the middle of peeling and chopping two hundred seventy onions,
My eyes tear-blind and mad with stinging,
I smashed in its skull with a stone.

Night after night…

I think about the former Yugoslavia.
On the spot where Gavrilo Princip took aim and shot,
The impression of a pair of pointy-toed shoes
Is sunk in the sidewalk. Preserved in bronze.
I stood in them. They were just my size.

So many spots where I stood in Kobe
Waiting for all those job interviews, the trains at Sannomiya.
Waiting and watching as Black Vans rolled.

Impossible to not think about the Holy Land.
Tonight another bombing of another bus in Jerusalem…

Somewhere down the street a car backfires.
It startles me. I turn around.

At the beginning of the twenty-first century
the thing that still amazes me
is how easily I startle.

© 2011 Peggy Landsman

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The Size of the World

As a small child, my mother lay in the long Scottish night dreaming of places worlds away—Rio, San Francisco, Zanzibar.
Now, she lies on a hospital bed, her limbs like sticks, her shanks encased in a diaper which she plucks with her fingers. “I don’t want this,” she whispers, but it is too much to expect nurses to clean her when there are so many to tend.
Her name is Harriet Flora Craig Stark Stannard—so much for such a little person. She no longer answers to Mrs. Stannard or Mother, or to the nurses when they call her Harriet, for she has always gone by Flora. I explain this when I can, but there is always someone new who doesn’t understand and writes on her chart: No Response.
Even I must call her Flora, as if she were my child. Then she stares at me with blue bright eyes. I remember to put on her glasses, but most of the time, they lie in the drawer by the side of the bed. Without them, she sees only shapes.
One day, she asks for her coat. “It’s time to go,” she says. I say nothing. A day later, she asks again “Where’s my coat?” I promise to bring it.
On my next visit, I walk past the nurses’ station with her winter coat over my arm. They follow me with their eyes as I pass. When I enter the room and put on her glasses, Mother sees the coat. She lifts the covers with a trembling hand until she can raise her leg. Both hang in the air as she tries to gather strength.
I do not help her. I do not speak. She lowers her leg and the covers. I hang the coat in the empty closet. “When you’re ready, it’ll be here,” I say. She never mentions it again.
As the days pass, I move closer to her body when I talk to her. I stroke her hand and brush her hair. I sing, just for her. This woman, who traveled to all the places of her childhood dreams now lives in a world smaller than a baby’s in a crib.

© 2011 Aline Soules

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hangover and sleeping pills

hangover

it’s not the

lack of belief

that has

caused me to

crucify myself

on a

thousand

crowded

nights

 

it’s the sun,

how it rises

every morning,

 

reminding me

that I have

empires to

build and

faces to

remember, so

 

remember me please

 

not this

version

of me,

in cobwebs,

breaking

the dawn

of a

still

unfinished

plan

 

© 2011 David LaBounty

 

 

 

sleeping pills

can I meditate on this,

 

this beginning

like a deep

dark lake

 

can I wade

out to my

chest and

take that

one sudden

step where

the bottom

falls away

 

and god, you

are my god

 

will you let

me fall

so quickly

under, grabbing

me by the

paleness of my

ankle and

keep me down

 

until it’s over

 

or until

another

moon

falls again

 

© 2011 David LaBounty

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20 Miles Home

I glance down at running, 5:13 AM. My mother and I have already run 5 miles. She is ahead of me, and in the harsh glare of the streetlight I see her sinewy arms and bobbing head as she bounces along effortlessly. We are training for a marathon, my first and her second and today we have 15 more miles to go. I call out to her in a grunt. She turns, jumping about in place as I lunge into the bushes and throw up.
“Again?!!!” She yells.
I am used to throwing up. I have in the past years perfected the art of making myself throw up. But today I do not welcome it. Today, more than ever, I hate what I’ve done to myself.
When I was a child and my mother read to me, I wouldn’t look at the pages of the book. I gazed at her; her pale skin, contrasted her deep black hair, she was breathtaking. I loved her because she was so beautiful. But when I was 13, I began to love her less because of her beauty. It seemed only to taunt me, remind me of what I wasn’t or at least what I believed I wasn’t.
One day, at the gym I saw the outline of her stomach muscles bulging as she did bicep curls. Even the muscles in her forearms were defined. She resembled a dinosaur; lean, cold, hard. I hated her and as obsessed with my wanting to be like her. It was my jealousy that wouldn’t let me love her.
Everything she did infuriated me. Her cackling laughter. The tap of her teeth against her fork as she ate her egg-white omelet. Her constant vacuuming, sweeping. Her rigid and controlling behavior, especially around food. She made her food separate from the family’s: salad without dressing, bagel without butter, oatmeal without cream. If she wasn’t going to eat anything with fat, I would beat her at her own game. I would eat less of everything. My journal from those years consist of food entries: “ December 18th: ½ C fat free cottage cheese, 15 carrots sticks, 1 T balsamic vinegar, 1 apple slice.” The more I hated her, the less I ate. A torture precisely for her. And yet, she hardly noticed. She was happy as always, her cheerfulness fraudulent. Her smile was like touched-up photo, covering up what was most imperfect in our lives. She refused to acknowledge anything was wrong. Her denial fueled my obsession.
I often began my runs at dinnertime so that I could avoid eating dinner. I slipped out of the house before my mom had a chance to question my intentions. I ran for about 30 minutes and began to feel the dizzying sensation in my head I had grown accustomed to. A direct result of either not eating or throwing up; I heard my heart as if it were outside my body, like the noise of cars swooshing by. The throbbing grew heavier. Then, all sound would cease. I fainted. Sometimes it only lasted a moment; sometimes I would wake up on the ground. I imagined my mother finding me like this, if not unconscious, then dead. I hoped she would know it was her fault.
My mother and I continued to run throughout these years, though we hardly ever ran together. My anger towards her isolated us. She didn’t know how to help me and remained untouchable, indifferent.
By the time I finished my freshman year of college, my eating disorder took over all that I did. The dean informed me I could not return unless I saw a psychologist. I made a commitment to get better and entered my first stage of recovery.
Four years after this initial therapy, I had regained a sense of myself and my mental and physical heath returned to well state. In a moment of hope, I suggested to my mom that we train and run a marathon together. My doctors approved though my mom was apprehensive.
For the next few months, we trained but I automatically threw up whatever I drank anything during a run. Most days, I battled through it and kept running. But on this particular day, after throwing up three times, I had no battle left in me.

I call out to my mother.
This time, she comes to me, pulls me to her. And for the first time in years, I don’t cringe with her embrace. I let her hold me, press my face into her chest and hear our labored breathing settle in a synchronized calm. Her sweat drips onto my cheek and it rolls into my mouth. We stay like this for a long time. I keep my eyes closed and feel her arms around me. In these moments, she is no longer the cold, hard dinosaur, but instead, my mother: human, safe.
After some time, she begins to run and I follow. Slowing her pace, she stays in front of me. Suddenly, she speaks.
“Lani, repeat after me. ‘I deserve to run.’”
I decide to trust her. “I deserve to run.”
“ I deserve to be healthy.”
“I deserve to be healthy.”
“I deserve food. I deserve water. “
Whenever I am too tired to speak, I repeat the phrase in my mind. My mother does not stop affirming the acknowledgement I have craved for so long. We finish running the 20 miles home, and with each step I forgive my mother. And in many ways, myself.
I do not throw up again.

 

© 2011 Lani Scozzari

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Reluctant Dragon

She wanted her first car
to be a red dragon,
to breathe fire, rev,
lift up off the dealer’s
parking lot and fly.
The seats, hand-sewn
red leather; headlamps,
glowing a high-intensity
Halogen; tires, clawed
in a deep biting tread.
Her father buys her
a Beetle instead,
a pastel Easter egg
on a roller skate, a small
scoop of vanilla ice milk
on sugar cookie wheels,
no nuts, no cherry.
The engine, a knockoff
of her Granny’s old
Singer sewing machine,
stitches down Main Street
as she pumps the foot
pedal trying to zip unseen
past the guys on the corner.
She parks the guttered
firedrake behind the house
as the fire in its belly,
and hers, slowly fizzles.

© 2011 Patricia Budd

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Mother at the Piano

Her piano, tall, dark, no-nonsense – upright like an unmarried uncle, followed us from house to house.  After a bed and chair, it was the next piece of furniture my father bought her.

All music seemed hers. “I’m Called Little Buttercup” flowed into “Just a Song at Twilight,” then “Welcome Sweet Springtime,” words set to a Chopin prelude. Sometimes, at parties, she’d improvise under a beery tenor as Nels Nelson tried to sing “Jeg Elsker Dig” like Jussi Bjørling.

Sometimes, when she was sad, she’d play “I’ll Take You Home Again Kathleen” to bring forth a shadow sadness from me. Yes. I did not want my mother to be sad. Even more, I was afraid of her longing for Sweden.

When my father died, she moved 600 miles back to an apartment in a town where there were still Swedes. What happened to the piano?  Was it given away, sold for a hundred bucks, or just left behind to find its own way? I was in California.  My brother did this arranging.

When she had to leave that apartment for the old people’s home. I was the son to fly back. She was 80 and filled with grief at the necessity of even more change.  She’ll last maybe a year, I thought to myself, but she lived to be almost a 100.

There was a piano, lonely, yes, like an unmarried uncle, in the lounge of Friendship House. But it would smile as towards the end she’d have an attendant push her wheelchair up to its keys, lean forward, and watch her fingers bring forth, accurate as a music box, “Edelweiss” from The Sound of Music.

One of the other women, in the thin exasperations of old age, said to me, “We wish she’d play something else once in awhile,” but she played – by heavens, she played.


© 2011 Nils Peterson

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The Ordination of Woman

As a young woman I went to church.
I would wiggle in the pew, only still
when the men and women sang hymns
and the organ swelled. We all prayed
the Lord’s Prayer, dipped bread, the Body,
into the red wine, the Blood. But I longed

to dance down the aisle. Stretch my long
legs from beneath the wooden church
pews, touch the curves of my new body
while the devout stayed bowed and still,
to wave my hands, shout songs of praise
to God that weren’t found in my hymnal,

my mouth a round O as I sang hymns
of devotion. I really wanted to belong
there, for my palms pressed in prayer
to become a steeple high atop the church’s
sanctuary, asking forgiveness. But still,
I went to bed each night rubbing my body

until I quaked, whispering psalms to nobody
until morning. Thought, I’m unworthy of Him,
as I watched good Christian women, so still
while good mister preacher shouted long
sermons every Sunday morning in church.
As I watched the Christian women pray

I imagined tiny gazelles—running prey—
swerving down the curves of their bodies
from neck to waist to hip. The church
frowned on lust, but I wrote love hymns
to womanhood, hummed them all night long
until my love of God and women distilled

into one lion’s roar, my song to Sharon, still
but loud: let me kiss her, I would pray
with the kisses of her mouth, lips oblong
and blood red. I wished to taste the body
of this divinity. Wash her feet with hymns
woven from my mane, build her a church

where the quick stillness of sloped bodies
was the only prayer, the words of every hymn
sang out lust and longing: a woman’s church.

© 2011 Laura E. Davis

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My Mother

It’s December 26th. I’m sitting on the right side of my mother’s hospital bed, away from the tangle of machines on the bed’s left— the cardiac monitor and respirator, the suction tubes and IV. The cardiac monitor blinks red and green. The respirator makes dying bird sounds. The room smells, of lotion and disinfectant, dried blood and urine. A portable dialysis machine is just outside.
I hold my mother’s swollen, bruised hand. I squeeze gently and hope for a response that doesn’t come. Her hand feels dead to me, the jaundiced skin tightly stretched and cool. The remnants of her white pearl nail polish are leftovers from a time when she read fantasy novels by the dozen, played with her gray tabby cat, did crossword puzzles and went to the North Berkeley Senior Center.
My black fleece tights and charcoal sweater are too warm for the overheated room. Without central heating, my Oakland apartment was frigidly cold last night. When I dressed this morning, I felt I’d never be warm. I shivered then. I’m sweating now. I’m trembling now. Letting go of my mother’s hand, I remove the vermilion-framed glasses that match my hair and wipe my damp eyes.
I look at my mother, a too small figure under institutional sheets. Just 5 feet tall, her once round body is shrunken and diminished. Her dentures were removed prior to the surgery. She wore them until the last minute. Does she know she’s toothless? She seems unaware. Except for the time her Haldol wore off, when with flailing arms she tried to sit up, her frantic eyes despairing and questioning, a disturbing horrible episode I witnessed alone.
This is the Medical ICU at Kaiser Hospital, in San Francisco. My mother was transferred here four days ago, after three weeks in Surgical Intensive Care. She didn’t recover from her bypass surgery, her heart isn’t working properly. She needs a respirator, but not the high-tech interventions of the Surgical ICU with its bustling, rushing, strained staff.
Here the pace is slower and the staff calmer, the atmosphere is one of hopeless resignation. The rooms circle the nurses’ station. The patients are extremely sick. Most of them are dying. Each patient has their own R.N. The doctors’ visits are occasional. Relatives visit day and night, with few restrictions.
Through the open doorway I see my mother’s nurse approaching. She’s wearing purple and pink flowered scrubs. In the Surgical ICU the nurses’ scrubs were plain blue. We exchange greetings. She checks my mother’s machines.
“Any change?” I ask.
She shrugs, then smiles thinly and shakes her head no.
“I have the shampoo,” I tell her.
During yesterday’s visit, the nurse told me to get a special shampoo for my mother’s long, matted, gray-blond hair. Even at 82, Mom dyed her hair blonde. She liked to be stylish, and wore long black skirts with colorful tunics. She favored short boots and dangling arty earrings. This morning, before coming to the hospital, I went to three beauty supply stores before I located one in south Berkeley with Klorane Extra Gentle Dry Shampoo, at $19.00 for 3 ounces.
“It’s good stuff. Wait ‘til you see,” the nurse tells me. Then she suggests I leave. “So I can tend to your mother, clean her up.”
“I’ll be back in an hour,” I say.
“Don’t rush,” she says.

I take an empty elevator to the 1st floor cafeteria. When my mother transferred from the Oakland Kaiser, before her surgery, I was impressed with the varied menu. I was happy with the vegetarian selections. But since the surgery, I don’t care about the food. I don’t care about a lot of things.
I order a grilled black bean burger and go to an isolated corner booth. A group of nurses at a large center table are laughing and talking. I feel pissed and resentful. I want the world to stop and comfort me.
I’ve been a social worker for twenty-five years. I understand grief. I studied Kubler-Ross in grad school. I wrote a paper on Death and Dying. I know my anger isn’t rational. Understanding doesn’t help.
I keep telling myself Mom will recover. That she’ll breathe on her own and her cardiac function will improve. Was her color just a little better this morning? Did she open her eyes for a second? I search my brain for signs she’s getting well, but come up cold.
My burger is bland and dry. I’ve had too many hospital lunches since my mother’s surgery, usually alone, but sometimes with one or both of my brothers. My father died at 54, twenty-seven years ago. There’s just the three of us. The last time we were here together, we had a painful conversation.
“It could be worse,” I said.
“How?” my brother, the gynecologist, asked. He lives in wealthy Hillsborough. He’s been a Kaiser doctor his entire career and has a reputation here.
I didn’t know how. It’s like I was channeling my mother, looking for something positive to say.
“What if she doesn’t get better and has to stay on the respirator?” my other brother, the lawyer-musician asked. He lives in liberal Berkeley.
“She wouldn’t want that,” I said.
We all agreed. We decided together. When the time came, if the time ever came…
We were hopeful then. I’m hopeful now. She has to get better. She’s my mother.

After lunch, I leave the cafeteria through the side exit to Geary Blvd. I have nowhere to go and nothing to do. A couple of weeks ago, I walked all the way to Ocean Beach. I had to take a bus back to the hospital. Today, I don’t have the energy for a long walk, but head west anyway.
The sunlight is dazzling, the cloudless sky winter blue. Geary is bustling with cheerful post-Christmas shoppers.
Step by step, I trod along. I flash to an image of the jail where I work, to the mental health inmates in their small outdoor courtyard, walking in circles and going nowhere.
Four teenage Latina girls, walking arm-in-arm, giggle as they bump into me. I smell heavy vanilla-musk perfume. They’re all wearing lavender hoodies. I envy their youthful good looks and exuberance. They’re at the plush stage of life. When they walk into the Cost-Plus World Market, I aimlessly follow.
The store is crowded. The air smells stale. I get jostled and pushed. Sale items are prominently displayed, with huge after-Christmas discounts. People seem frantic to buy.
“Look at these bangles. Do you think they’re real bone?” a middle-aged blond asks her balding, bearded companion.
“It says they’re from Africa on the tag,” he tells her.
I wander the store, feeling superior, like I’m above the crowd. Then I remember my mother and realize if she wasn’t sick, we’d likely be shopping ourselves, taking advantage of the sales. I wonder if we’ll ever go shopping again. I already miss her so much.
“Yeah, all the Christmas ornaments are half-off,” a sales clerk reassures three elderly women with full shopping baskets. The clerk has blotchy, sallow skin and keeps yawning.
I close my eyes to shut out the world and see orange-sparked blackness. I think of the Amtrak tickets for my mother and me, sitting on my desk at home. We’d planned a February trip to celebrate her birthday, taking the California Zephyr to Chicago, then the Lakeshore Limited to Penn Station in New York. I was going to sight-see while Mom visited her younger sister in New Jersey.
We both knew she was too sick, weak and debilitated from a September bout of meningitis, but couldn’t admit it. Or maybe it was just me who couldn’t. I bought the tickets in October, like having them would ensure her recovery. “You’ll be well enough by then,” I kept telling her.
My mother loved our “trips” during the ten years she lived in the Bay area. She was seventy-two when she left the San Fernando Valley after forty years to be near her children. Because I lived just south of Napa, she settled there.
At least twice a year we’d driven to L.A. to visit relatives. Mom loved any kind of traveling. We usually stopped at the Harris Ranch Restaurant in Coalinga. Because I’m vegan, she always worried I wasn’t getting enough protein.
Mom never minded the long, tedious ride down Hwy 5, the flat brown dryness, the cattle stench, the glaring sun. I did all the driving, first in my white Toyota and then in the green New Beetle Mom encouraged me to buy. We both loved that car.
Although my mother usually avoided emotional conversations, something about being in a car in the middle of nowhere made her open up.
“I worry about you. Get out and make friends. Not spend all your time with an old lady. I won’t be around forever,” she’d say.
“I’m fine,” I always answered.
Our last trip, just six months ago, was hard. Mom was testy with our relatives, she seemed fragile and exhausted. She wanted to be home. On the drive back, she kept falling asleep, sitting up in the passenger seat, with her head back and her mouth open. I kept checking to see if she was breathing. I was afraid then. I’m more afraid now.
I feel so lost and alone. Like my life is crumbling. For the first time, I regret not staying married and having children. Maybe my mother was right to worry about me.
A loudspeaker-voice announcing a reduction on Cost-Plus holiday fruitcakes brings me out of my reverie. Although it doesn’t seem possible the store is even more crowded. People are grabbing Christmas ornaments. The combined smells of perfume, popcorn, chocolate, espresso, sweat and pomade are nauseating.
“Excuse me, I’m feeling sick,” I keep apologizing as I rush toward the exit. Nervous sweat trickles from my armpits.
I’m almost at the front door when I see the mask on the wall. I stop cold, drawn to its enigmatic face. There’s no tag that says where it’s from or how much it costs. The hollowed-out wood is painted pale tan and peach. The carved eyebrows and pursed lips are black. My heart tightens. I swallow hard. It’s a woman’s face, with a long narrow nose and deep-set eyes.
Although it seems impossible, the mask looks like my mother. The resemblance is uncanny. I grab it from the wall and rush to the long check-out line. I have to buy it. I need the mask to save my mother. “Please god,” I mumble aloud. “If I buy this mask, let her recover.” I know I’m being irrational, but don’t care.
After an endless wait, I reach the cashier, who calls the store manager for the price. The manager takes the mask and leaves. The cashier touches up her lipstick. I’m impatient. So are the grumbling people behind me.
Finally the manager returns. “It’s $85.00, not a sale item,” he says. He wipes sweat from his forehead with the back of his hand.
I don’t care about the cost. “I want it,” I say.
I remember being with my mother in Sonoma, in a shop with Zuni artifacts. Like it was calling me, I was drawn to a soapstone bear. I would’ve paid any price for it. I still keep the bear on my coffee table. When I feel stressed, I stroke it for good luck.
I feel the same way about this mask. Finding a mask with my mother’s face has to mean something.

By the time I get back to the hospital there’s been a shift change. My mother’s evening nurse is a pleasant middle-aged woman who works weekends and holidays.

“How’s my mother?” I ask the nurse.

“Done some shopping?” she asks, looking at the Cost-Plus bag I’m carrying.

“I guess my mother’s the same then?”

“She’s resting quietly,” the nurse says.

It’s a practiced response which means nothing. I’m so angry and frustrated, I feel like shaking her to get at the truth. My ears pound with suppressed rage.

But it’s not until I’m in my mother’s room that I feel like crying. I look at her lying there, with her head supported by two pillows. Her eyelids flutter lightly. She’s heavily sedated. And her hair…Her hair is in a ponytail on top of her head, with a pink ribbon tied in a bow.

I’m sorry I bought the goddamn shampoo. Better off with tangled hair, better off with no hair, than this. My god, how she’d hate having her hair done up like an infant, or a senile, ridiculous old lady.

I go to my mother and remove the ribbon, then smooth her hair back on the pillow. A lone tear trickles from her right eye. I’m shaking, trying not to cry.

When I get home that evening, I hang the mask on the living room wall. It still looks like my mother. I trace the mask’s features with my fingertips and kiss its lips.

It’s December 29th. Like everyday this week, I’m at the hospital with my mother. My brothers have visited in the past two days, but now I’m alone. We’re all discouraged and exhausted. My one brother and his wife have a music gig New Year’s Eve. They should be excited about it, but instead are stressed. My other brother has his wife and three children to consider. I have nothing else going on.
The past two years have been hard for my mother, having to admit she couldn’t handle living alone, leaving Napa for Berkeley, moving in with my brother. I moved to Oakland then, but there was no place for her in my one-bedroom apartment.
Every Saturday, I’d take her out for lunch and grocery shopping. Her health kept getting worse, especially after the meningitis. She had trouble breathing and walking. We didn’t talk about her deteriorating condition. It was too hard.
I’m sitting by my mother’s bed when the resident enters the room. She introduces herself and asks if I’m the daughter. We go into the corridor to talk.
“When will my mother get off the respirator?” I ask.
The resident shakes her head. Her dark Asian eyes look sad. “She won’t,” she says.
“Not ever?” I ask. Like I’m the one with heart problems, my chest is tight with pain.
“Her diaphragm is paralyzed. I’m sorry. I thought you knew.” Her face twists with embarrassment.
My mind fills with questions I’m too upset to ask. How do you know her diaphragm is paralyzed? How long have you known? Wasn’t anyone going to tell us? But I can barely breathe, never mind talk. And in the end, what does it matter?
The resident tries to comfort me. “Can I do anything for you?” she asks. “Call someone?”
“No,” I tell her.
I go to my mother’s bedside. I’ve never felt so empty and alone, so emotionally dead. I can’t believe this is happening.
I need my mother to get better. She can’t stay on the respirator. She can’t live without it. I can’t let her go.
I leave to call my brothers.
On December 30th, we have a family meeting with my mother’s doctor—me, my two brothers and my Berkeley sister-in-law. The doctor confirms what the resident said. My mother’s diaphragm is paralyzed. One side was paralyzed before surgery, the other during the surgery, from the cold metal instruments. It’s a complication that happens sometimes. If there’s talk about how long the staff has known, I don’t hear it.
We agree on taking Mom off life support. We know it’s what she’d want. Still, it’s impossibly hard.
We decide there’s no use waiting. We don’t want to prolong her suffering, or ours. At first, I don’t think I can stand to watch her die. But in the end, I know I have to.
The doctor leaves. We wait to be called into my mother’s room. They’ve removed the respirator, but have her on the cardiac machine. She’s sedated. We stand around her bed, holding hands, crying, hearing Mom’s laborious breath.
It’s the most intense, overwhelming, excruciating experience of my life. More than an hour goes by. My doctor brother makes an awkward joke about how long it’s taking. We laugh hysterically. We watch the beats of her heart register on the cardiac machine and obsessively watch the numbers. Her heart doesn’t want to give up.
My mother’s doctor returns. He asks if we want to speed the process up. He doesn’t say her death. We leave briefly. When we return, Mom is quieter. A friend of my doctor brother, a nursing supervisor, comes into the room. She turns off the cardiac monitor, so we won’t watch the numbers.
“You can talk to her,” she says. “Tell her it’s okay to go.”
I look at my mother, really look at her. She’s trapped in a body no longer hers, hanging on and suffering. I have to let her leave. I think what I can’t verbalize. It’s okay Mom. Just let go. I want you to. We all want what’s best for you.
Then I say my final words to my mother. “We’re all with you. We love you.”
My mother’s eyes open for a brief moment. I see her looking at us. Then she dies.
We leave the hospital. I can’t stop crying. We’re all crying, my brothers, my sister-in-law and me. I spend some time at my brother’s house in Berkeley. Then I go home.
I feel afraid as I park in the carport. With weighted legs, I climb the steps to the front entrance. My hand shakes as I unlock my door.
My apartment is cold. It feels empty. I feel empty. I get undressed and open a bottle of Zinfandel. I sit on the living room couch. I don’t listen to music, or watch TV. I sip wine and cry.
The Zuni bear sits on my coffee table. My mother’s mask is on the wall. But I’m still alone.

© 2011 Myra Sherman

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MY MOTHER’S KEEPER (With Introduction by Stacy Furrer)

Dear Readers,

First, I must confess.  David Ulin is my hero.  He helped me make sense of my own story in the MFA program at UCR Palm Desert.  When I was mired in the painful details, he bade me, “Dig deeper. Break this open and find the truth.” When I wanted to be pulled out of the muck, he showed me that the way out was down, so one reason I asked him to write for our September issue was to see how he did it himself.

His story shows how tiny details reveal more than what the eye sees:  they lay bare raw emotion, as in his description of the “fright-mask smiles” of the cheery nurses, or when he steps across the sidewalk to take his mother’s hand.  He embeds the past in a chemotherapy visit, framing it with his initial aversion to watching the needle puncture his mother’s skin and his final decision to watch the nurse pull the needle out, accepting more than just that little spot of blood.

This is not simply a story about a chemotherapy treatment but about the universal nature of the relationship between mothers and their children. I took from it the realization that counting things in hospital rooms must be a natural reaction to trauma–I’ve done it myself.  I hope that others connect with David’s piece and take away a sense of connectedness, too.

Thanks for reading,

Stacy Furrer

The chemotherapy rooms at Memorial Sloan-Kettering’s Breast Cancer Center are small. Maybe eight by ten, maybe less. They have recessed Formica counters, white kitchen-style cabinets, and the kind of neon lights I associate with hospitals or principals’ offices, places where what awaits you is a needle’s prick or a reprimand. Speakers hidden in the ceiling pipe in new age chimes and synthesizers, while sliding doors of blond wood and translucent Plexiglas separate you from the world outside. There are nine rooms, arranged around an interior courtyard; in the center, a skylight glows with rays of dirty New York sunshine, but everything else is white-glove-test clean. Cheery nurses and volunteers in lab coats flash fright-mask smiles, asking in low tones how you’re feeling as they hand out cups of liquid or set up IVs. While they work, I check out the women in the other treatment rooms; some, like the startled looking blonde in the baseball hat and jeans, seem so young I wonder who she’s visiting, until I see an assistant help her to a seat and start probing the top of her hand for a vein.
Any other day, I’d probably fixate on that woman, obsess about the horror of someone so close to my age having to confront her own mortality, and wonder what must be going through her mind. But this Tuesday morning, my attention flickers past her and returns to the room in front of me, where I am sitting with my mother, who is about to undergo chemotherapy for the eighth and final time. Six months ago, a surgeon excised a 1.6 centimeter malignant tumor from her right breast, then removed some lymph glands from under her arm to make sure the cancer hadn’t spread. When all this is finished, after chemo and a six week course of daily radiation, she will have a 92% chance of complete recovery, but for the moment, the only thing she’s concerned with is that her white blood cell count might be too low. During our last visit, on Friday, she was sent home without treatment for precisely that reason, and it’s been a long weekend of worrying, of sullen silences and little girl pouts, of raging against the body my mother feels has betrayed her, and the physicians who can’t work fast enough to make her sickness go away.
Chemotherapy is an inexact science, and it often seems as if the doctors are fighting one poison with another, as if the only way to kill the unhealthy cells is to kill the healthy ones, as well. So I breathe a silent sigh of relief when a lab assistant comes in and tells us that everything can go ahead as planned. As the nurse hangs the drip bag and prepares the solution, my mother puts a pillow over her hand so I won’t have to look at the place where the IV enters her flesh. “I know how squeamish you are about needles,” she says, and flashes me a hollow smile. It’s a small human moment amidst the tension, and I find myself touched by her intention, by her attempt to mother me even now. Still, it doesn’t stop me from thinking about how much this place is like the suicide parlor in the movie Soylent Green, so quiet and polite and euphemistic, with everybody smiling at you as if by sheer indirection you could somehow forget the reason you’re here.

To watch one of your parents get sick is an unsettling experience. More unsettling even than the first time you realized they didn’t have all the answers, that the things that infuriate you about them are probably the very things that infuriated them about their parents, all those unresolved issues passed on and on. The illness of a parent makes you think about their basic human frailty, makes you consider the inevitability of them not being around. At the same time, things get complicated, since, disease or no disease, you’re still who you are, still burdened with a lifetime’s worth of emotional baggage, with that peculiar parent/child dichotomy of resentment and love.
When it comes to my mother and me, that dichotomy is especially strong. Over the years, we’ve had a tricky relationship, by turns affectionate and contentious, defined equally by hope and disappointment on both sides. From the time I was nine or ten until I went away to college, we fought like sparring partners, spending weeks at a time passing hardly a civil word. Even today, it’s hard to think back on those years without remembering all the things we could not be for each other; just this morning, in fact, on our way into the hospital, my mother mentions that she wished she’d raised my brother and me to be more dutiful, to give up little pieces of our lives for hers.
“What do you mean?” I ask, hackles rising. “I’m here, aren’t I?”
“For now. But you live so far away.”
I stare into her face, try to read the set of her jaw. This has been a running controversy ever since I gave up New York for Los Angeles, but cancer has magnified her emotions, made her feel more alone.
“Listen,” I say. “Don’t you get tired of this? I was never going to move in next door.”
She looks up, eyes wide, irises a washed-out brown like the yolks of runny eggs. The Cancer Center doorway is a looming shadow a few feet ahead of us; I can feel its pull. Stop, I say to myself, don’t pick a fight, and I recall how easy it is for me to upset her, how I can push her buttons as easily as she can push mine. I take a deep breath, study the worry lines around her eyes. Not now, I think again, then step across the sidewalk to take her hand.

An hour and a half later, my mother is receiving treatment, and we are making small talk, as I think about what almost happened on the street. In another time and place, I would have never walked away from that argument, but one thing I have learned is that cancer has its own geography, a shadow landscape that seems to exist a step or two from normal life. In it, my relationship with my mother has been turned upside down; since her diagnosis, I have become my own version of the dutiful son she so badly desires, visiting New York three times in six months to be with her and my father as they try to navigate this brave new world. I, too, am testing the territory, constantly unsure of how I should behave.
In fact, my mother’s cancer has cast our entire family into suspension, as if the tumor has infiltrated each of us, as if there were some strange, collective component to the disease. When I see the hollows take shape across her bony face, the way the chemo drugs weaken her body and soak her with perspiration, I am struck by the sense that, no matter what happens, we’ve come to an entirely new phase in our lives. It’s not the first time I’ve thought about this; the possibility has been in my mind ever since a winter afternoon two or three years ago, when I saw my mother slip on a patch of ice and nearly fall. Before she went down, I reached out and grabbed her, and as my hand closed around the thin cord of her upper arm, I realized how small she was, how she seemed to me lighter than air. All of a sudden, I had a vision of her as an old lady, bones brittle, birdlike, carefully negotiating these very streets. And in that moment, I could imagine what it might be like to help her, as her frailty continued to emerge.
Back then, of course, all this seemed like a marker, a whisper of a future that, I felt secure, was decades down the line. A couple of years later, however, that future — or a temporary version of it — has arrived. It’s not a development I’m particularly comfortable with, but things could be worse. During the last few months, two friends have buried parents, and my wife has had a similar experience to mine with her own father, who’s been fighting cancer since 1991. It’s an inevitable process, I suppose; both my parents went through it also, my father with his mother, who died of breast cancer when she was two years older than my mother is now, and my mother with her father, whose lingering death of Altzeimer’s sucked all the energy out of his wife and children, leaving his family a desiccated shell. But I thought I’d have a few more years before anything like this happened, and that, when it did, I’d somehow feel more prepared.

In the chemo room, the drip bag has run out of solution, and the nurse comes in to disconnect the IV. “Don’t look,” my mother says, as she moves the pillow, but I’ve decided to face it, whatever it is. The nurse peels off the adhesive tape, then gently eases the needle from where it is lodged beneath my mother’s skin. My mother winces, and a spot of blood bubbles up, but we are done.
Outside, we walk a block or two along Third Avenue. Traffic snarls at intersections, and businessmen brush past on their way to lunch. It’s a crisp fall day, and a cool breeze lacerates my brow. But my mother is sweating, poison rippling through her system like a storm.
“How’re you doing?” I ask. Before we left the Cancer Center, I called my father at his office; he will meet us at home, with champagne waiting, to celebrate the chemo’s end.
“I’m okay,” my mother tells me. “But maybe we should find a cab.”
“Sure,” I say, and raise my arm. Taxis jockey for position up and down the avenue, and within seconds, one screeches to a stop. My mother steps off the curb, her face all red, her back wet, and her hair beginning to mat against her scalp. I watch her for a moment, thinking that, soon, we’ll return to our lives.
Then I reach out, put my arm around her, and lead her to the waiting car.

© 2011 David L. Ulin
A previous version appeared as “Cancer’s Lessons”, in the Los Angeles Times, Volume CXV, Number 280, September 8, 1996.

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