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Assistant Head Wrapper

Editor’s Note: This piece was awarded an honorable mention in the Pulse writing contest, “On Being Different.”

I’m an antique. I started working as a junior copywriter at Time in 1972. I was a token Jew, a token hippie and a token “female professional” among hordes of perky typists and preppy males. The executives wore Cartier cufflinks engraved with initials and numbers, like GSW III or CMJ IV. My bosses were George the Third and Christopher the Fourth, while I was J, the only.

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The Quest of a Lifetime

Editor’s Note: This piece was awarded an honorable mention in the Pulse writing contest, “On Being Different.”

From a young age, we’re encouraged to stand out—to be who we truly are and to be proud of that person. We strive to understand both our strengths and our weaknesses. In doing so, we’re driven to move forward, knowing we’re doing our best. But sometimes we get stuck in a rut and can’t find our way. That’s where my story begins.

In the mid-Seventies, at age sixteen or seventeen, I was diagnosed with a genetic disorder called Klinefelter syndrome. There were no computers or internet, which meant no easy access to medical knowledge. Living in rural Northern Michigan complicated matters further. Our small town had no medical specialists, and medical journals

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Under the Microscope

I was walking into my kitchen with an armful of groceries when my cell phone rang. It took a second to register the caller’s name: Dr. James. The surgeon I’d met two weeks earlier.

I wasn’t expecting this call. My biopsy had occurred only a few days ago, and I’d been told that, because of the Christmas holiday, the results would be delayed.

Why is she calling?

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None of My Mom Friends Are Dying

Editor’s Note: This piece was awarded an honorable mention in the Pulse writing contest, “On Being Different.”

I’m squarely in the middle of my friends, in terms of when we became “mom friends.” However, one aspect sets me apart: None of my mom friends are dying.

None had excruciating pain during pregnancy, unrelenting constipation or unexplained blood in their stool. None went septic five days postpartum or were ultimately diagnosed with stage IV colon cancer with liver, lung and peritoneal metastases. None are parenting a two-year-old, knowing that they might not see him turn three.

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A Duplexity of Maladies

Editor’s Note: This piece was a finalist in the Pulse writing contest, “On Being Different.”

I have a body besieged by two chronic illnesses, namely multiple sclerosis (MS) and bipolar disorder. My health profile has been described as “abnormal,” but I’ve always resisted that term in favor of “atypical,” for my poor health renders me unusual but not inhuman.

Still, the truth is that I am essentially and profoundly sick. My imbalanced body frequently aches, hurts and falls, my labile mind races or crawls. While medications can ameliorate my symptoms, they cannot cure my illnesses.

My body betrayed me when I was on the cusp of adulthood.

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The Genesis of Forgetfulness: A Poet’s Journey

“The poet’s job is to translate unspeakable things on to the page…” – Roger Robinson

In the beginning, the Lebanese civil war barely seeped through the ceiling of our living room. It didn’t shatter windows or infiltrate through cracked walls. It became a slow fixture at our dinner table, nibbled on Mama’s delicately wrapped grape leaves, inhaled Father’s unfiltered cigarettes, listened to my older brother practice scale after scale on the upright piano and sat on the Persian carpet with my younger brother to rearrange his Matchbox cars. In our Armenian family of five, the war felt mute—a sixth character without words, an unobtrusive intruder who was given permanent residency.

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Lessons From the Heart

This can’t be happening to me, I thought. Yet here I was, on a gurney being wheeled into a cath lab for an angioplasty and possible stent.

This can’t be happening, I thought again.

But it was.

A little background: I have always thought of myself as healthy.

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My Castle

Moving to an independent-living facility requires finding a balance between controlling the things that you can, and accepting help, or changes, with the things that you can’t. It also means striking a balance between being part of a more regimented community and being part of the outside world.

I’m nearly seventy, which is young for this move. But my hearing and balance are not what they were. I’ve had no family for twenty years, having outlived parents, husband and brother. Friends who have helped me in the past are aging into their own disabilities. My apartment of twenty years needed renovations that needed me gone. The timing felt right.

But my transition comes with extra challenges, because I’m congenitally and totally blind.

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Saved

It was a spring afternoon in Kottayam, Kerala, India, and I was a seventeen-year-old student, doing my final two years of high school at a local college, as could be done in India. I was the student-body president, with just two months to go until graduation.

And in another five minutes, I was going to end my life.

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Due Date

It’s the bright orange color that catches my eye. Nestled in a box under my home office desk, alongside unused breast pads and pumping supplies left over from the birth of my first daughter.

My first, because there should have been a second. A girl.

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What Remains From the Pediatric Ward

I wake up in a hospital isolation room, where everything smells weird. It’s 1967 in Galway City, Ireland, and I’m four years old.

The worst smell is the antiseptic—a word I don’t know yet. The second smell is the crayons and newssheet coloring books on the nightstand. Christmas is gone, so how can these be for me?

The family lore would say that I spent nearly seven weeks in that hospital. That’s forty-nine days or 1,176 hours’ worth of temperature checks, dosages, white-coated doctors.

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Into the Unknown

On March 17, 2015, I was diagnosed with early-stage breast cancer. Initially it was thought that I would need only a lumpectomy and radiation, but the biopsy changed everything.

The pathology report said that the tumor was HER2-positive and estrogen/progesterone positive. The HER2 protein makes the cancer more aggressive, so I would need, in addition to surgery and radiation, eighteen weeks of standard chemotherapy, a year of two other infused drugs and a hormone-blocking oral drug.

Still, the cancer was stage 1a with a decent prognosis, according to my oncologist, who said, “The good news here is that we have treatments for every part of your cancer. You are lucky.”

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