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Stories

Overkill

Daniel Lee

Primum non nocere. First, do no harm.

I learned that in the first year of medical school. “Nonmaleficence” is the fancy name given to this sentiment, and it’s one of the four pillars of modern bioethics. In real life, it’s an impossible standard: We harm patients all the time. But the spirit behind the principle is what matters. Do the least possible harm to patients as they go through the medical system. Do only what is necessary. Act only when the benefits clearly outweigh the costs.

As a third-year medical student on rotation in the intensive-care unit (ICU), I admitted David, an elderly man transferred from another hospital because a severe lung infection was making it hard for him to breathe.

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Tales Out of School

David Power

I am a professor of family medicine at the University of Minnesota Medical School. During their third and fourth years, students must complete a four-week clerkship in family medicine. The clerkship includes a “significant-event reflection” project, in which students discuss patient encounters that they’ve found especially meaningful.

Over nearly a decade as a facilitator for these groups, I have heard many powerful and emotional stories. I’ve often felt deeply moved–and admiring of the students for their honesty, courage and humanity. Here are three of many whose stories I carry with me.

“Sure, I’ll go first!” said Rob. A fourth-year student, he was about to enter a radiology residency. Rob had a bright, open face and quick smile, and knowing that family medicine wasn’t his chosen specialty made me appreciate his enthusiasm all the more.

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Never Say Die

Christine Todd

In November of my intern year, I had trouble finding the sun. It was dark when I woke up for work, and it was dark when work was done and I headed back home. I’d picked up the service on the cancer ward from an intern named Bob, and Bob had left me six handwritten pages on the subject of Jim Franklin.

And this was the deal: Jim Franklin, thirty-seven years old, had been living on the cancer ward for the last three months. He had a two-foot-high stack of records, and the pity and admiration of nearly every nurse, tech and doctor in the hospital. He’d been diagnosed with Hodgkin’s lymphoma four years earlier, treated with chemotherapy and thought to be cured. A year ago his cancer had recurred, and he’d been failing therapy in what could only be called a spectacular manner ever since.

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Selfie

Melanie Di Stante

In 2000, my husband Brian was diagnosed with Stage IIIB Hodgkin lymphoma, which has since become a prominent part of our lives. My children and I belong to Gilda’s Club, a cancer support community, and recently we were asked to help record a promotional video to be featured at a fundraising gala for the local chapter and on the club’s website.

I’m not a “spotlight” kind of girl, and I don’t feel drawn to video cameras or speeches, but I’ve been going to two Gilda’s Club programs–a caregiver-support group, and a writing group–for nearly five years. Everyone is nurturing, supportive and so nice. My son Marco and daughter Gabriella also attend a group, where they do projects to help build resilience for kids impacted by cancer. It’s priceless, and it’s free.

If this is something I can do to give back, I thought, I’ll do it. My kids were on board as well.

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A Mother’s Son

Hugh Silk

“Why do you want to go into family medicine?” my internal-medicine preceptor asked.

It was an innocent enough question. I’d known from day one of medical school what I wanted to do, so I answered with confidence, and perhaps a bit of a chip on my shoulder.

“I love being with people and getting to know them,” I said. “I’ve always been this way, so it makes sense that’s what I would do for my career. I’m looking forward to having the long-term relationships and seeing where they go.”

A raised eyebrow, followed by his knowing Irish brogue: “I applaud that. My own father was a GP in Ireland. But I’m afraid you won’t find much of that in one month on the wards. This will be a chance, however, to learn your medicine well.”

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A Conversation About Race, Fear and Connection

Paul Gross

In the wake of recent events, many speak about the need for conversations about race. In our country, the implications of race are a moral issue, a humanitarian issue, a justice issue and, yes, a medical issue. (One need only examine how racial categorization affects rates of death.) But what would this conversation about race look like?

Today, Pulse’s editor provides one offering. In August, we’ll invite all Pulse readers to join in with their stories, when Race will be the theme of More Voices.

I grew up in Stuyvesant Town, a middle-class housing development just north of Fourteenth Street on the east side of Manhattan. Built after World War II, Stuyvesant Town was a leafy and desirable place to live. There was a long waiting list to get in, and priority was given to World War II veterans, like my father.

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Killer Shrimp Ceviche

Kristin Hirni

It’s October, and I’m a second-year medical student. My best friend Carly and I have just finished a backpacking trip through South America. We fly out tomorrow from Lima, Peru, and we have just one thing left to do: eat shrimp ceviche, the classic South American dish of raw seafood marinated in lime or lemon juice, oil and spices.

We wander along the busy streets until we find the restaurant our hostel’s desk clerk recommended. It’s a small, dingy joint that doesn’t look up to the current health code, but I don’t give that another thought once a giant bowl of amazing shrimp ceviche is placed in front of me.

It’s incredibly delicious, and we quickly demolish it.

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Blindsided

Alice Y. Kim

When Teresa showed up forty-five minutes late for her appointment, I sighed. I knew this would disrupt our clinic’s afternoon schedule.

That was nothing unusual, though. The clinic treats large numbers of patients who are undocumented, homeless and uninsured, and many must walk or take public transportation to get here. After seven weeks on rotation here as a third-year medical student, I knew that appointment times were flexible.

As I read Teresa’s notes and recent lab results, the nurse came in.

“Teresa’s blood pressure is 210/122,” she told Dr. Fuentes, the attending physician.

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Happy Feet

D. Micah Milgraum

It’s a typical chaotic day on the hospital’s hematology and oncology floor. I’m sitting in a side room with one of my fellow medical students, doing paperwork and making follow-up calls for our medical team.

That’s when the music starts. The sounds of two guitars, a tambourine and a few maracas drift down the hallway. I can’t make out how many people are singing, but the happy voices and the song’s upbeat tempo make me curious: I never thought I’d hear this type of music on the “cancer floor.”

As I look up in surprise, Kevin, our team’s intern, appears in the doorway.

He catches my eye, and after a moment, we both start bobbing our heads to the beat. He makes swaying motions, as if he wants to dance.

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Showing Up

Sarah Bigham

Years ago, as I left my college dorm room, the posters caught my eye. Plastered everywhere, they announced a bone-marrow drive led by a fellow student in search of a match for his brother, diagnosed with cancer.

A confirmed needlephobe, I’d recently fled a Red Cross blood drive at the mere thought of the tourniquet. Registering as a bone-marrow donor seemed like a terrible idea–but the sibling connection grabbed me and wouldn’t let go. The eldest of four, I pictured my sisters and brother at home, two states away. If any of them had developed this terrible illness, I knew that I, too, would implore my classmates to be tested. So, with several friends, I made the trek across campus to register and have my blood drawn.

I hope someone here is a match, I thought, looking around at the crowd.

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Pain

Ronna Edelstein

When my friend Madeline turned seventy, she celebrated in a big way: She walked a half-marathon; she hosted a cabaret for family and friends at which she sang and told stories; she traveled to China. Now, six years later, this dynamic woman has become a virtual prisoner in her apartment. She has undergone back surgery, suffered a nearly fatal intestinal infection and, after a fall, had bolts and screws placed in her hip. Her voice, which once broadcast her energy and joie de vivre, has dwindled to a whisper.

The thread that links all of these bodily assaults is pain. Chronic, intense pain has drained away my friend’s energy and quality of life. No doctor has definitively diagnosed the source of her pain–or been able to find an antidote.

I feel a special sympathy for Madeline because, like her, I live a life in which pain plays a constant role.

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Chemo Brain

Rick Monteith

One weekend about nine-and-a-half years ago, I flew from Minneapolis, where I live, to Atlanta for a publishing conference. A colleague and I were to make a presentation to the vice-president of one of our major customers.

For a couple of weeks I’d been plagued by a sore throat, but I’d written it off as allergies or a virus. When I tried to begin the presentation, though, all that came out was a squeak. The VP was very sympathetic, and fortunately my colleague was able to handle the meeting.

I flew home that afternoon. The next morning, I saw my primary-care physician, who referred me to a radiologist for a CT scan that very day.

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