Hi-Tech/Lo-Tech by John Graham-Pole

Holly helps me befriend “high-tech,” perhaps for the first time—I can clearly picture those frozen embryonic cells as babes-to-be. And I’m transported back to hard-scrabble Glasgow, Scotland. To Annie, a fourteen-year-old lassie from the Gorbals, Glasgow’s biggest slum, who’d just given birth, on New Year’s Eve, 1973, to micro-preemie twins (father unknown). Far from being yearned for, these new arrivals were decidedly unwelcome—at least to their great-grandmother, already raising three other children, alongside Annie, in a single tenement room with a multi-family outdoor privy. 

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Writing as Self-Care for Nurses by Linda Kobert

Mayhew and McArthur focus mainly on the value to patients and families of having nurses “courageously” see their patients’ experiences and document those observations with compassion. In these narrative records, which clearly move beyond the confines of formal healthcare documentation, it seems important to also recognize that, in formulating this narrative for others, the nurse also benefits on a personal level. 

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Is There Anything Good About Parkinson's? Dr. Ronald Lands Talks About A Poem That Explores That Question

Adler’s poem illustrates with elegance what I experienced personally and what my wise patient tried to teach me. If there is anything good about Parkinson’s, pulmonary fibrosis or any other chronic, incurable disease, it is the time it gives to remember, to appreciate, to love in spite of a different theology or political leaning and time to prepare for the inevitable appointment that modern medicine might postpone, but never cancel.

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Narrative Secrets: Why Disclosure Day is the Hardest One for Clinicians by Maureen Hirthler

“Disclosure day in the clinic is the hardest,” says Kathryn Cantrell in her essay of the same name. As a child life specialist, her job is to encourage disclosure—the naming of illness and the sharing of that name with loved ones. Yet her own story is suppressed: “My advisor said I shouldn’t disclose—that a hospital won’t hire me if I tell them I had cancer, that I understand the process.” 

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Sick with Desire: A Conversation by Lisa Kerr

In my poem “Borrowed Car,” I suggest that life-threatening illness may transform the body into an unfamiliar vehicle over which a person no longer feels she has ownership or control. This loss of perceived ownership may begin with the naming that comes with diagnosis, an act of labeling that seems a necessary part of the treatment process. However, as Arlene’s Weiner’s speaker demonstrates in “Line of Beauty,” a patient may ultimately resist certain labels and perceptions of her body as a means of reclaiming authority and determining what the literal and metaphorical scars of illness will signify.

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The Paradoxical Role of Paradox by Jeffrey L. Brown, MD

Moral and ethical considerations can greatly increase the complexity of medical decisions. The dilemmas described in Ellen Kolton's essay (“Ethics Consult: To Tell or Not to Tell;” The Intima, Spring 2015) and those that I experienced as a military doctor (“The Moral Matrix of Wartime Medicine;" The Intima, Fall 2015} share a similar frustration – the inability to find “correct” answers for difficult questions. 

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We All Suffer by April Brenneman

In the Intima Fall 2013 edition, Dan Luftig confesses a secret: he wants an anonymous person to have a stroke during his first hospital rotation. In his Field Notes piece: “Paradoxical Wishes,” Luftig describes this furtive hope. It seems a logical way of attaining every ounce of knowledge and skill through first-hand experience. He recognizes his inner quandary as he “hopes” to rid himself of the “hope” that his patients have a specific diagnosis that he, because of his education, suspects they have. He struggles with the disconnect between his wishes as a doctor and his patient’s wish for health. What a strange juxtaposition.

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