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Where She Will Be

Francie Camper ~

City snow blankets my little mother in her hospital
bed in her bedroom, no wonder she is confused,
pointing to things in the air, on the ceiling that only
she can see. She might be hailing a cab. She raises
her head to tell me, Four members of the Isenberg
family came to visit and one was Mima Ettel,
who is already buried in the plot and she doesn’t
seem to know this. A land of the living and a land
of the dead, why should she have to remember
the difference? We paid a thousand dollars to move
her grandfather’s monument to make room for her.

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The Look on Your Face

Priscilla Mainardi ~

Your skin pale with worry,
your mouth a straight line,
the fear in your eyes–
all this told me,
more than the nausea,
more than the fact that I couldn’t move my head,
that something was really wrong.

You thought I wouldn’t see.

I looked up at the ceiling,
at its pattern of dots,
white, and brighter white,
that could mean anything, or nothing,

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The Caregiver’s Mantra

Patricia Williams ~

If one more person tells me to be sure to take care of myself, I’m going to bury my face in a pillow and scream.

“Go for a walk, take a vacation,” they advise. I know they’re trying to help, but really? Giving me one more thing to do? Oh well, they’re just doing the best they can.

I moved my folks across the country, from Florida to Washington State, and into an apartment near me so that I could care for them in what seemed to be their final months. My brother, who’d been looking after them, was leaving to get married, and we didn’t think they were safe on their own.

They’d always been fiercely independent, but

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Simple Acts

Dianne Avey ~

One night on my nursing shift in the cardiac intensive-care unit, I received a new patient from the operating room: an eighty-eight-year-old woman who had suffered a major heart attack and had just undergone emergency coronary-artery bypass surgery.

Her bed was wheeled into the room along with the usual accoutrements: six different IV drips, a ventilator, an aortic balloon pump and various other lines and monitoring devices. Her name, I saw on the chart, was Mrs. Green.

The young surgeon took me aside.

“I don’t care what it takes, just keep her alive for twenty-four hours,” he told me, clearly more worried about his surgical-outcome stats than he was about Mrs. Green’s welfare. The hospital and insurers kept

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Standing Up by Speaking Up

My parents immigrated to the U.S. from Korea when I was two, in 1972. We were lucky we left when we did, or my father, a pro-democracy professor at Korea University during Park Chung-Hee’s regime, might have been jailed. We were also lucky my mother was a pharmacist, as the U.S. was accepting pharmacists and nurses then. We moved to Seattle and made our home there.
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An Act of Love

For sixty-seven years, my dad was my best friend. We enjoyed walking and talking, taking long drives while licking ice cream cones, traveling, and just sitting in companionable silence.

We were best friends, but we always respected each other’s physical privacy. All of this changed when I became Dad’s caregiver.

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One Afternoon at Teatime

Marilyn Hammick

Arthur stops close to where we sit waiting
for the person you call the activities lady
to serve us drinks and biscuits.
He moves his wheelchair with slippered feet,
so we become another group.
You introduce me, This is my sister,
I nod to Arthur and watch his mouth form words
that seem reluctant to reach me, hang
in the air unsteady, diminished.

He continues to speak, I continue to nod,
I think he’s asking about my name,
you seem to understand, or do you guess?
I’m trying to work out if there’s a knack
I’ve yet to grasp, a way to hear
the hush and lisp of

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A 3:00 a.m. Phone Call

 
When the phone rang at 3:00 a.m., as I reached out my hand to answer it I knew the call was bringing bad news. On the other end of the line, I heard my dad’s croaky, Parkinsonian voice stammer,”Rozzie, I’m so cold. Come here and help me; I can’t reach the blanket to cover myself.” It seemed like forever before he was able to squeeze out the additional information that he’d called the front desk at the assisted-care facility where he lived, but Jose, the night attendant, had said he was alone and couldn’t leave the desk, even for a few minutes. 
I told my dad I’d take care of the problem, dialed the front desk number, and listened to Jose explain that the

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Homecoming

Ronna L. Edelstein

For years, and especially as he entered his nineties, my father kept begging me not to “dump” him into a nursing home. He had seen too many of his cronies abandoned in this way by family members; his visits with these friends left him feeling depressed and hopeless for days. I assured Dad that I’d never put him in a facility.

It was an easy promise to make. I didn’t want him in a One Flew Over the Cuckoo’s Nest setting with a Nurse Ratched supervising his care. I didn’t want him waking up at night disoriented and lonely. Because he was inching closer to death, the greatest unknown, I didn’t want a facility, with all of its unknowns, to

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My Father’s Girl

Maureen Hirthler

I’m walking very slowly with my dad down the produce aisle at the local supermarket, past the colorful waxed apples, Mexican mangoes and Rainier cherries, and imagining my life’s blood trickling onto the floor from an invisible wound.

As I pass by the misting system spraying the bins of green, red, yellow and orange peppers, past the lady reaching for carrots, past the stock guy balancing the heirloom tomatoes into a precarious stack, I want to scream. The sense of loss is overpowering.

But no one notices as I inwardly watch my life’s blood–my father, age eighty-six–flow away, here in the grocery store.

I feel as if we’ve walked these aisles together forever. When I was a child, my

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(Not So) Golden Years

Madge Kaplan

When I read news articles about caring for elderly parents at a distance, I sometimes shake my head. There’s a tendency to put the best spin on the experience: as long as you contact the right people, get the right information and treat the ups and downs as just part of life’s challenges, you’ll be fine. You can do this!

I find myself wondering when the author last talked to a caregiver at her wits’ end–emotions and finances drained, logistics spiraling out of control.

I was a long-distance caregiver for twelve years. I believe it’s best to resist a formulaic approach in favor of one informed by the details–and always, always, humbled by the truth.

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Concierge Care

Deborah Pierce

I am a family physician. Like most of my colleagues, though, I must sometimes step out of the comfort of my clinical role to take on the role of patient or family caregiver.

Generally, these trips to the other side of the exam table inspire a fair amount of anxiety.

During visits to the doctor, I find myself noticing many details and comparing the quality of care to that in my own practice. I worry about how the doctor will relate to me–will I be viewed as a knowledgeable colleague, or as someone who knows relatively little? Will my background be treated with respect? Will my needs as a patient or caregiver be acknowledged? The uncertainty eases only when the physician wins my

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