Origin Story
When we met, she was in her first year of residency and had just finished an 80-hour work week. “It’s been hard to lean into the excitement,” she said. Growing up in a rural town, adjusting to city life was tough. “I have strong connections to rural communities,” she shared.
To cope with the demands of residency, she ran. “Running helps me reset. I value the brightness and warmth of the sun, but my favorite run is when it’s raining, and the sun is out. It gives me back more than I give.”
When asked why she chose medicine, she said her motivation had changed over time, but she was drawn to the intersection of science and service. Aspiring to be a colorectal surgeon, she liked the physical labor aspect of surgery – a mindset rooted in her upbringing on a farm. “I would choose it again, but think hard about it,” she admitted. “We grew corn and soybeans and raised pigs,” she said. “As a kid, I was always dirty. People are surprised to discover I’m into fashion and art now, but where I come from is the most important part of my life.”
On why she chose colorectal surgery, she explained that the colon is an intimate and essential part of the body that people often ignore due to self-consciousness. “It’s being human at our most vulnerable. Poo is taboo, but everyone does it. It’s natural,” she said. She wanted to help people feel comfortable and transform the shame around colon issues. “I want to talk about things that matter, the things people don’t want to discuss. I want to help them feel okay talking about it.”
D’ete Blackshire, Listener Poet
Stories from Residents and Fellows for the KNN, Vol. 1
May 2024
Crab Shell
By D’ete Blackshire, Listener Poet
As children
we’d played in the mud like pigs.
We didn’t claim manners
but our revelry
and bathed in dank soil
between snort and squeal
to retreat from searching for ways
to reinvent ourselves.
Our impolite bodies belonged
to the Earth.
Now I run through sunbeams and raindrops.
Dragging my shoelaces through the mud
collecting in puddles on sidewalks.
Secretly hoping they ripple through the civility of our self-image.
And when my rubber soles
bounce off the concrete
I draw strength and energy from the alliance.
It’s assurance that
our bodies still belong
to the Earth.
We may try hard to be polite
but we still need to shit to live a healthy life.
After the rain
I inhale the mingled scent of
wet terra and pavement
to humanize my mindset.
I see nature in Us.
But to find us in the world...well
This house of flesh and bone we inhabit
is a crab shell.
Invincible in its shameless vulnerability.
When we are in it
without disguise
perhaps we can arrive
home.
Interspersed with the joys and worries of being a gramma, she recounted her own grandparents – challenges and opportunities of caring for them, grief of losing them, gratitude for being loved by them, and the everyday experiences of now living in their home.
What is pain without a diagnosis? This is what occupied this patient before she even received her breast cancer diagnosis about a year ago.
She told me that she picked her battles more and was trying to be less of a people pleaser.
He ended up talking about his son, who is now his daughter. Another part of his experience of continual growth and soul-opening.
Her values and perspective on life had changed as she considered ways to spend more time with her husband.
“When I see an old dude who’s optimistic, living his life, I always stop to talk to him to try to find out what he has done.”
This nurse was considering leaving a position where she spent many years due to issues she experienced and witnessed at her hospital.
Many of the people he worked with had to develop a new identity in the context of their caregiving responsibilities. “It’s as if they need to become a new variant of themselves.”
“We’re taught to enter a room with a specific goal... with assumptions... with a hypothesis about what may be going on with the patient.”
She believes that most of those who have connected with ACS began with a personal connection, but then, according to her, “you evolve, and you shift.”
With her background in counseling and psychology, she works to bring people together and support patients.
Although at times she becomes discouraged about the inequalities in the world, she is determined to do her part by making sure everyone has access to quality healthcare.
This person radiated gratitude and hope. She shared that she discovered she was expecting a son just before receiving a lung cancer diagnosis at the age of 31.
She had an epiphany as a child — that love could heal the world. Now, as a seasoned physician, there’s still a part of her that believes in the power of love, but not with the same idealism she once held.
He talked about recently speaking with a patient who experiences migraines: she is seeking the truth, he is seeking the truth to find a way to work with her, wanting to give more than a diagnosis and prognosis.
To her, the surgical world has felt like “a wheel that keeps spinning,” a seemingly endless pursuit towards an undefinable goal.
While she kept an open mind throughout medical school, the field of OB/GYN ticked off all the boxes for her.
“I was at a birth recently and thought: This is why they are so afraid of us. They can’t control this” She sat on her couch with a mug of coffee. She is a queer, femme, mother of two who has worked in reproductive health for over two decades.
“The historic traumas of African-American women — all African-Americans — lead us to not be the first people at the doctors, nor the first to get surgery.”
“Sometimes I feel so helpless,” said this resident, reflecting on all of the challenges faced by the young patients and their families whom she served. Over the last several days, she has become increasingly overwhelmed by events in the news and has questioned her ability to make a difference in the world.
“It’s hard to watch the decline and sometimes hard to visit but it weighs on me not to,” she said. Her father had always been an elaborate storyteller and an alive, vibrant man with a big voice.
The Good Listening Project was honored to once again take part in the annual KNN conference in Minneapolis this year. Jenny closed the session by writing this harvest poem that captured the voices and sentiments shared.
After a history of crippling endometriosis, this woman had an arduous, ongoing struggle with her healthcare community for the right to have a hysterectomy. She was finally granted approval at the age of 29. “It had been like pulling teeth, but finally I felt free,” she told me.
Her childhood was infused with Hawaiian-Polynesian music and dance, taught to her father by his mother. Today, her life’s work is to connect the unbelievable discoveries of molecularly focused pre-clinical research directly to the patient experience of treatment.
She is a single mother born to a single mother and had to grow up fast. She is juggling a sticky work situation, her own anxiety and depression, and being away from home and her kids.
I was invited to create a group poem for forty participants at the Arts in Healing luncheon, hosted by the Inova Health Foundation in partnership with the board.
What does it mean for people living with Sickle Cell Disease to be seen, heard, and understood? For this person, it meant finding – and using – her voice to advocate for herself and for others.
“I’ve experienced a lot of big losses,” she said. “I want to be a beacon of hope and light, keeping the flame lit for cancer prevention.”
Professionally, for this person, Henrietta Lacks’ story represents the need to critically examine our research infrastructure.
