“‘O ka mele” by Julia McDonald
Her childhood was infused with Hawaiian-Polynesian music and dance, taught to her father by his mother. Today, this poemee is the Director of a PhD program in Biomedical and Translational Sciences. She has used HeLa cells for decades. Her life’s work is to connect the unbelievable discoveries of molecularly focused pre-clinical research directly to the patient experience of treatment.
“I think we’ve lost sight of the connection to patients,” she says. She learned this lesson firsthand when her father died. “There’s just a lack of humanity in truth and treatment by the medical industry,” she remembered, grief etched in her face. “No information, no permission…”
“Faith is my foundation,” she says, “and my opposition to rage is fun stuff, creative things, the legacy from my father. I sing the way my dad taught me.”
Julia McDonald, Listener Poet
Listener Poet Session
January 2025
‘O ka mele
By Julia McDonald, Listener Poet
What is Spirit if not the
eternal vibration of song?
Music echoing through generations,
like shifting chords on a ukulele,
each progression a history poured
from vessel to living vessel,
songs and prayers to unseen
descendants, each note
scented smoke rising
from a swinging thurible: “Those who
live and believe in me will never die…”
Immortality does not mean
unchanging: A population of billions
may all originated from one, yet
each roundish or more cuboidal offspring
is a tune played a million times—
never exactly like your father.
No one sings it exactly like you.
Tiny differences with every passage
forever and exponentially altering
the future.
Her childhood was infused with Hawaiian-Polynesian music and dance, taught to her father by his mother. Today, this poemee is the Director of the PhD program in Biomedical and Translational Sciences. She has used HeLa cells for decades. 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.
Instead of the usual Listener Poet format – listening to one person’s story and responding with a framing narrative and custom poem – 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, referencing the passing of a grandfather and two uncles who did not survive their cancer diagnoses. “There were others too.”
Professionally, Lacks’ story represents for her the need to critically examine our research infrastructure generally. “We need to pay more attention to the sustainability of research,” she explained. “Private companies benefit from publicly-funded research without a requirement to give back to ensure the viability of future research.”
“The fact of my life is a miracle,” she told me. Living with multiple chronic illnesses, this patient spoke to me of her journey with alopecia. Of how, in witnessing her body transformed by the condition, she continues to move at once through grief and reclamation.
“I can’t see a future outside of our relationship,” she tells me, “but I also can’t see a future outside of residency.”
“I always believe, no matter what the doctor says, that I will be cured,” she says as her sister sits next to her.
“I wonder if these medical professionals, in caring for people who face such insurmountable odds, walk around all the time carrying this weight I’m hauling now.”
He had been trying to cope with the grief ever since and was on a quest for soul-searching and meaning-making.
She spoke about the ways this traumatic event shaped who she is today: a person with an “unshakeable peace” born of deep faith,
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.
When we met, she was coming off a stretch of nine 14-hour shifts. She was tired but in good spirits.
She reflected on how her resilience was born from moments of shared mirth amid life's trying chapters.
“Life is complex and dirty, but digging in is important to me,” she said. “Maybe if more of us understood history, we could understand each other better.”
We are expected to research, contribute to scholarship, earn grants – all on our own time.
We are expected to research, contribute to scholarship, earn grants – all on our own time.
Every day, I try to see through the patient lens, and I ask: what can we do to change this broken system?
This past year, he was a right defensive tackle on his school football team, but for the past two and a half years, he’d been caring for his dad, who had cancer.
She was very proud of her daughter and has hopes for “a bright future that’s as pain free as possible”
“I’m trying to focus on doing little things to make people feel better during everything that’s going on in the world,” she told me.
“It’s hard to see others struggle,” she said. “How can I help with their struggle without struggling myself?”
"I'd tell her it's OK to be loud...it's OK to challenge and to bring all of you into these spaces where no one looks like you..."