She Checked the Organ Donor Box at 16, Now She’s Waiting for Someone Else’s Lungs
I’m Aware That I’m Rare: the phaware® podcast
Episode 594 - Kirsty McGeown
Canadian pulmonary hypertension patient, Kirsty McGeown signed up to be an organ donor as a teenager, believing it was a simple act of kindness. Years later, Kirsty found herself sitting on the opposite side of that decision. Now, she’s focused on reclaiming life’s normal moments, holding onto hope, and dreaming of one day becoming a grandmother.
The Impact of Exercise and Fitness on Improving Patient Outcomes
I’m Aware That I’m Rare: the phaware® podcast
Episode 593 - Lana Melendres-Groves, MD
Pulmonary hypertension patients are often handed powerful medications, but rarely something just as transformative: movement. Dr. Lana Melendres-Groves reveals a shocking truth that fewer than half of PH patients are ever referred to pulmonary rehab, even though research proves it can dramatically improve strength, breathing, and quality of life. This missing prescription may be the one that gives patients their lives back.
Participate in the PHenomenal Hope Run/Walk — New Mexico Saturday, October 17th at 10 AM
A Mom of Three, a Hidden Killer, and the Specialist Who Saved Her
I’m Aware That I’m Rare: the phaware® podcast
Episode 592 - Wendy Mercado
Balancing life as a full-time teacher, wife, and mother of three, PAH patient, Wendy Mercado, put herself last until her body forced her to stop. After years of bouncing between doctors and medications, a PH specialist finally sat down, drew her heart on paper, and said the words Wendy needed to hear: We’re in this together. That moment didn’t just change her treatment plan, it changed her future.
23 Years of Survival and Still Fighting the Darkness No One Sees.
I’m Aware That I’m Rare: the phaware® podcast
Episode 591 - Jenn Lalonde
Surviving a rare disease isn’t always heroic. Sometimes it’s depression, isolation, and wondering if you’re even “sick enough” to deserve the label anymore. Canadian pulmonary hypertension patient, Jenn Lalonde, battles imposter syndrome on her good days and crushing heaviness on the bad ones. Because even when your body stabilizes, your mind doesn’t always follow.
“Get Your Affairs in Order”: She Told Her Doctor She’d Be Back in 20 Years
I’m Aware That I’m Rare: the phaware® podcast
Episode 590 - Lynn Bouseman
In 1994, before there were any FDA approved therapies for pulmonary hypertension, Lynn Bouseman was told to prepare for the end. Her pressures were sky-high. Her heart was failing. A specialist suggested she might only have months to live. Lynn looked him in the eye and said, “No,” she had two small daughters waiting at home. Survival would require one thing above all else: a refusal to surrender.
PH Didn’t Just Change One Life, It Changed an Entire Family
I’m Aware That I’m Rare: the phaware® podcast
Episode 589 - Abby and Ari Borstein
When pulmonary hypertension changed their father, Eric Borstein’s life, sisters Abby and Ari refused to let the disease write the ending. Instead, their family turned heartbreak into hope by creating a community "Where is EB?" 5K dedicated to raising awareness, honoring their dad, and supporting others facing the same rare disease.
What began as one family's response to unimaginable adversity has grown into something much bigger, a movement proving that every step taken can bring hope to someone still searching for answers.
She Didn’t Just Survive Being Rare. She Made Meaning Out of It.
I’m Aware That I’m Rare: the phaware® podcast
Episode 588 - Donna Wallace Harmon
PH patient, Donna Wallace Harmon can’t fly. She lives with limits. She knows tomorrow isn’t guaranteed. But Donna refuses to live waiting for “someday.” Her motto is simple and defiant: Do the best I can when I can, because nobody knows what tomorrow holds.
Pulmonary Hypertension Tried to Shrink Her World. She Made It Bigger.
I'm Aware That I'm Rare: the phaware® podcast
Episode 586 - Sherri Odusanya
Being prescribed oxygen broke PAH patient, Sherri Odusanya, in a way her diagnosis hadn’t. Sleeping beside a roaring machine. Dragging tanks through daily life. Crying in the car after picking up her daughter from school. Then came the real gut punch… doctors warning she might never fly again. For a woman who loved travel and had family across the ocean, it felt like her world was closing in.
The Dream She Lost at 18 and the Child Who Gave It Back
I’m Aware That I’m Rare: the phaware® podcast
Episode 583 - Amanda Chickie
One of the first questions Amanda Chickie asked after her pulmonary hypertension diagnosis wasn’t about life expectancy, it was about motherhood. The answer devastated her. Told that pregnancy was too dangerous, Amanda reflects on what it means to mourn children you’ll never carry, how that grief shaped her mental health, and how hope slowly returned in a form she never expected.
A New Mother’s Greatest Fear: “Am I Going to See My Daughter Grow Up?”
I’m Aware That I’m Rare: the phaware® podcast
Episode 582 - Lisa Harder
When Lisa Harder became a new mom, she never imagined that shortness of breath would lead to a rare, life-altering diagnosis. Lisa shares how uncertainty nearly stole her future and how breakthrough treatment, advocacy, and hope gave it back.
Why a Social Worker Might Be the Most Important Person on a PH Care Team
I’m Aware That I’m Rare: the phaware® podcast
Episode 580 - Evan Holm, LMSW, SWCM
When pulmonary hypertension finally gets a name, fear rushes in fast. Social Worker, Evan Holm, is often the first person patients lean on after their right heart catheterization at University of New Mexico Hospital. As a support group leader for PAH, he is passionate about providing emotional and educational support to patients and their families while assisting them in navigating the healthcare system. His work proves that access, advocacy, and compassion can be just as lifesaving as medication @UNMHSC
Who Cares for the Caregiver When Everyone Else Comes First?
I’m Aware That I’m Rare: the phaware® podcast
Episode 579 - Laura Camponeschi
Behind every pulmonary hypertension patient is someone quietly running on empty. Laura Camponeschi pulls back the curtain on caregiver burnout — the emotional, mental, and physical toll that builds when someone is “always on” and never feels safe stepping away.
Three Generations. One Gene. A Rare Disease She Couldn’t Outrun.
I’m Aware That I’m Rare: the phaware® podcast
Episode 578 - Dawn Ogden
Dawn Ogden has lived her entire adult life under the shadow of pulmonary hypertension. After losing her sister and watching her father battle the disease, Dawn learned it was genetic — and that she carried it. What followed was a lifetime of testing, fear, and impossible choices as she faced the reality that the same gene could shape her children’s futures.
She Went Looking for Answers and Ended Up Building a Support Group
I’m Aware That I’m Rare: the phaware® podcast
Episode 577 - Carla Kinsey
Before Zoom, before Facebook groups, pulmonary hypertension patient, Carla Kinsey, had only a voice on a phone line. That loneliness pushed her to do something terrifying: start a support group herself. What began as a need for connection became a lifeline for countless patients navigating rare disease.
PH Tried to Isolate Her. She Turned Loneliness into a Lifeline for Others
I’m Aware That I’m Rare: the phaware® podcast
Episode 576 - Karen Sawyer
Pulmonary hypertension nearly stole Karen Sawyer’s sense of self. Instead, Karen rebuilt it through advocacy, education, and human connection, proving that no one should face a rare disease alone.
A Silent Blood Clot, a 10-Hour Surgery, and a Second Chance at Life
I’m Aware That I’m Rare: the phaware® podcast
Episode 575 - Carol Stokely
Canadian CTEPH patient, Carol Stokely was healthy, active, and unstoppable, until the day she couldn’t breathe. After months of being told nothing was wrong, she collapsed into ICU with life-threatening clots in her lungs. Hear how a once-in-a-lifetime surgery gave her breath, strength, and life back.
Why “The Walking Guy” Trusts His Therapist as Much as His Cardiologist
I’m Aware That I’m Rare: the phaware® podcast
Episode 573 - Eric Borstein
For PAH patient, Eric Borstein, walking started as a way to survive medication side effects. Now, it has become a way to survive himself. Each step pulling “EB” further from an ICU bed and closer to an identity that isn’t defined by illness. Mental health has reshaped his recovery, and has become one of the lifelines he believes should be prescribed alongside life-saving therapies.
Don’t Let PH Ground You: A Real-World PH Travel Playbook
I’m Aware That I’m Rare: the phaware® podcast
Episode 572 - Nicole Dempsey
For Nicole Dempsey, travel has always meant freedom. After being diagnosed with pulmonary hypertension, that freedom suddenly felt fragile. Nicole shares how she continues to explore the world, raise her family, and find freedom beyond fear, proving that even with a rare disease, life doesn’t have to stop.
He Sent 100 Emails to Save His Wife… Only 3 Doctors Answered
I’m Aware That I’m Rare: the phaware® podcast
Episode 571 - Florin Dumitrescu
From a devastating diagnosis to a lung transplant that changed everything, Florin Dumitrescu shares how mindset, persistence, and community carried his family through their darkest moment and how survival transformed into advocacy for pulmonary hypertension patients across Europe.
She’d Never Been Sick - Until a Rare Disease Hit Like a Brick Wall
I’m Aware That I’m Rare: the phaware® podcast
Episode 570 - Terrie Keplinger
Terri Keplinger went from healthy and unstoppable to fighting for breath after unexplained swelling and a shocking ER visit led to a pulmonary arterial hypertension diagnosis. In this episode, she shares how denial turned into purpose, and how she transformed her fight into advocacy, support, and a mission to help others get diagnosed before it’s too late.