Hosted by Laura Bonnell · 🇺🇸 US · EN · 199 episodes
Established thought leaders with verified media credentials.
Living with cystic fibrosis: the challenges and triumphs along the way. Live-Breathe-Inspire
Laura Bonnell hosts Living With Cystic Fibrosis, a society show with 199 episodes published.
Jon Gay and I had a great time recording this podcast because we not only talked about podcasting, but also reflected on our years in the broadcast business and what people should know before starting a podcast of their
“Take in your final breath before your first new one.” Those were the words Jillian heard before her double lung transplant—words that would mark the end of one life chapter and the beginning of another. Jillian is 34 ye
Chrisy and Dr. Kingzett, two women I met when we were all trying to raise our rare voices a little louder. Christine “Chrisy” Klavitter and Dr. Kristen Kingzett are both rare disease advocates, but more importantly, they
“Behind every breakthrough are countless failures no one ever sees—but that’s exactly what makes progress possible.” Dr. Thomas Kaiser. When I have scientists on the podcast: they’re some of the coolest, smartest, funnie
Living Fully with CF: Christopher Cornejo’s Journey from Diagnosis to Avatar This fast-moving and deeply engaging conversation features Christopher Cornejo, who brings a fresh and powerful voice to the cystic fibrosis co
A mother, advocate and one woman's global fight for access. Beth Vanstone is working to ensure rare disease patients don’t have to wait for the treatments they need to survive. Sometimes the most powerful friendships beg
Bridging Two Countries, One Mission: Cesar and Nora Hernandez Fight for Spanish-Speaking CF Families “When Alex was diagnosed, we felt fear and responsibility. If we had access to information in Spanish, other families s
Finding Strength After Loss: A Conversation with Margarete Cassalina I first met Margarete Cassalina when we were hosted for dinner by Bob Emmelkamp at the North American Cystic Fibrosis Conference (NACFC). We connected
Education, connection, and community are at the heart of our CF community. On Saturday, April 18th from 11:00 a.m. to 1:30 p.m. we gathered at the Next Step Gallery in Ferndale. Set in a bright gallery space surrounded b
“Being a CF aunt has shaped so much of my life. Now I get the opportunity to turn that love and connection into helping even more people at Breathe Strong CF." Julie Dunn Eichenberg didn’t just find the cystic fibrosis c
Men with CF and Infertility: The Science, The Options, The Hope. Pete Proimos is an entrepreneur, a chronic illness advocate, and the founder of the Filotimo Foundation, a nonprofit dedicated to supporting individuals an
Three decades caring for patients with CF, that’s Dr. Alan H. Cohen. His experience continues to shape everything he does today. As a pediatric pulmonologist (board-certified) , he has walked alongside patients through s
I’ve known Julie McCaffrey for years. She lives about 40 minutes from me, in Romeo, Michigan. Julie and her husband, Curtis, are raising four daughters, and their oldest, Jenna—now 20—lives with cystic fibrosis. What sti
“What if a blood draw didn’t have to feel terrifying, Abby Rose is a child life specialist. And if you have never taken advantage of all they have to offer when your child is hospitalized, you’re going to want to connect
Diagnosed with cystic fibrosis at the age of fifty, Sheri Boyd brings a rare and powerful perspective to the CF community, one shaped by decades of undiagnosed illness, years of caregiving, deep resilience, and a strong
“Patients are waiting…” Those simple but profound words from Dr. Steve St. Onge set the tone for this conversation, and for why this work matters so deeply. Science has always fascinated me. I often joke that I’m not sma
"Ever moment, every day is worth celebrating." Somer Love Somer Love has spent her life choosing hope, dreaming big, and showing up fully for each day. Diagnosed with cystic fibrosis at just 11 months old, Somer has grow
When Insurance Gets Between Doctors and Patients Dr. Elizabeth Ames and Dr. Caleb Bupp are deeply committed to their patients. But like so many clinicians today, they’re spending an extraordinary amount of time battling
Innovating Medicine: How Science, Collaboration, and Curiosity Transform Patient Care It is always inspiring to speak with true innovators on this podcast, the people who don’t just follow the science, but actively push
Daelyn James, is someone who understands the power of owning your story. Diagnosed with cystic fibrosis at just four years old, she remembers what it felt like to go from a carefree childhood to one filled with treatment
Jillian
Youth Coordinator · Gut Personal
1 appearance on this show
Cesar Hernandez
Mexico national football team
1 appearance on this show
Abby Rose
Regenerative Agriculture Entrepreneur · North American Cystic Fibrosis Conference
1 appearance on this show
Shawn
Dad Formula · Elite Fitness
1 appearance on this show
Dr. Wendy Chung
clinical and molecular geneticist, Chief of Pediatrics at Boston Children's Hospital, Mary Ellen Avery Professor at Harvard Medical School · Boston Children’s Hospital
1 appearance on this show
Chris
Pastor · unknown
1 appearance on this show
Deana
Pastor · Surviving Toxic Relationships
1 appearance on this show
Liam
lead vocalist · Fujifilm
1 appearance on this show
Abbie Stockard
2025 Miss America · Auburn University School of Nursing
1 appearance on this show
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Living With Cystic Fibrosis is hosted by Laura Bonnell. The show is categorised under society (culture) and has published 199 episodes.
Living With Cystic Fibrosis has published 199 episodes.
Living With Cystic Fibrosis regularly covers society, culture, documentary. It sits in the society category, with a culture focus.
Living With Cystic Fibrosis is accessible for guests with genuine society expertise. A personalised, episode-aware pitch will still outperform a generic one every time.
Living With Cystic Fibrosis hasn't explicitly signalled guest openness in recent episodes. That doesn't rule out pitching. your hook just needs to be especially compelling and relevant to their recent content.
Episodes of Living With Cystic Fibrosis average 42 minutes. a focused format where a clear narrative arc and tight preparation matter most.
Our data rates Living With Cystic Fibrosis's guest bar at 80/100 (Premium tier). Established thought leaders with verified media credentials. Sign in to PitchCentric to see how your own Pod Score compares against this show.
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