Cystic Fibrosis Podcast 204: Multitasking as a CF Mom
In Jerry’s latest video podcast, he speaks with Kelly Hatfield about being a mom to three boys with cystic fibrosis and a
Cystic Fibrosis Podcast 203: Thankful at the Holidays
Happy Holidays from Jerry Cahill. In his latest podcast, Jerry Cahill sits down to reflect on the holiday season – when he was growing up, why he is most thankful today, and how to make…
Cystic Fibrosis Podcast 202: Being Grateful
Don’t forget – registering to be an organ donor can save a life! Register today: donatelife.org. With the holiday season approaching, everyone starts to think about why they are grateful. In this video, a number…
Cystic Fibrosis Podcast 198: The Art of Healing
In the latest Cystic Fibrosis Podcast, Jerry met with Dylan Mortimer – a 38-year-old artist who lives in New York City with
Cystic Fibrosis Podcast 194: One-year post-transplant checkup
In the latest CF Podcast, Jerry Cahill sits down to answer some of his colleague’s questions about life post-transplant
Cystic Fibrosis Podcast 193: Why do you exercise with Faith Stone?
Jerry sat down with Faith Stone in his latest #cysticfibrosis podcast to discuss why she exercises. Faith is a 20 year old CFers who attends West Virginia University. Her parents always encouraged her and her…
Cystic Fibrosis Podcast 192: Emily’s Entourage
In the latest Cystic Fibrosis Podcast, Jerry speaks with Emily Kramer-Golinkoff about the role of a patient advocate organization in driving drug development in rare disease.
Cystic Fibrosis Podcast 191: ‘Why do you run?’ with Ben James
In his latest podcast, Jerry Cahill sat down with Ben James, a 19-year-old college student who was diagnosed with cystic fibrosis at 4 years old.
Cystic Fibrosis Podcast 189: Immune Tolerance Research for Lung Transplants
In the last installment of The Path Forward with CF series, Dr. Megan Sykes, Director of the Columbia Center for Translational Immunology (CCTI) and Director of Research for the Transplant Initiative at Columbia University Irving Medical Center/NewYork-Presbyterian Hospital,…
Cystic Fibrosis Podcast 188: Stem Cell Research
In this feature of The Path Forward with CF series, Dr. Hans-Willem Snoeck, Professor of Medicine (Microbiology and Immunology) at CUMC, sits down to discuss stem cell research as it relates to CF.
Cystic Fibrosis Podcast 187: The Pre-Transplant Process with Dr. Emily DiMango
The latest video in The Path Forward with Cystic Fibrosis series, Dr. Emily DiMango, Director of the Gunnar Esiason Adult CF Program at Columbia University Medical Center, discusses the lung transplant process through the lens…
Cystic Fibrosis Podcast 186: Ex Vivo Lung Perfusion for Transplant
In the latest edition of The Path Forward with Cystic Fibrosis, Dr. Frank D’Ovidio – the Surgical Director of the Lung Transplant Program and Director of the Ex Vivo Lung Perfusion Program at CUMC –…
Cystic Fibrosis Podcast 184: Involvement in the CF Community
Today, Jerry interviews Mark Levine, a 48-year-old husband, stepfather, tennis player, traveler, engineer, and cystic fibrosis patient. Mark lost his younger brother,
Cystic Fibrosis Podcast 183: You have a new set of lungs! What should you expect next?
In the latest edition of The Path Forward with Cystic Fibrosis, Dr. Arcasoy from Columbia University Medical Center is back to explain what happens after a patient has a double lung transplant. He discusses pain…
Cystic Fibrosis Podcast 182: You got the call for transplant, now what happens?
In Jerry Cahill’s latest edition of The Path Forward with Cystic Fibrosis, Dr. D’Ovidio and Dr. Arcasoy from Columbia University Medical Center explain what happens once a patient receives the official phone call for his…
Cystic Fibrosis Podcast 181: I’m on the transplant list, now what?
Dr. Selim Arcasoy from Columbia University Medical Center discusses what happens once a patient is on the transplant list.