Cystic Fibrosis Podcast 272: Overcoming Physical, Emotional, and Social Barriers with PTLD
Andrea Eisenman is a 57-year-old living with cystic fibrosis who received a double lung transplant in April 2000. 17 years later, she
Cystic Fibrosis Podcast 271: Life with a Rare Disease - Living with PTLD
Jenna Strickland is 32-years-old living with cystic fibrosis and received life-saving double lung transplant in 2015. Just eight months later, she was
Cystic Fibrosis Podcast 270: 65 and Alive Post-Transplant
During his annual Bike 2 Breathe ride, Jerry Cahill had no idea just how sick he was becoming. What he thought would
Cystic Fibrosis Podcast 269: Gearing up for Freshman Year with CF
In the latest CF podcast, Michael Caruso Davis – 18 and living with CF – shares some of his story and how
Cystic Fibrosis Podcast 268: Gearing up for Senior Year and Post-Grad Life
Dugan Reilly, a 22-year-old living with cystic fibrosis, discusses his college experience in the latest CF Podcast. He talks about struggling his
Cystic Fibrosis Podcast 267: Bike 2 Breathe 2021
The Bike 2 Breathe team was back in action! For their 8th ride, Jerry and Em biked from New Hampshire to Coney
Cystic Fibrosis Podcast 266: Being a CF Mom
In Jerry’s latest podcast, we meet Beth Gerritsen – mother to Charlie, who has cystic fibrosis, and Willie, who does not. From
Cystic Fibrosis Podcast 265: CF Siblings Supporting Each Other
In his latest podcast, Jerry chatted with Charlie, 11 with CF, and his older brother Willie about the CF-sibling relationship. They talk
Cystic Fibrosis Podcast 263: Patient and Family Education – ZephyRx
In the latest CF Podcast, Jerry speaks with Dwight Cheu, CEO of ZephyRx, a home-based respiratory diagnostic testing and therapy that allows patients to
Cystic Fibrosis Podcast 262: Dealing with Post-transplant PTLD
The You Cannot Fail Rare Disease podcast series was created so that the Boomer Esiason Foundation can shine a spotlight on other
Cystic Fibrosis Podcast 261: Advocating for Your Rare Disease
The You Cannot Fail Rare Disease podcast series was created so that the Boomer Esiason Foundation can shine a spotlight on other
Cystic Fibrosis Podcast 260: Accepting Cystic Fibrosis
“I believe in enjoying life and living it to the fullest, having fun, and just enjoying time.” Brayden Walsh, a 16-year-old living
Cystic Fibrosis Podcast 259: Importance of Exercise and Nutrition
In the latest CF Podcast, Anthony Esposito, aka Espo 2, shares why he loves fitness and nutrition. While he doesn’t have CF
Cystic Fibrosis Podcast 257: COVID-19 – A terrible virus & the wonderful humans who cared for me
“I’ve always felt gratitude for the hospital staff, but this was over and above. We all know how contagious this is, and
Cystic Fibrosis Podcast 256: Going through a Pulmonary Exacerbation
In Jerry Cahill’s latest podcast, he spoke with 30-year-old Enid Katz, who was diagnosed with CF when she was 3. Enid’s passion in
Cystic Fibrosis Podcast 255: Talking to Kids about CF
Jerry Cahill spoke with Dr. Kelsey Finn about her book, “Having Cystic Fibrosis is a lot like being a Super Hero,” which