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
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During his annual Bike 2 Breathe ride, Jerry Cahill had no idea just how sick he was becoming. What he thought would
In the latest CF Podcast, we meet Griffin Taylor, a 15-year-old who loves lacrosse and squash, is on his school’s robotics team,
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
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
Jerry Cahill spoke with Dr. Kelsey Finn about her book, “Having Cystic Fibrosis is a lot like being a Super Hero,” which
“I would tell a caregiver or a spouse of someone with CF that – all of those things you are feeling, the
In part 2 of Managing Your Life as a Teenager, Jerry sits down with Sean Randles… 6 years after their first podcast.
All parents worry about their children – but parents of kids with cystic fibrosis have additional stressors and concerns. In the latest
In Jerry’s latest CF Unmasked podcast, he sits down with Greg Love for an uncensored look at what it’s like growing up
“I am not defined by my disease. I have CF, but I am not CF. I can do what everyone else can
“Keep pushing. Know that people are working for a treatment for the extra group of our friends who don’t have a treatment.
Quarantine. Social distancing. Isolation. These words are very familiar to those of us living with chronic illnesses. I am 63-years-old, eight years
In the latest CF Podcast, Jerry Cahill sits down to answer some of his colleague’s questions about life post-transplant