Cystic Fibrosis Wind Sprint 61: How to Use and Care for Nebulizers and Spirometers
Jerry shares his organizational habits for using his nebulizers, spirometer, and testing his oxygen levels.
Cystic Fibrosis Wind Sprint 60: Extended Hospital Stays and Total Body Workouts
In this wind sprint, Jerry demonstrates a 5-minute total body workout.
Cystic Fibrosis Podcast 176: Importance of Nutrition for CF Patients
In this podcast, we meet Molly Bigford, a Registered Dietitian for the Adult Cystic Fibrosis Care Team in Grand Rapids, Michigan.
Cystic Fibrosis Wind Sprint 59: Extended Hospital Stays and Stretching
In order to stay fit and healthy during an extended hospital stay, Jerry is sure to stretch every single day.
Cystic Fibrosis Wind Sprint 58: Extended Hospital Stays and Leg Workouts
Jerry reviews the various leg stretches and workouts he uses during an extended hospital stay.
Cystic Fibrosis Wind Sprint 57: Extended Hospital Stays and Upper Body Workouts
In response to an email from Paul, Jerry reviews the various workouts he uses to work his upper body during an extended hospital stay.
Cystic Fibrosis Wind Sprint 56: Extended Hospital Stays and Core Workouts
In response to a Facebook message from Alexandra, Jerry reviews the core exercises he uses to stay in shape during an extended
Cystic Fibrosis Podcast 175: Being a CF Mom featuring Cheryl Esiason
Tune in to hear from CF mom, Cheryl Esiason.
Cystic Fibrosis Podcast 174: Rare Disease Series featuring Duchenne Muscular Dystrophy
Jerry interviewed Jonathan, who lives with Duchenne muscular dystrophy, a rare inherited disorder of progressive muscular weakness that is most typically found in males and affects only about 20,000 people.
Cystic Fibrosis Podcast 173: Becoming a Parent and Overcoming Infertility with Cystic Fibrosis
Chris Kvam, cystic fibrosis patient, husband, and father, discusses the process of becoming a parent.
Cystic Fibrosis Podcast 172: Exercising while in the Hospital
Jerry Cahill reviews several ways that he stays active in the hospital with cystic fibrosis exacerbations.
Cystic Fibrosis Podcast 171: The Daily Grind with Cystic Fibrosis featuring Pam Gauvin-Fernandes
In this podcast, we hear from Pam Gauvin-Fernandes, whose journey is truly unique.
Cystic Fibrosis Podcast 170: Jerry’s Five Year Transplant Anniversary
Jerry Cahill, 5 years post transplant, shares the ups and downs of his journey as an organ donor recipient.
Cystic Fibrosis Podcast 169: #MyNewLungs
In this podcast, cystic fibrosis patients share their inspiring double lung transplant stories.
Cystic Fibrosis Podcast 168: Sports and Cystic Fibrosis with Matt Mitchell
Matt Mitchell, 19, shares his journey with cystic fibrosis, exercise, and team sports.
Cystic Fibrosis Podcast 167: Living Life with a Terminal Illness
Michael is 24 years old with CF and 5 months post double lung transplant. Michael is from Nebraska, and loves fishing, hunting,