In this cystic fibrosis podcast, Johnell Garmany, President and CEO of Garmany, discusses the history of his family and store as well as the reasoning behind their generosity. Founded by Johnell’s father around 43 years ago, Garmany has become known READ MORE
Originally on the cystic fibrosis podcast series around three years ago, Lizz returns to discuss her life after her double lung transplant in March 2016.
Faisal is 18 years old and currently resides in Concord, CA. He recently graduated from High School and is headed to college in the fall. Faisal plays soccer for the Diablo FC in the National Premier League and was a member of the Afghanistan U19 National Team.
In this podcast, we meet Molly Bigford, a Registered Dietitian for the Adult Cystic Fibrosis Care Team in Grand Rapids, Michigan.
Tune in to hear from CF mom, Cheryl Esiason.
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.
Chris Kvam, cystic fibrosis patient, husband, and father, discusses the process of becoming a parent.
Jerry Cahill reviews several ways that he stays active in the hospital with cystic fibrosis exacerbations.
In this podcast, we hear from Pam Gauvin-Fernandes, whose journey is truly unique.
Jerry Cahill, 5 years post transplant, shares the ups and downs of his journey as an organ donor recipient.