Colleen Caul — whose little sister, Katie Rose, has cystic fibrosis — ran from St. Louis to New York City in 65 days to spread awareness of cystic fibrosis, raise funds toward a cure, and share stories with others in the community.

Josh Mogren, who lives with cystic fibrosis and cerebral palsy, discusses overcoming obstacles, including the loss of his sister to CF.

Marc Smolowitz, making his directorial debut, speaks about “The Power of Two” documentary film.The film offers an intimate portrayal of the bond between half–Japanese twin sisters, Anabel Stenzel and Isabel Stenzel Byrnes, their battle with cystic fibrosis, and the miraculous survival through double-lung transplants.

Recently, we tagged along with Jerry Cahill on the way to Milwaukee, where he spoke to packed house at Children's Hospital of Wisconsin. Jerry's message was clear: Everyone with CF should be exercising and getting involved in the CF community. Jerry talks about his lifelong struggle with CF and his no-nonsense approach to managing CF on a daily basis.

Jerry Cahill celebrates a milestone with his 100th CF podcast! Check out humorous outtakes, and clips from a range of interviews.

Eileen Minogue, Director of Operations for Patient Airlift Services (PALS), discusses arranging FREE air transportation for patients with in CF in need of medical diagnosis or treatment.

Maggie Sheehan, 22 years old with cystic fibrosis, talks about her great experiences attending the CFRI Retreat in Northern California. The retreat takes place off the beaten path under the ?redwoods," just minutes from Stanford Hospital. CFRI is a great organization that empowers the CF Community to attain the highest possible quality of life.

Travis Flores, 18 years old with cystic fibrosis, grew up in Ohio and is attending college in New York City. Besides going to school, Travis has written a children's book, has two websites that are raising awareness and funds for cystic fibrosis and is a "Heroes of Hope" award recipient. Travis is living, breathing and succeeding with CF.

Paul Drury is 42 years old with cystic fibrosis and is post-lung and -kidney transplant. Paul is happily married, working for the Cystic Fibrosis Foundation (Connecticut Chapter), a mentor to the CF community, and LIVING, BREATHING and SUCCEEDING on a daily basis. 24/7 for the CF community is what Paul Drury is all about. Not only does he live with the disease; Paul works for the CFF in fundraising and speaks to many people with CF on a daily basis.