A new set of standardized screening recommendations from the Cystic Fibrosis Foundation aims to reduce missed or delayed ...

A boy with cystic fibrosis is planning to complete a half marathon to raise money for a charity that supports people with the ...

Close to 2,000 people in West Virginia and Ohio were living with Cystic Fibrosis in 2023, according to the Cystic Fibrosis ...

Breathing—a natural and essential process—can be an incredibly labored process for people with cystic fibrosis. CF, a genetic ...

Cystic fibrosis follows an autosomal recessive inheritance pattern, meaning both parents must carry a defective gene copy for their child to develop the condition. This inheritance pattern affects ...

When Jordana McMurray was working night shifts as a pediatric respiratory nurse at the Hospital for Sick Children (SickKids) ...

Garriga-Grimau L et al. First results from the international paediatric bronchiectasis registry (Child-BEAR-Net Registry) ...

Navigating my newborn’s CF diagnosis during the height of the COVID-19 lockdown was one of our hardest moments — yet it was only the beginning of a journey filled with unexpected joy and hope.

Due to another upcoming weekend of expected rain, the team decided to switch from a Saturday to a Friday lunch event, but ...

The event is a fundraiser for Piper’s Angels, a local nonprofit that supports families affected by cystic fibrosis.

Children with those genetic mutations are typically diagnosed late and can suffer permanent organ damage with dire consequences. When Andersen published her description of cystic fibrosis in the ...

When he was about 14, Pete Proimos learned a soul-crushing statistic about the cystic fibrosis he'd endured since birth: Patients back then didn't live much past high school.