We are an integrated disease management program for children with cystic fibrosis, caring for patients from diagnosis on through adulthood.

Cystic Fibrosis in Children

Cystic Fibrosis (CF) is one of the most common genetic (inherited) diseases in America. It is also one of the most serious. It mainly affects the lungs and the digestive systems, causing breathing problems and problems digesting foods. It is a chronic disease that currently has no cure.

The pediatric specialists at Lucile Packard Children’s Hospital Stanford work closely with the Stanford Hospital team to deliver care for kids with cystic fibrosis.

We are pleased to offer a dedicated multidisciplinary team to manage our patients. Our pediatric pulmonologists work closely with gastroenterologists, ear, nose and throat specialists, and endocrinologists to manage this complex disease.

Our Cystic Fibrosis program is the only one in Northern California and is the only CF Foundation-designated Therapeutic Development Network center in California, Nevada and Oregon. We participate as a national leader in clinical trials  and the development of novel therapies.

Cystic Fibrosis Care Team