Cystic fibrosis is an inherited chronic disease that affects the lungs and digestive system of about 30,000 children and adults in the United States (70,000 worldwide).

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Children and young adults with cystic fibrosis (CF) go to school and college. They can be expected to and do take part in school activities, including sports and other extracurricular activities.

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Today’s healthcare landscape can be hard to navigate. A growing number of people with cystic fibrosis are finding themselves facing difficult choices about their or their child’s healthcare — even postponing care and cutting back on medications —

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The Cystic Fibrosis Foundation produces a variety of publications and videos designed to inform and educate those in the CF community about important topics relating to science investments and discoveries, as well as medical treatment and progress.

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Children and young adults with cystic fibrosis (CF) go to school and college. They should be expected to and take part in school activities, including sports and other extracurricular activities.

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Charity Spotlight: Cystic Fibrosis Foundation Cystic Fibrosis (CF) is an inherited chronic disease that affects the lungs and digestive system of about 30,000 children and adults in the United States.

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Most people with cystic fibrosis can lead active lives – depending upon the severity of their disease – with routine therapies and regular visits to a Cystic Fibrosis Foundation-accredited care center.

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