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Cystic Fibrosis

Cystic fibrosis (CF) is an inherited disease of the mucus and sweat glands. It affects mostly your lungs, pancreas, liver, intestines, sinuses and sex organs. CF causes your mucus to be thick and sticky. The mucus clogs the lungs, causing breathing problems and making it easy for bacteria to grow. This can lead to problems such as repeated lung infections and lung damage.

The symptoms and severity of CF vary widely. Some people have serious problems from birth. Others have a milder version of the disease that doesn't show up until they are teens or young adults.

Although there is no cure for CF, treatments have improved greatly in recent years. Until the 1980s, most deaths from CF occurred in children and teenagers. Today, with improved treatments, some people who have CF are living into their forties, fifties, or older.

Source: National Heart, Lung, and Blood Institute
Ohio State is recognized by U.S.News & World Report as one of the nation's best hospitals in pulmonology, and Ohio State's Lung Center is the only comprehensive lung and pulmonary center in central Ohio. Schedule an appointment with Ohio State's lung experts. Call 614-293-4925.