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This involves using an inhaled spray to deliver normal copies of the cystic fibrosis gene to the lungs.
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With improved treatment there has been a dramatic increase in the survival of people with cystic fibrosis over a period of 20 years or so.
In the 1960s and before, most babies born with cystic fibrosis only survived for a few months or years.
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Today, many people with cystic fibrosis are living into their late 30s and beyond.
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Other medication to improve lung function for example, ibuprofen and azithromycin may also be recommended in some cases.
TREATMENTS FOR PANCREATIC PROBLEMS Nutrition The enzymes needed to digest food are greatly reduced in most people with cystic fibrosis.
Therefore children with cystic fibrosis need a high fat and carbohydrate diet.
A dietician will usually give detailed advice.
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