Cystic fibrosis (CF) is a chronic genetic disease where a defective gene and its protein product cause the body to produce thick, sticky mucus. This mucus clogs the lungs, leading to life‐threatening lung infections, and obstructs the pancreas; preventing natural enzymes from helping the body absorb and break down food.
Approximately 30,000 children and adults suffer from CF in the U.S., and it is known as the #1 genetic killer of children. Before 1990, very few children lived to attend elementary school. Now, the median life expectancy is 37. In less than 20 years, advances in research and treatment have extended the life expectancy of CF patients more than 30 years! Research and care improvement are truly making a difference.
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