Cystic Fibrosis

Cystic Fibrosis is a genetic disorder, marked by abnormally thick mucus build up in the lungs and digestive tract. This can lead to severe respiratory problems, as well as difficulty digesting food. Cystic Fibrosis affects about 30,000 people in the United States and approximately 1 in 2,500 babies born with the condition. There is currently no cure for Cystic Fibrosis, but treatments like antibiotics, nutrition, and physical therapy can help reduce symptoms and improve quality of life. Research is ongoing to find a cure and to understand the cause of the disease. Cystic Fibrosis is an important condition to consider in the evaluation of any individual who presents with recurrent respiratory or digestive problems.