Cystic fibrosis (CF) is a life-threatening, genetic disorder that affects the lungs, digestive system, and other organs in the body. It is caused by a defective gene that causes the body to produce thick, sticky mucus that can clog and damage the lungs and digestive system. Although there is currently no cure for CF, treatments have improved significantly in recent decades, leading to a dramatic increase in life expectancy for those living with the disorder.
The average life expectancy of someone with cystic fibrosis is now around 37.5 years, according to the Cystic Fibrosis Foundation. However, life expectancy can vary greatly depending on a variety of factors, including the severity of the disease, access to medical care, and overall health.
For example, those with milder forms of CF may live significantly longer than those with more serious forms of the disorder. In addition, those who have access to specialized treatments and care, such as lung transplants or enzyme replacement therapy, may have a longer life expectancy.
Finally, the overall health of an individual with CF plays an important role in their life expectancy. Eating a healthy diet, avoiding smoking, and getting regular exercise can all help to improve overall health and potentially extend life expectancy.
Overall, while there is currently no cure for cystic fibrosis, advances in medical treatments and therapies have led to a dramatic increase in life expectancy for those living with the disorder. While the average life expectancy is now around 37.5 years, access to specialized treatments, overall health, and the severity of the disorder can all affect life expectancy.