It said that 95% of people with cystic fibrosis in England will now be eligible for modulator therapy. The new drug, also ...

Hundreds of cystic fibrosis patients become eligible for ‘life-changing’ therapy - Some people with the rarest forms of the ...

Children born in the 2020s with cystic fibrosis often have more treatment options and potentially better outcomes than those born with the disease in previous decades.

With Vertex's cystic fibrosis drug Trikafta, death no longer looms so close for many patients. But now, they face unfamiliar worries about careers, money, and old age — “the existential threat ...

Ann & Robert H. Lurie Children’s Hospital of Chicago is leading an awareness campaign that aims to reduce missed or delayed diagnosis of cystic fibrosis after newborn screening, especially in ...

The cystic fibrosis transmembrane conductance regulator has been studied for years but the new efforts have yielded important insights.

Advances in cystic fibrosis diagnosis and treatment haven't equally benefited people of color. One couple seek to change that.

Cystic fibrosis is a genetic disorder that causes mucus-producing organs to malfunction and produce abnormally thick, sticky mucus. This causes problems in those organs, such as the lungs, the ...

GRAND RAPIDS, Mich (WOOD) – Cystic fibrosis is an inherited chronic disease that affects the lungs and digestive system of about 30,000 children and adults in the United States. One in 3,500 ...