Cystic Fibrosis Ireland (CFI) is a voluntary organisation set up by parents in 1963 to improve the treatment and facilities for people with cystic fibrosis in Ireland.

CFI are supported by fundraising and voluntary contributions and are solely concerned with the well-being of people with Cystic Fibrosis.  

Cystic Fibrosis Ireland aspires to be a leading advocacy group in Ireland that professionally represents its membership with empathy while achieving results by improving the quality of life, health and medical care for people with Cystic Fibrosis so they can lives to their full potential.