Cystic Fibrosis Ireland (CF Ireland) is a non-profit organization established in 1963 by parents aiming to enhance treatment and facilities for individuals living with cystic fibrosis (CF) in Ireland. The organization is dedicated to improving the welfare and interests of those affected by CF through advocacy, support, and collaboration with healthcare professionals.

CF Ireland focuses on several key activities, including providing information and resources to help individuals with CF live independently, advocating for their needs, and working with healthcare providers to enhance treatment standards. The organization also engages in fundraising efforts to support research and initiatives that benefit the CF community.

Additionally, CF Ireland collaborates with the Cystic Fibrosis Registry of Ireland, which collects clinical data to improve care quality. The organization serves individuals diagnosed with CF, their families, medical professionals, and researchers interested in CF treatment and welfare.