Cahir O'Hagan was 25 when he died from cystic fibrosis while waiting for a lung transplant.

A man whose brother died waiting on a double lung transplant says more work is needed to make Cystic Fibrosis drugs available.

People who rely on Creon to digest food say supply issues are making them scared for the future.

Two people with cystic fibrosis say they are eating less and rationing pills due to the shortage.

Drugs to help tackle the root causes of cystic fibrosis will be made available on the NHS in NI.

Hannah Richards needs Creon so she can take a life-changing drug but supplies may be low until 2026.

A deal has been reached to give NHS patients Kaftrio, Symkevi and Orkambi.

Sophie Holmes says hopes her achievement will inspire other people living with the condition.