People with cystic fibrosis have to do daily nebulisers as well as take a lot of medication. They have to make sure they excerise take medication when they eat anything and a lot more. We as a family had to fight to get the drugs to keep our daughter healthy and well. We ask you give what you can . Thank you.
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 t