Cystic Fibrosis (CF) is an autosomal, recessive disorder, arising from defects in the CF transmembrane conductance regulator (CFTR) gene (Riordanet al., 1989) and affects many aspects of function and daily living for people living with CF (PwCF) (Elborn, 2016;Sawickiet al., 2011). This evidence concerns the gene CFTR and cystic fibrosis.