What do Tess and family wish for...
Back to school: Cystic Fibrosis and me
Tess, aged 9, tells us what it's like to manage cystic fibrosis at school
Babies, bright lights, blood-thinners and more: Cochrane evidence round-up
It’s probably best to draw a veil over many of the things done in English boarding schools by past...
Newer nebulisers cut treatment times for people with cystic fibrosis
Key message: Nebulisers don’t all perform the same. Some newer types such as adaptive aerosol delivery and vibrating mesh...
Helping the management of bleeding disorders to spread out of the wealthy world
This guest blog has been written by Dr Alfonso Iorio and Nikki Jahnke from the Cochrane Cystic Fibrosis and Genetic...
Spotlight on inborn errors of metabolism
28th February is Rare Disease Day. This guest blog has been written by Nikki Jahnke and John Walter for...