5 years ago, we received the devastating news that our beautiful baby girl, Esme, was born with Cystic Fibrosis, a genetic disease that causes irreparable damage to organs and the respiratory system. Thankfully, Esme is currently fit and healthy, and that in no small part is down to the support the Trust provides. We know there are other families that rely on the Trust just as much as we have, and would like to help raise funds for them, so that they may continue their vital work.

A little bit about CF

Cystic fibrosis (CF) is a genetic condition which causes sticky mucus to build up in the lungs and digestive system. It affects more than 10,800 people in the UK. One in 25 of us carries the faulty gene that causes it, usually without knowing.

Cystic fibrosis comes with challenges, affecting our physical health, mental wellbeing and how we choose to live our lives. But our community is uniting towards the ultimate goal of effective treatment for all.

Cystic Fibrosis Trust is the charity uniting people to stop cystic fibrosis and allow those with it to have a life without limits.

Thank you for your support.