Cystic Fibrosis Trust Homepage

Visit our COVID-19 hub

Find out more

We provide information and support to help everyone with CF live life to the full

We fund cutting edge research into new therapies and treatments

We campaign hard for better care, service and access to medicines

Information & support

Get involved

We need your support this Christmas

Research can’t wait - we need your support now more than ever. Will you support us this Christmas as we race towards life-changing treatment for all?

I want to help

Latest news and blogs

See all news

Blog - 02/12/2021

“During Hannukah, I feel the miracle of light inside me”: Elle’s story

Elle, 20, from Russia, tells us about her CF journey – and celebrating the Festival of Lights in her far eastern hometown

Blog - 30/11/2021

Looking to the future

Hear from our Chief Executive, David Ramsden, on why we remain committed to uniting for a life unlimited

Blog - 25/11/2021

The effects of the COVID-19 pandemic on people living with rare diseases: a doctor’s view

For people living with rare diseases like cystic fibrosis (CF), the impact of the COVID-19 pandemic has been far reaching, with both positive and negative outcomes. Dr Jamie Duckers, Consultant in CF and Respiratory Medicine at Cardiff and Vale University Health Board, talks about how the CF community has been affected by the pandemic.