Cystic Fibrosis Trust Homepage

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

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We fund cutting edge research into new therapies and treatments

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

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Great Strides My Way

This June, take on Great Strides in your own way – on a treadmill, doing laps around your local streets or by mapping out a route in your local area!

Latest news and blogs

Feature -

Join us for a tour through the Trust’s cutting-edge research

This year, our annual UK Cystic Fibrosis Conference (UKCFC) will be held entirely online for the first time, on Wednesday 12 May 2021. The conference is an informal opportunity for the CF research community to share their results, generate new ideas and spark interest in new collaborations. Read on to find out about some of the exciting research being presented at UKCFC this year.

Blog -

Tim's story: 50 years of living with cystic fibrosis

When Tim was diagnosed with cystic fibrosis (CF) in 1971, his parents were told he would only live to his teenage years. Instead, he celebrated his 50th birthday earlier this year. Tim, who has the double Delta F508 mutation, works full time as a Communications Manager in South London, where he lives with his wife, Katie, and 13-year-old son, Felix. In this blog, Tim takes a look back on how CF treatments have evolved over the last 50 years and reflects on key moments that changed his life, including cross-infection risks and Kaftrio. 

News -

UK CF Medical Association's statement on coronavirus

Here, the UK CF Medical Association (UKCFMA) gives feedback on the monitoring of data collected through the UK CF Registry about the number of people with CF who have had coronavirus (COVID-19). It also advises how people with cystic fibrosis and their families can help minimise their risk of COVID-19.

Events

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Captain Tom 100

Captain Tom believed in a better tomorrow, and so do we. Sign up to the Captain Tom 100, raise funds for the Cystic Fibrosis Trust and create a...

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