Cystic Fibrosis Trust Homepage

Physically Well 

Together, we can live without the physical challenges of cystic fibrosis. 

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Mentally Well 

Together, we can manage the mental pressures of cystic fibrosis. 

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Fulfilment

Together, we can lead the life we want as part of a connected community.

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Current issues

Find out about Creon shortages, I-neb nebulisers, and the cost of living crisis, what we're doing to help resolve these issues, and how we can support you.

Latest news and blogs

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Swansea University students saddle up for an epic cycling challenge

On September 18, our amazing supporters Tom, Louis, Rory and Nathan will be setting off on an epic challenge, cycling 270 miles from London to Paris on a four-person tandem bike.

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Taking on the Great Scottish Run for Cystic Fibrosis Trust

Claire shared the story behind her biggest motivation to take on the Great Scottish Run - her husband Bob, who is living with cystic fibrosis (CF).

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CTAP reaches exciting clinical trial milestone!

We set up our Clinical Trials Accelerator Platform (CTAP) eight years ago to increase opportunities to take part in CF research studies and get new treatments to people with CF faster. Through CTAP, we’ve supported a huge range of studies and helped thousands of people with CF to take part. To celebrate the 4,000th research study enrolment, we look at how UK clinical trials are growing in numbers and how you can shape the future of CF research by getting involved.

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Permanent access agreements for modulators

Kaftrio, Orkambi and Symkevi have been permanently approved on the NHS in England, Wales, Scotland and Northern Ireland.

Events

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Event Date:

Carols by Candlelight

Join us for Carols by Candlelight 2024

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CF never lets you have a day off

Cystic fibrosis is a life-limiting, genetic condition without a cure. It dominates thousands of lives every day. You never get a day off when you have CF. 

More from Cystic Fibrosis Trust

Helpline

Contact our friendly Helpline team who can provide you with information about any aspect of living with cystic fibrosis.

Contact us

Get in touch with us if you have any questions or are in need of guidance.

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