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Travel insurance – listening to our community
In May 2015 the Cystic Fibrosis Trust launched a travel insurance survey in response to concerns...
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When the Trust began in 1964, people with cystic fibrosis would be lucky to live past five years old. Now, according to the UK Cystic Fibrosis...
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Rob
Depending on the job I do, I have different ways of managing my CF treatments. When I first started work at the age of 16, I was lucky that...
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Looking for a job if you have cystic fibrosis
As far as possible, CF should not be allowed to limit your choices. For many jobs, reasonable adjustments...
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From genotypes and genetic influencers to the world around you and the way you live your life, a combination of building blocks makes you the...
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Cystic fibrosis studies
Any new treatments or changes to the way care is delivered have to be proven to be safe and effective, which requires...
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Ciara faces the challenge of managing her calorie intake each day to make sure she stays healthy and has the energy required for all her treatments...
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Sammie loves being creative and going to gym classes, and has had a varied range of careers, but currently feels unable to work owing to her...
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Liam’s daughter Rachel, aged 24, was diagnosed with cystic fibrosis when she was just six weeks old. Today, she has a Masters in psychology and...
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Thank you for supporting the Cystic Fibrosis Trust at your upcoming fundraising event! We want to give you as much tailored fundraising support...