We sat down with James, who has cystic fibrosis, to talk about the impact CF has had on his life, his biggest challenges – and his hopes for the future
We spoke to Jane, an anesthetist and member of our Sixty Five Roses Club, about her son William who has CF and her upcoming plans to run three marathons this year, two of which will be in the same week!
New analysis from Cystic Fibrosis Trust, published today, reveals that many people with cystic fibrosis (CF) are struggling to afford basic daily essentials such as food and energy bills, with more people than ever needing financial assistance. This is taking a huge toll on their mental health, with 9 in 10 worried about the future.
Everyone living with cystic fibrosis (CF) is unique and will have their own experiences. Find support, advice and resources to help you manage symptoms and live well with CF.
Kieron Smith, 26, was the face of our latest #CFTruths awareness campaign, ‘You don’t see CF,’ that launched across the UK in April this year. As part of this, his face appeared on billboards and adverts to raise awareness of the realities of cystic fibrosis.
Dr Tim Lee is the lead consultant for the Leeds Children's Cystic Fibrosis Centre. In the latest edition of CF Life, we caught up with him to learn more about how he started his career in CF, his interest in genetic therapies and his useful barbeque tip!
Improvements in lung function, reduced numbers of IVs and 140 women with CF having babies are just some of the highlights from this year’s Registry data report
