Our body image booklet features people with cystic fibrosis discussing how they feel about their own bodies and how they have dealt with body image challenges.
This Strategic Research Centre (SRC) aims to bring together exercise specialists, parents and adolescents to prescribe physical activity more effectively.
As we publish the findings from our second experience survey in paediatric CF care, Dr Jana Witt, Clinical Quality Improvement Manager at the Trust, recaps some of the key findings
Last month, over 180 CF professionals gathered in Birmingham for our MDT (multidisciplinary team) conference, which explored hot topics and emerging issues in CF clinical care. Jacqueline Ali, Head of Information and Support at Cystic Fibrosis Trust, shares some of the key takeaways.
Transition from paediatric to adult care is different for everyone with cystic fibrosis (CF). Cicely's transition didn't quite go to plan but here she reflects on the experience and the great work she has done with her new CF team.
Our fourth Your Life and CF report shows the reality of life with cystic fibrosis in 2025 – long daily treatment routines, rising living costs and growing concerns about mental health. We’re calling on the Government to act now and make meaningful change.
