To mark World Antimicrobial Resistance Awareness Week, we reflect on some of the milestones of 60 years of CF microbiology research, highlighted by Professor Jo Fothergill in a presentation last month.
As winter starts, a little preparation can make all the difference. The colder months bring new challenges, but with a few simple steps, you can stay well, manage costs, and find support when you need it most. Rachel, Cystic Fibrosis Trust’s Welfare Officer, shares helpful budgeting tips, energy-saving ideas, and explains how you can get more money help. We're here to help make winter feel a little brighter and a lot more manageable.
Cystic Fibrosis Trust held their 60th anniversary awards ceremony to acknowledge the outstanding efforts of the CF community, the event was hosted by celebrity ambassador Richard Madeley.
Developing CF diabetes (CFD) is one of the most common complications of cystic fibrosis. In fact, one in three adults with CF in the UK is currently living with the condition. Anabelle is a medical writer from Surrey. She has CF and CFD and is expecting her first child in January. To mark World Diabetes Day on 14 November, we spoke to Annabelle about her CF journey, her experience of dealing with CFD and her top tips for managing it.
Most people with CF in the UK need some kind of pancreatic enzyme replacement therapy (PERT) and we’re aware that the supply issues are having widespread and varying impact on the CF community. That's why we're calling on the Government to find lasting solutions which will resolve and alleviate the impact of supply issues.
To mark Men’s Mental Health Awareness Month this November, Duncan, dad to Charlotte, shares his experience of processing his daughter's CF diagnosis, while navigating parenthood as a single father.
