Hi everyone, my name is Tilly. I’m 15, and I have CF and CF diabetes. Today, I want to talk to you about the Trust’s Youth Advisory Group (YAG) and what it means to me.
Understanding more about the bacteria that cause serious CF lung infections can help prevent the spread of infection in the future. Cystic Fibrosis Trust-funded researchers Dr Aaron Weimann and colleagues at the University of Cambridge have made some important discoveries about how the bacteria Pseudomonas aeruginosa cause infections. These results are published today in the prestigious journal Science.
More than 1,000 children and adults with CF have now joined the CF BioResource project. The project is aiming to create a register of people with CF based on their genetic information. This has the potential to change CF research and improve our understanding of CF in many ways. Here are five ways the CF BioResource project could help people with CF.
At Cystic Fibrosis Trust, we’re here for families every step of the way and have created a new resource for parents and carers whose child has just received a cystic fibrosis (CF) diagnosis.
We're uniting so everyone with CF can live a life unlimited. This means funding research, campaigning hard to drive change, and supporting people with CF and their families. Here are five highlights from our 2022-2023 impact report.
Many people with cystic fibrosis face the possibility of a transplant, but adjusting to life after transplant can be difficult. We're here to support you.
