In this blog, we talk about the work that the Trust is doing to ensure policy makers understand how important Creon is to the health of people with CF, and that all steps are being taken to address and reduce the impact of shortages.
For 60 years we've worked together, sharing moments of frustration, despair and hope, overcoming challenges, and celebrating breakthroughs. Always learning and moving forward. This CF Week, we’re reflecting on how far we’ve come and looking to the future. Because we won’t stop until CF does.
Thiago was diagnosed with CF at five weeks. Now eight months old, his mum Shanique and dad Rico reflect on their journey with cystic fibrosis and what they hopes the future looks like for her little boy.
We chatted to Tammy, 44, from York, about her home education business – and the confidence boost winning a Helen Barrett Bright Idea Award has given her
Our latest Your Life and CF survey, published today by Cystic Fibrosis Trust shows the huge physical, mental, and financial burden people affected by cystic fibrosis (CF) face, where 43% worry about their future every day.
