The 2024 UK general election has brought significant changes to our political landscape, and at Cystic Fibrosis Trust we want to seize every opportunity to advocate for improved CF care and support. Our advocacy work puts the needs of people with CF, their families, and professionals working in CF care at the heart of everything we do.
Today (17 July) a new Parliamentary session has begun with the State Opening of Parliament and the King’s Speech. This is read out by the King but written by the Government and sets out the laws they intend to pass this parliamentary session.
School’s out for summer! Lian, mum to Henry, 9, who has cystic fibrosis (CF), shares her experience of planning for a family holiday when your child has CF. We also hear from others in the CF community about their top travel tips.
Cystic Fibrosis Trust, and CF clinicians, dietitians and pharmacists are working hard to ensure that the impact of shortages of Creon on the health and wellbeing of people with CF is minimised.
Consultant clinical psychologist Helen Oxley and principal clinical psychologist Rachel Massey-Chase highlight the work of CF psychologists and the importance of Cystic Fibrosis Trust’s new guidelines.
Whether you are running your own business, applying for this year’s Helen Barrett Bright Ideas Award, or building an influencer channel; join our digital marketing webinar and find out how to grow your business in an affordable way.
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.
