Ask YAG: Young people with CF answer parents' questions

Xander's family at Christmas – Wishing for a brighter future

Cystic Fibrosis Trust 60th Anniversary Awards

Outcomes and experiences in adult CF care | CF LIVE

60 years of the Trust: Rob's story

Meet Xander and his family – Wishing for a brighter future

Penelope's diagnosis story | Your Baby's CF Diagnosis

Applying for an emergency grants | Support

How do you feel about restrictions on joining further genetic therapy trials? | Involvement Group

How do you feel about starting a nebulised genetic therapy? | Involvement Group

What would you expect from a genetic therapy? | Involvement Group

Applying to our Home Essentials Fund | Support

Shanique talks about the forum | Your Baby's CF Diagnosis

Come with us to soft play | Your Baby's CF Diagnosis

Arlo's story | Your Baby's CF Diagnosis

Nicole and Martyn talk about their reactions to Arlo's diagnosis | Your Baby's CF Diagnosis

Nicole and Martyn discuss childcare and the Individual Healthcare Plan | Your Baby's CF Diagnosis

Nicole and Martyn discuss talking about CF to friends and family | Your Baby's CF Diagnosis

Tilly interviews her parents about her CF diagnosis | Your Baby's CF Diagnosis

Dhyuti's story | Your Baby's Diagnosis

CF Week 2024: Stuart's story

CF Week 2024: Thiago's story

Cystic Fibrosis Trust research support offer

No day off: Jon's story | #CFTruths

No day off: Charlotte's story | #CFTruths

Cystic Fibrosis Trust: Since 1964 | 60th Anniversary

Managed Migration: being moved to Universal Credit | Support

How can you get involved and influence the work of the Trust and future research? | CF LIVE

Paediatric CF care – Insights from the UK CF Registry and our patient experience survey | CF LIVE

Flexible working at the Trust | Our culture

CEO David Ramsden's end of year message | 2023

Researcher profile: Dr Emily Granger | RESEARCH

🌟 Dame Judi Dench cordially invites you to join us for the 21st Carols by Candlelight! ✨ | FESTIVE

Researcher profile: Hollie Leighton | RESEARCH

Unite with us this festive season | Festive 2023

UK Cystic Fibrosis Conference | CF LIVE

Session 4: Underlying cause of CF & closing remarks | UK Cystic Fibrosis Conference 2023

Session 3: CF Lung infections | UK Cystic Fibrosis Conference 2023

Session 2: Symptoms and complications of cystic fibrosis | UK Cystic Fibrosis Conference 2023

Welcome to UKCFC and opening session | UK Cystic Fibrosis Conference 2023

Rita and Asra's story | Living in poverty with #cysticfibrosis

NICE modulator appraisal: what does this mean for the CF community? | Access to medicines

Crucial insights in children’s CF care | Patient-reported experience measure surveys (PREMs)

Prescription charges should be free for everyone with #CF | Campaign for free prescriptions

Would taking genetic therapies modify my DNA? | CF LIVE

Genetic therapies could be available for everyone regardless of the form of CF | CF LIVE

Genetic therapies offer a potential cure for CF | CF LIVE

Carl's art | Helen Barrett Bright Idea Awards

Gut health | CF LIVE

Inside the lab, we chat with scientist Arthur Mitchell about his PhD studies in CF research

Genetic therapies | CF LIVE

What is Professor James Shaw working on? | CF WEEK 2023

CF diabetes: a message from a researcher | CF WEEK 2023

What does Professor James Shaw love about his job? | CF WEEK 2023

How do you get the genes into the cells? | CF WEEK 2023

Our experiences of campaigning for the Trust | CF WEEK 2023

How are genetic therapies different from medicines like Kaftrio? | CF WEEK 2023

Is gene therapy for everyone? | CF WEEK 2023

Q&A on genetic therapies | Research

Who could benefit from genetic therapies? | Research