Cystic Fibrosis Trust
Cystic Fibrosis Trust is the charity uniting people to stop cystic fibrosis. Our community will improve care, speak out, support each other and fund vital research as we race towards effective treatments for all.
We won’t stop until everyone can live without the limits of cystic fibrosis. Join us.
Ella's story | CF Week 2025
Jane's story | CF WEEK 2025
Aiden's surf school: Aloha Kakou | Helen Barrett Bright Ideas Awards
The story behind the Helen Barrett Bright Ideas Awards
Chloe's story | For everyone
Autogenic drainage | Physio
Posture and cystic fibrosis | Physio
Pelvic floor health | Physio
OPEP (Oscillating Positive Expiratory Pressure) | Physio
PEP (Positive Expiratory Pressure) | Physio
Infant PEP and Percussion | Physio
Bubble PEP | Physio
Active Cycle of Breathing Techniques (ACBT) | Physio
Vicky talks about her sons' neurodivergence | Vicky and Aiden's story
What children told us about living with cystic fibrosis | Have your say
A round up of our 60th anniversary year
What young people told us about living with cystic fibrosis | Have your say
Ask YAG: Young people with CF answer parents' questions
Inside the lab with Issie | RESEARCH
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