Find out how you can get involved with Cystic Fibrosis Trust and help to fight for a life unlimited by cystic fibrosis (CF) for everyone affected by the condition.
People with cystic fibrosis are fearing the financial cost of the coming winter months, reveal insights from Cystic Fibrosis Trusts’ frontline support services.
At Cystic Fibrosis Trust, we fund lots of amazing research – but how do we decide which projects to fund? That’s where our Research Grants Review Committee comes in, also known as the RGRC for short. The RGRC is a group of CF clinicians, researchers and people from the CF community who review applications for funding from the Trust and our partners. To find out more about the importance of CF community representation on the RGRC, we spoke to a few current members of the RGRC about their experiences.
Judy Ryan spent over 15 years supporting CF clinical trials in hospitals in Cambridge, retiring last summer. We spoke to her about the changes in CF care she’s seen over the years – and some of the highlights of her career
"Being a 41-year-old man living with cystic fibrosis, I am now able to look back over my lifetime and marvel at the progress made and the increased awareness of the condition." We chat to Simon about his journey with CF, his hopes for the future and the importance of being kind to yourself.
