A new global report using UK Cystic Fibrosis Registry data shows the number of people with cystic fibrosis (CF) who have become seriously ill or died from coronavirus (COVID-19) is low worldwide.
Gaming is a great way to connect with others, play the games you love and, increasingly, to raise vital funds that can provide people with cystic fibrosis (CF) with the support they need, when they need it most. Two gamers with CF will be starting a gaming challenge today, playing Pro Evolution Soccer for 24 hours to raise funds for the Trust.
The Trust’s Clinical Trials Accelerator Platform (CTAP) has received a £2.1 million funding boost from the Cystic Fibrosis Foundation (CFF) to help expand access to trials and accelerate the development of new treatments.
Dr Caroline Elston, Consultant Physician for King’s College Hospital Adult CF Centre, undertook one of the Cystic Fibrosis Trust’s Clinical Training Fellowship posts in 2006. Hear about her journey into CF care, and what her fellowship meant to her.
15-year-old Issy hasn't let cystic fibrosis or a broken leg come between her and Irish Dancing's World Championships in Glasgow, thanks to her fighting spirit, supportive family and a little help from the Nuffield Health CF exercise programme.
The Cystic Fibrosis Trust is partnering with Nuffield Health and cystic fibrosis (CF) centres across the UK to expand free access to gyms and health clubs and provide specialist one to one personal training to children and teenagers with the condition.
