When Pippa Kent received her double-lung transplant last year, she was also given a list of foods that she could no longer eat because of the new drugs she was taking to keep her lungs working. Taking these new restrictions in her stride, Pippa is raising money for her cook book, ‘Now What Can I Eat?’ which will be full of recipes suitable for people taking immunosuppressant drugs. Read on to find out more.
We met with artist Kate Hughes at her new exhibition ‘Island Collaborations’, an art project exploring the environment of people with cystic fibrosis (CF) staying on Foulis Ward at Royal Brompton Hospital in London. Kate, who has CF, collaborated with other people who had stayed on Foulis Ward to create beautiful images, sounds and animations that represent a stay in a typical room on the ward.
After a significant few weeks David Ramsden, Chief Executive at the Cystic Fibrosis Trust, discusses the latest developments in life-saving drugs and how you can help to keep cystic fibrosis (CF) at the top of the political agenda.
Make your fundraising event even more special by using our materials to help you spread the word about CF, ready to use materials to print out at home, and editable materials to give your event a personal touch.
Find out how to include a gift in your Will to the Cystic Fibrosis Trust that could have an incredible impact on the lives of people with cystic fibrosis (CF) and their families.
Caitlin has been on a clinical trial for a modulator therapy for the past three years at Leeds Hospital. Find out about her experiences in taking part in a clinical trial and what her hopes are for cystic fibrosis being represented in the media.