With your support, we have provided laptops so that people can work from home and hospital, we’ve funded training courses so that people can qualify in areas that allow them to work flexibly around their health commitments.
We’ve donated to people’s honeymoons and family holidays so they can create incredible memories that will stay with them and their families forever.
We recognise that life with Cystic Fibrosis is tough beyond words and will consider each and every application we receive.
Katie suffers from Cystic Fibrosis and sadly lost her brother and cousin to the same condition. Her mother then had a stroke which left her completely dependent on Katie.
At the same time as caring for her mother and managing her own condition, Katie was completing a PhD about the educational experiences for children and young people living with Cystic Fibrosis.
We encourage our applicants to tell us what would make their lives a little easier and in this instance we were asked to provide some relaxation time at a spa – we were happy to oblige!
