April 2023 marks 10 years since Personal Independence Payment, or PIP for short, was first introduced. Sangeeta, Welfare and Rights Advisor at the Trust, shares her reflections on this huge welfare reform and includes some of her tips for making your case stronger.
Elena - a Mental Health Nurse - tells us about her son Joshua’s cystic fibrosis (CF) journey, her training to climb Ben Nevis and Snowdon this year and her advice for other CF parents.
As part of our #CFTruths ‘You don't see CF’ campaign, Izzie, Content Lead at Cystic Fibrosis Trust, shares her experience of living with an invisible condition.
Cystic fibrosis (CF) is often described as an invisible illness. As part of our #CFTruths ‘You don't see CF’ campaign we hear from Siobhan, who shared her experience of living with an invisible condition.
Cystic fibrosis dominates thousands of lives every day. You never get a day off when you have CF. As part of our latest #CFTruths campaign, our supporter and volunteer Lian, whose son Henry has CF, shares what everyday life is like in their home.
Our amazing supporter Richard, 38, ran the TCS London Marathon for the Trust last year, and will be pounding the London pavements again at the 2023 event in April. Here he shares a typical Sunday of training, jobs, and spending time with family.
Ahead of the London Marathon this Sunday, we sat down with Colleen, mum to five-year-old Ewan, who has cystic fibrosis (CF), to hear all about him, her fundraising and how she’s feeling about the Marathon.
