Cystic fibrosis (CF) is often described as an invisible illness. As part of our #CFTruths ‘You don't see CF’ campaign we hear from Matt, who shared his experience of living with an invisible condition.
Applying for these benefits when you have an ‘invisible’ condition can be extremely challenging for people with cystic fibrosis (CF), especially since the rules for claiming PIP are notoriously strict.
Here Jake* shares his experience of switching from Disability Living Allowance (DLA) to Personal Independence Payment (PIP).
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.
