This guest blog was contributed by Dr Jill Edwards, School of Healthcare, Leeds University.
When I was born I was not expected to live long enough to go to school, but a few months ago I celebrated by my 50th birthday. I have cystic fibrosis (CF).
Ageing with CF is now a reality for many people with the condition (nearly 9,000 in the UK). Most people with CF used to die before they became adults, but now there are more adults than children with this disease. And over the last 30 years, the life expectancy of people with CF has increased drastically, with a median age of survival ranging between 35.9 and 48.1 years. More and more people with CF are now likely to face ‘old age’, yet it is not known how prepared we are.
Cystic fibrosis is a serious, inherited, long term condition. A fault in a gene prevents salts (sodium and chloride) from passing in and out of cells in the body properly. This results in the production of thick, sticky mucus in organs. To be born with CF a baby must inherit two faulty genes, one from each parent. Continue reading “Guest blog – A new ageing population: People with Cystic Fibrosis”