Cystic fibrosis (CF) is a condition that some people are born with. It mostly affects how the lungs (for breathing) and the tummy (for digesting food) work but can impact other parts of the body too.
Everyone’s body are made up of genes. People with CF have a gene which causes their body to make very thick and sticky mucus (like extra gooey slime).
This sticky mucus can:
Block the lungs, making it hard to breathe and causing lots of chest infections
Block the pancreas (a part of the tummy), so the body has trouble breaking down food and getting the goodness from it
How CF affects people:
It can be different for everyone
Some people with CF are more unwell than others
Doctors and nurses work together to help people stay as healthy as possible
Some signs someone with CF might have:
Skin that tastes very salty
A lot of coughing, sometimes with mucus
Frequent chest infections
Trouble breathing or feeling out of breath
Finding it hard to grow or gain weight, even if they eat well
Tummy problems, like difficulty in or unusual poo
In Ireland, quite a lot of people have CF, but there are special medical teams who help care for them and support them to live as well as they can. Cystic Fibrosis Ireland are also here to help people with CF in Ireland.