There's no cure for cystic fibrosis, but a range of treatments can help control the symptoms, prevent or reduce complications, and make the condition easier to live with.
Regular appointments to monitor the condition are needed and a care plan will be set up based on the person's needs.
People with cystic fibrosis are treated by a team of healthcare professionals. Sometimes the condition will require treatment in hospital.
People with cystic fibrosis may need to take different medicines to treat and prevent lung problems. These may be swallowed, inhaled or injected.
Medicines for lung problems include:
Any kind of physical activity, like running, swimming or football, can help clear mucus from the lungs and improve physical strength and overall health.
A physiotherapist can advise on the right exercises and activities for each individual.
A physiotherapist can also teach techniques to help keep the lungs and airways clear.
Eating well is important for people with cystic fibrosis because the mucus can make it difficult to digest food and absorb nutrients.
The pancreas often doesn't work properly, making it even harder to digest food.
A dietitian will advise on how to take in extra calories and nutrients to avoid malnutrition.
They may recommend a high-calorie diet, vitamin and mineral supplements, and taking digestive enzyme capsules with food to help with digestion.
The Cystic Fibrosis Trust has information on eating well with cystic fibrosis and nutrition advice factsheets for adults and children.
In severe cases of cystic fibrosis, when the lungs stop working properly and all medical treatments have failed to help, a lung transplant may be recommended.
A lung transplant is a serious operation that carries risks, but it can greatly improve the length and quality of life for people with severe cystic fibrosis.
The Cystic Fibrosis Trust has information on lung transplants in cystic fibrosis.