Cystic fibrosis

Cystic fibrosis (also known as CF) is an inherited condition in which the lungs and digestive system can become clogged with thick, sticky mucus. It can cause problems with breathing and digestion from a young age. Over many years, the lungs become increasingly damaged and may eventually stop working properly.

Most cases of cystic fibrosis in the UK are now identified through screening tests carried out soon after birth. It's estimated that 1 in every 2,500 babies born in the UK has cystic fibrosis.

A number of treatments are available to help reduce the problems caused by the condition, but unfortunately average life expectancy is reduced for people who have it.

For more information about cystic fibrosis and support offered, visit the Cystic Fibrosis Trust

• HOW WE HELP PATIENTS
• The story behind the image
• From mountainside to bedside
• Learning from life at the limits
• Acute mountain sickness, HACE and HAPE
• Acute Respiratory Distress Syndrome (ARDS)
• Blue Baby Syndrome
• Congenital heart disease
• Cystic fibrosis
• Chronic obstructive pulmonary disease (COPD)
• Oxygen deficiency
• Sepsis/septic shock
• Information about ICU and support offered