What Is Cystic Fibrosis?
Cystic fibrosis 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.
The RACH Respiratory Team
At RACH we have a team of specialists in respiratory conditions, including paediatric consultants and specialist nurses.
Contact Details
Karen Brown
Respiratory / Cleft Team Lead
Royal Aberdeen Children’s Hospital
Tel: 01224 552725
Mobile: 07971 505065