The School and Cystic Fibrosis publication aims to provide information about all aspects of Cystic Fibrosis (CF) and its implications at school.

It is intended to provide information:

• For teachers who may have little or no experience of children with CF and their needs
• For parents whose children with CF are just starting school, changing schools or have a new teacher
• For parents of children with CF who find they need additional support and information as their children progress through primary and secondary school.

At the outset, it is important to understand that every child with CF is different and there are different degrees of CF severity and symptoms associated with the condition. It is crucial that a parent or teacher has a solid comprehension of the medical status and day-to-day needs of a child with CF.

Download your copy of the School and Cystic Fibrosis booklet below