Parents and children
The early years of a cystic fibrosis (CF) diagnosis can be complex, but we're here to support you every step of the way.
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Newborn diagnosis
We understand that a new diagnosis of cystic fibrosis (CF) can be very difficult, and there's a lot for you and your family to think about. We are here to help.
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Early years
Children's early years are really important for their development.
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Pre-school and primary school
Starting pre-school or primary school can be an exciting and daunting time for parents, particularly if your child has cystic fibrosis (CF).
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Secondary school
We have information for parents and young people to help prepare you all for the move to secondary school, and resources to help teachers support their students with CF.
My friend has CF
Here, young people can find out more about the condition and how they can support their friends or people in their class who might have it.
CF youth
Are you a young person with CF, or close to someone with the condition? We have loads of events, support and opportunities for you to get involved with!
How is CF diagnosed?
Find out more about cystic fibrosis (CF) diagnosis, including the processes of newborn screening, carrier testing and diagnosis in adulthood.
Page last reviewed: October 2024
Next review due: October 2027