Congratulations on your new baby!

We understand that a diagnosis of phenylketonuria (PKU) can be very difficult. There is a lot to think about and you need to take it one step at a time. We are here to help.

In this short film, produced by parents and friends of children with PKU, we answer some of the questions you might have.

[FILM]

If you would like to talk to someone, call our helpline or send an email.

We produce a New parent pack which you should have received on your early clinic visit. If you haven’t received one let us know.