Are you a parent of a child up to the age of 18, who has PKU?
If so please take some time to help us collect evidence about the need for home monitoring of PKU, by doing this survey:
Helpline: 030 3040 1090 • Celebrating 50 Years and Counting!
The National Society for Phenylketonuria (NSPKU)
NSPKU is the only UK charity dedicated to improving the lives of people living with the rare condition PKU. Our goal is to support individuals and families living with Phenylketonuria across the UK.
