Vaccines and PKU 2024
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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.
The Adolescent Brain and PKU – are there any issues? This article was written by Claire Stephenson, a mum of […]
A downloadable photobook about savoury low protein alternatives is available here This book is kindly provided by the Birmingham Children’s […]
Here is a downloadable photobook about low protein sweets. This book is kindly provided by the Birmingham Children’s Hospital […]
Here is a downloadable photobook which covers drinks suitable for people with PKU – this has been developed and kindly […]
This is a 25 page photo book showing special low protein foods available on prescription Thank you to Anita MacDonald […]
This is a downloadable list of the low protein foods available on prescription for patients with PKU – last updated […]
This is a downloadable guide to the amount of low protein foods which can be prescribed for patients with PKU […]
Dietary Information Booklet : This booklet explains everything about the PKU diet
This is a 24 page downloadable list with examples of exchange free foods in 19 different categories. Thank you […]