Helpline: 030 3040 1090 • Celebrating 50 Years and Counting!

Facebook
Twitter
Instagrame

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.

MENUMENU

Home
About PKU
Living With PKU
- - - Throughout Life
    - New diagnosis of PKU?
    - During childhood
    - As a teenager or young adult
    - As an adult
    - During and after pregnancy
  - - Advice and Guidance
    - School and Nursery
    - Holidays and Travel
    - Living with PKU – Claiming Benefits
    - Blood test advice
    - Carers of people with PKU
    - FAQ’s
  - - Treatments
    - Clinical centres for PKU
    - Dietary Information
    - Non-Dietary Treatments
    - Untreated or late treated PKU
  - - Other information
    - Useful Documents
    - Useful Links
Get involved
Research
About us
Documents
News
Contact us
DHPR Deficiency

Baby Weaning Choices

Version
Download 1702
File Size 2 MB
File Count 1
Create Date 01/07/2020
Last Updated 01/02/2024

Download

Description

A guide to low protein choices during different stages of weaning - this has been developed and kindly shared by Anita MacDonald and the team of metabolic dietitians at Birmingham Children's Hospital.

Share on Facebook

For more information use our Contact page or helpline: 030 3040 1090

For PKU Unplanned Pregnancy Emergency Advice please contact your local centre.

You can also use our documents library to access lots of important information

THE NATIONAL SOCIETY FOR PHENYLKETONURIA (UNITED KINGDOM) LIMITED is a charity
registered with the Charity Commission (Company No. 01256124 Charity No. 273670 )

We use cookies to ensure that we give you the best experience on our website. If you continue to use this site we will assume that you are happy with it.