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

Author: Iain Williamson

AGM 2023

01/10/202312/12/2023 Iain WilliamsonLeave a Comment on AGM 2023

NOTICE TO GUARANTOR MEMBERS OF THE SOCIETY Notice is hereby given that the 50th Annual General Meeting of the National […]

News

Search for:

AGM 2023

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