Update on availability for sapropterin for PKU
NHS England has today (17 December 2021) announced that it will make the medicine sapropterin for PKU available to […]
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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.
NHS England has today (17 December 2021) announced that it will make the medicine sapropterin for PKU available to […]
NICE recommendations about sapropterin (Kuvan). What they mean for patients with PKU: Who is NICE and what has […]
Who is NICE and what are they doing? NICE is the “National Institute for Health and Care Excellence”. It […]
This survey is for children aged 18 or under (the carer/parent or guardian to complete) and the survey is about […]
This survey is for everyone with PKU aged over 18 (or their carers, parent or family member) and the survey […]
In 1951, Sheila Jones was the first person in the world to be treated for Phenylketonuria (PKU) at Birmingham Children’s […]
In 1951, Sheila Jones was the first person in the world to be treated for Phenylketonuria (PKU) at Birmingham Children’s […]
Click here to down load the list: NSPKU_Branded_Exchange-free_A4_5 This is a list giving examples of foods in 20 […]
CONSIDERATIONS FOR PEOPLE LIVING WITH PKU People living with PKU may be concerned about the impact of Coronavirus (COVID-19) and […]