Are you aged between 13 - 17 years old and have PKU?
This event is for you!
Read moreJoin the Vitafriends team for a day that all the family can enjoy:
Read morePlaces are limited. Please secure you space by contacting
Tamsin Mann by 28th April 2023
Email: tamsinmann@vitaflo.co.uk
Text: 07595 070307
PKU explore™
6 Months - 5 Years
PKU squeezie™
6 Months - 10 Years
PKU cooler®
PKU express®
PKU express™ plus
PKU air®
3 Years+
PKU sphere ®
PKU sphere® liquid
ProZero™
Vitabite™
Mini Crackers
Mevalia Pane Casereccio
Mevalia Ciabattine
Mevalia Pan Carre
Mevalia Bread Mix
Mevalia Penne
Mevalia Fusilli
Mevalia Spaghetti
Mevalia Cookies
Mevalia Frollini
Mevalia Fruit Bars
Mevalia Chocotino
Mevalia Ditali
Mevalia Rice
It’s said that an average of one in ten thousand babies are born with the rare genetic condition, phenylketonuria (PKU). That’s the equivalent of just nine people in a full capacity Wembley crowd. Yet, despite extreme rarity, and against huge odds, my newly wedded wife, Nichola, and I - both diagnosed at birth - recently celebrated an ‘all PKU’ marriage. Now, with our big day existing only in our memories, these are our tips for organising a PKU wedding:
