The first animation of the Kans for PKAN Children foundation is a fact! It premiered on Rare Diseases Day 2020, February 29th, 2020. The animation dwells on information that is needed when you as parents have just heard the diagnosis PKAN for your child. In the future, a number of animations will follow, on topics that are important when your child has PKAN. It will cover medical topics, but also what it means for the brothers and sisters. The animations will also be translated in English, for worldwide usage. If there are topics that you want to see, email us at! The animation was made by Henk Visser of DigiEmotion and the beautiful voice is by Marlies Zomers. Animation 1: “After the Diagnosis”