The Isabelle Lottie Foundation was formed in February 2014 by the family and friends of Isabelle following her diagnosis and treatment for Medulloblastoma. Izzy was just two when she was diagnosed, and she and her family have since embarked on a life-changing journey through diagnosis and treatment.

 

From the family's experience, the aim of The Isabelle Lottie Foundation is to support children and their families following the diagnosis of a brain tumour and also to campaign for a better understanding of the early signs of brain tumours in children and young adults across health professionals and people who work with children including parents.