The foundation aims to improve the quality of life of children suffering from Leukodystrophy. Fuelling this is the growing need to address the limited research towards the diagnosis and clinical treatment and this forms the core of our Foundation.
Our goals are:
1. Create awareness of pediatric white matter disorders and screening
2. Increase the quality of life to leukodystrophy children which includes working with affected families
3. Work together with researchers for the development of easier screening methods and to develop the clinical treatments