Leukodystrophies are rare genetic disorders that mainly affect the white matter of the central nervous system. They are usually degenerative, causing symptoms such as impaired mobility, vision, speech and hearing, incontinence, inability to swallow and loss of cognitive skills. This often leads to a reduced or limited lifespan.

We support patients and their families by providing information, connecting affected people and campaigning for better educational services and research into treatments and early diagnosis to increase life expectancy.