The AKU Society is a patient-led group for the debilitating genetic disease alkaptonuria (AKU). It is designed to unite all people affected by AKU: patients, their families and their doctors.

Our aims:

Support AKU patients, their families and their caregivers
Provide reliable, up to date information about AKU
Raise awareness of AKU
Research into the causes, effects and treatments of AKU
Bring together all the resources needed to find a cure for AKU

Here at the AKU Society, we're in urgent need of supporters. You will help us by raising money, but you're also guaranteed to have a brilliant time doing it. Previous fundraisers have done everything from obstacle races to Marathons.