We use a cookie to remember charities you favorite on this device. It's only set if you accept — see our Privacy Policy for details.
£100k · Collected in 25
Founded
2024
Legal Status
CIO
We fund research with the aim of improving clinical management, developing treatments, and finding a cure for rare, terminal paediatric mitochondrial diseases, such as Alpers-Huttenlocher Syndrome. We raise awareness among the public and healthcare professionals through events and training and support affected families with information, services, resources, and financial aid.
Year ending 25
Europe