About us
Our vision is for a world in which every mitochondrial disease patient has a voice and access to treatment, support to improve their life and, ultimately, a cure.
helps us provide our ‘Guide to Mito’ to newly diagnosed families
supports cutting-edge research into rare mitochondrial diseases
helps fund family access to support weekends so no one faces mito alone
monthly
means a family can reach out to someone who understands
monthly
funds our virtual coffee mornings to create a community for patients
monthly
helps build the new UK Mitochondrial Disease Research Institute
