Cure Mito Foundation

We are a leading patient advocacy organization dedicated to advancing research on Leigh syndrome and empowering families affected by this devastating mitochondrial disease. Our mission is to unite the global Leigh syndrome community to accelerate patient-centered research, treatments, and cures. We fund critical research and offer comprehensive resources for the community, including the Leigh Syndrome Global Patient Registry, an educational website (AboutLeighSyndrome.com), a directory of healthcare providers, our annual virtual Leigh Syndrome Symposium, support tools for families, and opportunities for free genetic testing, among other initiatives. Your donation is 100% tax-deductible and goes directly toward research dedicated to mitochondrial diseases. You can learn more at our website: You can donate at: You can learn more about Leigh syndrome global patient registry at: