Cure Mito Foundation
The Cure Mito Foundation is a patient-led advocacy organization focused on Leigh syndrome and other mitochondrial diseases. It unites the global Leigh syndrome community to accelerate patient-centered research, treatments, and cures, operates the largest Leigh syndrome patient registry (400+ participants across 40+ countries), and provides resources and support to affected families worldwide.
About Us
Our Mission
Uniting the global Leigh syndrome community to accelerate patient-centered research, treatments, and cures.
Our Values
Community. Commitment. Urgency.
Contact Information
Conditions We Support
Other Rare Disease
- Leigh Syndrome
Genetic Disorders
Supportive Care
CNS (Central Nervous System)
If you've been diagnosed with any of these conditions, we're here to help.
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