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ABOUT US
The Foundation is named for David Campbell, a red-headed, blue eyed little boy. who, at three and a half years old, died from a mitochondrial disease called Leigh's Syndrome.
Our Vision
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Goals
We are on a Search & Rescue Mission for Mitochondrial Disease!
We are searching for stopgap therapies to treat the symptoms of these diseases.
We want to rescue mitochondrial disease from the depths of the unknown:
- Demystify mitochondrial disease through national awareness efforts.
- Create patient support mechanisms to help patients and parents learn how to manage the disease and delay its effects.