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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.

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Facts about Mitochondrial Disease

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.
But, ultimately, we want to help find a cure for children and adults who suffer from any mitochondrial disease.