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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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For more information please contact:
Cathy Campbell - Founder
David P. Campbell Foundation for Pediatric Mitochondrial Disease Research 

Wish Upon a Cure
6661 Feather Drive,
Huntington Beach, CA
92648
info@wishuponacure.org


So Cal Benefit on Oct 8 brings attention to children diseases

Nation’s First-Ever Clinical Fellowship in Mitochondrial Medicine