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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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Would you like to receive updates on the progress we make in fighting mitochondrial disease? We’ll send you our twice-yearly newsletter and any critical updates on the fight to cure these diseases.
Just click on “Contact Us” and email us your name, address and email, and we’ll make you a part of the family and send updates directly to you.