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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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Share your story...
Do you have a similar story as ours? We'd love to hear from you and would be glad to share your story along with ours. The more people that know about this disease the more we can get focus on finding a cure.
Please provide your story but don't worry as we will contact you and then we can gather pictures as well as any other information to properly complete your story.