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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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YES! The David P. Campbell Foundation for Pediatric Mitochondrial Disease Research can count on my support!

Please make a Donation

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I would like to become a founding member of the Wish Upon a Cure Society:
Sponsor a Mitochondrial Child: $1,000 per year for 5 years
Sponsor a Clinic Day of Mitochondrial Children: $25,000 per year for 5 years
Endow a Fellowship in Mitochondrial Medicine:$20,000 (to be paid over years)
I would like to contribute in other ways:
Contribute $ for years
Please contact me. I have other thoughts to share
PAYMENT:
My check is enclosed, made payable to: OCCF/David P. Campbell Foundation
Please charge my Visa/MC
Visa/MC# Exp:
Please contact me about paying my pledge with stock
My company will match my gift.
We will bill you every November for your annual pledge unless you request otherwise:


If you feel uncomfortable submitting this information over the Internet Please print out this page and mail it to: Attn: Marylou Biddiscombe David P. Campbell Foundation for Pediatric Mitochondrial Disease Research 6661 Feather Drive, Huntington Beach, CA 92648