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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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Facts about Mitochondrial Disease

YES! The David P. Campbell Foundation for Pediatric Mitochondrial Disease Research can count on my support!
Date
Name
Organization
Address
City
State
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Day Phone
Evening Phone
Email Address
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