Losing a child is indeed one of the hardest things on
Cathy and Dan Campbell created the David P. Campbell Foundation
for Pediatric Mitochondrial Disease Research in memory
of their son, wanting to transform their suffering into
hope for others.
Their wish is that through David’s struggles and courage,
we can advance awareness of mitochondrial diseases so that
other children and their families will not have to suffer without answers,
as they did.
|The Foundation’s mission is to:
||Raise national Awareness of this orphan disease
class so that appropriate
||Research and funding will come to mitochondrial diseases,
with the goal of finding a
||Cure in our lifetime.