Our Mission
'To become the leader in
providing camping, sports activities, and education
program opportunities for all children and young adults
with heart disease or a history of heart disease'.
Our Organization
EXECUTIVE & ADVISORY BOARD
Lisa Knight, RN Executive Director &
Co-founder
Kevin Shannon, MD Medical Director & Co-founder
Glenn Knight, CRM CEO-Board Member
Tom Klitzner, MD, Ph.D. - Board Member
Bill Cabeen, MD - Board Member
Janene Hogan - Board Member
Michael Paseornak - Board Member
Mark Plunkett, MD Medical Advisory Board
William G. Stevenson, MD Medical Advisory Board
John R. Shiner, Esq. - General Consul
Camp del Corazon Inc. is a 501(c)(3) Non-profit
corporation, providing a free of charge summer camp for
children with heart disease. All proceeds are spent on
the camp, and it's programming, and staffed entirely by
volunteers.
Founded
in 1995, Camp del Corazon was the first medically
supervised free camp specifically for children with
heart disease in the Western United States. We remain
the largest camp of our kind on the West Coast.
Since its inception, camp has grown
from one weekend session of 49 campers to three 5-day
sessions now accommodating approximately 400 campers
each year.
Camp del Corazon is fully accredited by
the American Camping Association.
Camp del Corazon is a 501(c)(3) non-profit
organization funded entirely by grants, fundraisers and
private donations.
All programs are staffed entirely by
volunteer doctors, nurses and counselors.
The camp features a fully-equipped infirmary
and sick campers can be transported by boat or
airlifted, to the mainland quickly and safely while at
Catalina Island, and all local authorities are on
medical alert standby while camp is at the Malibu site.
Camp del Corazon has created additional
programs which offer new and exciting opportunities for
children living with heart disease such as a Tall Ships
Program and a Mammoth Mountain Snow Weekend.
Camp del Corazon has created a PACE Program for
young adults ages 18-25 who are going thru transitional
changes into adulthood. The PACE Program consists of
weekend retreats with peers and mentors to address the
issues of living as an adult with congenital heart
disease.
The American Heart Association funds a yearly
Family Symposium which provides an opportunity for
families to learn from experts in the field of Pediatric
and Congenital Cardiology.
Our Family Symposium also creates an
environment for families to network and share stories
and seek advice from others dealing with similar issues
and for the siblings to share in our programs.
Lisa Knight, RN, Executive Director
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