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Our mission
is to improve the quality of life for all people affected by Lupus and
to promote efforts for the diagnosis, treatment, prevention and cure of
Lupus.
The Lupus Foundation
of Colorado, Inc. (LFC) was established in 1972 for the purpose of
providing support, education and training to everyone that is affected
by the disease of Lupus. Our programs and services are designed to assist
people with Lupus and their family and friends in dealing with the frustrations
that may be encountered daily, living with a challenging and chronic illness.
When a person inquires about Lupus, we respond immediately, realizing
our job is to address the concerns, fears, and lack of knowledge about
Lupus. We also strive to bring community awareness about the disease and
the programs the Lupus Foundation of Colorado offers. Both awareness and
education can be the key to saving lives.
Our Board of Directors
is comprised of professionals many of whom have a direct relationship
with Lupus. Their hands-on work to benefit the foundation is critical
to the success of our work. The Health Advisory Board includes physicians
representing different specialties who treat people with Lupus.
Our staff consists
of a Chief Executive Officer, Director of Development, Director of Community
Programs, Data Base Manager, and Office Manager as well as valued volunteers
who all help make a difference in the lives of people living with Lupus.
| Skip
Schlenk, CEO |
| Debbie
Lynch, Director, Development and Administration |
| Gayna
Warren, Office Manager |
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