This is the MySpace group for the S.L.E. Lupus Foundation. Our members represent the Voices of Lupus -- the more than 1.5 million Americans affected by this devestating disease. We are spreading awareness and supporting research that will one day realize our dream of a "life without lupus."

Visit www.LupusNY.org - the website of the S.L.E. Lupus Foundation - for the latest information on lupus research, education programming, support services, and more!

With headquarters in New York City and offices in Los Angeles, the S.L.E. Lupus Foundation is one of the nations leading lupus organizations. It provides patient services, education, public awareness, and funding for lupus research.

Founded in 1970, the Foundation helps people with lupus, as well as their families and friends, cope with the anxieties and frustrations that often accompany daily living with a chronic illness. Sharing information and networking among patients and their families further helps dispel myths and provides daily support to those learning to live with lupus. We invite you to take full advantage of our comprehensive resources.