Sumac speakes out for lupus with Bart Buchards and a trend of Thought in the background playing a version of Riviarra Parradise

The Lupus Research Institute is the only organization exclusively funding novel lupus research, casting a broad net to identify and support scientists with the brightest new ideas that have the potential to unlock the mysteries of lupus. Since its founding in 2000, the Lupus Research Institute has invested almost $20 million in novel lupus research, providing funding for 73 studies at 43 academic medical institutions in 22 states. To learn more about lupus and the Lupus Research Institute, visit www.lupusre

Comments With Dr. James Haney Presents*the Lupus Foundation, with AJones and RDavis, Part 2 of 3

Check out this 30-second public service announcement for the Lupus Foundation of America. Model Tomiko Fraser Hines narrates.

SLE Lupus Foundation Gala Video, 2006

The S.L.E. Lupus Foundation, headquartered in New York and with offices in Los Angeles, is one of the leading lupus organizations in the country providing patient services, education, public awareness and funding for lupus research. The Foundation vigorously addresses minority outreach through its Lupus Cooperative of New York—a community based national model demonstrating the effective management of chronic disease among minority women. To date, the Lupus Cooperativ

Candace Baptiste, a young woman living with lupus, speaks at the opening of the Lupus Cooperative of New York outreach center in Brooklyn, NY on June 15, 2007.

Lupus affects millions.

Individuals discuss the symptoms of lupus that have affected themselves, their friends and family members.

With nearly 300 chapters, branches and support groups in 32 states, the Lupus Foundation of America (LFA) is the nation's leading non-profit voluntary health organization dedicated to finding the causes and cure for lupus. Our mission is to improve the diagnosis and treatment of lupus, support individuals and families affected by the disease, increase awareness of lupus among

Lupus targets people of all age and ethnic groups. Individuals discuss the symptoms of lupus that have affected their friends and family members.

With nearly 300 chapters, branches and support groups in 32 states, the Lupus Foundation of America (LFA) is the nation's leading non-profit voluntary health organization dedicated to finding the causes and cure for lupus. Our mission is to improve the diagnosis and treatment of lupus, support individuals and families affected by the disease, increase awareness o

Lupus LA, the west coast division of the S.L.E. Lupus Foundation founded by renowned physician and author, Daniel J. Wallace, MD, serves the needs of people with lupus and their families in Los Angeles County and across southern California. Lupus LA raises awareness, conducts advocacy and community outreach, and supports novel lupus research on the national level. Visit www.LupusLA.org for more info.

This segment aired on the morning of Thursday, August 31, 2006.

Lupus affects millions.

Individuals whose lives have been greatly affected by lupus describe the suffering caused by disease and offer ways that you can help find a cure.

With nearly 300 chapters, branches and support groups in 32 states, the Lupus Foundation of America (LFA) is the nation's leading non-profit voluntary health organization dedicated to finding the causes and cure for lupus. Our mission is to improve the diagnosis and treatment of lupus, support individuals and families affected by the d

Information about lupus from real life lupus survivors. Very moving.

What happens when you know your child is sick, but no one can tell you what's wrong...sometimes for

The Lupus Research Institute is the only organization exclusively funding novel lupus research, cast

S.L.E. Lupus Foundation, 2007

For nearly 40 years, the S.L.E. Lupus Foundation has helped people wi