About Lupus LA

Lupus LA, a non-profit health organization, was founded in 2000 by a concerned group of lupus families spearheaded by Daniel J. Wallace, MD, attending physician in the Division of Rheumatology at Cedars-Sinai Medical Center and a clinical professor of medicine at UCLA’s David Geffen School of Medicine. Lupus LA serves the needs of people with lupus and their families in Los Angeles County and across Southern California. Lupus LA has a full-time staff of five and an annual operating budget of $1.5 million.

Lupus LA raises funds for its patient programs, local rheumatology fellowships and research partners at the Lupus Research Institute (LRI) and the Alliance for Lupus Research (ALR). Since the year 2000, Lupus LA has raised over $10,000,000 dollars for the cause, primarily through special events – the LA Marathon, the Orange Ball, Get Lucky for Lupus LA Celebrity Poker Tournament, and the Hollywood Bag Ladies Luncheon.

Raising awareness is also an important part of the Lupus LA mission. While lupus is widespread, awareness and accurate knowledge about it are lacking. Research shows that although 1.5 million people in the U.S. have lupus, nearly two-thirds of the public knows little or nothing about the disease. In fact, more Americans have lupus than AIDS, cerebral palsy, multiple sclerosis, sickle-cell anemia and cystic fibrosis, making it one of this country’s most prevalent medical problems. In Los Angeles County alone, there are over 60,000 people suffering from lupus.

Lupus LA raises awareness through events along with extensive local, regional and national media coverage – in print and on TV, radio and the Internet. This is made possible through the support of Hollywood – both celebrities and industry executives.