With 41 chapters and 220 support groups in 32 states, the Lupus Foundation of America is the nation’s leading non-profit voluntary health organization dedicated to improving the diagnosis and treatment of lupus, supporting individuals and families affected by the disease, increasing awareness of lupus among health professionals and the public, and finding the cure. Research, education, and patient services are at the heart of the Lupus Foundation of America’s programs.

The LFA . . . .

• Provides direct support to researchers related to the diagnosis, treatment and cure of lupus

• Supports and stimulates a greatly increased public and private investment in medical research on lupus

• Promotes public information and education campaigns to increase knowledge and understanding of the disease

• Provides information, education and referral to individuals affected by lupus and their families

• Educates physicians and other health professionals about lupus