We offer an extensive variety of programs, services and resources for people living with lupus, including family members, caregivers and other members of their support systems
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Join us for South Florida Walk to End Lupus Now at our new location at Marlins Park! Pease join us as we rally together to create awareness of lupus while raising funds to fight this terrible disease.
Join us for a fun afternoon as we raise awareness for lupus at our second annual Walk to End Lupus Now in Melbourne!
LFAFL’s Team No Lupus program is an opportunity for individuals and teams to increase awareness of lupus and raise funds for a cure. Members can walk, run, ride or swim in the event of their choice while making a difference in the lives of over 100,000 people living with lupus in Florida! Every step you take and every dollar you raise supports the Lupus Foundation of America and its efforts to solve the cruel mystery of lupus.
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Under Investigation: Preventive care on the horizon
Not all patients who share a certain organ involvement can be treated with the same medicine at the same dose. In this piece, Foundation Medical Director Dr. Joan Merrill argues that improved classification of lupus can lead to better treatment.
Off-label drugs for the treatment of lupus symptoms represents the standard of care for people with lupus, but current regulations make it difficult for doctors and manufacturers to communicate. Read Sandra C. Raymond's remarks now.
Results from a study of epratuzumab were released today. It did not meet its primary endpoint of clinically reducing the severity of lupus in people with mild to moderate disease. The following is a statement from Sandra C. Raymond, President and CEO