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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We're asking YOU to design our 2016 Walk to End Lupus Now t-shirts to be worn by Walk participants all across the country.
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.
Latest News See all stories >
The Lupus Foundation of America research grants will support important studies on immune cells, pediatric lupus, stem cells, biomarkers, and environmental triggers of lupus.
A new Congressional report includes an article contributed by the Lupus Foundation of America on health disparities among people with lupus and current efforts to improve treatment and diagnosis in minority communities.
It is important that those with lupus receive a flu vaccine as soon as they are available. Sarah Stothers, RN, BS, provides an update for the 15-16 flu season.
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.