Thank you Palm Beach for coming out to Walk to End Lupus Now. You have until July 5 to turn in your donations and help us reach our goal.
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Join us at Marlins Park for 2016 Walk to End Lupus Now! Come and spend your afternoon at the ballpark while helping us raise awareness!
Join us at Wickham Park for a fun afternoon while raising funds and awareness for those suffering from the cruel mystery of lupus.
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!
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The Lupus Foundation of America applauds the U.S. Senate Appropriations Committee for voting to pass the bill, which now moves to the full Senate for consideration.
Today, the Lupus Foundation of America announced results of a first-of-its-kind study that could expedite the delivery of new and safer therapies to people with lupus.
Losing your hair can be a scary side effect of lupus. Fortunately, there are many ways to tackle this issue and get back to feeling like yourself!
Lupus Now® editor Jenny Palter did one thing right and one thing wrong when it comes to sun safety and UV protection. Her story highlights the importance of not getting complacent when it comes to dealing with the symptoms of lupus.
Lupus organizations announce groundbreaking collaborative initiative to inform lupus drug development.