by | May 11, 2025 | Lupus Foundation of America
Having been diagnosed with lupus over 20 years ago, Kristine Falk occasionally had to call in sick to work due to her lupus symptoms. But on a fall day in 2011, she was off work for a different reason: to support her daughter, Kaz Brown, who was a sophomore playing in...
by | May 7, 2025 | Lupus Foundation of America
Lupus advocates from across the country gathered in Washington, DC for the National Lupus Advocacy Summit, held May 4-6. Hosted by the Lupus Foundation of America (LFA), the Summit is the largest lupus advocacy event in the nation, bringing together hundreds of lupus...
by | May 6, 2025 | Lupus Foundation of America
New data highlights urgent need for improved education and diagnosis of lupus nephritis (lupus-related kidney disease), a serious complication of lupusA global survey conducted by the World Lupus Federation reveals that 47% of people living with lupus report kidney...
by | May 1, 2025 | Lupus Foundation of America
New Lupus Foundation of America survey shines a light on cruel and mysterious disease during Lupus Awareness MonthA new survey commissioned by the Lupus Foundation of America (LFA) for Lupus Awareness Month in May, reveals that lupus remains mostly unknown and...
by | Apr 29, 2025 | Lupus Foundation of America, News & Events
A new literature review explores the emerging application of CAR-T cell therapy in treating people with Systemic Lupus Erythematosus (SLE). Preliminary data suggests that CAR-T therapy may significantly improve both serologic and clinical outcomes in people with SLE,...
by | Apr 29, 2025 | Lupus Foundation of America, News & Events
In a new study, researchers evaluated the potential relationship between disordered eating attitudes and nutritional status in women with systemic lupus erythematosus (SLE). The cross-sectional study consisted of 46 premenopausal women between the ages of 18 and 40...
