The Lupus Foundation of America (LFA) is excited to announce Karen Costenbader is the recipient of the LFA’s 2024 Predict and ...

The unpredictability of lupus can be overwhelming at times, especially when attempting to navigate a maze-like healthcare system. It is important to know how to self-advocate by knowing your rights ...

Use your power! Find your walk and register your team today. Fundraise We provide you with all the tools you need to fundraise for lupus research, support and education services all while earning ...

Neuropsychiatric systemic lupus erythematosus (NPSLE), or central nervous system lupus, can be challenging to diagnose ...

The U.S. Food and Drug Administration (FDA) has placed a clinical hold on Kezar Life Sciences’ zetomipzomib, an ...

Drug-induced lupus is more common in men because they are given these drugs more often; however, not everyone who takes these drugs will develop the disease. Specific criteria for diagnosing ...

New study finds that Black children and those identifying with more than one race have higher disease activity and are less likely to achieve low lupus disease activity state compared to White ...

A support group is a gathering of people facing common issues to share what’s troubling them. Through the sharing of experiences, they can offer support, encouragement, and comfort to the other group ...

Annually, we detail our impact as we move ever closer to cure lupus and bring relief and help to millions. We take seriously our responsibility to the lupus community. Our mission is to END LUPUS. Now ...

Learn the many different ways you can support people with lupus and fund vital research. Click here to make a one-time gift, tribute gift, or monthly recurring gift. Donate By Mail Click here to ...