Following the U.S. Food and Drug Administration’s approval of Gazyva® (obinutuzumab) for the treatment of adults with #lupus nephritis, Dr. Brad Rovin, Chair of the Lupus Foundation of America’s Medical-Scientific Advisory Council and investigator in the REGENCY trial, shares what this milestone means for people with lupus. 🎥 Hear his insights and learn more in our new resource answering what you need to know about Gazyva: https://buff.ly/9CFUWAS | Lupus Foundation of America

🎥 Have questions about the new systemic lupus erythematosus (SLE) guidelines? Following yesterday's #ACR25 session, Dr. Lisa Sammaritano, rheumatologist at Hospital for Special Surgery and Principal Investigator for the American College of Rheumatology’s SLE Guidelines team, shared insights on what’s new, what’s changed, and how these updates will shape #lupus care moving forward. Watch the video and read more: https://buff.ly/nxiWOHq | Lupus Foundation of America

355 reactions · 183 shares | Lupus is a cruel mystery—but together, we can solve it. With RAY: Research Accelerated by You, people with lupus and caregivers can share their experiences on the Lupus Foundation of America's online patient registry and help researchers develop new treatments. Sign up today to be the solution to lupus! | Lupus Foundation of America | Facebook

From the onset of symptoms, it takes an average of six years to get an accurate lupus diagnosis. We’ll be with you every step of the way. Visit the National Resource Center on Lupus for more information about symptoms and treatment options. | Lupus Foundation of America

March is #AutoimmuneAwarenessMonth. Let's shed light on lupus, an autoimmune disease affecting millions worldwide. Common symptoms include extreme fatigue, joint pain, skin rashes, fever and more. Help us spread awareness this month by watching and sharing our brief video. | Lupus Foundation of America

Most symptoms of lupus aren’t often visible, but can affect every aspect of someone’s life physically, mentally and emotionally, relationships etc. Just because people can't see the impacts of lupus, doesn't mean they don’t exist - help us Make Lupus Visible this Lupus Awareness Month! | Lupus Foundation of America