Lupus low disease activity state (LLDAS) is an attainable and effective treatment goal for people with #lupus nephritis. Read the study: buff.ly/NJ70lSn

🚨💜 It’s the last day of #ResearchWeek! Match ends at midnight! This week, we shared Cassidy’s story. She grew up watching her mom live with #lupus — her story reminds us why predict & prevent research matters for millions. 🔬 Watch and give today: buff.ly/voEjMHA

We’re deeply saddened by the passing of Dr. Annette Shelby — a devoted advocate, supporter of lupus research, and cherished member of the LFA family. Her impact on lupus research will never be forgotten. Our condolences go out to Senator Shelby and the entire Shelby family.

⏰ Just hours left! Your chance to make 2X the impact for #lupus research ends at midnight. Your gift tonight can help unlock answers to devastating symptoms like relentless fatigue and serious pregnancy complications. 💜 Donate today: buff.ly/b4MlAWi #ResearchWeek

New study finds an association with Plaquenil use and early and long-term benefits on kidney function in people with #lupus nephritis. Read the study: buff.ly/lx9aKd4

💼 Today is the Anniversary of the Americans with Disabilities Act (ADA) — protecting the rights of people with disabilities in the workplace. If lupus affects your job, you can ask for changes like a flexible schedule or ergonomic tools. 💜 Learn more: buff.ly/AufXNA1

Here are July's top 20 Facebook birthday fundraisers! We’re so grateful for your impact and dedication. 💜 🎂 Got a birthday coming up? Celebrate with a Facebook fundraiser for the Lupus Foundation of America and help fuel research, support, and care: buff.ly/51War5e

☀️ Sunscreen plays a vital role in protecting your skin, especially for those with lupus. Aim for a minimum of 30 SPF and remember to reapply every two hours! Explore our resource for more information: buff.ly/iKACqWh

🚗 Have a vehicle you’re no longer using? Donate your car, truck, boat, or RV to the Lupus Foundation of America and help fund critical #lupus research, support programs, and resources. 💜 It’s an easy way to make a lasting difference. Learn more: buff.ly/QU8Avel

This #InternationalDayofFriendship, learn 7 steps to build and grow the support system essential for managing #lupus. 💜 It takes a community of friends and loved ones to provide emotional, physical, and spiritual support. Read our guide: buff.ly/uUf0UrZ

We’re proud to announce the appointment of Brad Rovin, MD, as Chair of our Medical-Scientific Advisory Council! His leadership will help shape the future of #lupus research, treatment access, and health equity. Read the full announcement: buff.ly/AqSzOBS

Jo hosted a fundraiser with friends to honor her best friend and support the fight against #lupus. With local businesses involved, it was a true community effort. Want to make your mark? Start your own fundraiser: buff.ly/rGNQszl