🔥The 9th Round of Easy Loan, Earn $40 Reward is in progress❗️ ⏰ Promotion Period: January 15th - Feburary 15th, 2025 👉 Register now and check more details at gate.io/campaigns/358

What causes the immune system to turn against the body in lupus? Thanks to Dr. Deepak Rao’s pioneering work, just recognized as the 2025 Lupus Insight Prize recipient, we're closer to finding answers. In this video, he shares how his research is uncovering key drivers of immune

☀️✨ Happy #NationalSunglassesDay! Wearing sunglasses isn't just a style statement but also a crucial step in protecting your eyes! Exposure to UV light is harmful to everyone but can cause even more damage in people with #lupus. Remember to protect yourself year-round to

The Lupus Research Alliance honors the life and legacy of Margaret “Peggy” G. Dowd — former Co-President and Co-CEO, and a tireless champion for the lupus community for nearly 25 years. Her vision helped shape the future of #lupusresearch, and her impact continues. Read more:

📣 Research community! The LRA is soliciting applications for the 2025 Empowering Lupus Research Administrative Supplement. These “ELR Supplements” provide up to $30,000 for up to 2 years to promising trainees from varied backgrounds who reflect the communities and populations

✨ Up next in our #MyLupus series showcasing the unique stories of individuals in the lupus community, meet Brian Ung. ✨ Brian is a proud member of the Lupus Voices Council and lives with SLE, Lupus Nephritis, and Scleroderma. Diagnosed at 31, he understands the toll lupus can

Are you an early-career scientist or junior investigator committed to a career in rheumatology and lupus research? The LRA/RRF Empowering Lupus Research Partnership is now accepting applications for funding that supports innovative, transformative lupus research. This is your

🚨 Registration is now open! 🚨 Join us on October 18 for the LRA Virtual Walk with Us to Cure Lupuson Instagram Live! 👟 ✨Walk from anywhere, connect with our lupus community, and help raise funds for critical research. 🔗 Sign up today: bit.ly/WALK25-VIRTUAL

This #WorldSocialMediaDay, stay connected with the #LupusResearchAlliance. 🙌📲 Follow us across our social platforms and subscribe to receive emails on the latest updates on #lupusresearch. 🔗 Lupusresearch.org

Just heard the word “lupus” for the first time? It’s okay to feel overwhelmed, we’re here to help you make sense of it all – from information, symptoms to treatments and much more. Start learning: lupusresearch.org #Lupus #LupusAwareness #LupusResearch

July is recognized as UV Safety Awareness Month. Did you know about 50% of people with lupus develop a butterfly-shaped rash across the cheeks and nose, often triggered by sun exposure? ☀️ Because many with lupus are photosensitive, protecting your skin from the sun is

Happy 4th of July from all of us at the Lupus Research Alliance!

Fatigue, pain or swelling in joints, skin rashes and fevers could be signs of #lupus. Knowing these symptoms can be helpful in getting diagnosed. Understanding the symptoms is a powerful first step. Learn more about lupus and how you can help raise awareness in your community:

✨Support lupus research that changes lives. Lupus affects millions, yet research remains underfunded. Every contribution to the Lupus Research Alliance helps drive the discoveries we need for better treatments, and ultimately, a cure. 💜 Donate today and make a meaningful

🌟 Dallas, let’s do this! 🌟 Join us for the Lupus Research Alliance Walk with Us to Cure Lupus event on October 18 at Glencoe Park! Be part of a powerful community walking to accelerate lupus research, fund breakthroughs, and bring us closer to personalized treatments, and one

The Lupus Research Alliance and clinical affiliate Lupus Therapeutics are proud to be selected as strategic collaborators for the new life sciences investment firm, Vie Ventures. Learn more: bit.ly/4lNoh9Z

Living with lupus can mean navigating chronic pain, fatigue, and mental health challenges. But support, movement, and the right treatments can make a real difference. Read expert-backed tips in HealthCentral — including resources from the Lupus Research Alliance  — to help you

“What is lupus?” It’s a question we hear often - especially on #ChronicDiseaseDay 💜 Lupus is a chronic autoimmune disease where the immune system attacks healthy tissues, causing inflammation and damage in organs like the skin, joints, kidneys, and brain. It’s complex, often

#DidYouKnow, approximately 50%-90% of people with lupus identify fatigue as one of their primary symptoms. ☀️😴 Summer heat can sometimes also take a toll on your energy. On those warmer days, it’s important to listen to your body and prioritize your well-being. Whether that

As we enjoy the season, it’s the perfect time to gear up for our Fall Walk with Us to Cure Lupus events. 👟 Start a team, spread the word, and help raise critical funds for lupus research. Every step you take moves us closer to a cure. Be part of the movement: