The LRA has launched the DREAM (Data Repository, Exchange and Analytics platforM), a cutting-edge knowledge-exchange platform for both researchers and people with lupus that aims to accelerate precision medicine. Learn more bit.ly/LRA-DREAM #Lupus #LupusResearch…

#LupusTherapeutics, the clinical affiliate of Lupus Research Alliance, looks forward to connecting with the world’s leading rheumatology experts at #ACR24. Tomorrow, visit Booth 2000 to learn more about groundbreaking #lupusclinicalresearch. 🔬Read more: lupusresearch.org/press_release/…

About half of people with lupus experience a “malar” rash or color change that may appear across the cheeks and bridge of the nose in the shape of a butterfly.       Hear from #lupus warriors in our community about their experiences with lupus and skin.…

Visit #LupusTherapeutics and LRA at #ACR24 Booth 2000 for updates on: 🔬Groundbreaking #lupusclinicalresearch 🩺Joining the #LupusTherapeutics Healthcare Provider Directory 🤝New #LupusTherapeutics collaborations and initiatives Read more: lupusresearch.org/press_release/…

Thank you to our incredible sponsors for making the 2024 Forum for Discovery possible! Your support empowers leading researchers to come together, share breakthroughs, and drive progress in #lupusresearch. Together, we’re making strides toward a brighter future for the…

This #NativeAmericanHeritageMonth, we spotlight in our #CommunityInspiration blog an extraordinary leader in health equity—Dr. Kent Kwoh. Dr. Kwoh is deeply committed to improving lupus care for Indigenous communities, where the disease disproportionately affects American Indian…

The LRA is excited to kick off its 2024 annual scientific conference, Forum for Discovery, in New York City! This scientific meeting serves as a pivotal gathering where leading LRA-funded researchers from across the globe convene to share their recent breakthroughs and exchange…

Anyone who is a current or retired federal, postal, or military employee can support the Lupus Research Alliance by making a pledge through the 2024 Combined Federal Campaign (CFC). This year’s #CFC campaign called #GIVEHAPPY launched on September 1st and ends January 15, 2025.…

✅ Pleasure and honor to be a Scientific Advisory Board member for the @LupusResearch Alliance, the WORLD LEADING non-profit health organization funding #Lupus research 💪 We are all meeting in NYC for 3 days of top-level #SLE discussions to fast-forward ⏩ lupus research 👍

It’s National Nurse Practitioner Week - A great time to acknowledge and give a huge THANK YOU to all nurses for their hard work being done today and every day to make a difference! 👩‍⚕️👨‍⚕️💜 #ThankYouNPs #NPWeek

Research Community! The LRA is soliciting Letters of Intent for the inaugural Mechanistic Clinical Award (MCA) to advance a precision framework for therapeutic development in #lupus. 📅 Intention to Submit (LOI) due: November 13, 2024 Apply now! bit.ly/RFA-MCA

Dallas, you truly rocked the Walk with Us to Cure Lupus event this year! 🙌 A big shoutout to everyone who joined us and raised funds for #lupus research, we are so grateful! If you couldn't be there, you can still experience the event through our photos: bit.ly/dallas-24

💜 Today, the Lupus Research Alliance launched DREAM—a new platform to advance lupus research! With secure data sharing for researchers & an engagement hub for patients, DREAM empowers the lupus community. Proud to partner with @lupusresearch & @lifebitai on this!…

🌟 Today we are very proud to announce @LifebitAI’s partnership with the @LupusResearch and working with @sanogenetics to establish DREAM, a secure data platform to enable lupus research and new treatments. 🌐 Powered by our Trusted Research Environment, DREAM will bridge data…

We’re thrilled to welcome @tamronhall back to host this year’s #BreakingThroughGala on Nov 25 at 7PM EST in NYC! 🎉 We appreciate her continued dedication to the #lupus community. Join us for an evening of breakthroughs in research and powerful stories of resilience. 💜 RSVP:…

Congratulations to Timothy B. Niewold, MD, FAACR, (@TimothyNiewold), Vice Chair for Research in the HSS Department of Medicine, who has been named among the recipients of the @LupusResearch Translational Bridge Award. lupusresearch.org/lupus-research… #HSSRheum

It’s #FertilityAwarenessWeek, and we’re shedding light on lupus and pregnancy. For so many women, especially those with an autoimmune disease, pregnancy can be complicated. In our special pre-recorded webinar, experts discuss the realities of family planning with lupus—covering…

The LRA is pleased to announce five recipients of the brand-new Translational Bridge Award, designed to translate groundbreaking research into potential treatments and diagnostics for #lupus. Read more about these exciting projects: bit.ly/LRA-TBA24 #LupusResearch…

📢 Calling all Researchers! @BreakthroughT1D , LRA, and the @mssociety have once again joined forces to identify common mechanisms of #autoimmunity. 🔬 These three leading autoimmune disease organizations are proud to launch the 2025 Common Mechanism in Autoimmunity Insight…

Living with #lupus can be challenging, and stress can be a common trigger for flares. Being mindful of stress levels and practicing relaxation techniques, staying active, and reaching out for support can help manage symptoms. Share ways you find helpful to manage stress.…