Lupus Research Alliance

📢 Calling all Researchers! The Lupus Research Alliance is seeking nominations for the 2025 Lupus Insight Prize recognizing and honoring an outstanding investigator with a documented record of creativity and innovation who has made a novel research discovery in scientific domains relevant to lupus between 2020 and 2024. Nominations due: December 20, 2024 To nominate a colleague from academia or industry, please review the Request for Nominations. Learn more: https://bit.ly/LIP-2025 #Lupus #LupusResearch #LupusGrants #LIP

This August, as we recognize National Make-A-Will Month, take a moment to plan for the future. Crafting a will is a meaningful way to protect your loved ones and support the causes that matter to you. The Lupus Research Alliance is proud to partner with FreeWill, to offer you a simple, cost-free way to create or update your will. Learn more: https://lnkd.in/gaEZKjcV #MakeAWillMonth #EstatePlanning #PlanAhead

Thank you Kathleen Arntsen, Dave Arntsen, and Lupus and Allied Diseases Association, Inc. for all you do to support the community and lupus research! Proud to have been a sponsor of this year's Annual Lupus Charity Golf Classic.

Wherever you are across the globe, you can Walk with Us to Cure Lupus. Gather your friends, family, and team and let’s make an impact for lupus research! 👟 Join us on 10/19 for the 2024 Virtual Walk with Us to Cure Lupus. 🙌 Register now at bit.ly/walk-virtual2024 #LupusWalk #WalkwithUs #LupusResearch #ManyOneCan

August is National Hair Loss Awareness Month. ✨ Hair loss is a common symptom of lupus. In this video, hear how nine lupus champions describe their experiences with hair loss and hair thinning. 
 Share your experiences with hair loss. #NationalHairLossAwarenessMonth #lupus #symptomsoflupus #SLE #lupuscommunity 

🎉 Get ready, Dallas! The Walk with Us to Cure Lupus is happening on October 19 at Glencoe Park, and we can’t wait to see you there! Together, we’re pushing the boundaries of lupus research to find personalized treatments and, ultimately, a cure. 💜 Don’t wait—sign up today! https://lnkd.in/gzhpPKyW #WalkWithUs #ManyOneCan #LupusWalk #Lupus #LupusResearch #lupuscommunity

#ICYMI: Drs. Radic and Schett, recipients of the 2024 Lupus Insight Prize for their groundbreaking work in using CAR T cell therapy, share more about their research and how they hope it could potentially revolutionize lupus treatment. We eagerly anticipate the continued advancements that will improve outcomes for people with lupus. Watch the video to learn more from this year’s Lupus Insight Prize recipients! 🧬 #LupusResearch #CARTCELL #CARTTHERAPY #Celltherapy #LupusTreatments

📢 ✨ Make a difference and to #TakeItToTheDistrict for lupus research funding! Members of Congress are in their home districts this August, and your voice is crucial. Connect with your Representative this August at local town halls, personal meetings, and public events to advocate for: 🟣 $15 million for the Department of Defense's lupus research program 🟣 $51 billion funding for the NIH Together, let's ensure the final bill supports lupus research. Use our toolkit to guide your conversation and find supportive Representatives. Your advocacy can make a real impact! https://lnkd.in/g3he4eY2 #LupusAdvocacy #LupusResearchFunding #Lupus #LupusAwareness

Join us for National Kidney Foundation-led's Patient-Focused Drug Development Meeting on Lupus Nephritis! Share your input on living with #lupusnephritis, even if you can’t attend. Your feedback will shape the discussion. Survey responses are confidential. Learn more: https://lnkd.in/giQG7uCG #PatientVoice #KidneyHealth #Lupus #LupusResearch

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 in the comments ways you find helpful to manage stress. 👇