Lupus Research Alliance

What an incredible day at the LRA Walk with Us to Cure Lupus — thank you to our incredible walkers, volunteers, sponsors, staff, and the entire lupus community who joined us in New York, Dallas, and Virtually! Your energy and support drive lupus research forward, bringing us closer to more personalized treatments and a future free from lupus. We couldn’t do it without you! ✨💜🙌👟 #LupusWalks #LupusResearch #LupusCommunity #WalkWithUs #Lupusawareness #Lupus

👟🙌☀️ Today’s the day! We can’t wait to see everyone at the LRA Walk with Us to Cure Lupus! Whether you’re in NYC, Dallas, or joining Virtually, let’s come together as a community to celebrate, raise awareness for lupus, and take steps toward better treatments and, ultimately, a cure. Every step you take makes a difference! 📍 NYC – Intrepid Museum Check-In & Festivities: 8:00 AM ET Walk Begins: 9:30 AM ET (Note: Other walks/marches in NYC may affect travel; please plan accordingly.) 📍 Dallas – Glencoe Park Check-In & Festivities: 9:00 AM CT Walk Begins: 10:00 AM CT 💻 Virtual – LRA Instagram Live: 9:30 AM ET 📸 Don’t forget to share your photos and tag us—we can’t wait to see your moments! 👉 It's not too late to register! lupuswalks.org #LupusWalks #LupusResearch #Lupus #WalkWithUs #ManyOneCan #LupusCommunity

💫 👟Tomorrow is Walk Day! Join Stephanie and the lupus community on October 18 for the LRA Walk with Us to Cure Lupus!   📍 NYC: Intrepid Museum (Please note that we are aware of other walks and marches taking place in New York City on Walk Day, which could make commuting more difficult. We recommend all participants plan accordingly and allow extra time) 📍  Dallas: Glencoe Park 💻 Virtual: Instagram Live Every step counts, and if you can’t #walkwithus, you can still make a difference by donating. 👉 It’s not too late to sign up or give! lupuswalks.org    #WalkToCureLupus #LupusAwareness #LupusWalk #LupusWarriors #LupusResearch #LupusResearchAlliance

Join us in just 2 days for the LRA Walk with Us to Cure Lupus — happening October 18 in NYC, Dallas, and Virtually! ✨🎉 📍 NYC: Intrepid Museum (Please note that we are aware of other walks and marches taking place in New York City on Walk Day, which could make commuting more difficult. We recommend all participants plan accordingly and allow extra time) 📍 Dallas: Glencoe Park 💻 Virtual: Instagram Live Every step will help advance life-changing lupus research and bring us closer to more personalized treatments and a cure. 👉 To register and for more information visit our website: lupuswalks.org #LupusResearch #WalkWithUs #LupusWalk #ManyOneCan #LupusCommunity

Preventing joint pain caused by lupus is just one reason why we are so committed to funding the world’s most innovative science that can lead to promising treatments. Listen to the stories of nine lupus warriors describe their joint pain. Watch now! #lupus #lupusresearch #jointpain #symptomsoflupus #BoneJointWeek #BoneAndJointActionWeek

People living with autoimmune diseases often face fatigue, flares, and uncertainty, which can make physical activity feel daunting. Dr. Saira Sheikh, Chair of the Lupus Clinical Investigators Network (LuCIN) overseen by #LupusTherapeutics the clinical affiliate of the Lupus Research Alliance, underscores why movement should be guided by self-awareness and flexibility — not pressure. Her perspective in WebMD bridges the gap between research and real-life experience, empowering patients to find what works for them. 🔗 Explore more: https://lnkd.in/g2JbCTRR #Lupus #LupusResearch #AutoimmuneDisease

Self-advocacy is powerful — especially for women navigating autoimmune disease. In HealthCentral Corporation, Dr. Diane Kamen, a member of the Lupus Clinical Investigators Network (LuCIN) overseen by #LupusTherapeutics the clinical affiliate of the Lupus Research Alliance, shares how tracking symptoms and speaking up can help in the path to diagnosis. These tips and resources are incredibly important as 90% of people living with lupus are women. 🔗 Learn more here: https://lnkd.in/gbckN7Ed #Lupus #LupusResearch #WomensHealth #AutoimmuneDisease

¡Haz que cada paso cuente! Este sábado, 18 de octubre, únete a nuestras caminatas y ayuda a marcar la diferencia para la comunidad de lupus. 📍Dallas: Glencoe Park 📍 NYC: Museo Intrepid (Tenga en cuenta que somos conscientes de otras caminatas y marchas que se llevarán a cabo en la ciudad de Nueva York el día de la caminata, lo que podría dificultar el transporte. Recomendamos que todos los participantes planifiquen con anticipación y consideren tiempo extra) 💻 Virtual: Instagram Live Para registrarte y obtener más información sobre cierres de calles y retrasos en el tren, visita nuestro sitio web: lupuswalks.org ___ Make every step count! This Saturday, October 18, join our walks and help make a difference for the lupus community! 📍Dallas: Glencoe Park 📍NYC: Intrepid Museum (Please note that we are aware of other walks and marches taking place in New York City on Walk Day, which could make commuting more difficult. We recommend all participants plan accordingly and allow extra time) 💻 Virtual: Instagram Live To register and for more information on street closures and train delays, please visit our website: lupuswalks.org #LupusWalks #Lupus #LupusResearch #LupusCommunity #WalkWithUs #LupusResearchAlliance

Thank you to the Hispanic and Latino/a/e lupus community for your strength and stories that inspire us all . 💜 As #NationalHispanicHeritageMonth comes to a close, we remain committed to sharing resources and amplifying your voices all year long. ✨ Explore our Spanish-language section to learn more about lupus, its symptoms, diagnosis, and other resources: https://lnkd.in/g94FvJ6x ___ Gracias a la comunidad hispana y latino/a/e con lupus por su fortaleza y por compartir sus historias que nos inspiran a todos. Al concluir el #MesNacionalDeLaHerenciaHispana, reafirmamos nuestro compromiso de seguir compartiendo recursos y amplificando sus voces durante todo el año. ✨ Explora nuestra sección en español para aprender más sobre el lupus, sus síntomas, diagnóstico y otros recursos: https://lnkd.in/g94FvJ6x #Lupus #LupusAwareness #LupusResearch #LupusResearchAlliance

The Lupus Research Alliance is seeking nominations for the 2026 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 2021 and 2025. To nominate a colleague from academia or industry, please review the Request for Nominations. Nominations due: December 1, 2025 🔗: https://bit.ly/46Nyn65