Lupus Foundation of America

Lupus Foundation of America

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@lupusorg

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The latest news, resources and opportunities for those with lupus and their friends and families.

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Recent posts

➡️ Swipe to take a look at highlights from #ACR26! 💜 Our team had the opportunity to share important lupus research findings, engage in meaningful conversations about the future of lupus care, and connect with researchers, healthcare professionals, and advocates from around the world. Explore our recap for LFA research findings and updates shared throughout the event (🔗 LINK IN BIO). 14 Nov 2026 💜 Calling clinics and healthcare providers who care for people with #lupus! The Lupus Foundation of America is offering up to $9,000 in funding to help clinical settings connect patients with free, evidence-based lupus self-management resources. Through our Clinical Referral Mini-Grant Program, eligible clinics can receive funding to refer patients to tools that support symptom management, stress reduction, and overall well-being. 📅 Applications close December 1, 2026! Click the link in our bio to apply today. 13 Nov 2026 The support someone needs while living with #lupus can change over time. Staying connected through open communication can help you navigate those changes together. 💜 This #NationalFamilyCaregiversMonth, Heather Rose Artushin, LISW-CP, explores communication, boundaries and self-care, and introduces our new Care Partner Toolkit with resources to support your loved one and yourself. Read our new blog (🔗 LINK IN BIO) 13 Nov 2026 That’s a wrap on #ACR26! This year’s LFA-led research explored #lupus diagnosis, research participation new ways to measure treatment response, and more. 🔗 Click the *link in bio* to read our full recap. Thank you to everyone involved for helping advance #LupusResearch and care forward. 12 Nov 2026 💜 Supporting someone with #lupus can look different from day to day. Whether it’s providing emotional support, helping with daily tasks, or attending medical appointments, every act of care can make a difference. This #NationalFamilyCaregiversMonth, we’re recognizing the important role care partners play while reminding them that their own well-being matters, too! Click the 🔗 link in bio to explore tips for supporting your loved one and yourself. 12 Nov 2026 Join us on December 9 for our free national Lupus & You virtual education event where we’ll explore what current research tells us about nutrition and #lupus, better understand the connection between gut health and the immune system, and learn practical strategies to support your overall health. CLICK LINK IN BIO to register today! 11 Nov 2026 🎉 The Lupus Foundation of America is proud to honor three outstanding #lupus researchers at the 2026 Evelyn V. Hess Reception! Dr. Mary (Peggy) K. Crow and Dr. Gary S. Gilkeson are this year's Evelyn V. Hess Award co-recipients. Dr. Crow's research focuses on the immune system's role in lupus, while Dr. Gilkeson's work explores lupus genetics and new treatments. Dr. April Jorge received the Mary Betty Stevens Young Investigator Prize for her research on personalized lupus treatment and patient outcomes. Click the 🔗 link in our bio to learn more about this year's honorees and their research. 09 Nov 2026 🏃💜 Just two weeks until @Philly_Marathon Weekend. Our Racing to End Lupus runners have already raised over $50,000 to support our mission to end lupus! Join us in cheering them on as they put their training into action, raising funds and awareness with every step. Feeling inspired? Racing to End Lupus will be back in Philadelphia next year! Learn how you can get involved (🔗 LINK IN BIO). 08 Nov 2026 We are at ACR Convergence 2026 (@acrheum)! Our team will present eight abstracts exploring #lupus diagnosis, treatment decision-making, access to care, clinical trial participation, CAR T-cell therapy, health equity and more. 🔗 Click the *link in our bio* to learn more about the research we’re presenting and its potential to advance lupus care and treatment. #ACR26 06 Nov 2026 #FactFriday 💜 Living with #lupus can make everyday activities challenging, especially when dealing with chronic pain. Working with your doctor to understand what’s causing your pain and developing a personalized management plan can help. Click the link in our bio to explore strategies for managing lupus pain. 06 Nov 2026 Mark your calendars! #GivingTuesday is 12/1, and we’re coming together to make a difference for people living with #lupus. Together, we can raise lupus awareness, fuel research, and provide vital resources and support to people affected by lupus. 📅 Click the 🔗 link in bio to save the date and join us in creating a world without lupus. 05 Nov 2026 💜 This National Family Caregivers Month, we’re recognizing the family members, friends, and loved ones who provide care and support to people living with #lupus. Whether you’re new to being a care partner or have been supporting a loved one for years, our Caregivers Information Center offers resources to help you navigate your role, build a support network, and care for yourself along the way. Click the *🔗 link in bio* to explore resources and tips for care partners! 05 Nov 2026

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DfuX7cfl5jn➡️ Swipe to take a look at highlights from #ACR2…
Dfsfju9F8my💜 Calling clinics and healthcare providers who c…
DfrvjUll82rThe support someone needs while living with #lup…

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