Lupus Research Alliance

🌴✨ Exciting news, South Florida! The 2025 Walk with Us to Cure Lupus is officially OPEN for registration! 🙌 Mark your calendars for Sunday, March 2, and meet us at Lynn University in Boca Raton for an empowering day to support lupus research. Don’t miss out—register now! https://bit.ly/WALK25_SF #WalkWithUs #LupusWalk #LupusResearch

Using vagus nerve stimulation to treat lupus? ⚡ Building off her previous successful clinical trial results, Cindy Aranow, MD, professor in the Institute of Molecular Medicine, recently received a $450,000 Translational Bridge Award from the Lupus Research Alliance to further study how this innovative treatment could ease the pain and fatigue associated with the chronic autoimmune disease. Find out more here: https://bit.ly/49mHEl6

Lupus is an autoimmune disease affecting various aspects of daily life. Hear from people living with lupus in our community on how the disease affects their quality of life. #Lupus #LupusResearch #InternationalQualityofLifeMonth

Lupus is one of the more complex autoimmune diseases and it affects each person differently. By learning about the signs, symptoms, and complications of lupus, you can better understand the disease and access resources to support yourself or a loved one. Learn more: https://lnkd.in/gx2cTxuK #lupus #lupusresearch #SLE #LupusSymptoms #Autoimmune

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. Make your mark on lupus research. Choose the Lupus Research Alliance CFC 37283 as the recipient of your 2024 pledge! https://lnkd.in/gXWugWrZ #LupusResearch #Lupus

A planned gift is a powerful way to drive new breakthroughs…and no matter your income level, your impact can be greater than you think. Learn how you can join champions like Jennifer in making a difference: https://lnkd.in/guGTxakz #Lupus #LupusResearch

Es importante comprender cómo el lupus puede impactar en su salud mental y emocional. Conéctese con otras personas de la comunidad de lupus para reflexionar de manera significativa sobre la salud mental: https://lnkd.in/g94FvJ6x #lupuscommunity #LupusEnEspanol

🌟 IDEAL Initiative: New Clinical Research Funding Opportunity! 🌟 The IDEAL (Investigate Dietary Approaches for Lupus) Initiative, established by Lupus Therapeutics, the clinical research affiliate of the Lupus Research Alliance, is accepting applications. This RFA addresses the need for well-controlled studies assessing the impact of diet and microbiome on lupus. 🔍 Details Funding: Up to $500,000 each over two years Focus: Proof-of-concept pilot clinical study designed to evaluate the impact of diet on the lived experience of lupus Eligibility: Multidisciplinary teams focused on diet intervention with scientific and clinical outcome measures; encouraged to keep patients at the center and include patients as research partners 📅 LOI Deadline: January 8, 2025 at 11:59 pm ET This is an opportunity to help transform lupus care. Learn more and apply: https://bit.ly/3AIWcPg #LupusClinicalResearch #IDEALforLupus

Lupus can be difficult to diagnose because it affects every person differently, can impact almost any organ, mimics other diseases, and can even change within the same person. Here are symptoms and measures doctors use as a guide to determine if a person has lupus. Learn more: bit.ly/Lupus-Diagnosis #ManyOneCan #Lupus #LupusResearch #lupuscommunity

Special Lupus Research Alliance cleats are on auction until January 5! 🏈 nyjets defensive tackle Javon Kinlaw was inspired to raise #lupusawareness and support #lupusresearch through #MyCauseMyCleats after learning about the Lupus Research Alliance, and we’re so thankful! Javon wore his custom cleats in support of the LRA in the NY Jets December 1 game vs. Seattle. Now through Jan 5 - you can make a bid on Javon’s amazing custom cleats to support LRA: https://bit.ly/cfc-jk