🎉 Dallas, it’s time! Join us on October 19 at Glencoe Park for the Walk with Us to Cure Lupus. Every step we take drives lupus research closer to a cure. 💜 Sign up today: bit.ly/WALK-DALLAS24 #WalkWithUs #ManyOneCan #LupusResearch #lupuscommunity

August is #NationalHairLossAwarenessMonth! ✨ 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. #lupus #symptomsoflupus#SLE #lupuscommunity

Wherever you are across the globe, you can Walk with Us to Cure Lupus on 10/19. Gather your friends, family, and team and let’s make an impact for lupus research! 👟💥 Register now at bit.ly/walk-virtual20… #LupusWalk #WalkwithUs #LupusResearch #ManyOneCan

Thank you Kathleen Arntsen, Dave Arntsen, and Lupus Association 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.

📢 LRA 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. bit.ly/LIP-2025

Lupus is marked by a staggering gender imbalance -- about 9 of 10 people with #lupus are women. Knowing the reason why could unlock novel treatments and revolutionize outcomes. In recognition of #WomensEqualityDay, we share several groundbreaking findings by Dr. Howard Chang,

It’s #NationalDogDay! 🐶 🐾 To all the animal lovers, tag us in your favorite walk photos with your pet. We can't wait to see you all at our 2024 Walk with Us to Cure Lupus fall events! 🍂👟 Join us: Lupuswalks.org #WalkwithUs #ManyOneCan #lupus #LupusResearch

If you feel stressed out and have lupus, you’re not alone! Research has shown stress is common among people with a chronic disease like lupus. Here’s ten of our favorite tips to help manage #stress from Priscilla Toral at Hospital for Special Surgery (HSS).

El lupus puede ser difícil de diagnosticar porque afecta a cada persona de manera diferente. Estos son los síntomas y las medidas que los médicos usan como guía para determinar si una persona tiene lupus. Más información: bit.ly/lupus-diagnost… #Lupus #LupusResearch

Warm thanks go to Lupus and Allied Diseases Association, Inc. for the very generous donation of $150,000 to support #lupusresearch projects funded by the LRA. Lupus Association President & CEO Kathleen Arntsen presented the check at the organization’s 24th Annual Lupus Charity Golf

The LRA is proud to have helped launch this year’s football season at the New York Jets Annual Kickoff Luncheon. In addition to introducing the 2024 team roster, the event spotlighted the worthwhile causes supported by the New York Jets. With the support of more than 500 passionate

📢 Diversity in Lupus Research Program Letters of Intent are due Sept 6! 🔬 Supports underrepresented talent in #LupusResearch & #autoimmunity by fostering growth & building a strong community of scientists & clinicians 🏆 $600K for Career Development & $200K for Postdoctoral

You’ve registered for the Walk with Us to Cure Lupus and want to know what next steps are? Here are the next steps to maximize your Walk experience! 🟣 Select a team name, begin to recruit fellow team members and build your team: Your team can be one, two, ten – or hundreds! 🟣

🌞 As we kick-off a holiday weekend, remember to protect yourself from the sun. It’s important to be mindful of sun exposure year-round to help manage #lupus and your overall well-being. Dr. Werth shares tips for the summer for those with lupus. ☀️

What is lupus? Lupus is a debilitating autoimmune disease that affects each person differently. This complexity makes it one of the hardest diseases to diagnose and treat. Learn more about #lupus, signs and symptoms, treatment and more. bit.ly/4bOKTSM

The Lupus Research Alliance wishes you a healthy #LaborDay! 🇺🇸

📢 The LRA is accepting Letters of Intent for the Diversity in Lupus Research Program, due September 6. 🔬 This program supports exceptional underrepresented talent across different stages of their scientific careers, promoting research in #lupus and #autoimmunity. Awardees gain

🎉 Have you checked out our brand-new Walk with Us to Cure Lupus website? It’s now easier than ever to find an LRA Walk near you, create and promote Walk teams and more. Visit today! bit.ly/4bjVQLS

Anyone who is a current or retired federal, postal, or military employee can support us by making a pledge through the 2024 Combined Federal Campaign (CFC). Make your mark on #lupusresearch. Choose the LRA CombinedFedCampaign 37283 as the recipient of your 2024 pledge! bit.ly/CFC-lupusresea…

✨ Today is #InternationalDayofCharity! Our mission at the LRA is to transform the lives of people with lupus through the power of science 🔬, and this is an opportune moment to let you know how we are perceived as a charity by independent organizations that help donors evaluate