Meet Tamara. 💜 Diagnosed with #lupus at just 10 years old, her journey has included hospital stays, moments with family by her side, and learning to live with lupus. All while showing remarkable courage and hope.

The holidays can make it tough to keep up with healthy habits, but you don’t have to do it alone! 🎁💜 Our free SELF program sends text reminders with quick tips and encouragement to help you stay on top of your health. Sign up today: buff.ly/7yAf8Wn 📱

🚨 Medicare Part D Open Enrollment Ends Soon! This year, new benefits include a $2,100 out-of-pocket and the Medicare Prescription Payment Plan (MPPP) for monthly installment options. Read our Open Enrollment Guides and make your selections before 12/7: buff.ly/XKTlh9C

Swipe to see how #lupus warriors, families and supporters showed up across the country this #WalktoEndLupusNow season! 💜 There are just two walks left — North Carolina and South Carolina! Join us and make your steps count: buff.ly/ftR8yCA

Phase III ALLEGORY study for Gazyva® (obinutuzumab) shows significant reduction in disease activity in adults with #SLE. The study met all primary and secondary endpoints, showing greater improvements compared to standard therapy. Read more: buff.ly/dG6PvsJ

Managing #lupus requires consistency in nutrition and treatment, and disruptions to paychecks and health coverage can make it difficult to maintain that stability. 💜 Our new blog shares food assistance programs, medication support, and tips: buff.ly/QOK420k

Congratulations to our inaugural Lupus Foundation of America team for completing the 2025 #TCSNYCMarathon! Your 26.2 miles inspire lupus warriors everywhere. Watch highlights and learn how to join next year’s team: buff.ly/UAbGkgX

We’re less than a month away from #GivingTuesday — the biggest day of the year to rally together for #lupus warriors! 💜 Save December 2 on your calendar and get ready to rise as one to fuel research, deliver support and ignite hope. Together, we can make an impact that lasts.

💜 We extend gratitude to caregivers for National Family Caregivers Month. Our Caregivers Information Center provides resources from basics to practical tips for #lupus care. You’re not alone on this journey. Build your support team today: buff.ly/KF37VgI

Today’s the day! Our inaugural Lupus Foundation of America marathon team is running the 2025 #TCSNYCMarathon — 26.2 miles to end lupus and bring hope to millions. Wish them a strong finish below! www.lupus.org/start-a-fund...

Join us in honoring #NativeAmericanHeritageMonth! 💜 This #NAHM, we’re raising awareness about lupus in American Indian and Alaska Native communities and working together to address disparities and improve outcomes for lupus warriors nationwide. Reply with a 💜 to show support!

We want to hear from you! 💜 How has the Lupus Foundation of America community made a difference in your life? Share your feedback, a quick quote or reflection and help other #lupus warriors discover programs, resources & support that make a difference: buff.ly/1KdpxqJ

With changes to SNAP and food assistance, we know many are struggling to access food and other essentials. 💜 If you or someone you know needs support, the Lupus Foundation of America offers information for assistance with food, housing, and more: buff.ly/jdOQgTL

Good luck to our inaugural Lupus Foundation of America marathon team running the 2025 #TCSNYCMarathon this Sunday! They’re #racingtoendlupus to raise awareness and make their miles matter - 26.2 miles in NYC. Wish them luck in the replies! buff.ly/UAbGkgX

💜 From massage therapy to meditation, many people with #lupus explore complementary & alternative medicine to help manage symptoms. These therapies can offer comfort but always consult your care team to find options that are safe for you. Learn more: buff.ly/F7FPJUs

The next generation of #lupusresearch starts here. Our 2026 grant opportunities support mentorship, career growth, & innovation in basic, translational, & clinical research—helping scientists improve lives of people with #lupus. 🔗 Apply now: buff.ly/8algCI0 #Medsky #Rheumsky

Missed our latest Lupus & You event? Our new blog covers top Q&As from experts on living well with #lupus at every age — from navigating changes over time to staying strong, independent and connected while aging with purpose. Read more: buff.ly/uozz64H

🔬 Catch up on the latest innovations in #lupus care from #ACR25 in Chicago! The Lupus Foundation of America proudly shared 8 studies and sessions—from treatment breakthroughs to tools improving communication and inclusion in research. Read our new recap: buff.ly/ilFTdwy #Rheumsky #Medsky

At #ACR25, LFA’s Care & Support Services team shared findings from a study evaluating disease education through the virtual Lupus & You program. 💜 With 20K+ registrants over 4 years, results show a strong need for virtual #lupus education. Read more: buff.ly/QAvOvMl

🎥 Have questions about the new SLE guidelines? Dr. Lisa Sammaritano, rheumatologist at Hospital for Special Surgery and Principal Investigator for the American College of Rheumatology SLE Guideline team, shares insights on the new SLE Guidelines shaping #lupus care: buff.ly/HbP3nma #ACR25

🎉 We're honored to present the Evelyn V. Hess Award to Dr. Karen Costenbader for advancing #lupus research and care, and the Mary Betty Stevens Prize to Dr. Andrea Fava for innovative research driving progress in lupus science. Learn more about their research: buff.ly/cn8xViK

In case you missed it, the Lupus Foundation of America’s research was featured at this year’s #ACR25. 💜 Our research advances #lupus self management, quality of life, and more. Highlighting the innovation driving lupus research forward. ➡️ Swipe to explore each study.

Today, at #ACR25, the American College of Rheumatology held a discussion of the new guidelines for the treatment & management of systemic #lupus erythematosus (SLE). The new guideline includes detailed recommendations for a wide range of management options: buff.ly/GfoD9cn #rheumsky #medsky

Increasing diversity in #lupus research is key to advancing clinical trials. At #ACR25, LFA shared new Research Accelerated by You (RAY) Registry findings on boosting participation, trust, & outreach—especially in Black/African American communities. Read more: buff.ly/BHqFjL8

#NationalFamilyHistoryMonth is about more than our past, it’s about protecting our future. 💜 With FreeWill, create or update your will in 20 minutes—for free—and choose to include a gift to the Lupus Foundation of America to make an impact. Get started today: buff.ly/oc8MoKJ

We’re proud to share the Lupus Foundation of America’s research presented at this year’s #ACR25! From advancing lupus diagnosis & treatment to improving quality of life, each study reflects collaboration between researchers, clinicians & people with lupus. ➡️ Swipe to explore.

Test how well you know #lupus! Watch as our Be Fierce. Take Control. mini-grant recipients from Bowie State University raise awareness and spark conversation about lupus on campus. 🎯 Take the Know Lupus Quiz and challenge your loved ones to test their knowledge too: buff.ly/Yejr9eg

#FactFriday 💜 Living with #lupus can be unpredictable, but having a plan can help you feel more in control. Preparing for flares, leaning on your support system, and talking openly with loved ones can make daily life easier. Find more tips for living well with lupus: buff.ly/bxRAdzL

🆕 New episode of The Expert Series! Protecting your matters more than ever with #lupus. Dr. Amit Saxena shares how vaccines can protect your immune system and prevent serious infections, especially if you’re on lupus meds. 💜 🎧 Listen now: buff.ly/zdAJ4lC

💜🆕 New Resource: Acthar® Gel: What You Need to Know. This FDA-approved treatment has been used for some autoimmune diseases, including #lupus, since 1952. Learn how it works, who it’s for, and what makes it different from other lupus treatments: buff.ly/96RWrNe

We’re gearing up for this year’s American College of Rheumatology Convergence Conference! We’ll bring you the latest updates in #LupusResearch, including new abstracts from the Lupus Foundation of America. Follow us on LinkedIn for updates: buff.ly/q2iByzr #ACR25 #Medsky #Rheumsky

🎥 Following the @fda.gov’s approval of Gazyva (obinutuzumab) for #lupus nephritis, Dr. Rovin, Chair of our Medical-Scientific Advisory Council and REGENCY trial investigator, explains what this milestone means. 💜 Watch the full video and learn more: buff.ly/YQrB4qb

💜 The Lupus Foundation of America is proud to share new #lupus research at #ACR25, kicking off 10/24 in Chicago — from digital health tools to studies advancing inclusion in clinical trials. Discover how our work is shaping the future of #lupusresearch and care: buff.ly/BHqFjL8

💜 Living with #lupus can affect every part of life. But you don’t have to face it alone. Our new tips for living well with lupus offer practical steps for managing symptoms, talking with loved ones, and planning ahead. 📘 Learn more: buff.ly/bxRAdzL

What an incredible #TwitchConSanDiego! 💜🎮 We’re so grateful for all the love and support we felt throughout the weekend. The energy doesn’t stop here — the countdown to Game On! To End Lupus 2026 starts now! #GameOnToEndLupus

BREAKING NEWS: The FDA has approved Gazyva® (obinutuzumab) for the treatment of adults with #lupus nephritis. Gazyva is the fourth therapy for lupus to receive regulatory approval since 2011. Read the announcement: buff.ly/81tYgo7

💜 It’s #EstatePlanningAwarenessWeek — a time to protect what matters most. With FreeWill, you can create or update your will for free and leave a legacy to support the Lupus Foundation of America and families affected by #lupus. Get started today: buff.ly/9g4KAqi

#TwitchConSanDiego is in full swing! 🎮 💜 Don’t miss your chance to connect with us at our Meet & Greet tomorrow (Sunday) at 2pm in the Charity Zone, booth 3444-CH. We can’t wait to see you there!

Thank you to everyone who joined Lupus & You: After Dark! Missed the event? No worries—catch the recording and event resources here: buff.ly/llyMbVB

#TwitchConSanDiego, we’ve arrived! 🎮 💜 We’re thrilled to reconnect with alumni and meet new streamers ready to join Game On! To End Lupus 2026. Come find us at booth 3444-CH in the Charity Zone. We can’t wait to see you!

How well do you know #lupus flares? 👀 Watch the video and take our quick quiz! 💬 Comment your score + share this post to support lupus awareness and education. 💜 Learn more about lupus flares: buff.ly/KIx34pK

The TCS New York City Marathon is just 2 weeks away! Our Lupus Foundation of America marathon team is racing to end #lupus — help us cheer them on in the comments! #TCSNYCMarathon

💜 Lupus warrior Ivette joined NBC 6 to raise awareness about #lupus and the upcoming #WalktoEndLupusNow - South Florida happening this Saturday, October 18 at loanDepot park! Watch her inspiring interview and learn how you can join the movement: buff.ly/6REoPj9

➡️ Swipe to see some of the amazing moments from last weekend’s #WalktoEndLupusNow events! 💜 #Lupus warriors, families, and friends came together to raise awareness, hope, and funds to end lupus. 👟 Walk season isn’t over yet — find an event near you: buff.ly/Xfxq0dw

Tonight’s the night – join us at 7 PM ET for Lupus & You: After Dark! This free, virtual event will explore how lupus can impact sexual health, intimacy, and menopause, featuring expert insights and real experiences from lupus warriors. Register now and we’ll see you virtually! buff.ly/llyMbVB

Flu and COVID season is here — and for people with #lupus, prevention is key. Our new resource shares ways to stay protected this winter, from vaccines to everyday precautions. Learn how to prepare, protect, and stay healthy through the colder months: buff.ly/5K7DaBZ

Our commitment to the Hispanic/Latino #lupus community goes beyond #HispanicHeritageMonth. 💜 We offer 150+ expert reviewed Spanish-language resources, plus support groups to ensure you have information & connection every step of the way. Learn more: buff.ly/ZDt0zOS

An estimated 1.5 million Americans live with #lupus, facing pain & uncertainty each day. Your workplace gift brings hope, resources, & crucial research. Designate the Lupus Foundation of America in your campaign to help build a future with breakthroughs: buff.ly/rCtWI7G

This Thursday, join us for Lupus & You: After Dark! This free virtual event explores #lupus, sexual health, intimacy, and menopause with experts and lupus warriors. Register now: buff.ly/llyMbVB

What is your life with #lupus like? 💜 We're looking for photos that show the real experiences of people with lupus - the ups, the downs and everything in between. From butterfly rashes to quiet victories and big accomplishments. 📷 Submit photos here: buff.ly/1UN4yNT