Dublin, we're cheering you on! 🏃♀️🏃♂️💜
Our amazing LRA Team Life Without Lupus runners are hitting the streets of Dublin today, taking on 26.2 miles in celebration of the 45th anniversary of the Irish Life Dublin Marathon and in support of lupus research.
Every mile brings us closer to a world without lupus, and we couldn't be prouder of this team for going the distance for the lupus community.
Join us in wishing our runners good luck! 👏
#LifeWithoutLupus #LupusResearch #IrishLifeDublinMarathon
NYC, you showed up for the lupus community! 👟💜
To our incredible walkers, generous sponsors, dedicated volunteers and everyone in the lupus community who supported today’s Walk, thank you!
Seeing everyone come together for lupus research is a powerful reminder of what we can accomplish together. We’re one step closer to a world free of lupus.
#WalkWithUs #LupusResearch #Lupus #LupusWalks
Today’s the day, NYC! 💜
We’re so excited to welcome you to the Intrepid Museum for the NYC Walk with Us to Cure Lupus.
Whether you’re walking with us or cheering us on from afar, you’re part of a community working toward a world free of lupus. Let’s do this! 👟
#WalkWithUs #LupusResearch #Lupus #LupusWalks
See you tomorrow, NYC! 💜👟
LRA President and CEO Albert T. Roy and lupus advocate Maddy Bustamante Cocchiarella joined CBS New York to talk about tomorrow’s NYC Walk with Us to Cure Lupus and the importance of coming together to support lupus research.
A big thank you to CBS News New York for helping us spread the word!
🎥 Catch the interview: bit.ly/4eSjy5B
#Lupus #LupusResearch #WalkWithUs #LupusWalks
Tomorrow’s the big day, NYC! 💜👟
We’re so excited to come together for the LRA NYC Walk with Us to Cure Lupus!
Whether it’s your first walk or you’ve joined us before, we can’t wait to see you at the Intrepid Museum as we take steps toward a world free of lupus.
📍 Intrepid Museum, NYC
📅 Tomorrow, October 24
⏰ Check-in and festivities begin at 8:00 AM
👟 Walk begins at 9:30 AM
It’s not too late to join us! Register here: bit.ly/WALK26_NY
#Lupus #LupusResearch #WalkWithUs #LupusWalks
We couldn't be happier to honor Drs. Gregory Barton and Olivia Majer at #ACR26! Congratulations to you both. Your groundbreaking discoveries are helping deepen our understanding of lupus, and we're excited to see where this research leads.
#ACR26 Must-See Session 🔎 TLR7 from Discovery to Translation: Lupus Research Alliance Lupus Insight Prize Lectureship
The 2026 @LupusResearch Lupus Insight Prize Lectureship at ACR Convergence will honor Gregory Barton, PhD, and Olivia Majer, PhD, for complementary discoveries that illuminate how regulation of innate immune sensing pathways governs susceptibility to lupus. Their work centers on the UNC93B1–TLR7 axis, a critical pathway controlling responses to RNA, and demonstrates how disruption of this regulatory system can lead to aberrant immune activation and inflammatory pathology relevant to SLE. Learn more → acr.tw/4yYLMDL
ACR Convergence is almost here! Complete your registration → acr.tw/44pY0G8
Step inside the Global Walk! Tune in to our Instagram Live on October 24 at 9:30am ET to meet some of the people walking for #LupusResearch worldwide, and find out how you can bring the Global Walk to your own community — anywhere, anytime.
Learn more: LupusWalkGlobal.org
For people living with lupus, better biomarkers - measurable molecules that provide information about a person’s health - could mean earlier diagnosis, more precise treatment, and fewer invasive procedures. A new publication outlines a roadmap developed as part of the Lupus Research Alliance Biomarker Roadmap Initiative for how cross-sector collaboration and consortium-based partnerships can help overcome longstanding barriers and bring the next generation of lupus biomarkers into clinical practice.
Read more: bit.ly/4z3071Z
#LupusResearch #LupusAwareness
We’re thrilled to welcome Maxwell of 103.5 KTU, “The Beat of New York,” as host of this year’s #BreakingThroughGala on Monday, Nov. 16 in NYC! 🎉
Join us for an evening of inspiring stories of resilience and hope for the lupus community.
💜 RSVP: bit.ly/4iaWG2e
#Lupus #LupusResearch
When your joints ache, moving more might be the last thing on your mind. But staying active could actually help.
In @EatingWell, NYU rheumatologist and Lupus Research Alliance-funded researcher studying lupus and the gut microbiome, Gregg Silverman, MD, joins other experts to share why it may be time to rethink how you manage joint pain.
Learn more about joint health: bit.ly/4y9VVNs
#Lupus #LupusResearch #LupusAwareness
This Saturday, we're coming together for the 2026 NYC Walk With Us to Cure Lupus! 👟💜
Ahead of the walk, our Chief Advancement Officer, Nicole Capossela, joined NIna del Rio on @1067Litefm Get Connected to share what makes this event so special for the lupus community and how it supports research that brings us closer to a world free of lupus.
🎧 Listen to the conversation and learn how you can be part of this Saturday's walk: bit.ly/4sdeLBp
#Lupus #LupusResearch #WalkWithUs #LupusWalks
The countdown is on! 💜👟 We're just days away from the LRA NYC Walk with Us to Cure Lupus!
This Saturday, we're coming together at the Intrepid Museum to walk toward a world free of lupus. Whether you're walking for yourself, someone you love, or the entire lupus community, we can't wait to see you there!
📍 Intrepid Museum, NYC
📅 Saturday, October 24
⏰ Check-in and festivities begin at 8:00 AM
👟 Walk begins at 9:30 AM
There's still time to join us! Register today: bit.ly/WALK26_NY
#Lupus #LupusResearch #WalkWithUS #LupusWalks
From diagnosis to making a difference. 💜
After being diagnosed with lupus at 11, Alex Moy brought together family and friends through Alex’s Superheroes to raise nearly $200,000 for lupus research.
Her story is a reminder of what can happen when personal experience becomes purpose.
Read more about Alex and get her top tips for DIY fundraising: bit.ly/47nX8Fu
#Lupus #LupusResearch
This #PatientCenteredCareAwarenessMonth, we’re recognizing its importance for people living with lupus.
Lupus affects everyone differently, and your care should reflect your unique experience. You deserve a care team that listens to your concerns and works with you to find ways to manage lupus that fit your needs and daily life. 💜
What helps you feel heard and supported by your care team? Share below. 👇
#Lupus #LupusResearch #LupusAwareness #PatientCenteredCare
Diagnosticada con Lupus a tan solo los 9 años, Miah Andrade conoce de primera mano el impacto que Lupus puede tener a cualquier edad.
La próxima semana, puedes unirte a ella y a la comunidad de Lupus en la Caminata 2026 de Nueva York para Curar el Lupus (Walk with Us to Cure Lupus) 💜
Es una oportunidad para unirnos y dar un paso más hacia un mundo libre de Lupus
📍 Museo Intrepid, Nueva York
📅 Sábado, 24 de Octubre
⏰ El registro comienza a las 8:00 a. m. | La caminata comienza a las 9:30 am
Camina con nosotros! Inscríbete hoy: bit.ly/4rW0IzR
—
Diagnosed with lupus at just 9 years old, Miah Andrade knows firsthand the impact lupus can have at any age.
Next week, you can join her and the lupus community at the 2026 New York City Walk with Us to Cure Lupus. 💜
It’s a chance for us to come together and take another step toward a world free of lupus.
📍 Intrepid Museum, NYC
📅 Saturday, October 24
⏰ Check-in begins at 8 AM | Walk starts at 9:30 AM
Walk with us! Register today: bit.ly/4rW0IzR
#WalkWithUsToCureLupus #LupusResearch #LupusAwareness #Lupus
It’s #BoneAndJointActionWeek! 💜
If you live with lupus, you know how much joint pain can affect everyday life. That’s one reason we’re so committed to funding research that can lead to new and better treatments.
Hear from nine people living with lupus as they share what joint pain feels like.
Watch now. 📹
#Lupus #LupusResearch #JointPain #LupusAwareness
As #HispanicHeritageMonth comes to a close, we’re highlighting lupus advocate Erika Reyna and the difference she’s making in the lupus community. 💜
Erika uses her voice and lived experience to help others feel seen, heard, and empowered to speak up for their health - including using her platform to raise awareness about lupus.
Learn more about Erika’s story and the experiences that inspire her work here: bit.ly/47jPFHu
#NationalHispanicHeritageMonth #LupusAwareness #Lupus #LupusResearch
Go inside the Global Walk! On October 24, join our Instagram Live to celebrate walkers supporting #LupusResearch — and learn how easy it is to organize your own walk, anywhere and anytime, to help move the world closer to a cure.
Learn more: LupusWalkGlobal.org
Qiana Alexander, Ambassador for the LRA NYC Walk with Us to Cure Lupus, has been walking with us since 2014 - and she keeps showing up for the lupus community, past, present, and future. 💜
Every step and every dollar raised helps support lupus research and brings us closer to a world free of lupus.
Can’t join us in person on October 24? You can still be part of the day by making a gift.
👉 Give today at bit.ly/4rW0IzR.
#WalkToCureLupus #LupusAwareness #WalkWithUs #LupusResearch #Lupus #LifeWithoutLupus
Lupus can affect your joints, too. 💜
Joint pain and swelling are common symptoms of lupus, and noticing changes can be an important part of managing your care.
If something feels different, talk with your doctor.
👉 Explore lupus resources at LupusResearch.org.
#WorldArthritisDay #BoneAndJointActionWeek #BoneJointWeek























