🧬 Make your mark in shaping the future of lupus research!
Each case of lupus is unique, and so is your voice, your experience, and your impact. 💜
Join the Lupus Landmark Study and help accelerate groundbreaking medical research for a cure. By donating a small sample of blood and other biological samples, along with health data from your personal experience with lupus, you’re giving scientists the tools they need to better understand, treat, and one day cure lupus.
✅ Confidential
✅ Your participation could help save lives
📍Be part of the next breakthrough. Learn more: https://t.co/j9QCUrcwW7
#Lupus #LupusResearch #LupusAwareness #LupusLandmarkStudy
As summer is in full swing, it’s important for people living with lupus to pay attention to sun exposure.
Learn from Jillian Richmond, PhD, Assistant Professor, Tufts University about how you can stay safe in the sun – and how research is making the future brighter.
See the tips: https://t.co/rs2raOZjPA
#Lupus #LupusResearch #SunSafety #UVSafety #UVSafetyAwarenessMonth
This #ChronicDiseaseAwarenessMonth, we recognize everyone living with lupus and the realities they navigate each day.
Behind every diagnosis is a unique journey. That's why we're committed to advancing research that improves lives today and brings us closer to a future free of lupus.
#ChronicDiseaseMonth #LupusCommunity #LupusResearchAlliance #HopeInAction #TheFutureOfLupus
Happy #SocialMediaDay! 💜
To everyone who follows, shares, comments, advocates, and helps raise awareness for lupus—thank you. You are this community.
Together, we're driving awareness, advancing research, and bringing hope to everyone affected by lupus.
Stay connected by following our channels, signing up for our newsletter, and exploring ways to get involved. Visit the link to join us: https://t.co/jBEPDTafLX
#SocialMediaDay #Lupus #LupusResearchAlliance #TogetherForLupus
🤝 Emmitt Henderson III knows the power of community.
What began as a search for connection after his lupus diagnosis has grown into a mission to support other men living with lupus through Male Lupus Warriors.
Read Emmitt's inspiring story of turning isolation into impact: https://t.co/ZYf5No35oE
#LupusResearchAlliance #LupusCommunity #LupusAwareness #StrongerTogether #MensHealthMonth
Check out the Lupus Voices Council (LVC) Guide to Lupus Resources! 💜
Created by the #lupus community, this guide provides information, tools, and programs to strengthen clinical trial education and support people living with lupus.
The guide features information on:
✔ Community-driven projects
✔ Guidance on participating in clinical research
✔ Resources for people with lupus, caregivers, and advocates
Whether you’re a person living with lupus, caregiver, researcher, or advocate, this guide offers ways to learn, connect, and take action.
Explore the full guide here: https://t.co/BTCxPUNrER
#LupusABC #LupusResearch #LupusVoices
🔔 In Case You Missed It: Our First Hope in Action Fireside Chat
LRA President & CEO Albert T. Roy was joined by Saira Sheikh, MD—Linda Coley Sewell Distinguished Professor of Medicine in Rheumatology, Allergy & Immunology at UNC Chapel Hill and Chair of LuCIN, overseen by #LupusTherapeutics—for an inspiring conversation on the latest progress in lupus research.
Together, they explored the power of collaboration, advancements shaping the future of lupus care, and the reasons for hope across the lupus community.
🎥 Watch the discussion on demand and hear more about hope in action: https://t.co/YAeUHTUhaD
#HopeInAction #LupusResearch #LupusTherapeutics #Collaboration #Innovation #Lupus
Are you an early-career scientist or junior investigator committed to a career in rheumatology and #lupusresearch?
The LRA/@RheumResearch Empowering Lupus Research Partnership is now accepting applications for funding that supports innovative, transformative #lupus research.
This is your opportunity to:
🟣Investigate novel pathways in lupus biology
🟣Drive breakthroughs in autoimmune disease
🟣Bridge the gap from bench to bedside
Two award mechanisms are available:
~ Scientific Development Award - up to $225,000 over 2-3 years
~ Investigator Award - up to $500,000 over 3-4 years
LOI Due: July 1, 2026
Learn more and apply at https://t.co/v9SW6SzJl3
Every act of generosity moves lupus research forward. 💫
Whether you're making a gift today or planning for the future, there are many ways to support the Lupus Research Alliance's mission:
🔹 Stock Donations
🔹 Matching Gift Programs
🔹 Payroll Deductions
🔹 Combined Federal Campaign
🔹 Vehicle Donations
🔹 Planned Giving & Bequests
🔹 Donor-Advised Funds (DAF)
🔹 Contributions to the Lupus Brain Bank
No matter how you choose to give, you're helping drive discoveries and bring hope to people living with lupus.
Learn more: https://t.co/hdbtJr3sKg
#GiveYourWay #SupportLupusResearch #HopeInAction #TheFutureOfLupus
💜 What happens when a community comes together with a shared purpose?
On Monday, sports stars, advocates, and friends of the Lupus Research Alliance gathered for the 12th Annual Willie Colon Golf Outing, hosted by former NFL player, Super Bowl Champion, and current sports analyst @WillieColon66, whose dedication continues to help advance lupus research.
We're grateful to Willie and @AikishaHolly Colon, the Golf Outing Chairs, and everyone who made this event possible.
🔗 Read the full recap to learn more about the day: https://t.co/lfZp0GjMX6
#LupusResearchAlliance #LupusResearch #Lupus #LRA #WillieColonGolfOuting #WillieColonGolf4Lupus
Recent evidence may reveal a link between ADHD and certain health conditions, including lupus.
Hear from Meggan Mackay, an LRA-funded researcher, rheumatologist, and professor at the Feinstein Institutes for Medical Research, as she discusses these connections with The @washingtonpost.
#Lupus #LupusResearch
Evidence suggests that people with ADHD face a higher risk of anxiety, disordered eating, autoimmune disease, migraines, long COVID, and chronic pelvic pain.
What remains unclear is whether there is a biological link between ADHD and these conditions. https://t.co/VeoUlbVCb2
💫 Today’s the day! Join us at noon ET for the next webinar in our series, Lupus & Life: Science, Support, and Self-Care, to explore the connection between lupus, nutrition, and the microbiome.
Topics Covered:
🟣 What is the relationship between lupus, diet, and the microbiome?
🟣 What impact do diet and nutrition have on inflammation and autoimmune diseases?
🟣 How can nutrition potentially impact lupus activity?
Whether you're living with lupus or care for someone who is, this webinar is a chance to learn and feel empowered.
Register here: https://t.co/WZBfHe9rbg
#Lupus #LupusResearch
💫 Don't miss this opportunity - there's still time to register for the next webinar in our series, Lupus & Life: Science, Support, and Self-Care. Join us as we take a closer look at lupus, nutrition, and the microbiome.
📅 Live Webinar: June 24
⏰ 12:00 – 1:00 pm ET
Topics Covered:
🟣 What is the relationship between lupus, diet, and the microbiome?
🟣 What impact do diet and nutrition have on inflammation and autoimmune diseases?
🟣 How can nutrition potentially impact lupus activity?
Whether you're living with lupus or care for someone who is, this webinar is a chance to learn and feel empowered.
Register today: https://t.co/WZBfHe9rbg
#Lupus #LupusResearch
We’re back on the green for another unforgettable day at the annual Willie Colon Golf Outing! ⛳️
The Lupus Research Alliance is proud to partner with former NFL player with the New York JETS and Pittsburgh Steelers, Super Bowl Champion, and current sports analyst with the NFL Network and FS1 @WillieColon66.
Now in its 12th year, this special event honors Willie’s late mother, Jean Davis, and has raised over $3 million to advance lupus research. With the support of over 300 golfers, including an incredible lineup of athletes and advocates, this outing continues to drive real change for the millions impacted by lupus worldwide.
💜 Thank you to Willie and @AikishaHolly Colon, and everyone who continues who show up year after year to move forward lupus research.
#Lupus #LupusResearch #WillieColonGolfOuting #WillieColonGolf4Lupus #LupusAwareness #LRA
💫 Diet and nutrition can play an important role in overall health and well-being, whether you live with lupus or not. Join us for the next webinar in our series, Lupus & Life: Science, Support, and Self-Care to take a closer look at lupus, nutrition, and the microbiome.
Live Webinar: June 24
⏰ 12:00 – 1:00 pm ET
Topics Covered:
🟣 What is the relationship between lupus, diet, and the microbiome?
🟣 What impact do diet and nutrition have on inflammation and autoimmune diseases?
🟣 How can nutrition potentially impact lupus activity?
Whether you're living with lupus or care for someone who is, this webinar is a chance to learn and feel empowered.
Register today! https://t.co/WZBfHe9rbg
#Lupus #LupusResearch
💫 Diet and nutrition can play an important role in overall health and well-being, whether you live with lupus or not. Join us for the next webinar in our series, Lupus & Life: Science, Support, and Self-Care to take a closer look at lupus, nutrition, and the microbiome.
Live Webinar: June 24
⏰ 12:00 – 1:00 pm ET
Topics Covered:
🟣 What is the relationship between lupus, diet, and the microbiome?
🟣 What impact do diet and nutrition have on inflammation and autoimmune diseases?
🟣 How can nutrition potentially impact lupus activity?
Whether you're living with lupus or care for someone who is, this webinar is a chance to learn and feel empowered.
Register today! https://t.co/WZBfHe9rbg
#Lupus #LupusResearch
The Lupus Research Alliance honors #Juneteenth as a time to reflect on freedom and progress. We remain committed to advancing lupus research and care, supporting all those impacted. Together, we continue to strive for a world free of lupus.