Lupus Foundation of America

➡️ Swipe to meet Rahul and Samantha, two athletes who turned their own races into something bigger for the #lupus community through Choose Your Own Race. Join them and turn an 5K, 10K, half marathon, marathon, triathlon or ultra into something charitable: buff.ly/b19EUrk

A new study explores the biomarker potential of IgG sugars for #lupus nephritis using a lectin-based test. Read the study: buff.ly/j4VlUjX

There's still time! Use the free SELF app for four days in July and you could receive a special gift from the LFA. Track medications, #lupus symptoms, or read the Activity of the Day. Supplies are limited! Start today: buff.ly/rLKgyFz

We're proud to announce Dr. Wobma from @HarvardMed as the 2026 Michael Jon Barlin Pediatric Lupus Research Grant recipient. Her study explores using CAR-Treg therapy for immune balance and achieving drug-free remission in children with #lupus. Learn more: buff.ly/F6QviP2

For many people, a barrier to participating in #lupusresearch is not knowing what to expect. ➡️ Swipe to learn about clinical trials, what participation looks like, and how your rights are protected. 🔗 Get involved in a trial today: buff.ly/LsxHWSR

Up to 80% of people with #lupus experience brain fog. A new tool, the Lupus Brain Fog Severity Scale, helps assess and track these cognitive symptoms. Read the study: buff.ly/6O988Yf

DYK up to 60% of people with #lupus may experience #lupusnephritis? Lupus warrior and LFA Director of Care and Support Services Wendy Rodgers joined At the Table with Greg & Elliott to explain the importance of kidney health. Learn more: buff.ly/nQqw24N

What a weekend at #EssenceFest! 💜 Thank you to everyone who stopped by our booth, shared their stories, and kept the conversation going. ➡️ Swipe to see some of the moments we captured. Together, we keep fighting for everyone impacted by #lupus.

New @Penn research sheds further light on molecular mechanisms that lead to #lupus and other autoimmune diseases most common in women. Read the research: buff.ly/0iXwueS

Today is #ChronicDiseaseAwarenessDay. 💜 #Lupus is a chronic autoimmune disease that can cause inflammation throughout the body. 9/10 people with lupus are women, and symptoms look different for everyone. Help us raise awareness and learn more: buff.ly/kBYEjRh

Ready to get involved in #lupusresearch but not sure where to start? From the RAY® #Lupus Registry to the Lupus Clinical Trial Finder, there are tools designed to help you explore opportunities and make informed decisions. Learn more: buff.ly/IbmD2Fo

Looking for a way to make an impact? 💜 ➡️ Swipe to see how our Purple for Purpose partners are turning everyday purchases into impact. A portion of every purchase goes directly to #lupus research, education, support and advocacy. Shop with purpose: buff.ly/BmAh0bW

📣 Nominations are still open for our Evelyn V. Hess Award and Mary Betty Stevens Young Investigator Prize. Whether they're an early-career or seasoned #lupus researcher, nominate someone who has made incredible contributions to #lupusresearch by 7/20: buff.ly/887Txqa

Do you live with #lupus, care for someone who does, and are 18+? We want to hear from you. Your responses are anonymous and will help shape the future of lupus care, education, and support. Take our online survey by 8/20 to share your experience: buff.ly/suP7TB0

Happy #NationalVideoGameDay! 🎮 DYK you can stream and play games anytime of the year to help end #lupus? Turn your stream into a fundraiser or join #GOTEL in May to raise money for lupus research, education and support programs 💜 Learn more: buff.ly/PAI5y8w

We're proud to share that Lupus Science & Medicine, LFA's open-access journal, has achieved a 2025 Journal Impact Factor of 4.2, up from 4.0. We're also pleased to welcome four new members to our Editorial Board. Explore the latest #lupusresearch: buff.ly/MGcOquI

Each breakthrough in #lupus treatment starts with people like you.  Clinical trials are how new treatments are born, and every participant brings us closer to better options for everyone living with lupus.  Find a trial near you: buff.ly/HcXMDpn

👟 The #WalktoEndLupusNow is more than an event, it's community. Hear from our CEO Louise Vetter, #lupus warrior Kayla, and lupus advocate Lynn on what makes the day so meaningful to those living with and affected by lupus. Find a walk near you: buff.ly/47f0gOC

☀️ DYK 40% to 70% of people with #lupus find that UV exposure makes their symptoms worse? From sunscreen to covering fluorescent bulbs with UV filters, there are steps you can take to protect yourself indoors and out. Learn more: buff.ly/tiMhusd

Put yourSELF first this July! 💜 Use the free SELF app for four days this month and you could receive a LFA purple on-the-go bag and pillbox. Track #lupus symptoms, track medications, or read the Activity of the Day. Supplies are limited! Start today: buff.ly/6b5bQU0