Lupus Foundation of America is the only national force devoted to solving the mystery of lupus while giving support to those who suffer from its brutal impact.
Washington DC
Joined February 2009
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We're proud to share our research at #ACR26 (@ACRheum)! Our studies explore #lupus diagnosis, treatment, access to care & patient priorities, reflecting collaboration between researchers, clinicians & people with lupus.
Learn more about our research: buff.ly/dUR9Ikp
🏃💜 Congrats to our Racing to End Lupus team for completing the 2026 TCS @NYCMarathon! They took on 26.2 miles to raise funds and awareness for people with #lupus. Thank you to everyone who supported them!
Learn how to join us next year: buff.ly/muofxyD
#TCSNYCMarathon
We are at #ACR26 (@ACRheum)! Our team is presenting eight abstracts on #LupusResearch, from diagnosis and treatment to access to care and more.
Learn more about the research we’re presenting and its potential to advance lupus care and treatment: buff.ly/dUR9Ikp
Stay tuned! Follow us on LinkedIn for research highlights and updates from #ACR26: buff.ly/iHYIgdP
One week until #TwitchCon! 🎮 Find us at booth 3444-CH in the Charity Zone to connect with the team, catch up with GOTEL alumni and learn how you can get involved with #GameOnToEndLupus. We can’t wait to see you in San Diego! 💜
#FactFriday 💜 Pain can affect daily activities for people with #lupus, but there are ways to manage it. Working with your doctor to identify the cause and explore options like physical therapy, sleep and at-home strategies can help.
Learn more: buff.ly/SLuWbTN
Mark your calendars! On December 1, join us for #GivingTuesday to raise #lupus awareness, fuel research, and provide resources and support to people affected by lupus.
📅 Save the date and make a difference: buff.ly/b57OaBE
💜 This #NationalFamilyCaregiversMonth, we recognize care partners supporting loved ones with #lupus. Our Caregivers Information Center offers tips & resources to help you build a support network and care for yourself.
Learn more: buff.ly/2OKzyUX
Update: The @US_FDA has granted breakthrough therapy designation to CIMZIA® (certolizumab pegol) for the prevention of adverse pregnancy outcomes in women with antiphospholipid syndrome and #lupus anticoagulant. Read the announcement: buff.ly/uFn8W6y
🚨💊 Medicare Part D Open Enrollment is underway! Medicare Part D covers prescriptions for over 56 million Americans, including people with #lupus.
Read our updated blog for resources to help you compare plans and make informed decisions before 12/7: buff.ly/qyqzrSh
💜 November is #NationalHospiceandPalliativeCareMonth!
Did you know palliative care isn’t just for end-of-life care? For people living with #lupus, it can help manage symptoms, provide support, and improve quality of life at any stage.
Learn more: buff.ly/hRbZevH
🆕 A new episode of The Expert Series is live!
Dr. George Tsokos explains how #lupus arthritis differs from other forms of arthritis and discusses common symptoms, flare triggers, lifestyle strategies, and more.
🎧 Listen now: buff.ly/QSk3cQM
This episode of The Expert Series was sponsored by @Biogen. The Lupus Foundation of America would like to thank Biogen for their support of education programs for people with lupus.
Join us in recognizing #NativeAmericanHeritageMonth! 💜 #Lupus disproportionately affects American Indian and Alaska Native (AI/AN) communities.
Explore our latest blog for resources to help raise awareness and improve outcomes: buff.ly/vJIJvTa
🏃💜 NYC, come cheer with us! Our Racing to End Lupus team is taking on the TCS @NYCMarathon tomorrow!
📍 Join our cheer section in Long Island City, Queens, just before mile 14 at Vernon Blvd & 47th Rd. Look for our purple Racing to End Lupus signs and banners!
#TCSNYCMarathon
The #WalkToEndLupusNow community continues to make an incredible impact this season! 💜
Join us in recognizing the top fundraising teams and individual walkers leading the way so far.
Find ways to get involved: buff.ly/s2rMhX2
San Diego, here we come! 🎮💜 We’re headed to #TwitchCon in just two weeks.
Stop by booth 3444-CH in the Charity Zone to meet the team, connect with the community and learn how you can join the fight against #lupus through #GameOnToEndLupus.
#FactFriday 💜 Understanding #lupus and its impact on children can help parents make informed decisions about their care. Staying informed about symptoms, treatment and daily health needs is an important part of managing the disease.
Learn more: buff.ly/JKZ1HCz
Want to take part in a #lupus study? A new clinical research study is now evaluating the safety and effectiveness of an investigational medication in adults with lupus.
Answer a few questions and see if you qualify: buff.ly/BwtgvTH
Meet Joanna. 💜 Diagnosed with RA and #lupus at 24, she remembers being terrified and wondering if her life was over before it started. At 40 now, she has earned a doctorate, traveled the world, and chosen to fight every single day.
Read her full story: buff.ly/jZbGrK5
