Lupus Foundation of America

Can a heart enlargement measure predict major heart and brain events in people with systemic #lupus erythematosus? A new study finds a connection. Read the study: buff.ly/8XTLMlX

🚨 Don't forget: the deadline to book your hotel room with the group discount and register to meet with your members of Congress in April is two days away! Register now: buff.ly/YgJnEWk

@CocoConfession 💜💜💜

💜T-minus 43 days until GAME ON! TO END LUPUS💜 First timers that register by Monday 3/23 will get the official GOTEL tee! Join us! Registration and Discord link below! DMs on Discord open for questions! 🤘🏽

You don't have to do this alone. 💜 This #KidneyMonth, meet Raena — diagnosed with #lupusnephritis at 21 and now a co-facilitator of LFA's National #Lupus Kidney Care support group. Free. Virtual. Open to all. Find your community and join today: buff.ly/IvDsrn3

Thank you to everyone who joined our Lupus & You event: Protecting Your Kidneys! If you missed the event, don’t worry! Check out all of the resources available and the event recording, and keep an eye out for our next event: buff.ly/2kIVLIl #KidneyMonth

🏠 NJ & NY: Your spring cleanout can fight #lupus! Donate gently used clothes, shoes, and household items to support vital lupus research in your community. Free pickup, tax-deductible, and every item makes a difference. Schedule your pickup today: buff.ly/tEWegky

🧠 It’s #BrainAwarenessWeek. From brain fog and memory challenges to headaches, neuropathy, and more, #lupus can impact the brain, spinal cord and nerves in different ways. Learn how lupus can affect the brain and what to watch for: buff.ly/VNa3GHj

@LoreVQ Hi! Thank you for your interest. Research Accelerated by You (RAY®) is currently available only in the US. We'll be sure to share your interest with our team!

@LupusOrg This is only USA or maybe people in Latin american too

You can share your experience living with lupus in our patient-powered registry called RAY. This will help with understanding #lupus and support the development of future treatments & cures that may benefit you & the entire lupus community. Learn more: buff.ly/1ezfLW1

Tonight’s the night – join us at 7 PM ET for our free #Lupus & You event: Protecting Your Kidneys! Hear from experts as they discuss how to protect your kidneys, the importance of early detection, which labs to watch, and treatment options. Register now: buff.ly/1HFUk0H

One week away! ⏳💜 Conquer Your 6 at the 2026 Virtual 6 Challenge, March 24–29 — get active your way, fundraise, and raise awareness of the 6 years it takes to diagnose #lupus. Every step supports research, education, advocacy & care. Sign up today: buff.ly/OozdiB5

It’s not too late to register for tomorrow's #Lupus & You event, which covers how to protect your kidneys, the importance of early detection, which labs to watch, treatment options, and next steps if dialysis or a transplant is needed. Register today! ⬇️ buff.ly/2kIVLIl

Want to make your #GOTEL 2026 stream bigger? Bring in creators for a collab fundraising event — tournament, challenge run, or D&D campaign. More streamers = more chaos & more impact! With 2 months to go, drop into our Discord for help along the way: buff.ly/ek0x9Er

During last night’s @TheAcademy #Oscars show on @ABC, @ConanOBrien insensitively used #lupus as a joke, highlighting the need for lupus awareness & education. Lupus is a chronic disease that can cause inflammation, pain & can be fatal. Read our statement: buff.ly/f8WO7Zy

Meet Joanna. 💜 She's conquering her 6 one run at a time. However you Conquer Your 6 — spin, run, walk, hike, or stretch — join us March 24–29 to fundraise and raise awareness of the average six years to diagnose #lupus. 👉 Sign up now: buff.ly/C5JD3U2

⏰ Have you registered for the 2026 National #LupusAdvocacy Summit in DC yet? One week left to book your hotel room with the group discount & sign up to meet with your members of Congress. Join #lupus advocates April 19–21 to make your voice heard: buff.ly/144pzi2

Has kidney health become overwhelming? 💜 Join Timeka & other experts 3/18 for Lupus & You: Protecting Your Kidneys to learn about early detection, key labs, treatment options, & advanced kidney care options. Register today: buff.ly/1HFUk0H #NationalKidneyMonth

Big news! The LFA's Community Health Workers Mini-Grant Program has awarded up to $4,500 each to Augusta Family Practice, Roots Community Health, MHP Salud & Gamma Pi Rho Lupus Sorority, Inc. to expand access to lupus self-management resources for communities that need them most.

@khal Thank you for your support! We would recommend calling our Northeast home goods partner's customer support line at 1-888-44-LUPUS (1-888-445-8787).

@LupusOrg what do i do if i schedule a donation pickup and they don't show up?