One of the things announced yesterday was our @lupus.org Game On! To End Lupus campaign of this year! We will have our fundraiser on May 16th in an extra long stream! Make sure to clear your calendars! If you want to participate, signups are still open! Scan the QR code to get all the information!

After his sister was diagnosed with #lupus, Andrew found his way to make a difference — one mile at a time. The LFA is building our inaugural team for the 2026 Philadelphia Marathon Weekend! 5 spots per distance. Join us and apply by April 13th: buff.ly/LVO9aVt

Can't make it to the National #LupusAdvocacy Summit in-person? Virtual Advocacy Day is just 2 weeks away — and you can still raise your voice for #lupus research, education, and care from anywhere. Sign up as a Lupus Foundation of America advocate today: buff.ly/xG5U3xB

🧠 Ever have trouble finding the right word, remembering details or concentrating? Up to 80% of people living with #lupus experience brain fog at some point. 💜 Learn more about lupus brain fog, what causes it, and ways to manage it: buff.ly/XDyUFT3

💜 For the #lupus community, stress management may directly impact flare frequency and severity. Small changes to how you manage stress can go a long way. Learn tips for managing stress with lupus: buff.ly/fFv3icz Reshare this post to help raise awareness!

Missed our latest #Lupus & You webinar on kidney health? 💜 Our new blog recap covers everything from recognizing early warning signs and monitoring to treatment options, lifestyle habits, and advocating for your care with confidence. Read more: buff.ly/KmKykMj

💜 This #StressAwarenessMonth, we're thinking about the #lupus community. For people with lupus, stress can trigger flares and worsen symptoms. The good news? There are steps you can take to manage it. Check out our stress management tips: buff.ly/fFv3icz

🎮 1 month away — #GOTEL is almost here! Whether you stream video games, make music, craft, or create art — you can be part of the fight against #lupus. Join hundreds of creators worldwide May 1–3 or keep the momentum going all May long. Sign up today: buff.ly/XXfvXfs

Doctor visits. Medications. Insurance battles. The financial weight of #lupus is real. This #FinancialLiteracyMonth, remember our Health Education Specialists are here to help connecting you with non-medical resources for free. Reach out today: buff.ly/u8Covx0

🎉 Here are March's top 20 Facebook birthday fundraisers! We’re so grateful for your dedication and impact. 🎂 Got a birthday coming up? Celebrate with a fundraiser for the Lupus Foundation of America! Fuel #lupus research, support, education, and more: lupus.org/facebook

Update: Phase 2 results for litifilimab for treatment of cutaneous #lupus erythematosus show a significant reduction in skin disease activity and continued improvement over time in trial participants. Read the announcement:

As #NationalKidneyMonth comes to a close, kidney health matters all year long 💜 For people living with #lupus, understanding #lupusnephritis & knowing when to get screened can make a difference. Learn more about symptoms, testing, & treatment options: buff.ly/DubOrPM

This #NationalDoctorsDay, we celebrate the health care teams who support people with #lupus. Having the right team matters! 💜 Our free SELF app helps you build a team. Start today and select “working with your health care team”: buff.ly/Pveb73z

Hey look! It’s me! 😄 Join us in May to raise funds for Lupus research and support programs! We are one month away!

New study finds no connection between early use of Plaquenil in pregnancy and reduced risk of preeclampsia or preterm birth in women with #lupus. Read the study: buff.ly/awsQVHA

Meet @cococonfession.bsky.social, #lupus warrior, streamer, Twitch partner & ambassador. In 2020 she united creators to build #GOTEL. 7 years later we’re on the road to $2M for lupus research & support programs. Join Coco and 2026 GOTEL team May 1–3 and all May long: buff.ly/XXfvXfs

Easter is almost here. 🌸🐣 If you’re sending flowers to celebrate, consider ordering through our partner Crayola Flowers. 10% of your purchase supports the Lupus Foundation of America and helps improve the lives of millions affected by #lupus. Shop now: buff.ly/hzP3Dw9 #PurpleForPurpose

🚗 Have a vehicle you’re no longer using? Donate your car, truck, boat, or RV to the Lupus Foundation of America and help fund critical #lupus research, support programs, and resources. 💜 It’s an easy way to make a lasting difference. Learn more: buff.ly/RXAEW4N

Have questions about #lupus? 💜 Our Health Education Specialists are specially trained to provide free, non-medical support, disease education, and resources to help you find answers and live your best life with lupus. Reach out today: buff.ly/u8Covx0

🎮💜 Gamers and content creators, there's still time to join us! Stream, fundraise, and win prizes May 1–3 and all month long! Sign up for #GameOnToEndLupus 2026 to help raise #lupus awareness: buff.ly/XXfvXfs

🏃 The Lupus Foundation of America is now an official charity partner of the 2026 Philadelphia Marathon Weekend! Apply to join our inaugural team — choose the Marathon, Half Marathon, or 8K & race to help end #lupus. Apply by April 13: buff.ly/OdGgEqr

#Lupusnephritis may not show symptoms right away. That’s why understanding kidney health is an important part of living with #lupus. Learn how lupus affects the kidneys, signs to watch for, testing options, and treatments in our resource: buff.ly/Gz0o5Dg

This #NationalKidneyMonth, caring for your kidneys starts with caring for your whole self. 💜 Our free SELF app helps people with lupus manage symptoms, medications, stress, and care coordination. 📲 Download SELF today: buff.ly/Pveb73z

💜 Your story matters. Voices of Lupus is a living collection of real stories from real #lupus warriors that brings hope and awareness to others. Submit your story and read others' today: buff.ly/SKIUXrM

#FactFriday 💜 Fatigue is one of the most common symptoms of #lupus — and daylight saving time can make it harder to manage. Small changes to your rest routine can make a big difference. Learn tips for better sleep with lupus: buff.ly/PUlW4Rm

Because kidneys can’t talk, it’s up to us to check in them to see if they are being impacted by your #lupus. Early monitoring is key, as symptoms aren’t always obvious. Have you talked to your doctor about monitoring kidney health? Repost this to raise awareness! 💜

💜 Meet Kacey. Diagnosed with #lupus at 17. For 18 years, she tried to live like lupus didn’t exist. Now, she’s choosing to live fully — on the trails and slopes — refusing to let lupus define her. Read her full story today: buff.ly/Sb4gKEH

A new episode of The Expert Series is live! 💜 Living with #lupus affects more than your body. Dr. Skoufalos joins us to discuss identity loss, medical gaslighting, finding the right mental health support and reclaiming your sense of self. 🎧 Listen now: buff.ly/mapcv1F

We are proud to welcome Genentech as the National Presenting Sponsor of the Walk to End Lupus Now. 💜 This partnership strengthens our efforts in #lupusresearch, education, & support programs for the people living with #lupus. Read the announcement: buff.ly/0mc8mge

💜 Your athleisure can help end #lupus. Our partner Inspira is proud to donate 1% of every purchase from their curated collection to advance #lupusresearch and awareness individuals and families affected. Shop now and make an impact: buff.ly/hzP3Dw9 #PurpleForPurpose

💜 Meet @forthebiscuit.bsky.social. A #GOTEL streamer on a mission to show the world that #lupus is more than a punchline — it deeply affects people's lives. Join ForTheBiscuit and others May 1–3 — and all May long — as we stream, fundraise, and raise lupus awareness: buff.ly/XXfvXfs

You’re invited to take on the Virtual 6 Challenge, taking place March 24-29! 🏆 6 miles in 6 days, however you like to move, representing the average time of 6 years it takes to get a correct lupus diagnosis I’m fundraising for @lupus.org to find a cure for this mysterious autoimmune disease

It's Day 1 of the Virtual 6 Challenge! 💜 Show us how you're conquering your 6 — post & tag us! Every move raises awareness of the average 6 years to a #lupus diagnosis & fundraises for research, education, & care. 👇 Not too late to join, register today: buff.ly/mE4rbLN

💜 Meet Cheri. Diagnosed at 34, she found a shining light in the LFA during one of the darkest times of her life. Now she's an active advocate for herself and everyone living with #lupus. ➡️ Share your life with lupus: buff.ly/xKd0TPs #KidneyMonth

Meet Curtis. 💜 After losing his daughter Rashara to #lupus, his family formed DeLynn’s Dashing Squad—carrying her legacy through the Virtual 6 Challenge. Rashara loved to run. Now they get active for her. Read his story & join us this week, March 24–29: buff.ly/JDClo58

A #lupus diagnosis can feel overwhelming. 💜 But you don't have to figure it out alone. Whether you're newly diagnosed, supporting a loved one, or want to understand this cruel disease, our resources are here to help you take the first step. Learn more: buff.ly/KKeeP5Q

🚨 The Virtual 6 Challenge starts in 2 days. There's still time to sign up & get active your way. Run, walk, stretch, or anything in between from 3/24–29. Help raise awareness of the 6 years to diagnose #lupus & fundraise for research, education, & care: buff.ly/mE4rbLN

🚨 Today’s the last day to register for meetings with Congress members! Be a part of #LupusAdvocacy and help make a difference for everyone living with #lupus. Sign up now: buff.ly/Cb0Xaq6

The fight against #lupus needs YOU. 💜 Walk, fundraise, advocate, raise awareness, or partner with us - when you show up, it makes a difference. Join a community of people committed to ending lupus. Learn how to get involved today: buff.ly/EqceujX

💜 Meet Jami. Diagnosed with #lupus at 15. From high school to a career in engineering, her path has included challenges & growth. Today, she listens to her body, knows her limits, & continues building the life she wants. Your story matters. Share today: buff.ly/SKIUXrM

What if diagnosing #lupusnephritis didn't require a kidney biopsy? This #NationalKidneyMonth, learn how Dr. Fava from John Hopkins Medicine and recipient of LFA's Career Development Award is bringing earlier answers & better outcomes. Learn more: buff.ly/ERVnXs3

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/y8LdGPA

🚨 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/Cb0Xaq6

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/YDxFZjG

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/vWE0GQB #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/d8NxlQJ

🧠 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/BmGE0le

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/vWE0GQB

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/6tqZEtN

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/vWE0GQB