Lupus Foundation of America

#MakeLupusVisible this May for #LupusAwarenessMonth! 💜 While many symptoms of #lupus aren't visible, the impact is real. Join us all month long as we raise awareness for the millions living with this cruel disease. Learn more: buff.ly/3OCV73t

How much do you know about #lupus? Play @lupusorg’s #KnowLupus game to find out and join me in making lupus visible! lupus.org/knowlupus

We made the video and did the thing! WE STILL RAISING MONEY TOO!

💜 Meet Samantha. At 7, her mom helped her out of bed every morning. 2 years later, a #lupus diagnosis changed everything. Now, a lupus advocate and Miss Potomac's Teen 2026 — she's asking you to take the #KnowLupus Quiz and share it with your loved ones: buff.ly/mKgepMN

Ahh snap. We made the video 💜

Hey look! It’s me! What an incredible month so far and we still have so many more events to go! 💜

Its time to play more games and raise more awareness! Happy Lupus Awareness Month! Check out @LupusOrg to learn even more about lupus! Episode 4 of Marvel's Spiderman Remastered starts now! Lets get those donations today! Twitch.tv/steveanger

#GOTEL is in full swing! Content creators worldwide are helping end #lupus. In 2 weeks, 200 streamers raised over $150,000 for lupus research, education, & support. Whether you play games, make music, or craft, join us all May & keep the momentum going: buff.ly/MhTIpXA

May marks both #LupusAwarenessMonth and Women’s Health Month. In the latest Bio.News story, @LupusOrg discusses the ongoing challenges facing lupus patients, the latest advances in research and treatment, and why greater awareness remains critical - particularly as lupus disproportionately affects women, especially women from historically underserved communities. Read the full story on Bio.News: bio.news/latest-news/lu…

Later today! Join me for my post-birthday hangout stream where we'll be checking out a ton of @womenledgames demos, games, and raising money for @LupusOrg!

#FactFriday 💜 No two cases of #lupus look the same — and neither do treatment plans. Managing lupus often means finding the right combination of medications and lifestyle changes that work for you. Learn more about treating lupus: buff.ly/uBNiRHy #LupusAwarenessMonth

Join us May 20 as our speakers break down what Phase III #clinicaltrials & FDA Fast Track therapies mean for people living with #lupus — hear real patient stories, current opportunities, and what's ahead for lupus care. Register and submit Q&A questions: buff.ly/dOkJqvF

LFA advocate Scarlett was 3 when doctors gave her a 1/10 chance of leaving the hospital. After 118 days in the ICU, she was diagnosed with #lupus. Her story is a powerful reminder of why early awareness and diagnosis matter. Read her story in @People: buff.ly/psneMqB

@hallyuhamkke Thank you for all the support! 💜

Game on To End Lupus donation event is live! There will be a place to donate on the check out page of the website until the end of May. All customers that donate will receive a free gift with their purchase! Thank you for another year of allowing us to fight with you, @LupusOrg~!

@WarriorButtrfly 💜

Living with #lupus has taught me that information is power & #clinicaltrials are the next chapter of lupus care. Join me 5/20 for a free @LupusOrg webinar on Phase III clinical trials, hear patient stories, current opportunities, & more. Register today: lupus.org/events/the-nex…

What exactly is lupus — and why is it so difficult to diagnose and treat? During the GOTEL (Game On to End Lupus) charity campaign, SciAnts_Streams sits down with Dr. Joy Buie for an in-depth discussion on the science of lupus, autoimmune disease, and the future of immunotherapy. From B cells and autoantibodies to CAR T-cell therapy and precision medicine, this interview breaks down complex immunology into accessible, engaging science communication. Dr. Buie explains how lupus causes the immune system to attack the body itself, why the disease can affect nearly every organ system, and why diagnosis often takes years. The conversation also explores the latest lupus treatments, including biologics, monoclonal antibodies, interferon inhibitors, and emerging therapies that may one day “reset” the immune system entirely. Whether you’re interested in immunology, autoimmune disease research, medical science, or patient advocacy, this episode offers a fascinating look at one of the most complex diseases researchers face today. @LupusOrg youtu.be/W3dMGH88i0M

Our #KnowLupus Quiz is live—are you up for the challenge? It’s time to test what you REALLY KNOW about #lupus. 💜 Take the quiz, post your score, tag us, and we'll reshare! Let’s #MakeLupusVisible! Play now: buff.ly/mKgepMN

💜💪 2 weeks left in #LupusAwarenessMonth and there's still time to make an impact! Start a Facebook fundraiser. It's quick, easy, and every dollar raised helps fund the #lupus research, education, and resources that change lives. Create a fundraiser: buff.ly/5SPjGKK

Understanding #clinicaltrials is key to the future of #lupus treatment. Phase III trials are the final stage before regulatory approval to confirm new lupus therapies are safe. Want to get connected to a trial? Join us for a free webinar on 5/20: buff.ly/dOkJqvF

This #JewishAmericanHeritageMonth, #lupus warrior Shira is shedding light on the unique challenges people with lupus face within faith communities, and how those communities can show up in ways that truly matter. Read her story: buff.ly/aCa2Wda