Lupus Foundation of America
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lupus.org
Lupus Foundation of America
@lupus.org
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. 💜
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Have you ever thought of joining a support group? They offer a place to build community in an understanding environment where people with #lupus come together to share & help each other. Find out more about our support group network: buff.ly/LTFhDUC
Lupus blood tests can feel overwhelming. Our Glossary of Lupus Blood Tests breaks them down, explaining what they mean and how they help diagnose #lupus. Understanding these tests is an important step in managing your health.

📖 Learn more: buff.ly/edcQtGC
January 21, 2026 at 1:01 PM
🎮 Game On! To End Lupus 2025 brought the energy, hitting the $1 million program milestone! Relive the magic and get ready to join us for #GOTEL2026, May 1–3, and all May long!

Stream, fundraise, and help improve the lives of people living with #lupus: buff.ly/JyhcxxM
January 20, 2026 at 3:03 PM
Have you heard of Inside #Lupus Research? It's your one-stop location for learning about the most important #lupusresearch news that matters to you.

Stay on top of the latest, check out the current headlines and subscribe to get them straight to your email: buff.ly/zQt0t4K
January 20, 2026 at 1:01 PM
💜 Meet Titilayo. Diagnosed with #lupus at 34, her year quickly became a cycle of flares, hospitals, and surgeries. She shares her journey to remind others living with lupus that even in the hardest seasons, hope can still exist.

👉 Read her full story: buff.ly/08JwuFq
January 19, 2026 at 1:02 PM
If your company has an employee matching gift program, you can maximize your support for the #lupus community throughout the year by doubling or even tripling your next donation to the Lupus Foundation of America!

Visit our site to learn if your company has a similar program: buff.ly/dFKUJY8
January 18, 2026 at 5:00 PM
Calling clinics that serve people with #lupus. The Lupus Foundation of America is offering Clinical Referral Mini-Grants of up to $7,000 to support referrals to the LFA SELF app, a free, evidence-based lupus self-management tool.

Apply now: buff.ly/jiZM1tb
January 18, 2026 at 2:01 PM
Meet Anthony. Diagnosed with #lupusnephritis at 19. Standing with #lupus warriors, he saw the power of advocacy when we come together. 📣 Registration for the LFA's National #LupusAdvocacy Summit is open. Join us in DC on 4/20-21.

Save your spot today: buff.ly/LYWn0Vy
January 17, 2026 at 2:00 PM
January is #ThyroidAwarenessMonth. DYK thyroid disorders may be linked to #lupus? An Inside Lupus Research article explored the autoimmune connection & why people with lupus may face higher risk.

Read more & sign up for the latest #lupusresearch news: buff.ly/apBKFkG
January 16, 2026 at 1:00 PM
Thank you to everyone who joined our Lupus & You event: Be Your Strongest Voice! 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/RusNwjK
January 15, 2026 at 8:30 PM
Can herbal supplements pose a risk to people with autoimmune diseases like #lupus? A new study identified 15 herbal supplements with immune-activating properties that may increase the risk of potential flare activity. Read the study: buff.ly/jvDleil
New study identifies 15 herbal supplements to potential skin flare activity in people with autoimmune skin diseases
In a new study, researchers examined herbal supplements with immune-activating properties that could trigger or worsen autoimmune skin conditions, such as in people with cutaneous lupus erythematosus…
www.lupus.org
January 15, 2026 at 6:48 PM
Community Health Workers and community-based organizations — we’re funding you!

Apply for up to $4,500 to distribute #lupus self-management guides to community members who aren’t using digital tools. 📅 Applications close January 31, 2026.

Apply now: buff.ly/Xerlj54
January 15, 2026 at 1:01 PM
Tonight’s the night – join us at 7PM ET for our free Lupus & You event.

Hear from our dynamic panel of speakers as they discuss how to clearly communicate with your medical team, advocate for your care & navigate difficult situations.

Register today! ⬇️
buff.ly/RusNwjK
January 14, 2026 at 2:00 PM
The next generation of #lupusresearch starts here. Our 2026 grant opportunities support mentorship, career growth, & innovation in basic, translational, & clinical research—helping scientists improve lives of people with #lupus.

🔗 Apply now: buff.ly/Z4wO34L

#Medsky #Rheumsky
January 14, 2026 at 12:01 PM
Reposted by Lupus Foundation of America
it's that time again! the incentive that gets met every year for GOTEL @lupus.org ! BAD RETRO GAME NIGHT! be there this friday for the chaos you will surely go down!
January 13, 2026 at 2:49 AM
It’s not too late to register for our Lupus & You event tomorrow night, which focuses on how to clearly communicate with your medical team, advocate for your care and navigate difficult situations where you do not feel heard!

Register today! ⬇️
buff.ly/RusNwjK
January 13, 2026 at 12:00 PM
Advocating for your care can feel overwhelming when living with #lupus. Lupus warrior & retired LCSW Racquel knows the power of feeling confident in medical conversations.

💜 Join Racquel & expert speakers for our free virtual Lupus & You webinar on 1/14: buff.ly/RusNwjK
January 12, 2026 at 1:02 PM
UPDATE: AstraZeneca announces positive Phase III trial results for the self-administered subcutaneous version of Saphnelo. Study finds a meaningful reduction in disease activity in adults with #lupus. Read the announcement:
New Phase III study results support self-administered Saphnelo as an effective treatment option for systemic lupus erythematosus
AstraZeneca reported positive results from a Phase III TULIP-SC clinical trial.
buff.ly
January 11, 2026 at 5:31 PM
💜 Meet Desiree. Diagnosed with #lupus at 29. Behind her everyday moments are flares, infusions, hair loss, and learning new limits. She’s learned to move at a different pace. She shares her story so others feel less alone.

➡️ Share your life with lupus: buff.ly/svPUdtJ
January 10, 2026 at 2:00 PM
Feeling dismissed in medical settings is something many people with #lupus face.

💜 Join Brian and other expert speakers for Lupus & You: Be Your Strongest Voice on January 14 — a free virtual event focused on advocating for your care.

Save your spot: buff.ly/RusNwjK
January 9, 2026 at 9:01 PM
Johnson & Johnson has announced positive topline results from the Phase 2b JASMINE study of nipocalimab for adults living with active lupus, meeting primary endpoints. Read the announcement:
Phase 2b JASMINE trial of nipocalimab demonstrates positive results for treatment of systemic lupus erythematosus
Johnson & Johnson announced positive topline results from its Phase 2 randomized placebo-controlled JASMINE study. The drug therapy, nipocalimab, met its primary endpoint and multiple key secondary…
buff.ly
January 9, 2026 at 7:00 PM
Reposted by Lupus Foundation of America
Our biggest event of the year is BACK💜Game On! To End Lupus 2026 is all May long, raising funds for @lupus.org

If you're interested in participating as a streamer, sign up through the link in the message!
#GameOnToEndLupus is back in 2026! 🎮

Join gamers and creators May 1–3, and all May long, to stream, connect, and help raise lupus awareness and funds to support people living with lupus.
Get involved: buff.ly/MrhO4s9
January 7, 2026 at 8:23 PM
Reposted by Lupus Foundation of America
I’ll be registering for this again this year. If you’re looking for a great cause to fundraise for, this is one of them 😄💜
#GameOnToEndLupus is back in 2026! 🎮

Join gamers and creators May 1–3, and all May long, to stream, connect, and help raise lupus awareness and funds to support people living with lupus.
Get involved: buff.ly/MrhO4s9
January 7, 2026 at 11:53 PM
Reposted by Lupus Foundation of America
Yall know this charity is important to me as a lupus warrior myself. But lupus warrior or not, if you know anyone interested in raising money to help find a cure and continue researching treatments, the 2026 registration is now live!

www.lupus.org/fundraise/ga...
January 8, 2026 at 2:18 AM
January is #NationalBloodDonorMonth 🩸, a good reminder about the importance of blood donation and how #lupus affects the blood.

Blood disorders are common with lupus, often impacting platelets and red and white blood cells. Learn more: buff.ly/ZcoDgTf
January 9, 2026 at 1:00 PM
Conquer Your 6 to End #Lupus in 2026, March 24–29. Run, walk, bike, hike, paddle, dance, stretch - whatever you choose, while raising awareness for lupus diagnosis delays and supporting research, education, advocacy, care, and services.

Register now: buff.ly/bvaGW3Y
January 8, 2026 at 8:00 PM