Lupus Foundation of America

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.

[Lupus Foundation of America @LupusOrg]

Behind every step at #WalktoEndLupusNow is a reason to walk. Maybe it's for yourself, maybe it's for someone you love, maybe it's both. Every step brings us closer to a future free of #lupus.

Who are you walking for? Comment below and find a walk today: https://t.co/xborYDG3nc

[Lupus Foundation of America @LupusOrg]

💜 Meet Yolanda. Diagnosed at 49. Through the LFA, she found a community that helped her understand #lupus and reminded her she is not alone. Her photos capture the highs and lows of a journey that is uniquely her own.

➡️ Share your life with lupus: https://t.co/CLWVrMK1yd

[Lupus Foundation of America @LupusOrg]

A new study finds people with systemic autoimmune rheumatic diseases like #lupus and clinicians describe flares differently, especially in how quickly they start, how they are recognized, and whether they require changes in treatment.

Read the study: https://t.co/aYIolCaIrf

[Lupus Foundation of America @LupusOrg]

This #PainAwarenessMonth, we're highlighting the link between chronic pain and #depression for people with #lupus. Our new blog with Heather Artushin, MSW, LISW-CP, explores this connection and shares 6 evidence-based approaches that can help.

Learn more: https://t.co/URfytXFEdG

[Lupus Foundation of America @LupusOrg]

Fall #WalkToEndLupusNow season is almost here! 👟💜 Communities across the country are coming together to raise funds and awareness for everyone living with #lupus.

Find a walk near you and register today: https://t.co/xborYDG3nc

[Lupus Foundation of America @LupusOrg]

Researchers identified two molecular subtypes of lupus nephritis that differed in immune activity, kidney function and chronic kidney damage. They also identified APOL1 as a candidate biomarker that may help distinguish between the subtypes.

Learn more: https://t.co/farpNNau5Y

[Lupus Foundation of America @LupusOrg]

Meet the 2026 Racing to End Lupus TCS @nycmarathon team! 💜

This November, nine runners will take on 26.2 miles while raising #lupus awareness and funds to help end lupus.

Get to know the team: https://t.co/M4eGqDgeoc

#TCSNYCMarathon

[Lupus Foundation of America @LupusOrg]

Want to make an impact for #lupus community from your phone or computer? Start a Facebook fundraiser to rally your network for a meaningful cause. Every dollar funds LFA research, education, resources for millions with lupus.

Get started today: https://t.co/d5IIIUjPCU

[Lupus Foundation of America @LupusOrg]

Novartis and Bristol Myers Squibb have paused their CAR-T trials for #lupus and other autoimmune diseases to review safety concerns. CAR-T remains experimental, and continued research is needed to understand its benefits and risks.

Read the announcement: https://t.co/lIPRag9hWr

[Lupus Foundation of America @LupusOrg]

Many people with #lupus experience skin problems like rashes and sores, and for some, lupus affects only the skin.

This #SkincareAwarenessMonth learn the signs to help you recognize symptoms early and find treatment.

Read more: https://t.co/VyzRHVZE57

[Lupus Foundation of America @LupusOrg]

@TiffanyWitcher Thank you for supporting the lupus community and for putting together such a meaningful event in honor of your mother. 💜

[TIFFANY - The Benevolent Bard Coming 2027 @TiffanyWitcher]

My biggest Charity Concert yet! More singers, duets and even group songs. This will be for the @LupusOrg in honor of my Mother on October 4th! Be sure to check out all these talented singers joining!

I have worked super hard on this!

[Lupus Foundation of America @LupusOrg]

🆕 A new episode of The Expert Series is live!

Dr. Susan Goodman shares what people with #lupus should know before surgery, from medications and care coordination to recovery and recognizing a possible flare.

🎧 Listen now: https://t.co/Ape6Ej9FIe

[Lupus Foundation of America @LupusOrg]

🎉 Here are August'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: https://t.co/fUVSm8x8MI

[Lupus Foundation of America @LupusOrg]

Lupus Foundation of America Ambassador and Asian Community Support Group facilitator Karen Ng shares how her experience with #lupus nephritis became a mission to educate, connect and support others. 💜

🔗 Read her story: https://t.co/D53zFL2npF

[Great Plains ADA Center @ADAGreatPlains]

Upcoming learning opportunity happening September 6!
#DisabilityEmployment

[Lupus Foundation of America @LupusOrg]

August is #MakeAWillMonth. Planning ahead brings peace of mind and protects loved ones. With @FreeWill_HQ, making your will is free & secure. Include a gift to the Lupus Foundation of America to support #lupus research, education, & advocacy.

Start now: https://t.co/BRMqyrkM6z

[Lupus Foundation of America @LupusOrg]

💜 Tierney shares what so many in the #lupus community know. Flares can be relentless, and the people around you don't always see it. Check on the ones you love.

Share this resource with friends and family to start the conversation: https://t.co/mHquM24ndq

[Lupus Foundation of America @LupusOrg]

It’s the final week with @AUProSports, and we’re proud to cheer on lupus warrior and LFA Ambassador @MayaJohnson_SJA, who chose LFA as her charity this season. Thank you for continuing to bring visibility to the #lupus community, Maya. Finish strong!

[Lupus Foundation of America @LupusOrg]

Join us on September 16 for our free national Lupus & You: Answers. Advocacy. Action. virtual education event where we’ll discuss workplace accommodations and Social Security Disability Insurance (SSDI).

Register today! https://t.co/GA9fuI4Osn