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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El #lupus afecta a las comunidades hispanas/latinas a tasas más altas y puede causar complicaciones. 💜 Este #MesDeLaHerenciaHispana, estamos compartiendo información clave para ayudar a crear conciencia.
Descárgala ahora: buff.ly/5GfnYNR
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#Lupus affects Hispanic/Latino communities at higher rates and can lead to complications. 💜 This #HispanicHeritageMonth, we’re sharing key information to help raise awareness of lupus symptoms, risk and warning signs.
Download now: buff.ly/5GfnYNR
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Immunovant shared results from a proof-of-concept study of imeroprubart in cutaneous #lupus. While the study did not meet its primary endpoint, findings may help inform future research in lupus and autoimmune disease.
Read the press release here: buff.ly/HhJc412
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La música, el amor propio y la comunidad han ayudado a Natalis a sobrellevar su experiencia con el #lupus. 💜
En este #MesDeLaHerenciaHispana, descubre cómo conectar con los demás se han convertido en una fuente de fortaleza.
Encuentra apoyo: buff.ly/EuCNxcu
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Music, self-love and community have helped Natalis navigate her journey with #lupus. 💜
This #HispanicHeritageMonth, hear how sharing her story and connecting with others have become a source of strength.
Find support and resources today: buff.ly/EuCNxcu
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💜 @WMAR2News featured LFA ambassadors and member of LFA’s Board of Directors, Dr. Ashira Blazer, sharing their stories and why they join Baltimore's Walk to End Lupus Now.
Following this weekend’s Maryland Walk, hear why every step matters: buff.ly/1AkXcpZ
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🆕 A new episode of The Expert Series is live!
Dr. Paul Hoover discusses obesity, how GLP-1 therapies work, and what researchers are learning about their potential role in #lupus and related health outcomes.
🎧 Listen now: buff.ly/ZxjmIrw
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Black/African Americans make up 43% of #lupus cases nationally & face worse outcomes. For treatments to effectively address this community's health needs, it’s crucial that Black/African Americans share their lupus experience w/patient-registries like RAY: buff.ly/J2kkg3F
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Why do you walk? 💜 Members of the #lupus community share what brings them to Walk to End Lupus Now and why every step is personal.
Join us at a Walk near you and make your reason part of the movement: buff.ly/No6tAZi
💬 Share why you walk in the comments.
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Meet members of the 2026 Racing to End Lupus @Philly_Marathon team! 💜
This fall, 34 runners will take on the marathon, half marathon and 8K while raising #lupus awareness and funds to help end lupus.
Learn the stories behind the miles: buff.ly/C2wsAXG
#phillymarathon
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Managing #lupus takes more than one strategy, and this #SelfCareAwarenessMonth, SELF is here to help. Our free app helps you manage symptoms, stress, medications, and your relationship with your health care team.
Download the SELF app today: buff.ly/NfMcyYx
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New research found that people with #lupus had a higher risk of stroke, including increased risks of both ischemic and hemorrhagic stroke, reinforcing the importance of cardiovascular health in lupus care.
Read the study: buff.ly/Hot3set
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Lupus Foundation of America retweeted
Wildcat Red and Gorlock Blue make Lupus Purple. Thank you to @GorlokWBB for joining us today at the @LupusOrg walk. It was a great way to raise awareness! @HWHSactivities
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Lupus Foundation of America retweeted
Lupus & You: Practical Tips Guaranteed to help people living with #SLE #lupus @LupusOrg
piped.video/watch?v=jXCd68-U…
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Join us on October 14 for our free national Lupus & You virtual education event where we’ll explore practical tips on protecting your skin from UV exposure, navigating cosmetic procedures safely, and choosing the right products.
Register today: buff.ly/QGmjGGe
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Looking for a place to connect with others who understand life with #lupus? 💜 LupusConnect is a free online community for people with lupus and their loved ones to share experiences, find emotional support and discuss tips for daily life.
Join today: buff.ly/asMmNfD
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🏃 Race to End Lupus at the 2027 Double TCS @LondonMarathon!
Join our inaugural team for this historic two-day event and make your miles matter for people impacted by #lupus.
Apply by October 2: buff.ly/1p7jQSs
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Durante tres generaciones, el #lupus ha formado parte de la historia familiar de Yvette. En este #MesdelaHerenciaHispana, ella comparte cómo la familia, la fe y la defensa de sus propios intereses marcaron su trayectoria de 30 años.
💜 Lee más: buff.ly/Y2a3P0q
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For three generations, #lupus has been part of Yvette’s family story. This #HispanicHeritageMonth, she shares how family, faith and self-advocacy shaped her 30-year journey. She hopes more Hispanic families will talk openly about health.
Read her story: buff.ly/Y2a3P0q
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