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Lupus Foundation of America

@lupus.org

1.1K followers 36 following 770 posts

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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Lupus Foundation of America @lupus.org · Jul 3

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

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Lupus Foundation of America @lupus.org · 41m

Flu and COVID season is here — and for people with #lupus, prevention is key. Our new resource shares ways to stay protected this winter, from vaccines to everyday precautions.

Learn how to prepare, protect, and stay healthy through the colder months: buff.ly/5K7DaBZ

Lupus Foundation of America @lupus.org · 1h

Nuestro compromiso con la comunidad hispana/latina con #lupus va más allá del #MesDeLaHerenciaHispana. Ofrecemos más de 150 recursos en español revisados por expertos, además de grupos de apoyo para asegurarte de que tengas información y conexión en cada paso del camino. Aprende más: buff.ly/ZDt0zOS

Lupus Foundation of America @lupus.org · 1h

Our commitment to the Hispanic/Latino #lupus community goes beyond #HispanicHeritageMonth. 💜 We offer 150+ expert reviewed Spanish-language resources, plus support groups to ensure you have information & connection every step of the way.

Learn more: buff.ly/ZDt0zOS

Lupus Foundation of America @lupus.org · 8h

An estimated 1.5 million Americans live with #lupus, facing pain & uncertainty each day. Your workplace gift brings hope, resources, & crucial research.

Designate the Lupus Foundation of America in your campaign to help build a future with breakthroughs: buff.ly/rCtWI7G

Lupus Foundation of America @lupus.org · 1d

This Thursday, join us for Lupus & You: After Dark! This free virtual event explores #lupus, sexual health, intimacy, and menopause with experts and lupus warriors.

Register now: buff.ly/llyMbVB

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Lupus Foundation of America @lupus.org · 1d

What is your life with #lupus like? 💜 We're looking for photos that show the real experiences of people with lupus - the ups, the downs and everything in between. From butterfly rashes to quiet victories and big accomplishments.

📷 Submit photos here: buff.ly/1UN4yNT

Lupus Foundation of America @lupus.org · 1d

💜En este #MesDeLaHerenciaHispana, hemos enaltecido voces e historias hispanas/latinas con #lupus y compartido recursos clave.

Nuestro trabajo continuará. Únete para honrar su fortaleza y explorar herramientas paraq ayudar a cada travesía por el lupus: buff.ly/Lz1yld4

Lupus Foundation of America @lupus.org · 1d

💜 This #HispanicHeritageMonth, we’ve uplifted the voices & stories of the Hispanic/Latino #lupus community while sharing key resources.

Our work continues year-round — join us in honoring their strength & explore tools to support every lupus journey: buff.ly/Lz1yld4

Lupus Foundation of America @lupus.org · 2d

Have questions about #lupus? Tomorrow, we’re hosting an Instagram Q&A with our Health Education Specialists, Lety & Lupe! 💜

👉 Submit them today on our Instagram Stories (in English or Spanish) & we’ll answer during the Q&A: buff.ly/mDlTa3N

Lupus Foundation of America @lupus.org · 4d

💜➡️ Diagnosticada a los 15 años, la Dra. Meléndez convirtió su travesía en una misión de esperanza. Hoy, es reumatóloga y facilitadora del grupo de apoyo en Puerto Rico.

🔗 Explora nuestros grupos de apoyo en español: buff.ly/7GgvFr3

Find Support Near You

The Lupus Foundation of America and our national partner network run lupus support groups nationwide. Find a group near you.

www.lupus.org

Lupus Foundation of America @lupus.org · 4d

💜➡️ Diagnosed at 15, Dr. Meléndez turned her journey into a mission of hope. Today, she’s a rheumatologist and facilitator for our Puerto Rico support group, helping others find connection.

🔗 Explore our Spanish-speaking support groups: buff.ly/7GgvFr3

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Lupus Foundation of America @lupus.org · 5d

💜 Watch as #lupus warrior Mo’Nay takes you through her day at the Los Angeles #WalktoEndLupusNow — from getting ready to joining the crowd and walking to end lupus!

There’s still time to take part this fall! Find a walk near you: buff.ly/nbH3oNE

#DayInTheLife #DITL

Lupus Foundation of America @lupus.org · 5d

🎥 Our CEO Louise Vetter and #lupus warrior Lynnore joined PIX11 to raise awareness about lupus & share the impact of the #WalktoEndLupusNow – NYC at Pier 17. Their conversation highlights the power of community & support.

💜 Watch the full video: buff.ly/aHXDVlS

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Lupus Foundation of America @lupus.org · 5d

We’re just one week away from #TwitchCon San Diego! 💜 Stop by booth 3444-CH in the Charity Zone to meet the team, reconnect with GOTEL alumni, and learn more about #GameOnToEndLupus 2026. Don’t miss our Meet & Greet Sunday at 2pm! 🎮

Lupus Foundation of America @lupus.org · 5d

🎥 #Lupus warriors, Linda and Racquel, joined @12OnYourSide.com to share how to get involved in the #WalktoEndLupusNow - Richmond, happening tomorrow at Midtown Green! 💜

Hear their inspiring stories and learn how to take part: buff.ly/HMlF2XS

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Lupus Foundation of America @lupus.org · 5d

Living with #lupus can be unpredictable. Talking with the people in your life is key to getting the support you need. Together, you can plan ahead and make managing flares a little easier.

Learn practical ways to care for your health and find support: buff.ly/HPdsaYV

Lupus Foundation of America @lupus.org · 5d

We’re halfway through the fall #WalktoEndLupusNow season! Shoutout to the top fundraising walkers & teams leading the way!

There’s still time to register & rally your family & friends: buff.ly/nbH3oNE

Lupus Foundation of America @lupus.org · 6d

📅 Mark your calendars for our October 16 Lupus & You event! Join us next week as Ken, Jeanine, and other speakers discuss sexual health and #lupus, including how menopause can affect intimacy, confidence, and connection.

Register today ↓
buff.ly/57s7BXR

Lupus Foundation of America @lupus.org · 6d

New study finds women with systemic #lupus erythematosus and with mild cognitive impairment exhibit measurable brain changes. Read the study: buff.ly/EYappPE

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Lupus Foundation of America @lupus.org · 6d

💜 It’s Donor-Advised Fund (DAF) Day! Make a gift from your DAF to power #lupus research & support services. No DAF? You can still give through stock, IRA, or legacy gifts — every contribution brings us closer to a cure.

👉 Give today: buff.ly/SnlLHG4

#DAFDay

Lupus Foundation of America @lupus.org · 6d

🆕💜 Nuestro blog del #MesDeLaHerenciaHispana incluye historias personales y recursos. El lupus tiene un profundo impacto en la comunidad hispana/latina, y la concientización y los recursos son importantes.

👉 Lee el blog: buff.ly/Lz1yld4

Lupus Foundation of America @lupus.org · 6d

🆕💜 Our #HispanicHeritageMonth blog now includes featured personal stories and resources.

Lupus has a profound impact on the Hispanic/Latino #lupus community making awareness and resources especially important.

👉 Read the updated blog: buff.ly/Lz1yld4

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Lupus Foundation of America @lupus.org · 7d

💜 Living with #lupus can take a toll on your mental health as well as your body. Our resource shares practical ways to care for your emotional well-being. From finding support to improving sleep, there are many strategies to explore — and even more in the full guide.

Read here: buff.ly/C5XVpPR

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Lupus Foundation of America @lupus.org · 8d

Congratulations to the 2025 Nobel Prize winners in Physiology or Medicine for groundbreaking discoveries in T-cell response and immune regulation—paving the way for better understanding and treatment of #lupus and other autoimmune diseases.

Learn more: buff.ly/S6XDYVn

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Lupus Foundation of America @lupus.org · 9d

¡Nuevo Episodio! El dolor es uno síntoma común del lupus. Hablamos con la Dra. Kromo sobre qué causa el dolor de #lupus, cómo puede afectar tu vida diaria y tu salud mental, y estrategias para manejarlo.

💜 Escucha ahora: buff.ly/I8Ppsni
#MesDeLaHerenciaHispana