Lupus News

05/27/2025

Did you know that the Lupus Foundation of America provides free education and support services to people with and caregivers? 💜 From support groups to educational programs, the Lupus Foundation of America is here for you — every step of the way.

Learn more: https://buff.ly/xurzOiq

05/27/2025

Ninety percent of people with are women, with Black, Latinx, Indigenous, Asian and Pacific Islander people disproportionately affected, both in prevalence and severity.

Since lupus affects each person differently and symptoms can change over time, continued research that includes adequate representation of women and people of color in lupus clinical research is essential to the development of effective new therapies.

Learn more this : https://bit.ly/ManyOneCan2025

05/25/2025

💜 doesn’t follow a script. Early signs can be subtle, change over time, or easily missed. But with more awareness, more people can get the answers they need.

🔗 Click the link in our bio to learn more about lupus and help raise awareness this .

Reposted@lupusorg

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💜 doesn’t follow a script. Early signs can be subtle, change over time, or easily missed. But with more awareness, more people can get the answers they need.

🔗 Learn more about lupus and help raise awareness this : https://buff.ly/fRQwUks

05/24/2025

05/24/2025

05/22/2025

05/22/2025

05/14/2025

Breaking News: The American College of Rheumatology has released new guidelines for the treatment and management of systemic lupus erythematosus. The guidelines are another critical step in improving care in line with advancements in treatment and understanding of lupus. Read the summary: https://t.co/NUMmNnuBRJ

05/14/2025

📍Live from Washington, D.C.!

The Lupus Research Alliance is in Washington DC today with passionate advocates, researchers, and supporters, calling on Congress to prioritize lupus research funding.
Our panelists are bringing personal stories and expertise to help drive lasting change. We’re urging Congress to:

🟣 Increase funding for lupus research at NIH & DoD
🟣 Restore and grow support for the DoD’s Lupus Research Program
🟣 Back the Lupus ABC public-private partnership
🟣 Say NO to cuts that would slow progress toward a cure
📣 We’re here to raise our voices for those living with lupus. Stay tuned as we share more.

05/11/2025

Happy Mother's Day to all mother figures! Your strength and love are truly remarkable. 💜❤️

05/10/2025

It’s ! 💜 Like Izzy, show your support and help make lupus visible by rocking your best purple outfit or accessories today! 💜✨ Join the global lupus community and take action to raise awareness.

📸 Drop a pic of yourself in purple in the comments or post on your own page with !

Learn more about how you can get participate and raise awareness: https://buff.ly/qHvUgoP