Women are disproportionately affected by lupus. Black/African American and Hispanic/Latino/a/x/e women are 2-3x more likely than white women to develop #lupus and have severe symptoms. #ManyOneCan learn more about #lupus research: bit.ly/ManyOneCan2024  #LupusAwarenessMonth

Happy National Women’s Health Week! ✨ Let’s empower women to prioritize their health, particularly those living with #lupus . While lupus can affect anyone, it predominantly impacts women, with about 9 out of 10 adults diagnosed being female. 
 
#LupusAwareness #WomensHealthWeek

When our community joins together and speaks up, our elected officials listen. Anyone can advocate for the #lupusresearch funding needed to bring us closer to a cure. Learn about advocacy efforts and how you can help: bit.ly/ManyOneCan2024 #LupusAwarenessMonth

Join @hspecialsurgery as they host free virtual and in-person programs in honor of #LupusAwarenessMonth ! hss.edu/lupus-awarenes…

● Hospital for Special Surgery (HSS) is hosting a virtual LANtern® Support Group on 5/18 for the Asian lupus community, led by Eliza Ngan-Dittgen, Program Supervisor, LANtern® (Lupus Asian Network). Register at: hss.edu/lupus-awarenes… #AANHPIHeritageMonth #HealthEquity #LupusAwarenessMonth 3/3

Check out our partners' initiatives in honor of the month: ● FDA Minority Health and Health Equity invites you to listen to the newest episode of the Health Equity Forum podcast, “Engaging Native Hawaiian Communities in Clinical Trials.” Listen here:  fda.gov/consumers/heal…

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This month the LRA honors the cultures and traditions of Asian American, Native Hawaiian, and other Pacific Islander communities. Lupus disproportionately affects #AANHPI populations, highlighting the urgent need for greater awareness and support. ✨

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It's not too late to make your voice heard! The LRA's new Social Media Toolkit makes it easy with sample posts, images, and content that can be shared during #LupusAwarenessMonth .

#ManyOneCan make a difference. Download: bit.ly/ManyOneCan2024

#lupus research #lupus

This #LupusAwarenessMonth , learn about Project CHANGE by Lupus Therapeutics, the clinical research affiliate of LRA, which aims to increase diversity in #lupusresearch . bit.ly/4dmc2Og

Despite higher prevalence, communities of color are underrepresented in clinical trials. #ManyOneCan get involved with research funding that diversifies clinical trial participation. Learn more: bit.ly/ManyOneCan2024 #LupusAwarenessMonth

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

#Mothersday #Lupus

Thank you to the sponsors and all attendees at this year’s #LuCINCommunity Meeting! We're grateful, hopeful, and inspired by the dedicated #lupus community and our shared mission to ensure people with lupus have equitable access to safe & effective therapies and clinical trials.

Interesting panel discussions happening today at the #LuCINCommunity Meeting on the critical need for diversity in #lupus clinical trials to help bring us closer to more effective treatment options. Learn more about #lupus research bit.ly/LuCIN2024

Wearing purple and sharing the importance of funding Lupus Research - Happy #WorldLupusDay

Join us in 1 month for our Northern Michigan Walk with Us to Cure Lupus event on 6/8 at Mineral Springs Park!  The Walk is a fun way to help raise funds for important research for #lupus .  Register now! bit.ly/walk2024-NM 
 
#ManyOneCan #LupusAwarenessMonth

Honored that on #WorldLupusDay we are surrounded by a team of leaders in the #lupus community and having discussions on #lupus clinicalresearch and cell therapies paving the way for more treatment options in #lupus at #LuCINCommunity Meeting 2024 #LupusTherapeutics .

💜 Today is #WorldLupusDay ! Let’s take time today to shine a light on #lupus , honor every lupus champion, and celebrate all who are making a difference. We stand together! You are not alone. #ManyOneCan get involved: bit.ly/ManyOneCan2024 #LupusAwarenessMonth

#LupusTherapeutics , the clinical affiliate of the LRA is honored to host the 4th annual Lupus Clinical Investigators Network (LuCIN) Community Meeting, together with clinical investigators, study coordinators, individuals with lupus, research & industry partners. #LuCINCommunity

We’re proud to stand with the Lupus Agencies of NYS at the NYS Capitol and others representing the lupus community during #LupusAwarenessMonth . Together, we're dedicated to raising #lupus awareness  and support for those affected by #lupus . 💜