LRA is accepting nominations for the 2024 Lupus Insight Prize, which honors a remarkable investigator who has made a groundbreaking discovery in lupus-related scientific fields between 2019 and 2023. Nominate a fellow academic or industry professional: bit.ly/LRA-LIP24

The NY Jets and LRA will host #lupusAwarenessDay 12/3 today, at MetLife Stadium when the Jets take on the Atlanta Falcons. This event aims to increase awareness of #lupus and raise funds supporting critical research. Huge thanks to the @nyjets and good luck in today’s game! 💜🏈

Check out our resource center for helpful information like a glossary of lupus-related terms and downloadable educational information for the lupus community: bit.ly/lupusresources  #lupusresources #lupusinformation

Neuropsychiatric lupus affects 80-90% of people with lupus. It’s important to speak with your health care provider about all of your symptoms to be able to find the right treatment for you. Learn more lupus-related terms at lupusresearch.org/glossary #neuropsychiatriclupus

Exciting news: Three young women who ran on behalf of LRA’S Team #LifeWithoutLupus in @nycmarathon were featured in a FOX News Channel story, showcasing their dedication in running the marathon for Rosie, their beloved friend diagnosed with #lupus. 🔗bit.ly/marathon-news

At the recent annual meeting at #ACR23, important #lupus clinical trial data and breakthrough foundational research were presented - many from studies which were supported by the LRA or our clinical affiliate Lupus Therapeutics. Read more: bit.ly/LRA-ACR23

Thank you @malikjefferson for supporting the LRA and raising #lupusawareness! 💜🏈 twitter.com/dallascowboys/…

It’s important for those with lupus to prioritize self-care and seek support from loved ones, healthcare providers, and lupus support groups."✨ #MyLupus #Lupus #ManyOneCan 🧵3/3

“One aspect of lupus that is not often talked about is the emotional toll it can take on individuals and their families. Lupus can be a challenging disease to live with, as it often involves unpredictable flares of symptoms and can require significant lifestyle changes. 🧵2/3

Next in our series highlighting the unique experiences of individuals in the #lupuscommunity, we introduce you to Precious Otiora. Precious was diagnosed with SLE at 23. She shares this hopeful message on the importance of prioritizing self-care when living with lupus. 🧵1/3

#GivingTuesday

Thank you to our #BreakingThroughGala host @tamronhall for supporting the LRA and #lupuscommunity and sharing awareness on her show today! youtu.be/Qe_kUbUij2k

Celebrating @GivingTuesday with @Classy_org and @gofundme on the @Nasdaq stage, ringing in a day dedicated to generosity and positive impact. 🙌✨

Double your Impact this #GivingTuesday! Your gift before midnight TONIGHT will be MATCHED up to $20,000 thanks to a generous supporter of the LRA! Your gift will fund promising projects, find new and personalized treatments, and one day a cure for #lupus: bit.ly/LRAGIVE23

Lupus can be difficult to diagnose because it affects every person differently, can impact almost any organ, and can even change within the same person. Here are symptoms and measures doctors use as a guide to determine if a person has #lupus. bit.ly/Lupus-Diagnosis

50-90% of people with lupus identify fatigue as one of their primary symptoms. Share how you recharge.😴 #lupus  #SLE  #autoimmune  #fatigue

Join our social media communities and stay connected! #LupusResearchAlliance

Thanks for making this year's Walk with Us to Cure Lupus unforgettable! Your steps, stories, and generosity mean the world. Although the 2023 Walk season has ended, you can still support #lupusresearch until 12/31. Your donation makes a difference! 💜 bit.ly/walk-give

Happy Thanksgiving holiday! We hope you have a wonderful day with family and friends! 🦃🍁

📸: Travis W Keyes Photography, ​​​Tamara Fleming Photography

THANK YOU to all who joined us at our #BreakingThroughGala, raising $2 million for #lupusresearch! Gratitude to honorees Kate & David Kies, Laura Kies Gever, and Louis Shapiro. Special thanks to @tamronhall & @ChloeFlower for an unforgettable night.💜🔗: Bit.ly/LRAGala2023

Last night was moving, inspiring, powerful! @LupusResearch twitter.com/LupusResearch/…

✅ After a high-level @LupusResearch meeting, what a joy to see the Empire state lighting up with the colors of #Lupus awareness. The #LRA is funding amazing #SLE research and it is truly an honor for me to be part of their scientific advisory board 👍 twitter.com/LupusResearch/…

Enjoying supporting #lupus research at the @LupusResearch Gala in NYC! For once @alhkim was not my favorite guy in the picture, my husband came too!

THANK YOU for the AMAZING outpouring of support at tonight’s 2023 Lupus Research Alliance #BreakingThroughGala Fundraising Event!✨

Lupus warrior Laura Kies Gever shares her own personal experience living with #lupus for more than 30 years at our #BreakingThroughGala. Thank you!💜

2023 Gala honoree David M. Kies, Board of Directors, gives a touching speech on how #lupus has affected his family and why progess is important. #BreakingThroughGala

LRA recognizes honoree Louis A. Shapiro, Advisor, Past President and CEO, @HSpecialSurgery. Louis shares why he’s so passionate about #lupus research and progress during his speech at our #BreakingThroughGala!

@LAlupusLady @Annezab @LADAOrg @ACRheum Thank you 💜

It’s not too late to help us reach our goal for the #BreakingThroughGala! Text to Pledge NOW to make an impact on #lupus research and progress: 📲 646-749-2572 👉 Type Your Name/Company Name 👉Amount of donation 👉 Send!