We’re leading the charge in the future of #lupusresearch with the #LupusLandmarkStudy — powered by Lupus Nexus. Hear how this study, led by Devon Kelly, LRA Director of Lupus Nexus, will make a difference in the lives of people living with lupus.

Today we are meeting to celebrate the first anniversary of #LupusABC , a partnership uniting individuals with #lupus and industry, clinicians, researchers and government to identify and pursue ways to accelerate lupus drug development. Visit bit.ly/LupusABC #lupus voices

BREAKING: The Lupus Accelerating Breakthroughs Consortium ( #LupusABC ) announced an expanded partnership with FDA Biologics to advance engineered cell therapies, a huge step in #lupusresearch and lupus drug development. Read on to learn more bit.ly/LupusABC01

#lupusvoices

No single test can determine whether a person has lupus. The doctor will look at the entire picture — medical history, symptoms, and test results — to determine if you have #lupus .

Here are a few ways to prepare for your visit with your health care provider.

Join our Northern Michigan Walk with Us to Cure Lupus event on Saturday, June 8 at Mineral Springs Park! ☀️ 👟🙌

Sign up as a team or individual and kick-start your fundraising efforts! bit.ly/walk2024-NM

#ManyOneCan #lupus #WalkwithUs #lupus community

El lupus es una enfermedad autoinmunitaria crónica y compleja. Los síntomas más comunes son cansancio extremo, erupción malar, inflamación de las articulaciones y fiebre sin causa aparente.

Obtenga más información: bit.ly/lupusespanol

#LupusEnEspañol

FUNdraising for #Lupus in NYC this May with Jøyus

'Songwriter Showcase at Joanne Trattoria NYC Supporting Lupus Research Alliance'
eventbrite.com/e/songwriter-s… @Eventbrite RSVP Now!

We’re pleased to announce the team of industry partners working together to bring the Lupus Nexus to life. Lupus Nexus is a first-of-its-kind lupus registry, biorepository, and data exchange platform to accelerate #lupus drug development and patient care. bit.ly/LNx-LRA

It's #NationalSiblingsDay ! We share the story of TwoBeingHealthy -- two sisters and strong social media voices - Em & Kate - who are so close they seem like twins. They went to the same college, see the same doctors, and share the same diagnosis - #lupus . bit.ly/EM-KATE

It's time to gear up for an unforgettable day at the 2024 New Jersey Walk with Us to Cure Lupus on 5/4, at MetLife Stadium. 🙌

Join us and the #lupus community for a day filled with celebration, family-fun activities, music and more! Register now! bit.ly/NJ-WALK24

It’s #NationalPoetryMonth ! 💜

Shanelle Gabriel, singer/poet/lyricist/advocate for lupus awareness, shares her inspiring original poem 'Living While Living with Lupus' as a message to encourage fellow #lupus warriors. 🎤✨

#lupus awareness #lupus poem #LupusResearch #lupus voices

🌍 On #WorldHealthDay , let's spread #LupusAwareness . The cause of lupus remains unknown, but there is solid evidence that genetics, epigenetics, environmental factors, viruses and infections play a role.

Learn about #lupus symptoms, treatments, and more: bit.ly/aboutlupus

It’s #NationalVolunteerMonth ! We are so grateful for our community and every individual that volunteers with the LRA. Your support is extremely valued and makes a difference. Thank you! 💜

No individual can do it alone, but together #ManyOneCan !

This April, we're spotlighting J. Christopher Reed in our #CommunityInspiration blog as he urges taking action on healthcare disparities for minorities during #NationalMinorityHealthMonth ! He's passionate about fair representation in #lupustrials .
bit.ly/communityblog-…

We’re 1 month away from the New Jersey Walk with Us to Cure for Lupus! Join us on Saturday, May 4 at MetLife Stadium! Register for the Walk as a team or individual and begin fundraising! bit.ly/NJ-WALK24

#ManyOneCan #lupus #WalkwithUs #lupus walk

Celebrate #NationalWalkingDay by taking a step forward in finding a cure for lupus! Join forces with the lupus community to support groundbreaking lupus research through our Walk with Us to Cure Lupus events this season. Visit Walk.lupusresearch.org to get involved! 👟🙌

We can't wait to come together as a community for this year's Northern Michigan Walk with Us to Cure Lupus event on Saturday, June 8 at Mineral Springs Park! Register now! bit.ly/walk2024-NM

#ManyOneCan #lupus #WalkwithUs #lupus walk

Lupus is a complex disease that can be difficult to comprehend, especially for children. Mack the Molecule is here to help!

Download this poster explaining lupus in a way kids can understand, too! bit.ly/lupusresources

#lupus #lupus research #lupus awareness #symptomsoflupus

Join us for our New Jersey Walk with Us to Cure Lupus event on Saturday, May 4 at MetLife Stadium! Register for the Walk as a team or individual and begin fundraising! bit.ly/NJ-WALK24

#ManyOneCan #lupus #WalkwithUs #lupus walk

In honor of #NationalDoctorsDay the Lupus Research Alliance would like to thank all the doctors who are working so hard today and every day! 👩‍⚕‍👨‍⚕‍ #DoctorsDay