Lupus Foundation of America, Lone Star Region

03/18/2026

Join us for the Dallas Lupus & You: Empowerment Conference, an inspiring event that celebrates and supports lupus warriors, care partners, family, and friends. Connect with others, hear from expert speakers, and gain tools to help navigate life with lupus.

Hosted by the Lupus Foundation of America, Lone Star Region on Saturday, May 9, 8:00 AM – 12:30 PM at the Scottish Rite Hospital Conference Center.

Register today: https://www.lupus.org/lonestar/events/2026-dallas-lupus-you-empowerment-conference

03/06/2026

It takes an average of 6 years to receive a correct lupus diagnosis. That’s 6 years too long. Join the Virtual 6 Challenge and help raise awareness and funds to reduce the time to diagnosis.

Run, walk, bike, dance. Conquer your 6 your way, anywhere.

Register today! https://www.lupus.org/fundraise/virtual-6

03/03/2026

Lupus nephritis is a serious complication of lupus that causes kidney inflammation. It affects up to 60% of people, often within five years of diagnosis, and can lead to kidney damage if untreated.

If you have lupus, talk to your doctor about screening and visit our Information Center to learn more. https://www.lupus.org/lonestar/resources/lupus-nephritis-resources

02/24/2026

Join us the LFA for a patient-friendly webinar exploring this exciting area of . Learn how T-cell engagers aim to help “reset” the immune system, where these therapies are in clinical trials, what participation looks like, and what to know about safety and side effects.

Register now: https://www.lupus.org/lonestar/events/tcell-engagers-what-lupus-patients-need-to-know

We’re just one day away from our free webinar on T-Cell Engagers!

Join us tomorrow for a patient-friendly webinar exploring this exciting area of . Learn how T-cell engagers aim to help “reset” the immune system, where these therapies are in clinical trials, what participation looks like, and what to know about safety and side effects.

Register now: https://buff.ly/A9KPT5W

02/19/2026

Hair holds deep meaning in the Black community, and lupus-related hair loss can feel isolating. You’re not alone. Understanding how affects hair and scalp health can help you choose care and styles that work best for you.

02/12/2026

Registration is open for the 2026 National Summit, April 19–21 in Washington, DC!

Join lupus advocates nationwide to meet with lawmakers, push for more research funding, and improve access to care. Help us turn Capitol Hill purple.

Register today! https://www.lupus.org/lonestar/events/2026-national-lupus-advocacy-summit

02/11/2026

01/18/2026

Meet Anthony. Diagnosed with nephritis at 19. By standing alongside others who understand living with and are using their voices on Capitol Hill in support of important lupus policies, Anthony experienced what advocacy looks like when a community comes together.

📣 Registration for the Lupus Foundation of America's National Summit is open. Join us in Washington, DC on April 20–21 and add your voice to the movement for change. Save your spot today:

The Summit unites lupus advocates to learn, connect, and raise their voice on Capitol Hill in support of federally-funded lupus research and education programs. Join lupus warriors April 19-21 at the 2026 National Lupus Advocacy Summit!

12/10/2025

Please join us on December 11th @ 6:00pm CT for the Lone Star Virtual Town Hall! https://lupusfoundationofamerica.regfox.com/lone-star-town-hall

12/07/2025

Attending Flutter Fest for Lupus & feeling inspired by these amazing high school students from Prosper, TX raising critical funds & awareness in our fight to end lupus 🩷

12/03/2025

Help support Flutter for Lupus this Sunday @ Flutter Fest! Donate now & help support the Flutter for Lupus team from Prosper, TX as they team up with the Lone Star Region in our Fight to End Lupus! https://support.lupus.org/site/TR/MYM/TeamMakeYourMark?pg=team&team_id=39179&fr_id=2215

12/02/2025