Fundraising has officially begun and registration is now open for the 2026 Walk to End Lupus Now events in St. Louis and Kansas City. • St. Louis Walk to End Lupus Now Join the Heartland lupus ...

Immunovant has announced topline results from a proof-of-concept study evaluating treatment imeroprubart (IMVT-1402) in ...

My name is Ray Cora. I’m 32 years young, from the Bronx, New York, and I was diagnosed with lupus when I was 24. One of the hardest parts of living with lupus is that I often don’t look how I feel.

In this episode of the Lupus Foundation of America's The Expert Series podcast, Dr. Paul Hoover discusses what we know about obesity and its impact on people living with lupus, how GLP-1 therapies ...

A new systematic review and meta-analysis found that people with systemic lupus erythematosus (SLE) had a significantly ...

I was diagnosed with lupus at the age of 15. I'm 17 now, trying to live with an illness I have no clue about was hard. Not going outside, always feeling tired, not being able to be a regular teen was ...

I was sick before I ever had a name for what was happening to me. I spent my junior and senior years of high school sick, and my senior year I was homebound. While other teenagers were planning ...

Hi, my name is NiCraisha and I was diagnosed with lupus when I was in high school. My symptoms started out with me having red blisters on my fingers and the tips of my toes. I started out with a ...

The Lupus Foundation of America’s Lupus & You: Philadelphia Empowerment Conference is an in-person event that celebrates, inspires, supports, and uplifts lupus warriors, care partners, family, and ...

A new study found that non-Hispanic Black individuals with systemic lupus erythematosus (SLE) experienced the highest rates ...

In this Lupus & You recording, experts and guest speakers discussed legal rights at work, the social security disability insurance (SSDI) process and ways to manage the emotional impact of stepping ...