Cynthia shares her lupus journey, from diagnosis and a major flare to finding strength, community and hope through Walk to ...

Join us and thousands of walkers in cities across the U.S. and Walk to End Lupus Now! Each event provides people affected by lupus and their families and friends with the opportunity to come together ...

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The start of a new school year often brings excitement and even some first-day butterflies. But for children and teens living with lupus, the back-to-school season can also bring a unique set of ...

"Bringing awareness to a disease that effects 1.5 million Americans is a big part of what the organization does, but on a smaller scale, brings together people who really need a support team." Lindsey ...

A new study identified 39 candidate measures for an updated tool to better assess long-term organ damage in people with ...

We support everyone affected by lupus. Whether you are living with lupus, a parent, spouse or loved one - we're your partner on this journey. The Lupus Foundation of America provides education and ...

Before my diagnosis, I had been sick for a couple of weeks and then developed a rash, but I did not think much of it at the time. I was also feeling extremely fatigued, but I assumed it was just ...

Hello my name is Quan’Tahnece! I was diagnosed with lupus at 34 years old. I am currently dealing with multiple organ issues due to lupus. My lupus flare is currently in severe mode (heart, stomach, ...

One year ago, I was given a name for something that had already begun changing my life: lupus SLE. At first, it felt like everything I knew about myself—my energy, my plans, even my sense of ...

What started as a hopeful pursuit to grow my family quickly turned into an odyssey marked by pain, emotional and physical suffering, and moments of hopelessness. In 2020, I did fibroid surgery as part ...