A big obstacle for kids with a chronic illness like lupus is the uncertainty of their condition. They may feel fine one day and unwell the next. Add the stress of school to this and, understandably, ...

Using isobaric tags for relative and absolute quantitation (iTRAQ) screening technology, a new study published in Lupus ...

The Lupus Foundation of America is pleased to announce six recipients of the 2024 Gina M. Finzi Memorial Student Summer ...

In a new study, researchers looked to understand the changes in the molecular structure of systemic lupus erythematosus (SLE), looking specifically at disease remission and discovered several genetic ...

The Lupus Foundation of America works to improve the quality of life for all people affected by lupus through programs of research, education, support and advocacy.

When your rheumatologist asks you, “Are you getting enough exercise?” what’s your response? For many with lupus, the answer may be “no.” It’s not lack of desire that’s holding people back, though.

We are excited to announce the formation of a NEW Lupus Support Group in Augusta. Please fill out the form below and we will keep you posted.

We educate, empower, and connect you to resources and support so that you can live your best life with lupus. Our educational video series features empowering presentations from leading lupus experts ...

In a new case report, investigators recommend that in women with systemic lupus erythematosus (SLE), physicians must work closely with the woman to determine whether in vitro fertilization (IVF, a ...

I was diagnosed with Lupus in August 2014 at the age of 34. I had bad tingling in my hands and feet. My hands then turned blue and I was placed on antibiotics and sent home. I then had fever and a ...

Hi, my name is Charisma Atkins from Decatur, GA and I have been living with Lupus for nearly 25 years. I was first diagnosed with Lupus SLE as a graduate student in 2001 but as I look back over my ...