Everyone should have an emergency preparedness plan and, in addition, for people living with lupus make sure you have a “lupus kit" ready to go. Being prepared now will keep you healthy and safe.
Join us for the 2022 Walk to End Lupus Now season! We are happy to announce that our Florida walks will be returning in-person, and we will also have a Virtual Mid-South walk this year for our Kentucky, Alabama, and Tennessee warriors and their families.
Our health education specialists are specially trained to provide people affected by lupus with non-medical counseling, disease education, information, and helpful resources. You have lupus, but you are not alone. Let us know how we can help.
No matter how long you’ve been living with lupus, the SELF online self-management program has the tips and tools to help you better manage your disease. Learn more.
Visite nuestro Centro Nacional de Recursos sobre Lupus en Español. Visit our National Resource Center on Lupus in Spanish
September is National Pain Awareness Month. Many people with lupus experience pain in their joints and muscles. Read here to learn how you can manage pain with the help of a doctor or at home.
A free educational series where people with lupus, their family and friends can learn more about the latest in lupus research and managing the disease
A birthday party. A bake sale. A 5k. A half marathon, marathon, or triathlon for lupus. There's no limit to how you can raise money to fight lupus. Here are some popular ways lupus advocates like you around the U.S. are bringing their communities closer to raise critical funds for lupus research.
In order to protect our patients, loved ones, and facilitators during COVID-19, we have moved our support groups online, and we invite you to join us virtually via Zoom. Please click the link to RSVP for the groups.
Help us create more meaningful moments for lupus warriors. Your support and generous contributions to the LFA supports life-saving research, education and advocacy initiatives to bring an end to lupus.
Many companies will match donations made by employees and retirees to eligible charitable organizations, like the Lupus Foundation of America. Find out if your company does and double your impact.
A tribute donation to the Lupus Foundation of America is a thoughtful and lasting gift to honor or remember someone whose life has been impacted by lupus and a way to join the movement to end lupus.
Itolizumab shows promise for the treatment of lupus nephritis.
In a new study, scientists improved the prediction accuracy of adverse pregnancy outcomes (APOs) using machine learning.
In a new study, researchers found that lack of sleep was associated with increased risk of lupus in women.
The latest phase III trial investigating ustekinumab (Stelara) found there was not sufficient evidence to support its use as a lupus treatment.
We are following all developments as they relate to Covid-19 and lupus and will keep you updated as they happen.Read More