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The Latest | Southeast

Every 32 Minutes Someone Is Diagnosed with Lupus

People living with lupus are at the heart of everything we do.

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March Lupus News and Resources
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Lupus and the Kidneys

March is Kidney Month! The kidneys can be significantly impacted by a condition called Lupus Nephritis. If you have lupus nephritis or know someone who does, we have information available for you. Learh more about it here. 

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2024 Lupus & You: Empowerment Conferences

We are thrilled to hit the road with stops in South Florida, South Carolina, Nashville, Orlando & more. You will have access to leading medical experts who will provide insights on lupus treatments, gain tips on managing lupus, engage in a wellness activity, & connect with others.

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2024 National Lupus Advocacy Summit

Join lupus warriors from all over the country for the largest lupus advocacy event of the year in Washington, DC from May 19–21. Don’t miss your chance to turn Capitol Hill purple once again! Learn more. 

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Newly Diagnosed with Lupus? Start here.

Getting a lupus diagnosis can be overwhelming, and not just for the worry about your health. We’re here to help you through this difficult part of your new life with lupus. Read more here.

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Contact A Health Educator

You have lupus, but you are not alone. Our health education specialist provides people affected by lupus with free non-medical support, disease education, information and helpful resources. Contact them today! 

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Join the Champions for Hope Movement

Champions for Hope are our passionate monthly givers who are providing year-round support for life-transforming research and expert and compassionate support to people living with lupus. 

Sebrina WTELN Jacksonville
Supporting the LFA’s mission is essential because it has given a voice to those battling this invisible illness. It has provided a hub for information and education. The LFA has been on the front lines with being an advocate for those who suffer with lupus, as well as those who care for them. Without support, all of the programs that the LFA provides wouldn’t be possible and the information would not be getting to those who need it the most.
Sebrina S., Lupus Warrior
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