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We're committed to partnering with those living with lupus, their loved ones, friends, and the medical community to fulfill our vision of a life free of lupus.
The nation's largest lupus advocacy event is going digital again in 2021! Join us from March 2-4, 2021 as thousands from the lupus community come together virtually for two days of educational and networking opportunities focused on lupus advocacy, research, and drug development. Finally, meet virtually with your members of Congress to advocate for policies to improve the quality of life for everyone affected by this disease.
Please join us for our upcoming online Lupus & You program: Managing Pediatric Lupus During the Pandemic on March 30th at 4pm. This online education program will focus on navigating disease management during the pandemic, for both patients and their caregivers.
This April Fool’s Day we are bringing the laughs to you! On April 1st at 8pm we will be hosting an online Comedy Night from the comfort of your own home. Comic, lupus warrior and LFA friend Ayanna Dookie will be hosting a night of comedy as she alongside other lupus warrior comics perform an evening of fun and side-splitting laughter.
Please visit this landing page for information on the coronavirus and lupus. It contains information from the Lupus Foundation of America regarding the coronavirus, updated as needed, with additional FAQs from our National Health Educators.
Nearly 1.5 million Americans live with lupus, a chronic illness, yet those who suffer may not "look sick". Learn the facts about this cruel and mysterious disease and resources for managers, employees, and their family members. We'll share essential tools and information about how you can help the Lupus Foundation of America.
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