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Join the Lupus Foundation of America, Dr. Jillian Rose, AVP Community Engagement, Diversity & Research, Dr. Ashira Blazer, Assistant Attending Rheumatologist at Hospital for Special Surgery, and a patient advocate, for an important presentation on navigating bias in the healthcare setting. We will learn how our own biases may impact medical decision-making, how to identify bias in the medical setting, and tools & strategies to strengthen your voice as a lupus patient.
May is Lupus Awareness Month! It’s an opportunity for the lupus community to join together across the country to raise funds and awareness of the physical, emotional, and economic impact of lupus. Let's Make Lupus Visible!
Join the BWH Lupus Center at our annual Spring Lupus Forum! Lupus patients, family, and caregivers are invited to attend and hear from our Lupus Center physicians and invited speakers on important topics in lupus such as new medications and trials, cardiovascular disease, and navigating life with lupus.
Registration is open for the 2022 Walk to End Lupus Now Season!! Thank you for all of your continued support.
We are pleased to welcome Michele Insley to the LFA Northeast team. In her new responsibilities, Michele will be managing the Walk to End Lupus Now events in Boston and Hartford. Michele can be reached by email at insley@lupus.org.
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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