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My Lupus Night Light
From An Outsider’s Perspective
I’ve always been a curious person. Curious about how things come to be. I love to learn and expand my knowledge in anything my brain can get its hands on. When I got hired at the LFA, GOC, my knowledge on lupus was...
Applying for Social Security Disability and Lupus
This article was written by Emily E. Warren, Esq. for the September issue of our Living With Lupus magazine...... The Social Security Administration recognizes Lupus as a medical condition that may prevent a...
Advocate, Educate, Celebrate
This quarter, Living with Lupus magazine is focused on taking the reins of your lupus and making the most of life with a chronic illness. Over the past decade that I have worked for the Lupus Foundation of America,...
Getting the Most Out of Your Relationship with Your Lupus Doctor
How to Get the Most Out of Your Relationship with Your Lupus Doctor By Maria J Antonelli, MD A person finds himself or herself in a vulnerable position when they seek medical care. They are asking for advice on what is...
Our Trip to Capitol Hill
2024 National Advocacy Summit By Suzanne Tierney, Lupus Patient First The 2024 National Lupus Advocacy Summit was held in Washington D.C. from May 19th through May 21st. The purpose of the Summit is to bring lupus...
Spring Cleaning Tips
Spring Cleaning Tips for Life with a Chronic Illness Life with a chronic illness is hard. Lupus patients often have fatigue, joint pain, strained ligaments, muscular pain, headaches, and a host of other symptoms. These...