We hope that you’ll consider joining a Walk to End Lupus Now in your community this fall and raise much needed funds. Here is a short guide on how you can be successful in your walk fundraising efforts.
Rowan Mulligan turned her lupus diagnosis into an opportunity to change her community and raise money and awareness for those affected by lupus. Read her story.
Off-label drugs for the treatment of lupus symptoms represents the standard of care for people with lupus, but current regulations make it difficult for doctors and manufacturers to communicate. Read Sandra C. Raymond's remarks now.
Preguntale a Los Expertos es una serie de charlas educativas y presentaciones sobre una variedad de temas diseñados para proporcionarle información importante sobre la vida con lupus.
August 2015 - Dr. Donald Thomas answered your 15 questions about lupus diagnosis.
In honor of National Friendship Day, we’re sharing some of your advice on how friends could better support people with lupus in maintaining a social life.
Attorney by day, romance novelist by night, Chloe Barlow found her inspiration to write after struggling with the realities of chronic illness. Read her story now!
Lupus wasn’t Alex's disease at all — it was her mom’s. That all changed when she was diagnosed at 16-years-old but her dream to create films has not dampened. Read her story.