Increasing funding for lupus research is a top priority for the Lupus Foundation of America. We urge Congress to robustly fund the National Institutes of Health (NIH), the largest source of biomedical research (and lupus) funding in the country.
Join Nick and the many others who are sharing their stories by becoming a media spokesperson. Learn more!
Farah Jasmine, author of the blog High Heels and Training Wheels, discusses some of the difficulties of taking part in some of the most typical parts of being a parent: back to school shopping and school activities.
Health advocates are part of a new profession to help patients remove barriers to the care they want and need. This emerging field helps patients by building skills and connecting them to resources so patients can participate and drive their health care experience and make the best decisions possible.
Valentina Vergati and her husband Eric are the recent winners of Brides Live Wedding 2014. Valentina, whose father and younger sister were both diagnosed with lupus, is an active member of the Lupus Foundation of America, Lone Star Chapter and explains what lupus means to her.
In her blog, Sara Chang, Senior Manager of Advocacy and Government Relations writes about the importance of participating in surveys.
Thanks to your actions this Lupus Awareness Month, we reached more people than ever before to help raise the profile of lupus. Take a look at what we achieved together.
Global Ambassador Julian Lennon is featured in the Spring 2014 issue of NIH MedLinePlus. Learn more.