Everyone who participates in a Walk to End Lupus Now™ does so for a different reason. But all of us are working toward a common goal: to raise funding and awareness for lupus research and education. Crystal Torres is just one of them.
Spring is officially here and Walk to End Lupus Now™ is in full swing. See our upcoming Walks from around the country.
After years of suffering from symptoms invisible to most people, Savannah Knudtson decided to start speaking out about what lupus means to her life and the lives of her loved ones. This is her story.
April 2015 - Sharon Mack, Health Educator for the Lupus Foundation of America, provides helpful tips and advice about caring for a loved one with lupus while caring for yourself as part of the Ask the Experts program.
Earlier this month, the Lupus Foundation of America was honored to play a role in the launch of Geek & Sundry’s Twitch.tv channel. Read more about the event that raised more than $160,000 for lupus research and awareness programs and how you can host your own fundraiser.
Chris Joyner always looked up to his sister Dawn. Their shared love of music helped Chris become a professional musician but her life with lupus inspired him to write a song about her struggles. Read more.
This year, the Lupus Foundation of America is implementing numerous projects to achieve our goals to increase federal support for lupus research and services to benefit people with lupus, their families and caregivers. Find out more about two of our exciting endeavors in this letter from our CEO, Sandra C. Raymond.
On the outside, Josie Pearce seems like your average 17-year-old. You’d never know that just a few years ago Josie’s parents were taking her from doctor to doctor, trying to figure out why their once energetic daughter now spent days lying on the couch unable to move or attend the ballet classes she loved.