Mahlia was diagnosed with lupus at just 8-years-old. Now 11, she is finally starting to speak up about her disease, starting with her participation in the Lupus Foundation of America's new KNOW LUPUS public service announcements.
Before lupus, Allie was fiercely independent and faced every challenge head on. She thought that would all have to change when she was diagnosed with lupus. But with the help of her mom, Allie has been able to triumph over the obstacles that come from a life with chronic illness.
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.
Bonds that stand the test of time - and lupus
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.