When Lisa Walters was diagnosed with lupus last month, she didn’t expect to feel relieved. But after eight years and around 50 doctors, Lisa had rarely left an appointment feeling satisfied with the answers she received about why she was experiencing painful symptoms. Read about her journey to diagnosis and the importance of never giving up.
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.
Foundation grantees Dr. Jill Buyon and Dr. Jane Salmon recently presented results from their research on pregnancy in women with lupus. Read more.
You have questions, we have answers. Watch now.
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
Julian Lennon is a long-standing supporter of the Foundation, and our thoughts and prayers are with him and his family during this time.