A new study supported by the Lupus Foundation of America and published in Arthritis and Rheumatology offers clinicians and researchers a new way to better understand how various treatments may impact the quality of life of children and adolescents living with lupus.
Lupus Foundation of America activist, Mallory Dixon, reflects on her life living with lupus and shares her incredible lupus journey over past year. Read Mallory's story and learn why she is grateful for her lupus diagnosis and how she lives each day to the fullest.
A recent review of lupus quality of life studies found five common themes that describe the experiences of adults living with lupus. Healthcare providers can now use these themes to develop and expand patient-focused care and support services that will improve health and treatment outcomes.
As 2013 comes to an end, Sandra C. Raymond, President and CEO, reflects on the advances Lupus Foundation of America has made over the years, and speaks about the key priorities for the future.
Jody Gehrmann shares her experience of living with lupus and staying physically active and the journey she and her husband are taking to climb Mount Kilimanjaro.
New study reinforces need for Patients’ Access to Treatments Act (H.R. 460) to reduce excessive financial burden placed on people with chronic diseases