Statement from Sandra C. Raymond, President and CEO of the Lupus Foundation of America
Results show how disease takes a toll on life for people with lupus and lupus caregivers
New study reinforces need for Patients’ Access to Treatments Act (H.R. 460) to reduce excessive financial burden placed on people with chronic diseases
Studies Focus on Advancing Research and Improving Quality of Life for People With Lupus.
Professional Soccer Player and Olympic Gold Medalist Shannon Boxx Scores New Goal As Lupus Awareness
The Lupus Foundation of America’s Summer Issue of Lupus Now® Magazine highlights Shannon Boxx' journey as a professional soccer player living with lupus.
Spring Issue of Lupus Now® Magazine highlights how Maurissa Tancharoen Whedon found support through her all-star network of friends and family.
LFA Funded Studies Focused on Advancing Research and Improving Quality of Life for People with Lupus
Investigators Present Research Findings at 2011 American College of Rheumatology Scientific Meeting.
The HealthWell Foundation® announces the launch of a new fund supporting treatment for Systemic Lupus Erythematosus.