Our mission is to improve the quality of life for all people affected by lupus through programs of research, education, and advocacy. In fulfilling our mission, we provide a variety of services and support for those living with lupus and their support systems.
The philosophy of LFA support groups is to provide a warm and caring environment where people with lupus, their family members, caregivers, and loved ones can share their experiences, methods of coping, and insights into living with lupus. LFA support groups encourage and accept people as they are and provide a comfortable learning environment to help them develop the best coping strategies to reduce stress that often accompanies living with a chronic illness.
The National Resource Center on Lupus includes many helpful resources for people with lupus, their families and health professionals.
Share your experiences and find support.
Our health educators are available to answer your questions and give you the help you need.