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Whether you or your loved one just received a diagnosis of lupus or have been living with it for a long time—we are here to help you live better with lupus now and in the years ahead. No one fights alone!
We Are Here To Help
Receiving the diagnosis of lupus can be a stressful or frightening moment for both the patient and the family. It is important to realize that help is available and you are not alone. You can also fill out our Health Educator request form to have a health educator contact you directly.
Our health education specialists are specially trained to provide people affected by lupus with non-medical counseling, disease education, information, and helpful resources. You have lupus, but you are not alone. Let us know how we can help.
LFA support groups, led by trained facilitators, offer a warm and caring space for people with lupus, their families, caregivers, and loved ones to connect, share experiences, and find support in managing the challenges of this chronic illness.
Each year, the regions host empowering programs with local and national experts in lupus diagnosis, treatment, and research, featuring insights from medical specialists and inspiring stories from lupus warriors and caregivers.
In addition to the support and services our chapter provides, we maintain a list of resources and other helpful organizations to support you and help you live better with lupus. Learn more about these helpful resources.
Our living collection of trusted, up-to-date lupus resources is created by doctors, scientists, health educators, and people with lupus, providing you with expert information to better understand the disease.
The Expert Series is a monthly educational podcast featuring leading lupus experts sharing insights to help you live well, with new episodes released every third Thursday—subscribe for email notifications!
Stories from lupus warriors, caregivers, family and friends highlighting their courage and power. Personal stories help us find hope and remind us that no one fights lupus alone.
SELF: Strategies to Embrace Living with Lupus Fearlessly. No matter how long you’ve had lupus, the SELF program offers tips and tools to help you manage better. Explore SELF now.
The Be Fierce. Take Control. ™ campaign by the Lupus Foundation of America aims to raise awareness and reduce diagnosis time for young Black/African American and Latina/Hispanic women, who face a higher risk of developing lupus.
Take Charge is a 12-week education email series designed to empower people with lupus, including those newly diagnosed, by providing weekly tips, resources, and skills to help manage the disease and its daily challenges.
Lupus Connect offers individuals with lupus and their loved ones a space to share experiences, find support, and exchange practical tips for managing daily challenges.
We're expanding our list of lupus-aware physicians (Nephrologists, Dermatologists, Cardiologists, Rheumatologists). Help us connect lupus patients with specialists who understand their unique needs. Please fill out the form.