Welcome to Georgia | Georgia
Over 55,000 Georgians are living with lupus. Whether you are living with lupus or loving someone with lupus, we are here.
We are back IN PERSON for our 2022 Walk to End Lupus Now! We can't wait see you at parks and stadiums across Georgia! Let's gather and celebrate our successes and imagine the possibilities of a world without lupus.
REGISTER TODAYBuilding relationships is the most important aspect of advocacy. Relationships with legislators will provide you with opportunities to work more closely with them to get bills introduced, assist in drafting bill language, shape the debate and, ultimately, get legislation signed into law. Dorothy Leone-Glasser, RN, HHC, Executive Director of Advocates for Responsible Care will facilitate a discussion exploring the importance of building relationships with our elected officials.
Register Now We have something for everyone, from caregivers, family, and friends to men living with lupus. Please join us for our Summer Webinar Series led by Courtney Mitchell, RN, BSN, CFNP, Patient Engagement Liaison with GSK.
A new online self-management program designed to help people with lupus build and enhance skills in four pillars of lupus self-management: managing symptoms, managing stress, managing medications and working with their healthcare team.
Give SELF a try nowCheck out the ways our passionate supporters across Georgia are turning their events into fundraisers benefitting the Lupus Foundation of America, Georgia Chapter. Imagine what you could do? Let us know if you are interested in hosting a third-party event, contact Teri Emond at temond@lfaga.org for more information.
Check Out Our Inspiring Third-Party Fundraisers We are following the developments regarding a COVID-19 vaccine and booster shots very closely. As we learn more we will keep you up to date on what is important for people with lupus.
The Pfizer COVID-19 vaccine has received full approved by the FDA and we anticipate Moderna and Johnson & Johnson are soon to follow.
Let's Talk About It is a series of monthly webinars designed to provide you with important information about living with lupus and better managing your symptoms. Live webinars are accessible through a link provided after registration.
You sleep plenty (you even nap), but you’re always tired. Some days, the pain in your joints and muscles makes you feel three times your age. You work hard and take care of business—but there are times when it feels like your body is fighting against you. Lupus can be like that. Learn More.
Take Charge is a weekly education email series for people with lupus, including those recently diagnosed. Each week for 12 weeks, you'll get an email from our Health Educators with tips and resources that can empower you to take charge of your health.
IMPORTANT NOTE: The well being of our patients is our highest priority. Due to COVID-19 and in accordance with CDC guidelines, all support will be held via teleconference until further notice. Our Support Network is essential to all the Chapter’s efforts, working tirelessly to support patients, our programs and events and advocate for awareness.
A lupus activist engages in educating their federal, state, and locally elected officials about the cruel mystery of lupus. Whether through a letter, email, phone call, or face-to-face meetings with elected officials, lupus activists are the vital voice on legislation and policies issues impacting people with lupus and their families. An activist’s voice makes a difference.
We have SO much to offer the Lupus Community in 2020 and we are looking for some dedicated volunteers and committee members to help us reach our goals!
The GOAL project, lead by the Division of Rheumatology at Emory University. to better understand how lupus may impact patients' lives. We need to hear from you to build the wealth of knowledge needed to transform health care and improve health outcomes.
The mission of the GCLEA is to improve the lives of Georgia residents who live with lupus by raising public education and awareness, improving access to resources for patients and family members, obtaining information that will inform current and future public health efforts, and increasing appropriate diagnosis of lupus by non-rheumatologists. Read more.
Stay up-to-date on coronavirus news, reliable information, and resources, all geared toward people affected by lupus. Even in these challenging times, we are here to support you.
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Researchers found the skin cells in people with lupus have a unique “signature” that influences skin cell behavior and increases skin disease risk.
The deadline for researchers to submit a pre-application for any of the three opportunities is August 16, and applications must be submitted by September 1.