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.
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.
Learn More "Every day, every time you give your love and hope to another who is in need, it might not seem like a lot but stacked with others you might be part of a miracle!"
- James Stroker
You might be a part of that miracle!
We all feel stressed from time to time, but the holidays offer their own special stressors that can make us feel even worse - gift shopping, family obligations, finances, and perhaps, the grief and sadness that accompanies the loss of a loved one. Stress can be unhealthy. Join Dr. Adair F. White-johnson, best-selling author and motivational speaker as she provides tips , tools, and strategies for thriving this holiday season.
Register TodayWe hope you will join us on December 13th for a special presentation by Aurinia to learn about lupus nephritis, an inflammation of the kidneys caused by lupus, and a different treatment option from rheumatologist/nephrologist Elizabeth S. Clayton, MD . We will also hear from a person living with lupus nephritis who will share her personal journey.
Register Today These meetings are so important because they remind us that we are not alone in our stresses and struggles of having a child with lupus. We'd love to hear your child's story, or you can just join to listen to others experiences with lupus. Either way, we'd love to have you!
Second Sunday of Each Month
If you have lupus, you’re at higher risk for infections like the coronavirus, also known as COVID-19. Some people with lupus may also be at risk for more serious complications from catching the coronavirus.
Join S. Sam Lim, MD, MPH as he provides up to date information on a monthly basis about what we know and don’t know about COVID-19 and how it may impact those living with lupus in Georgia. Watch the November 14th recording on the right.
NEXT MEETING: December 12th at 9 PM
Send your questions to info@lfaga.org
Thank you to everyone who has sent their photos and videos. We love them!!
Here's how to send your walk photos/videos!
The file sizes of videos are often large. To send the video, we recommend using WeTransfer. Go to WeTransfer.com from your computer, or phone if you filmed on your phone, upload your video file and send it to walk@lfaga.org.
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.
Read more about all of the lupus research that was shared at this year’s American College of Rheumatology Convergence 2021.
New research uncovers an association between a potential chemical imbalance and poor cognitive performance in people with lupus.