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 MoreLearn the effective points of a flare plan and receive additional resources to get started, including a guided worksheet to fill out your own flare plan.
Register Today 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 bi-weekly basis about what we know and don’t know about COVID-19 and how it may impact those living with lupus in Georgia. Watch last week's recording on the left.
NEXT MEETING: November 8th at 9 PM
Send your questions to info@lfaga.org
You may not know that all walkers and teams can still raise funds to earn our Club 100 Walk t-shirt and one of the upper level prizes until our October 31st deadline. To date we have raised close to $200,000! In previous walks, more than 10 - 20% of our walk total was raised AFTER the walk.
Check out our NEW incentivesNEXT MEETING: November 8th | CLICK FOR ZOOM INFORMATION: Join Dr. S. Sam Lim, MD, MPH as he provides up to date information on a weekly basis about what we know and don’t know about COVID-19 and how it may impact those living with lupus in Georgia.
The telephonic support group is available via a toll-free conference call, held on the first and third Tuesday of every month from 7:00 - 8:00 pm. Register to receive call-in information and an email reminder. Feel free to reach out to info@lfaga.org with any questions, or call our office at 770-333-5930.
Ask the Experts is a series of monthly educational teleconferences designed to provide you with important information about living with lupus and better managing your symptoms. Live teleconferences last one hour and are accessible through a toll-free phone number. All registered participants will receive call-in/log-in information before the event along with any support materials.
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.
A series of live and archived educational teleconferences on a variety of topics designed to provide you with important information about living with lupus. Don't miss this opportunity to learn from the country's leading lupus experts from the comfort and privacy of your home!
Learn from the Comfort of Your Home