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
It is times like these that the lupus community needs your support now more than ever! Please consider giving the gift of hope for someone you know with lupus!Give the gift of hope 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 22nd at 9 PM
Send your questions to email@example.com
This four-part webinar series is designed to help parents understand lupus and how to care for a child or teen with the disease. Parents and children will learn how to work together to manage symptoms, maintain a healthy lifestyle, and successfully transition to adulthood.Register for Part 2
NEXT MEETING: November 22nd | 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 firstname.lastname@example.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