Can anyone else relate? I truly can! Sunscreen has become my best friend because the sun, photosensitivity and my lupus do not mix! My left arm is so severely discolored due to the sun that it has become quite embarrassing. But who wants to wear long sleeves in 100 degree weather? And who wants to… Read More The Sun And It’s Affects On Lupus Sufferers!
While there are countless songs out there that have helped people through difficult health moments, there’s something extra special about songs inspired by the ups and downs of living with a health condition. Below, we rounded up 18 songs that were written about an individual’s experience with chronic illness — whether that person is the… Read More 18 Songs I Bet You Didn’t Know Were About Chronic Illnesses!
Be sure to join in on this teleconference. You won’t want to miss it! Chime in on Thursday, August 15, 2019 as Dr. Mohammad Kamran, member of the LFA GA Chapter’s Medical Advisory Board, touches on some interesting tips to help you get on the best treatment plan. “The medications prescribed to treat lupus can… Read More Managing The Side Effects Of Medication Teleconference!
Tuesday | September 10, 2019 | 8:15 am – 2:15 pm It’s tee time at the ONLY Tom Watson-designed championship golf course in Georgia. Raise funds for the fight against lupus at the 12th annual golf tournament. Mark Strickland’s leadership in memory of his mother has raised more than $240,000 for the fight against lupus.… Read More The Drive To End Lupus NOW 12th Annual Golf Tournament!
Dr. Samuel Pegram is a Rheumatologist in Houston, TX. He is affiliated with multiple hospitals in that area. Dr. Pegram is the principal investigator and founder of the Rheumatic Disease Clinical Research Center and has practiced Rheumatology for more than 20 years. Dr. Pegram has built a reputation for treating complicated cases of lupus… Read More Lupus Clinical Trials Teleconference
Good Morning Lupies, Doesn’t it feel good to know that someone is thinking of you? With all the daily stresses that come with living with an autoimmune disease such as lupus, we often forget that there are people in our corner. We often forget about our support systems, those rooting for us, praying for us,… Read More To Know Someone Is Thinking Of You…
Over 55,000 Georgians are living with lupus and thousands of walkers raised their voice to a lupus ROAR at the 13th Walk to End Lupus Now at Georgia State University Stadium. We walked. We hugged. We cried. And we shouted,“END LUPUS NOW!” So, the Lupus Foundation of America, Georgia Chapter is bringing together good food and great friends… Read More Lupies, Celebrate Your Success!
So Lupies, it’s about that time where people experience annoying dry coughs, runny noses and the sniffles. It’s about that time where we spend lazy days in bed not because we want to but because we HAVE to. It’s the time for the fuzzy slippers and the gigantic Kleenex piles, over indulging in chicken noodle… Read More Catching A Cold When You Have Lupus!