Sickle Cell Program
July 24, 2025
Sravani Gundarlapalli, M.D., Joins UAMS Division of Hematology Oncology

Sravani Gundarlapalli, M.D., has joined the University of Arkansas for Medical Sciences (UAMS) as a hematologist oncologist and assistant professor in the UAMS College of Medicine’s Division of Hematology Oncology in the Department of Internal Medicine. Board-certified in internal medicine, Gundarlapalli joins the state’s most experienced hematology oncology team that leads Arkansas’ only stem cell…
July 8, 2025
UAMS Adult Sickle Cell Program Announces Support Group, New Director

The University of Arkansas for Medical Sciences’ (UAMS) Adult Sickle Cell Program celebrated World Sickle Cell Awareness Day on June 19 by announcing a support group for adult patients with sickle cell disease, as well as a new director. During a free information session held on the 10th floor of the UAMS Winthrop P. Rockefeller…
December 13, 2024
‘I’m Still Here’: Sickle Cell Patient Lives on Her Own Terms

Susan Johnson, 62, of North Little Rock, has fought sickle cell disease her entire life. She was first diagnosed decades ago, before early screenings were common and when care was still evolving. So to make it to this point in her life as a sickle cell patient, Johnson said, is remarkable. “My brother didn’t see…
October 11, 2024
UAMS Adult Sickle Cell Program Celebrates 10th Anniversary at Annual Symposium

The University of Arkansas for Medical Sciences (UAMS) Adult Sickle Cell Program celebrated a decade of providing care for patients across Arkansas during its annual symposium. Speakers at the event, which included several patients, reflected on the past while looking with hope toward the future. The Sept. 19 event was held on the 12th floor…
August 30, 2024
Sickle Cell Patient Offers Message of Hope: ‘Don’t Let the Sickness Stop You’

Briana Pringle, 22, of Little Rock, is pretty busy these days, and that’s a good thing. The Helena-West Helena native studies at the University of Arkansas for Medical Sciences (UAMS) during the week and works on weekends. She barely has time to visit her family back home. Sickle cell disease is an unwelcome part of…
September 21, 2023
Sickle Cell Disease Symposium Looks Ahead to “New Era”

The University of Arkansas for Medical Sciences (UAMS) hosted its annual Sickle Cell Symposium on Sept. 12, bringing together leading researchers, clinicians, patients and community advocates to share the latest advancements in sickle cell disease and treatment. The fall event, held in the 12th floor auditorium of the Jackson T. Stephens Neurosciences & Spine Institute…
August 21, 2023
UAMS Hosts Free Sickle Cell Disease Symposium Sept. 12

LITTLE ROCK — The University of Arkansas for Medical Sciences (UAMS) will host its annual Sickle Cell Symposium on Sept. 12. The symposium brings together leading researchers, clinicians, patients and community advocates to share the latest advancements in sickle cell disease research and treatment, identify current challenges and gaps, and develop strategies to accelerate progress…
July 28, 2023
‘Roll With the Punches’: Sickle Cell Patient Keeps a Positive Outlook on Life

Sickle cell disease hasn’t made life easy for Xavius Hymes, 27, of Pine Bluff, but he hasn’t let it keep him from dreaming big. In fact, he uses the disease as fuel to keep going. “If anything, I feel like sickle cell anemia has made me mentally stronger,” Hymes said in a YouTube video. “It’s…
May 26, 2023
For Hot Springs Woman, Sickle Cell Disease “Didn’t Prevent Me from Doing Anything”

After years of learning how to handle pain crises when they come and developing a routine for care, Cyncere Tidwell says sickle cell disease is just another part of her life. “Other than the pain crises, sickle cell doesn’t bother me,” she said. “I’ve been dealing with it for so long that it’s nothing new…
September 6, 2022
New Mother with Sickle Cell Comes to UAMS to “Get Rejuvenated and Go Back to Life”

Sickle cell disease is just another part of everyday life for Jada Mosby, 24. And as a new mother, she doesn’t plan on letting it slow her down anytime soon. “It’s just part of my life,” she said. “It is my life, but it’s nothing to me.” As a baby, Mosby was diagnosed with sickle…
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