Sickle Cell Program

September 6, 2022

New Mother with Sickle Cell Comes to UAMS to “Get Rejuvenated and Go Back to Life”

Benjamin Waldrum

Jada and TJ Mosby

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…

July 8, 2022

Father Fights Sickle Cell’s ‘War on the Inside’ to Spend More Time with Family

Benjamin Waldrum

Tyrrence Sanders

Tyrrence Sanders, 31, wants his children to know they can do anything they put their minds to. And he plans to be there with them, every step of the way. “Spending time with family is the most important thing to me,” he said. It’s a feeling that’s deeply embedded in his own experience. Sanders grew…

June 22, 2022

Annual Sickle Cell Disease Symposium Highlights Multiple Barriers to Care

Benjamin Waldrum

Stella Bowers and Rebecca Camp

Adult sickle cell patients continue to benefit from increased awareness and newly available therapies. However, lack of research funding and access to care, as well as perceived bias from health care professionals, are still impediments to better care. That was the message from the annual UAMS Sickle Cell Symposium, held virtually June 10. The symposium…

February 17, 2021

Symposium Spotlights Social Burdens of Sickle Cell Disease Treatment

Ben Boulden

Collin Montgomery, APRN, lower right, was one of three featured speakers during the recent, virtual Sickle Cell Symposium at UAMS.

Racial bias, the opioid crisis and the stigma of suspected drug use often make getting access to treatment a frustrating struggle for adult sickle cell patients. In a short video that opened the UAMS Sickle Cell Symposium on Feb. 2, sickle cell disease patients spoke about the attitudes of physicians and nurses that often seem…

June 15, 2020

Cured: Arkansas Man’s Sickle Cell Disease Eliminated by Bone Marrow Transplant

Ben Boulden

Phillip Sanders, right, with his wife and young son, has been cured of sickle cell disease as a patient at UAMS Adult Sickle Cell Clinical Program and Johns Hopkins in Baltimore.

While Phillip Sanders’ journey to a cure for his sickle cell disease was ultimately successful, it was a path with peaks and valleys and struggles and challenges. It’s beginning was relatively undramatic and took place during a conversation in October 2017 just after the conclusion of the Sickle Cell Symposium organized by the UAMS Adult…

February 25, 2020

Patient Moves Forward in Sickle Cell Care and in Life

Ben Boulden

Jayla Buford recently transitioned into the UAMS Adult Sickle Cell Clinical Program from Arkansas Children's Hospital.

Feb. 25, 2020 | Maturing into adulthood often means leaving familiar things behind while embracing new ones, and Jayla Buford did just that in late 2019 as a sickle cell patient. Buford had been receiving care through the sickle cell program at Arkansas Children’s Hospital since she was 4. In late 2019, now an adult,…

October 1, 2019

Symposium Focuses on Past, Present, Future of Sickle Cell Disease Treatment

Ben Boulden

Issam Makhoul, M.D., lectures on the state of sickle cell disease treatment and research at the annual Sickle Cell Symposium at UAMS.

One patient with sickle cell disease can experience severe pain and other symptoms while another with the same disease type only has moderate or even mild pain crises, said UAMS’ Issam Makhoul, M.D. “What makes that disease so severe in one individual over another one?” he asked. “That’s what we need to learn more about….

January 22, 2019

Living with Sickle Cell, Pine Bluff Woman Retains Joy

Katrina Dupins

Doris Carter, 53, was diagnosed with sickle cell anemia when she was 3.

Doctors told her mother she wouldn’t live past childhood. But Doris Carter proudly announces that she has her hands full at age 53 working as a nurse’s aide in Pine Bluff, having raised two daughters and now keeping up with seven grandchildren. When she was 3, Carter was diagnosed with Sickle Cell Anemia, an inherited…

October 2, 2018

Symposium Spotlights Psychology of Sickle Cell Disease

Ben Boulden

The Rev. Johnny Smith talks about the faith community and attitudes toward illness and health.

By 2014, Shamonica Wiggins had reached a point where she couldn’t cope with her sickle cell disease. She felt lost and defeated until a therapist helped her try a new approach.

August 31, 2018

Sickle Cell Symposium Sept. 18 to Focus on ‘Mind, Body and Soul’

Ben Boulden

People with sickle cell disease, their families, health care professionals and the public are invited to the 2018 annual Sickle Cell Symposium at 6 p.m. Sept. 18 at the University of Arkansas for Medical Sciences (UAMS). The symposium is free.

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