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Blood, Sweat, Cells: Real Talk About Sickle Cell Disease

Blood, Sweat, Cells: Real Talk About Sickle Cell Disease

By: Valerie Bey
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About this listen

Blood, Sweat, and Cells: Real Talk about SCD is a podcast that provides in-depth, educational information about sickle cell disease (SCD). Each episode features interviews with patients or family members, doctors, and researchers who share their insights and experiences living with and treating this chronic condition. Our primary aim is to educate and advocate for patients with SCD and help them live their best quality of life.2024 Hygiene & Healthy Living Social Sciences
Episodes
  • Cure No Longer Out of Reach: Half-Match Bone Marrow Transplant
    Aug 30 2025

    On this episode of Blood, Sweat, and Cells, host Valerie Bey sits down with Dr. Robert Brodsky from Johns Hopkins to talk about a groundbreaking half-matched bone marrow transplant, opening the door to cures for more sickle cell patients than ever before.

    Learn how this breakthrough procedure compares to gene therapy and what it means for the future treatment of patients with sickle cell disease.

    For anyone who’d like to learn more about this procedure, you can visit https://www.hopkinsmedicine.org/transplant/programs/bone-marrow

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    13 mins
  • Half-Matched Bone Marrow Transplant: KeAndra's Story
    Aug 18 2025

    Born with sickle cell disease, KeAndra Hickman endured years of painful crises, countless hospital stays, and constant uncertainty about her future. Then she discovered a groundbreaking option—a half-matched bone marrow transplant—and decided to take the leap.

    In this episode of Blood, Sweat, and Cells, host Valerie Bey sits down with KeAndra for a powerful and deeply personal conversation about the highs, lows, and ultimately life-changing outcome of her transplant journey.

    Most people with sickle cell disease will never find a perfectly matched bone marrow donor. But the good news is that almost everyone has a half-match. KeAndra shares how her successful transplant at Johns Hopkins, under the care of Dr. Robert Brodsky, transformed her life—and why this option could bring hope to so many others living with SCD.

    If you’d like to learn more about this procedure, visit hopkinsmedicine.org/transplant/programs/bone-marrow.

    And stay tuned for a future episode featuring Dr. Robert Brodsky himself, where he’ll discuss the latest research and explain who makes the best candidates for a half-matched bone marrow transplant.

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    11 mins
  • Super Campers Always
    Feb 24 2025

    Imagine a place where kids facing unique health challenges can just be kids. A place filled with laughter, friendship, and adventure, where medical needs for children with sickle cell disease are understood and met with expertise and compassion. That's exactly what Super Campers Always provides. Camp dates for 2025 are July 6-11.

    We'll be talking with Lulu Moeller, Director of Recreation Center & Youth Services with Melwood Community Services. They will share the inspiration behind this unique camp, the impact it has on campers and their families, and how it creates a supportive and empowering environment for these incredible young people

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    16 mins
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