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

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.

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

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.

We all want to take charge of our health, and with new technology, there are more tools than ever to help us manage it. But sometimes, the greatest gains come from something more human: connection. For people living with chronic health conditions like sickle cell disease, the healthcare system can sometimes feel impersonal and focused solely on the physical aspects of the illness.

In this episode, we're diving into a vital aspect of well-being that goes beyond medical charts and treatment plans: the power of peer support. We'll explore how connecting with others who understand your journey can make a profound difference in living with sickle cell disease. Guests: Donisha Holley, Social Worker and Support Group Organizer from the Inova Adult Sickle Cell Center, and Sickle Cell Warrior Sunday Coleman.

Discover the incredible story of a young man and his bone marrow transplant experience. In this episode, we hear from a courageous young man and his supportive father as they recount their transformative journey through a bone marrow transplant that cured his sickle cell disease. Despite facing numerous obstacles and enduring many hardships, their unwavering determination led to a successful outcome. Now, they share their triumphant story of hope, perseverance, and ultimate happiness.

🎧 Listen now to be moved by their tale of overcoming adversity and achieving medical miracles. Don't miss this inspiring episode!

#Podcast #BoneMarrowMiracles #SickleCellAwareness #MedicalBreakthroughs #FamilyStrength #Inspiration

On this edition of Blood, Sweat and Cells: Real Talk About Sickle Cell Disease,

We delve into the unique challenges women face when managing sickle cell disease, from menstrual issues to fertility concerns. Join us as we have a candid conversation with Dr. Sheinei Alan, an expert in sickle cell disease and its impact on women's health.

Discover what you need to know about pregnancy complications, genetic counseling, and optimizing the chances of a healthy pregnancy and childbirth. We'll also explore the emotional and psychological well-being of women living with sickle cell disease and discuss specific concerns for older women.

This sickle cell awareness month, the Heart of Gold Sickle Cell Foundation of Northern Virginia invites you to discover the significance of knowing your sickle cell status.

Our guest, Dr. Sheinei Alan, sheds a light on understanding the distinction between sickle cell disease and the sickle cell trait. We'll explore family planning for couples who carry the trait and the impact of the sickle cell trait on those engaging in strenuous sports activities.

Raise your awareness and foster understanding about the unique experiences of individuals with the sickle cell trait.

Remember, knowledge is power. Together, let's create a more informed and compassionate world during Sickle Cell Awareness Month!

In this heartfelt episode, join host Valerie Bey and her guest Dr. Clarence Pearson as they dive into a deeply moving conversation with a courageous father who opens up about his journey of raising a daughter with sickle cell disease. Through his candid storytelling, listeners gain valuable insights into the profound challenges and triumphs faced by families affected by this condition.

As our guest shares his experiences, we explore the immense strength and resilience required to navigate the complexities of managing sickle cell disease on a daily basis. From coping with daunting hospital visits and treatments, to cherishing cherished moments of joy amidst adversity, this interview offers a raw and honest portrayal of the life-changing impact of this illness.

While discussing his daughter's life, we delve into the intricacies of her medical journey and the complications that ultimately led to her passing. This emotional exploration sheds light on the gravity of sickle cell disease and its far-reaching effects on both patients and their loved ones.