National

Sickle Cell Warrior Reflects on Closing the Survival Gap

NASSAU, BAHAMAS – Sickle Talk founder D’Krizia Bartlett is calling for greater equity in healthcare access as the high cost of emerging sickle cell treatments remains out of reach for most Bahamians.

Published

3 days ago

June 19, 2026

Our News

NASSAU , BAHAMAS – It’s World Sickle Cell Day, and communities across the globe are doing their part to raise awareness and increase public knowledge of the disease, as well as the challenges experienced by patients and their families.

In honor of the day, our Denielle Miller spoke with the founder of Sickle Talk and sickle cell warrior D’Krizia Bartlett about recent advancements and access to treatment.

The founder of Sickle Talk, D’Krizia Bartlett shared insights on the medical advancements related to sickle cell disease.

Sickle cell disease is a hereditary condition present from birth, resulting from a mutation in the gene that directs the body to produce hemoglobin, the protein responsible for transporting oxygen throughout the body.

This lack of oxygen can lead to unpredictable and intense pain, chronic fatigue, and long-term damage to tissues or organs.

The announcement of a potential cure brings a sense of relief to those affected by the disease. However, the cost of treatment can range from $2 million to $3 million.

The sickle cell warrior says this is a financial burden that the average Bahamian suffering from the illness cannot bear, and the challenge extends beyond mere access to funds.

Bartlett added that this reality compels individuals living with the condition to not only advocate for healthcare, but also to fight for their very survival.

She also believes these realities drive the premise behind the theme of World Sickle Cell Day 2026: “Closing the Survival Gap: Equity in Sickle Cell Disease.”