Ghanaians grief the passing of the renowned gospel musician KODA, whose death has brought to light details about his battle with G6PD deficiency, a condition that may have contributed to his passing.
In a viral video, KODA revealed that he had unknowingly taken the wrong medication for eight months, which could have worsened his condition.
G6PD deficiency, or glucose-6-phosphate dehydrogenase deficiency, is a genetic condition where the body lacks enough of an enzyme called G6PD, which is crucial for red blood cell function.
Without this enzyme, red blood cells can break down faster than normal, leading to a deficiency of red blood cells in the body (anaemia), particularly in response to certain medications, infections, or other stresses.
This condition is inheritable and more common in males and individuals of African, Asian, and Mediterranean descent.
Symptoms of G6PD deficiency may include fever, jaundice (yellowing of the skin, eyes, and mouth), weakness, dark urine, and abdominal or back pain.
These symptoms typically occur when triggers such as infections or certain foods and medications cause harm to the blood cells, resulting in hemolytic anaemia.
Treatment for G6PD deficiency focuses on managing symptoms and avoiding triggers. While there is no cure, most people recover in a few days without treatment.
It’s crucial for individuals with G6PD deficiency to inform healthcare providers about their condition before taking any new medications, as certain drugs can trigger hemolytic episodes.
In light of KODA’s experience, raising awareness about G6PD deficiency and its management is essential. People with this condition should be vigilant about avoiding triggers and seeking appropriate medical care when needed to prevent complications.