BUJUMBURA, February 18th (ABP) – Sickle-cell disease or drepanocytosis, sometimes called sickle-cell anemia, is a dangerous disease for human health. It is also genetic, affects hemoglobin and causes potentially serious complications, especially in children. This was revealed on Thursday, February 13, 2025 by Boaz Nibitanga, general practitioner at Johnson Hospital at Gihosha in Bujumbura City, during an interview with a check by ABP.
Regarding the symptoms of sickle-cell disease, Nibitanga cites, among others, acute or chronic anemia, sensitivity to infections and painful crises caused by poor blood circulation. Since sickle-cell disease is an incurable disease, its treatment consists of treating opportunistic diseases, and blood transfusions are often necessary. According to him, sickle-cell disease is a chronic disease for which there is currently no cure. However, screening at birth allows for early medical care, which is the key to a better prognosis and a preserved quality of life.
Mrs. Nah. E. testifies: “I am married to a man who carries this disease while I do not have it. We had three children with my husband and two were affected by the disease. They are weak all the time, and eat selectively. Their exposure to the sun makes them have crises and I often go to the hospital for their healthcare. I am already desperate about their state of health.
I carry a heavy cross on me. I would ask the government to put in place a law requiring future spouses to be screened before deciding to be together for life, so as not to increase the number of patients. For those who are already affected, I advise forming associations so as not to feel discriminated against in society,” she concluded.