Noor Haba, a young mother in Bangladesh, pulls her headscarf close around her face with one hand. With the other hand, she strokes the back of her seven-year-old daughter, Shahara, who lies semi-conscious on the hospital bed. Shahara is being treated for thalassaemia, a genetic blood disorder.
Sharaha is the second of Noor Haba’s five children to suffer from thalassaemia, and Noor Haba has to bring them both to hospital every two months for blood transfusions. As there is no blood bank, she relies on people coming to the hospital voluntarily to give blood—usually a simple matter. Because of the pandemic, they’ve been waiting for a blood donor for three days now. Many people are scared to come to a medical facility for fear of catching the virus, while lockdown measures have made travel difficult.
“We’re searching everywhere,” Noor Haba says. “Normally we can easily find someone to give blood. But this time I can’t find any blood donors due to the COVID-19 situation. No one wants to come to the hospital because they feel afraid.”
The MSF nurse inserts a needle into Shahara’s arm and draws blood into a syringe. As the child cries out and squirms on the bed, her mother soothes her. Shahara’s legs and arms are stick thin; her belly is extended from the swollen spleen caused by her condition and exacerbated by malnutrition. Thalassaemia causes decreased haemoglobin levels and can be fatal if not treated with regular blood transfusions.