Amilia Eva Gabba, Programme Coordinator of the Sickle Society Sierra Leone |
The Sickle Cell Disease (SCD) is causing devastation in Sierra Leone amidst little
attention to the genetic condition from the public health system, patients and
a campaign group say.
SCD, also known as Sickle Cell Anaemia, is a condition
caused by the abnormal growth of the red blood cell, leading to suffering among
patients. The condition is hereditary, meaning it can transfer from parents to
their offspring.
In Sierra Leone many sufferers dye in silent agony due to
lack of proper care, say the Sickle Cell Society of Sierra Leone (SCS-SL),
noting that it is also a leading driver of maternal and infant deaths in the
country.
A normal red blood cell is round. An abnormal one is shaped
like a crescent or sickle [the shape of the agricultural implement]. Unlike the
normal red blood cells, sickle shaped red blood cells do not live for long. And
since these red blood cells are responsible for the transportation of oxygen through
the body, sickle cell patients often lack enough blood due to the short-live
span of their red blood cells. This condition is called anaemia.
In addition, because of their shape, sickle cells tend to get
stuck in blood vessels, blocking blood flow. This can cause pain and organ
damage, as does constant deprivation of oxygen-rich blood. This
organ damage is what makes sickle cell a fatal condition.