Sickle cell anemia and Thalassemia

Thalassemia and sickle cell anemia are two genetic blood disorders that affect the production and shape of red blood cells in the body.Thalassemia is a group of inherited blood disorders that affect the ability of the body to produce hemoglobin, which is a protein in red blood cells that carries oxygen throughout the body. People with thalassemia have a reduced amount of hemoglobin and may experience anemia, fatigue, and other health complications.Sickle cell anemia is another inherited blood disorder that affects the shape of red blood cells. People with sickle cell anemia have abnormally shaped red blood cells that can become stiff and sticky, leading to blockages in blood vessels and reduced oxygen flow to organs and tissues. This can cause pain, organ damage, and other health complications.Both thalassemia and sickle cell anemia are chronic conditions that require ongoing medical management and treatment to help manage symptoms and prevent complications.

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