Thalassemia is an inherited blood disorder that affects hemoglobin production, leading to anemia and other health complications. Since it is a genetic condition, the risk of developing thalassemia depends largely on family history and ethnicity. People of Mediterranean, South Asian, Middle Eastern, and African descent are more likely to carry the genetic mutations associated with the disorder. If you experience symptoms like persistent fatigue, weakness, pale skin, or slow growth in children, it may be worth assessing your risk. This assessment will help you determine if you may be at risk for thalassemia based on factors such as family history, ethnicity, and symptoms. While this is not a diagnostic tool, it can provide valuable insights into whether further medical evaluation is necessary. Take the assessment to gain a better understanding of your risk and learn about the next steps for managing your health.
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