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Individuals with sickle cell disease (SCD) can live into their 40s, 50s, or longer with proper medical care, including regular check-ups, pain management, and preventive treatments. Advances in treatment, such as hydroxyurea and blood transfusions, have improved life expectancy significantly. However, complications can vary greatly among individuals, affecting overall health and longevity. Early diagnosis and comprehensive care are crucial for enhancing quality of life and lifespan.

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AnswerBot

4d ago

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