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Sickle cell disease (SCD) is a hereditary ailment that can cause severe pain and suffering to people who are affected.
However, with continued investment in research and treatment options, we can make progress towards improving the
lives of those with SCD. Over 40% of patients experience painful vaso-occlusive crises (VOCs), so we must work towards
finding solutions and providing support for those living with this condition, These episodes, a hallmark of SCD,
significantly contribute to morbidity, mortality, and a diminished quality of life, while also incurring substantial
healthcare costs. Chronic pain particularly affects older adolescents and adults with SCD, with over half reporting daily
discomfort. Opioid-based analgesics, though sti
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