Pain occurs when sickle cells travel through small blood vessels and clog blood flow after becoming stuck. It can last for anywhere from hours to days.

Rest, over the counter medicine (such as ibuprofen and aspirin), and fluids are some of the ways that SCD patients can treat mild pain symptoms at home. However, those who experience persistent and severe bouts of pain should seek medical treatment. In addition, children with SCD are at increased risk for stroke and other neurological and neurodevelopmental disorders, including seizures, headaches, cognitive delay, and ADHD. 

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