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In the United States, pediatric patients younger than age 18 with Sickle Cell Disease (SCD) have more options than adults for ongoing health management through
Adults with sickle cell disease (SCD) shared their insights in a panel discussion at the 2018 Management of Sickle Cell Disease Conference held by the Sickle
An expansion of research interest in adult-onset complications of SCD, meaning secondary symptoms that are likely to first appear after childhood, has revealed new information.
On November 9th, 2018 Beverly Francis-Gibson, President & CEO of the Sickle Cell Disease Association of America (SCDAA), spoke at the 2018 Management of Sickle
People living with sickle cell disease (SCD) can experience changes in the ways that their brains process information. These changes can be seen and measured,