Patients and others battling sickle cell disease (SCD) — a devastating genetic disorder primarily affecting African-Americans, but also Latinos, Arabs, and Indians — may now pre-register for no-cost access to oneSCDvoice.com, an empowering online community that will launch in December. Promoted as “A Sickle Cell Community Tailored to You,” oneSCDvoice seeks to provide trustworthy information that will help patients increase their knowledge of the disease, acquire greater understanding of available clinical trials involving promising new therapeutics, and more easily obtain the support they need.

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