The Maryland Sickle Cell Disease Association, Inc. (MSCDA) is a 501 (c)(3), tax exempt non profit organization that was incorporated in 2006. MSCDA was formed by concerned parents and interested individuals seeking to improve the lives of persons affected by Sickle Cell Disease in Maryland.
MSCDA affairs are governed by a Board of Directors with day-to-day operations being facilitated by various other staff members.
Our team consists of the following people:
MSCDA Board of Directors:
Derek Robertson, President
Benjamin Joseph, Vice President
Shantá Robertson, Executive Director