About 2017-06-19T15:34:01+00:00

About the MSCDA

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 seeks to work collaboratively with patients, families, healthcare providers, federal and state agencies and other community based organizations to promote advocacy, education, research and excellent healthcare delivery.

Our mission is to improve the quality of life for those affected by sickle cell disease by promoting advocacy, education, research and excellent healthcare delivery.

MSCDA Team

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.

MSCDA Board of Directors
Derek Robertson, President
Benjamin Joseph, Vice President
Shantá Robertson, Executive Director

To learn more about our services and how we can help, get in touch with us today.

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