The Black Down Syndrome Association is a non-profit organization dedicated to providing Black families with the resources and support they need for their loved ones with Down Syndrome.
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Founded in 2022 by two Black mothers who have Black sons with Down Syndrome, the organization works to create a culturally competent, safe space for Black families and their loved ones with Down Syndrome.
At the Black Down Syndrome Association, we strive to create a community of support and understanding and to provide a platform for Black families to share their stories, experiences, and needs. We are committed to advocating for the rights of Black persons with Down Syndrome and to ensure that they are given the same opportunities and respect as everyone else.
Mission
The mission of the Black Down Syndrome Association (BDSA) is to connect Black families in the Down Syndrome community with resources to improve their lives in a more meaningful way by addressing the many inequalities present that increase barriers to access, support, and education. We strive to fill the gap for the families we serve.
Vision
Transformative change often begins with a single, focused idea and grows through intentional strategy and collective commitment.
The Black Down Syndrome Association is grounded in the belief that meaningful, sustainable impact requires coordinated action, strategic investment, and community accountability. Through a growing portfolio of initiatives, we intentionally align our expertise, partnerships, and resources to advance clearly defined goals and measurable outcomes.
BDSA is committed to strengthening the long-term well-being of Black individuals with Down syndrome by expanding access to culturally responsive information, resources, and opportunities that support full participation, autonomy, and quality of life across the lifespan.
