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Delawareans with Special Needs: Medicaid Managed Care Panel
Every person is a unique individual with strengths, gifts and dreams. As parents, families and friends of children and young adults with Down syndrome, the DSA of Delaware members have discovered that every person has something special to offer. The individuals in their lives with Down syndrome may have different needs than those who do not, however their ability to enrich, teach and challenge is the same. Founded in 1979, the DSA of Delaware is a statewide non-profit support group, organized and managed by parents of people with Down syndrome. DSA aims to be a supportive resource, advocating for the acceptance and understanding that allows individuals with Down syndrome to achieve the same level of access and opportunity as their peers.