The Down Syndrome Association of Delaware (DSA of DE) is a non-profit organization dedicated to supporting individuals with Down syndrome and their families. Founded in 1979, we aim to provide resources, education, and advocacy to promote inclusion and improve the quality of life for individuals with Down syndrome. Originally founded by a small group of parents of children with Down syndrome, our organization now serves over 600 individuals with Down syndrome throughout DE and surrounding states. Our organization is one of the most robust and prominent Down syndrome organizations in the country.
Through a variety of programs, events, and support services, DSA of DE fosters a community where individuals with Down syndrome can thrive, develop their full potential, and enjoy meaningful connections. We work to raise awareness and advocate for the rights of those with Down syndrome, ensuring they are recognized as valued members of society.
Our mission is to support families, promote community involvement, and encourage a lifetime of opportunities for people with Down syndrome. Join us in our commitment to support, educate, and inspire!
Our Mission
The Down Syndrome Association of Delaware supports families, promotes community involvement, and encourages a lifetime of opportunities for people with Down syndrome.
Our Vision
We envision a community in which individuals with Down syndrome are healthy, happy and successful. They and their families are effective advocates for their needs.