The Down Syndrome Association of Delaware was founded in 1979 as a non-profit parent association. We aim 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.
As a volunteer organization 100% of contributions received are directed to the education and support of DSA of DE members and its mission - including and but not limited to: New Parent Info Packets, Educational Seminars and workshops, Camp and Convention Scholarships, and Social events for families, teens and adults.
|Address||PO Box 747
|Type||Inclusive Extracurricular Programs|