Finding out that your baby is going to have Down syndrome can be a very emotional and confusing time. Please know that you are not alone! Many of our families have been through the experience of receiving a prenatal diagnosis, and they stand ready to share with you. The National Down Syndrome Congress and the Global Down Syndrome Foundation have produced a brochure that explains the different prenatal tests available. You can download it in English or Spanish, using the links below.
New Parents First Call Program
Trained volunteers are located all over the state and will talk with you over the phone or meet with you in person at any time during your pregnancy. We offer emotional support, information, and as much continuing connection to our community as you need.
Our First Call support continues for as long as you need it. We offer all new parents of children with Down syndrome a welcome package, and if needed, we can connect you with medical specialists and family support groups – both within and outside of our own organization.
Complimentary Membership
There are nearly 3,000 families in the State of Connecticut who have children with Down syndrome. Many have joined together through DS ACT to find answers and comfort and to explore all the possibilities life has to offer their children. We welcome you to our community with open arms. Our First Call coordinator can set up a complimentary one-year DS ACT membership, so you can attend our events and have ready access to the fellowship and resources we make available to our members.
For those who are seeking information about adoption, the Down Syndrome Association of Greater Cincinnati supports the National Down Syndrome Adoption Network, which has a waiting list of more than 100 families waiting to adopt a child with Down syndrome.
Additional online informational resources and recommended reading are located on our New Parents page.
Contact our First Call Coordinator Patty Alessandro for confidential information and support at firstcall@mydsact.org.