Lettercase’s featured resource is “Understanding a Down Syndrome Diagnosis.” It received input from representatives of National Society of Genetic Counselors, the American College of Obstetricians and Gynecologists, the American College of Medical Genetics, the National Down Syndrome Society, and the National Down Syndrome Congress. It is available for free as a web app, and copies are available for purchase with medical practitioners being able to receive one free complimentary copy.
DSP, for short, is an online support resource for expectant mothers who have decided to continue their pregnancy after a prenatal test result. DSP provides a free, downloadable book, “Diagnosis to Delivery” that was written by mothers who received a prenatal diagnosis and has been reviewed by medical specialists. DSP maintains a blog with interactive comments on issues and questions expectant mothers may have. DSP also provides a helpful resource for family members, another free, downloadable booklet titled, “Your Loved One is Having a Baby with Down Syndrome.”
The National Down Syndrome Adoption Network maintains a registry of families from across the nation who wish to adopt a baby with Down syndrome. Adoption is an option to consider in pregnancy management decisions following a prenatal test result, and NDSAN makes adoption a very viable option. For those practitioners and expectant couples interested in learning more, NDSAN is available to provide non-directive support. You can also visit DSACK’s link about Adoption.
“What Parents Wished They’d Known: Reflections on Parenting a Child with Down Syndrome” contains the responses of parents of a child with Down syndrome to the question, “What do you know now about parenting a child with Down syndrome that you wish you’d known from the start?”
© 2022 Down Syndrome association of central kentucky