Down Syndrome: “Gregory”
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On April 19, 1983 we heard these words from a doctor, “I believe your newborn son has Down’s Syndrome. I encourage you to take him home from the hospital, but he probably won’t be able to go to school, run, read or write.” Those words were very sobering concerning our son’s prognosis. They were also words we chose not to … Read More

John and the Art of Learning
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by Jenny Marrs When John was born in the fall of 1994, we were devastated with the diagnosis of Down syndrome. We were so scared about what kind of future he would have. Among the tons of literature we were given to help us understand Down syndrome, I found no silver lining, and I only became more fearful. Not only … Read More

Language Acquisition in Children with Down Syndrome: The significance of auditory function and the developmental costs of teaching signing or “Total Communication”
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by Robert J. Doman Jr.   In order to determine appropriate treatment approaches for children with Down Syndrome (DS), one must first, look at “normal” development, and then explore how and why the DS population differs. When considering language acquisition we encounter historic problems that are not dissimilar from those of any of our special needs populations. The primary problem … Read More

Down Syndrome Perspectives: A Message to Parents of Down Syndrome Children
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by Robert J. Doman, Jr. In 1972 I sent my first Down Syndrome child off to her first day of school, in regular class, in a “normal” public school with “normal” expectations, and no special services. Linda was entering first grade, having spent two years with me at the George Crother’s Memorial School. Linda entered 1st. Grade at the head … Read More

IN SEARCH OF JOSHUA
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My story begins on June 7, 1992, when my husband and I received a call about a baby born in another state with Down Syndrome. On June 8, 1992, at approximately 2 p.m., one of the most beautiful babies I had ever seen was placed in my arms. As I looked into his beautiful blue eyes, I felt he was … Read More

Scott – A Father’s Story
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More than ten years have gone by since my son was born. He came into our lives loved and wanted from the very start. In fact, this is true of all my children. I love my children unconditionally. Which doesn’t mean I like all the decisions they make, but right or wrong, I’ll stand by them. There was no instruction … Read More

Down Syndrome: “Daniel”
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My firstborn, Daniel, was born with a chromosomal abnormality known as Down Syndrome. The medical term for Daniel’s condition is Trisomy 21. This means that he has three #21 chromosomes instead of two. This extra chromosome blocked proper nutrition to all the cells in his body before and after birth, resulting in a very weak and poorly developed baby. Daniel … Read More

Down Syndrome: “Cindy”
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Cindy Cherie Wade was born May 22, 1976, in Salt Lake City. When the doctors told us that Cindy was born with Down Syndrome, they described a very bleak future and we found the first months of her life to be very discouraging. Not knowing where to turn we searched for help from individuals and organizations, but found little that … Read More

Philosphy and Rationale
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Robert J. Doman, Jr. NACD’s developmental and educational programs are designed to lead each child toward developing his/her fullest potential. These programs are designed through the expertise of Robert J. Doman, Jr., and represent an eclectic approach to child development. These programs are implemented by the parents and other family members under the training and auspices of The NACD Foundation. … Read More

OUR JOURNEY TO NACD CHANGED OUR LIVES
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by Joan Burns Seems like just yesterday (seven years ago) a tiny bundle of love was handed to me, his bright eyes seemed to say “thank you for being my mom.” This was and is true of our son as he shows his love and appreciation for everything we teach him. “Your son has Down Syndrome” the doctor said in … Read More

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