by Jeannie Cummings When Michael and Mark were born 3 1/2 months prematurely, no one expected they would live through the day*. But they were fighters, and despite several setbacks they came home from the hospital at 3 months old, which was 3 weeks before their due date. Yet, I soon began noticing developmental delays;…
by Joanna May, as told to Iliana Clift Existing in survival mode—day… after… day… after… day—is downright exhausting. This was my reality. My son screamed incessantly, hid under the kitchen table, refusing to come out for an inordinate amount of time; played for hours with spinning wheels, or stared dreamily as “Dora the Explorer” and…
by Christi Petrucka Isaac had been struggling with reading and expressing himself for so long, that by the time I heard about the NACD in May 2012, when he was 16, I knew that I was quickly running out of time to help him. It’s not that I hadn’t done anything up to this point….
by Kristina Houser & Lyn Waldeck In the years I have been associated with NACD, I have worked with a many wonderful families. Since I have been around long enough now (20 years + in one capacity of another), I have gotten the pleasure of watching many children become wonderful adults. At a recent evaluation…
by Vidya Guhan, NACD Developmentalist and Coach As a coach, this tends to be the number one concern that I address with parents. As a parent, I always come home from an evaluation feeling good, feeling like I have a plan and can make some real progress. Then I receive my program, and I feel…
by Roxane Sarrazit, NACD Mom For as long as I can remember, I have never liked running. I have always been poor at it. So since there was so much room for improvement, it seemed to be the perfect sport for me. I took up running in February 2011 at the old age of 33….
By Ellen Doman As we increase the number of Skype evaluations that we do and continue to request videos through our coaching program, we need to look at why we are doing videos and how to make the most of these opportunities. As evaluators we have a perspective regarding your child based on our own…
by Sara Erling I remember talking to David’s mom, Holly, prior to her starting the NACD program. She was familiar with NACD because when she was a girl in the 80s, her mom had helped do program with three children. So when her own son, David, was diagnosed with a sensory processing disorder, anxiety, and…
by Ellen Doman Have you heard about the latest supplement that fixes autism? Have you heard about this reading program that fixes dyslexia? There is this new exercise that immediately reorganizes the brain! Every day there are new fixes out there. With our internet access we are bombarded with new information and the latest immediate…
Arianna is 13 years old. She happened to have been born with one extra chromosome, a fact that is neither positive nor negative but certainly has been a challenge for her in many ways. As parents we learned that the medical term is designated Trisomy 21. We feel very strong about using that term. Verbalizing…