In addition to staying on top of the latest research and various modalities that affect our children, NACD also likes to take advantage of cutting edge and current technology in order to provide greater service to our families. NACD is pleased to announce that we have begun utilizing Facebook as a tool to unite the…
A Message from Bob Some of the areas that I am particularly concerned about are issues relating to speech and language development, as well as feeding and oral motor issues. We have two speech pathologists on staff to address these issues. Lori Riggs, the Director of our Center for Speech and Sound, is really…
by Sue Lesch With our current economic times, it’s now more important than ever to make sure you’re taking advantage of every possible way to save money. I’m writing this to tell you about my family’s experience using our Flexible Spending Account (FSA) to pay for our NACD expenses. For those of you…
by Lisa Jamieson, Co-author of Finding Glory in the Thorns As a mom, I wear many hats. As an NACD mom, I’ve worn even more. And just like our ever-changing Minnesota weather seasons require different kinds of hats, my life’s seasons often require that I take on different roles and wear different “hats” to make…
by Elisa Delfino How do I even begin? There was a time that I didn’t understand the new perfect angel that the Lord sent to me. I thought, “What do I do? Cry? Cuddle her and wish it wasn’t so?” As a mother I thought, “What can I do to fix the situation?” This time…
by Debbie Frederickson When Ammon was born he had oxygen problems that weren’t detected until he was six weeks old. When he was three, the Sparks Clinic in Birmingham evaluated him and they said he was “mentally retarded.” When he was about five, we discovered that he had a hearing loss. We were told that…
by Ashley Lammons I have three children on the autism spectrum and they have been on NACD’s TDI Targeted Developmental Intervention® for 9 months. I have six-year old twin girls and a son who is now 3 ½. Hannah and her sister Lauren were born prematurely at 25 weeks. Hannah is legally blind. When we…
by Ellen Doman I am going to start this off by asking you to think of your child first. That precious child of yours who needs and deserves every opportunity to advance and grow is what this is all about first and foremost. It is the job of the parent to ensure that their child…
by Sara Erling “Thanks again for the wonderful time during the NACD Rendezvous! Your hard work did not go unnoticed!” —Steve and Lori Lane “My husband and I also want to extend a BIG THANK YOU to everyone there for the great times and opportunities you presented for the NACD families. What a joy it…
by Robert J. Doman Jr. I recently returned from our Chapter in Southern California with renewed faith that our families there are really “getting” the importance of working memory/sequential processing. More importantly, they understand that they can really change it—dramatically! But before I tell you their specific stories, let’s look at the key they discovered…