Throughout the years, Nicholas has been in many therapies. He's been in speech therapy since he was 2 for apraxia. But before there was speech, there was occupational. At his 4-month old checkup, I told the pediatrician I noticed he wasn't putting any weight on his legs. Thus began his "career" with Early Intervention and private therapy. He was diagnosed with having a gross-motor delay, and by the time he was 15 months old, he was walking, but not without a lot of hard work. I remember those therapy visits. The therapist would make him put weight on his legs and he would scream. And when we left, the people in the waiting room would look at us with sympathy, because they all heard the screams from where they sat.
Because of his global apraxia, he has also had fine motor delays and has been in occupational therapy again two different times. His pencil grasp is what has concerned us most recently, so back to therapy we went this summer (thanks Mimi and Pipi for making sure he got there each Monday). What we found interesting was that his therapist mostly worked on core exercises with him, telling us that if his core wasn't strong, his hand strength wouldn't be either. So we did situps (I could have done a few more) and we did jumping jacks (I could have done alot more) and we did pushups (I have weak wrists and I'm sticking to it!).
And weeks ago he surprised us with coming home from therapy and could tie his shoes! We celebrated! He was so proud of himself and I will never forget the smile of satisfaction he had on his face.
And fast-forward to today:
I love the determination on his face:
And if there was ever any question on who his father is (which there wasn't!)...
Nicholas Robert, we are so proud of you!!!