It’s hard for me to believe that tomorrow, my “baby” will be 25! Unlike Casey, Rob doesn’t seem to care about his birthday. When asked what he wants, his answer is always “presents.” Trying to ask for specific things, all the while trying to use a statement (tell me what you want) instead of a question is difficult for both of us. But, that doesn’t matter because it will his day and I’ll do everything I can to make sure he knows how special he is.
When I think back to when the kids were little, it’s amazing to me just how different they were. It seems I should have seen the autism in Rob earlier. I was concerned and even talked to Casey’s neurologist and our family doctor about him. They both agreed with his history, I needed to wait before I panicked.
For the first three years of his life, Rob managed to end up in the ER every six months or so. As soon as I would get a bill paid off, he would end up there again. He tumbled as a toddler and split his forehead open – stitches. He had pneumonia. He fell down the basement steps and got to ride on a helicopter to a children’s hospital (he wouldn’t wake up). He had a seizure after getting a set of vaccinations. He jumped down the steps and broke his collar bone. Need I go on? I often said that had he been first, there wouldn’t have been another.
So, when he didn’t talk much, no one was very concerned. He didn’t have routines that he needed to follow. He didn’t have sensory issues when he was a toddler. However, since he was language delayed, our school district put him in their preschool when he was 3. It was the same one both girls had gone to and he was so proud to be there. He played beside other kids, but rarely played with them.
But, he followed Mandy everywhere at home. She would tell me what he wanted, so he never needed to use his voice. She was the ultimate big sister to him and he still leans on her. The years she was in Texas were especially hard on him. Casey knew Mandy would come home and would watch the calendar for those dates. He just knew she was gone.
Since he didn’t show many signs of autism, we waited. He was going to preschool and getting speech. There wasn’t much I would have done differently had he had a diagnosis. When it was time for Kindergarten, though, the signs were becoming more obvious. He went to our county board of DD Kindergarten and had a one on one aide that he adored. I also made an appointment with the neurologist for him. It didn’t take the doctor long to agree that he had autism, too.
I wasn’t surprised. I didn’t feel much of anything, really. It was what it was and a diagnosis didn’t change any of us. It wasn’t till a few days later when Casey had one of her hours long meltdowns that it occurred to me he may start doing that, too. And I cried. I wasn’t strong enough to handle two screaming, kicking kids.
God was watching over me. While Rob does have his issues, meltdowns have never been one of them. He rarely gets angry and when he does, he tends to cry (like his mom!). Rob was happy to go to school with Casey and his teachers were awesome with him. His aide, Beth, went with him and stayed with him through elementary school. He still talks about “My Beth” – that’s what he always called her.
Sensory issues were Rob’s biggest obstacle. He hated most shirts, but jeans and tennis shoes were no problem. He wore a hat everywhere he went. He had hunter ear protection that he wore through his school day to add pressure to his head and block unexpected loud noises. He had a huge platform swing in his classroom that he used all of the time. Beth discovered while he was laying in his swing, he could spell and read and recite math facts much easier.
When he became stressed, he squeezed his jaw or flapped at his ears. He still does the flapping, but now it’s by his jaw and it doesn’t happen often. In some ways, his sensory issues have gotten better. He is willing to try new foods, new places and new clothes, for short periods of times. In others, it’s become harder for him. Crowds bother him more. Being hot is extremely uncomfortable.
Rob is a grown man now, but that little boy is still inside him. He still loves Dr. Seuss and his Power Rangers. Willy Wonka and The Wizard of Oz will always stop him in his tracks. He still builds trees and power poles with his Legos. “Where did Robbie go?” will always get a smile and giggle from him. He is still Mom’s boy and still leans on Mandy.
He doesn’t like to get dirty like he used to. He hates anything gooey on his hands. He doesn’t like to wear jeans (though part of that is trying to find a pair that fits well!) and doesn’t always have a hat on. His interests are not those of a grownup, but he is a happy guy.
To him, the best part of his birthday will be that Grandma Rose and Grandpa Mack, Mandy and Cory will be here and we will have Long John Silver’s for supper. He’ll grin as we sing to him and blow out his candles. He’ll open presents and say thank you. And then he’ll be done with being the center of attention and disappear into his room.
I know many of your reading this have little ones. I know you have days when you wonder how you can keep going because you are so darn tired. I had those days and I can tell you, it does get easier. It may not be a perfect life, but no one has that. You will always have hard times, but you are strong enough to handle it.
I didn’t always believe in myself, but we are making it, day by day. I can sit and remember how far the kids have come and some day, you will do that same. Your journey won’t look like ours at all, but it will still be a good one. The ups and downs average out – even when the downs seem to never end. Always believe in yourself and your child.
As for me, I’m going to go wrap Rob’s presents and hope he likes them. I’m going to look at his scrapbook and know that little boy is still around – as cute and as ornery as ever. I’ll be grateful he doesn’t climb to the roof and jump anymore and that he finally seems to have a small awareness of danger. Some day, you will look back and be proud your child has come just as far.
