We went to get the last of Robbie's shots at public health today. I ended up talking to the nurse about some of his issues. He has real sensory issues. He can't stand to wear shoes and socks, when we go out he takes them off every 10 minutes. When he gets home, he can't stand to be dressed and strips to a t-shirt. He does not like me to brush his teeth, as he doesn't like his face held. He has certain food aversions, he won't eat mashed food (just like me.)He is obsessed with plastic food and groceries. His gross motor is a little behind, he can't ride his tricycle or hop on one foot and is clumsy. He won't let me teach him to draw or print, or colour in the lines. And in the winter he is clingy, and just out of control behaviour wise. We had the Autism talk, and I helped her rule that out, his speech, comprehension, understanding of others and communication skill are beyond excellent. The nurse referred him for physiotherapy and occupational therapy. And I had a call from a social learning program, he was referred to this at his 3 and half year check-up, in the winter. It is a program to help him with transitions and social interaction with peers, all which are problem areas. So, he has an assessment for that, to see which group he will go to (they try to fit together similar children). I was telling her about my talk with the nurse, and she was concerned too. She said she would carefully screen him and would probably refer him to a developmental specialist and their team.
I don't how to feel. His problems have overwhelming me, tiring me out and worrying me. His ped. brushed us off when I saw him for the winter behaviour. I am relieved someone is listening and going to get him help. Now, is the time, as he goes to school in 2009.
The other part of me is upset. I feel he has a lot of good qualities. He is loving, affectionate, a great conversationalist, has a wonderful imagination, good with babies and pets. He is very advanced verbally and doing well with early reading skills. Maybe these are his quirks? Maybe 2 kinds of therapy, a social group and his play group is overkill? Maybe he will grow out of his issues or they won't be as significant as he gets older (I dealt with my own texture problems and motor skill problems).
Also, how did this happen? Did I hand him down some crappy genes, as I have had some of these problems myself. And is this because I am a bad parent? Shouldn't I be able to handle all this myself. Shouldn't my MA in child studies and my almost finished PhD in education made me see these problems earlier? Shouldn't my background enable me to help him, without a bunch of interventions?
I am just going to suck it all up. Follow the steps and get my son the help he needs. I am happy he is getting help he needs and someone listened. But, I am also confused and baffled. And sad, I want his life to be smoother, an average kid. With my motor problems, lack of social skills and big brain, I had trouble making friends and fitting in. I wanted better for him. Maybe the help will help us find a better spot. I am just sad we have to go there.