‘How old is he?’ you ask at the gym session we both go to.
I always thought that was a straight-forward question with an obvious answer. William was born in January 2010, so he is 5 years and 3 months. Simple maths. But then my youngest came along.
Now whenever I get asked that question, I hesitate. What do I say? “He’s three, but…”
I’m not sure when I really started to worry. It was a gradual thing, I suppose. He sat up a little later than some babies, but that was fine. He didn’t wave good-bye but he did learn to clap earlier than his brother. He didn’t crawl until eleven and a half months; I was just grateful that he would still stay where I left him so I could chase the other one. Walking was at 18 months – an acceptable age. But there were so many other little things. With my first I would read the books avidly every month and crow at all the things he had mastered early. With my youngest, I gave up as he never did any of the things he was “supposed to” by a certain age. But some children just do things a bit later, don’t they? I used to joke that he was backward, but after a while it began to niggle at me.
People say a mother knows her own child, and to trust your instincts. My mother and sister were both worried about him too. Yet it’s hard to stick to your guns when a health professional tells you that there is nothing to worry about and to come back in 6-12 months if you’re still concerned. I managed to leave it 9 months before I went back.
“He’s three, but his understanding is limited.” So when I ask him to do something and he runs off instead, he isn’t being naughty. He doesn’t understand.
“He’s three, but he’s bigger than a lot of 4 year olds.” So when he pushes your daughter out the way to reach his ball, believe me, I’m watching him even closer than you are. I’m very aware that he might hurt her, but I know he doesn’t intend to.
“He’s three, but he’s got…” And there it is. I just can’t say those words. Developmental delay. Additional needs. That’s what they’re saying in all these appointments we’re having now. Speech and language, exploratory play, coarse features, portage, Specialist Early Years: I’m having to learn a whole new language myself. Of course I understand what they’re saying, and I know how important it is to ensure he gets the support he needs. But when it comes down to it, I look at his chubby, grinning, open, wonderful little face and can’t bear to label him like that.
He is progressing all the time, and I’m overjoyed at each new thing – walking upstairs by himself, doing an action to a song, and saying “moo” when seeing a cow have all been major achievements lately. I’m so proud of him.
Apart from my sister and a couple of wonderful friends, it is hard not to feel isolated from other mums though. I’m not one of the mothers of “normal” children who mean well, but hurt me more than they realise when they say breezily, “Oh, they all develop at different rates. My Jack didn’t talk until he was three, but he understood everything of course!”
Yet my life is so easy compared to others coping with autism, cerebral palsy or other unbelievably difficult conditions. I’m a fraud stuck on that terrible cliche, the emotional roller-coaster.
When the Speech Therapist first admitted that yes, there was indeed a problem, I found it such a relief. Someone was finally taking me seriously. That lasted all of a week and then the reality began to sink in.
I’m afraid about what will happen when I’m not able to watch him every minute; that he’ll be rejected by other children in the school playground for not knowing the rules.
I’m envious when I see your two year old trot happily along next to you on the school run. I tried it once – Danny spent half the time trying to run in the wrong direction, and the rest lying down in protest when I wouldn’t let him. I had to carry him in the end, which is no easy matter – he’s over a third of my weight now.
And worst of all is guilt. Believe me, I’m a master at the guilt thing – most mothers are. I went through all the normal ones with my first. Was I right to give him a dummy? Will it hurt him if he has the occasional bottle? Should I really let him watch that much TV? But they pale into insignificance compared to my latest ones. I feel guilty that I often get bored spending time with my own child. I feel guilty that sometimes I wish he was more like his over-achieving brother. I feel guilty that I look forward to the mornings that I leave him at preschool. And worst of all, I feel guilty that maybe it was me that did this to him – that my ancient, worn-out eggs have failed him somehow.
But as when all the evils of the world came pouring out of Pandora’s Box, at the bottom there lay hope. We don’t know what the future will hold. Sure, the gap between him and his peers may widen, but there is every chance that it will narrow or even disappear completely. Sometimes I have to remind myself to keep hold of that hope and cherish it. Why? Because of the still point at the end of that roller-coaster. Love for my boy whose smile lights up my world. Love for my boy who, after I’ve been away for half an hour, greets me as if it was a year. Love for my curly-haired, freckle-faced boy who will chat happily to anyone and anything. My little Pumpkin, amazing and unique just the way he is.
Which is why I need to relearn the answer to that question.
“How old is your son?”
“He’s three. How about yours?”
Editor’s Note: Sally’s son has since been diagnosed with Hunter Syndrome. May 15 is MPS Awareness Day.
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