My eldest son, Jacob, played his first solo show last Friday.
My husband and I took the rest of the kids to hear him and we had a nice time, or as nice a time as any 40-something adults can have in a large crowd of teenagers. There is deep joy in watching our teens circulate among their peers. Abbie, my 15 1/2 year old daughter, ran into some boys she knew from school and spent the time flirting with them and bragging (oh-so-subtly) that the guy on stage was her brother. Spencer, my 14 year old stepson, hung out with some of Jacob's friends, eager to test his social prowess before he officially starts high school in August. Jacob took the stage and although he was visibly nervous, he performed wonderfully. The audience was caught up in the off-center humor with which everything Jacob creates is infused.
Of the hundreds of things that Carter's illness (bipolar with psychotic features, among other things) has robbed from us, one of the saddest is the tempering of joy. I try very, very hard to be in the present, but I'm rarely 100% successful. I couldn't help thinking that Carter will probably never enjoy the social successes that our other children have achieved. His heart is as generous as any of his siblings, but his illness too often covers his kindness. He wants to make friends, but his bizarre conversational tics and habits scare other children.
So I'm proud of Jacob. Wildly proud. Warm from my head to my toes proud.
But also sad.
Carter, in the past year or so, has become increasingly aware that he is different. Most of the time, he's caught up in his own concerns—the hallucinations, delusions, obsessions, anxieties, and compulsions that propel him through his life—but lately, in his more alert moments, he knows that most people don't struggle like he does.
That awareness tears him apart. It causes me to have a bizarre not-quite-wish that he was just a little sicker—sick enough not to understand what he doesn't (and likely won't ever) have: play dates and sleepovers, parties and performances, teams to join and extracurricular activities to enjoy. Friends that everyone can see and hear. Confidence, contentment, and fun.
As he gets older, we are less and less able to prevent his dawning awareness and the violent self-hatred that results from it. His siblings are so much older than him that he has, until recently, not compared himself to them. They were Big Kids who did Big Kid Things, vastly different from the things that he did. At 8 1/2, 6 1/2, and 5 years older than Carter, they were almost a different species. Lately, though, there are questions. "How old was Jacob when he had a sleepover the first time?" "How many friends did Abbie have when she was the same age as me?" "Was Spencer scared to go to school when he was in second grade?"
I always knew that Carter's innocence (about this one thing, at least; he's innocent about so little) wouldn't last forever. I knew that my basic explanations (Everyone has a hard time with some things, and this is what's hard for you.) wouldn't hold water for long. It's sort of like teaching my other kids about reproduction. At first, I gave vague descriptions of babies who grow in women's bellies like magic beanstalks, or some such. And at first they were satisfied. Eventually, though, I had to talk about eggs and sperm, and how one got in contact with the other.
That was a piece of cake compared to this, because as much as teaching my kids about sex was a little uncomfortable, it was a natural thing to be doing. I was explaining a normal part of life to kids who would one day experience it (much as I don't want to even consider that!). But Carter's illness is a perverse twisting. A wrongness. A misery-creating beast.
My husband and I talked long, long into the night last Friday, contemplating all that Carter suspects, knows, and fears. We discussed what to tell him, and how, and when. How do we help him understand the reality of his illness, while helping him remain hopeful? How do we teach him to let go of expectations that are tied to what everyone else does, and grasp at goals that are within his reach? Will he be relieved or devastated?
I don't know, and sometimes that's the hardest thing. I just don't know.
I'd shrug if I could stop imagining Carter's pain if I get it wrong.
Adrienne Jones lives in Albuquerque, New Mexico with her husband and children. She writes the blog No Points for Style.
My son is the same age and becoming more aware that there is something different about him. I too am struggling with what and how to tell him about his challenges. So far we are taking what sounds like the same approach as you. As he asks questions I will answer them honestly, providing pieces of information at a time. Eight just seems so young for such a heavy conversation.ReplyDelete
Pickles, liike Carter is starting to realize. Just a little bit. I will offer you to join me hiding in the closet until this time passes by.ReplyDelete
I feel like through your story I'm taking a peek at my future. I agree with you that it is very hard. I'm sure you will find a way to handle the situation so that it works for your family. Sending positive energy your way.ReplyDelete
I hated that part. Explaining to Tim that he was different. He knew - he knew when he wasn't able to do things his older brother was, but his younger sister could. He had a very black and white sense of how things should go. Big brother does them first, then him, then little sister. That is the natural order. But when she read first, had a sleepover, went to camp, his natural order was upset, and so was he.ReplyDelete
He gets it now. But he's nearly 17. He was upset about it years ago. He's made piece with it. Now he seeks out kids like him, actively wants to help them. I'm proud of him. But I hated how down he was on himself during the time to get to where he is now.