It has been seven years since Schuyler was diagnosed with bilateral perisylvian polymicrogyria.
I think I can safely say that I've never experienced as much change, as much growth and heartbreak and joy and failure and LIFE as I have in these past seven years. In a very real sense, I feel like a different person than I was that beautiful summer day in Connecticut when our world came crashing down around us, albeit soundlessly and invisibly to the rest of the world and particularly to Schuyler. I remember how on that sunny afternoon, she kept spinning in her little private, wordless world, the one she still visits from time to time but no longer seems to live in.
Our world fell apart, but it came back together again, completely different and not pretty, but somehow stronger. The worst case scenarios we were given were mostly not to be. Schuyler has a few things she can't eat and a few tasks she finds difficult to accomplish with her clumsy hands, but she's otherwise completely ambulatory and mostly unmarked by her disability. She sometimes experiences a strange anomalous electrical storm on the left side of her brain when she sleeps, but it doesn't seem to be doing anything other than just happening. Schuyler's not having the seizures that we were told were probably inevitable, and I am beginning to feel ever so slightly comfortable with imagining a future without them ever arriving. School is hard for her, and I am no longer confident that her team really understands her or what she's capable of. But she's also in a good program where even when they get it wrong with her, they are getting it more right than most schools ever would. She's delayed and unable to speak, and she might always be, but she's not trapped in her secret world anymore. She's trying with all her heart to be a part of this one, this beautiful, hateful, hard grand world that has never understood her but which has mostly welcomed her just the same.
As for me, I've come to see my weaknesses, as a husband and as a provider, and as a father. As aware as you may believe you are of the things at which I have failed, I hope you'll understand that I am even more acutely aware of them. But at the same time, I've grown as a person. I've become a better father, and I've learned to trust my instincts with Schuyler, because even when I'm wrong about what she can do, I like to believe that I mostly err on the side of overbelieving in her. I've learned that everyone needs people who love them enough to overbelieve in them. In Schuyler's case, she has a funny way of ultimately meeting those expectations, albeit in her own time and in her own way.
I've learned over the past seven years that when Schuyler stumbles, when she doesn't meet academic expectations or fails to communicate the things that are happening inside her broken but beautiful brain, she usually does so because someone out here in this world has failed her. Her teachers haven't found the tools to teach her or the methodology to reach her. Or her parents have dropped the ball in some way or another, or the technology that is supposed to help her is inadequate to the task.
Perhaps that overbelieving is informing my perspective, but I believe that most of Schuyler's failures are ours more than hers. And in seven years, I've learned to embrace the ancient wisdom of the Chumbawamba. We get knocked down, and we get up again. Oh yes.
Schuyler's diagnosis didn't change who she was. She's had her monster since before she was born, since before she even looked like a tiny little human fetus. She had her monster when she was a guppy, and probably before we even knew she was coming.
No, her diagnosis changed who we were, and who we are today. And if it wounded us, it made us stronger, too. Not like an athlete whose body becomes beautiful and efficient through training and exertion, but like some old scarred animal who has been bitten and scratched and chewed up, but who always comes back for more, desperate to protect its young from the biting monsters and an unforgiving world.
So there it is. Seven years.
Robert Rummel-Hudson is the father ten-year-old Schuyler and the author of Schuyler's Monster: A Father's Journey with His Wordless Daughter (St. Martin's Press, 2008). He is also a contributing essayist for My Baby Rides the Short Bus: The Unabashedly Human Experience of Raising Kids with Disabilities (PM Press, 2009). His work has appeared in Good Housekeeping and Wondertime. Robert's adventures with Schuyler can also be found at his blog, Fighting Monsters with Rubber Swords.