I crashed into a wooden model of a building at school when I was 11. One moment, I was walking and chatting with my friends, the next, I was sprawled on the floor with splinters all over. I had smashed the model like a tornado tearing through the Oklahoma plains.
I went home in a state of panic, saying, “I didn’t see it! I don’t know what happened!”
My mother told me why I hadn’t seen it.
The model had been in the peripheries of my vision, which was full of blind spots. Blind spots that were growing larger with each passing day. “Your peripheral vision will get worse and start to close in” – my mother brought her hands together, imitating a circle constricting into a single point – “and then you won’t see much.”
That was how I found out I would one day go blind.
This news would gut anyone, but it was an especially devastating blow for me. I had been born Deaf. Although I had received a cochlear implant at age six, I remained absorbed in all things visual. Everything I loved from books to Sign to art all were things you see. Now my mother was telling me that all these things would fade away, a retinal cell at a time. “By middle age” was the only prognosis I got for when my sight would move from “impaired but manageable” to “blind.”
My mind has erased the conversation and the accident from my memory. My mother has recounted all of this to me, saying that I got up and retreated into my room without a word. I didn’t cry – at least not in front of her. I might not remember the events, but I remember what I felt. I felt as if I were a natural disaster, wreaking havoc on everything in my path. I also felt the light of my future dim. Not extinguished, but it lost its luster.