These shoes. Tiniest little white Nikes you’ve ever seen. In this picture, my youngest daughter Hannah is wearing them, standing next to big sister Sophie in her barefeet. We’ve just been traipsing around the yard. But once upon a time, they were Sophie’s shoes.
Sometimes I unpack a box full of Sophie’s things for Hannah and just savor the fond memories of Sophie’s younger days. Her cute little diapered butt crawling around in that ruffled skirt. A fancy church dress with all the frills. The t-shirt she wore in this picture or that. Other times, I pull out an item like these shoes, and I’m transported back to a very different time in my life.
Why would anyone buy lace up shoes for a baby? You might wonder. And they look to be hardly worn! Being Nikes, we all know they weren’t cheap. Was this just a first baby thing where you splurge on a super cute tiny version of something? No. These were Sophie’s therapy shoes. They had to be lacers because she had custom made braces for her ankles. Her little ankles were hyper-mobile, too flexible for her to stand up when she should have been able to. Because of her hypotonia, Sophie started physical therapy at about five months old. These tiny shoes take me right back to those home therapy visits. And boy do they make me realize exactly how far we’ve come. It’s hard to see that in the day to do. I forget the challenges that Sophie has already overcome, her grit, her determination, her pride in finally being able to do something that was difficult for her. Sometimes it’s all too easy to focus on the every day struggles of autism. It’s much more difficult to keep in mind what an overcomer my Sophie is.
This week she started kindergarten. It felt a little anti-climactic to me because it’s like the fourth year I’ve taken her to her first day of school. But these tiny shoes made me realize exactly how huge this moment is for us. The fact of the matter is that any number of very serious conditions were on the table in Sophie’s first year of life, when she wore these tiny shoes. But exactly NONE of those conditions were ever found to be her diagnosis. Autism. Yes, it is still very hard. But it is so important for me to remember what it is NOT for Sophie, based on those early days of her journey.
A kind lady in my church, a follower of Sophie’s story, recently asked me, “Does it ever get easier to accept?” speaking of our autism diagnosis.
In all frankness, I told her, “No.” But today I would add to that “not yet.” Because today I have the perspective of the past.
And, not the least bit coincidentally, the same day she asked me this, my pastor taught on “Anticipating Heaven” and having a “God’s Eye View” of the troubles of this life. Yes, autism is very hard to accept, but someday, this diagnosis will be a memory, just like her physical therapy days. And someday, when all things are set right, my sweet girl will be free of this neurological disorder forever. She, like the rest of us, was created for far more than this broken world allows. We live with autism in this life, but we anticipate a life of wholeness, for all of us, in what is to come. And in this there is hope.