A few months into the ordeal of Maisy's hospitalization, multiple surgeries, seizures, collapsed lungs, pulmonary embolism, etc., a neurologist came into her room. In the haze of memories I have from that experience, I remember my heart pounding, my mind swimming, and telling him that neurology was not an exact science. That for every study he could use to prove his point I could find another to refute. That children compensate and that the brain was marvelous beyond our understanding. I decided at that point I would take things as they came. In my heart, in my dreams, in my mind I could see my daughter playing, talking, laughing, happy. She was just a baby with so much ahead of her. When she looked into my eyes there were things no MRI or neurologist could ever see. I even had a dream one night that she was sitting at a piano on a stage playing for a large audience.
But sometimes in the day to day I lose sight of those strong feelings. Communication is a big issue, I sign to her she signs a little back. But neither one of us is getting our message across. Sometimes my three-year-old is throwing and kicking and crying out of frustration, and I too want to do all three because I am just as frustrated. Because Maisy doesn't eat she uses her tongue like a hand and just as you or I would touch something to sense it, Maisy might lick that same thing for the very same reason. Those are the times I forget what my heart feels or I wonder if some of those feelings stem from wishful thinking.
Then on Friday she tore the book and I took it away. She cried, I felt bad. That night as I told Evan the story, Maisy cried at the mere mention of Knuffle Bunny. So I read it to her again, but this time as I watched her I realized that my beautiful little girl was relating to this book. That she was understanding what it was like for Trixie to not be able to tell her dad what she needed. That she was so proud of Trixie for those wonderful first words brought on by a much loved friend. I also realized that every time I had read the book to Maisy she had been trying to form words.
I know in my heart that Maisy is capable of more than she is given credit for. One therapist told me that she believed Maisy would eventually catch up to her peers. I don't know what her future will hold. I have fears of teasing and broken hearts, sitting and crying with my daughter. I know that she is wonderful beyond what a sideways glance will tell. I know that whatever her future holds it will defy CT scans and doctors notes. This week it was not only nice to see a small glimpse of that potential,but for this mom, its my own little miracle.







3 comments:
Miracles are all we have sometimes Somer. Maisy will do whatever you wish her to do. She has you as a mom and that's the first miracle. They will continue. Love you.
What a gift. Our Father in Heaven has that kind of insight into us, all the time! Amazing. You are amazing. Give Maisy a hug from me.
hey there...i got on your blog from mo willems' website. my heart goes out to you and your family, somer. i'm a kids songwriter, and i wrote a couple of songs back in the spring about signing for a friend of mine that teaches sign. the little girl in the song is called "maisy". i'll send you an mp3 when i demo it. it's nice to have a face with the name now. i hope to meet you all someday. don't give up.
bill
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