I am raising a boy whose on the spectrum. He is becoming more than I ever dreamed of. More than I ever hoped for. More than I ever thought he would become. He is also doing it his way. Sometimes his ways are out of sight. We are all astound. Here is a boy that barely said a word at 3. A boy for whom meltdowns were all he knew. Until things changed. I still pinch myself as I have not really taken the time to truly uncover all we did in the beginning. And we did a lot.
If you told me back then that we would get to this place one day, I would not believe you. He was kicked out of his first school at age 2 after attending for 2 days. The odds were completely against us. My own child was kicked out of school before he could say his name. I still remember crying by myself that day wondering where to begin. I remember calling a helpline for special needs kids in Georgia that day too. The person on the other line had to have been an Angel. After briefly chatting with her calming me down, she asked what we both did for a living. I said I was a researcher and dad was a resident in neurology. Her response, I wouldn’t worry to much about your son then. I asked why. She said because we would both use our gifts for him and that’s more than most kids on the spectrum would have. Looking back, she was right. When we learnt through research that a drug for cancer had speech properties, my son was on it. When he had a series of nonstop laughing episode, and my husband remembered something about the brain and laughter, my son’s brain was observed via EEG which uncovered mini seizures while he slept. Our gifts were indeed useful for him.
Today at age seven, I keep pinching myself every time I have a heart to heart with him or watch as he reads a book. These days Dog man’s series are all he knows. All he is obsessed about. That he reads makes my heart swell. His ways are still forming, still making sense of this world, still stimming, still repeating things that make no sense, still involves play that makes no sense too, but all of it, all his ways are perfect by design. These days, I would not trade any of this for any sense of normalcy. Not with him. He is perfect by design and even when he tries, all his ways are good. It’s the smallest things with him, the hugs, the meltdowns too, all of them combine, remind me just how blessed we are as a family. To be in the midst of a child on the spectrum is a blessing. One that I am extremely thankful I got to witness with my own eyes. Today he is in a Christmas play in school. The boy who barely spoke at 2, was kicked out of school at 2 as well, is in a play at school at 7. His ways remain out of sight with great days and days with good tries. The sky is not a limit and I remain hopeful for what the future will bring his way.
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Makes my heart joyful to read the hope, the sunshine breaking through the clouds to reveal greatness and warmth! Keep soaring kid! Keep soaring while your parents keep outing into your growth!