Thursday, March 14, 2019

Sweet Raspy Voice

It’s been so long since I have expressed my deepest feelings on paper.  Maybe it is the hectic environment in which I live, maybe it’s the denial that splashes my mind every morning, or the guilt that is seeded deep within me.  Uncertainty is my demon that gnaws away at my confidence to parent the way I need to.   It is difficult to grasp the concept of my everyday jealousy of ‘normal parents with normal children.’  Our life is anything but. Some days my life consists of washing smeared feces off the carpet and wall, or feeling numbing bites from my beautiful child who can’t verbally communicate her frustrations. It’s the constant monitoring of heavy duty drugs like clonazepam.  My Aspen started having seizures at 4 and a half months old. Every seizure I witnessed the pain and worry of what part of the brain was being damaged Every. Second. Of. Every. Seizure. My hope was being shattered. At first my Aspen hit every developmental milestone. She started talking and would put two words together.  Then at fifteen months of age, she regressed and she stopped talking.  My God, how I wish I would have video-taped her first words and sweet raspy voice when she would speak those words, I now only can hear them in my dreams.  I struggle when the world gives me glares and watch as she flops down on the concrete just to feel the texture on her face.  They have no clue.  Autism is messy, it is painful, it can shatter a whole family.  We rely on faith and taking things minute by minute.  Sometimes I have to remind myself to breathe and allow the tears to flow while I give my little Aspen a tight squeeze and allow her to hold me while I mourn the loss of a ‘normal’ life for her.

3 comments:

  1. I get it. Every thought. We have never dealt with the medical problems Aspen endures. You have a whole different level of worry there. Three years ago I promised myself I would not look up, look at other peoples' faces when Ronnie act as up in public. And I have never broken my promise to myself. My heart cant take the judging eyes. Love you guys and everything about you--especially the abnormal parts.

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  2. Ohh your writing and true and honest and I couldn't have said it better. My smart, kind, and oh so beautiful 7yr old was diagnosed with autism at 3.5yrs old. We dont face your medical problem. God knows I dont know how you handle that ontop of autism. I too mourn the loss of my daughters "norma" life. Every single day. I just dont know how to get past that. I am doing my best to prepare her for an independent functioning life. When I'm honest with my self she will never be independent or have a "normal" life. My fears for her take over my mind body and soul. I am fighting to be the best mom and wife.

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