Monday, June 18, 2018

Day Three

Pink wants to know if today is the day that I won't sleep on the couch for hours at a time. She asks how long it usually takes for jet lag to wear off. I explain to her about depression, so then she starts telling me the best jokes she knows.

Stow wants my attention. He comes to me frantic about his train, his tummy, his sister, his window. He hits me in frustration when my responses are slow and sloppy. I turn him away when he asks me to go downstairs and play with him. I can't possibly muster the energy it would take to play.

My chest feels like someone has filled it with quick drying concrete that hardens as it seeps into my stomach and down to my legs. The simplest tasks feel insurmountable. I'm able to make it through the grocery store but can't face putting gas in the car or picking up a prescription. The kids have a swim lesson that I'm not sure I will make it through.

This pizza felt like a herculean achievement.
Ren's patience wears thin. Under his breath, but loud enough for me to hear, he says, "She's back, but I am still doing everything myself." Supine on the couch, I don't disagree. Sleep beckons me in the middle of the day. At night I lie awake hour after hour as it eludes me replaced by anxiety dreams and a buzzing in my brain that can't be shut off.

This is not my A game, or my B game, or even my C game. This isn't really even coping. In my head, I know that it will get better (it always does), but I also know that it could take awhile. I don't have awhile; being a mom in a special needs family means I'm operating on borrowed time already. Still, my only choice is to put one foot in front of the other, to wake up each morning and to try again, to hope that tomorrow will be a little easier than today, and to pray that somehow everyone else can keep it together just enough to avoid complete catastrophe.


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