Showing posts with label disability. Show all posts
Showing posts with label disability. Show all posts

Monday, June 10, 2019

Up, In, Out, Down


It’s late. The sun has long set and Evie has surrendered to sleep. Her body is the most pliable when she is asleep. She doesn’t fight me as hard when I work with her legs. After years of sitting, her knees have become stiff, not too bad though. I’ve seen much worse. It makes it difficult to get an accurate measurement of her length. I start working her legs a little bit doing some of the movements I have done during my gym classes. I guess I hope it will loosen the tightness. It probably won’t. But I try anyway.

Up, in, out, down.

Over and over. Smooth and slow measured movements. It’s quiet. I’m left to my thoughts while my hands manipulate her legs. I realized I’m living a comedy routine once aired on Amy Schumer’s show years ago. It was a bit about not really wanting to work out and if you were rich enough you could just pay someone to move your body for you. People laughed in amusement. In this moment, it is not as amusing as I may have thought 9 years ago. I must help my daughter move her body. Everyday. We attend therapy where other people help her move her body. When she is in school, her teachers, aides, and therapists help her move her body. If we don’t, muscles grow weaker, they shrink, they tighten, they hurt, and skills we fight hard to maintain slip away.

Up, in, out, down.

A pang of sadness washes over me as I move her legs. What would these legs have done if not for Rett? Run up and down a soccer field? Help her twirl in a ballet recital? Propel her onto the pommel horse at gymnastics. How many scraped knees would I have kissed and bandaged by now? Would she have used those legs to steal a base during a ballgame? Climbed the spiraling steps of a lighthouse? Will they stay strong as she ages? Will they ever be strong enough for her to stand? Take a step?

Up, in, out, down.

First the left, then the right. Moving her legs to the soft sound of her even breathing. I finish exercising her, start her tube feed, and tuck her in bed. She stirs a little, but her eyes never open. She is completely calm and unnaturally still. Sleep is where she finds the most peace and where I find myself the most restless. The morning brings another day of helping her move and live the best life we can offer her.