At my writing group last night one of the women wrote about care-giving for her father who had Alzheimer’s. She wrote of herself as a reluctant caregiver. She found a lot of reasons why she didn’t want to make the 2-hour drive to Columbus and stay overnight at her parents’ house.
I applauded her for her honesty.
And then I started to wonder about myself. Did I resent feeling a responsibility to take care of Mom and Dad over the past years? I don’t remember not wanting to go visit them. I don’t remember it being a burden. What I remember most was being driven to try to fix the problem, to help ease their pain, to scramble to make things better somehow, someway. It was a vocation for me.
I’m sure there were days when I might have preferred to stay home, but I really can’t recall feeling that way.
And it makes me wonder whether I am now in denial, or whether my personal history has made me approach or feel differently about care-giving than some others might. I learned care-giving from a very early age as I stooped to pick Annie’s toys up off the ground where she dropped them, or straightened her up in her chair, or fed her a meal. When I moved away from home it wasn’t very many years before I was giving care to what would eventually be four children in our family.
I know there were times when I grew tired, or frustrated, but I don’t think I would ever refer to myself as reluctant. I wanted to help my parents. I was desperate to make things better.
When things fell apart last December, I spent nights on a sofa in the lobby of a hospital, on a sofa at my Mom’s house, on a Hospice chair that converted to a very hard bed, on an air mattress on the floor, in a recliner beside my father’s bed. I wanted to be there. I went home and slept in my own bed only because I knew that if I didn’t take breaks I would not be able to sustain the level of support I wanted to give.
But in this place of grief where I now dwell, I wonder if I will ever know the truth of any of it anymore. Can we ever really know the truth?