The Waking Dreams of My Father

So I'm just going to "talk" about it, rambling and writing whatever comes out.
This is something I never imagined, ever, in the first 54 years of my life.
When my Dad started to slow down in his late 70s, and after he moved into his 80s and slowed down more, I sometimes thought that when we said goodbye at the end of one of our frequent visits to Arlington, it might be the last time.
I thought, "Maybe this is it. Maybe I'll never see him alive again in this world." I thought about that possibility. I won't say I was prepared for it, but I saw it on the horizon.
When his motor coordination and memory began to decline gradually last year, I figured it was the initiation of a slow decline.
But Dad was dependable. He was always basically the same (at least as I perceived him). He took care of my Mom. He took care of my brother and me, taught us the value of hard work and being professional, but without goading us. Worldly success was not an inflexible imperative; when health problems brought my own career crashing down, he was there to help and to be quietly understanding.
He loved his grandchildren and they loved their "Papa." When the kids were little, they saw my parents a lot. We would spend many weekends (and longer visits during the Summer) at their place, with the kids in sleeping bags on the floor in the living room.
Then came the year 2018. What is probably an Alzheimer's related dementia rapidly accelerated in a few months to the point where he now only occasionally manages to speak a coherent sentence. He has also completely lost the ability to walk.
He seems adjusted to his new physical surroundings after 6 months (though he doesn't really know where he is; sometimes he thinks still at home, or in a hotel, or at a conference, or we don't know because he says words that don't make sense). He gets frustrated because he can't remember what he wants to say to us, or how to say the words.

My father lives in a world of obscurity, of waking dreams. Thank God he is being well cared for, and that we can spend time with him.
It has taken me a long time just to realize how difficult it is for me to accept that my Dad is incapacitated. When he says things that make no sense, it's not my fault that I can't understand him.
It's not my fault. That would seem obvious, but it's different when it's your own father's face in front of you, still with some of the expressions you have seen--and the voice you have heard--ever since you were born. This is the face and the voice that raised you, that you respected and that always made sense. Around your own middle age, you finally began to realize how much sense and how much wisdom and how much love came from that face and that voice.
It's still there. Occasionally something flashes through, suddenly and rapidly. He grabbed my shoulder today and said, "Solid fellow. Solid fellow." He is still the same living breathing human person; he is just handicapped by a terminal illness. He can still give and receive love. And we have to remember that as the illness progresses and he can no longer grab our shoulders or even open his own eyes.
I know there is deep down mysterious suffering for my Dad. I pray for him all the time, and trust in God who knows him entirely and loves him completely. God knows what my Dad needs in this last season of life, and for eternity.
Well, that's enough rambling from me. I'm battling to keep my own head above water. Even though I often feel useless, I also see (as much as a human being can see such things) that my task in this life is not yet completed. Even if it seems like nothing, I'll do what I can for each day and throw myself upon the mercy of God.
Published on September 19, 2018 20:52
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