So, if this comes off as whiney & “oh, poor me” I apologize in advance. My blog is a place that I go to for working things out in my head, and this is one that I need help with. Bloggy help. Open-up-the-burdens-of-your-heart help. So, read on if you want some major whining. I guess sometimes we have to have a pity party before we pick up and move on with the changes in our lives. Ok, now I've warned you…
I’ve talked a little about my Dad on this blog. In October of 2005, we found out he had alzheimers. Things hadn’t been right with him for about a year. Even when Ben was born the previous February, my dad wasn’t himself. He complained that his memory wasn’t good. He had a haunted look in his eyes the night he met Ben. Something was wrong, but I hoped against hope it was depression or something less…I don’t know. Less permanent. Less like looking down a long dark tunnel to a depressing end.
Flash forward through time with me. June 2006: I visit my dad and take him on a trip to the bookstore. I read him a bit of one of my favorite books; he asks me to buy it for him, and I do, knowing he probably can’t read it anymore. December 2006: dad complains that the newspaper he’s reading doesn’t make any sense. July 2007: my mom finally sells his car, because he hasn’t been able to drive for months. February 2008: Dad comes to Ben’s birthday party at my house. He can say hi to those who speak to him first, and, in a suprising moment of clarity, tells me he likes it when he comes to my house (but he calls it “Becky’s house.”) May 2008, mother’s day: a silent dad eats what is put in front of him, stands where his daughters tell him to stand while they take pictures. Even simple words like “Hi” and “bye” and “I love you” are spoken in a halting voice, the concentration that it takes to even say these words almost tangible.
June 1, 2008. It’s two weeks away. It’s 6 days away from his birthday. It’s also the day that he will no longer live at home anymore. It’s the day when his clothes and few possessions will be transferred to a nursing facility, the same nursing facility I remember visiting my Grandpa in 6 months before he died. That will be my dad’s new home.
I know it’s a necessary step. I don’t fault my mom for making this decision; she has done as much as she can to keep him home, and I know that this is hard for her as well. But when I found out last night that the timeline of my dad’s “home” vs “nursing facility” would be two weeks, TWO WEEKS, it hit me hard. I’m more mad at circumstances and stupid diseases that take away our loved ones. I hate it that I can look at a man that looks like my dad, but is really a stranger inhabiting his body. I hate it that he can’t do any of the things he loves anymore, like reading and mowing the lawn and telling old random stories from 30 years ago and laughing over stupid jokes and. And. And.
I just miss my dad. And I wish he didn’t have to go through this trial, and I wish I didn’t have to watch him go through this trial. I hate that he’s right there in front of my face, but miles away, in his mind, trying or not trying to puzzle it all out.
Two weeks. Alzheimers REALLY sucks.