In my previous post I commented on how talkative Kate was this past week. We had another good conversation on Friday. It was an ordinary lunch at Applebee’s, but it was a time when we both felt the impact of the words we exchanged. We talked about how much each means to the other. We briefly touched on the subject of re-marrying if one of us died. At this point, that is something neither of us can imagine. Each of us expressed our feelings about the other and the difference that made in our lives.
Kate asked me about a number of things. She was soon overwhelmed with information and asked me to stop. She said, “You know I won’t be able to remember. I will have to ask you again.” I told her I would always be there to answer any of her questions. I also reminded her of a nickname she had given me in the early years after her diagnosis – “MM” for “My Memory.” It was no surprise that she hadn’t remembered. I would have been surprised if she had.
It was a moment when each of us spoke very candidly. She was clear about not remembering. I was equally clear in my commitment to be with her whatever the future holds. That commitment is an important source of strength for me. I believe it keeps me from dwelling on the sad aspects of living with Alzheimer’s. There is no doubt that caregiving is stressful, but it has its rewards. I think of it as a privilege to care for Kate during this last chapter of her life. Overall, I still believe things are going “remarkably well.”
