Somedays my 24/7 caregiving responsibilities are quite manageable. Then there are days like yesterday and today that make me wonder "can I continue?" It sure would be nice to take a break but that is not to be.
The current challenge is an old one, Bill can't see. He has macular degeneration. He's legally blind. Yet he insists on doing things like his eyesight was perfect. All he succeeds in doing is making life harder for me and for him. But I can't seem to get through to him. He's stubborn. He always has been.
Yesterday he somehow managed to break the wire to the headphone jack to his portable transistor radio. It was a clean break. For the life of me I can't figure out how he did that but he was lost without his headphones and listening to his radio, the only station of which he can get in clear is the local Fox Propaganda Network. I've warned him if he listens too much to those lies propagated on that Treason Network his brain will turn to mush. He'll be one of those Far Right Zombies. Wouldn't that be nice to care for? But break the wire he did so I ordered a new one from Amazon. But it won't be here until next week. What? They have to get it from China?
Well, we couldn't wait that long so I took him down to the local Walmart. Yes, I fought that Friday night summertime August beach weekend traffic to go to the Rehoboth Beach Walmart to get new headphones for Bill. I had to get the kind with a jack because he can't figure out how to operation the wireless ones. They had one left, $4.97. It works, thank God.
For a backup I bought another set of cheap headphones at Walmart because he will break this one I just bought him and I'm leaving the order into Amazon.
Bill's downstairs vacuum cleaning his bedroom now. He can't see of course what he's vacuum cleaning but he wants to be "doing something." I understand that. Earlier he was calling to me (which I was brushing my teeth) in desperation. I thought "What? Did he fall?" No, he was trying to plug in the light to check if there is a leak near the sewer pipe exit out our bathroom wall. He can't see of course but he's "checking" nonetheless. Now I'm not totally heartless, I know he wants to be "doing something" but all he's succeeding is doing now is making my life more difficult.
HE CAN'T SEE!
For some reason (his stubborness) he refuses to accept that fact. I can understand now why so many inmates of nursing homes spend most of their days drugged with their heads on their chests, sleeping the day away. If Bill was in a nursing home he would be one of the primary candidates for Drug Therapy. Even when I visited him at the rehab facility in Dover, they had him so drugged up that I couldn't understand him and he didn't even know who I was. I asked why they drugged him (which they denied by the way) and they told me "Mr. Kelly sometimes gets agitated." Agitated? That's Bill. If he doesn't get his way.
I do have to admit he has changed somewhat in the year and a half since his strokes and he's home now. And this is where I want him so I can take care of him. I couldn't sleep at night knowing he's in some sterile, heartless "facility", rotting away. I just couldn't do that to him. But I do wish he would work with me a bit here at home while I am caring for him. I don't expect to ever be in the situation that he's in now but if I was and someone was caring for me, I know I would do everything possible to make my caregiver's life easier. But we're all different. Bill is always used to "doing something."
I used to worry, "What if I die before Bill?" I don't worry about that anymore. One less worry. Whatever will be, will be. Things will sort themselves out. One day at a time folks, one day at a time.