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If your dad tries to hop around on one leg I would imagine he is a handful and I don't know about you but when my dad was in skilled care I never saw this ghost of a Dr. I heard about, much less ever talked to him. Is your dad eligible for hospice, childofvet? If he is I would highly recommend it. Our idiotic Dr. at the nursing home refused my father hospice and only approved it when my dad was circling the drain and was way past the point of being able to appreciate everything hospice had to offer. It might be worth inquiring about. Our hospice people were amazing. There was little they could do for my dad (although they made damn sure he was on the appropriate medication at the appropriate dosage for his situation, something the staff at the facility cared little about) but they did monitor him and send out aides who would trim and shape my dad's beloved beard. My dad was barely conscious at this point. The hospice nurses came by often and advocated on our behalf with the facility which was such a burden that was lifted. In a nursing home our parents are just one among many but in a hospice situation our folks are the only patient. I don't know how I would have gotten through the last couple of weeks of my dad's life without hospice.
Doped up or agitated are not good choices, I agree. How committed is his Dr. to working on this? There has to be a medium.....there IS a middle ground, the Dr. just has to be committed enough to want to find it.
When my dad lived with me I thought about him every second of the day. He was my #1 priority. When he had to go into skilled care that didn't change. I worried about him constantly, worked like a dog to get him what he needed, visited him all the time, and when I wasn't visiting him I was on the phone taking care of his business or advocating on his behalf at the facility. The caregiving certainly does not end and I think I know how you're feeling. We still have to take care of them whether they're with us or not. And it's stressful and exhausting.
I'm going to go out on a limb and blame it on the dementia. Dementia is progressive and people with dementia are often combative. I work in home healthcare and I've been socked in the chin a few times myself. But it was easy for me to not take it too personally. For you it's very personal. And you've learned one thing: Dad will pipe down when your husband is around. That's good to know.
Is dad in a skilled nursing facility now? Can you request that he be given the anti-anxiety medication (or whatever kind of med he was on) more regularly? I know how difficult it is to get things accomplished when a loved one is in skilled care but once it goes through the Dr. and let's say the Dr. okays it, you can call and check that your dad is getting the medication.
Is he losing his mind? Yes. That's dementia. Just because he knows your name doesn't mean that his dementia isn't progressing. My dad knew my name but he also told me that there were people trying to kill him and they had guns and knives. That he still knew my name meant little to me.
At this point all that can be done is getting the combative behavior under control. Even though he has dementia, your dad can't be happy feeling combative a lot of the time. You can't reason with him anymore. What you're left with is medication. You have to be your dad's advocate right now. It's up to you to see that he gets what he needs because he can't express what he needs anymore. This is your job. I had to do the same thing with my dad while he was in skilled care and it was like a full-time job that made ME crazy and caused me to lose almost 30 lbs from stress (it was 20 lbs but I keep losing).
But now it sounds like, if you want to communicate or just 'be' with your dad you're going to have to crawl into his dementia because he's unable to be with you in your world anymore. Don't fight it. Try to get it managed with medication and be with your dad wherever he lives now mentally, if that makes sense.