Well, we were are still hanging on together.
I think I'll ask about playing Taps at the gravesite.
Steve came out on Steve-time. He was the only person to visit on Sunday and I am lucky that he came.
I'd told Steve that he could stay inside while the nurse visited and we had our discussion of plans. He always went outside to be out of the way.
Ariel, Steve, and I were the last ones to exchange a conversation with Rich. With the systems shutting down gradually, the verbal communication had left him. He still would open his eyes when spoken to but rarely respond vocally to any questions.
Muscle twitches and movements were random now. It seemed that Rich was reaching and grasping for things. [This is a normal part of the body shutting down the control over muscle movements]
His breathing was comfortable. The nurse and I washed him up a bit and changed his briefs. There is a trick to changing sheets and briefs with a patient that can't assist you anymore. I had no idea. Perhaps I should have been watching YouTube for a tutorial.
The nurse decided that we were low on one medication, so we searched for an open pharmacy. I was exhausted from the long night of watching over a very animated Rich who often tried to climb out of the safety rails and pulled off his cannula.
Steve volunteered to run to town only to come back and tell me that the only open pharmacy in our little town had none of that med. The Hospice nurse at the 'hot' line searched and called pharmacies and found one an hour away that had the meds we needed for early morning.
Steve grabbed his keys and set off for a 2 hour journey to get medications for his best friend.
The rest of the afternoon was pretty quiet. My neighbors to the west [the one who brush hogged the pasture] came over with a wonderful array of chopped vegetables, crackers, and cheese. I snacked on those items most of the afternoon. The rest of the day was spent reading a book and nodding off for short naps between medication doses to keep him from having pain in the struggle to breath.
By evening I felt as though I was becoming an expert at catnapping between two hour med doses.
I kept moving the cannula back on his face and talking quietly to him.
I told him that Fred [his beloved mule] was waiting for him as well as his father. I retold the story of our meeting and our long distance courtship and asked if he'd greet me on the other side too so we could one day be together forever.
He settled down and finally seemed comfortable.
The night terrors visited Thursday night around 11pm. He awoke with a start and became extremely agitated asking me what that noise was.
I turned on all the lights as he asked and listened.
Nothing.
But he heard it. And said: Something's trying to kill me. [It came out a bit garbled, but he repeated it several times sometimes missing parts of words]
He tried sitting up and couldn't. But there was no stopping him. It was awkward, but I got him up sitting safely. He took off his 02 cannula and claimed it was upside down. It took forever to have him see that the cannula was indeed okay to use.
Everything was wrong and he kept grabbing his O2 hose and tried to pull out his catheter.
Since I recognized it as hallucinating and agitation, I offered his meds to calm him down. He actually raised his voice and told me to go away. He seemed very angry.
Having lived with his severe PTSD for many years I wasn't too fazed. At least not right now. The anger hurt but I understood he was just lashing out and I was in the room to receive it.
I made sure he was safe and went into the kitchen to prep some liquid meds.
I was quiet and calmly asked him to open up his mouth.
He did and I sat next to him and waited.
After 25 minutes passed, I could gave him his nebulizer treatment. More silent waiting while his hands adjusted invisible things. Those hands were busy. It actually looked as if he were talking with someone and expressing the conversation points as he used to all the time.
He then reached up and brushed his facial hair as if he had a long beard. The 02 line seemed to be a lifeline for him to hold. He held it in both hands as he looked across dim lit the room.
For a while he seemed lost. With the meds and the NEB, he was back to breathing in an acceptable manner. But his mind was in and out of places only he could see. Some of this is natural to his state of being right now and some of it is aggravated by the fact he can't swallow his meds well anymore.
Because his psych meds were stopped cold, it can lead to a number of difficulties that we have to try to deal with.
Why? In such a forlorn voice.
Oh did you? That is flat over...look.
Garbled, stop, isn't...the language turned into several grunts and many moans.
He sat up for nearly an hour with me sitting next to him. He fell asleep and woke, shut his eyes and swayed, then finally I asked quietly, "Do you want to lay down?"
Yes
Off and on for the next hour he made sounds and some words before falling back to sleep.
I fell back to sleep on the loveseat around 2AM. It seemed we'd made through one more big event.
This may seem odd, but I find this part of his 'journey' somewhat interesting.
Yes, it feels a bit scary too. I'm that person that studies it. I suppose it keeps me from freaking out if I look at what is going on with an analytical eye.
Friday morning was startling. Rich had pulled his cannula off while I was asleep and when I checked him his 02 was a mere 66. I put it on and he pulled it off again a while later. Another hurdle overcome as I changed cannulas and got a more comfortable one for him.
Steve and his daughter showed up early and Steve sat with Rich so I could sit and enjoy some coffee and chat with Steve's daughter [she is the one who got our horse '15' now ... named Honey]. Gina told me she had to come with her dad as he was pretty upset and anxious regarding his Fishing Buddy.
I'm happy to give Steve all the time in the world with Rich. He seems to know exactly how to be quiet or to chat a bit. Rich is calm when Steve is there.
Nurse Jason has been here every day and each day we construct a new plan to deal with his psychosis, anxiety, and end of life issues. This morning was pretty intense, but I'll talk about that later. Aside from being tired, I am doing what folks would say pretty okay.
Friends make the world go around...especially when they bring me something to eat.
So again today too many folks showed up. Tammy the respite worker was scheduled and she talked briefly with Rich to find out if he wanted Peanut butter cookies or a cooked lunch.
He couldn't exactly tell her what she wanted, he got stuck with the words which happened often after his stroke but was really exaggerated now. We asked Peanut Butter and he nodded.
She started to get things ready and we chatted while I cleaned up some dishes and gave her an idea of what was supposed to happen. Hubby's daughter and her husband showed up at the same time as life long friend Steve.
I'd already pulled the mattress off the double bed I'd been using and taken everything apart and tossed stuff in the wash. I'd washed the windows in the corner of the living room so he'd have nice clean windows to watch the outside world with. I moved bird feeders close in so the activity would be evident even if he wasn't watching for it.
We had decided to move his hospital bed to the best view in the house and he didn't want it at first. But the little bedroom is pretty boring. During the move of 'stuff' he got pretty agitated. I'd told everyone they had to stay outside while the nurse and I got things moved around.
Friend Steve took Charlie for a ride in his car [Charlie was over the moon]. The other two waited on the porch. [It was cold!]
Tammy understood what was going on and stayed out of everyone's hair.
I'll make it short. Once everyone was gone, hubby settled down and took a good nap.
He is moving into Terminal Delirium language. Fidgeting [Terminal Restlessness], making motions, and stopping mid speech. It is much worse in the afternoon to evening.
Terminal Delirium is a physiological sign that the body and the mind are slowly shutting down. He can be perfectly lucid one moment and nonsensical the next.
I've learned to just seem to understand and let it go. I never ask him to explain or elaborate. It passes.
I have noticed though that with his buddy Steve he is more animated and laughs a lot. Steve just waits when hubby shuts his eyes and when Rich is ready, he chats again telling him stories.
He was so happy to see his daughter but she kept asking too many questions. Finally he just waved his hands at her to go away. Questions are bothersome, soft chatting is better.
Too many folks at once irritate him. My bad--> Duh on my part.
He may be happy to say hello for a second or two, but two people is too many. This is something the Chaplain and one of the other nurses had warned us of.
One of the Home Health Aides suggested that I play some music that he likes softly in the background.
I did that this afternoon and watched as hubby tapped his hands against his legs in time to some of the songs. I'm beginning to recognize the beat of the music that effects him.
Things I am learning:
Music is a universal language.
All at once [visitors] is bad and distressing.
Quiet is good.
Bird watching is good.
Last note. He refused the peanut butter cookies and most anything I'm offering to eat now.
Shhhh...let's listen to the music and the bird song.
It's enough for me today.
I'm there, I finally made it.
Made it where?
He smiles at me and flutters one hand as if directing someone. It is 3AM, what a magical time.
Later, he stares intently at the the bedroom wall.
Hey. The chair moved. Who moved it. It moved.
I look and the chair is there where I left it earlier. I just nod because no answer is needed, he is just talking about random things.
Charlie slips into the room quietly and asks to get up on the bed. He lays next to Rich's feet quietly for hours.
Don't lose the keys.
Ok.
Later.
Wait until things hard up. He nods. I nod back.
We attempt some coffee and some cereal. Then he insists on getting up and I tell him he can't and explain why. It crashes his 02 and rockets his heart rate.
He thinks a while then says.
When CAN I get out of bed?
I'm not sure how to answer this as we've been through it for the past 3 days. He starts to try and get up and I have to tell him.
Not now.
Then when? He gives me a hard stare. When can I go fishing again. What day is it? I want to go fishing tomorrow. When can I go fishing again?
I'm not one to lie so I say. You may not be able to.
I'm stuck in bed now?
Yes.
Then I may as well be dead.
I don't know what to say.
Am I dying?
Yes.
Good, then lets get it over with.
We'd had this conversation yesterday about Hospice about dying and how they were making sure this part was not painful. I'd asked him if he was okay with it. He was. I asked if he was afraid. He wasn't. We talked about it for a while because no one else was around to bother us.
Things changed rapidly from Monday to Tuesday morning. The signs were there. The vacant stares and looks, the non-responses. Yet guess what, we still could eat ice cream or a few bites of it for breakfast. Because.
Why not? Because ice cream is his weakness. He loves his sweets.
Steve spent the most time with him after the nurse and social worker left. The two old coots chatted and laughed and life seemed almost as if it were normal if Rich hadn't been stuck in a hospital bed. Since the guys loved hunting together for years, Steve brought Rich an unusual pistol with a 16 inch barrel for him to admire.
By Tuesday night he didn't know who I was at times but still let me give him his liquid meds. Lucidity comes and goes. Sometimes he knows who I am and other times not. At least he still lets me attend him.
Alli who has seen him twice a week since he started Hospice came out 'off duty' last night to see Rich and to just give me some company and support. Some people go way above and beyond.
The progression continues with something like a wave of up and down. Good, a little less good, a little more good, a little less good, and eventually ending.
His daughter did show up late in the afternoon with a chiffon cake which made Rich bright eyed. She handed me a piece that she cut and put on a plate and I told her to take it and help her dad eat it. She gave me a side look when I handed the plate back to her.
Rich loved it and made a right mess of things while eating it. I handed his daughter some paper towels while I went back to washing dishes and folding clothes.
Her husband sat at the kitchen table most of the day at the kitchen table and stared at his phone. His daughter joined him while I tended to things. They had to leave early so they could go out to eat. [meow...never asked if I'd like something...😼]
I'm pretty sure I had some sort of expectations of them other than them parking themselves in my kitchen for the day.
So it goes. Family Dynamics can be strange at times.
The Progression continues. It could be a couple of days or a couple of hours. But I am here and that is what is important to me.
I woke Dennis up much later and took him outside to sit on the porch. We marveled at the stars and the Milky Way. He kept commenting on how many stars he could see. I could hear the awe in his voice even though I couldn't see his face.
It was a gift I could give him for helping so much.
In the morning, I got him up early so he could see the deer wandering through the meadow in front of the house. Then I had him watch the old oak tree so he could see the magical light in the fog .