How fast it all changed.

Love sent Rodeo. Agitation is a difficult part to face, no matter how much one knows or is told about it. Horrid emotionally at times. It was definitely the hardest part for me. I am very sorry. Thankful that you have so many loved ones around you to help you get through it all.
 
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Rodeo, I started reading this thread last night after returning from the hospital where my DH had what we hope was minor surgery. Will have to wait a few weeks for the results. I just wanted to give you some support in this difficult time for you. You sound like a brave, strong person. I will be thinking of you and your family every day to have the strength to get through this journey that we all face in our lives. You are not alone. Let your family and friends support you and your children through the healing that will come eventually. Hugs.
 
Combative is definitely the word of the day.

The nurses did tell me what kinds of things I may see at the end. They mentioned the mottled skin and the respiration. The day nurse was still there when I went back this evening. She said it would be best to bring the kids tomorrow, so that is our plan. DH is no longer eating. He is drinking very small amounts (he never finished the cup that was there for the whole afternoon) and I think will still chew on a Popsicle but not finish it. They have started using a sponge to wet his lips and mouth.

They now have him on a pump for his anti-anxiety medication - can't remember what this one is called. Hopefully that will do a better job of keeping him on an even keel.

It was a very up and down day. He wants me there, but then when I am he's pretty combative with me. Apparently he actually got out of bed last night, setting off his alarm, but made it to the window before the nurses got down to his room (he's the last one on the hall.) When they asked what he was doing, he said he'd been dreaming that he was supposed to meet me for danishes. Not anything we've ever done in our lives, but I had bought a package of them for the kids the week he was home from the hospital, so I guess that's what his mind is working with. He said he guessed he wasn't supposed to meet me and would go back to bed.

Even though he wants me there, he gets angry with because I won't help him get up and dressed and leave. I started off being more playful about it, but he wasn't responding to that and kept trying to get up - set the alarm off about nine times through the afternoon and evening. Finally I became more firm - "nope, sorry, I know you'd like to get up but it's for your safety. You're not strong enough to stand and walk on your own." That's when he got really mad. Oooohhh - if things were what they used to be and he wasn't working away at dying I'd have given it right back to him. He is definitely fighting it, which is very hard to watch. I worry about the kids seeing him like that, but both still say they want to be there. At least there are other areas they can go if it's too much - living room, family room, quiet rooms.

Soon after I got home tonight he called DD on her phone. She brought it to me and we talked for a few minutes. He seemed ok, although confused. I said we'd all be there tomorrow and he needed to get a good night's sleep so he'd be awake for us tomorrow. After he hung up I called the nurse. She said whatever I told him did the trick. He'd been agitated and angry with them for not letting him get dressed and go but calmed after I spoke with him. He refused his 10:00 pain relief but allowed it after we spoke which was around 11:45. So, pretty late and he was likely in a fair amount of pain by then. I'm going to discuss a pump for that also tomorrow. So I guess he's angry with whoever is with him and in his mind stopping him from what he wants to do.

I have been told that about the person hanging on until everyone leaves the room, but good reminder that I need to let my kids know that. That they may not be right there for his last breath and that's ok.

Oh Rodeo my heart is with you and your family tonight.

Your posts describe exactly what I experienced just last month with my mom who lost her battle very suddenly. My four sisters and I never left my mom's bedside for her final 12 hours on this earth and i can honestly say that nothing prepared us for what we witnessed.

Nothing I can say will make this any easier for you & I won't even begin to pretend that I understand since my husband is blessedly healthy. What I can tell you is that no matter what choices and decisions you make know that you aren't wrong. Whatever you need to do to survive these moments is the right thing. Don't feel the need to hide your emotions from your kids because then they will know that it's ok to me mad/sad/angry/hurt whatever emotion comes to the surface.
Our wonderful final nurse told us that they believe that while my mom might not have been awake it's extremely likely that she still could hear our voices so we turned on her final movie, White Christmas, and watched it 5 times while we talked and cried and shared memories. We talked to my mom, talked to each other, whatever came natural in the moment. Just do whatever you need to survive the moment.

I'm so very sorry you are going through this. Life truly isn't fair sometimes. Please know that you and your entire family will remain in my thoughts and prayers. ❤️
 


Rodeo it is breaking my heart to read how fast things are happening with your husband. It must be so hard on you and your kids to deal with so much so fast. You are giving me strength to deal with my situation based on how amazingly you are handling everything that is being thrown at you. I spent this week driving 4 hours each day to Victoria so my husband could get radiation, and I am finally beginning to accept what is happening. He was working until Tuesday and now he is so tired and weak. He sleeps most of the day and is out of breathe a lot. He has also stopped eating much. I just found out that he is in pain at night from his ribs which the cancer has spread to.
Like others, I teared up when you mentioned the sponge to moisten his lips. I was doing that for my Mum 2 years ago. I don't want to think about having to do that any time soon with my husband. You deserve so much more time. Every day you are in my thoughts. This is so unfair. Just remember that you are not alone, obviously. So much support from everyone here.
 
I had forgotten about the combativeness. When my dad was still in the hospital he kept trying to get up to go to the bathroom, but he was catharized so didn't need to. He would yell at us because we wouldn't help him up to go. It was heartbreaking. Even worse they had him restrained to the bed so he wouldn't get up and fall. It was horrible. It was such a relief when my mom finally agreed to hospice, he finally got to have some peace there.

I'm so sorry Rodeo you and your children have to go thru this.
 


Peace and grace to you and your family Rodeo. You all have been in my daily prayers for the past few weeks.
 
Rodeo. I'm in tears every morning reading your update. Your love for your DH and your children shine forth in every word.

Were I ever in your shoes I hope to face it with the grace, and dignity, and strength, and love that you are showing. Much love to you and your family. May you all be at peace.
 
Rodeo, continuing to send prayers to you all. I also hope this thread will give you some comfort. Things have happened so quickly & I am sure you are in shock. Having this thread as a timeline might help you later as you process everything you all went thru.

Excited family, still praying for you & your family as well. So sorry to hear your update. I hope your DH gets some relief from his pain. Radiation is just as hard on the body as chemotherapy. So hard to watch when the treatment seems to be making your loved one worse. :hug:
 
Just checking in Rodeo. Hope you are doing okay. Update us when you can. We are here for you.
 
I just wanted to drop by and see how things are going. I can't imagine how you and your kids feel. You are definitely not alone. :hug:

And neither are you excited family. :hug:
 
I wish I knew the right words to say :(

Rodeo, I’m thinking of you tonight and how much strength you are showing. I’m so sorry.
 
Rodeo it is breaking my heart to read how fast things are happening with your husband. It must be so hard on you and your kids to deal with so much so fast. You are giving me strength to deal with my situation based on how amazingly you are handling everything that is being thrown at you. I spent this week driving 4 hours each day to Victoria so my husband could get radiation, and I am finally beginning to accept what is happening. He was working until Tuesday and now he is so tired and weak. He sleeps most of the day and is out of breathe a lot. He has also stopped eating much. I just found out that he is in pain at night from his ribs which the cancer has spread to.
Like others, I teared up when you mentioned the sponge to moisten his lips. I was doing that for my Mum 2 years ago. I don't want to think about having to do that any time soon with my husband. You deserve so much more time. Every day you are in my thoughts. This is so unfair. Just remember that you are not alone, obviously. So much support from everyone here.

Excited family, please make sure you take care of yourself. That's a lot of driving, so try to find a way to stay well rested. Radiation is just as hard on the body as chemo, but for some reason people think radiation is easier. In this "new norm" you are experiencing, just as we've all said to Rodeo, remember to ask for what you need and to let people help you. Contact your husband's doctors ASAP and insist they manage his pain. All of this is so hard! Keep encouraging your husband to eat, regardless of what it is. Please don't feel like your struggle is secondary on this thread. So many of us have you and yours in our hearts and prayers, along with rodeo65 and her family. I cannot imagine the challenge of what you and Rodeo are facing every day. Know that you, too, have your DIS-family behind you. Please keep us posted. :hug:
 

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