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User
Posted 14 Mar 2019 at 22:22

Devonmaid,
“its always hard to know what to wish for when someone you love is so ill.”
You hit the nail on the head there, after the children and I talked all three of us agreed that although we want N to stay we all wished it was over for him.
I don’t think anything you have said is insensitive, I think you are honest and keeping thoughts like these to ourselves hurts because we feel so guilty for wanting it to be over even though the motivation for the thought is for your love’s relief from pain.
The sodium has taken a nosedive again and the hospice felt it would be a good idea to try the demeclocycline just one more time and that they didn’t think the previous attempts were the cause of the horrendous symptoms, just a really unfortunate coincidence. So, psychosomatic or not N is feeling pretty ropey today and has had 2 extra doses of anti sickness meds, lost his appetite and is very, very tired.
He’s also developed a phlegmy cough and bubbles when at rest but because he’s so deaf, I don’t think he can hear it, though I’m finding it quite distressing to listen to!
When I’m at the hospice, I change N, wash him, help cut up food etc, get drinks. The staff are always asking if I need help or want to take a break, I feel so useless just sitting there waiting for someone else to do it. He only asks me to take his dentures to be brushed, if I didn’t do it then he probably would have stopped using them. I also wash his fingernails, this is something they don’t do either in hospital or in the hospice, strange that they wipe bottoms but don’t use a nail brush…I don’t know why.
I hope the enza is having a positive impact and the chest pain was just a dream, love and hugs to you both.xx

Teacups,
Hoorah, I’m so glad you feel he is well cared for, it goes an enormous way to feeling that you can carry on when you know that they are being looked after when you are not there. There are always moments in any relationship that are hard to forget, mine would be when I was pregnant with my second and turned into a psycho, I punched N in the arm I was so angry, we both put this down to raging hormones and decided we would stop at 2! I suppose what I’m trying to say is those moments are often caused by something extraordinary, which is perhaps easier to live with than if they weren’t.
I hope today has been peaceful for you both. Love and hugs to you both.xx


Phil,
Thank you, I hadn’t really thought about it like that, I try very hard to support N but I can’t always know how he is really feeling or what he is actually thinking, I try to offer openings so he can tell me to “go home” or “stay the night” and when I think he doesn’t want to tell me but does really need to (if you know what I mean) I act all strong and capable and encourage him to share it so he doesn’t feel the weight of it on his own. Then when I go, I cry, a lot.
I read your profile, I get the needing to know, when you’re feeling uncertain and the worry is getting to you it can be so hard to get on with anything else. Best wishes and hugs too.xx

User
Posted 15 Mar 2019 at 21:45
A pretty rotten day for N, chronic nausea and tiredness. A combination of very low sodium and very strong anti nausea meds means he's confused and "out of it". I'm half expecting a phone call to go back to the hospice he seems so poorly. I didn't know whether to stay or come home, torn between our daughter and him. I know they'll call me but I just want to be sitting there.

I'm struggling today, I suppose because he has deteriorated again so quickly, from playing cards last week to not knowing what he's saying or doing today. It's like the third or fourth run at grieving the loss of "him" and I'm not sure he'll come back again this time.

To add to this stress a doctor asked to talk to me earlier, I thought about N's rapid deterioration but instead it was to say that it had been noted that I was doing most of N's personal care and that I was at the hospice a lot, I don't know if it was meant to come across as a negative or if that is just how I've taken it but I feel judged. I thought I was looking after him in the only way I can now but now I feel uncomfortable because they are taking notice of this. Then I wondered if perhaps N had said something yesterday or whenever and would like me to stop doing this, he was in no fit state to ask today but I'd stop if he wanted me to.

I'm too embarrassed to ask the staff if he did. I feel a fool, my previous post saying all the things I could still do to show him I cared and this evening I'm not sure whether to pour him another glass of water or not or to check if he's been to the toilet before I left.

I'm tied up in a knot of anxiety over ringing to see how he is, going back or going early tomorrow or just going at 9am like I have been.

User
Posted 15 Mar 2019 at 22:10

Dear Kentish,

I honestly dont know where you find the strength to carry on. I’m so sorry N is having a bad day, I’m praying he rallies after a good sleep. I’m sure its just out of concern for you the staff are mentioning the amount of help youre providing, and who wouldn’t help their loved one as much as possible. I think of you every day, and the struggles you and N are enduring, my heart breaks for you. I am so happy to read when you guys have had a ’quiet day” I’m praying you have many more.

Michaela xx

User
Posted 15 Mar 2019 at 23:19
You do whatever you think is best, he is your man not theirs. You are a 🌟.
User
Posted 15 Mar 2019 at 23:49

Kentish

Is there one of the staff who you get on really well with, could you discuss with them what has been said. 

Thanks Chris

User
Posted 16 Mar 2019 at 00:21

Oh my dear Kentish,

A deteriorating day is hard enough, isn't it.  Please don't feel they are judging you.  You need to do what feels right for you and N.  My instinct tells me that if a nurse or a social worker had spoken to you that the message might have been different.  A friend who was a nurse for many years had such a conversation with me the other day - but expressed as concern that I was close to burning out, and that I was going to need strength to get over this trauma. And that one way to do that was for other people to take some of the load.  I'll need the strength for me, but you'll need the strength for the kids too.

I hope tomorrow is a better day.

For us a quieter one - H was unsettled and hit out yesterday when they washed him, the one morning when I wasn't here. But the feeling is that his pain had increased.  An increase in the meds, and he was comfortable this morning, when I was pleased that I got here in time for the wash.  But sleeping all the time now.  As you said the other day, I don't want to imagine the life without him, but nor do I want to extend his suffering.  So, so hard.  And yes, it seems every step is another grieving one.

I hope you get some sleep.  I had a better night last night, and feel better for it today.

Sending the usual buckets of love.

User
Posted 16 Mar 2019 at 02:26

Originally Posted by: Online Community Member

To add to this stress a doctor asked to talk to me earlier, I thought about N's rapid deterioration but instead it was to say that it had been noted that I was doing most of N's personal care and that I was at the hospice a lot, I don't know if it was meant to come across as a negative or if that is just how I've taken it but I feel judged. I thought I was looking after him in the only way I can now but now I feel uncomfortable because they are taking notice of this. Then I wondered if perhaps N had said something yesterday or whenever and would like me to stop doing this, he was in no fit state to ask today but I'd stop if he wanted me to.
I'm too embarrassed to ask the staff if he did. I feel a fool,  

 

You are not a fool and you are not being judged. I am sure you know that N does not want you to stop doing these things for him. However, the staff at the hospice see these terrible times unfolding before their eyes day in and day out - some families arrange for hospice care precisely because they don't want to do the things you are doing so perhaps the doctor just wanted to be sure that you are caring for N's personal needs because you want to and not because you feel obliged. We often say on here 'don't forget to care for yourself' - who cares for the carer and who will pick up the pieces if you crumble? It is part of the hospice staff's job to care for you as well, and perhaps to make sure that when the time comes you feel able to just sit and be peaceful with him. 

I have been in that space a number of times and the one thing I have learnt is that if you do what feels right, you are in a better place in the weeks, months and years after because you have nothing to look back and regret or replay and over-analyse. The staff at the hospice have a great insight into how most people cope with the unbearable and they will undoubtedly have seen people collapse with the strain of grief but you will not be the only partner they have ever come across who coped by doing what feels right. I think I have told you before that I stole my mum from a hospice because my instincts told me that I could care for her better in my own way - others were shocked and the hospice staff were concerned but I have never regretted it for a second. 

Be brave and sure footed x 

"Life can only be understood backwards; but it must be lived forwards." Soren Kierkegaard

User
Posted 16 Mar 2019 at 07:53
As said above,

YOU need to make sure YOU care for YOU in all of this. You sound exhausted and confused, all signs of stress.

It is natural to want to do all you can, and everything they need, for a loved one. But, please don't get to your breaking point.

Could you speak to someone, to see what support you could get to enable you to carry on giving the care you have been?

What you're doing is incredible.

atb

dave

All we can do - is do all that we can.

So, do all you can to help yourself, then make the best of your time. :-)

I am the statistic.

User
Posted 16 Mar 2019 at 08:28
Thank you for all the replies, lots of sound advice. After a night spent waking almost every hour I'm just going back, I am tired but not exhausted and today I don't feel any happier about the conversation than last night.

I thought that the staff at the hospice "got me" I've said before that I've felt nurses, doctors etc have not understood where I am coming from and that "matter of fact" is my usual go to. A straight answer is very difficult to give with cancer but as near to is better than the unknown.

I wonder if this is taken for "denial", being pragmatic and not showing masses of emotion about changing N and doing the personal care. I just choose to cry at home, in the car, by myself. On the days where N goes to the loo 12-15 times, if i didnt clean him then I wouldn't see him. No sooner is he cleaned than he goes again. I would spend the day sitting in the corridor waiting to go back in, and then for example the last 2 days he hasn't been so I've just sat with him and reassured him when he comes to.

There are so many reasons for staying at the hospice all day, being there for the lucid moments, calling the kids to come at the best times and these outweigh the hours spent sitting, though I've done some sewing, birthday cake icing and lots of crosswords while I'm there. But I think I'm most upset at feeling I have to explain this, justify it. I watch the other wives go home after an hour or visit for a couple of hours in the evenings, they are in their 70's/80's, none of them physically able to do any personal care for their husbands. N and me and our family cannot be grouped with them.

I will just carry on this morning but I don't feel connected there now. Trust is a very fragile thing especially when there's a lot of stress. I felt confident that i was doing what is right for us all and now I don't.

Hoping N has had a restful night.

User
Posted 16 Mar 2019 at 09:22

My heart breaks for you reading this. It’s such a horrific time that frightens me to the core. I worked as a HCA in a nursing home for a year not long back. I nursed many men and women who were at end of life , including one end-stage PCa man who was 70. I think you are amazing and should carry on how you see fit , however I would add that at my home we didn’t like relatives doing too much care , mainly because of the paperwork ie knowing he is turned correctly re pressure sores , monitoring food and fluid intake etc. We did have one wife that was always in , and it did cause some issues , but we learnt to work round it with some boundaries. I know I don’t know you but I’m sending an enormous warm cuddle full of support and respect and strength xx

Edited by member 16 Mar 2019 at 13:25  | Reason: Not specified

User
Posted 16 Mar 2019 at 18:55

I had wondered that too Chris, they aren't monitoring food and fluid, no one checks he's restricted it except for him and me, they aren't measuring urine output and he's classed as "independent" regarding turning as he can move himself around the bed and readjusts himself regularly anyway. There is a poo chart to list when and what type/size and as they change him after I've gone and in the mornings they inspect for pressure sores at that point according to the charts at the end of his bed.
I wondered if I have been doing it wrong, not keeping him clean enough or putting enough barrier cream on, and when he's washing/being washed, not doing it the right way.
I don't know, I just know I feel like I am out of place, unsure of what to do and say, whereas before I felt comfortable in my role as his listener, caregiver, wife.

Country boy,  I didn't feel confused or close to breaking point until doubt crept in,  although yesterday was horrible it was bearable and I thought I was coping well enough. Perhaps I'm not. Second guessing myself is a bad place to be, not helpful in anyway and a useless mindset to have right now when N and the kids look to me for strength and support. Now I feel like those staff I looked to for support are doubting me and if they doubt me then am I doing what's right?

N was still very tired today but not sick so I asked him carefully if he wanted me to carry on cleaning him or if he'd rather the staff did it. He was adamant he would rather I do it as a general rule but understood that when the whole bed needing changing this morning and I asked him to bleep the staff to do it as they are much quicker and have the stuff for cleaning the bed too.
A friend came to visit and I offloaded this and asked what she thought, she thought that perhaps my age and willingness to get stuck in had thrown them and they weren't sure where the place for that is. I'm guessing home but that's not an option at the moment.
I don't want to be that "wife" who gets in the way and I suppose that's how I feel too. So I took a cue from the other wives and walked away when the meds came round, the flushes were done and when they changed the bed this morning. It didn't feel right and I probably won't do it again as N couldn't remember if he'd had a flush and asked me to get the nurse to come and do one. (She already had).
Regardless of this, if "this" even exists, I'm probably being over sensitive, N had a better day and both kids spent a couple of hours each with us in between working and their social lives. We played a game of rummy, albeit at a very slow pace for N, if the sodium doesn't improve then neither will his cognitive condition so another adjustment for the kids to make but easier than the horrible vomity situation of yesterday. Got to find that ray of sunshine in these dark skies.....

 

Edited by member 16 Mar 2019 at 20:09  | Reason: Not specified

User
Posted 16 Mar 2019 at 20:56
Thinking of you and hoping you will feel confident that you are giving N all the comfort he wants and that you do whatever feels right to you and to him.

I sat with my Mum when she was at the end of her life and I regret that I let the nurses do some of the things that I know she would have liked me to do but this was the nhs hospital not a hospice and relations were not expected to do much although when she was ill I did help her with her food and also others on the ward because they were often left to fend for themselves after having strokes etc due to there being too few staff to give them time.

I hope that if we reach this stage that we will be able to look after each other to the best of our ability and that we will be allowed to do it.

I am sure that you will work it out in your own way and that perhaps you could talk to one of the staff to check out what was meant by the comment. When we are under pressure and coping with things that are so difficult, we become extra sensitive to comments of others, which might not be meant in a negative way. They will be concerned for you too and aware of the strain on the whole family.

User
Posted 16 Mar 2019 at 22:09

Kentish

i think the person who spoke to you would be mortified if they thought they had caused so much stress, my thought is that they were giving you a way out in case you thought you had to do it. I’m pretty sure i wouldnt want to do it, but I can’t be sure unless and until the time comes. i think being in the hospice is meant to be a time for you both to be husband and wife and mum and dad, not nurse and patient, and they maybe thought you felt obliged. How long you stay there is your call i think, our local hospice has family accommodation to help with that situation. When John has been in hospital, I’ve stayed every minute i was allowed unless he needed a break or I did. I do think if this was me i’d have to ask them outright as I would feel uncomfortable. That is not what a hospice is for.

I think they think you need a break, but if so, why not just say so? Mostly they are usually just plain speaking aren't they.   

Bless you, you didn't need this worry on top of all of this. 

Big hugs from me today.

With love

Devonmaid xxxx

User
Posted 16 Mar 2019 at 22:33

I'm sure they probably did mean well but I can't shake the feeling of doubt. I thought I was doing good job of wifeing, and trying hard to be mum too and this has made me doubt that.  Just because I think I'm doing alright doesn't mean that's how others see it and they obviously don't otherwise nothing would have been said in the first place. Drawing attention to something I thought was a positive and questioning it makes it feel less so.

I can't change that it has been brought up, I think I might just sulk for a day or 2 more and then I'll probably get over it and carry on as before. I can hear how irrational and paranoid I sound, this is obviously a weak spot in my armour that I didn't know I had, thank you everyone for your kind words.xxxx

User
Posted 16 Mar 2019 at 23:02

Kentish, never doubt for a minute that you are doing the most excellent job of wifeing and mothering.  We each do it in our own way, and your way is right for your family. I hope they aren't judging you, but are badly expressing concern.

You aren't sounding paranoid, but just like me you are sounding tired after months and years of worry.  And we second guess everything we do, wondering if every step has been right.

Peaceful here, sitting with H, who can no longer respond to me.  Glad we came back in to familiar surroundings and staff.  His own room and music playing.

Sending love, and wishes for a better night's sleep.

User
Posted 17 Mar 2019 at 09:59

Teacups, 

My heart goes out to you, you sound so calm even though we know what must be going on under the surface. Please remember that we are with you in spirit and hoping for peace for you both. Hugs.

Kentish

I get what you are saying, it would leave me feeling discombobulated too, I think it's a shame that they have made you feel this way and I think they deserve to know as I really can't believe that was the intention. Why not give them a chance to explain what was meant? I know me, I would feel so upset I'd be seething underneath and questioning everything, not something you should be expending energy on at the moment, its so unfair. On the other hand I'm not good at holding grudges either, sounds like you are similar.

I hope you have had some rest overnight, and N has had a comfortable night (just about the best we can ask for isn't it?). I hope the children are ok, 

I wish I could convey how much I feel for you all

with love

Devonmaid xxxxxx

User
Posted 17 Mar 2019 at 23:08

Thank you Devonmaid, you do understand, I know.  And you do convey it. Calm on the outside, but even that is a very very thin veneer now.  Had to warn those outside the tight immediate inner circle yesterday, so a tough day.

I've been in here for a while this morning.  Still peaceful, and I'm running Jerusalem, Land of Hope and Glory and now some welsh hymns through our little speaker.  So all is as good as it can be in these terrible times.

Kentish - love to you.  I hope today has been OK.

Edited by member 17 Mar 2019 at 23:59  | Reason: Not specified

User
Posted 17 Mar 2019 at 23:17
You are on my mind, Teacups
"Life can only be understood backwards; but it must be lived forwards." Soren Kierkegaard

User
Posted 18 Mar 2019 at 09:09

Teacups

That thin veneeer, oh I know it. I’m living some kind of ”normal” life again at the moment, thanks to the Enza, but I find myself sounding off on social media about things that annoy me (the horrible B word, local politics etc) and I have had to remove myself from some groups because I'm becoming that person, so opinionated! It's a release i know but not really fair. I'm off on my annual jaunt to Portugal this week, a week in the mountains with the childless daughter, who works for Honda (bad news story, made me furious), no food or booze, just fresh juice, yoga, walks in the mountains, fresh air, freezing lake swims, Jacuzzi and like minded people. I tend to come back utterly renewed, 10 Lbs lighter and looking and feeling ten years younger. I booked it six months ago neve thinking i would be able to go, but I am. I will be able (just about) to catch uo from the mountains.

Kentish,

Hoping you had a reasonable night and that N is feeling a bit better today. much love coming your way both.

I wish you could join me in the mountains of Portugal, a healing retreat for the body and soul. Off to oncology today.

with love always

Devonmaid xxx 

User
Posted 18 Mar 2019 at 11:10

Lyn - thank you.  And Devonmaid - parts of your retreat sound absolutely wonderful (note that I said parts!).  And yes, it would be lovely if we could all go.  But it is so good that you can go.  Hope you do come back refreshed and renewed.

 
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