Hello, my husband (35 years old) has been fighting a rare bladder cancer for the past 5 years and in August this year we were told it had spread to rapidly and he had days to weeks to live. He had been on an experimental targeted gene treatment and we really thought it would work, we had so much hope. We were told separately, my husband on his own, while I joined on the phone at work. It was devastating. I didn’t know what to do with myself, I’d always promised him it would be ok and it wasn’t going to be. Since that day we’ve not heard from his oncologist (we had a relationship with her for the whole 5 years) after she passed us on to the hospice. I feel really angry about that. I feel abandoned and as it was only her and myself who supported Dan through this I feel like I’m the only one with the knowledge of what we really went through and what medications he can handle.
It’s now the end of October and my husband is still here. He was doing so well, but now his stomach is protruding, with a swollen liver and a tummy filled with fluid. He’s a deep yellow with jaundice and won’t stop itching, with little cuts from his nails all over him.
I’ve been trying to work out how long we have, I feel like this is going to go on for ever and it breaks my heart everyday seeing my love shrink and become someone I don’t really recognise. He seems to have no real interest in interacting, so I feel so lonely.
I have read about the dying process over and over again and it says the first thing to shut down is the digestive system and he will stop eating, but he is eating HUGE amounts and I worry that might harm his already very bloated stomach. Why is this so hard and why can’t I find any information about others who have died from secondary liver cancer and what to expect. The hospice nurse and GP don’t really know what’s going on.
Even writing this made me feel a lot better, I feel I can’t share with anyone.
Thank you for listening to me and I wish you and your loved ones peace x
Hi. Your post really resonated with me. Yesterday my brother who is 55 was told no more treatment. After chemo, radiotherapy and immunotherapy, we go for scan results and that’s it!
The consultant was so matter of fact that I had to ask twice what he actually meant.
Pain and comfort management is the only road for him.
I feel like I have lost it. I’m wandering around, I feel guilty for even thinking about what to make for dinner as he isn’t even able to eat.
Like your Dan, Richard is almost unrecognisable from the vibrant, corny joke telling man I knew. Everyone else seems so strong and I’m a mess.
So now we wait. How long no one knows. You get told, that’s it, the cancer has won this unfair battle that he fought so hard only for cancer to up its game and make a dirty stab in the back when he took a moment to rest.
I can honestly say I would rather have been told he had died in a car accident yesterday than this. Yes, it would have been so incredibly sad but for him, a quick end.
The reality now is, pain and comfort management, while every day we all wonder, is it going to be today.
My parents are in their 70’s and it’s killing my Mum but she plays the factual ex nurse who isn’t going to show her emotions in front of anyone. Me on the other hand am like a hose pipe full of holes that someone periodically turns on the water to to watch the tear and sorrow parade.
In short I guess if I’m asking one question it is this, what the hell do we do while we wait.
I’m so so sorry to hear this. it’s the same with Dans parents, they are in their 70s and I try to do most of the caring because it will take it out of them. It gets so tiring.
I hope that you are able to take some time out for yourself during all this, do you have hospice help? I’m getting counselling and massage therapy (haven’t had that part yet) I find the talking to someone completely out of the picture is really good, hard at times but sometimes you really just want to download.
It sounds like Dan and Richard would get on well . I really hope that he is as ok as he can be and I’m sending you all strength. I feel like some people take most of the weight of the grief so other people don’t have to, I think maybe you and I are doing a bit of that.
If ever you just need to chat or vent please do message me on here.
x
Hi, I too am in a very similar situation and am new to these forums.
My husband has just turned 49 and has been diagnosed with terminal secondary liver cancer after starting to feel unwell only a couple of months ago. No other warning signs or anything. Similarly, my husband was told his prognosis while he was on his own and he in turn then had to tell me.
In the space of 2 months our whole world has turned upside down and he is now in hospice care on pain management.
Surgery was out of question due to where the tumour was on his liver and his general health took a massive downside as a result of the cancer, massive fatigue, shortness of breath so he wasn’t suitable for chemo. He decided he wanted quality over quantity. He is basically bed bound due to the fatigue, weakness in his legs and the massive water retention that he has.
We have lots of family and friends who are supporting and visiting but I too sometimes feel like I’m playing a waiting game. I’ve spent the last 3 weeks with him, 2 in the hospital and 1 so far in the hospice as he understandably doesn’t want to be in his own. We have been given a time frame of high weeks but in reality nothing can ever be exact.
I am also dreading what comes after, we have no children so it will just be me. Don’t get me wrong, I have sisters and friends that are and will be looking out for me but they’ll never be my husband.
Thinking of you and sending you strength x
Thank you so much for sharing your story. I’m so sorry for the diagnosis, it’s so hard to get your head around it, especially as your husband had no symptoms. We’re caring for my husband at home with my in-laws (which is also a challenge) and sometimes I wish he was in the hospice so I knew he was being given the best care possible, I try to do everything I can, but I’m so tired.
I really hope your time together will hold some happy special moments. Always here if you need to talk.
Wishing you both peace during this time xxx
we are in the process of telling his friends and family at the moment which is tiring in itself.
some people seem to think there is a miracle on its way ‘ you never know’
it’s hard to get across the ending of the treatment is because it’s not working.
I think my brother and his wife are having ‘ the ‘ conversation today about how, when and where.
I understand how you are both feeling
Hi my partner is 55 and we was on holiday in August. A few days after we came back he started to feel really tired and off balance. Straight to docs who sent him for mri which confirmed inoperable brain cancer Glioblastoma grade 4. We were given a prognosis of 12/18 over the phone. We was devastated. Our whole world turned upside down. We visited Guys cancer centre and they then told us to look more like next 2/3 months I couldn’t even get my head around 12/18 months let alone 2/3. He had lost feeling in his left side and was in a wheelchair by this time. Then few days later he had a bad seizure where I had to give him cpr. Docs said next 24 hours were crucial. I was heartbroken I sat by his bed all night and then in the morning he woke and said any chance of a cup of tea !!! I couldn’t believe it. He lost all feeling in his body coordination and was bed bound. That was 5 weeks ago. He is at home has gained feeling in his right hand so he feeds himself again and can hold his drink. He eats and drinks as normal and they are weaning him off steroids now. He also got a blood clot in his leg and I give him injections in his stomach twice a day. He has a hospital bed in the living room and I have slept on the sofa next to him since he’s been home. We don’t know how much time we have left but I appreciate everyday we have together. I think he will deteriorate but for now I count my lucky stars we are still together. I’m good one day then can’t stop crying the next thinking we had so many plans for our old age together why is life so cruel. Love to everyone who is going through this battle x
I’m so sad to hear your story, everyone of these stories are hard to hear because I feel exactly what you’re going through and it’s a really really lonely place to be. At least we all have each other and know that we’re here in the dark when you need us. Stay strong, you can do this, we are now in a hospice and it’s taken a lot of the caring stress so I can just spend time with my Dan. Xxx
It’s so hard because he’s eating and drinking even though he’s bedbound and it’s just the not knowing what’s gonna come next he hasn’t been able to have any type of surgery or radiotherapy as they dn’t think he will tolerate it.
I just wanted to say your resilience, stoicism and grateful attitude are astounding. This all sounds so incredibly difficult, particularly given the speed from initial symptoms to diagnosis and prognosis. So I just wanted to say you sound incredible, that I hope you get all the support you need, and that you and your partner are in my thoughts x
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