Metastatic Prostate cancer and heart failure

  • 4 replies
  • 29 subscribers
  • 96 views

Hi, 

I haven’t written anything for a while because I really don’t know where to begin. Tonight I just need to vent my thoughts and feelings. My husband was diagnosed with metastatic prostate cancer just over a year ago. It has spread to his spinal cord and in spite of having radiotherapy he is still unable to stand or to walk. A few months ago he developed an infection which resulted in a six week stay in hospital where doctors battled to keep him alive. He is back home now. Doctors have told me he might survive three or four months or maybe another year depending on his ability to resist another infection. The prostate cancer is less of a worry than the heart failure. The heart failure causes fluid retention and builds up in his chest making breathing difficult. 
my husband has never accepted his diagnosis and being admitted to hospital when seriously ill, he has little knowledge or recognition of how unwell he actually is. He is understandably frustrated at being bed bound. Physiotherapists are working with him at home to see if he will be able to stand up again, 

needless to say life is difficult for us both. We have carers coming in but recently they seem so concerned about the way they are being treated by the care agency,m they pay little attention to my husband’s care needs. The agency came highly recommended and were great at first but since their return after my husband’s last hospital stay, they seem to have gone downhill. Lots of carers who my husband trusted have resigned and the registered manager never replies to my emails and phone messages. 
I am feeling lost and alone. Medication is keeping my husband alive and his quality of life is not being improved by it. I think medical science has gone too far in keeping people alive when they have no quality of life. My husband lays in bed waiting for me or carers to move him, put him on the bed pan, empty the catheter etc., there is no joy in life for him. I have to cut up hi food so he doesn’t spill it all over himself trying to eat laying in bed. He has about eight pillows to support him but still isn’t able to sit up to eat. 
Where is all this leading to? How long does my husband have to tolerate this kind of life and how can I help him to get enjoyment out of this situation when can barely cope. 

  • I just wanted to send you some gentle love and hugs. In terms of keeping things enjoyable, does he have much contact with friends? I know he may not want people to see him this way but maybe some trusted close friends to have some ‘boy’ time. A cuppa and a chat about anything and everything. At times like this friends and family mean the world. 
    what about a movie afternoon? I know it sounds really silly but although my situation is not the same but I have to think outside the box. Things we enjoyed doing we still do but abit differently. Quiz nights in bed of an evening with people on teams, movies afternoons with soft food you don’t have to worry about eating. 

    people sometimes think grand gestures to make things easier but for my partner is the normal things he misses 

  • Hi Teatowel,.

    I've read your post and your profile. 

    All I can offer is empathy to reinforce your own amazing strength. Even if you don't believe that you are strong. 

    My husband started 2nd time around for Mets chemo at the start of the month. Not going well. 

    I can only wish you respite from pain and hope for peace. 

  • Hi Sierraoscar, 

    I am sorry you are going through all this stuff. Thank you for your reply and you kind words. It means so much to me. My husband’s oncologist has told us my husband isn’t suitable for chemo. His immune system is compromised enough without chemo. My husband wants surgery to fix him….he is unlikely to survive the anaesthetic let alone the surgery. We have a particularly difficult few days but I am hoping he is through the worst of it for a while. He is watching football on tv now…rubbish is all I can say! 
    we will keep plodding on and try to live one day at a time. 
    I hope things improve for your husband. Do keep in touch. HuggingHeart

  • Hi Exhausted and frightened , 

    thank you for your help suggestions. My husband is in a hospital bed, an air flow bed,in our living room. I sit in an arm chair next to him. We do quizzes, watch game shows on TV and join in. I try to remind him of the importance of the day to day stuff of life but he gets so frustrated it is hard to know what to suggest. I have bought him books, drawing materials, arts and craft stuff but he has lost interest. Our friends are busy…run for the hills. I have asked our local hospice if they can find a male companion to visit but no luck so far. My husband is focusing on being able to get back into his power chair…then it will be the next thing. 
    I hope things are ok for you and your partner. Thank you for the hugs…sending hugs back to you. xxx