Stage 4 - husband not supporting me the way I need

Hello all 

Well I'm up at 4 a.m. as couldn't sleep, started to cry with my sadness at the situation between me and my husband of 25 years. I was diagnosed stage 4 in November 2019. Spread to various organs. Have been on immunotherapy treatment since then which is keeping things stable so far but my kind of cancer does not have a long prognosis. Living between 3 monthly scans. We are both late 50s and have 3 children youngest is 17.

Obviously I have been and still am devastated about the cancer itself and that I probably won't make it to 60, leaving my children way too soon etc. But I now have a second source of pain which is my husband's response. To start with at stage 4 I had lots of pain, was in shock and bedridden, constantly going to hospital, he was very helpful and 100% there for me. But since things have improved physically now I'm on treatment and I don't have pain, I'm fairly active again, look like I'm 'ok', we have very different ideas on how he can support me. My emotional needs are huge but he doesn't seem to get it. I do my best to get plenty of other support, I have a counsellor twice a week, I talk to other friends regularly (obviously with lockdown it's harder to access but I do my best) so I'm not only relying on him. But his view is that he will support me 'when it suits him'. He 'has to draw a line, other things are also important to him, he needs choice' etc.

He will help me by getting me drinks or doing practical things at times, or will do an activity with me if it's something he enjoys (hard to find these things). But he mainly spends his time on political campaigning, he has found a new obsession since my illness which he thinks is incredibly important. (He took early retirement a couple of years ago).

We have talked about it endlessly, I feel like I spent most of last year trying to get him to understand, begging for more support but to little avail. When I read on here last night the accounts from people's partners of their dedication to making the last part of their partners life as good as possible, I was in tears wishing so much that my husband would be feeling the same. He used to adore me so I thought, where has that gone now I really need him by my side? I feel more like I am single now.

I would love to hear from anyone who can relate to this - whether you are the person with cancer or the family member or partner - or suggest anything that could help. No questions about my actual cancer please it's the emotional issues that are my reason for being on here atm.

Thanks for reading if you got this far.

Tess.

 

 

 

  • Hi Tess and hello to our lovely forum.  So I've been posting daily since 2017 when my husband was diagnosed stage 4 lung, now liver, trust me its been a roller-coaster of feelings, some days I felt like a nurse, provider of support and all I could see was that cancer had taken our retirement from us, so you begin to get angry about what could have been.  He would get nasty, look at me as though he hated I was well and he wasn't.  But he's also on immunotherapy now and the last ten months have been more pleasant despite the lockdown.  So what to do?  Men do not have the coping gene that we do, they seem to not want to discuss the issues that are important to us and it becomes a vicious circle.  He's not giving you what you want but he is probably scared and worried also, you sometimes distance yourself from the incurable partner as you k ow, just know that you will be left to cope on your own, left with the family, the life you thought was secure is no longer there, you start being busy to keep sane, anything to not think of the future without the love of your life.  He does adore you, as does mine me, he tells me so, but he is struggling to cope as well.  Give him space,, you talk about living between scans, yes we do that as do many others, he doesn't want his life planned out in three monthly pieces, he wants today, not three months time.  I truly know how you are feeling as I see it in my husband's face, he also will not be able to see our family grow up but we live for today and make the best of that.  If you want to a lot of friends have been made on my page Dor06, those who have lost loved ones, those coping with cancer, so join us if you wish or message privately as you can say more and no one but me will know!!  Take care Tess and I'm sure others will pop by and give their thoughts as well.  Hugs your way, love Carol 

  • I hop your hubby gets better 

  • Hi Tess 

    Can understand about you and your husband, I've been on palative care since 2016 and looking after my darling wife she has Alzheimer's and Parkinson's sometimes she's ok others she's cursing at me because she's scared I'll go first and leave her .

    Hope things go ok for you because nothing is easy with this virus.

    Take care and keep positive.

    Billy

  • Thanks I appreciate your care.
  • Thanks Billy. What a tough situation. Staying positive is a good idea and I try but it is hard sometimes (a lot of the time of I'm honest). 

    Take care

    Tess

     

     

     

  • Hi Carol thanks so much. I wrote a long reply to your message which seems to have disappeared which is very annoying, do you know where it might have gone? Anyway i just read quite a bit of your blog which is very touching and got really useful perspectives in it. Take care.

  • Hi Tess, we often write replies that fly off into cyber space, what I do now is push post now half way through to save it then you can edit it and add more.  Thanks for reading my blog it's therapy to write it all down because keeping it in your head drives you bonkers.  Please write again if you feel lost, ignored, fed up and unappreciated, it's a hard time for you and your family.  Here if you need me.  Carol x 

  • Very helpful tip thanks, all the best x