Living with grief

FormerMember
FormerMember
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I lost my husband 5months ago to lung cancer I feel like you go through loosing them twice because cancer takes so much away from before anything happens .I was with my husband from The age of 16 dealing with this is extremely hard people around you try to understand but they dont really and there is so many stages you go through with grief as well.

  • Hello, I understand completely. I couldn't cuddle Ken or get a hug for months before he passed. It wasn't his fault, and of course the daily life you used to have changes and shrinks as the illness progresses. The feeling of loss started for me almost upon diagnosis. I almost feel as though I have been widowed for longer than the 2 weeks I have. There is no shock, just the dull ache that sits in your belly and sucks away the colour. 

    Love is eternal
  • It's been over 6 months since my wife passed some days are just bearable most days are like walking in a nightmare it just sucks  the life out of you very hard to come to terms with it

    Ian
  • When my husband was ill and dying all our focus was on making his last days as comfortable and safe as we could. Teams of nurses, doctors, family and friends came and went. New nurses with different responsibilities took over from not quite dying to definitely dying. I did all his personal and emotional care and I would not let anyone else take this from me. What I realise from this support group is that there is little  time given to the fallout of the one person who loved their partner more than life itself. All the medicine all the drama all the tears all the making other people feel okay strips your soul down to the when will it end. When it ends you rush around with the funeral and then nothing. Nothing and nothing for day after day, week after week, month after month. Perhaps cancer research et al could look to the left behind. 

  • Absolutely, you have described it perfectly. I have often thought it would be interesting and helpful if there was a questionnaire for us all to fill in asking about our feelings about the journey we are on. What we feel could be improved on and asking for suggestions. These could be used to help the medical profession with their care. It could also be used as guidance for others in our situation. We could also say how we feel and what we wish for from friends, family and neighbours  before and after the bereavement. I know we are all different but it could be helpful. I have  been so angry with people who appear only  to call for gossip and never really bothered before. I feel like saying if you want to come in and interrogate me then there is a £10 charge which I will donate to macmillan. Then we would see who genuinely cares. I guess I'm a bit angry, take no notice. I hope that you find your path much love Pam x

    Love is eternal
  • FormerMember
    FormerMember in reply to Needing friends

    Hi Pam, 

    I absolutely agree with you. I would only add one more thing. A guidance for workplaces as they have no idea, how to deal with bereaved people.

    I had a horrible experience from my own line manager, who said this, when my husband was in hospital

    ' You wouldn't think, how much money the NHS is wasting just by keeping people in hospital '.

    My husband died three weeks later. 

    I cannot forgive her for saying this. This was the most painful thing to hear from my own line manager. It still terribly hurts Sob

  • Dear Owl58

    I  experienced a similar situation from our McMIllan nurse associated with the local hospice plus the supporting medical nurse who made home visits before Anne was hospitalised. (  Anne unfortunatly never got into the hospice.) Our McMillan nurse couldn't do enough for us on a day to day basis whilst Anne was dying in hospital. All smiles and empathy. Then Anne suddenly passed away and  it all went dead. Not a single courtesy phone call from either of them to say they'd  heard Anne had passed and so offer condolences. I felt as if all their support had just been part of the job  - and so onto the next person.  About a month later I got a letter from the hospice offering counselling. Too late for me I'm afraid. That missing phone call would have meant everything. 

    Love and Light.

    Geoff.

    At the end of all our journeying will be to find ourselves back where we started knowing the place for the first time. TS ELIOT.

  • I had the same Macmillan nurses were brilliant my wife went into critical care she passed in there 1 and a half days later I have had nothing from the hospital from that time till now you would think something could be put in place to help the ones left behind  not just blank

    Ian
  • Dear Andrea 

    The most heartless and pragmatic people always end up in senior positions. They have absolutely no idea of people skills which personally I don't think can be taught. They get to those positions because they support the corperate ideology: profit and efficiently.

    Remember we used to have a Personel Department who dealt with people - persons?  Now it's named Human Resources. How cold and inhuman is that term?  People are just a resourse these days like a cog in a machine.

    Love and Light 

    Geoff.

    At the end of all our journeying will be to find ourselves back where we started knowing the place for the first time. TS ELIOT.

  • We feel lost, there is no script to follow, we are left without guidance. Many of us have been full time carers and that job is gone, we are left drifting. Our future is in our hands, but we don't know what to do with it. Perhaps we can help each other. 

    Love is eternal
  • Hi Needing friends,

    You have said it so well in your post: Those of us who were fulltime carers, but also those who were not fulltime carers but still always there throughout the long or sometimes not long journey through cancer, are suddenly lost now because that purpose, that task, that meaning in our lives is gone. I used to feel this a lot in the months after Paul died but also now I feel this sort of pointlessness, being-without-purposeness, from time to time. I felt it, for example, when I came back from my Christmas holidays: Here I am at home again, only having to look after myself, noone to care for, noone to help, noone whose life I can try to make better with my love and care... As you say: I am drifting, my future is in my hands, but I have no idea what to do with it. It's a feeling that sometimes causes me a feeling of panick when I go into it too much.

    Helping each other is what we do on this forum I think. But it would be lovely to meet up with others on this forum in person sometimes. If only we were living closer to one another.

    By the way: I am traveling to the UK tomorrow to do my end-of-life companion course. If any of you live in the Lewes/Brighton area, I would be very happy to meet up for a coffee or glass of wine in the evening.

    Love, Mel

    I don't like the term "moving on" because it sounds to me like we are leaving our loved ones and the life we had with them behind. I like the term "moving forward" as it implies that, while life goes on, our loved ones are still with us in our hearts and minds.