Caring and it’s impact on other relationships

FormerMember
FormerMember
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My dad has small cell lung cancer which was diagnosed in Jan this year. He has now finished all the treatment available to him and at the last consultant appointment 3 weeks ago he was given weeks left to live. He is single and lives alone. I am his only daughter. I have supported him all the way with going to every appointment with him, being there during his chemo and staying at his on an off when I’ve needed to. I’ve managed this around working full time and also studying.

as he is now on palliative care I have come to stay with him to care for him. I am currently off sick from work due to the emotional impact of supporting him through this stage of his illness. I have paused my studies and I am living away from my partner (and Catt). I had only been with my partner 6 months when my dad got the diagnosis. I moved in with my partner around that time. we have now been together just over a year. Therefore 6 months of that year I have been in the worst state of my life going through this ‘living grief’ and now I am away from him and all my other life’s responsibilities whilst I care for my dad. I know he thinks I should leave this to ‘carers’. It’s hard to explain to him how little carers/nurses can provide and also how important it is for me to be with my dad at this time.

How do people carry on with their lives whilst caring for a loved one? Is it possible to continue relationships when your whole world has fallen apart? I’m happy to put my life on pause to care for my dad but I cannot expect my partner to wait too. I feel very lost.

  • Hi

    Sorry to hear about your father and the impact that is having on your live and that of others you care for. You are right of course that what professional care can do for your dad tends to be quite limited, from what I hear typically 4 visits a day is maximum above which people are generally pointed towards either assisted living or a care home.

    Has your dad had a needs assessment from the local authority and you a carers assesment? These can be very helpful in getting someone to look at the care needs in a systematic way and can often highlight support that might be available to you. It might help to look at our publication getting support as a carer.

    <<hugs>>

    Steve

    Community Champion Badge

  • FormerMember
    FormerMember in reply to src60

    Thank you for your reply Steve. I’ve been relying on the palliative care nurses to tell me what we need and when. I hadn’t thought of a needs assessment. We have just started having district nurses done in every other day but more just for a general reassurance and questions at the moment rather than much physical care. I am guessing they are trying to get to know my dad so they know him more when the they will need to care for him more.

  • Hi,As Steve has said a needs and carers assessment can be helpful.My situation was different as I was the person with cancer.I was caring full time for my elderly mother who was disabled after a brain haemorrhage.I managed to get assessments for us both and Mum was eligible for extra help.She is now in a nursing home with end stage dementia.It is difficult regarding relationships.I had been with my partner a couple of years when mum became ill in 2004.Despite lurching from one crisis to another we are still together.Even if we are unable to meet up we keep in touch everyday by text or phone.You are there for your dad and that is so important.Love and best wishes Jane xxx

  • FormerMember
    FormerMember in reply to winkers60

    Thank you Jane.

    Just an update my dad moved into a hospice now. I am still devoting all my time to be with him as thankfully I can stay here too but it is huge relief to know there is also a team of others caring for him. 

    Thankfully my partner is being a bit more understanding about my need to be with my dad at this time.

  • It must be a comfort to know you can stay with your dad at the hospice.I’m thinking of you both.Love Jane x