Secondary Liver cancer

FormerMember
FormerMember
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Hi

Ive been reading through all these amazing posts and felt great hope, sadness and support. Thought I’d put out my feelings regarding my mums situation because partly I’m still in denial about her cancer and secondly I just don’t know where else to ask these questions.

So my mum was diagnosed with stage 3 lung cancer at Christmas, it was in operable but she completed chemotherapy and the tumour hugely reduced in size, she also received some radiotherapy treatment for some lymph nodes around her throat!

fast forward 8 months we have just come back from a lovely family holiday where she was great, still tired but looking well. This is something we thought we’d never do again 8 months ago so a real boost in confidence.

Yesterday she had her consultation with oncologist and scan review and it appears she now has 3 small tumours on her liver. He was as shocked as were we! Apparently he wasn’t very good at explaining things and due to the shock my mum probably didn’t ask all the questions I would have done but here goes...

Removal of these tumours was not discussed? Just treatment- she is to start immunotherapy treatment once she has had bloods done, is this common? 

She mentioned a pain down her side and in her elbow? He brushed that off as unrelated and just said see her GP and take ibuprofen. 

I suppose I’m just in panic mode and would like to hear from anyone with any words of wisdom, I live 1,5 hours away from my mum and have 3 small children at home. I want to be here with her all the time but realistically that’s not possible.

whats the best way to offer support? I know every patient is different but  right now I’m finding it difficult and battling with the thoughts that the end could be near and fighting talk!!!! I can see in her eyes she thinks this is it!!!! It’s heart breaking!!!!

Thanks in advance if you have taken the time to read this waffled post! X

  • FormerMember
    FormerMember

    Hi NGoode, 

    Sorry to see your post, I know how confusing and scary everything must feel at the moment.

    My situation is that my mum was diagnosed with secondary liver cancer back in May this year, it was picked up on her final follow up scan almost four years after her primary cancer had been removed. 

    I'm no expert I'm afraid but have asked a lot of the same questions you're asking, so here goes.

    First question on surgery, with secondary liver cancer removing the tumours surgically is not possible apart from in a very small minority of cases (I think if the primary is bowel cancer then sometimes it can be removed). Immunotherapy to control the cancer is a fairly common treatment, it wasn't an option in my mum's case (chemo only) so I don't know anything about treatment etc.

    Pain in the elbow - I've not heard of that with liver cancer before, it can bizarrely cause shoulder pain, although pain in the right side could be a symptom of the liver.

    With questions for oncologists I find it helps to write down questions before I go, and take a notepad and write down the answers. If not I find everything just becomes a blur after you've left. Also, has your mum's hospital got Macmillan nurses? If so, ask to be put in contact with them as my mum and I both find they are fantastic at dealing with questions and worries, and are really good at translating doctors' comments into a more understandable form of English! 

    I know it's hard not to panic over your situation, and all I can advise to take each day as it comes. Everybody's story is a little bit different, but everyone on here can relate to what you're going through so feel free to rant and rave on here. Personally I've found it a great help at times.

    I know the distance between you and your mum makes things even more difficult (my mum is a four hour drive away from me), but all you can do is be there whenever you can. The hospital will have a lot of support available, helplines etc, all I can suggest is that you use everything they offer. Don't feel like you're being a pain or bothering them, it's their job to be there and they genuinely want to help. 

    My mum is currently halfway through her 6 cycles of chemo, and it's been a bumpy ride so far, but to look at her you wouldn't think she was ill at all. We won't know whether the chemo is working for another 9 weeks yet, so it's one day at a time till then.

    Take care

    C

  • FormerMember
    FormerMember in reply to FormerMember

    Thanks very much for your kind words and advice. I’ve reconnected with her palative care nurse which has eased the worry and reinstated support for my mum which is a relief. 

    Good luck on your journey too! Much love xxx

  • FormerMember
    FormerMember in reply to FormerMember

    Hi

    That's good to hear. This place is a good place to offload so if things get tough then just remember that everyone here is more or less in the same boat.

    Take care