Tumor and kidney removal- in shock

FormerMember
FormerMember
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Hi, just got back from the hospital- got my CT Scan result- really large tumor so they will be removing kidney in next 3 weeks. Told highly likely cancer, 90% chance as its large. Then he said it will be about monitoring to see if it has spread anywhere. He said cancer may not spread and first couple of years important , and will have scans.  Such a shock. I'm 58, just wasn't expecting it. My partner doesn't really want to talk about it as has always struggled to talk about health issues- has a we have to get on and can't do anything approach, won't change it if we talk about it.  But its tough, feels like a lonely place to be.  Be nice to hear how others cope. thanks everyone

  • FormerMember
    FormerMember

    Yea, had a shock  diagnosis myself in May which showed  tumour in tubing just below my kidney, and kidney etc was removed within weeks. Feeling OK now, just had another scan for the Oncologist and waiting to hear what and how much chemo I need.

    First month after op was worst, felt quite sore and took some time to get my appetite back.

  • FormerMember
    FormerMember in reply to FormerMember

    Thank you so much for your reply. I feel really isolated and unable to talk to my family about how I feel, so just to hear how you have come through the last few months gives me comfort. So glad you are feeling ok- but its the waiting, just constantly waiting for results - it is something i shall have to come to terms with. How to cope and keep positive, i really don't know yet. I wish you all the best.

  • FormerMember
    FormerMember in reply to FormerMember

    Yes,the waiting is the worse part. I waited a month after surgery to hear from my Consultant. Then he failed to organise another ct scan for Oncology and its taken a month to get my scan so now I have to wait again for an Oncology  appointment to hear what my further treatment will be. 

    I found the best way to cope for me is focusing on my recovery. From the day after the op I started walking.  I walked the hospital corridors over and over each day, catheter bag in hand and continued walking each day since as well as focusing on my diet. Eating what I enjoy to help with initial loss of appetite, but lots of salads and fruit as well in increasing amounts since. Loving strawberries on cereals for breakfast at the moment.

    I try to set myself some tasks each week at the same time being gentle and forgiving of myself when I don't always accomplish them. I find I'm beginning more and more to realise what is important and what doesn't really matter that much.

    For myself I have faith that God will be with me as he has been, whatever the future holds.

    I hope things work out well fir you in the coming days. The surgeons doctors and nurses are truly incredible a d will hp you l thet can. Have the tel number of the loc district nurse team to hand fir when you come home from surgery. They are brilliant , don't be afraid to ask them for help.

    All the best.

  • FormerMember
    FormerMember in reply to FormerMember

    Goodness your waiting period sounds so hard- i can just see so easily how they did not organise the appointments, seems so unfair.

    Thank you so much for your practical suggestions as well, I will definitely think about all of these things. You have given be a boost today- just to know others are going through all the same things, I will need to be determined and try and keep positive.

    I wish you well with your treatment, thanks again