Kidney cancer with secondary in lungs

I am no different to anyone else, I think. I have my own family tales of cancer.

My mother battled and beat cancer twice; as she puts it, now she’s rattling around inside. Grandad smoked all his life, but didn’t die of lung cancer; it was everywhere else though. My father-in-law didn’t smoke and lung cancer took him. There is no rhyme or reason to the havoc cancer wreaks.

These events were rarely spoken about. I certainly pushed them to the back of my mind, preferring to remember the people not the disease.

Now, it’s my turn. I went into hospital with sepsis and high blood pressure, came out with type 1 diabetes, kidney cancer with secondary cancer of the lungs. I’m not sure I won that round. Certainly, I was down but I’m not out. Not yet.

The cyst on my liver is benign and the MRI on my brain didn’t necessitate any stay in hospital or panicky phone calls telling me to get myself back there PDQ. 

Not like when they found a blood clot on my lung. Funnily enough, that upset me more than when I was told I had cancer. I don’t know why. Maybe it was the thought of another night in MAU; the experience wasn’t enjoyable when I had sepsis.

I thank all the NHS staff from the cleaners through porters, nursing staff, doctors, registrars and consultants – even the four radiographers of the apocalypse – for the kindness, decency and professionalism, especially in the moments when my illnesses stripped me of all human dignity. When I was low, they picked me up, dusted me down and set me off and running again. OK, stumbling.

So, the upshot of it all is that I’m having my kidney hooked out in a week or so, with the consultant “confident” he can do it via keyhole surgery. Once I’ve recovered, a course of chemo for the lungs which I’m told may be fun. Mother Nature beat the pills to hair loss as my sister pointed out, hot on the heels of my wife telling me my head is egg-shaped after a trip to the Turkish barbers. 

Sorry if I’ve rambled or offended anyone with the levity; that’s my way of dealing with it all. And remember, you aren’t as offended as I was when a man wearing orange crocs told me I had cancer. 

Orange crocs. Orange blooming crocs.

  • Hi muttley welcome to the forum, whats wrong with orange somethings you see nowadays nearly blind you, hope you've still got sence of humour when they start on you, we could do with more like you, sorry you've got a few problems, do you know how they get a kidney through a keyhole is surgeon a magician now you see it now you don't,. Your welcome any time.

    Billy 

  • Thanks, Billy

    Now you've mentioned it, all I can envision in my head in David Frost and Loyd Grossman telling me about my cancer. "What lives in a body like this?" "David, it's over to you..."

     

  • Hi never been here before please excuse me for any mistakes, my husband who is my rock and my world has been diagnosed with kidney cancer that has spread how far we dont know but there are spots in his lung, been told he will have the kidney out but not by key hole, what gets me he will not have the operation until the second week in July surley the cancer will have time to keep spreading i cant show him that i am upset, as he is so positive that he can beat it i hope pray he is right, feel so bad been here as i am not the one fighting this disease! 

  • Hi gutted,

    Sorry to hear of your husband’s cancer.

    I guess the waiting times vary widely around the country. I was due to have my op in mid-May but they put me on blood-thinners and forgot to tell my consultant so it’s not been completely smooth. 

    My wife suffers more anguish than I do, or at least outwardly, but her worries are compounded by making sure the boys are alright - oldest goes to uni this summer, youngest is currently sitting GCSEs - when I’m in hospital.

    I’m more concerned about her health than my own because the stress isn’t doing her any good. You shouldn’t beat yourself up about cancer. A family suffers it, not just the patient. 

  • Hi muttley can you please reply to misseyA, she is very worried about her dad. 

    Billy 

  • Thank you Muttley for replying, hope your op will be soon, July the 9th seems so far away but i realise its only 5weeks and a few days, please give a cwtch from me to your wife, we as partners of cancer patients feel so useless and yet need to keep the ordinary live going with a smile on our face, failing sometimes but that is only because we care!

  • Hello Everyone, My husband was diagnosed with Reno Cell cancer 8 tears ago, thought we beat it, the cancer went to his lungs, he is 58years old. We have fought it with immunotherpy, was on opdivo, for almost two year, and now he is on cabometyx, which is really taken a toll on his body. I joined the site tonight in hopes that I can find out more information or hopeful help some that are battling like we are.

  • Thank you for replying, my husband has just had a appointment(through the post this morning) to have 3 units of blood on the 1st of July a week before his operation no one has said why though the assessment nurse wasnt happy with his blood results( anemia,)went to see our gp yesterday and he said that there is nothing to worry about the result of the blood tests, just feel as if i am knocking my head against  a brick wall!  How do you keep your spirits and your husbands up!  I havent heard of cabometyx but as we are only just starting this horrible journey i havent a clue, but hearing from you has giving me a lot of hope and  realise  that you must be a strong lady keep battling on  thinking about you.

  • Hi mut 

    When are you starting treatment or operation.

    Billy 

  • Hi Billy

    The op is Monday morning. Got to pitch up at an ungodly hour but was told today that I’m first on the list. By the time it comes to the big day, I’ll probably be last :cry: