Hi all my name is Dave haven't been on this forum before but have been on the bowel cancer group. I was diagnosed with anal/rectal cancer July 2022 had radiotherapy, chemotherapy then surgery and am presently all clear. As it happens my wife had ongoing bowel problem. And was on waiting list for surgery so our surgeon did a bogoff and we had ops on same day and in same ward (wierd). My wife had a touch of nuemonia after but soon recovered. In October she had what we thought was a chest infection but 2 different antibiotics and steroids didn't help so an xray then which showed a shadow. So after ct scan and pet scan she is waiting for a camera in lung and biopsy. Gp has told her definitely cancer in right lung lower lobe and since pet scan says it has spread to lymph nodes and thyroid. So basically I am asking for anyone with similar symptons to get in touch with any advice on future treatment. I know we are all different and my own experience means I know what the shock of the diagnosis is like but if there is anything I can find out for her to try and help I would be grateful. Google is of course full of scare stories an animal excrement. Thanks Dave
Hi Dave,
I just wanted to treat out to you and share my experience so far as my dad has recently been diagnosed with lung cancer.
My dad has a 5.6cm lobe in the right upper lung with spread to the r4 lymph node in the mediastinum. Because of where the cancer is, and the lymph node being near the heart cavity, they are unable to operate so my dad is receiving 12 weeks of treatment - 4 cycles of 3 weekly chemo and 6 weeks (in between) concurrent radiotherapy. He is then being offered 1 year of Durvalumab.
With the diagnosing for your wife, it will all depend where the cancer is, how big it is and where in the lymph nodes it has spread as to what treatment they offer. We were told no surgery due to the location of the tumour and spread to that lymph node - it is stage 3B locally advanced lung cancer my dad has been diagnosed with. He starts chemo on Monday. I think the biopsy will be an important part of the jigsaw piece in terms of treatment because they do histological testing on the cells and tissue to see what kind of cancer it is specifically with gene/ mutation testing which is important when looking at treatment options.
It might be worth speaking with the lung cancer nurse in the respiratory department that your wife will have been referred to? At our final apt before the treatment plan, the lung cancer nurse said they'd known from early on that surgery wasn't an option. You could always ask, hypothetically with the info that they have now - is surgery an option, is it not? what other treatments MIGHT they offer. They might be reluctant to say now as to not get your hopes up but you could always say that you understand things might change but you're just wanting to try and gauge where things are.
Please reach out if you have any other questions
Adele
Hi Adele thanks for the reply my wife's tumor is7.8cm and in the lower right chamber but that and the pet scan showing nymph lode spread is as far as we have got so I can't say much more at this stage. My wife is 69 so lots of living yet to do. I will try and ask the lung cancer nurse next appointment. Hope your dad's treatment works out well and he has many good years after all the treatment stuff is over. For me personally I feel healthier than I did before my diagnosis so it can be done ,good luck .Will let you know how things progress
Thanks
Hi Dave,
I am so sorry to hear this news about your wife and to hear that you are still in the throes of treatment yourself. It's a very heavy load for anyone to bear. Like you I sometimes wonder why Mother Nature (or the powers that be) overloads some people and spares others. Some of us get more that our fair share of ill health.
I hope your surgery and treatment goes as well as possible and that you return to good health. I am sure that your dearest Linda is looking out for you.
Take care
Miranda
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