My wife has lung cancer diagnosed in 2020. From the start the tumor has been inoperable due to the proximity to major blood vessels. She has been through radiotherapy without any improvement. The first chemo did not go well and she ended up in hospital for a few days, so that was abandoned. Immunotherapy was the next treatment initially it seems it was successful in reducing the tumour, but after a short while it stopped working and had to be abandoned. She developed fluid around the affected lung which was drained but returned. An IPC drain was fitted and this controlled the fluid build up. Chemo was restarted but she ended up in hospital for a week with an infection, something she is very reluctant to repeat as it was not very good experience. More recently the drain was removed as there was no more fluid coming out. Since returning home after the infection she has not really improved, to put it in context she has not been in the kitchen for nearly 6 weeks now. She is very weak, has lost a lot of weight, while she is still able to move around she is using a trolley for support.
Heather doesn't want more treatment, each time she has had chemo it hasn't gone well. We don't have any timescale, but in her current condition it would not take much to finish her off. She is prone to infections as the left lung is almost completely blocked off by the tumour.
She is now in bed a lot of the time. Off to bed at 20.00. She gets up at 10.00 but often lies in bed after getting dressed. She gets up for a couple of hours at lunch time and again at 17.00
I am her sole carer, we have no children and she doesn't want to involve any other family (we are all getting on a bit anyway). It is only recently that I have accepted that I am her carer. A role that I am not well suited to as not having children my experience as a carer could be written on the back of a stamp, I had a minor role in caring for my mother. This was filling in gaps in her care by others, so different from the current situation.
She tells me to plan the meals for the week ahead, this is all very well but I can't tell from one day to the next what she fancies eating. As a cook I get by but am much more comfortable feeding myself. Heather is more choosy than me when it comes to food, whereas I eat just about anything.
I'm starting to find things are more difficult for me emotionally. Writing this I find the tears are not far away.
How about M & S or Co-op ready meals they are exspensive but some in the frezzer for the days you feel low may help sorry my spelling is bad.
Hi Terry D ,I’m glad you found it helpful in any way .i also am new to this ,well in as much as it’s a new diagnosis for another cancer .not sure I ever felt of myself as a career before more just someone’s partner who did .i don’t know your circumstances but we are all having to deal with different things but knowing we are not really alone helps ,that someone is facing similar difficulties to me is a big help ,like being part of a support group for each other .i hope your situation is not too difficult for you and that you cope ,or at least have a support network that can help you ,but I will say anytime you want to chat I’m here ,sorry it’s taken me a little while to reply but it’s all been going on ,but please feel free to message and I will get back to you .have a positive day .you are not alone .M
Good idea .most major supermarkets do some good ones .
Hi it is just over a year since Husband diagnosed and I don’t really have a support network, my husband & I are over 70 with no children & my sisters are a long way away, I am reluctant to contact & ask for help as they are older and have problems themselves. When I noticed that is was more then a year for this our latest chalange I struggled and did not feel up to another year. So I am trying to get help with my stress I think this is going to help me. The awful thing is seeing that people have it harder then me. So I feel that I should try to cope better. I have told my GP I have contacted Macmilli & I have told my husband that I am struggling and asked him to help me help him. It will take time but I have more hope today then I had last week. I will look at the carriers site and try to take some of the good things from it. I know I am lucky to still have him and his bloods are good. But it is the side effects and general feeling (his) feeling poorly that make me feel I am not good at the catering bit. I got my COVID vacs all 3 the lady said are you a career I said my husband she said like all us then. I love how Nurses talk don’t you. Thank you for your kind thoughts and take Care.
Only problem is that we are both gluten free. The options from the general supermarkets is very limited. M&S have a handful, Tesco a few, once you exclude the dishes Heather won't eat it is not really an option.
Wiltshire have reasonable range of GF meals.
Sorry you have so many things to deal with I remember a shop on Mll Rd and one on King Hedged that as my husband would say funny food, he is a meat & 2 Vedge man. I bet someone can remember there name it was near to the old post office on Mill Rd.
Hello fellow Scottish person!
I am new to the website. Yours was the first message I read. I really really feel for you. I am finding it a very lonely place . My partner has had two dose of chemotherapy. But just before got covid. So didn’t go into it in the best place . Lost loads of weight and felt very low.
I am glad you found Wiltshire meals, I used them a few years ago when my mum was ill. Now he’s eating, school dinners he calls them! Before that, the whole eating thing caused loads of fights and arguments (I eat really healthy stuff…boring I know , but he just wasn’t interested) we’ve only been together two and a half years. Both have children, so finding it all a mine field. He only wants to talk to me and not tell his kids what he’s feeling. But it’s too much sometimes.
I get the ‘going to bed early thing too! And staying in bed!
I just feel helpless! But reading a few of the messages on here I realise I am not on my own .
sending luck hugs and good wishes x
Hi Elephant 21 I understand where you are coming from. Initially Heather didn't want others knowing about her condition or treatment. This was so hard for me, because she didn't speak to me too much either. She has always dealt with health issues herself on basis "my body, my illness". Her mother hated family being ill, possibly after after losing her first child to gastroenteritis. Unlike you we have been together over 30 years so I understand her way of thinking, not that it always makes it easier to cope with.
Heather's poor appetite is a continuing problem. The Wiltshire catalogue arrived yesterday and we will have a look at it over the weekend.
Big hugs to all out there in the same position.
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