my husband knows about this group, but I’m the one who asks the questions. He’s not into these, or any kind of groups. So I give him my input from you
as his wife , I am so worried about his dx. I know there’s a good cure rate but I still worry. Once you have cancer it’s easy to get a recurrence or secondary cancer. How do I, as his wife get thru this without nagging or letting him not know that I’m worried. His post treatment scan isn’t until April and he doesn’t seem phased but I dread going to that appt Please I worry constantly about the future. I know what I should be doing but it’s so hard to change my mindset. I cry all the time w worry. I dint want to lose him cannot imagine my life without him. TYIA
Hi
Difficult situation for loved ones, I'm sure everyone will have a different take on the situation, I was diagnosed with colorectal cancer in 2017, a big shock at the time for both of us...we just made the best of a bad situation and helped each other deal with it...got the all clear in December 2022...Feb 2023 diagnosed with tonsil cancer...big setback...knew this was going to be tougher...for both....no choice again but to deal with it...It was challenging for both of us ...oncology support teams were first class....treatment finished and the 'new normal' starts....scans are part of the 'new normal', scanxiety is part of the new normal...worry lessens as time passes....we try to give ourselves things to look forward to ...meals out, days out...sunshine breaks....no point in hiding from cancer....we just have to live with it.
Take care
Peter
Hello
I feel for you. My husband went through pretty much what you describe during my treatment. I’ve said it before, but I think this treatment, hard as it is for those of us going through it, is any number of orders of magnitude worse for partners who are in the unenviable position of having to watch and wait.
I don’t know your husband obviously, but don’t kid yourself that he isn’t aware that you are worried. I was never worried for myself. I’m quite fatalistic about these things. My Dad , a WW2 veteran of at least two of the major theatres, always said that if your number was on the bullet there was nothing you could do about it. I knew my husband was worried (just how worried I confess I hadn’t realised) but I couldn’t get him to open up about how he was feeling either to me or to anyone else, which was hard….for both of us. We have since talked about it, but I would have preferred to have done so at the time. Support is a two way thing.
From the point of view of the patient I fully endorse your desire not to nag!! In the latter stages of treatment and the weeks afterwards when I had a real crisis with eating it was quite hard to deal with both the dietitian and husband being on my back! They were right, but since when did being right make any difference?!
It’s quite a leap from being in the immediate aftermath of treatment for something which, as you acknowledge has a high cure rate, to imagining life without him. I know it’s so easy to imagine the worst…but dealing with what is is hard enough without going into overdrive about future scenarios which really may never happen. Easy to say, and we all react to this sort of stress differently.
Do you have access to a counselling service? We were given details by the hospital, and I’m not sure, but I think MacMillan have their own services. You are certainly not alone and sometimes it helps to talk.
April isn’t that far off. I wish you both well and have my fingers crossed that it will be good news and a weight off both your minds.
Take care of yourself
Liz x
Please I worry constantly about the future
Hi
It is hard but as you have pointed out your husband has come to terms with the situation and as you intimate he doesn't need to be worried about you. You sound desperately unhappy and depressed so to my mind you need to seek professional help for his sake but most of all for yourself.
See if your GP can help both with medication and pointing you to counselling. Macmillan's counselling is for cancer patients and sadly it is about to be axed anyway.
I don't mean to be harsh but you are facing a harsh reality and you need help. No amount of reassurance from us is sufficient.
Once you have cancer it’s easy to get a recurrence or secondary cancer.
Not this one. It's not easy...It's damn hard
Dani
Base of tongue cancer. T2N0M0 6 weeks Radiotherapy finished January 2019
Hi Dani
Didn't realise that it had been axed....Finances?....The Bupa counselling service is now closed | Macmillan Cancer Support
Afraid so. Some financial services are being farmed away too.
It's about surviving to provide the more important services. If Macmillan have to cut their cloth can you imagine what the smaller charities are facing?
Dani
Base of tongue cancer. T2N0M0 6 weeks Radiotherapy finished January 2019
Hi we make it through because we have to it’s fight or flight scenario. I trusted my team and my husband was there for me every step,of the way. Don’t waste a moment thinking of the what if think if the what now. We have one life and I’m certainly living it. I don’t intend to waste a moment thinking what if
Typing this from southern Spain living a great life please be aware your hubby would do the same for you just be there for him and trust the treatment I did
hugs Hazel
Hazel aka RadioactiveRaz
My blog is www.radioactiveraz.wordpress.com HPV 16+ tonsil cancer Now 6 years post treatment. 35 radiotherapy 2 chemo T2N2NM.Happily getting on with living always happy to help
2 videos I’ve been involved with raising awareness of HNC and HPV cancers
Yes..and, so far yes. My 3 month scans were clear and a recent scan at 13 months triggered by a swollen lymph node (caused as it turned out by an infection) was also clear. Obviously I’m still being monitored…but I feel fine and am putting the last 18 months firmly in the past.
Try not to worry…but I know it’s tough.
Happy to answer anything you want to ask…..and if I can’t, there will be someone else on this forum who can.
All the best to you and your husband
Take care
Liz
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