Hello we are a year into my husbands diagnosis of Acute Myloid Leukemia. He has been amazing, told 3 times to prepare for worst, amazing though he pulled through.
Long story short, he has been in out hospital a lot 1st half of 2023. Lots of appointments and on chemo for life (his life is limited)
After diagnosis and the real rough weeks that followed, I coped and still worked (still am working). It was the anniversary of diagnosis this month and i feel I am less coping than this time last year. I feel I am grieving possibly because everything feels different, I also lost my dog 2 months ago and I just feel everyone I love is being taken away. I can feel myself feeling really angry and annoyed. This sounds awful but my husband falls asleep a lot and he does this because he is poorly but I am starting to feel even a bit angry at that, (as I write this it sounds ridiculous but I will keep writing) I am upset, annoyed, angry that this blood cancer is taking my husband away, in somewaya it feels like it has already taken him, its hard to explain really.
I have good family and great friends but I can't tell people how I feel because it sounds mad. I feel like I am living a ticking time bomb knowing it will go off. Thanks for listening if you have got this far. X
Hi notagain3
I almost lost my wife to sepsis even before she was, eventually, diagnosed with Leiomyosarcoma so totally get the idea of being prepared for the worst and then being called back from the brink.
We have quite a good page on anticipatory grief that I think matches quite nicely with your "already taken him" comment.
I did a living with less stress course that really helped me, friends though often feel very uncomfortable talking about cancer - not the easiest conversation point though in the last could of years I have lost friends to all sorts of reasons, including one who has a massive heart attack.
<<hugs>>
Steve
Dear notagain3,
I think you are coping well! You are a human being, frail as your husband but in a different way. Openly accept your feelings of anger, it is against your husband’s illness, the frustrations of being a carer and and because you are emotionally drained. How do I know this feeling? My partner died from a rare and horrible neuro-degenerative disease 3 months ago. I had cared for him for the four years of his illness. During that time he had a ruptured spleen, a stroke, sepsis, Covid and lymphoma. I often told him how much I loved him and how much I hated his illness! Try to take breaks when you can. Even a twenty minute walk a day will help, maybe whilst your husband is snoozing. Your friends and family will be admiring your love and care and will understand your frustrations I’m sure. They may feel sad that they are unable to help as much as they would like. Listening to you, however you feel will help you all. Carry on caring … and shouting… you are being wonderful!
Thank you so so much for your words, they mean a lot and I am sorry to hear what you have been through. Yesterday my husband was taken to hospital with covid and sepsis, he is doing ok and I am doing ok, just another set back. I will keep reading your message it has made me think differently Thank you x
Oh no! Another mountain to climb! You are in my thoughts. Lean heavily on your support network and try to rest and have a change of scene whilst your husband is being cared for elsewhere. It is so important to guard your own physical and mental health so that you can support your husband. You are doing a wonderful job! You are not called to be perfect, just good enough!
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