hi everyone
its been a while since i posted on here and its been a bit of a rollercoaster ...
saw the oncologist 4 weeks ago who promptly admitted my husband to the hospital as he felt he was too unwell for any kind of treatment so hes been treated for an infection and put on steroids and some stuff to help clear away mucus from his lung ..we call them the spit shit tablets as they sound very similar to the pills he takes for his thyroid .
he saw the oncologist last week and hes now been offered a targeted drug therapy for the mutation of his cancer....it wont cure the cancer but should hopefully slow it down and give him more time...we are both numb at the moment although i still cry when no one can see me...
my husband is trying to do more for himself although the cancer is eating away at him and he does look frailer now ...hes still got his attitude and we do argue mainly because he gets so frustrated and of course im the one in the firing line ...
our local surgery has not been helping very much as they dont seem to understand what the hospital letters mean in terms of medication for my husband ..its like fighting battles on all fronts with them ...but the macmillan nurses are amazing and are very helpful so thats not too bad
at the moment im having health issues and my surgery has been less than helpful but im coping so far ...i spend a lot of time mentally telling everyone to eff off lol ...worried my mental thinking is going to cross with my actual verbal saying ..but thats my cross to bear ..never knew i could swear so much and with style either ! ........
its hard to face the prospect of my husband dying when we havent had a life time together and he feels the same but we have been lucky in what we have done together so far so i shouldnt complain ...
its the hurry up and wait mentality that drives me crazy ....but i know the oncology doctors and nurses are doing all they can for him and thats all i can ask of anyone ..my kids have been fantastic and that helps ..rest of my family not so much but thats ok ...im used to that
so now we wait and see if the new drugs will help ....the oncologist mentioned chemotherapy as a last resort so life is till worth fighting for as far as im concerned but then im an eternal optimist as opposed to my husband who is a natural pessimist !
hope everyone has a good day today
Hi greyhoundsrule I think we have spoken before. Your post made me smile at the prospect of you swearing with style? Love it! It sounds like it is all very frustrating trying to get all the different parts of services to talk to each other and you not having to chase everyone. That's not the way things should be..I don't know what to say about the prospect of the loss of a loved one but hey hubby is here , frail but OK and he has a wife that loves him dearly who is gona make sure he has all services he needs to keep him comfortable .. you keep that optimism.up and also venting at times of frustration because that's OK to do that..Best wishes for now Gailx
hi granny59 ..thank you for that ..ive decided that best way is to walk away when my hubby gets angry and frustrated with life ..walk away swearing though lol .......
its hard to get everyone to accept that he wants me to speak on his behalf ...our surgery wants an official letter saying they can talk to me on his behalf so they are going to get one which they will probably file and forget about as per normal ..
i know more about his medication than our gp probably ..,,my husband gets frustrated with our surgery as they insist that any letters from the hospital have to processed by them before they can do anything about medicine changes ordered by the cancer unit ...
so much for a paperless society! ...its the little things i find frustrating ..when hes in hospital everything is sorted out and explained clearly ,,but at home trying to get help from our gp is not so easy ...getting an appointment to see a gp is nigh on impossible but we keep trying ...
the other morning he woke up and first words out his mouth were .." im dying " ...i froze and said well we all die ..your just getting there faster ..tactless i know ,,but it made me cry because he actually used the " d" word and i didnt know how to react ..i think we have both accepted that hes not going to reach 100 years old !! ..but hearing him say it out loud like that was a shock ...
thing with cancer is it takes away everything you love bit by bit..once you accept that its not nice but you try and deal with it day by day ..
best wishes for you and your hubby too
sarah xx
Thanks for sharing this.
this week Weds 16 July my husband age 44 has been diagnosed with stage 4 bowel cancer which has spread to 5 organs. We have 2 teenage daughters and this is the hardest thing we have ever had to face as a family.
we currently wait for oncology at addenbrookes to let us know what treatment they want to start but he is frail he has lost over 2 stone in 3 months, he is so tired and his iron has dropped below 4 hence his 5th infusion coming up on Monday.
please how do you cope with this sort of thing? I’m broken. I don’t know how to carry on. He is my soulmate and best friend.
thank you and I am routing for your husband at this difficult time and stay strong if you can xxxx
i am so sorry to hear about your husband ..i know how devastating it is when the specialists talk about cancer and stage 4 and treatment ...and options
im still trying to cope with it all and some days are harder than others ...
my husband is angry about the cancer and gets very stroppy and because im his carer and general manager i get the full force of it ..but we did talk and he realised he was taking it out on me and promised to try not too ..that meant a lot to me ..because the cancer has taken half of his vocal chords away and i need to be his voice with the doctors and nurses and anyone else ...
i do get resentful of what cancer has done to him ....hes frailer now and more prone to infection so we have to be careful about where we go and what we do .and also not having too many people around us ....
i dont think about the future anymore im just grateful to get through the day with no drama or emergency hospital visits ...
the cancer team at the hospital have been so good and im grateful for the macmillan nurses as they have been brilliant in explaining things to us both .and offered advice about diet and therapy for us...my husband doesnt want to talk about the cancer and i cant do face to face therapy ,,im happier writing about it on here as i can express how i feel better ...
theres no easy way to cope as when i feel overwhelmed with it all ...i try and take some time for myself even if its only a few minutes away in another room where i can cry or just be alone ..my kids have been very supportive and worry about me but i dont want them to take on too much ...
its hard to accept that life has changed and i know what you mean about about best friend and soulmate ..its accepting the fact that life is not what you hoped for and making the best of what you have now......
im still broken and devastated but i cant change anything so i have to accept that for now i can only live my life with what i have now...
im rooting for your husband and your family and hope that you have better news soon
take care xx
Whatever cancer throws your way, we’re right there with you.
We’re here to provide physical, financial and emotional support.
© Macmillan Cancer Support 2025 © Macmillan Cancer Support, registered charity in England and Wales (261017), Scotland (SC039907) and the Isle of Man (604). Also operating in Northern Ireland. A company limited by guarantee, registered in England and Wales company number 2400969. Isle of Man company number 4694F. Registered office: 3rd Floor, Bronze Building, The Forge, 105 Sumner Street, London, SE1 9HZ. VAT no: 668265007