Hi everyone
I'm Steph from the Community team
Here is a new thread for carers, family and friends. This is a space for you to chat, share experiences and support each other through issues related to your loved ones bowel cancer. The previous thread will shortly be locked as it was getting rather long which can make it difficult to navigate.
Please remember that we also have other dedicated spaces on the Community for carers, family and friends. These spaces exist so you can support each other away from members of the forum who might be dealing with their own cancer diagnosis:
Supporting someone with incurable cancer forum
You would be welcome to set up another new thread like this in one of the above forums. Please just let us know if you would like any help?
We hope you will continue to find lots of support from each other and the Community. We're here to help, so please do let us know if you have any questions or support needs by emailing us at community@macmillan.org.uk
Jkee Les calls him his therapy dog and has a reason to get up and walk him. Les does take his phone with him as well. I think the same as you but when we got him after the ops etc we thought it would be preventative chemo and he was really well. It is 6 am and sat in the dark as don’t want to wake Rufus up. The things we do xx
Good morning all. Well I have tears in my eyes but still can’t cry. I am in such a state with no one to talk to. Les has been really curt with me in anything I say. I feel completely useless and helpless and he is blaming me for the way I am when I have put up for years with others coming first. I felt dreadful yesterday and asked him to put Rufus away for me while I went to bed, The first time in 4 months, he took umbrage and this morning hardly spoke. My tummy is doing summersaults, my lips keep going numb, headache etc etc. I really wish I had someone near I could just go and have a chat. I have sort of become a recluse and now get really bad anxiety if I have to go out. Just needed to get this off my chest.
jkee I hope you being strong and how is Simon doing. Love and strength to everyone xxxx
Maggie we are here for you first of all everything that you are going through ditto we have had a rough week Simon had to go to hospital Friday he had targeted therapy Wednesday Thursday Frida you couldn't see his skin it was red raw plus painful piles very snappy with me he wanted to give up blamed me for this chemotherapy saying he didn't want it at that I don't understand . Of
urse we can't understand I just want the love if my life to be here but I understand where he is coming from absolutely had enough so unfair . Maggie get in touch with your local hospice ours
ve been there for me counciling and a day of spa treatments vonce a week just gives me a break and once a month coffee morning for carers. I have only made one treatment spa like you a recluse
t it was relaxing even though I cried telling her everything it was exhausting but lovely they let me just of load . We don't have a easy answer my stomach is in pain daily on high alert watc
ng but can't have people here soo unfair luckily our relationship is strong and so is yours cancer is evil it effects all the family love to you
Hi jkee I knew you were going through the same as are others on here. Les can’t have targeted therapy or immunotherapy. Will find out on Wednesday the best way forward which like you I am dreading. I don’t think Les would be happy if I said I was going to get in touch with the local hospice (bearing in mind I did agency work at ours). He would think it would giving in. I can’t stand the tummy aches etc. yes our relationship is strong but by heck I could sometimes walk out after he has had a go at me, but obvious I don’t, like you I hold it in. Just reading your post makes me so sad as we are living the same lives. I really wish I had someone near and to talk to.
just love the photo of him. Rufus is asleep at the moment so getting quiet time xx

as you can see he has chewed his towel. I will buy a new one for him.
Maggie if you want to keep in touch private for a chat not sure if we can but yes we are are the same path Simons face is bleeding looks awful have a feeling treatment will be delayed and yes Simon didn't want to be involved in hospice but they remind me they are here for the living not just the dieing. Do you have a Maggie center near they are brilliant for partners to vent ours is in the hospital but a hour away x
Jkee no we don’t have a maggies place near, just the butterwick hospice. Which is next to the hospital and only about 15 mins away. I don’t think we can do it privately. I am sure if I could cry I would feel better, instead I get angry and iron or something whatever it is. My friend in Australia since I have known since 1st year senior said she would fly over but I said no as she has family herself in Australia. I can’t believe his face is bleeding. Les has come out in cold sores and mouth ulcers. They are so strong and I have to remember that. Gosh jkee I wish we all lived near xxxx
Whatever cancer throws your way, we’re right there with you.
We’re here to provide physical, financial and emotional support.
© Macmillan Cancer Support 2026 © 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