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 just hang on in there. It won’t be long now. Just popping out will speak when I get back xx
Hi Jkee
Really feeling for you . My mum’s electrolytes would get knocked off easily and she was a bit similar to what you are describing. Hopefully it’s something that can be quickly sorted . Struggled through a few emergency admissions and it’s so stressful.
Thinking of you both .
Court
Helpline Number 0808 808 0000
He got a ambulance at 6pm in a&e had bloods ok going for a brain scan no idea what's going on in one way hoped the blood would show something nothing yet xx
Jkee sorry I did not reply again. Pleased he got to AandE. my thoughts and prayers are with you and fingers crossed it is just one of those things. Nothing I can say will make you feel better but thinking of you both. Stay strong xx
Thanks Maggie. In the early hours of yesterday morning he was transferred to ward 3 at James Cook. Bizarrely that is the diabetes and contagious infections ward. However, the doctor we saw there (not cancer specialist) is probably the best one we’ve seen in terms of bedside manner (he lost his father last year and so was very empathetic). The plan is to try to build him up for discharge early next week, but with full care package in place. We already have some equipment at home from when he was discharged following discovery of the spinal fracture and we suspect he will be completely bed-ridden from now so probably won’t need any more equipment, just carers. They’re talking about him only having a matter of weeks now, and there was mention that 2 weeks might be realistic x x
Thank you, Karen. He seems to be over the confusion now. He was completely lucid yesterday afternoon and is back to making his usual terrible dad jokes, which is a good sign. That’s a bit of a relief because he seemed very agitated when he was confused - fidgeting, looking around, seeing things. It was pretty scary x
Hi Jkee. I’m so sorry to hear this. This disease is so cruel - you get a little bit of positive news and then something else comes along to pull the rug out from under you. I hope the doctors are getting to the bottom of it and that they are able to address Simon’s symptoms. I hope you’re managing to take care of yourself too. Sending love and hugs to you x x
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