Treatment any advice

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Following the diagnosis of rectal cancer I have been booked in on Friday to have more biopsies taken under anesthesitic. They are going to form a stoma as I will then be having chemotherapy and radiotherapy which they have said can affect the bowel functioning due to the location of the tumor lower in the rectum. 

Feeling really nervous now that things are starting to happen, any advice with regards to the stoma, how I may feel after surgery? 

  • Hi . I had my stoma as part of my operation but I know the reversal of it was a much smaller operation. You will be encouraged to get up and about after surgery and the nurses will help you with your stoma initially. The stoma nurses will visit you to show you how to clean the stoma and change the bag. It’s a bit daunting at first but you’ll quickly get into a routine knowing when it’s quiet and the best time to change it. I’m going to tag a couple of people who might also be able to offer some insight  and 

    Hope it all goes well on friday

    Take care

    Karen x

    Macmillan Support Line - 0808 808 00 00, 7 days a week between 8am-8pm
  • Hi Happy14

    Your story is similar to mine, low rectal cancer. Do have a look at my profile. Having a stoma can be a bit difficult at first, it’s quite a thing to get your head around. Reading posts on here over the last few months, it seems that, for most people, once it settles down and you get used to the new routine, it quickly becomes part of your life with no problems.  It took me a few weeks (yes, I hated it at first!) but the stoma nurses are incredibly kind and supportive. At first it took me up to half an hour to change my bag, whereas now it is less than 2 minutes.
    A month after my stoma op I started on 4 cycles of Capox chemotherapy. I found it hard because of the side effects (which not everyone has). But I became extremely grateful for my stoma, because it coped  easily with the rapid changes from constipation to extreme diarrhoea  - and saved me having to rush to the loo and sit on it for ages when feeling quite poorly. It also meant that the pain in my rectum disappeared, perhaps because it was no longer being irritated by stools trying to get past the tumour. I finished the chemo a month ago. It worked brilliantly at shrinking the tumour and I can honestly say I feel great.

    I  am starting my radiation next week.. I am not looking forward to it, but I am looking forward to getting it out of her way! Another part of my treatment done and dusted. Do have a look at the “Ileostomy, colostomy and stoma” forum on here. Everyone reacts differently, both mentally and physically, I know. There is a lot of support on here, and some great success stories, which genuinely helped me get through the difficult times.

    I wish you the very best with your treatment. It is completely normal to feel nervous, but you are not alone -  do ask if you have questions or concerns xx

  • Thank you veggie lady, your message is really helpful and I'm really pleased your treatment is going well xx