Hi all
My first post: I'm a bit uncertain about which Forum is most appropriate for this issue, so all advice or redirection welcome.
Brief history: tumour in lower colon and rectum found last year, successful removal. Temporary colostomy stoma, reversed April 2022. Bowel problems thereafter, consistent with Low Anterior Resection Syndrome. Unfortunately, later-stage prostate cancer discovered in post-operative biopsies, which required early and wide-area radiotherapy, from which the bowel could not be screened.
I"ve just finished my 39-session course. As predicted, during the last weeks of treatment classic side effects of fatigue and bowel problems (compounding the LARS and leading to sleep-deprivation), which are expected to continue for some weeks or months more. All a bit of a Christmas-spoiler.
My question relates to managing, or part-managing, the pretty constant diarrhoea. Laperomide really does nothing, 30mg codeine tablets sometimes help; diet doesn't seem to affect it unless I'm foolish enough to have a blow-out, when it all goes really crazy for a while. I've been on probiotic supplements, approved by the specialist nurses, since the reversal, and eat kefir, sauerkraut and kimchee when I can.
But the worst thing is the burning rectal/anal pain from all the diarrhoea. I have special barrier creams and standard antiseptic creams. Washing repeatedly in warm water is essential. I've been warned off haemorrhoid creams, especially hydro-cortisone ones. The nurses' overall advice is in effect 'you'll have to live with it; as the radiotherapy effects die away it should get gradually better'.
Does anyone have comparable experience, and any tips?
Hi and welcome to the board. Yes the burning pain is horrible and I would normally suggest haemorrhoid cream but you’ve already covered that. Hopefully the radiotherapy side effects will wear off quickly as you seem to be taking all the normal precautions and medications.
I’ve just posted a link on another post that was a talk given by a gastroenterologist about LARS and bowel control which might be of interest?
We also have a reversal /LARS board on here - see link below - and there’s also a LARS page on a popular social media site which you can apply to become a member of
Ileostomy, colostomy, urostomy and any other stoma support
Take care
Karen x
Karen
Many thanks for this. Mr Andreyev's Q&A is certainly useful, and reassuring in the sense that the LARS issues are recognised as significant (the attitude of my team has been a bit "well, yes of course, what would you expect?"), even if there's not been much specialist study of management techniques. I'll check out the other groups and forums.
Viszla
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