Does anyone have any experience of radiation enteritis after treatment has been over a while? I understand it is commonplace during treatment.
The position of the tumour & affected lymph nodes plus a lack of mesorectal fat has led my onc to call me in again to discuss the above. Anyone know of anything that can reduce the long term risk?
I am due to start therapy on Tuesday, but really do not want my life sitting next to the loo, wearing incontinence pads, nor being so restricted in what I can eat that it takes verything away from being me.