So here’s a thing I saw a reference to what I have as mud pies and I think it fits quite well. I had stage 3 colon cancer diagnosed in may 2016, radiation and then the main op in October 2016, then chemo and my reversal in may 2017. Since they removed part of my rectum things have never been the same, gradually getting better but I now get mud pies. As in mud like ‘crap’ that oozes sometimes, and I don’t know about it until after the fact. It’s not all the time, some days it doesn’t happen, other days it’s a few times and my diet doesn’t really vary that much. Anybody else have/had this problem? What did you do!!
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Cancer Council NSW would like to acknowledge the traditional custodians of the land on which we live and work.We would also like to pay respect to elders past and present and extend that respect to all other Aboriginal people.