So I’ve been on TPN over a week now, seems to be helping with energy, but not so much with weight yet. And I tried eating here and there, and then days of not eating, and my stomach feels the same regardless. It get’s burbly and distended and a bit painful even if I don’t put anything in it… So why should I go hungry entirely. And just sips of water… I ended up eating most of a salt packet yesterday, cos I was desperate for some flavour. (Not all at once ofc)
Managed to find a pic of the actual salt packets they have at this hospital. How sad am I?
So bacon with too much fat on is apparently a very bad idea. I can’t think what else messed up today, so it must have been the bacon muffin I had after my gastro appointment(will elaborate later). But it seemed to just sit in my stomach all day till I hurled in the evening. Tmi I know, but most folks with Crohn’s and IBD have to get used to talking about bodily functions, so it’s probably not that shocking.
I know some things I’ve read have said that fat in general is harder to digest, and therefore bad for Crohn’s. Which I’ll go with, since processed hot dogs and stuff like that seem to bother me, during a flare up anyway. Even though I ate canned/jars of hot dogs loads before. And beans… I miss baked beans… but right now thinking of food isn’t what I wanna do. But there are good fats we need too right? Either way, I went from feeling meh, to feeling seriously bleh… literally.