I have finally had my biopsy results; it turns out they have no idea what has caused the inflammation in my small bowel. No signs of Crohn’s, (which is great, by the way. One auto-immune disease is enough) but also no signs of infection either. They literally said they have “no clue what has caused the inflammation”. They want to see me again for another flexi in about a month so maybe they’ll find something then.
For now, I’m still on the modulen. I’m awaiting a prescription of it which apparently can take over a week as it’s not something a pharmacy would stock. I’m going to try and have small amounts of soft foods like yoghurt or mashed banana or potato for a few days to see how my gut handles it. So far, it’s been fine with smashed potato, and I had some banana last night which also went through me fine. I’m going to take it slow and only have it in the evening. That way, if my gut does protests, I’ll be at home where I can deal with it and not at work where I can’t.
Considering how quickly I responded to the antibiotics, I didn’t think it was Crohn’s (and nor did my GI or surgeon) but as there is no sign of infection, it does make me wonder what on earth my gut is playing at. It’s very frustrating.
So, I have spent today doing not a lot because of having had my biopsy yesterday, and I can honestly say I’m glad I did; my right side and shoulder have ached most of today but it’s gone down a bit this afternoon. It hurts if I cough or move my torso too much but the nurses said that should get better over the next couple of days. I’m going back to work tomorrow but I work in an opticians so it’s not like it’s heavy lifting or terribly physical work.
Biopsy all done. It’s a little uncomfortable but I’ll be ok in a few days. I’m hoping to get the results during my consultation with my surgeon next month.
I’m waiting to be picked up by my parents who are coming with me to the hospital for my biopsy today. I know what to expect so I’m not feeling nervous, but I still don’t want to have it done because it’s a whole day in the hospital.
I’m allowed to drink water until 8:30am (so, for the next 20 minutes or so), but I’m not allowed to eat anything until after I’ve had it done. I’m just having a read through the Patient Information leaflet I was given at the pre-assessment.
I’ll likely be home from work tomorrow so I’ll try and keep you all updated.
I’ve got my second MRI this afternoon. It’s so they can take a better look at my liver but it’s the biopsy that’ll tell for definite.
I worked out that I have eight appointments coming up in the next two months; six are at the hospital, one’s a stoma check that’s been pushed back since before Christmas, and the last one is to sort out my Pills. I just hope my work can arrange my days off so I don’t have to change any of them.