I’m trying to learn more about IBS as my GP has suggested this is the cause of some problems I’ve been having but it doesn’t sound typical to me. I’d love to hear from anyone who has something similar & can set my mind at rest that there’s nothing more sinister going on. It may be that I’ve just misunderstood how IBS presents itself.
I’ve been struggling with lower-right abdominal pain since March 2019. It’s a permanent dull ache that has been constantly present for over 5 years now. Sometime it eases off a little but it never goes away completely. When it’s bad I can think of nothing else & it can keep me awake at night. Having had a look at a ‘map’ of the body I would guess that it’s at the lower end of what I believe is called the ascending colon. When it’s bad it then feels like it radiates up the colon, as if there’s some sort of inflammation. (I’m not a medical person so I may not be using the right words here - one of the problems I’ve had throughout this whole process is finding it quite hard to describe what I’m feeling & even struggling to pinpoint exactly where the pain comes from). But it’s not sharp or cramping pain which I think is what I always imagined IBS to be.
I haven’t had too much trouble with bowel movements although I would say everything is a bit more sluggish in that department. Whereas I would have had a good BM every day, I now sometimes skip a day or two & sometimes what I get is small & pellet-like. But I’ve never really felt that anything I’m experiencing is affected in any way by what I eat. I’ve put my slight changes in BM down to age (I’m in my mid-50s).
Back in 2019-20 my then GP ordered a number of tests: a pelvic US which looked at ovaries etc (all normal), an abdominal US (which showed a well distended gall bladder & several mobile gallstones but otherwise normal) & an MRI of my hip area because I was also getting pain in the adjacent hip & I wondered if it was somehow related (all normal too). I realise looking back at these results now that nothing ever seemed to look directly at my colon, presumably because I have always said that my pain doesn’t seem to be affected by my food or digestion.
Since then, the pain has increased & I have been back to various GPs about once a year asking for help. Blood tests about 2 years ago showed that I now have very low iron (although I’m not apparently anaemic). At first I was put on a big dose of an iron supplement for 4 months which brought my levels up to normal (although not, my GP said, what they might expect given how much iron I’d been taking). When I stopped taking it my iron levels dropped again & they are now the lowest they have ever been. None of the GPs have been concerned by this & don’t seem to think it necessary to work out why my iron levels are so low. I have a pretty varied diet & eat red meat & most of the other foods that are apparently rich in iron so I’m fairly sure this deficiency isn’t diet-related. My other main symptom is awful fatigue which I’m guessing is related to this. I’ve started taking an iron supplement which hopefully will help with this (but last time I got constipation from it so I’m just taking a small amount for now).
The result of all this was that my GP thinks I have ‘a little bit of IBS’ & referred me to a dietitian. I get a phone call every 6-9 months & I’ve been experimenting with eg low FODMAP, eliminating wheat & dairy, adding lots of golden linseed. Nothing has made the tiniest bit of difference to the pain & I’m still not convinced that what I’m feeling is food-related.
I did a stool test to check for blood & that was negative thankfully so my GP doesn’t think there’s anything sinister there. He also said that if it had been anything bad I would have known about it by now! Presumably meaning that if I’d had something like cancer it would have got to a point after 5 years when it would have become very obvious. He declined to order a colonoscopy because, as he said “you really wouldn’t want to have one of those”.
So, I suppose my question is (& I am so sorry everybody for such a long post, but it’s really been helpful for me to write it all down for the first time!) does this constant dull ache sound like a typical IBS symptom? And am I missing something I can try to sort this out? I’ve put up with it for more than 5 years now but as it gets worse I’m struggling more & more, especially as the fatigue gets worse. I’ve actually just given up work as a last resort - hopefully just a career break - in the hope that some rest & self-care might help. I used to love walking but I’m struggling with that too now - how much would I love to get back to that!
Thank you so much everyone for letting me get all this off my chest!