Broken up stools and incomplete BM's

Posted , 26 users are following.

Hi all,

I've been having this problem for a while now. When I have a BM, my stools are often broken into many pieces. I can't remember the last time I had a well formed "log". After I'm done it often feels like there's still some left inside my anus. Soon after eating I get discomfort, not pain, in my lower/middle intestinal area and flatulance/belching. It's enough to make me restless or irritable. It's like a slight urge to have a BM after every meal. Anyone experience these symptoms? Can someone recommend something that will help get me regular again?

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  • Posted

    I'm just curious, does anyone experience heightened sensitivity to touch, or even somewhat itchy/prickly skin when they have the feeling of incompleteness or the slight urge to have a BM? This is another symptom I experience. It adds to my irritability and restlessness when I have this feeling.
  • Posted

    Update:

    Been a little while since I lasted posted on this discussion, thought I'd update.

    Not long ago my gastroenterologist diagnosed me with IBS after testing for celiac and intestinal inflammation. The results were negative. He recommended I go see a dietician to try a low FODMAP diet, who I'm seeing today. 

    I noticed some of you mentioned that you have ASD and anxiety which I have too. Anxiety and stress I think probably do contribute to our IBS symptoms. I wonder if any of you have any food intolerences too? I noticed if I drink milk it sometimes makes me feel sick or gives me the runs, and if I eat nuts it gives me pain or discomfort in my tummy the next day. Also, eating bread seems to make me more constipated as does taking a fibre suppliment. I've recently drastically cut out alcohol from my life (I was drinking daily to cope with anxiety/stress) because it made my IBS symptoms worse. I also stopped smoking cannabis because it was raising my anxiety. It seems like my body reacts negatively to quite a few things going into it, I will have to be careful what I eat and drink from now on.

    • Posted

      Yes to ASD, no to food intolerances. Almonds help me re: nuts. I limit my bread intake. I used to devour 2 loaves a week and now I make 1 last longer than a week. Exercise also helps although I have developed vein problems so that limits but this is not uncommon in fit people apparently. I am currently teetotal. Milk has no effect on me. I eat too many non Fodmap foods which help me to go Fodmap. I can only think of apples for now. I have devised my own food strategy. It has taken 3 - 4 years but it works in a non workplace environment. Add in work and I am all over the place again but that is stress and anxiety.
  • Posted

    After years of trying various medicines and herbs including Anti depressants and what not, what seems to work for my IBS is to have Tramadol Hydrochloride medicine just after my first bowel movement. I accidentally discovered it after having one pill after my first BM and found out I did not have another BM that day- which was very odd but interesting. Try with a small dose 50 mg and if it doesnt work, try slightly higher dose without overdosing.

    For me, this drug has worked wonders especially when I want to avoid multiple bowel movements while traveling or in a party or important office functions and after a pizza party. I get some side effects of gas passing and sleepiness but when properly used or when your system is used to the medication, the sleepiness can be managed. Slightly offtopic, but I use Shreddies underwear to manage the gas passing/flatulence while traveling- which has helped a lot in filtering the fragrance.

    I used to pass stools like 4-5 times daily for atleast 2-3 years.

    Finally, after a series of antibiotic treatments (2-3 antibiotics were given at the same time which felt aweful during treatment), the pain of IBS and excessive gas passing symptoms disappeared and I thought I had a better forming BM but with decent intake of fiber daily.  Do your research and try Tramadol if you like. Let us know how you felt about it. 

  • Posted

    Well guys I decided to go back to my gastroenterologist and book a colonoscopy. It's happening at the end of this month. I'll also be taking part in a study where they place a fibre-optic pressure sensing catheter into my colon during the colonoscopy which will record my bowel contractions and determine what is normal or abnormal. I will need to stay at the hospital for up to ten hours whilst the catheter is inside me, but I will be allowed to eat and use the toilet.

    For those of you who have had a colonoscopy before, how was it? how did you feel afterwards? I'm a bit nervous about it, but I guess it's worth it if they find anything and if not at least it might help put my mind at ease.

    • Posted

      Congrats Sounds like you are being listened to so can not say fairer than that.
    • Posted

      I got the colonoscopy done about a week ago and they didn't find anything which is a relief, but I also feel clueless about what is causing my issues, I mean is it really just IBS? I'm still experiencing the same symptoms I have been since I started this whole business of seeing doctors and getting tests done. I suppose I need to work on reducing my stress but how do you do that when your symptoms are largely what are causing you stress. It doesn't seem to matter what liquid or solid goes into my gut, it gives me discomfort (even water) and my stools come out unformed (they're still flat, and broken up into pieces). I've noticed they're flaky, fluffy too on occasion with undigested food in them.

      Does anyone else have any more recommendations about what might help? I feel pretty much clueless at this point.

    • Posted

      This is horrible advice!! Painkillers are the most constipating meds out there along with NSAIDS.
  • Posted

    Hi @jaseinspace I am dealing with similar problems at the minute I think. I seem to have excessive gas, bloating and flatulence which is often triggered by eating. I get relief from going to the toilet but I don't seem to be fully evacuating and will need to go 2 or 3 times a day. I am a long time sufferer of ibs, had a sigmoidoscopy 4 years ago and results were fine so I'm kind of hoping that still stands as I know nasty things take longer to develop than 4 years. Usually I have struggled with the bloating but constipation, now my bowels have become more active but not fully evacuating. It doesnt help that I am currently on holiday and supposed to be enjoying myself but I think I may try the fodmap diet and cut out onions and garlic and certain fruits etc.

  • Posted

    I am wondering how many people on this thread might be gluten intolerant and not know it. It is a simple blood test. I suspected my daughter had gluten intolerance after after a few years of loose bowel movement, occasional vomiting from breading and pizza, general malaise after eating wheat products. She USC now waiting for celiac testing. I myself would get headaches, malaise, dizziness, loose stool, inflammation in my skin from gluten. Since I've largely cut it out I have lost weight and have none of those symptoms. I cut the gluten and most processed foods.

  • Posted

    It's all about a good diet, alot of the times it is allergies too, honestly it's good to have some alcoholic beverages. it helped me so much! give it a try.

    • Posted

      I think stress plays a large part too for example if I were able to chart illness by day it would be heavily skewed to the weekend and Sundays in particular. This is because the weekend is when we relax and in theory release stress. 

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