Bowel accidents

Hi, 

I have always had bowel issues, even as a kid. The dr said back then I had a spastic colon. In my thirties, I had a magic eye & was told I had IBS. In my early forties another magic eye & again nothing found. Two years ago my bowel habits changed. I was constantly running to the toilet. I had another magic  eye & polyps were found & removed & I was told all was ok. Now, things are much worse & have been for over a  year. I am up through the night going to the toilet & cant leave the house as I am having bowel accidents even at home, despite my stools being normal. I just cant hold onto a stool anymore. 

My dr said as my magic eye was normal, its just IBS. I have recently seen a consultant who said I need a flexible sigmoidoscopy & it will be around 2 months before I receive an appt. I have also passed blood in my stools which was dark & cant understand why he isnt doing another colonoscopy. I am so worried & so embarrassed having accidents. I have told no one. 

I am also worried about having an infection in my bladder, due to having so many bowel accidents. I have to throw my underwear away each time.

The consultant asked if I had normal delivery on my two children, which I did. I asked if he would examine me but he refused & said the sigmoidoscopy was what was needed for my symtoms. Then he asked if I had felt or found any lumps around my bottom.

I am just so worried & I have to keep making exscuses why I cant go shopping with my friends at the weekends. 

I did have an abnormal smear 15 years ago & it was a CN3. It also said it was caused by the HPV virus. The consultant at the time said as I had always had regular smears, that my smear results had been misread for many years to get to be a CN3. I am now thinking maybe they have misread my smears again & its now spread to my bowel. 

Any advice greatly appreciated.

thanks

Molly

 

  • The FODMAP plan (I can never remember what the letters mean) is hard work, and you need to be really good for at least three months.  You'll have to exclude whole groups of food (no gluten, no lactose, no fructose, little soya, and much much more excluded). So, most dairy is excluded, except for hard cheeses. No fruit or honey. No milk in tea or coffee, but you can get Lactofree which is ok.  No butter, but olive spread is ok. No wheat products, but there are some nice (well, acceptable) gluten free substitutes. You'll probably find you're scouring the free-from section of every shop you go in, and reading the ingredients list of every prepared food! 

    Fortunately, it isn't permanent and after 3-4 months (once your symptoms have settled down) you can cautiously re-introduce foods until you find one which triggers your symptoms.  Then you know  what you have to miss out.  It turns out I can't eat beans nor mushrooms.  I can only take dairy in small quantities, so I've switched from milky lattés to americano or filter coffee with a small quantity of milk, or sometimes a soya latté when I want a treat. 

    I hope your doctor is able to refer you, but if not it might be worth seeing a dietician privately.  It's not like you'll need to see them very often. I think I saw my dietician just four times over 6 months, with maybe a couple of emails in between.  She gave me LOTS of booklets and leaflets on the FODMAP plan which made it a little bit easier. 

    Good luck. Please let us know how you get on. 

  • Hi Telemando,

    Sorry so late in replying to you, I have a virus! I rang my dr who said there would be quite a wait on the NHS to see a dietition so I am going to go private. Things are so bad now, I will do/ try anything just for a normal day. 

    I don’t eat any dairy, apart from those plain bio yogourts & I have used soya milk for decades. I do eat lots of fruit though but will happily stop if it helps me leave the house.

    I avoid eating bread as somehow that makes my stomach really swell, so much so that I cant fit into my jeans after estimg it so obviously something there that dont agrre with me.

    I will let you know how it all goes. Thank you for all your  help.

    Molly x

     

  • Hi Molly33.

    At least your doctor didn't condemn the idea. It's a pity there's a long wait on the NHS but by going private you're taking control. It seems to me that there are definitely some candidate trigger foods in your diet. Let's hope this is the beginning of taking your life back.  

    If you need any encouragement then I'll be here for you.  I've been through the FODMAP process and I know what it's like.  The first couple of weeks are a nightmare, but it gets better once you settle into a routine.  

    This isn't strictly a cancer topic, but I suspect that your experiences will prove useful to others.  I don't think the moderators will ask us to take the discussion elsewhere.  Nevertheless, if you prefer to talk privately then feel free to send me a friend request now or any time in the future.