Hello all,
My name is Tim. I was diagnosed with post infectious IBS three and a half years ago, after suffering from a bout of gastroenteritis. I have severe problems with my diet. I cannot tolerate dairy, soya, herbs, spices, fried food, juices, fizzy drinks, alcohol, wheat, any cakes or biscuits (Even if they are lactofree/wheat free), crisps and some other things. Basically, I ate only skinless potatoes with some veg and salad, meat, and some lacto-free products. I also have porridge with maple syrup, and I eat some dark chocolate on occasions. I control my symptoms if I 1) stick to my diet 2) do not talk whilst eating - talking always leads to diarrhea 3) sit for extended periods after eating, from 30mins to over an hour depending on the size of my meal.
I have spent the last few years working out what I can eat. The frequency of my attacks have certainly decreased, but I feel that my food sensitivity has increased.
I do not fell tired with my illness unless I have diarrhea, which usually only happens in the mornings occasionally if I keep to my diet (if I ate freely I would have diarrhea multiple times a day). I do not suffer from fevers, I only have pain when I'm going to be ill, and my weight is under control (I'm 5 10 and around the 10 stone mark, which has been consistent for 12 months or so).
However, I have other symptoms which are consistent with IBD conditions. I have had blood in my stools with more frequency over the last six months, which also appears on the tissue paper after wiping. This does not happen always, and sometimes not for weeks at a time, but it does happen. I also have some arthritis in my back, and I occasionally get eczema.
My father suffers from IBS-D, my mother has bad arthritis, and I also have a cousin with IBS. 2 more distant family members on my mother's side have died from bowel cancer. I had a blood test sometime ago which did not show any unusual inflammation.
I would really like to know the opinions of some on here, and whether they thought I likely had an IBD condition. I plan to get tests when I can get them, although I dread the inevitable colonoscopy.
My name is Tim. I was diagnosed with post infectious IBS three and a half years ago, after suffering from a bout of gastroenteritis. I have severe problems with my diet. I cannot tolerate dairy, soya, herbs, spices, fried food, juices, fizzy drinks, alcohol, wheat, any cakes or biscuits (Even if they are lactofree/wheat free), crisps and some other things. Basically, I ate only skinless potatoes with some veg and salad, meat, and some lacto-free products. I also have porridge with maple syrup, and I eat some dark chocolate on occasions. I control my symptoms if I 1) stick to my diet 2) do not talk whilst eating - talking always leads to diarrhea 3) sit for extended periods after eating, from 30mins to over an hour depending on the size of my meal.
I have spent the last few years working out what I can eat. The frequency of my attacks have certainly decreased, but I feel that my food sensitivity has increased.
I do not fell tired with my illness unless I have diarrhea, which usually only happens in the mornings occasionally if I keep to my diet (if I ate freely I would have diarrhea multiple times a day). I do not suffer from fevers, I only have pain when I'm going to be ill, and my weight is under control (I'm 5 10 and around the 10 stone mark, which has been consistent for 12 months or so).
However, I have other symptoms which are consistent with IBD conditions. I have had blood in my stools with more frequency over the last six months, which also appears on the tissue paper after wiping. This does not happen always, and sometimes not for weeks at a time, but it does happen. I also have some arthritis in my back, and I occasionally get eczema.
My father suffers from IBS-D, my mother has bad arthritis, and I also have a cousin with IBS. 2 more distant family members on my mother's side have died from bowel cancer. I had a blood test sometime ago which did not show any unusual inflammation.
I would really like to know the opinions of some on here, and whether they thought I likely had an IBD condition. I plan to get tests when I can get them, although I dread the inevitable colonoscopy.