IBS Information

Well, I'm still in the situation where consultants refuse to officially declare me as suffering from PCOS (even though it's been acknowledged that "anecdotally" (ie, I've got several severe symptoms of PCOS but not in the right combination for the clinical diagnosis) I've got PCOS).
Four months ago, I had a foot operation. Because some of the medication they gave me clashed with the Pill, I came off the Pill (I wasn't going to sacrifice the painkillers!). My GP told me to stay off the Pill for four months to see what's going on with my body (I've been on the Pill for years without a break - ironically all the PCOS-detection tests have always been done while I've been on the Pill, I've always expressed concern about that, but doctors kept saying it didn't make a difference - I'm not convinced).
Just had a visit from Auntie Flo for the first time in months, and I was in agony from cramping and bloating. I have been for the past two years, really, but I had post-op infection complications, so they slapped me with some very high-dose antibiotics. The side-effects hit me hard, but the nurses decided they were hitting me too hard - even for the antibiotic I was taking (which is apparently notorious for side-effects). The doctor agreed and ended up concluding I've got IBS.
All my doctor really said to me was that I should eat a high-fibre diet, and gave me mebeverine and told me I could back this up with mintec if I wanted. I was a bit wary - for the past two years, I've been relying on a cup of fennel tea after food to ease my digestive problems, but peppermint tea makes issues... worse.
I made an appointment to see my dietician, and she was very useful on the advice about IBS (such as telling me the doctor's advice of eating a high fibre diet isn't necessarily good advice, I need to explore my food and find out what my triggers are).
I find it somewhat ironic that doctors are refusing to give me a clinical diagnosis of PCOS (or more accurately, recinded the clinical diagnosis they originally gave me in 2006), and now I'm found to be suffering IBS - they told me that PCOS and IBS is linked, although the actual nature of the link is a bit of a mystery.
Is there any advice people can give me about handling IBS? Any literature worth reading? What about diets? I had been trying the low GI diet, which my dietician said had a good reputation with PCOS sufferers, but now it's known I've got IBS, she admitted that a low GI diet isn't necessarily the best option for an IBS sufferer - after comparing my GI recipes books with the dietary fact sheet she gave me, I can see why!
I was thinking of becoming vegetarian, but my dietician has asked me to rethink that now. The trouble is that I already know that meat is a trigger for me - red meat I avoid like the plague, and even chicken is beginning to affect me now, so I've cut right back on it. The only meat I get on with is fish. As a result, I'm a bit stuck on how to plan my diet now that I know I've got IBS. Any advice would be appreciated.
Four months ago, I had a foot operation. Because some of the medication they gave me clashed with the Pill, I came off the Pill (I wasn't going to sacrifice the painkillers!). My GP told me to stay off the Pill for four months to see what's going on with my body (I've been on the Pill for years without a break - ironically all the PCOS-detection tests have always been done while I've been on the Pill, I've always expressed concern about that, but doctors kept saying it didn't make a difference - I'm not convinced).
Just had a visit from Auntie Flo for the first time in months, and I was in agony from cramping and bloating. I have been for the past two years, really, but I had post-op infection complications, so they slapped me with some very high-dose antibiotics. The side-effects hit me hard, but the nurses decided they were hitting me too hard - even for the antibiotic I was taking (which is apparently notorious for side-effects). The doctor agreed and ended up concluding I've got IBS.
All my doctor really said to me was that I should eat a high-fibre diet, and gave me mebeverine and told me I could back this up with mintec if I wanted. I was a bit wary - for the past two years, I've been relying on a cup of fennel tea after food to ease my digestive problems, but peppermint tea makes issues... worse.
I made an appointment to see my dietician, and she was very useful on the advice about IBS (such as telling me the doctor's advice of eating a high fibre diet isn't necessarily good advice, I need to explore my food and find out what my triggers are).
I find it somewhat ironic that doctors are refusing to give me a clinical diagnosis of PCOS (or more accurately, recinded the clinical diagnosis they originally gave me in 2006), and now I'm found to be suffering IBS - they told me that PCOS and IBS is linked, although the actual nature of the link is a bit of a mystery.
Is there any advice people can give me about handling IBS? Any literature worth reading? What about diets? I had been trying the low GI diet, which my dietician said had a good reputation with PCOS sufferers, but now it's known I've got IBS, she admitted that a low GI diet isn't necessarily the best option for an IBS sufferer - after comparing my GI recipes books with the dietary fact sheet she gave me, I can see why!
I was thinking of becoming vegetarian, but my dietician has asked me to rethink that now. The trouble is that I already know that meat is a trigger for me - red meat I avoid like the plague, and even chicken is beginning to affect me now, so I've cut right back on it. The only meat I get on with is fish. As a result, I'm a bit stuck on how to plan my diet now that I know I've got IBS. Any advice would be appreciated.