Newly Diagnosed UC After Having My Head in Sand for Years


I’ve had colitis symptoms most of my adult life, but only in the last year has a massive flare-up with blood and so many near-misses almost crapping my pants made me go and seek medical help. I’m glad I did.

What is different about me is that I’m over-weight. This seems out of the ordinary as most Cronhs/Colitis sufferers seem under weight, especially when at the conditions worst.


Hi. I’ve degrees of ‘runny poo’ for most of my adult life, in fact I can remember running out of University exams cross-eyed and in a cold sweat! Years later I’m now in my mid thirties, and things got a whole lot worse for me. In the first half of 2010 I noticed the first signs of blood in my stool. Very light red in colour and sort of weepy. Anyway being a guy I ignored it of course and figured it would go away. Well it didn’t, and reading the stories of you all on this site I can identify with what you all have been through, because I have gone through it now too. The blood got darker and more frequent. There was upwards of 6-8 bowel movements a day. Feeling like you urgently have to poo straight after pooing! So nearly crapping my pants that many times now. I would emerge from the bathroom clammy and pale. Time to see the doctor.

I’ve been to GP and then the Gastroenterologist. I’ve had the colonoscopy and saw the photos. Ulcerative colitis all up the left hand side of the colon. I was shocked at what I saw and even more so to learn that according to modern medicine, the condition is ‘curable’ totally only by having a colectomy!!!!

But it is treatable. I’m on the drugs now, and they are working. So far it’s going really well. i’m on a declining dose of cortico-steroid prednisolone, and am taking Salofalk Mesalazine tablets 4g daily. The steroid is a sucker punch for the inflammation and the mesalazine to treat the condition. My Gastro says the mesalazine is long term and at this stage has no plans to take me off it.

I’ve heard it’s not good for your kidneys, ad i notice I have to pee real bad during the night. I guess I would like to be off it long term, and have read with much interest the experience of others on the SCD diet. I have actually done a similar diet to this to lose weight in the past. Interested to know

Very interesting to report that the Gastro has no confidence that any dietary approach can treat the illness. He says I need to eat ‘low-residue’ diet – low in fibre etc. Great so eat McDonalds and pop my pills and all will be cool.

I’m going to try SCD and I’m really interested to know the stories of others on this eating plan. I think I can make it work and if it gets my mesalazine dose right down if not to nothing then I’ll be sweet. But please dont get me wrong, compared to just a few months ago – man I’m cruising!



PS Adam – I make your shakes about 3 times a week and really enjoy them :-)


Medications: As I said, I’m on mesalazine and at the moment on 30mg prednisolone.


Bennett’s story is now entered into the 2011 Ulcerative Colitis Writing Contest!!! You Can Join too, click here for details

3 thoughts on “Newly Diagnosed UC After Having My Head in Sand for Years”

  1. Hi Bennett,
    I’m glad you’re on your way to feeling better. My husband was diagnosed with UC in September 2010 and he messed with Asacol and Rowasa for about 3 months, then had a colonoscopy that showed widespread colitis sohis GI doc wanted to put him Imuran and Pred. Neither of us could stomach the thought of these drugs. Instead, together we decided to try the SCDiet. Within the first five days on the diet, his symptoms were completely gone, and he is medication free. We’re 64 days in, and we’ve definitely had our ups and downs, but it’s worth trying for sure. We are documenting our journey on a blog: Good luck!

  2. Sadly the diet did not work for me at all. 6 months the first time and 4 months the second time was the duration. My doc finally said to not do it anymore.

    Its so frustrating to see that it works for so many and does not affect me whatsoever it seems.

    1. Hi Erin,

      From what I can see everyone is different it seems! It’s unfortunate you have not had the success of others. I showed the diet plan to my mum, she is a GP. She thinks that although it might help, it doesn’t address the cause of the problem, that is the inflammation caused by the immune system. I have yet to try it myself, but think it’s worthwhile having a go.

      Most important to listen to your Doctor I guess.

      Best of luck, hope you’re feeling better before too long.

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