Does fruit make you bloated?

Natural (and/or added) sugar in the fruit can cause abdominal bloating if you have an overgrowth of candida.

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Diagnosed with ulcerative colitis spring 1999

I think I way overdid it. I had to take two phyzame and another priolosec. I have learned a lesson!

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Tabitha

100mg Azathioprine, 2 Fibercon, Colazal-9 a day (attempting to cut this down to 6 by slowly tapering), acidopholis pearls, just added Prilosec OTC

http://www.healingwell.com/donate
Co-Moderator UC Forum

I'm sorry, but for me, it is about candida. I just thought I'd toss that possibility out there for consideration. Everyone has different issues.

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Diagnosed with ulcerative colitis spring 1999

fruit doesnt seem to bother me any worse then anything else

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34 year old Male
First Flare was February 2005. Diagnosed June 2005-left-sided Colitis, suspect it has since spread. Started 4000 mg Oral Salofalk June 2005-stopped January 2007. Remission until November 2006.
Been in a flare to various degrees since November 2006 to February 2007. Currently in remission.
Presently on 0 mg Prednisone-down from 60 mg!
Nightly 4000 mg Salofalk enemas.
Daily 4000 mg Salofalk oral.
Started Omeprazole 40 mg February 2007.
Co-Moderator-UC Forum

Fruit doesn't seem to make me bloated. I eat a lot of berries, bananas, pears, apples and kiwi.

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23 years old
Diagnosed with UC March 2007

Asacol 4 tablets 3x/day

princesa, OK...(firstly, it wasn't my intention to be rude, you perceived it as rude)...now let me rephrase it so there won't be any inflection..how do you know you have yeast? Is it what you believe or did you get tested? or was it through trial and error?

Eric...I have never said i was anti-SCD...I think it's a well-rounded diet with good food intake. I suggest it often. What I don't support is people NOT eating or going on a "white" diet or bowel rest..etc.

I never suggest people need to eat grains or starches to live a healthy life. I never believed it in the '80s and I don't believe it now.
I always suggest protein and a well balanced diet. I also suggest that whole grains are a source of B vitamins...and for those who don't consume them to get their B12 checked and to possibly take a good brand multi B vitamin (not mega dosages, however).

I do say that I don't believe candida/yeast/fungus/food is a cause of UC, UC flares or will heal them. That will never change...but one might have that issue in conjunction with UC.

I do believe that if certain foods bother someone...don't eat them. Plain and simple.

It's unfortunate the both ends approach didn't work for you..treating that way (5ASA to start) is a base-line med regimen that many doctors don't even offer to their patients. I didn't say it works for everyone...but if anyone isn't on it, they should at least try it.
Of course...many are enema/suppository phobic and will avoid it like the plague, and I even believe some doctors have another motive for not suggesting it..which I don't quite understand.

I pretty much say the same things.....I don't, however, believe anyone has to read between the lines with what I have to say. You must read more of my postings to get the "well rounded" personality and suggestions of mine you're missing.

quincy

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I don't think it's the cause either. However, when your colon is in such bad shape for so long all those things can build up to where it causes major symptoms.

"Common yeast
Heavy fungal infection with the common yeast (shown) displaces good bacteria. Such heavy infections can cause dysbiosis and other intestinal disbalances. Dividing (multiplying) yeast indicates that damage is being caused to the intestinal lining. The same phenomenon is also observed in dividing Candida."

"Dysbiosis
A disturbance in the bacterial flora of the alimentary canal with resulting gut dysfunction, which may result in diarrhoea, malabsorption, or the absorbing of toxins from the gut with a wide range of symptoms. This condition is probably very common, and up to 50% of the population may be affected at some time. Effective treatment usually requires dietary manipulation to discourage the growth of pathogenic organisms, and it may also be possible to recolonize the gut with ‘friendly’ bacteria, available in the form of ‘probiotics’ such as Lactobacillus acidophilus."

http://www.parasitetesting.com/picturesofparasites/

So you see, if you research on it instead of just "beliving things" you can see a huge connection to why some people just can't get into remission with flares for such a long period of time. There is no way around it except to treat it.

Quincy, have you ever had a quality lab check for parasites/yeast? I'm not talking about local labs either.

Post Edited (Eric704) : 8/27/2007 12:11:04 AM (GMT-6)

Quincy, If you read the first sentence I made, I said I don't belive they cause UC either. I'm not suggesting you didn't research it, but when you use the word belive, I don't know what to make of it. :)

Yes, I too was like you. I didn't think I had to worry or care about having a yeast build up because I know a hardcore ammount of stress triggered my UC back when I was 16. This wasn't typical stress, and I wont get into details.. It was pretty bad though, nothing any kid should go through.

I did have the www.parasitetesting.com lab do a test to see if I did infact have any parasites. When I got the results I was surprised that they did find diving yeast (no, it's not good for you and no you shouldn't just ignore it) I was expecting maybe a bug or something, who knows. But not dividing yeast.

Now I'll tell you this. Back in last August I stopped all my meds and started the LDN (low dose naltrexone) because it's supposed to help with all kinds of auto-immune diseases. Before on my meds and such I had watery stools like 20 times a day. I got used to it for 6 years after my doc shoved every kind of prescription down my throat and I always thought it was the best option. After I stopped taking the scripts and started taking LDN I was going 4-7 times a day on the same diet I always had. I was like "wow this thing actually works I wonder how long it will take me to get into remission." Well, 6 months later and it was still at the steady pace. So I figured I got the auto-immune part taken care of maybe I have some bugs I have to kill off or something.

That brings us back to the test. I honestly think if I can get rid of the yeast/fungus build up from my colon being damaged all those years, I might finally go into remission after never being in remission once for 7 years since I got this disease.

Also, I remember my doctor showing my a colonscopy picture he was concerned about. He showed me this colorful stuff he said looked to be "pre-cancerous cells." Yeah, well first thing I thought of when I seen it was it looked like some sort of fungus build up. He also said it could just be a yeast/fungus build up but paid no attention to it and rather just focused on it being precancerous cells (which I don't belive it was.) This was 2-3 years ago.

So as you can see, once you ACTUALLY put the effort into seeing what's really in your colon with a professional lab (studies say 98%(?) of labs don't know how to test for parasites properly). I only paid $100 for the test, $25 for the kit. Well worth the money for all the information they give you. They will send it to your doctors office but I would also ask for a copy so you can research the findings on your own also.

Hope that clears some stuff up on my take on yeast/fungus (which I also chose to ignore, like you, for so long.)

Looks friendly to me. Perhaps re-read?

Well after I made my reply I tried to edit it to say "I forgot about how it started off" which was alittle unfriendly. But it ended friendly.

But that's just how forums work. One topic leads to another.