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Pancreatine vs Peptizyde

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Peptizyde starts doing its stuff in the stomach (which is what many of these

kids need), Pancreatin does it fiurther on the process, I beleive they are

usually enteric coated to get through the stomach, they can;t be crushed or

emptied like a pep foe ease of use for those not swallowing caps, you need to

use more pancreatin, so is it really cheaper and my sons stool qulaity was

damned near 'pefect' after 10 days of Pep which 3 years of everything else had

not touched :)

Try them and you'll see the difference :)

Mandi in UK

I would like to know why Peptizyde is a more effective enzyme for

autists than animal enzymes like Pancreatine, which are much cheaper

and much more powerfull *in improving stool quality* than Peptizyde.

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Hi

I would like to know why Peptizyde is a more effective enzyme for

autists than animal enzymes like Pancreatine, which are much cheaper

and much more powerfull *in improving stool quality* than Peptizyde.

Thanks in advance!

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Which other enzymes had you tried first? We have had no success so

far with enzymes. I have a cow's milk protein intolerance and saw no

difference, and there was no difference in my son's stool consistency

either. My daughter has an egg intolerance (which I believe is

presenting as mucus in her stools), and there was no change in that

either. As a matter of fact, they have complained of stomachache far

more on the enzymes.

nat

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>

> Which other enzymes had you tried first? We have had no success so

> far with enzymes.

Enzymes did not help my son with all foods. You might try removing

the foods you KNOW are problems, see if you notice any difference.

If your child has a yeast issue, that can interfere with what you

notice regarding enzymes.

>>My daughter has an egg intolerance (which I believe is

> presenting as mucus in her stools), and there was no change in that

> either.

Mucus in the bm was yeast for my kids.

Dana

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Honestly I am totally confused. I am going to take a break with the

enzymes for a week or so, and restart with the Houston enzymes.

We have been GF/CF for several months (son has positive

transglutaminase and endomysial IgA, daughter with presumed gluten

sensitivity and definite egg intolerance, which we just discovered,

and is in all of her GF/CF food substitutes), with occasional

transgressions with the CF part. After I started the enzymes they

both complained of stomachaches, and one day my son had pure diarrhea

(no odor, though). Then my son had a stool that looked like he had

gotten " glutened " , and my daughter continued to have mucus strands in

her bms. I couldn't tell if it was from the enzymes, from the dairy

that we reintroduced, from their guts still going through the healing

process--which can take up to two years from going gluten free--or if

it could be yeast die-off/bacteria die-off, or do they have parasites

that have not been diagnosed through the stool tests we have done?

It's difficult to tell because one of my children (my daughter) had

intermittently complained of stomachaches before I even started the

enzymes. Of course I also realize at some point I started a new

probiotic without regard to trying one new thing at a time.

Aaaack!! At this point I am seriously considering seeking out a

psychic's help. :)

And sadly, I know that I cannot seek out a GI's help, because I know

they are going to suggest scoping, which I prefer not to do, since

the outcome would probably just show inflammation in their intestines

or colon, with the suggestion of anti-inflammatory drugs.

I greatly appreciate all of your help. Without this message board, I

would never have even considered yeast die-off as a possibility.

nat

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