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      Frequently Asked Questions About Celiac Disease   09/30/2015

      This Celiac.com FAQ on celiac disease will guide you to all of the basic information you will need to know about the disease, its diagnosis, testing methods, a gluten-free diet, etc.   Subscribe to FREE Celiac.com email alerts What are the major symptoms of celiac disease? Celiac Disease Symptoms What testing is available for celiac disease? - list blood tests, endo with biopsy, genetic test and enterolab (not diagnostic) Celiac Disease Screening Interpretation of Celiac Disease Blood Test Results Can I be tested even though I am eating gluten free? How long must gluten be taken for the serological tests to be meaningful? The Gluten-Free Diet 101 - A Beginner's Guide to Going Gluten-Free Is celiac inherited? Should my children be tested? Ten Facts About Celiac Disease Genetic Testing Is there a link between celiac and other autoimmune diseases? Celiac Disease Research: Associated Diseases and Disorders Is there a list of gluten foods to avoid? Unsafe Gluten-Free Food List (Unsafe Ingredients) Is there a list of gluten free foods? Safe Gluten-Free Food List (Safe Ingredients) Gluten-Free Alcoholic Beverages Distilled Spirits (Grain Alcohols) and Vinegar: Are they Gluten-Free? Where does gluten hide? Additional Things to Beware of to Maintain a 100% Gluten-Free Diet Free recipes: Gluten-Free Recipes Where can I buy gluten-free stuff? Support this site by shopping at The Celiac.com Store.

Best Digestive Enzymes?
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12 posts in this topic

Okay, I take digestive enzymes before breakfast and dinner now, to deal with possible cross contamination.

Well, dinner was flounder, brown rice, carrots (in butter), and apple sauce. I took 2 enzymes before dinner, but after dinner, felt a slight blood sugar drop (I think) and a little strange in the forehead. But I didn't have any gastro symptoms, D, or other stuff I had with being glutened in the past (like the time after discovering I had celiac/NCGS that I ate breaded fish and got glutened by the bread, and had D several times in an hour). I rushed to take a bunch of L-glutamine. The symptoms began to disappear very quickly after that, though it's possible they were going to anyway, if this was caused by something else.

Do you think I was glutened somehow from CC? I'm still in the "hungry a heck of a lot" phase, so it could have been just a random sudden hunger onset (I've gotten that before without eating anything that should be glutening, like for instance, 2 hours after a normal dinner a few weeks ago. A sudden blood sugar drop and feeling strange in the forehead. It's rare).

Anyway, my digestive enzyme is AFP Peptizide. Manufacturer claims it can be used as a companion to or alternative to the Gluten-free Casein-free diet. Well, I use it to deal with CC issues. Does it help? Are there better (chewable!) enzymes I can take? I've heard GlutenEase is really good, but it's not chewable, nor in powder form.

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Ads by Google:

I can't promise you that they work just yet, but I just bought the chewable Super Papaya Enzyme Plus, and they taste good and so far (two days) I feel awesome on them. Worth checking out?

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I can't promise you that they work just yet, but I just bought the chewable Super Papaya Enzyme Plus, and they taste good and so far (two days) I feel awesome on them. Worth checking out?

I can't find info claiming that this particular product is designed to help with celiac disease. I'd try it if other people could vouch for it, or if you noticed it helped with glutenings (i.e. you knew for a fact that you accidentally ate gluten, but you took this and felt no symptoms).

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Hi Cgalley,

I don't know of an enzyme that you can take and have zero symptoms after CC. I don't think one exists currently.

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CGally - I got the papaya mixture because it has the enzymes in it that many told me help with digestion. I don't know if there is something out there to avoid all symptoms...otherwise, could we just eat wheat them? ;) But I didn't feel bad on the pill, and it's very chewable and tastes decent...I'll let you know after I've used it for a week.

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Anyway, my digestive enzyme is AFP Peptizide. Manufacturer claims it can be used as a companion to or alternative to the Gluten-free Casein-free diet. Well, I use it to deal with CC issues. Does it help? Are there better (chewable!) enzymes I can take? I've heard GlutenEase is really good, but it's not chewable, nor in powder form.

If this is being advertised as an alternative to the gluten-free CF diet I would return it and get your money back. I would not trust this drug. Your dinner sounds safe, why are you concerned with CC issues for this meal? Was it in a restaurant? If it was a homecooked meal you shouldn't need to worry about CC issues. I wonder if the daily use of enzymes before every meal isn't doing you more harm than good. There is nothing but time that is going to do away with a glutening, there are no pills that will magically remove gluten once it gets into your system.

The Papaya enzyme mentioned likely also contains papain if it is the same one I used. I took it for a while after an attack of pancreatitis when I was seeing undigested food in my stool. If you don't like to swallow pills then you can add pineapple to your meals as that will do the same thing.

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If this is being advertised as an alternative to the gluten-free CF diet I would return it and get your money back. I would not trust this drug. Your dinner sounds safe, why are you concerned with CC issues for this meal? Was it in a restaurant? If it was a homecooked meal you shouldn't need to worry about CC issues. I wonder if the daily use of enzymes before every meal isn't doing you more harm than good. There is nothing but time that is going to do away with a glutening, there are no pills that will magically remove gluten once it gets into your system.

The Papaya enzyme mentioned likely also contains papain if it is the same one I used. I took it for a while after an attack of pancreatitis when I was seeing undigested food in my stool. If you don't like to swallow pills then you can add pineapple to your meals as that will do the same thing.

Yeah, I think it's meant to be such an alternative only to those on the autism spectrum, who have a problem with gluten for different reasons. I'm on the autism spectrum myself, but just my luck that I randomly got NCGS or Celiac (without the 2 genes it's known for). I've heard Peptizyde makes things worse by breaking gluten down into smaller chunks that the immune system attacks anyway, but I assumed AFP Peptizyde was somehow different? I guess not.

I can't tell you how much I hate having no guard whatsoever against accidental glutenings. I can't take GlutenEase because it's not chewable. There's no known drug or anything you can take every day to guard against CC.

I very likely got sick from CC involving a bread crumb or something in the butter the carrots were dipped in. I can't imagine what else would gluten me, if indeed my blood sugar drop only a half hour after dinner was caused by gluten. And I did take my enzymes (2 of them, not 3 or 4) before dinner.

Is GlutenEase any good? I can't swallow pills; could it be taken in powder form? The company claims it's not "formulated to prevent celiac symptoms." But "proactively supports the gut, allowing proteins to be properly broken down and absorbed in their digested state; broadening the potential food groups a person may eat. GlutenEase may also be used by those who wish to remain on the Gluten-free Casein-free diet to ensure complete breakdown of proteins safe and effectively." Whatever that means. A small handful of testimonials say that they were able to eat gluten without symptoms.

Is anyone famliar with GlutenEase? There a similar product? Anyone here know of a digestive enzyme that has worked for you, after you accidentally consumed gluten?

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Hi again CGally,

Sorry to say it, but I think GlutenEase is just taking your money. It has not worked for me at all.

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Hi again CGally,

Sorry to say it, but I think GlutenEase is just taking your money. It has not worked for me at all.

So there really is, as yet, no known way to deal with possible cross contamination? That really sucks. I hold out hope that cures or treatments will be developed some day, but still...

Has anyone else tried any enzymes and knowingly had gluten (even a tiny amount), and vouch for if any brand works or not?

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Hi again CGally,

Sorry to say it, but I think GlutenEase is just taking your money. It has not worked for me at all.

A question: did you eat a trace amount of gluten and still get glutened, or did you try it for a normal-sized gluten food?

Supposedly DPP IV and Glucoamylase are the big things in enzymes now. Or do they only help people on the autism spectrum, and not celiacs?

Our silver bullet would probably be something that kills the gliadin.

There are people who say that enzymes do help repair damage done in the body and reduce symptoms, though. I'd love to find those types of enzymes in CHEWABLE form. It would be nice if they could help a bit. (Would I be able to break open the Glutenease capsule and just eat the powder?)

Also, if it means anything (because some say it might), I am not confirmed Celiac. I don't have the 2 genes associated with it. I may be non-Celiac Gluten intolerant. Same symptoms, of course... but apparently a different reaction. People were saying that enzymes might work for non-Celiacs. I don't know, but I hope something does.

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Also, if it means anything (because some say it might), I am not confirmed Celiac. I don't have the 2 genes associated with it. I may be non-Celiac Gluten intolerant. Same symptoms, of course... but apparently a different reaction. People were saying that enzymes might work for non-Celiacs. I don't know, but I hope something does.

Do you know what genes you do have? I would have been told I don't have celiac either if I had been gene tested before I was firmly diagnosed. There have recently been 7 other celiac related genes (most recognized as such in countries other than the US) that are now being acknowledged as celiac related here in the US. We can not go off gene testing for diagnosis.

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Do you know what genes you do have? I would have been told I don't have celiac either if I had been gene tested before I was firmly diagnosed. There have recently been 7 other celiac related genes (most recognized as such in countries other than the US) that are now being acknowledged as celiac related here in the US. We can not go off gene testing for diagnosis.

Allegedly, 95% of Celiacs have either HLA DQ2 or HLA DQ8, which I was tested for and do not have. Is the number lower than that? What are the other genes?

I do feel like while knowledge of Celiac/gluten intolerance is increasing, doctors are still not quite caught up to the newest knowledge. At my gastroentrologist's office, I was given a pamphlet on celiac disease with somewhat outdated information (i.e. that the immune system "is involved in some yet unknown way", and that "oats might or might not be acceptable"). I get the impression that even if I asked to be tested for certain genes, they wouldn't be able to test me unless they themselves knew what those genes were.

I'm going to an endocronologist later in the search for answers to both this and my constant hunger problem. I hope I get some. I don't know what kinds of answers I'd get, since I'm not sure what endocronologists do or what they might find.

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