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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 Celiac.com's FREE weekly eNewsletter   What are the major symptoms of celiac disease? Celiac Disease Symptoms What testing is available for celiac disease?  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 What if my doctor won't listen to me? An Open Letter to Skeptical Health Care Practitioners Gluten-Free recipes: Gluten-Free Recipes
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willabec

Yellow Stool

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Anyone out there have celiac disease as well as loose, yellow stools? i have them about once a week and i can't seem to figure out why, if it was something i ate at some point??

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Anyone out there have celiac disease as well as loose, yellow stools? i have them about once a week and i can't seem to figure out why, if it was something i ate at some point??

Pale yellow, greasy, foul-smelling stool: malabsorption of fat due to pancreatic insufficiency, as seen with pancreatitis, pancreatic cancer, cystic fibrosis, celiac disease.

Keep a food diary and document everything that goes in your mouth. Check your meds, vitamins, shampoos, lipstick, shaving cream and lotions.

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Yep. I've been having this problem since January. Sometimes it is just loose but many times I have D, there is undigested fat and and very malodorous. There has been times I have barely made it to the bathroom. In Feb. I had a gallbladder ultrasound (normal) and Hida scan (suboptimal but above the sugical thrrshold), some stool testing in March for parasites/pathogens (normal), and a repeat EGD and biopsy in April (esophagitis, gastritis, stomach ulcer but normal small biopsy this time). I went dairy free thinking it was causing my symptoms and also cracked down on potential CC. I got worse. I definately am not digesting fats well. Avocados and the almond milk will really set me off as well as anything greasy or fried. On my last visit I tried a trial of welchol to control the diarrhea. It helped some but not enough to care. The GI also suggested that I may have a pancreas problem because of the fat in the stool. I'm supposed to call back and let him know about the welchol. I also decided on my own to try some digestive enzymes. They helped more than the welchol (although I was not able to take it exactly as prescribed because of the drug interacting with my thyroid meds), but I ran out and I'm waiting on them in the mail. I think the reason I'm not digesting fats is because of my dysfunctional gallbladder. However the doctor said he thinks I would be hard pressed to find a surgeon to take it out when it is working at 48% when the threshold for surgery is 35%. He did say he likes to see the function at least 50%. I do have RUQ discomfort, but never severe pain. It's more of a pinching/pulling sensation that is very annoying. I'm going to go really low fat for awhile and see how I react. If I still have problems I may go in for more testing/surgical consult. I'm getting very discouraged by all this, tired and a sore butt! :lol:

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Pale yellow, greasy, foul-smelling stool: malabsorption of fat due to pancreatic insufficiency, as seen with pancreatitis, pancreatic cancer, cystic fibrosis, celiac disease.

Keep a food diary and document everything that goes in your mouth. Check your meds, vitamins, shampoos, lipstick, shaving cream and lotions.

i have tried the food diary, but i cannot figure out what the culprit is...about how long do you think it takes to eat something and then have it reek havoc on your system? for example...today was a bad day...yellow, frothy and very, very loose and went 3 times after lunch within a two hour time span....thoughts?

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Yep. I've been having this problem since January. Sometimes it is just loose but many times I have D, there is undigested fat and and very malodorous. There has been times I have barely made it to the bathroom. In Feb. I had a gallbladder ultrasound (normal) and Hida scan (suboptimal but above the sugical thrrshold), some stool testing in March for parasites/pathogens (normal), and a repeat EGD and biopsy in April (esophagitis, gastritis, stomach ulcer but normal small biopsy this time). I went dairy free thinking it was causing my symptoms and also cracked down on potential CC. I got worse. I definately am not digesting fats well. Avocados and the almond milk will really set me off as well as anything greasy or fried. On my last visit I tried a trial of welchol to control the diarrhea. It helped some but not enough to care. The GI also suggested that I may have a pancreas problem because of the fat in the stool. I'm supposed to call back and let him know about the welchol. I also decided on my own to try some digestive enzymes. They helped more than the welchol (although I was not able to take it exactly as prescribed because of the drug interacting with my thyroid meds), but I ran out and I'm waiting on them in the mail. I think the reason I'm not digesting fats is because of my dysfunctional gallbladder. However the doctor said he thinks I would be hard pressed to find a surgeon to take it out when it is working at 48% when the threshold for surgery is 35%. He did say he likes to see the function at least 50%. I do have RUQ discomfort, but never severe pain. It's more of a pinching/pulling sensation that is very annoying. I'm going to go really low fat for awhile and see how I react. If I still have problems I may go in for more testing/surgical consult. I'm getting very discouraged by all this, tired and a sore butt! :lol:

what digestive enzymes are you taking?

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i have tried the food diary, but i cannot figure out what the culprit is...about how long do you think it takes to eat something and then have it reek havoc on your system? for example...today was a bad day...yellow, frothy and very, very loose and went 3 times after lunch within a two hour time span....thoughts?

As you travel through the gluten free lifestyle, you will notice that your reaction time will vary. That makes it very difficult to pin point and issue. And sometimes, you never know. And everyone is different. You will learn your own clock, once you are healed.

You may be one who reacts to the slightest bit of cross contamination...at home, work or elsewhere.

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As you travel through the gluten free lifestyle, you will notice that your reaction time will vary. That makes it very difficult to pin point and issue. And sometimes, you never know. And everyone is different. You will learn your own clock, once you are healed.

You may be one who reacts to the slightest bit of cross contamination...at home, work or elsewhere.

well, i was diagnosed 8 years ago and on the gluten-free diet since then...i just don't know why the past 1-2 years "things" have gotten like this....it is making me nervous!

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what digestive enzymes are you taking?

Nature's Sources, AbsorbAid, 600 mg

Description

Family of Plant Enzymes

Aid for Digestion & Stomach Distress

Clinically Tested/Scientifically Proven

A Dietary Supplement

Suggested Use

Take 2 capsules with each meal. (More should be used by individuals with compromised digestive systems.) When you experience occasional indigestion, or for nighttime discomfort, open 2 capsules and mix in 2-4 oz of room temperature water.

Supplement Facts

Supplement Facts

Serving Size: 2 Capsules

Servings Per Container: 120

Amount Per Serving % Daily Value*

Calories 5

Total Carbohydrates 1 g <1 % *

AbsorbAid enzyme blend **

Lipase, Amylase, Protease [from Bromelain,] Cellulase, Lactase.

* Percent Daily Values are based on a 2,000 calorie diet.

** Daily Value not established.

Other Ingredients

2 capsules provide-Lipase (381 FIP), Amylase (2772 SKB/DU), Protease [from Bromelain] (12 GDU), Cellulase (99 CU), Lactase (300 ALU)

Vegetarian Capsule (HPMC and Water), Rice Starch, Plant Cellulose, Silicon Dioxide, and L-Leucine.

Contains no corn, sucrose, wheat, gluten, yeast, dairy, soy, preservatives, artificial colors or flavors.

Warnings

Keep in a cool dry place. Do not refrigerate. Keep container free of moisture. Heat destroys enzymes.

I have been taking Nature's Sourse Absorbaid. I found these at my local health food store. I did not want one with the betaine HCL or pepsin because I did not know if it would aggrivate my ulcer. So I got this one instead and it seemed to help some. At least the watery stool was gone. I still have soft yellow stool, but at least I'm not going all the time. I may look for one that has ox bile in it and see if that helps any better. I'll wait until I finish this new bottle. I'm also going to ask the doctor if if the betaine or pepsin would hurt me to take now since most of the digestive enzymes supplements with ox bile have the betaine or pepsin in it.

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    • The reason I think it was the shampoo? Process of elimination. Our house is almost entirely gluten free (except for this shampoo which slipped through the cracks until I read the ingredient label). My husband has bread that he eats at lunch, but he practices something that resembles aseptic technique from the lab when he's making his sandwiches. He's been doing this for years now and I've never been glutened from within my home. The previous week I hadn't eaten out, I cooked all my food, I don't eat processed food and I never eat something from a shared facility.  Usually if I get glutened it's a single dose sort of thing and it follows a very predictable course, to the point where I can estimate when I got glutened within 24 hours of when it happened. However, this time, I was feeling achy and arthritic and moody for about a week before it got bad enough for me to recognize it as the result of gluten exposure, at which point we went searching and found the shampoo (and conditioner, which does leave more of a residue than shampoo), which he immediately stopped using. Within three days I was feeling back to normal (which is the usual course for me).  Sure, it could have been something else, but I know how sensitive I am, and, as silly as it sounds, it was the only thing that made sense. The other thing you said: You're correct, mine was not a rock solid celiac diagnosis, but I have no doubt that gluten is the problem. I was SICK. I went through two different gluten challenges in an effort to get a more straightforward diagnosis during which I was a barely functioning human being. Consuming gluten may not have given me blunted villi or elevated antibodies, but it did inflame my gut, and actually started to damage my liver. If you look at my diagnosis thread, I had elevated liver enzymes, which have been correlated with celiac disease in the past. There was no alternative explanation for the liver enzymes, he checked EVERYTHING.  I too am a scientist and I have spent a lot of time with the literature trying to make sense of my condition.  https://www.ncbi.nlm.nih.gov/pubmed/26150087 I also have no doubt that gluten was damaging my intestines in some way, as any prolonged gluten exposure in the past has inevitably been followed by a severe FODMAP intolerance that goes away once I've eliminated the gluten and given myself a month or so to heal.  I also had a very fast diagnosis following the onset of symptoms (~1 year) so it's possible that the disease never had a chance to manifest as full celiac. I wasn't willing to eat gluten long enough to find out. As a result of my diagnosis, hazy as it was, I am *meticulously* gluten free. It is not a fad for me. I don't occasionally cheat. It is my life, for better or worse. All of that being said, I'm not sure what my diagnosis has to do with your question. You say you're not trying to be rude, but when you bring up my diagnosis in a thread that has nothing to do with diagnostics, it seems like you're trying to undermine the validity of my disease or the validity of my input in this forum. If I'm being hypersensitive, I apologize, but that's how you came across on my end. I'll admit that the fact that my diagnosis wasn't more straight forward does make me a bit defensive, but I promise that even if I didn't have a solid diagnosis, I interact with the world as though I did, and I'm not out there giving people the wrong idea about celiac disease by not taking it seriously. If there was a connection between your question and my diagnostics that I missed I would appreciate you giving me the chance to better understand what you were asking. 
    • I am just curious.  As a scientist (and I am not trying to be rude), how can you determine if hydrologized wheat protein from your husband’s shampoo was actually the culprit?  If I recall at your diagnosis, you were seronegative, Marsh Stage I, gene positive,  but your doctor still  suspected celiac disease.  You improved on a gluten diet.  Other than observation, how do you really know?  Could it not be something else that triggered your symptoms?   I firmly believe that even trace amounts of gluten (under 20 ppm), can impact sensitive celiacs.  But traces of a protein within a shampoo from someone else’s hair that was rinsed?    
    • I also can't have dairy but through a series of experiments and a lot of research I think I've pinpointed my problem. It may or may not be the same for you, but I thought I'd share.  There are two kinds of beta-casein protein A1 and A2. We'll call A1 "bad casein" and A2 "good casein". The two proteins differ only in a single amino acid, but this is enough to make it so that they are processed differently in your guy. Bad casein is actually broken down into a casomorphin, which is an opioid peptide. That does not mean that milk gets you high, or is as addictive as heroin, or anything like that, it just means that it can interact with opioid receptors (which the gut has a bunch of). It's worth noting that opioids cause constipation due to their interaction with the opioid receptors in the gut, and that a lot of people feel like cheese and dairy slow things down, but any connection between the two is pure speculation on my part at this point.  Now here's where things get weird. The vast majority of milk cows in the western world are derived from Holstein-like breeds, meaning black and white cows. In a few select places, you'll see farms that use Jersey-type cows, or brown cows (Jersey cows produce less milk than Holsteins, but many connoisseurs feel it's a higher quality milk, particularly for cheese).  Holstein-like cows have A1 and A2 casein (bad and good), however, Jersey-type cows only have A2 (good casein), unless their genetic line involved a Holstein somewhere in the past, which does happen.  A company in New Zealand figured out how to test their cows for these two genes, and selected their herd down to cows that specifically produce ONLY A2 (good) casein. You might have seen it in the store, it's called A2 milk. Some people have had a lot of luck with this milk, though it still doesn't solve the problem of cheese.  I have suspected, due to trial and error and a few accidental exposures, that I have a problem with A1 casein, but not A2. In line with this: I am able to eat sheep and goat dairy without any difficulty, so at least I can still enjoy those cheeses! I am also fortunate because I'm apparently not too sensitive, as I can still eat cow-milk butter. The process of making butter removes *most* (read: enough for me) of the casein.  However, if I eat cow cheese or a baked good with milk, I get really sick. It's a much faster reaction than if I get glutened. Within minutes I'm dizzy and tired and my limbs are heavy. I have to sleep for a couple of hours, and then, over the next couple of days, I'm vulnerable to moodiness and muscles spasms and stomach upset just as though I'd been glutened (though the brain fog isn't as bad). I actually haven't tried A2 milk yet, mostly due to lack of availability (and motivation, I don't miss milk, I miss CHEESE). However, last year, when I was getting ready to go on a trip to Italy, I had a thought. Once, in the recent past, when I'd been testing dairy, I'd had a slice of parmesan cheese. Miracle of miracles, I was fine. I didn't feel a thing! I was so excited that I ran out and got some brie to eat as a snack. That did not go so well... Turns out parmigiano reggiano is made from the milk of the Reggiana variety of cow which is, you guessed it, a brown cow (they say red). I did a little more research and found that dairies in Italy predominantly use brown cows. So I decided to try something. As some of you may know, Italy is something of a haven for celiacs. It's one of the most gluten-free friendly places I've ever been. You can say "senza glutine" in the smallest little town and they don't even bat their eyelashes. You can buy gluten free foods in the pharmacy because they're considered a MEDICAL NECESSITY. If travelling-while-celiac freaks you out, go to Italy. Check out the website for the AIC (Italy's Celiac society), find some accredited restaurants, and GO NUTS. While I was there, I decided to see if I could eat the dairy. I could.  Friends, I ate gelato Every. Single. Night. after that. It was amazing. Between the dairy being safe for me and the preponderance of gluten free options, it was almost like I didn't have dietary restrictions. It was heaven. I want to go back and never leave.  So that's my story. Almost too crazy to believe.  TL;DR: Black and white cows make me sick, brown cows are my friends.
    • I'm a scientist, and I did a little research into the study. Looks valid and it was published in a respected journal.  http://www.gastrojournal.org/article/S0016-5085(17)36352-7/pdf The science looks solid. As someone who didn't have a super clean cut diagnosis before going gluten free, I'd love to see something like this become available. Then again, there's no doubt in my mind that I can't have gluten, so any additional testing would be purely academic. But like I said, I'm a scientist. I can't help myself. 
    • Update: I have tried calling the company several times and have emailed twice. I have yet to talk to a person on the phone and no one has emailed me back.    I did a little research and they were are already involved with a class action lawsuit about being labeled as salt free and one of the first ingredients is sodium chloride.  I am done with this shampoo because this whole company seems a little shady now! 
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