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Is There Such A Thing As Mild celiac disease


jacobsmom44

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jacobsmom44 Newbie

I was diagnosed with celiac disease last month. I am doing ok, but not completely gluten-free yet. It all started when I joined Weight Watchers and started eating whole wheat and whole grains. I started getting stomach-aches. After being diagnosed, I gave up the wheat products and started feeling better. I have always had gastro problems but my doctor said it was Irritable Bowel. I don't feel like I get sick when I cheat. From what I read on some of these posts, people get horribly sick from "just touching bread". I can't say that has ever happened to me. The GI Doctor did a scope and he says he is 90% sure it is celiac disease, but why doesn't some of the foods bother me? Is it still going to hurt me in the long run if I continue cheating (even if it doesn't bother me)?

I need help?


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CarlaB Enthusiast

There is no such thing as mild celiac. You either have it or you don't. Even if you don't feel symptoms, you are causing damage to your intestines every time you consume gluten, even if it's a small amount. Typically, the longer you are off it, the more you feel it when you accidentally consume some. So, even though you don't feel it now, once you haven't eaten it in a while, you probably will start noticing, especially as your gastro problems start clearing up. Think of it like smoking, a smoker might have bad general health, so stops smoking. At first he notices no difference, but after a few months off it, even a single cigarette might make them ill. It's the same way with gluten.

Welcome!

AndreaB Contributor

If you have been diagnosed with Celiac (and it sound like you have), then you need to be 100% gluten free for life. Wheat, rye, barley and oats (unless you buy the exp uncontaminated kind) free. There are people who don't have obvious symptoms (and some are on this board) but are still doing damage. I am one that didn't have any obvious symtpoms before going gluten free. Now I get some stomach and intestinal distress until it clears my system, usually a day.

Also be sure to check you personal care products, including make up. You'll need your own toaster (if you toast gluten-free bread), your own non stick pan (if you use them, Stainless steel is ok), new colander. Basically, plastics and non stick pans cause the problems in the kitchen.

There is a learning curve to this diet. The most important is the food, then work your way through the list. Some of the quickness of getting through it depends upon the funds available to replace stuff. This forum is a great place to learn from a lot of people's experiences.

Welcome. :D

2kids4me Contributor

Each person will have different outward symptoms, some mild, some horrible and immediate. BUT all celiacs suffer the same internal damage - flattening of the villi, inflammation,and impaired absorbtion.

I have 2 children - one may experience some joint pain or mild stomach ache if he gets a big "gluten oopsie" (oopsie poopsie :o )

the other child gets severe migraines, neck, back pain and stomachache with nausea - within hours of even a teensie bit of gluten.

and guess what - the child with the most damage to the small intestine - was the one with the least outward symptoms (totally flat on all biopsies and visually the GI doc diagnosed celiac before the pathology was back).

This child was only checked cause he was diabetic and sibling was diagnosed celiac.

Do not rely on outward symptoms.

eKatherine Apprentice
Each person will have different outward symptoms, some mild, some horrible and immediate. BUT all celiacs suffer the same internal damage - flattening of the villi, inflammation,and impaired absorbtion.

Some people with severe intestinal damage may have no symptoms whatever, while some people actually don't get any intestinal damage. They may just wake up one day and find that they have neurological problems which prevent them from leading a normal life, and they may never recover.

mouse Enthusiast

I hope you decide to go completely gluten-free. There is not just a little gluten-free. You might find yourself with some auto-immune diseases that you do not want, somewhere later in life. My understanding is that a small amount of gluten will require 3 to 4 weeks of recovery time in your small intestine. The diet is really not that hard, once you get over the learning curve. I do most of my shopping in a regular grocery store. I go to the health food store a couple of times a month for things I cannot get in the grocery store. I also eat out several times a month. I am just very careful where I eat. This is really all very doable and well worth the extra effort. Good luck.

Mandy F. Apprentice

I think I fall into a similar category as you. I had no real symptoms before being diagnosed and for a couple of months afterward, I went sort of gluten free. I decided one day to test the daignoses and stayed completely gluten-free for 3 weeks and was extrememly careful. At the end of the 3 weeks, I had some powdered donuts (I really miss those... :rolleyes: ) and within 30 minutes, I was so exhausted that I could hardly move. Now, if I get glutened, I might have some gastric symptoms, but I'll know for sure when I get the sudden energy drain... Following the diet usually isn't really that bad. I'm still in the learning stages, but for the most part, I don't have any major problems. There are a lot of really good substitute foods and if you skip the substitutes, you're left eating a healthy well-balanced meal. Good Luck!


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    • trents
      Not necessarily. The "Gluten Free" label means not more than 20ppm of gluten in the product which is often not enough for super sensitive celiacs. You would need to be looking for "Certified Gluten Free" (GFCO endorsed) which means no more than 10ppm of gluten. Having said that, "Gluten Free" doesn't mean that there will necessarily be more gluten than "Certified Gluten" in any given batch run. It just means there could be. 
    • trents
      I think it is wise to seek a second opinion from a GI doc and to go on a gluten free diet in the meantime. The GI doc may look at all the evidence, including the biopsy report, and conclude you don't need anything else to reach a dx of celiac disease and so, there would be no need for a gluten challenge. But if the GI doc does want to do more testing, you can worry about the gluten challenge at that time. But between now and the time of the appointment, if your symptoms improve on a gluten free diet, that is more evidence. Just keep in mind that if a gluten challenge is called for, the bare minimum challenge length is two weeks of the daily consumption of at least 10g of gluten, which is about the amount found in 4-6 slices of wheat bread. But, I would count on giving it four weeks to be sure.
    • Paulaannefthimiou
      Are Bobresmill gluten free oats ok for sensitive celiacs?
    • jenniber
      thank you both for the insights. i agree, im going to back off on dairy and try sucraid. thanks for the tip about protein powder, i will look for whey protein powder/drinks!   i don’t understand why my doctor refused to order it either. so i’ve decided i’m not going to her again, and i’m going to get a second opinion with a GI recommended to me by someone with celiac. unfortunately my first appointment isn’t until February 17th. do you think i should go gluten free now or wait until after i meet with the new doctor? i’m torn about what i should do, i dont know if she is going to want to repeat the endoscopy, and i know ill have to be eating gluten to have a positive biopsy. i could always do the gluten challenge on the other hand if she does want to repeat the biopsy.    thanks again, i appreciate the support here. i’ve learned a lot from these boards. i dont know anyone in real life with celiac.
    • trents
      Let me suggest an adjustment to your terminology. "Celiac disease" and "gluten intolerance" are the same. The other gluten disorder you refer to is NCGS (Non Celiac Gluten Sensitivity) which is often referred to as being "gluten sensitive". Having said that, the reality is there is still much inconsistency in how people use these terms. Since celiac disease does damage to the small bowel lining it often results in nutritional deficiencies such as anemia. NCGS does not damage the small bowel lining so your history of anemia may suggest you have celiac disease as opposed to NCGS. But either way, a gluten-free diet is in order. NCGS can cause bodily damage in other ways, particularly to neurological systems.
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