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JBaby

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JBaby Enthusiast

Based on 3 week diet experiment, my several visits to her over 2 yrs with no answers vs symptoms that came back when off diet, she feels I have celiac disease. We did blood work anyway(celiac panel). Told me they may come back negative but that doesnt mean I dont have it, just means tests are not conclusive. Advised me to get a nutritionist to help me stay on diet.... which is incredibly hard to stay on diet.


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zeta-lilly Apprentice

I'm sorry that you're having such a hard time! Look on the bright side, it could be much much worse! I'm allergic to close to 30 foods. My diet is so limited. Q-doba is a great place to get gluten free food. Wendy's chili and baked potatoes are also gluten free. You can make gluten free tacos at home. There are some decent gluten free breads out there. If you slather butter on them and grill them in a pan, you won't be able to tell much difference between a gluten free grilled cheese and a regular one. Van's waffles taste pretty close to regular waffles. Rice and corn chex are both gluten free. Amy's mac and cheese is exceptionally good. It's hard to get started because it's a change in your mind set, but I don't think it's that bad once you get used to it.

Amyleigh0007 Enthusiast

It sounds like your doctor is really on top of it. That's good. You are lucky. My main motivation to stay on the diet is my son. I must be a good example for him. It also helps me to think about how I will feel the next day if I consume gluten. I can't leave the house due to restroom issues and fatigue. Gluten just isn't worth it to me. What are your symptoms? If they are bad, that could be your motivation to stay on the diet. Also, family and friends will take your diagnosis more seriously if you don't cheat. It really isn't incredibly hard to stay on the diet. It gets easier. Good luck!

hez Enthusiast

I have two very strong reasons to stay on the gluten-free diet. My children and pain! I get very sick from cross contamination let alone a huge chunk of gluten. I stay sick for about 4 weeks. By the fourth week I am starting to feel better. Is eating gluten worth a month of my life? No. Plus there is a strong chance my kids will someday have celiac. I need to be the example, show them that my life is rich and full without gluten.

Find what motivates you and realize your health and life are worth a gluten-free diet.

Hez

ang1e0251 Contributor

It will help you to get into the mindset if you start very simply with your diet. Eat whole foods that you prepare yourself for awhile and let yourself adjust to shopping, cooking and eating in this simple way. When you feel you have it mastered, then add new foods one at a time every few days. That way you won't be overwhelmed in the market or the kitchen and you can plan ahead easily. When you are past the simple beginning stage and ready to add new foods, sit and write down the 10 most common meals you prepare. Then convert them to gluten-free. If this seems hard, come here for advice. Many of us have become a whiz at converting recipes and substituting.

It will get easier, I promise. It seems daunting to change the way you look at food but it is doable and the great benefit is the healthy way you will feel. It's no fun to live so sick that you can't remember what normal feels like!

tarnalberry Community Regular

It seems silly, but one thing that will make the gluten-free diet easier is not paying a whole lot of attention to those who think the diet is really hard. It's not hard, but it's a big, huge, gigantic *difference*. So, I would argue that it's not the diet that's hard, it's the change. If you just try to twist your current foods to not have gluten, but not otherwise change, you may find yourself frustrated. But, if you're willing to take a little more license with your notion of what makes a meal, then it can be easier.

For instance - sandwiches are made on bread, right? Yeah, but gluten free bread is expensive, and it takes a lot of trial and error to find one (store bought or homemade) that you like, so you get frustrated, "I can't have sandwiches!". Well, what if you don't use bread for a sandwich. Corn tortilla? Rice cake? Lettuce leaf? (And those are just ones I've done, there are all kinds of options out there.) It's a lot about creativity and a positive attitude towards unrestricting what labels are for food in the mind.

Of course, there is definitely a steep learning curve to the technical side. What ingredients indicate gluten? What companies label gluten ingredients? What ingredients do I have to call for? (Here's a hint - the less things you buy with ingredients, the less you have to ask these questions. ;) ) (Ooo... I think the heat wave is making me snarky... :P) Know that you'll make mistakes - we all do. Know that you'll make mistakes even after you think you're over the hump - we all do. But know that you *can*, with a lot of patience and practice, learn the nitty gritty details and minimize those mistakes.

LDJofDenver Apprentice

I agree with tarnalberry, it's really not all that hard.

The hardest thing is that gluten can be in things you'd just never suspect, like soy sauce, spices, licorice, ice cream. That and eating out.

It's a little bit of a learning curve at first, but within a couple months you'll have it down.

A couple months after my diagnosis I found these grocery guides and, man, they made a big difference.

They list mainstream products (Kraft, Heinz, Kroger, Hormel, etc.) by category (soups, chips, dressings, spaghetti sauce, etc.)

Gluten-Free Grocery Shopping Guides:

Open Original Shared Link

Open Original Shared Link

About $25 but sooooooooo worth it.

My only other tip is be aware that


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    • captaincrab55
      Imemsm, Most of us have experienced discontinued, not currently available or products that suddenly become seasonal.   My biggest fear about relocating from Maryland to Florida 5 years ago, was being able to find gluten-free foods that fit my restricted diet.  I soon found out that the Win Dixie and Publix supper markets actually has 99% of their gluten-free foods tagged, next to the price.  The gluten-free tags opened up a  lot of foods that aren't actually marked gluten-free by the manufacture.  Now I only need to check for my other dietary restrictions.  Where my son lives in New Hartford, New York there's a Hannaford Supermarket that also has a gluten-free tag next to the price tag.  Hopefully you can locate a Supermarket within a reasonable travel distance that you can learn what foods to check out at a Supermarket close to you.  I have dermatitis herpetiformis too and I'm very sensitive to gluten and the three stores I named were very gluten-free friendly.  Good Luck 
    • rei.b
      Okay well the info about TTG-A actually makes a lot of sense and I wish the PA had explained that to me. But yes, I would assume I would have intestinal damage from eating a lot of gluten for 32 years while having all these symptoms. As far as avoiding gluten foods - I was definitely not doing that. Bread, pasta, quesadillas (with flour tortillas) and crackers are my 4 favorite foods and I ate at least one of those things multiple times a day e.g. breakfast with eggs and toast, a cheese quesadilla for lunch, and pasta for dinner, and crackers and cheese as a before bed snack. I'm not even kidding.  I'm not really big on sugar, so I don't really do sweets. I don't have any of those conditions.  I am not sure if I have the genes or not. When the geneticist did my genetic testing for EDS this year, I didn't think to ask for him to request the celiac genes so they didn't test for them, unfortunately.  I guess another expectation I had is  that if gluten was the issue, the gluten-free diet would make me feel better, and I'm 3 months in and that hasn't been the case. I am being very careful and reading every label because I didn't want to screw this up and have to do gluten-free for longer than necessary if I end up not having celiac. I'm literally checking everything, even tea and anything else prepacked like caramel dip. Honestly its making me anxious 😅
    • knitty kitty
      So you're saying that you think you should have severe intestinal damage since you've had the symptoms so long?   DGP IgG antibodies are produced in response to a partial gluten molecule.  This is different than what tissue transglutaminase antibodies are  produced in response to.   TTg IgA antibodies are produced in the intestines in response to gluten.  The tTg IgA antibodies attack our own cells because a structural component in our cell membranes resembles a part of gluten.  There's a correlation between the level of intestinal damage with the level of tTg antibodies produced.  You are not producing a high number of tTg IgA antibodies, so your level of tissue damage in your intestines is not very bad.  Be thankful.   There may be reasons why you are not producing a high quantity of tTg IgA antibodies.  Consuming ten grams or more of gluten a day for two weeks to two months before blood tests are done is required to get sufficient antibody production and damage to the intestines.  Some undiagnosed people tend to subconsciously avoid lots of gluten.  Cookies and cakes do not contain as much gluten as artisan breads and thick chewy pizza crust.  Anemia, diabetes and thiamine deficiency can affect IgA antibody production as well.   Do you carry genes for Celiac?  They frequently go along with EDS.
    • rei.b
      I was tested for celiac at the same time, so I wasn't taking naltrexone yet. I say that, because I don't. The endoscopy showed some mild inflammation but was inconclusive as to celiac disease. They took several biopsies and that's all that was shown. I was not given a Marsh score.
    • knitty kitty
      Food and environmental allergies involve IgE antibodies.  IgE antibodies provoke histamine release from mast cells.   Celiac disease is not always visible to the naked eye during endoscopy.  Much of the damage is microscopic and patchy or out of reach of the scope.  Did they take any biopsies of your small intestine for a pathologist to examine?  Were you given a Marsh score? Why do you say you "don't have intestinal damage to correlate with lifelong undiagnosed celiac disease"?   Just curious.  
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