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Amy's Meals


mcle8232

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mcle8232 Apprentice

I am very discouraged. I just got my endoscopy biopsy results back and after 2 yrs on the gluten-free diet my villi are still blunted. :( I went in for the EGD because I wasn't feeling as well anymore. My migraines, fatigue, skin rash... all came back. The thing is, I am SOOOO careful!! I don't eat out at all, and cook all my own meals, except I do eat alot of Amy's gluten-free/dairy free enchilada dinners when I'm crunched for time. I heard a RUMOR that Amy's Kitchen has had some contamination problems recently. Does anyone think there's any truth to this rumor? I really really need to pinpoint my gluten source. Thanks for any advice.


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KaitiUSA Enthusiast

Is there any way you could be getting a little bit in you? Do you prepare gluten containing foods? Does your spouse eat gluten and if so do they kiss you before brushing their teeth or mouthwashing the gluten out? Are all cosmetics gluten free...lipsticks etc..? Are shampoos, soaps gluten free? I'm wondering if anything is possibly slipping in.

As for Amy's meals...I eat them all the time. I know they are made in a factory where wheat is processed but alot of brands do that and clean in between. I have not found a problem with them.

Guest nini

I eat Amy's meals all the time too and I don't have any problems with them. I think because Amy's is more vigilant about AWARENESS of food sensitivities, they are careful to avoid cross contamination.

I would think that it might be from some other hidden source of gluten, like lipsticks or lip balms or other beauty care products... or something like that.

Nadtorious Rookie

The last time I checked with Amy's, their policy was that "gluten free" meant no ingredients contained gluten, but they were prepared in the same facility as their other products. Some of the ingredient labels even state this (as well as peanuts and other allergens). Why this isn't on every one of their labels, I don't know. I haven't checked their website or called in a long time, but this is from me calling last year. They may have changed their policy. Personally I have reacted to all the Amy's products I've tried (that's why I called them), so I avoid them, but I know other people can eat them without problems.

Peace-

Nadia

skbird Contributor

I only eat the mac and cheese as all the other gluten-free Amy's foods either have nightshades (tomatoes/potatoes/peppers) or tamari (can't eat fermented tamari sauce). I ate the veggies and brown rice bowl once but had an upset stomach after, plus didn't like the taste (it had tamari in it). But the mac and cheese has never caused me any trouble, except maybe being too many carbs at one shot for me. I lived on those this winter while my kitchen was being remodelled (I scored - they were on sale at the Grocery Outlet for 99 cents each! I bought about 20!)

Stephanie

Carriefaith Enthusiast

I've never reacted to frozen Amy dinners, however, I have reacted to their gluten-free canned soups.

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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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