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I Need Beer


heep70

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heep70 Rookie

Hi, I am new to the site. The doc says I have Celiac Disease. Having two issues with it. One which I have a handle on now. I like P&J sandwiches, but I have found a few good bread recipies.

Then #2. Where is the a list of Gluten free beers? I have a week spot for the harder achohol and need to stay with beer. Can anyone help me out? Would like to get it in a can if possible.

Thanks, and take care B)


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jmd3 Contributor

Redbridge by Budwiser is pretty good - but expensive. There is another I heard is pretty good too, but even more expensive - Bairds Tale

Teacher1958 Apprentice
Hi, I am new to the site. The doc says I have Celiac Disease. Having two issues with it. One which I have a handle on now. I like P&J sandwiches, but I have found a few good bread recipies.

Then #2. Where is the a list of Gluten free beers? I have a week spot for the harder achohol and need to stay with beer. Can anyone help me out? Would like to get it in a can if possible.

Thanks, and take care B)

I hadn't had a buzz in probably 10-15 years, but this past school year was so awful that I decided that I was definitely going to have a beer on the last day of school when I got home. Of course, being on the gluten free diet, I had to plan ahead, so I went to the Whole Foods Market and bought a six-pack of Bard's Tale Beer-Dragon's Gold (it even has a cool name). It's made from sorghum and is awesome! There were quite a few gluten free brands from which to choose, but that's the only one I've tried.

heep70 Rookie

I found some Redbridge. Not to bad if I must say. To bad it is pricey kinda like a micro. I t will do. I will just learn to savor it in an icy mug.

GeoffCJ Enthusiast

I have tried the New Grist Beer, and Redbridge. I like Redbridge better. It's pretty good.

I have never seen gluten-free beer in a Can. I think bottles are easier for smaller runs/batches/production.

kbtoyssni Contributor
I have tried the New Grist Beer, and Redbridge. I like Redbridge better. It's pretty good.

I have never seen gluten-free beer in a Can. I think bottles are easier for smaller runs/batches/production.

That's funny - I like New Grist better!

Guhlia Rising Star

Red Bridge by Anhueiser Busch - easy to find, tasty (picture Heineken mixed with Sam Adams and Sierra Nevada), priced the lowest

Bard's Tale - Dragon's Gold - the best IMO, harder to find, very pricey

New Grist by Lakefront - a lighter beer, harder to find, very pricey

Romapo Valley has a gluten free beer - never tried it, couldn't find it

There are a few more, but they're very hard to find. So long as you don't live in PA, you should be able to find Red Bridge at your local super Walmart or grocery store. The others are much harder to find. Red Bridge is the best priced as well. I'm sure Tom will pop up with some input as well. :) (Hi Tom!)


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  • 2 weeks later...
Piesmom Apprentice
Hi, I am new to the site. The doc says I have Celiac Disease. Having two issues with it. One which I have a handle on now. I like P&J sandwiches, but I have found a few good bread recipies.

Then #2. Where is the a list of Gluten free beers? I have a week spot for the harder achohol and need to stay with beer. Can anyone help me out? Would like to get it in a can if possible.

Thanks, and take care B)

heep70-

My husband likes Red Bridge, but also New Grist by Lakefront Brewery (out of Milwaukee).

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    • 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.  
    • rei.b
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