Jump to content
  • Welcome to Celiac.com!

    You have found your celiac tribe! Join us and ask questions in our forum, share your story, and connect with others.




  • Celiac.com Sponsor (A1):



    Celiac.com Sponsor (A1-M):


  • Get Celiac.com Updates:
    Support Our Content
    eNewsletter
    Donate

gluten-free Beer - What Do You Drink?


squirmingitch

Recommended Posts

squirmingitch Veteran

Both my hubs & I  have dh & the slightest amt. of gluten can set off an outbreak so we need to be extra careful. We would like to have some beer but worry about getting cc'd. What gluten-free beers have you guys tried & been okay with? I figure you will have the skinny on this question b/c if anyone is going to react, you guys will.


Celiac.com Sponsor (A8):
Celiac.com Sponsor (A8):



Celiac.com Sponsor (A8-M):



IrishHeart Veteran

Not a big beer drinker (I prefer gin)

 

but I have had: 

 

Green's

Bard's

New Planet

 

they all taste pretty good and I have never noticed a thing (except the buzz we hope for!)  :lol:

dilettantesteph Collaborator

I have tried several gluten-free beers.  I remember Greens, New Grist, Redbridge and Bard's Tale.  I think I only tried Greens and New Grist once and they didn't make me feel too good.  I have no proof that it was gluten reactions, but that is what it felt like.  According to many here there are many other things that can give you reactions that feel like gluten reactions.  Redbridge was pretty good, but Bard's Tale was the best as far as perceived reactions go.  Those guys really go out of their way to keep out cc possibilities.  Eventually I dropped that too.  I had a little sip yesterday though.

 

This is the super sensitive section and I am very sensitive.  A typical celiac shouldn't have problems with gluten-free beers.

 

Here is an article about more gluten-free beers: Open Original Shared Link

squirmingitch Veteran

Thanks IH & Steph. Steph, I am not a typical celiac. I don't get the gut & crappy feeling stuff you guys do. I have the celiac rash so if I get the slightest bit of gluten then the rash makes me pay for ---- ohhhhhh YEARS. You see, I would only know I was reacting when the rash flared & it then is depositing more antibodies under my skin which take literally years to go away. This is why I'm being ultra careful. So it looks like Bard's is the one to go with. I know about Redbridge but I just can't trust in a mega company like that, that there won't be "mistakes" --- someone forgot to clean the lines or didn't do a good job & a hundred other mishaps. To those who will say the world is full of gluten ...... fine, I understand, but that doesn't mean I shouldn't be as careful as I can be. And it looks like Bard's is the safest bet.

pricklypear1971 Community Regular

I've had Redbridge and another....without looking in the bar I can't remember. I'm ok with either. I don't really drink beer - I cook with it.

For drinking I hit the cider, wine, or Tito's. or mimosas. Or tequila, straight. Or good bourbon.

Apparently, anything but beer.

squirmingitch Veteran

I've had Redbridge and another....without looking in the bar I can't remember. I'm ok with either. I don't really drink beer - I cook with it.

For drinking I hit the cider, wine, or Tito's. or mimosas. Or tequila, straight. Or good bourbon.

Apparently, anything but beer.

 

:lol:  :lol:  :lol:

dilettantesteph Collaborator

I hope you do OK with the Bard's Tale.  I drink Metaxa Ouzo.  It's an acquired taste.


Celiac.com Sponsor (A8):
Celiac.com Sponsor (A8):



Celiac.com Sponsor (A8-M):



squirmingitch Veteran

Yes, I'm not sure I could "acquire" the taste! :lol:

Kate79 Apprentice

The best gluten free beer I've had is from a dedicated, 100% gluten-free brewery in Oregon called Harvester.  They've got several flavors and test out new ones frequently - I've had their Red Ale, Dark Ale, and IPA, as well as a few experimental flavors.  Unfortunately, they aren't widely available outside of the pacific northwest yet, but you can order online depending on the state you live in - www.harvesterbrewing.com.  It's expensive, but totally worth it if craft beers used to be your thing.

 

Green's and New Planet are my other favorites.  Both widely available and pretty tasty, with several flavors.  I also liked one called Celia that I had in New York last year.  Reminded me a lot of a Blue Moon -  I think it's only available in the northeast right now. 

 

Redbridge, Bard's and New Grist are all perfectly safe beers and widely availalbe, but in my opinion, they don't taste all that good.

 

Stay away from Omission and Daura and all the 'low-gluten' beers they're marketing these days.  Some people don't react, but a lot do - better to be safe than sorry!

MYSweetPea Newbie

I've been able to drink:

Dog Fish Head's Tweasonale - tastes like strawberry beer and

Angry Orchard Hard Ciders - Tastes like wine coolers though. 

  • 1 month later...
'lynrn Apprentice

Try omission beer. Gluten free and has all sorts of awards, even against regular beers! It is really good!

IrishHeart Veteran

Not everyone agrees with you about Omission, I am afraid.

While it tastes good (so I have heard), it is questionable about how "gluten free " it actually is.

The things I have read, leave me skeptical about its safety.

But if you have no symptoms after drinking it...cheers!  :) 

ndw3363 Contributor

I've only tried Bard's and Redbridge.  Bard's I didn't care for the taste...Redbridge is a weird story.  I started to notice that every time I had it, the next day I was an emotional wreck.  Every time!!  Didn't matter if I had one or four...didn't matter what else I ate that day (always gluten-free of course), the next day I was a mess of tears for no reason at all.  I want to try another brand, but haven't happened upon a weekend where it wouldn't matter if I was bawling all the next day.  Guess I'll stick to wine for now - been trying a couple ciders, but most are so darn sweet!!

killernj13 Enthusiast

Redbridge here but I was a Bud guy before celiac disease so I am not a beer snob at all.

 

As others stated stay away from the Daura beer which is made wiht barley but claim to remove the gluten.  Had that twice and got sick both time.

squirmingitch Veteran

We found some New Grist in our town & have been drinking that. We like it & have had no ill effects. Real beer aficionados probably would stick their tongue out at it but we weren't beer aficionados in the first place ~~~ beer always made me sick so it stands to reason right? I will say that it doesn't seem to have as much carbonation in it. It makes a nice head but the liquid itself isn't as fizzy as gluten beer. Personally that's just fine with me as I'm an odd bird who has never cared for too much carbonation in anything & that includes soft drinks. 

  • 1 month later...
becksss Newbie

You could try ciders.. They are delicious... Michelob makes one that is naturally gluten free!

notme Experienced

i was drinking redbridge, but recently tried bards and new planet.  my beer guy is going to hate me, i'm going to make him order bards and send back the redbridge.  

 

just another 'click' - the bards is nicer to my gut :)  and i like the taste better..   the new planet 'blonde' was absolutely delish but i can't find it around here.

  • 3 months later...
JoyMurphy Apprentice

This is a late weigh in, but I used to only like bards..... My new love? Glutenberg blond ale...... Omg!!!!!! I was in love! They are out of Montreal and started to import this year

dilettantesteph Collaborator

Does Glutenberg blond ale use a dedicated facility?  I haven't heard of them.

MJ-S Contributor

I've also never heard of Glutenberg beer. They claim to get 0ppm (as in zero) - that's quite a claim! According to their FAQ they are a gluten free facility: Open Original Shared Link

I'll have to see if we can get it in the Boston area.

 

This thread is timely for me because I was planning on resurrecting it too!

 

I just definitely reacted to Green's. Not a huge reaction, but definitely a reaction. I've been off gluten-free-beer all summer (cider is just more appealing to me when the weather is warm, btw I do fine with Crispin's cider). This week I decided to have a Green's. I've been ok with it in the past, but with some doubtful incidents. This time I was sure it was the Green's. I emailed the distributor who confirmed they test to 20ppm (not good enough for me) and are brewed in a regular brewery with other beers. So, sniff, I guess it's back to Bard's for me. 

 

I've also read a misconception on this forum (another thread) that Bard's is processed in a gluten-free-facility. It is not. I confirmed directly with them after the Green's incident. However, Bard's takes extra precautions to guard against cc with their raw ingredients and to super-clean their equipment. They also bypass the facility's grain handling system and test repeatedly to 10ppm. I've never noticed a problem with it, but it's been a while since I've had one.

dilettantesteph Collaborator

I thought that Bards was from a gluten-free facility too.  How did you confirm that?  I can't find it on their webpage.  I believe that I have reacted to Greens too.  Bards was better, but still a bit hit and miss so I haven't had any beer for awhile.  I looked up Glutenberg too.  I clicked on their "view the chemical analysis report" and it says 0.00 ppm gluten.  The method that was used is R5 Elisa.  It doesn't say whether it was competitive or sandwich, only the former is useful for detecting hydrolyzed gluten.  I think that the detection limits are such that there a few too many significant figures present in the 0.00 figure.  I remember working hard to teach that concept to freshman chemistry students.  This gives some information about the tests: Open Original Shared Link

 

I'm going to be in Montreal in the new year.  I think I'll look this up.

MJ-S Contributor

I emailed Bards directly and they responded right away. 

 

 

The 10ppm I read somewhere else (I think on their site somewhere?) 

I'm ok with other gluten-free products in dedicated facilities that test to 10ppm (Udi's, Namaste). I don't love the shared facility part, but I'd be comfortable going to back to Bards and trying it again. I just don't love the taste, but it's ok.

JoyMurphy Apprentice

you can get glutenberg in boston.  New England def has it.  Other areas not so much yet.   Not a fan of the American Pale Ale, but I don't like IPA and the red...it;s an aquired taste....but the Blonde....YUM!!!!!!!  And a cool oil can too!

I drove from Plymouth to Stoneham the day they got it in and cleared them out.  Now a lot of places have it.  Some restaurants carry it too.  I know there is a restaurant in JP that had a tasting dinner one night.

JoyMurphy Apprentice

daura is delicious but it gave me an instant headache...too many ppm.  

dilettantesteph Collaborator

JoyMurphy, I was posting to you in another thread where you said that you were on the Fasano diet.  I didn't think that it included alcoholic beverages.  I looked it up and it doesn't.  That may be another reason for ongoing symptoms.

Archived

This topic is now archived and is closed to further replies.


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,856
    • Most Online (within 30 mins)
      7,748

    Sonya Haskin
    Newest Member
    Sonya Haskin
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.4k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • Jillian83
      He is. Which makes everything even more difficult. I’m not a believer in “staying for the kids” but I have nowhere to go and it’s not just me, it’s me plus my babies. We live in a beautiful place, lots of land in the country and me and the kids love the place we’ve called home for their entire lives. But Im seeing that he’ll never change, that my kids deserve a happy healthy Momma, and that staying in this as is will be the early death of me. Then I look at the scars covering my entire body…this disease and the chronic stress I’ve been enduring for years that tell me I’m no longer beautiful and no one will ever look at me with interest again. I try self care, try to give myself grace so I can just start loving myself enough to gain strength but the slightest sparkle in my eye and skip in my step attracts his wrath and it all comes crashing ten fold. Life is just absolutely railing me from every single direction leaving me wanting to wave that white flag bc I don’t feel like there’s much hope no matter what happens. 
    • trents
    • Jillian83
      Hi, I was recently diagnosed with Celiac and dermatitis herpetiformis after years of suffering without answers. I lost my mind. I lost my job. I lost so much time. I lost Me. Conventional doctors are opulent come near me and the one who did sat across the room, misdiagnosed me, pumped me full of steroids which collapsed my entire hip for 6 months. So without answers I began my holistic journey. Fast forward a couple of years and still struggling with a mysterious whole body itchy, crawling “skin hell”, perfect teeth now deteriorating, thick hair now thinning rapidly and no more than a day or 2 at most relief….An acquaintance opened up a functional medicine practice. Cash only, I found a way. Within a month tests clearly showing my off the charts gluten allergy/sensitivity as well as the depletion of vital nutrients due to leaky gut and intestinal damage. dermatitis herpetiformis was more than likely what I was experiencing with my skin. I was happy. I thought this is easy, eat healthy Whole Foods, follow the diet restrictions and I finally get to heal and feel confident and like myself again very soon! 😔 Supplements are very pricey but I got them and began my healing. Which leads to the other major issue: not working, stay at home Mom of young kids, entirely financially dependent on my man of 7 plus years. He’s never been supportive of anything I’ve ever done or been thru. He controls everything. I’m not given much money ever at a time and when he does leave money it’s only enough to possibly get gas. His excuse is that I’ll spend it on other things. So my “allowance” is inconsistent and has conditions. He withholds money from me as punishment for anything he wants. Since being diagnosed, he’s gained a new control tactic to use as punishment. He now is in control of when I get to eat. He asked for proof of my diagnosis and diet bc he said I made it up just to be able to eat expensive organic foods. Then after I sent him my file from my doctor he then said she wasn’t a real doctor. 😡. I go days upon days starving, sometimes breaking down and eating things I shouldn’t bc I’m so sick then I pay horribly while he gets annoyed and angry bc I’m not keeping up with all the duties I’m supposed to be doing. His abuse turns full on when I’m down and it’s in these desperate times when I need his support and care the most that I’m punished with silence, being starved, ignored, belittled. He will create more of a mess just bc I’m unable to get up and clean so that when I am better, I’m so overwhelmed with chores to catch up that the stress causes me to go right back into a flare from hell and the cycle repeats. I’m punished for being sick. I’m belittled for starving and asking for healthy clean water. I’m purposely left out of his life. He won’t even tell me he’s going to the grocery or to get dinner bc he doesn’t want me to ask him for anything. I have no one. I have nothing. Im not better. My supplements ran out and I desperately need Vitamin D3 and a methylated B complex at the very minimal just to function….he stares at me blankly…no, a slight smirk, no words. He’s happiest when im miserable and I am miserable.  this is so long and im condensing as much as I can but this situation is so complicated and disgusting. And it’s currently my life. The “IT” girl, the healthy, beautiful, perfect skin, perfect teeth, thick and curly locks for days, creative and talented IT girl….now I won’t even leave this house bc Im ashamed of what this has dont to my body, my skin. Im disgusted. The stress is keeping me from healing and I think he knows that and that’s why he continues to keep me in that state. He doesn’t want me confident or successful. He doesn’t want me healed and healthy bc then how would he put the blame of all his problems on me? This journey has been hell and I’ve been in Hell before. I’ve been killed by an ex, I’ve been raped, robbed, held hostage, abused beyond nightmares but the cruelty I’ve experienced from him bc of this disease is the coldest I’ve ever experienced. I’ve wanted to give up. Starving and in tears, desperate…I found a local food pantry in our small town so I reached out just saying I had Celiac and was on hard times. This woman is blessing me daily with prepared gluten free meals, donations, educational info, people who know this disease and how they manage life and the blessings just keep coming. But it’s overwhelming and I feel like I don’t deserve it at all. He just glared and I know he’s going to sabotage it somehow. I don’t even know what to do anymore. I’m so broken and just want peace and healing. 
    • cristiana
      @Colleen H   I am just curious,  when you were tested for coeliac disease, did the doctors find out if you had any deficiencies? Sometimes muscle pain can be caused by certain deficiencies, for example, magnesium, vitamin D, calcium, and potassium.   Might be worth looking into having some more tests.  Pins and needles can be neuropathy, again caused by deficiencies, such as iron and B12,  which can be reversed if these deficiencies are addressed. In the UK where I live we are usually only tested for iron, B12 and vitamin D deficiencies at diagnosis.   I was very iron anemic and supplementation made a big difference.  B12 was low normal, but in other countries the UK's low normal would be considered a deficiency.  My vitamin D was low normal, and I've been supplementing ever since (when I remember to take it!) My pins and needles definitely started to improve when my known deficiencies were addressed.  My nutritionist also gave me a broad spectrum supplement which really helped, because I suspect I wasn't just deficient in what I mention above but in many other vitamins and minerals.  But a word of warning, don't take iron unless blood tests reveal you actually need it, and if you are taking it your levels must be regularly monitored because too much can make you ill.  (And if you are currently taking iron, that might actually be making your stomach sore - it did mine, so my GP changed my iron supplementation to a gentler form, ferrous gluconate). Lastly, have you been trying to take anything to lessen the pain in your gut?  I get a sore stomach periodically, usually when I've had too much rich food, or when I have had to take an aspirin or certain antibiotics, or after glutening.  When this happens, I take for just a few days a small daily dose of OTC omeprazole.  I also follow a reflux or gastritis diet. There are lots online but the common denominators to these diets is you need to cut out caffeine, alcohol, rich, spicy, acidic food etc and eat small regularly spaced meals.   When I get a sore stomach, I also find it helpful to drink lots of water.  I also find hot water with a few slices of ginger very soothing to sip, or camomile tea.  A wedge pillow at night is good for reflux. Also,  best not to eat a meal 2-3 hours before going to bed. If the stomach pain is getting worse, though, it would be wise to see the doctor again. I hope some of this helps. Cristiana    
    • Me,Sue
      I was diagnosed with coeliac disease a couple of years ago [ish]. I love my food and a variety of food, so it's been hard, as it is with everyone. I try and ensure everything I eat doesn't contain gluten, but occasionally I think something must have got through that has gluten in. Mainly I know because I have to dash to the loo, but recently I have noticed that I feel nauseous after possibly being glutened. I think the thing that I have got better at is knowing what to do when I feel wiped out after a gluten 'episode'. I drink loads of water, and have just started drinking peppermint tea. I also have rehydration powders to drink. I don't feel like eating much, but eventually feel like I need to eat. Gluten free flapjacks, or gluten free cereal, or a small gluten free kids meal are my go to. I am retired, so luckily I can rest, sometimes even going to bed when nothing else works. So I feel that I am getting better at knowing how to try and get back on track. I am also trying to stick to a simpler menu and eat mostly at home so that I can be more confident about what I am eating. THANKS TO THOSE WHO REPLIED ABOUT THE NAUSEA .
×
×
  • Create New...

Important Information

NOTICE: This site places This site places cookies on your device (Cookie settings). on your device. Continued use is acceptance of our Terms of Use, and Privacy Policy.