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

Sharp Pains From Bourbon?


Ys255

Recommended Posts

Ys255 Rookie

Looking back through the years, I remember getting quite severe stomach aches when I consumed bourbon (with coke), and this was around 5 yrs ago.

I was in my early 20's, without really understanding why I got this. 80% of the time I'd get cramps to a point I had to hunch over as it really hurt, like sharp stabbing pains and I couldn't walk much either. Being stubborn as I was, I kept at it, not understanding why I got this.

Being on a gluten free diet now, I've been looking back and this rings a bell to perhaps a reaction of some kind? I usually had beer, but maybe 10% I'd get these cramps but weren't as severe. Is there gluten in bourbon? Any ideas what was happening?


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



Celiac.com Sponsor (A8-M):



Pegleg84 Collaborator

As I told my Celiac aunt whilst sipping some whisky this weekend: if it's distilled, it's safe (she's been gluten-free longer than anyone else in my family, and said she just kind of glossed over that fact). I've been drinking a lot of bourbon lately, and aside from the usual affects of alcohol, and maybe a tad of heartburn, it causes no symptoms.

 

That said, some people are super super sensitive and still can't handle distilled gluten grain based alcohols. Also, some people just can't handle too much hard liquor (or any alcohol) in general because it is hard on the stomach in any case. If you were still consuming gluten at the time, then your gut was probably much more sensitive.

 

Another possibility is the mix: if you were always having it with coke, then your body might have not wanted to deal with alcohol and sugary-chemically stuff at once. I know I've mostly switched to drinking my liquor straight (which means drinking good stuff) since the mix is always what makes it go to my head faster. Why? Not quite sure. Something to do with the sugar, probably.

 

In any case, the majority of whisky/bourbon/rye (some bottom-of-the-barrel stuff with mash added into it at the end of the distillation might not be safe, but I couldn't tell you what brands those would be. If it looks uber cheap, it probably tastes like s$#&e anyway, so not even worth it) is perfectly safe for the majority of Celiacs/Gluten Intolerants. All I know is if it wasn't, I'd be in serious trouble.

 

Next time you're out, order a finger of it and find out. You might be one of the people who can't handle it, but you might be fine. Everyone is different. (for example, i'm fine with distilled alcohol, but after one attempt I won't go near those "gluten removed" beers, but some people are fine with those too)

 

Also, welcome to the Forum!

w8in4dave Community Regular

I don't drink but I do have a severe problem with coke. I used to drink it all the time. Becoming gluten-free I have cut back on every thng!! Especially coke, occasionally I would still have one. when I go out to eat. I thought I was being cc'd but , seems it was the coke all along. I was going shopping with a friend and she bought me a coke. I had nothing to eat or drink before we went shopping! Within a half hr. Cramps and in the bathroom I went! It was the coke. Fructose Corn Syrup. So no more Soda pop for me!! If I ever drink I will drink a gluten-free beer, or have a shot on ice maby a bit of water in it. I will not ever have another pop again. 

Archived

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

  • Get Celiac.com Updates:
    Support Celiac.com:
    Join eNewsletter
    Donate

  • Celiac.com Sponsor (A17):
    Celiac.com Sponsor (A17):





    Celiac.com Sponsors (A17-M):




  • Recent Activity

    1. - catnapt posted a topic in Related Issues & Disorders
      0

      anyone here diagnosed with a PARAthyroid disorder? (NOT the thyroid) the calcium controlling glands

    2. - catnapt replied to catnapt's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      6

      how much gluten do I need to eat before blood tests?

    3. - Jmartes71 posted a topic in Coping with Celiac Disease
      0

      Curious question

    4. - Amy Barnett posted a topic in Gluten-Free Foods, Products, Shopping & Medications
      0

      Question

  • Celiac.com Sponsor (A19):
  • Member Statistics

    • Total Members
      133,322
    • Most Online (within 30 mins)
      7,748

    avery144
    Newest Member
    avery144
    Joined
  • Celiac.com Sponsor (A20):
  • Celiac.com Sponsor (A22):
  • Forum Statistics

    • Total Topics
      121.6k
    • Total Posts
      1m
  • Celiac.com Sponsor (A21):
  • Upcoming Events

  • Posts

    • catnapt
      learned I had a high PTH level in 2022 suspected to be due to low vit D  got my vit D level up a bit but still have high PTH   I am 70 yrs old (today in fact) I am looking for someone who also has hyperparathyroidism that might be caused by malabsorption    
    • catnapt
      I am on day 13 of eating gluten  and have decided to have the celiac panel done tomorrow instead of Wed. (and instead of extending it a few more weeks) because I am SO incredibly sick. I have almost no appetite and am not able to consume the required daily intake of calcium to try to keep up with the loss of calcium from the high parathyroid hormone and/or the renal calcium leak.    I have spent the past 15 years working hard to improve my health. I lost 50lbs, got off handfuls of medications, lowered my cholesterol to enviable levels, and in spite of having end stage osteoarthritis in both knees, with a good diet and keeping active I have NO pain in those joints- til now.  Almost all of my joints hurt now I feel like someone has repeatedly punched me all over my torso- even my ribs hurt- I have nausea, gas, bloating, headache, mood swings, irritability, horrid flatulence (afraid to leave the house or be in any enclosed spaces with other people- the smell would knock them off their feet) I was so sure that I wanted a firm diagnosis but now- I'm asking myself is THIS worth it? esp over the past 2 yrs I have been feeling better and better the more I adjusted my diet to exclude highly refined grains and processed foods. I didn't purposely avoid gluten, but it just happened that not eating gluten has made me feel better.   I don't know what I would have to gain by getting a definitive diagnosis. I think possibly the only advantage to a DX would be that I could insist on gluten-free foods in settings where I am unable to have access to foods of my choice (hospital, rehab, nursing home)  and maybe having a medical reason to see a dietician?   please let me know if it's reasonable to just go back to the way I was eating.  Actually I do plan to buy certified gluten-free oats as that is the only grain I consume (and really like) so there will be some minor tweaks I hope and pray that I heal quickly from any possible damage that may have been done from 13 days of eating gluten.    
    • Jmartes71
      So I've been dealing with chasing the name celiac because of my body actively dealing with health issues related to celiac though not eating. Diagnosed in 1994 before foods eliminated from diet. After 25 years with former pcp I googled celiac specialist and she wasn't because of what ive been through. I wanted my results to be sent to my pcp but nothing was sent.I have email copies.I did one zoom call with np with team member from celiac specialist in Nov 2025 and she asked me why I wanted to know why I wanted the celiac diagnosis so bad, I sad I don't, its my life and I need revalidaion because its affecting me.KB stated well it shows you are.I asked then why am I going through all this.I was labeled unruly. Its been a celiac circus and medical has caused anxiety and depression no fault to my own other than being born with bad genetics. How is it legal for medical professionals to gaslight patients that are with an ailment coming for help to be downplayed? KB put in my records that she personally spent 120min with me and I think the zoom call was discussing celiac 80 min ONE ZOOM call.SHE is responsible for not explaining to my pcp about celiac disease am I right?
    • Amy Barnett
      What is the best liquid multivitamin for celiac disease?
    • Jmartes71
      I've noticed with my age and menopause my smell for bread gives me severe migraines and I know this.Its alarming that there are all these fabulous bakeries, sandwich places pizza places popping up in confined areas.Just the other day I suffered a migraine after I got done with my mri when a guy with a brown paper bag walk in front of me and I smelled that fresh dough bread with tuna, I got a migraine when we got home.I hate im that sensitive. Its alarming these places are popping up in airports as well.I just saw on the news that the airport ( can't remember which  one)was going to have a fabulous smelling bakery. Not for sensitive celiacs, this can alter their health during their travel which isn't safe. More awareness really NEEDS to be promoted, so much more than just a food consumption!FYI I did write to Stanislaus to let them know my thoughts on the medical field not knowing much about celiac and how it affects one.I also did message my gi the 3 specialist names that was given on previous post on questions on celiac. I pray its not on deaf door.
×
×
  • 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.