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

Any Other Sober Celiacs?


brooklyngal

Recommended Posts

brooklyngal Rookie

Hi all. Just wondering if there are any other celiacs here who don't drink – what do you do for fun? Sometimes I feel like all I can do is go to coffee shops!


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



Celiac.com Sponsor (A8-M):



kareng Grand Master

Bowling. Picnics. Walks. Kayaking. Movies. Places that play music - you don't have to drink. Juice shops. Play pool. Swimming. Fishing. Boating. Rent a paddle boat or board at a local lake. You can go to bars to socialize and dance.

bartfull Rising Star

Get a dart board and start a league with your friends. We used to play at a different person's house every week and the winning team won the right to wear the "Citizen Dart" t-shirts for a week. (And if you felt mean you could bring it back the following week without washing it first!)

 

If darts isn't your thing you could choose another game. Make it a party but make sure any food is gluten-free.

BlessedMommy Rising Star

I don't drink and never have--my religion forbids it. 

 

There's lots of stuff to do for fun! Today we went canoeing and tomorrow we're taking the kids to the water park.

GF Lover Rising Star

I don't understand why your social life would be limited by not drinking.  That's like a celiac not doing anything because they can't eat some of the food.  All establishments that sell alcohol also sell soda etc.  I went to a golf tournament today and there were many people drinking.  I didn't.  There was no problem and I would never consider not going because someone there might be drinking.  

 

Being Celiac and being Sober are very similar.  Both can be self limiting if you let it.  Your health depends on making good health decisions with any disease, condition, sickness etc. Be confident in yourself that you will make the appropriate decision if and when the time comes that you are temped.  This is about your health....nothing more, nothing less.  

 

Don't be upset by my comments.  I know well of the subject to which I speak.

 

Colleen

LauraTX Rising Star

I am a Celiac who doesn't drink.  I was never a big drinker, I just view it as unnecessary to me having a good time.  So I designated drive people when drinking is involved.  If we go to a bar, I get soda... if we are at a restaurant, I get something nice and talk the drinkers into paying for it.  But that is not a frequent happening, maybe once or twice a year.  If you are a recovering alcoholic who purposefully avoids tempting situations, then that is another thing.  But since you have not indicated that, I agree with GFLover/Colleen in that it should not be limiting of what you do.  I will go out to a nice restaurant that already has a wine glass at each spot, and when they ask what you want to drink give them your order and say "We won't be having any alcohol tonight"  to save them the spiel.  

 

I do avoid situations where there are rowdy crazy drunk people and/or there is drug use, because those are things I don't feel comfortable being around.  So, I like rock music, but don't go to the concerts.  I also have terrible asthma and can't hang out anywhere people are smoking, but with many laws nowadays there are few places that applies to.  But there are plenty of other things to do.  All of the ideas listed above are good ones.  I like to have people over to my house and just hang out, we have a single male friend and I like to make him a good home-cooked meal every so often since his family is far away.  You can volunteer, too... just pick something in an area you enjoy.

user001 Contributor

I don't even go to coffee houses because I can't drink coffee and im afraid to drink from a mug because I dont trust that people clean them properly and I'd feel like a fool drinking hot tea from a mug with a straw. I hang with my family for fun, invite my friends over for a chat and cook us up something delightful, or buy some premade gluten free treats and make us some teas and sip them on my porch. I always used to the be person to cook for friends before, so I figured why does it have to change? I also like nature walks, which often includes photography. I just learned how to swim and I love it because I can get really good exercise and it doesn't bother my joints, my friends like to come along if they are visiting. We go to the boardwalk at the shore (I bring a gluten free to-go treat) and play boardwalk games. I sometimes go out to 'eat' with friends, but I eat beforehand so it's not tempting. I get some water, with a straw and enjoy the company. Food is just so social and it tends to make people feel weird the first time you do this, just tell them you aren't there for the food, you are there for their company.


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



Celiac.com Sponsor (A8-M):



nvsmom Community Regular

As a young adult, I found having a bit of sugar and a big coffee before going out helped me have a good time more than alcohol ever did.  Being active helped me keep my energy levels up so I could keep up with friends at 2am.

 

You can go anywhere you want while sober.  In fact, I think drinking limits your activities more than sobriety.  When drinking you can't drive or boat.  All sports would be harder. Dancing is never as good (although you might THINK you look better LOL). Conversations are affected by drinking as is decision making.... If you think about it, drinking is pretty limiting.

 

If you want to go to the bars, that's fine too.  Drink a coke, dance the night away, beat everyone at darts, Get some phone numbers, and then be the designated driver to your friends.  Sounds like a good time to me.  :)

Archived

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

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

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





    Celiac.com Sponsors (A17-M):




  • Recent Activity

    1. - Scott Adams replied to Jhona's topic in Introduce Yourself / Share Stuff
      35

      Does anyone here also have Afib

    2. - Jacki Espo replied to CDFAMILY's topic in Related Issues & Disorders
      5

      Covid caused reoccurrence of DH without eating gluten

    3. - Mari replied to tiffanygosci's topic in Coping with Celiac Disease
      1

      New Celiac Mama in My 30s

    4. - Mari replied to Jmartes71's topic in Coping with Celiac Disease
      2

      My only proof


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,957
    • Most Online (within 30 mins)
      7,748

    Dogdad21
    Newest Member
    Dogdad21
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.5k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • Scott Adams
      If black seed oil is working for his Afib, stick to it, but if not, I can say that ablation therapy is no big deal--my mother was out of the procedure in about 1 hour and went home that evening, and had zero negative effects from the treatment. PS - I would recommend that your husband get an Apple watch to monitor his Afib--there is an app and it will take readings 24/7 and give reports on how much of the time he's in it. Actual data like this should be what should guide his treatment.
    • Jacki Espo
      This happened to me as well. What’s weirder is that within a couple hours of taking paxlovid it subsided. I thought maybe I got glutened but after reading your post not so sure. 
    • Mari
      Hi Tiffany. Thank you for writing your dituation and  circumstancesin such detail and so well writte, too. I particularly noticed what you wrote about brain for and feeling like your brain is swelling and I know from my own experiences that's how it feel and your brain really does swell and you get migraines.    Way back when I was in my 20s I read a book by 2 MD allergist and they described their patient who came in complaining that her brain, inside her cranium, was swelling  and it happened when she smelled a certain chemical she used in her home. She kept coming back and insisting her brain actually swelled in her head. The Drs couldn't explain this problem so they, with her permission, performed an operation where they made a small opening through her cranium, exposed her to the chemical then watched as she brain did swell into the opening. The DRs were amazed but then were able to advise her to avoid chemicals that made her brain swell. I remember that because I occasionally had brain fog then but it was not a serious problem. I also realized that I was becoming more sensitive to chemicals I used in my work in medical laboratories. By my mid forties the brain fog and chemicals forced me to leave my  profession and move to a rural area with little pollution. I did not have migraines. I was told a little later that I had a more porous blood brain barrier than other people. Chemicals in the air would go up into my sinused and leak through the blood brain barrier into my brain. We have 2 arteries  in our neck that carry blood with the nutrients and oxygen into the brain. To remove the fluids and used blood from the brain there are only capillaries and no large veins to carry it away so all those fluids ooze out much more slowly than they came in and since the small capillaries can't take care of extra fluid it results in swelling in the face, especially around the eyes. My blood flow into my brain is different from most other people as I have an arterial ischema, adefectiveartery on one side.   I have to go forward about 20 or more years when I learned that I had glaucoma, an eye problem that causes blindness and more years until I learned I had celiac disease.  The eye Dr described my glaucoma as a very slow loss of vision that I wouldn't  notice until had noticeable loss of sight.  I could have my eye pressure checked regularly or it would be best to have the cataracts removed from both eyes. I kept putting off the surgery then just overnight lost most of the vision in my left eye. I thought at the I had been exposed to some chemical and found out a little later the person who livedbehind me was using some chemicals to build kayaks in a shed behind my house. I did not realize the signifance  of this until I started having appointments with a Dr. in a new building. New buildings give me brain fog, loss of balance and other problems I know about this time I experienced visual disturbances very similar to those experienced by people with migraines. I looked further online and read that people with glaucoma can suffer rapid loss of sight if they have silent migraines (no headache). The remedy for migraines is to identify and avoid the triggers. I already know most of my triggers - aromatic chemicals, some cleaning materials, gasoline and exhaust and mold toxins. I am very careful about using cleaning agents using mostly borax and baking powder. Anything that has any fragrance or smell I avoid. There is one brand of dishwashing detergent that I can use and several brands of  scouring powder. I hope you find some of this helpful and useful. I have not seen any evidence that Celiac Disease is involved with migraines or glaucoma. Please come back if you have questions or if what I wrote doesn't make senseto you. We sometimes haveto learn by experience and finding out why we have some problems. Take care.       The report did not mention migraines. 
    • Mari
      Hi Jmartes71 That is so much like my story! You probably know where Laytonville is and that's where I was living just before my 60th birthday when the new Dr. suggested I could have Celiacs. I didn't go on a gluten challange diet before having the Celiac panel blood test drawn. The results came back as equivical as one antibody level was very high but another, tissue transaminasewas normal. Itdid show I was  allergic to cows milk and I think hot peppers. I immediately went gluten free but did not go in for an endoscopy. I found an online lab online that would do the test to show if I had a main celiac gene (enterolab.com). The report came back that I had inherited a main celiac gene, DQ8, from one parent and a D!6 from the other parent. That combination is knows to sym[tons of celiac worse than just inheriting one main celiac gene. With my version of celiac disease I was mostly constipated but after going gluten-free I would have diarrhea the few times I was glutened either by cross contamination or eating some food containing gluten. I have stayed gluten-free for almost 20 years now and knew within a few days that it was right for me although my recovery has been slow.   When I go to see a  medical provide and tell them I have celiacs they don't believe me. The same when I tell them that I carry a main celiac gene, the DQ8. It is only when I tell them that I get diarrhea after eating gluten that they realize that I might have celiac disease. Then they will order th Vitamin B12 and D3 that I need to monitor as my B12 levels can go down very fast if I'm not taking enough of it. Medical providers haven't been much help in my recovery. They are not well trained in this problem. I really hope this helps ypu. Take care.      
    • knitty kitty
×
×
  • 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.