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

Trapped Wind (Chest Pain) Constipation And Bloating?


Kirstie

Recommended Posts

Kirstie Apprentice

Hey everyone,

I've been suffering from trapped wind for three days straight now, its been really painful (especially on Saturday) and wakes me up at night.

I am also really bloated and constipated. I'm not sure if the trapped wind is a result from constipation, or different entirely?

Has anyone else suffered from this. I've taken laxatives, fibre supplements, prune juice, smoothies, effervescent salts, linseed and flaxseed and generally just been healthy! Jogging, lots of water and juice, no fatty foods or alcohol. They haven't done much except give me mild cramping.

I'm trying to give up dairy and have been avoiding it fine, except for occasional problems with milk in unexpected places.

I'm just so tired of being ill! There is always something wrong with me! My constipation really improved after quitting gluten, but its been bad this past week.

Can anyone recommend food or other things to help constipation, bloating and my digestion in general? I'm getting really depressed about this :(

Thanks again everyone x


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



Celiac.com Sponsor (A8-M):



GFreeMO Proficient

It sounds like you have been glutened. Thats how I feel when I have been. I also had to give up corn, corn syrup..especially in soda would make me feel like that for days. Anything with corn makes me horribly constipated.

I would drink lots of water to help get things moving and stick to a whole foods diet for a while. Maybe have some chicken with salt and some soft carrots. Things like that. Sometimes fruit makes things worse because it feels like it is fermenting in your guts and causes more gas and pain.

I hope you feel better soon!

Chad Sines Rising Star

This is also how i feel when i am having issues with fat intolerance which seems to be something many of us get. Same side effect of too much probiotic, dairy (if you have issues), soy (if you have issues), starting fiber, some of the wheat alternatives (at least for me), and even gut bacteria being off.

GFinDC Veteran

A big can of salty sauerkraut has some chance of getting things moving. Don't drain it real well, the salt is what makes it work.

For gas in the stomach peppermint is good. Peppermint Altoids work well. Also Betaine HCL. Mastic gum may help too but you need to take it for a couple weeks several times day.

nvsmom Community Regular

I like prunes (I know I know) and strong coffee along with extra fibre supplements. I also always have Gas Rx or something like that, on hand to help get the gas going (wind bloat is the norm for glutening for me).

When desperate, standing on your head or, from your knees, bend your head to the ground in a prayer-like pose... the gas seems to rise and, ahem, leave more easily... do without a spouse around to mock you... trust me. ;)

Ibuprofin seems to help with the pain a tad... Best wishes, I know that bloat can hurt.

FruitEnthusiast Enthusiast

I recently had trapped gas, which isn't a usual symptom for me and it was really painful, so I feel for you. Gas X usually works well occasionally when I need it. When constipation gets bad enough though, it's beyond fiber and dietary changes and you need to be more proactive: enemas work. It's not as bad as it sounds. I only use purified water enemas. I can give you more info if you like. Dulcolax suppositories work too, but cause irritation. Magnesium Citrate is another option but not too pleasant to use either.

  • 3 weeks later...
Skittles Enthusiast

This happens to me often. Even though you feel bloated, drinking water does help. Also, peppermint herbal tea really helps me!


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



Celiac.com Sponsor (A8-M):



justlisa Apprentice

My first question is: "Chest" pain?

Second question: How do you KNOW that the "chest pain"is "trapped wind"?

Third question: It's been a couple of weeks...how have you been doing?

Keshavdas Apprentice

Constipation and gas were my big indicators of Celiac disease. Haven't had it since going gluten free. Before going gluten-free - little things would set me off and couldn't move anything without stool softners for a month at a time.

Stool softeners don't work overnight like Dulcolax etc but they are gentler and the GI system doesn't seem to become as dependent on them as it does with strong stimulant-based laxatives.

I would take two with each meal until things started moving and then taper off as things would

get too loose.

Last time I was really desperate and nothing was helping I did a couple spoonfuls of coconut oil at night before bed. Castor oil is even stronger but not supposed to be so healthy to ingest - tho if the discomfort was severe enough I would use it. Lots of water of course as it's very easy to dehydrated when using any kind of laxative and as it's been pointed out numerous times here, not getting dehydrated is paramount for folks with Celiac issues.

In the end you need to figure out what is causing you to create so much gas, which is what is trapping everything in your bowel.

RonSchon Explorer

My guess is that you have an intolerance to something which causes gluten like reactions in your digestive system.

I've been running into the same thing. First nuts, then powerade, then gatorade, then other gluten-free labeled processed items.

I'm down to a very limited selection of things that seem stable and safe. From there, I try to bring things in on an individual basis so that I know they are ok.

Kind of a pain in the butt, and often leads to poisonings, but at least I know for certain if it is ok.

I keep it in a log online, so I know dates and items and a timeline, etc.

Lucy Lastic Newbie

I get that a lot. I have IBS in addition to my gluten issues. Any kind of vegetable or fruit that is insoluable fiber makes me very gassy so I try to avoid those.

Peppermint tea or Fennel tea helps me as does taking activate charcoal capsuals. Also, exercise helps me. I guess it forces the gas to move around until it comes out. Nothing is a cure all, though. I just have to wait it out several days until its gone. Hope you feel better.

RockChalkChic Newbie

Running or swimming help me. My daily probiotic (Culturelle) and my daily red wine intake :) seems to help most of the time. I used to get that "full up to my chin" feeling before going gluten-free and it was miserable. It was like I just wanted to let out one huge burp! gross! Sometimes eating a cup of brown rice seems to help me, too, or eating dried prunes. Good luck!

Oh, and watch the Altoid minis, they contain wheat!

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,963
    • Most Online (within 30 mins)
      7,748

    AlissaW
    Newest Member
    AlissaW
    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.