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

This Is My Opinion On Ibs


FootballFanatic

Recommended Posts

FootballFanatic Contributor

I do believe in "IBS" when it is a person who gets intestinal problems under extreme pressure, like my mom gets D when she gets under too much stress of a project or travel etc. My boyfriend gets D when he gets extremely nervous. My friend gets very painful cramping and nausea and indigestion when her emotions get a blow (like a breakup or a death).

But when people are sick on a daily basis....I think it's something more, like Celiac Disease for example.

Now today, I have a constant pain in my gut, don't feel much like eating, feel emotional and dizzy, and I'm not glutened I'm just SO NERVOUS because I'm running for an officer of a club tonight against 4 other girls.....Very high stress level, and I feel "IBS"

Anyone else still get symptoms due to nerves/stress when you haven't been glutened?

Sorry that was confusingly written, I told you, I'm a nervous wreck today!


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



Celiac.com Sponsor (A8-M):



Offthegrid Explorer

Sorry you are nervous -- good luck tonight!!!

My mom says she has IBS, but I personally believe it is gluten and dairy intolerance. (She refuses to be tested or to go off gluten to try it. Says there's no way she can give up bread. But that's another story.)

ANYhow, I've read that it's rare for celiacs to have IBS, but I'm certainly no expert. After going gluten-free and finally being strict about it, I still had tons of symptoms. I kept assuming I was getting glutened from something. After much trial and error, I've finally figured out that it's casein and soy intolerances. Who knew?

Could you possibly have other food intolerances?

That said, people do feel sick from time to time. I always assume gluten, but maybe there are times when you just get a bug or something.

Rya Newbie

Stress is powerful. Over 75% of people truly diagnosed with IBS were abused or neglected as children.

BRUMI1968 Collaborator

It is actually part of flight or fight to have to evacuate your bowels. Isn't that weird? Like a lion is chasing you and pooping your pants is going to help?

I am VERY influenced by stress. If I'm stressed out, I'll have tummy and bowel issues. I think that's normal, even for folks who don't have IBS or Celiac. But those of us that do have those things or other chronic digestive problems, are extremely sensitive to them.

Generic Apprentice

They call is spastic colon when your gut gets messed up from stress and or nerves. IBS is just a name for a collection of symptoms that basically say, yup you got a problem with your stomach but we don't know what it is.

ravenwoodglass Mentor
They call is spastic colon when your gut gets messed up from stress and or nerves. IBS is just a name for a collection of symptoms that basically say, yup you got a problem with your stomach but we don't know what it is.

I agree with this statement. I was under the IBS shroud for years, and years, and years. Since becoming 'really' gluten free no matter what stress I am under it does not effect my bowel function. Foods sure do though. In my case IBS stands for 'I Be Stupid' for listening to all the doctors who told me for years that I just have IBS, here have a prozac and just take immodium EVERY DAY and learn to live with it.

alamaz Collaborator

Before going gluten-free, anytime I became anxious or stressed I had explosive D. Before being DX'ed I also had horrible anxiety. Since being gluten-free/CF/SF I don't get as anxious as I used to (stressed still but not high anxiety like before) and I only occasionally have the tummy trouble to go with it. Now, I'll *think* I'm going to have trouble because I got so used to it but amazingly it doesn't happen every time. It's really only high stress situation like flying (I can't get on a plane since 9/11) or going to spend time with my family who I don't really get along with and on top of having to have a "special diet" just makes it that much harder to really want to go see them and be happy about it :D .


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



Celiac.com Sponsor (A8-M):



JNBunnie1 Community Regular
It is actually part of flight or fight to have to evacuate your bowels. Isn't that weird? Like a lion is chasing you and pooping your pants is going to help?

I am VERY influenced by stress. If I'm stressed out, I'll have tummy and bowel issues. I think that's normal, even for folks who don't have IBS or Celiac. But those of us that do have those things or other chronic digestive problems, are extremely sensitive to them.

HAHAHAHAHA!!!! I know, is the smell supposed to scare them off or something?

Anyway, I have stress-induced 'IBS' too. When my father was diagnosed with cancer last April, I spent two hours every morning for three weeks running back and forth to the bathroom. Which was kinda tough, because I worked at a hotel front desk and they don't like that................ I still do it when I get really nervous about something.

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,951
    • Most Online (within 30 mins)
      7,748

    SY8
    Newest Member
    SY8
    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

    • 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
    • DebJ14
×
×
  • 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.