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

Night-time Abdominal Pain


EJR

Recommended Posts

EJR Rookie

Hi Everyone,

I am a new member. I started following a gluten-free diet about 1 year ago. I seem to have made every classic mistake in dealing with this health issue. First of all, I started a gluten-free diet prior to my small bowel biopsy and blood work therefore I do not have a definitive diagnosis. Also, I have tried to reintroduce gluten a number of times throughout the year with disastrous results.

Just wanted to ask other members if their gluten intolerance symptoms cause them to wake-up from their sleep. I usually fall asleep for an hour or two and then wake-up with pretty awful abdominal pain and bloating. The bloating is often so bad that it presses on my diaphragm and triggers tachycardia. I have had tachycardia since I was 13 years old (due to an extra electrical pathway in my heart). Some nights the pain is already very bad when I go to bed and sleep is just not possible. I have a lot of what I think is pain from my lower bowel (spasms, cramping, bloating, feeling like I've been totally pressurized and may soon blow up). Perhaps the best description may be a feeling that my bowel is partially obstructed. It can be very, very painful.

I am lactose intolerant and have IgE tested allergies to a variety of foods including eggs, barley, beef, pork and so on.

Look forward to hearing if others have any similar experiences. Does your abdominal pain keep you awake at night?

Thanks so much

EJR


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



Celiac.com Sponsor (A8-M):



Mother of Jibril Enthusiast

Hi EJR,

Have you ever tried taking an H2 antihistamine before bedtime like Pepcid or Zantac? That might help with your symptoms while you're trying to find the cause. H1 antihistamines (Zyrtec, Claritin, Benadryl, etc...) help with the classic "allergy" symptoms like itchy eyes, runny nose, hives, etc... but the H2 antihistamines can help with mast-cell related symptoms in your GI system, nervous system, cardio-vascular system, bones and joints, etc...

It's a long explanation as to why this might work, but antihistamines are pretty safe and sold OTC. It might be worth a try.

mommida Enthusiast

If I have been glutened, it is impossible to sleep from the pain. I will have to run to the bathroom at some point too.

oceangirl Collaborator

When glutened the nights are THE WORST! BIG left side pain, bloating to the point I feel I can't breathe and NO relief until sometime in the morrow when, if lucky, I'll start to have a bowel movement. (sorry to be graphic but, there it is...) My left hip is usually in agony as well and I am not talking about discomfort, I mean PAIN! This can persist for days... I am AFRAID of gluten.

Hope you get some relief,

lisa

EJR Rookie
Hi 'Mother of Jibril'

Thank you so much for your response and suggestion. Unfortunately I have tried both Pepci and Zantac and they don't seem to help me. Zantac also affects my heart problem. I didn't know about the H2 antihistamine explanation that you wrote. I appreciate it very much and may have to think again about trying these.

EJR

Hi EJR,

Have you ever tried taking an H2 antihistamine before bedtime like Pepcid or Zantac? That might help with your symptoms while you're trying to find the cause. H1 antihistamines (Zyrtec, Claritin, Benadryl, etc...) help with the classic "allergy" symptoms like itchy eyes, runny nose, hives, etc... but the H2 antihistamines can help with mast-cell related symptoms in your GI system, nervous system, cardio-vascular system, bones and joints, etc...

It's a long explanation as to why this might work, but antihistamines are pretty safe and sold OTC. It might be worth a try.

EJR Rookie
When glutened the nights are THE WORST! BIG left side pain, bloating to the point I feel I can't breathe and NO relief until sometime in the morrow when, if lucky, I'll start to have a bowel movement. (sorry to be graphic but, there it is...) My left hip is usually in agony as well and I am not talking about discomfort, I mean PAIN! This can persist for days... I am AFRAID of gluten.

Hope you get some relief,

lisa

Hi Lisa,

Boy, am I ever glad to have received your response. I'm not glad that you also suffer this kind of pain, but I was starting to wonder if I was the only one that was often severely bothered at nighttime with the bloating and abdominal pain. I also feel it in my hip area and in my lower back.

You mentioned sometimes starting to get some relief towards morning. This also happens for me quite often (for me that is when I am finally able to release some of the painful, trapped gas).

Have you found anything that helps you at night when you feel like this? Do your symptoms sometimes occur even when you have avoided gluten? How long have you been gluten free? Did your symptoms abate fairly quickly after starting to eat gluten free or was it a slow, gradual kind of healing?

Thank you so very, very much for your response.

Joyce

EJR Rookie
If I have been glutened, it is impossible to sleep from the pain. I will have to run to the bathroom at some point too.

Hi Mommida,

Thank you for sharing this with me. As I mentioned I was starting to think that I was the only one with nighttime abdominal pain that makes sleep impossible. Does this only happen to you if you have been glutened or does it happen at other times also.

Thanks again,

Joyce


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



Celiac.com Sponsor (A8-M):



oceangirl Collaborator

Joyce,

I have been gluten free for going on 5 years but, prior to diagnosis, I was in so much agony at night I was certain I had something quite bad. If I ingest even the most negligible amount of gluten I will get that hideous bloat and trapped gas and PAIN! It feels like someone filled my whole insides with cement and, sadly, no, nothing seems to help except time. However, I will tell you I am not a fan of taking medication (never have been- pretty naturopathic French and Greek family passed on my suspicion of the pharmaceutical industry...)

I almost never eat out, eat almost NO processed food and eat only whole foods made by myself or Michael. Sometimes I will get the symptoms you describe (along with some other fun ones...) and not know where they came from. I've kept a food log every day for 4 years and it has been a very useful thing- I highly recommend it. And for two years I was gluten, soy, nightshades, eggs, dairy, legume and citrus free. I am now able to eat dairy, whole corn and nightshades, corn and eggs but I continue to avoid soy along with gluten. Also avoid at all costs any "fake" sugar like sorbitol. Oh yeah, and no high fructose corn syrup.

Here are some things I eat: Steak, fish, chicken, cabot cheddar cheese, Fage Greek yogurt, all veggies but no white potatoes (cooking helps at first), raw sugar, fruits (bananas are very good), Tinkyada pasta, cabot butter, sweet potatoes, Planter's cashews,almonds and macadamia nuts, corn on the cob, occasionally coffee with milk, occasional Larabar, homemade jams and Lundberg rice cakes.

Hope this helps. It DOES take time- nearly 2 years before I got things right. Trust your gut- if you hear hoofbeats think "horses"- that's what I remind myself when wondering if I could have been glutened. If it acts like gluten, it's probably gluten.

Take care,

lisa

mimommy Contributor

You've had some great replies here and I just wanted to say that when my 9 year old daughter is glutened, the night time abdominal pain is probably her first and worst symptom. Intially her stomach will hurt just below the ribs, then she'll feel the pressure and the need to use the bathroom (usually without much result). If it's bad enough she will cry and say, "Mom--my back hurts!". Before diagnosis this would involve diarhea and vomiting, but now it will usually be constipation. And the strangest thing of all is the sleepwalking! If she ingests even a microscopic amount of gluten she will sleep walk with absolutely no memory of it. Her symptoms always seem to start right around bed time, but I can sometimes see it in her face hours before it starts--it's like a puffiness and dark circles under her eyes.

  • 2 years later...
mikyraso Rookie

Hi Everyone,

I am a new member. I started following a gluten-free diet about 1 year ago. I seem to have made every classic mistake in dealing with this health issue. First of all, I started a gluten-free diet prior to my small bowel biopsy and blood work therefore I do not have a definitive diagnosis. Also, I have tried to reintroduce gluten a number of times throughout the year with disastrous results.

Just wanted to ask other members if their gluten intolerance symptoms cause them to wake-up from their sleep. I usually fall asleep for an hour or two and then wake-up with pretty awful abdominal pain and bloating. The bloating is often so bad that it presses on my diaphragm and triggers tachycardia. I have had tachycardia since I was 13 years old (due to an extra electrical pathway in my heart). Some nights the pain is already very bad when I go to bed and sleep is just not possible. I have a lot of what I think is pain from my lower bowel (spasms, cramping, bloating, feeling like I've been totally pressurized and may soon blow up). Perhaps the best description may be a feeling that my bowel is partially obstructed. It can be very, very painful.

I am lactose intolerant and have IgE tested allergies to a variety of foods including eggs, barley, beef, pork and so on.

Look forward to hearing if others have any similar experiences. Does your abdominal pain keep you awake at night?

Thanks so much

EJR

Hi EJR-

I have only had the blood testing done thus far and it was neg. But my 6yr old DD had Biopsy and bloodwork done and her bloodwork was neg. as well. So I don't have a formal diagnosis. However my night time symptoms are keeping me up most nights until 2am. My symptoms are nausea, my stomach feels like it just won't stop churning and popping and cramping, and then I also become very gassy. I did just get a prescription for something to help with the upset stomach but I am not we'll see. It seemed to help last night. .

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,948
    • Most Online (within 30 mins)
      7,748

    Stephanie94
    Newest Member
    Stephanie94
    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.