Jump to content
This site uses cookies. Continued use is acceptance of our Terms of Use and Privacy Policy. More Info... ×
  • 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

Distended Abdomen...celiac?


mezzo9673

Recommended Posts

mezzo9673 Newbie

Thank your for taking the time to view my post! For the past year I have had severe abdominal distention. When I wake up in the morning, it is only slightly distended, but bloats out a lot after eating ANYTHING (sometimes looks like I'm 5 or 6 months pregnant, and lasts for hours). I also frequently have excessive gas. I finally saw a doctor today who suspects I may have celiac disease, but I won't know for sure until we review my blood work @ my next appointment in 2 weeks. I've been reading a lot of the posts on this forum and am suprised to not have read anyone with the same abdominal distention as I have. I do also have symptoms sush as unexplained anxiety from time to time, gas, heart palpatations once in awhile, and fatigue/low energy... but I do not have any sort of pain or cramping (unless I eat something heavy) and my bowel movements are regular and healthy. I suppose maybe symptoms vary between individuals with this disease, but I'm wondering if anyone shares my problem with the "permanent" distended abdomen! Anyway, I'm very nervous to possibly find out I have this disease. Not only will it be a major lifestyle adjustment (never eating bread anymore OMG!), but possibly developing osteoporosis, anemia, or becoming infertile absolutely terrifies me :/


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



Celiac.com Sponsor (A8-M):



MsCurious Enthusiast

Thank your for taking the time to view my post! For the past year I have had severe abdominal distention. When I wake up in the morning, it is only slightly distended, but bloats out a lot after eating ANYTHING (sometimes looks like I'm 5 or 6 months pregnant, and lasts for hours). I also frequently have excessive gas. I finally saw a doctor today who suspects I may have celiac disease, but I won't know for sure until we review my blood work @ my next appointment in 2 weeks. I've been reading a lot of the posts on this forum and am suprised to not have read anyone with the same abdominal distention as I have. I do also have symptoms sush as unexplained anxiety from time to time, gas, heart palpatations once in awhile, and fatigue/low energy... but I do not have any sort of pain or cramping (unless I eat something heavy) and my bowel movements are regular and healthy. I suppose maybe symptoms vary between individuals with this disease, but I'm wondering if anyone shares my problem with the "permanent" distended abdomen! Anyway, I'm very nervous to possibly find out I have this disease. Not only will it be a major lifestyle adjustment (never eating bread anymore OMG!), but possibly developing osteoporosis, anemia, or becoming infertile absolutely terrifies me :/

Unfortunately, I too suffer from this... as does my sister. I look completely normal in the morning, and can eat one wrong thing and blow up just like someone used a tire pump on my stomach...its EXTREMELY uncomfortable. I think its pretty common... usually referred to here as "bloating"... you'll see it quite often. Hope you have success figuring out what's going on with you. Several of us are still in the "testing phase"... its a long wait. We're here if/when you need us. :)

mushroom Proficient

Welcome to the board, Mezzo. Keep reading on here - you will find oodles of post about abdomen distention, bloating, gas, heart palpitations. These are all classic gluten intolerance symptoms around here. It is an anxious time waiting for testing results, but even if your tests come back negative that does not mean that gluten is not the culprit. There is both a 20% error rate in the testing for celiac, and also, as is now being recognized by the doctors, a non-celiac gluten intolerance which requires a gluten free diet just as much as celiac disease does. Sorry to be a little joy-germ here :rolleyes: , but you may as well know it now as keeping your hopes up until after you get your results. For those who test negative (and many test negative on both blood and biopsy) the only present way of determining whether gluten is a problem is to eliminate it (which is, after all, a lot cheaper than a bunch of tests) :P You can also do the genetic testing to see if you have the predisposition for celiac, but just having the gene is not diagnostic - many people who carry the gene have no problems with gluten. There are also some other food intolerances that can mimic some of the celiac symptoms, like lactose/casein and corn, also soy, and sometimes we have to eliminate these too and then challenge them to see if they are a problem.

If you eliminate your food intolerances you should not develop any of the side effects that they cause if you do not already have them. That's the good news. It's like quitting smoking - after 5 years you go back to the normal population statistics. :D

mezzo9673 Newbie

Unfortunately, I too suffer from this... as does my sister. I look completely normal in the morning, and can eat one wrong thing and blow up just like someone used a tire pump on my stomach...its EXTREMELY uncomfortable. I think its pretty common... usually referred to here as "bloating"... you'll see it quite often. Hope you have success figuring out what's going on with you. Several of us are still in the "testing phase"... its a long wait. We're here if/when you need us. :)

MsCurious, I'm sorry you are suffering from this same problem, but truthfully it feels comforting to hear I'm not alone. What kind of tests are you getting done? I got my blood tested and sometime next week I go for an ultrasound. I really hope it doesn't take too long to figure out what's going on, this is just so scary..let me know how it goes with you please! P.S. How old are you? I just turned 25.

mezzo9673 Newbie

Welcome to the board, Mezzo. Keep reading on here - you will find oodles of post about abdomen distention, bloating, gas, heart palpitations. These are all classic gluten intolerance symptoms around here. It is an anxious time waiting for testing results, but even if your tests come back negative that does not mean that gluten is not the culprit. There is both a 20% error rate in the testing for celiac, and also, as is now being recognized by the doctors, a non-celiac gluten intolerance which requires a gluten free diet just as much as celiac disease does. Sorry to be a little joy-germ here :rolleyes: , but you may as well know it now as keeping your hopes up until after you get your results. For those who test negative (and many test negative on both blood and biopsy) the only present way of determining whether gluten is a problem is to eliminate it (which is, after all, a lot cheaper than a bunch of tests) :P You can also do the genetic testing to see if you have the predisposition for celiac, but just having the gene is not diagnostic - many people who carry the gene have no problems with gluten. There are also some other food intolerances that can mimic some of the celiac symptoms, like lactose/casein and corn, also soy, and sometimes we have to eliminate these too and then challenge them to see if they are a problem.

If you eliminate your food intolerances you should not develop any of the side effects that they cause if you do not already have them. That's the good news. It's like quitting smoking - after 5 years you go back to the normal population statistics. :D

Thank you mushroom for your advice. I will definetely keep that all in mind! My doctor recommended continuing to eat food with gluten for the next week, and going gluten free the following week to see if there's a difference in my symptoms, but after reading how gluten is literally a poison to people with celiac, I am terrified to eat even a piece of bread knowing it's damaging my intestine :(

MsCurious Enthusiast

Welcome to the board, Mezzo. Keep reading on here - you will find oodles of post about abdomen distention, bloating, gas, heart palpitations. These are all classic gluten intolerance symptoms around here. It is an anxious time waiting for testing results, but even if your tests come back negative that does not mean that gluten is not the culprit. There is both a 20% error rate in the testing for celiac, and also, as is now being recognized by the doctors, a non-celiac gluten intolerance which requires a gluten free diet just as much as celiac disease does. Sorry to be a little joy-germ here :rolleyes: , but you may as well know it now as keeping your hopes up until after you get your results. For those who test negative (and many test negative on both blood and biopsy) the only present way of determining whether gluten is a problem is to eliminate it (which is, after all, a lot cheaper than a bunch of tests) :P You can also do the genetic testing to see if you have the predisposition for celiac, but just having the gene is not diagnostic - many people who carry the gene have no problems with gluten. There are also some other food intolerances that can mimic some of the celiac symptoms, like lactose/casein and corn, also soy, and sometimes we have to eliminate these too and then challenge them to see if they are a problem.

If you eliminate your food intolerances you should not develop any of the side effects that they cause if you do not already have them. That's the good news. It's like quitting smoking - after 5 years you go back to the normal population statistics. :D

Mushroom ... that was such a nice, easy to understand, comprehensive summary... nicely done! :) Very helpful, to people just arriving, I'm sure! :D I speak from experience... your comments such as this... and those of other people sure helped me get through the terrified, confused, scared first days of "learning" on here. :) Thanks again for that!

mezzo9673 Newbie

I replied to both the responses from mscurious and mushroom, but I don't see them posted. Thanks so much to both of you! It sucks that we have to go through this, but comforting to know we're not alone. MSCURIOUS...please let me know about biopsy results! Mushroom..thanks for the advice, I will definetely keep that all in mind :)


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



Celiac.com Sponsor (A8-M):



mushroom Proficient

mezzo, for new members there is a delay until your posts appear because they do require approval by a moderator first. (I was having my dinner ;) ) Don't worry, you'll soon pass the threshold where they come through automatically. :)

JoLynneS Newbie

Thank you mushroom for your advice. I will definetely keep that all in mind! My doctor recommended continuing to eat food with gluten for the next week, and going gluten free the following week to see if there's a difference in my symptoms, but after reading how gluten is literally a poison to people with celiac, I am terrified to eat even a piece of bread knowing it's damaging my intestine :(

Definitely continue to eat gluten till you get tested. If you stop eating it, the test results won't be accurate. I tested negative a few years ago and I recently went off gluten. I feel awful when I do get a little bit by accident, so I'm assuming I have gluten intolerance. But in a way, it would be nice to have an official diagnosis.

Best of luck to you.

Cara in Boston Enthusiast

I would caution you against going gluten free before the tests are done.

I have all the symptoms (well, not all, but plenty). I tested positive on my original blood test. In the time I was waiting to meet with the GI doctor, I tried going gluten-free to see if my symptoms resolved (really, who can resist?) When I saw the GI doctor, he did another blood test and scheduled an endoscopy - after only 10 days of being gluten-free. Both came back negative. Maybe because of going gluten-free, maybe not? We don't know. Now I have to wait even longer (3 months eating regular diet) to have an opportunity to get a more accurate test done.

This is all very frustrating since I am pretty sure I have it (son tested positive too - coincidence? probably not) but I'd like to be as sure as possible.

Also, the 10 days gluten free was not really long enough to see a change. You are likely to feel WORSE in the begining. Trying it out for just a week won't really tell you anything but it may make further testing that much more unreliable.

Good luck -

Cara

NateJ Contributor

I would caution you against going gluten free before the tests are done.

I have all the symptoms (well, not all, but plenty). I tested positive on my original blood test. In the time I was waiting to meet with the GI doctor, I tried going gluten-free to see if my symptoms resolved (really, who can resist?) When I saw the GI doctor, he did another blood test and scheduled an endoscopy - after only 10 days of being gluten-free. Both came back negative. Maybe because of going gluten-free, maybe not? We don't know. Now I have to wait even longer (3 months eating regular diet) to have an opportunity to get a more accurate test done.

This is all very frustrating since I am pretty sure I have it (son tested positive too - coincidence? probably not) but I'd like to be as sure as possible.

Also, the 10 days gluten free was not really long enough to see a change. You are likely to feel WORSE in the begining. Trying it out for just a week won't really tell you anything but it may make further testing that much more unreliable.

Good luck -

Cara

I agree. I went gluten free before my biopsy and haven't not felt any better at all. Some days are worse than others probably depending on what i eat. But so far I haven't been able to find what my trigger is.

My scopes did show the inside of my stomach is completely red. But my glorious GI doesn't seem to think that is abnormal and has yet to call me with reviewed biopsy results or any type of treatment plan.

So, resolve is probably the key here. Thats what everyone preaches to the new people. Sticking with diets and following up with Drs. It is exhausting but hopefully there is light at the end of our tunnels.

JenHarris Apprentice

I definitely have similar symptoms to you. I've measured and found as much as a 5 inch difference in my waistline on days that I bloat. Prime example... I felt ok all day yesterday after being gluten free for the first time in a month (gluten challenge for testing). Then I went to dinner with some friends. The corn tortilla chips and tortillas were supposedly gluten free, but somehow I got dosed and I was up half the night with severe distension, nausea, severe stomach upset and cramping. I'm still bloated today and have cramping, but nausea is gone.

I get my blood test results on Monday hopefully. Hang in there.

karagog Newbie

I used to get the distended abdomen before cutting out gluten. I have not been diagnosed with anything yet, but after nixing gluten from my diet it only took 24 hours for me to notice a difference. I have been off gluten for 2 weeks now, and I have never felt better. No more bloating.

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      128,175
    • Most Online (within 30 mins)
      7,748

    Janice Emmendorfer
    Newest Member
    Janice Emmendorfer
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.1k
    • Total Posts
      70.7k

  • Celiac.com Sponsor (A22):




  • Who's Online (See full list)

    • There are no registered users currently online

  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • Wheatwacked
      Once you have removed the inflammatories, it is time to focus on the deficiencies.  A lot of them not specific to Celiac, but deficiency in them elicits symptoms associated with Celiac. According to research, celiac disease tends to be more prevalent in urban areas compared to rural areas.  Same is true with airborne viruses.  Because urban residents get less sunlight.  To top it off we use lotion and gear to block the little light there is.  This compremises the vitamin D blood level.  A virus attack further lowers vitamin D and the immune system loses control over the Celiac genes and they go into acute symptoms. 40% to 75% depending depending on country are vitamin D deficient. 50% do not eat the Adequit Intake for potassium (4700 mg a day) 90% do n ot eat the Adequit Intake for Choline. Iodine intake since 1970 had dropped 50%.  The western diet is typically excessive in omega 6 fatty acid compared to omega 3.  Above 14:1 by some estimates.  So they sell us expensive, processed oils to compensate.  Anyway after 10 years gluten free myself,  here is what has helped me in just the past few years; once I realized I was at a healing plateau and just GFD would not cut it, and reallized my deficiencies.  Most recently, I started a statin which I only took for two weeks before it started to cripple me.   Got a prescription for Nicotinic Acid to 2000 and am more flexible now Plus HDL went 29 to 44, eGFR from 55 to 79. I also learned if the pharmacist gets a prescription for Niacin that it is dealer's choice whether you get Nicotinic Acid or Niacinimide.  And it comes out of a regular vitamin manufacturer.   "likely deficiencies and what I take to boost my intake (I get anorexic at the drop of a hat so I take them to keep me stable):  the ones that helped me the most noticibly Was increasing vitamin D blood level to 80 ng/ml and Iodine to 500 mcg once or twice a day, Thiamine, Choline, and Iodine. 10,000 IU vitamin D 500 mg Thiamine or more Choline Iodine – 600 to 1200 mcg of Liquid Iodine Vitamin B2 helps break down proteins, fats, and carbohydrates. It plays a vital role in maintaining the body's energy supply.  500 mg Nicotinic Acid - increase capillary blood flow, lower cholesterol. I recently started 2000 mg a day instead of a statin which I cannot tolerate. I the first month my HDL went from 29 to 44. eGFR (kidney function) jumped from 55 ti 75. It also has make my whole body less stiff. The ichy, flushing with the first few doses goes away. The non flush forms of vitamin B3 do not work. It is the relaxing of the capillaries and tendons. 500 mg Pantothenic Acid vitamin B5 Omega-3 and Omega-6 Fatty Acids in Vegetables  Eating more of the vegetables low in omega six and high omega 3 can reduce inflammation Whole Milk Vanilla yogurt to which I add 100 grams of raspberrys, black berries and blueberries has lots of probiotics and makes my tummy and body happy. Red Bull has sugar (not high fructose corn syrup) and the vitamins (B2,3,5,6 need to metabolize to ATP energy and Taurine as an antioxident). It is a good source of energy for me because my genetic hyperlipidemia does not process complex carbs well.        
    • trents
      Gluten-like cross reactions to other foods are from the proteins that make them up. Dextrose is the sugar component found in corn.
    • Ryangf
      I just found out a few days ago that some salt like table salt contains dextrose that’s derived from corn. I’ve been thinking about getting rid of using table salt and just using my own kosher or Himalayan salt, but tbh I’m reluctant to do it. I’ve cut out a lot of things and I don’t really want to cut out anything else that I’m not sure will effect me…in a super small amount that it might be added to salts to stabilize the iodine. I don’t want to be further alienated when I have to go to a restaurant with my friends. Also most of the items at my house that have salt in it canned food etc. are some of the few quick things I can eat- because I’m not the one paying for the food in my household and i can only ask for so much. I’m not in a place financially where I can get a lot of my specialized items- although my family tries their best to get items I Can actually stand. I get I can bring a my own salt with me at a restaurant and ask for no seasoning but it feels like a lot to me- cause I already check for cross contamination and ask if the food has like a high volume of corn in it like cornstarch etc. I’ve also heard most dextrose is not derived from the Zein (corn gluten) portion of it- so it might be safe- but idk if that’s true. I just wanna know if anyone actually responded to it negatively.
    • Scott Adams
      For my first couple of years after discovering my celiac disease I also had to avoid cow's milk/casein and eggs, as well as other things, but could tolerate duck eggs and sheep and goat's milk products. I'm not sure if you've tried those, but it could be worth testing them out.
    • knitty kitty
      Hello, @Kwinkle, How are you doing?   Have you tried adding a Magnesium supplement?   The B Complex vitamins need magnesium to work properly, especially thiamine vitamin B 1.   Magnesium deficiency symptoms and Thiamine deficiency symptoms both include gas and bloating.  Thiamine deficiency symptoms also include loss of appetite and fatigue.   My gas and bloating resolved rather quickly when I took Benfotiamine (a form of thiamine shown to promote intestinal healing) and Magnesium Glycinate in addition to my B 50 Complex (all twice a day plus the following...).   I found Magnesium L-Threonate or Magnesium Taurate are better when taken with a form of thiamine called TTFD (Tetrahydrofurfuryl dusulfide) because all of these cross the blood brain barrier easily, which corrects the loss of appetite, fatigue and anxiety.    Like @Celiacandme said, keeping a food/mood/poo'd journal is a big help in finding problematic foods, and for making sure your diet is not carbohydrate heavy.  If you're eating a lot if processed gluten free facsimile foods, be aware they do not have vitamins and minerals added to them like their gluten containing counterparts.  For every 1000 kcal of carbohydrates, we need an extra 500 mg of thiamine to turn them into energy and not store them as fat.   Let us know how you're doing!
×
×
  • Create New...