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Stomache Bloating/gas Daily


campcour

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campcour Apprentice

i have never used this forum before so hopefully i am doing it right. anyways, i have been strictly gluten-free and dairy free for about 8 months now and feeling much better. but i still have severe stomache distention and gas almost every day. in the morning my stomache is flat and normal looking and feels really good. then about a few hours after eating anything, it starts getting bloated and gets more and more distended throughout the day. by the time i go to bed i look pregnant and my stomache hurts and is really gasy. please help! any suggestions are greatly appreciated. i don't know what to do anymore. :unsure:


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pturse Apprentice

I am going through the exact same thing. gluten-free for 8 months. In the morning after I have BM I feel great and my stomach is flat but as soon as I eat the smallest amount of food I get bloated and gassy no matter what I eat.

celiac3270 Collaborator

I'm gluten-free 7 months with bad symptoms -- not so much gas as vomiting/stomach pains -- sorry I can't help, but I'm in the same boat in terms of length of time (almost) passed w/o feeling better

burdee Enthusiast

Even after I eliminated gluten/dairy sources, I also still had symptoms of bloating, gas and cramping pain. When I tried to substitute soy for dairy, I had the same symptoms. So I also abstained from soy Avoiding those 3 things gave me some 'good' days of no pain, no bloating, very little gas. But whenever I had any accidental ingestion of any of those 3 ingredients, I experienced all the symptoms again. I have also noticed sensitivity to acidic foods like tomatoes, raspberries, alcohol, etc. so I have avoided those. I'm not sure what could have caused my last symptoms, but avoiding acid seemed to help. I read that as we restrict the main food intolerances like gluten/dairy/soy, we may discover other sensitivities which are related to damage to our intestines during longterm undiagnosed celiac disease. Since I've only been avoiding gluten 4+ months, dairy 2+ and soy 1+ month, I'm still learning to avoid sources and possible cross contamination from those 3 ingredients. So I'm not completely symptom free, but I'm a long ways from where I started 4-1/2 months ago. ;)

BURDEE

PS I also take digestive enzymes and probiotics and use 'beano' before consuming some notoriously 'gassy' veggies and beans.

tarnalberry Community Regular

There may be other foods you're eating that are causing the problem. Like burdee noted, soy could be an issue. Some other very common foods can cause bloating even though there's no intolerance issue - beans, peppers, etc. You may want to talk to your GI, due to the extremity of the situation (maybe bring in "morning"/"evening" pictures? ;-) ). I've heard some people say digestive enzymes have helped them, and you might find some variation on an elimination diet to find out what other foods you have problems with would help.

Carriefaith Enthusiast

I have also been on the gluten-free diet for a long time (6 months) and still have problems. Gas and bloating are a daily routine now <_< My other symptoms are getting better thankfully :)

My GI doc says that having celiac disease caused me to have an irritated bowel.

I personnally think that some celiacs have more extensive damage than others and require a longer healing time. I think that some of those people suffer through the whole healing process. That's just my opinion though.

-Carrie

campcour Apprentice

i was surprised to see how many people replied to my question and very excited that people are there to help and tell their story. it helps to know that others are going through similar things. i have been avoiding all soy/dairy and gluten very strictly but i am curious about the digestive enzymes. what are these? i have never heard of them. i have made an appt to see a gi speicalist again, but it takes a long time to get (3 months) in so in the meantime i am trying to do anything that might help me to feel better. thanks again for all the responses! i really appreciate it :)


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tarnalberry Community Regular

digestive enzymes are ... just like lactase, but for other things that need digesting. you can try googling the term, and checking out a local health food store for more information. I'm not well informed enough at the moment to speak authoritatively on them, but the idea is that, if your body isn't producing the enzymes you need to break down your food, you can take the enzymes with your food. (just like the lactose intolerant may choose to take lactase with their dairy-containing meals)

Canadian Karen Community Regular

Hi.....

I just wanted to mention that if you are taking anything for the gas/bloating, make sure it is gluten free. I made the mistake of thinking Gas-X was gluten-free and I was eating them like candy because my gas/bloating was so bad. Found out recently they actually contain gluten.

Just wanted to make sure you aren't making the same mistake.....

Good Luck!

Karen

burdee Enthusiast

I just thought of another source of gas and bloating which I now avoid. When I was looking at ingredients for gluten free/casein free toothpastes, I noticed most include sorbitol which can cause gas and bloating for many people. The only gluten-free/cf toothpaste I found WITHOUT sorbitol is Tom's of Maine. Also many sugar free candies and gums include sorbitol or mannitol (similar to sorbitol in gas/bloating effect). :o

BURDEE

ponita Newbie

My goodness, I am so glad I found this conversation today! I have been gluten-free for 12 weeks and have felt so much better until yesterday when I had a couple Tablespons of ice cream on an empty stomach. I have tolerated Blue Bunny ice cream with no problem after a meal (about a 1/3 cup serving), yesterday I started the abd. pain almost immediately and have been in gastric distress ever since and eating Gas X for 24 hours.

Thanks for bringing up this subject (not something you can easliy discuss with your friends over coffee at work).

I know what to do now, thanks!

Melissa

Guest jhmom

It seems as though a lot of us continue to have GI probs such as diarrhea, abdominal pain, nausea, etc.. even on the gluten-free diet. I have been gluten-free for almost one year with some improvement but not enough to say "I feel good".

I don't know if it takes some people longer to heal than others or the possiblity of another problem on top of Celiac. I suggest talking to your GI doctor about it and possibly requesting lab-work and or any other tests/procedures to be done. I recently switched GI docs and told him of my problems, his first thought was I was not sticking to my diet which is not true but has decided to do an endoscopy/biopsy to check things out. There has to be an underlying problem here. Personally I do not think my GI problems have anything to do with Celiac, I think there is another problem, the hardest part is waiting on the doctors to figure it all out.

Good luck to each of you and I hope each of you begin to feel better soon!

campcour Apprentice

thanks so much for all the suggestions! i bought some digestive enzymes last night and tried them... still felt really sick last night. but i have hope that they will help if i give them some time. but i am wondering if these don't work, what other things do people use for gas/bloating? i am looking for something sold in canada. thanks for your help!

burdee Enthusiast

Peppermint tea helps relieve the cramping pains from celiac disease reactions. For gas and bloating I do pilates or yoga exercises that put my knees to my stomach or over my head. That works EVERY time to push gas through. Also a hot shower with water spray concentrated on the painful area helps me. I won't take any drugs to treat celiac disease symptoms, because there's so many potential side effects from ingredients which I may not tolerate.

BURDEE

kabowman Explorer

After I discovered the lactose/casien intolloerance, I then discovered the gluten intollerance. Once those were eliminated from my diet. I discovered a peanut intollerance, a soy bean intollerance, a corn intolloerance, and a peanut intollerance. Corn syrup is used in a LOT of foods and a lot of foods contain soy bean products and/or are made using peanut/corn oil.

I though my regular mayo was safe, not so--soy bean oil. I thought a little bit of corn syrup each day wouldn't kill me, I was wrong.

Go completely, sauce free, only fresh veggies and fruit and meat for a few days until your stomach clears up (mine took almost a week) and then start adding things back in. I have now a wide selection of products to use that use real sugar, apple cider vinegar, rice, etc.

-Kate

burdee Enthusiast

Kate: HOW did you discover those other 'intolerances'? After relying on just fruit, vegies and meat for a while, did you add back each of those ingredients (peanuts, corn and soy) in an 'elimination' diet manner? I already have been diagnosed (Enterolab tests) with gluten and casein intolerances and reacted badly to soy. So as I ate my breakfast of PEANUT BUTTER on an Ener-G foods Brown Rice Sweet Potato muffin with CORN flour, I considered your post about those additional intolerances. :o Everytime I discover a food I REALLY enjoy, but doesn't give me any immediate, obvious symptoms (like acidic foods have also recently given me), I fear I may have problems with that food. :huh: I have MUCH less painful symptoms than I did before I eliminated gluten/dairy/soy, but I still have occasional twinges, gas and bloating. So when you avoided gluten/dairy/soy/peanuts/corn, what DID you eat for breakfast that wouldn't require extensive preparation? My symptoms (excruciating abdominal pain) are usually pretty obvious, so I don't think I react to peanuts and corn, but I sure do like those which makes me suspicious. :blink: Were your reactions to peanuts and corn much different from your dairy/soy/gluten reactions?

BURDEE

kabowman Explorer

Well, after my stomach calmed down, I added other foods back in, catiously. After eating peanuts as a snack a few days in a row and realizing, hey! my stomach hurts, I have gas, etc. I think this might be a problem. I have since discovered that even stuff I thought was safe, i.e., did NOT have peanuts even reading the ingredients but having the same symptoms, I would then, usually too late, re-read and discover it was made with peanut oil. Who would have thought???? Not me.

Well, that kind of goes for everything else. I have been drinking soy milk for years as I am lactose/casien intollerant and not thinking about it, added it to my coffee one morning and guess what...same problems. I just discovered my mayo, which I thought was safe was primarily made with soy bean oil. No wonder I was getting sick on what I thought was safe food.

Rice and potatoes are OK for me, corn was not - although I kept trying it, I was still getting sick so that has now been COMPLETELY eliminated from my diet. Talk about something that is in EVERYTHING - high fructose corn syrup, from gum to BBQ sauce to Margartita mix.

Breakfast: Lucky for me, my husbands makes eggs and bacon (which surprisingly I can eat) every morning (with olive oil, not any type of margarine since they all contain at least soy bean and/or corn and/or lactose). And on mornings he is gone, I eat fruit and almonds (just about the only nut not prepared with peanut oil), and sometimes pre-cooked bacon - not store bought but what we purchased then cook up in advance to make mornings easier. We do the same with dinner meats to make evenings with three kids, us both working full time, all the activities, etc. that much easier. We then just need to fix side dishes.

I have actually just had my first really good days in a couple of weeks. No corn syrup! Camping was a little difficult with 3 different families and all the sauces and milk products going around. I just ate as much of my food as I could but it ALL looked SO good, it was a little hard to pass up.

-Kate

strack2004 Rookie

I just posted a long list of foods I eat on the SCD diet on another thread. Forgot to write it down, but it was posted today, Sept 13. Upon reading these posts, I realize that one of the things I have eaten regularly for lunch is peanut butter. Last Tuesday was a day when I felt better than I have for awhile all day. That was possibly because I didn't eat peanut butter for lunch that day. Although I felt better in the morning, too, and I had had peanut butter the day before. Ruth

burdee Enthusiast

Thanks, Kate, for the reassurance. No, really, you reassured me by telling me you had SYMPTOMS after introducing each of those foods. I also had SYMPTOMS when I introduced soy products to substitute for dairy products. However, I have NEVER had symptoms after eating peanut butter or corn products. Before my gluten/casein intolerance test results, corn and peanuts were foods I could easily do without. I started eating peanut butter as a protein/fat source, since I could no longer have casein/soy products and don't like to take time to cook eggs for breakfast. <_< So I guess I really like peanut butter on muffins with corn flour because they FEEL good in my body, not because of any addictive craving. Unfortunately, I have previously eaten tomatoes, acidic berries and citrus fruit because I thought it was 'healthy' for me and ignored my symptoms. The biggest thing I've learned from my celiac disease diagnosis is NOT to ignore any discomfort after eating ANYTHING, healthy or not. As long as I stay gluten/casein/soy free and acid limited (including citric acid in diet sodas), I feel VERY good and symptom free. :D

BURDEE

tarnalberry Community Regular

I think it's a valid point, though... we go about replacing all these foods, and then end up eating potential allergens in large quantity... While there's no "proof" that repeated exposure to the allergen will cause it (well, a lot of allergists will tell you that... ;-) ), it means I try to not eat the same thing (if it's got a high allergen potential) day after day. I do worry about becoming sensitive to peanuts (I love peanut butter... fab food for hypoglycemics ;-) ) and soy (gotta have something for my cream of buckwheat!), but I'll cross those bridges if I ever have to.

CoolCat1 Rookie

I have been gluten-free for 2 months and I just recently found out that my favourite chocolate Lindt/Lindor has malt. Cheaper chocolates do not. I am looking for a comparable Swiss/Belgian chocolate. Anyone know of any? :angry: Chocolate withdrawal uck!

burdee Enthusiast

Tropical Source makes great gluten/dairy free chocolate bars (delicious DARK chocolate) in dark expresso roast, hazelnut, raspberry, almond and rice varieties. UNFORTUNATELY those contain SOY which may cause problems for others (like me). :( Has anyone found any gluten/dairy/soy free chocolate? I know Ener-G Foods makes gluten-free/df/sf chocolate chips as does EnjoyLifeFoods. But I'm still looking for gluten-free/df/sf chocolate bars. :unsure:

BURDEE

campcour Apprentice

just to let you all know that i have been taking digestive enzymes for about 5 days now and was SUPER SICK, but had been really sick before, so i thought they just took time. well, the health food store informed me they were gluten free and it said "wheat free" on the bottle (organika, digestive enzymes). but i made the mistake of trusting that and finally decided to contact the company. turns out there is gluten in them. so don't use! does anyone know a gluten free brand? preferably in canada? same with probiotics.. i was accidentaly using one with gluten in it. errr! i can't find a gluten free one in canada.

vany4 Newbie

Dove chocolate is gluten free.

sixtricks6 Newbie

Is there different levels of celiac disease? I get severe bouts that last a about a week to 2 weeks and then other days maybe just gasy, or maybe just nauseia or just bloating with a little cramping in between the severe attacks.

Cheryl

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      Welcome to the celiac.com community @EssexMum! First, let me correct some misinformation you have been given. Except in the case of what is known as "refractory" celiac disease, which is very rare, it is not true that the "fingers" will not grow back once a consistently gluten free diet is adopted. Celiac disease is an autoimmune condition whereby the ingestion of gluten triggers an inflammatory process that damages the millions of tiny finger-like projections that make up the lining of the small bowel. We call this the "villous lining". Over time, continued ingestion of gluten on a regular basis results in the wearing down of these fingers which greatly reduces the surface area of this very important membrane. It is where essentially all the nutrition from what we eat is absorbed. So, losing this surface area results in inefficiency in nutrient absorption and often to medical problems related to nutrient deficiencies. Again, if a gluten-free diet is consistently observed, the villous lining of the small bowel should rebound. "We was informed that her body absorbs the gluten rather then rejecting it and that is why she doesn't react to the gluten straight away, it will be a build up and then the pains start. " That sounds like unscientific BS to me. But it does sound like your stepdaughter may have a type of celiac disease we know as "silent" celiac disease, meaning, she is asymptomatic or at least the symptoms are not intense enough to usually notice. She is not completely asymptomatic, however, because you stated was experiencing tummy aches off and on. Cristiana gives some good suggestions about ordering "safe" food for your stepdaughter from restaurant menus in Europe. You must realize that as the step parent who only has her part of the time you have no real control over how cooperative her other set of parents are with regard to your stepdaughter's needs to eat gluten free. It sounds like they don't really understand the seriousness of the matter. This is very common in family settings where other members are ignorant about celiac disease and the damage it can do to body systems. So, they don't take it seriously. The best you can do is make suggestions. Perhaps print out some info about celiac disease from the Internet to send them. Being inconsistent with the gluten free diet keeps the inflammation smoldering and delays or inhibits healing of the villous lining. 
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    • cristiana
      Good evening @EssexMum You are quite right to be concerned about this situation.  Once diagnosed as coeliac, always a coeliac, and the way to heal  is through adopting and sticking to a strict gluten diet. That said... I have travelled twice to France since my diagnosis, firstly in May 2013 and again in August 2019.   My spoken French isn't bad, and whilst there I tried my best to explain my needs to chefs and catering staff, and I read labels very carefully when shopping in supermarkets, but both times I came away with worsening gastric symptoms and pain. Interestingly,  after the second holiday, my annual coeliac review took place the following month and although I'd been very careful to avoid gluten all year, thanks to that August holiday my coeliac antibodies were elevated,  Clearly I hadn't been imagining these symptoms and they must have been caused by gluten sneaking in somehow. When I spoke to my gastroenterologist on my return, who is an excellent doctor, he told me with a smile that this was a very common experience in France among his patients, and not to worry too much about it! In fact, before we went away in May 2013, which was just after I had been formally diagnosed, he told me not to even bother trying to adopt a gluten free diet until I returned, knowing what France was like, but I was feeling so awful at that time I ignored his advice and at least tried to make a start with it. (I ought to say - both these visits were some time ago, so perhaps things are a lot better there now.) So what to do?  I would say at least try to explain to catering staff the situation - they should be able to rustle up a plate of cheese, boiled eggs, tuna, salad and fruit, and if things like crackers and gluten-free pot noodle or oats can be packed in the UK, those can be produced at mealtimes.    Of course, most larger supermarkets in France do now cater for coeliacs, but when I was last there the the choice wasn't as wide a range as we have in the UK but I think that is partly because the French like to cook from scratch, whereas our gluten-free aisles have quite a lot of dried or pre-baked goods in them/convenience foods, because I think we as a nation tend to use them more. I would be worth doing a bit of research on the internet before the trip, - the words you want are 'sans gluten'.  I've just googled 'sans gluten Disney Paris" and this came up.  I do hope at least some of this is of help. https://www.tripadvisor.co.uk/Restaurants-g2079053-zfz10992-Disneyland_Paris_Ile_de_France.html  Whatever befalls in France, at least your stepdaughter can resume her usual diet on her return. On a related tack, would you be happy to post any positive findings/tips upon her return - it might be of use to others travelling to Disneyland Paris with children in future? Cristiana
    • EssexMum
      Hi, I am after some advice re my step daughter and her Coeliac Disease. She is 9 years old and had a very limited diet before being diagnosed (very fussy and very lenient parents), since being diagnosed it has become hard to find places out that will cater for her, but we manage.  History: She had been having severe tummy pains on and off every few months so had a bunch of tests and eventually was diagnosed with celiac disease a number of months ago. We was told that she is at a very high level and should avoid gluten for the rest of her lift, we was told that the gluten she has been eating has damaged the 'fingers' inside her and they will not replenish. We was informed that her body absorbs the gluten rather then rejecting it and that is why she doesnt react to the gluten straight away, it will be a build up and then the pains start. We was advised that by her not reacting straight away, it did not mean it wasnt harming her inside. We was given literature about buying a separate toaster and cutting board etc to avoid cross contamination and have been checking all food labels etc.  Problem: the issue is the novelty seems to have worn off with her Mum and we are now posed with a situation. They are going on holiday to Disneyland Paris for 3 nights and she phoned the hotel who said they cannot cater for gluten free. She phoned the GP and had a conversation and then told my partner that the GP had said it was fine for her to have gluten for the 3-4 days. He questioned it and she said no its fine, she hasnt had it for months so a few days wont hurt and she exposed to it anyway without knowing so it will be fine and shes not ruining her holiday etc.   My partner could see from the online notes that his ex wife had told the doctor that the child does not follow a strict gluten-free diet anyway - not true. At least not with us! My partner requested a call with the same doctor who told him that it is the mums discretion and that the child should be monitored for reactions - he explained that the issue is she doesnt react straight away. The GP said no its all mums discretion and she knows best. We are going to try to speak to the consultant at the hospital, but I just wanted to gauge some thoughts. It just seems bizarre to me that we can go from being told to avoid gluten for the rest of her life and how harmful it is to her body, to now it being ok for her to have it for a few days. Thanks in advance  
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