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

An Apple A Day......


Lizking531

Recommended Posts

Lizking531 Rookie

Alright - been thru the gamut of Dr's offices - long story short, after test & test & hernia surgery - ended up with a doc telling me I had bacteria overgrowth. Between diet, exercise & probiotics, had everything under control for the past year or more. Lately, eveything has been sliding back to how it was. Right now I have 3 specific foods that I try to avoid because they kill me. There's a few others I try to avoid as well (beer, processed food, sugar) but they aren't quite as menacing. Basically, I try to eat "real" food prepared simply. My go-to dish is my "white meal" - baked chicken breast, white rice, some sort of mild veggie.

The foods that kill me:

apples (uncooked - eating an apple "like an apple")

summer squash/zucchini

bananas

certain IPA beers

Each of those give me horrible gas, explosive BM (for lack of better term), irritability, feeling of a lump in my throat, and like a confused/dazed feeling. There's enough distension in my system that I can feel exactly where the mesh for the hernia was put.

Has any one experienced anything like this or have any suggestions/stories/anecdotes/etc for this situation?


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



Celiac.com Sponsor (A8-M):



ravenwoodglass Mentor

Are you gluten free? IPA beers are not something we can tolerate we have to drink beer without barley malt. Redbridge, New Grist, Greens gluten-free etc.

If your drinking them regularly, even just a couple a week, your keeping the antibodies active.

lucia Enthusiast

Have you seen an allergist? Perhaps you are actually allergic to these foods (not including the beer, which is gluten-based)?

Lizking531 Rookie

Are you gluten free? IPA beers are not something we can tolerate we have to drink beer without barley malt. Redbridge, New Grist, Greens gluten-free etc.

If your drinking them regularly, even just a couple a week, your keeping the antibodies active.

No, I started going that route, but I never made it completely to gluten-free - I read to keep gluten intake while testing, so I quit trying to change the diet for a bit. Once tests came back with bacteria overgrowth, I went to (what I call) a "whole food" diet - very little, if any, processed food & sugar, supplemented with probiotics.

Everything was more or less "ok" (never what I'd consider normal, but not bad) for the last couple years. I would still have 3-4 solid bm's per day (but much cut back from the 15+ not-solid per day previously). My energy was back up & I felt a lot better.

Now more recently I am back to having gas that causes sharp pain, lot's of gas, more floating stinky stools, stools more often, overall crappiness feeling, more fatigue & irritability, feeling "full" - not finished feeling. It also kinda feels like I have UTI - but I don't. I have also noticed more often that when I feel like crap, I also have the feeling of a lump in the back of my throat that I didn't really notice before.

One other note - I can eat a salad, but only every other day. If I eat a salad 2 days in a row - it will look almost identical on the way out as on the way in - like it never digested at all.

Could this still be celiac or is it more likely a food allergy?

- I'm fed up & skeptical with the Dr's so I'm looking to avoid that as much as possible.

I do see in hindsight that this question would've been more properly suited for a different topic - more of a pre or figuring it out, rather than celiac specific - pardon me...

Katie B Apprentice

I'm dealing with bacterial overgrowth and potential celiac disease - I have enough autoimmune things going on that I feel more comfortable eliminating gluten.

You should check out the low FODMAP diet. It limits the foods that will ferment and provide extra food for the bacteria. The team at Monash University in Australia is conducting the research and Sue Shepherd - Shepherd Works and Jaci Barrett at Diet Solutions are dieticians specializing in the diet.

I tried the specific carbohydrate diet and it worked but find that this diet allows a bit more variety - small portions of rice etc.

Apples are a huge problem for people with fructose malabsorption (not fructose intolerance) - they are highly fermentable. Safer fruits (at 1/2 cup per serve spaced out by 2.5 hours) are berries, kiwi, grapes, melon and more. I would limit your amount of fruit for a little while until you get things under control. Bananas can be problematic as well because they are a pre-biotic and feed bacteria. Apparently a full serve of banana is 1/2 a banana.

I can send you more info if you like. You can also order the booklet from Monash and get a more in-depth list. I should mention it does help to speak to the dieticians who are doing the research because all of the lists on the internet of "safe" and "unsafe" FODMAP foods conflict. They're also always testing new foods so the information is very recent.

Sue Shepherd also has a couple of cookbooks that I've yet to use (I still can't eat a lot of the foods).

I'd watch out for carbs too - those are what get me with the SIBO.

T.H. Community Regular

Well, just things to check to see if they might be of use?

1. Fructose Malabsorption: veggies, fruits, and whole grains can set this off. Often involves lots of gas and stool problems, and then other issues from poor absorption of other foods since your gut is messed up. Apples are a definite 'bad' food for this problem, but white rice is a definite 'good.' I believe fermented products are also not so good for this issue, as well, so might be worth checking out. just like celiac disease, the only cure is to alter the diet, and many people alter the diet to diagnose it, too.

This link lists some of the good/bad/in moderation foods for people with this issue:

Open Original Shared Link

Oh, and it's not genetic, it's caused, they just don't know by what. But seems to be more common in people who had other gut issues.

2. intestinal parasites or h. pylori infection. You might want to look up some parasite symptoms to see if they match any of your difficulties. Or H. pylori ones.

3. Crohn's disease. there can be trigger foods, and foods that cause more trouble. Steroids are what is needed to help this, for a while, and to figure out the trigger foods.

Wishing you good luck and hoping that you can find a solution and feel better soon!

cassP Contributor

yes- look up fructose malabsorption & the FODMAP diet...

i have this to an extent-

but i have to tell you- a lot of the times- Fructose Malabsorption &/or Lactose Intolerance go hand in hand with Celiac or Gluten Intolerance.

you may need to also get back to eating enough gluten for proper celiac blood panels


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



Celiac.com Sponsor (A8-M):



WheatChef Apprentice

Almost nothing should look the same going out as it went in (except for pennies, why are you eating pennies, oh no wait that's my dog who does that). I don't think the fructose malabsorption would specifically explain why you can't have raw apples but have no problems from cooked apples.

For bananas is it the same in regards to cooked/uncooked? If you chew on an apple for a while do you get itchiness in the mouth? Aside from the squashes, the apples/bananas/hops raw issues may be related to oral allergy syndrome (aka pollen allergy syndrome). It's basically a collection of foods that your body responds to as if they were really pollen, cooking breaks down the offending proteins however and renders the cooked substance safe. Itching occurs in the mouth and throat but if you swallow it the histamine response can also occur in your intestines leading to the issues you mentioned.

Lizking531 Rookie

Almost nothing should look the same going out as it went in (except for pennies, why are you eating pennies, oh no wait that's my dog who does that). I don't think the fructose malabsorption would specifically explain why you can't have raw apples but have no problems from cooked apples.

For bananas is it the same in regards to cooked/uncooked? If you chew on an apple for a while do you get itchiness in the mouth? Aside from the squashes, the apples/bananas/hops raw issues may be related to oral allergy syndrome (aka pollen allergy syndrome). It's basically a collection of foods that your body responds to as if they were really pollen, cooking breaks down the offending proteins however and renders the cooked substance safe. Itching occurs in the mouth and throat but if you swallow it the histamine response can also occur in your intestines leading to the issues you mentioned.

Hehehe - and quarters: if you get back 2 dimes & a nickel, ya got a problem :lol:

I cant' say I've ever noticed, or thought about, cooked bananas. I can't say I've had an itchiness in my mouth that stood out specifically (except maybe bananas), I'll have to pay attention better. Bananas can sometime taste kinda metallic/acidic to me, but I just thought that's how it was.

I've read about fructose malabsorbtion before. I'm may need to do a little more reading.

One other thing I feel I should add is that I quit smoking a few months ago. When all my troubles started intially a couple years ago, it was right after I tried to quit before. I made it a couple months but ended up smoking again because, unfortunately, it made my guts feel better. This go round it's been almost 6 months, but with no desire to smoke again. Although I do have a strong desire to get my guts in check.

Katie B Apprentice

So confusing eh?

Did you become constipated after stopping smoking? If you're eating highly fermentable foods and you're constipated then it compounds the problem because it gives the bacteria even longer to feast away.

I would highly recommend eating foods that aren't highly fermentable and making sure things are moving. There's some debate as to whether people with SIBO should take probiotics - I'm taking 1/2 packet of VSL#3 2 x a day.

Just as an FYI - wheat and milk products (containing lactose) are highly fermentable as well.

If you are constipated and need a laxative then avoid lactulose at all costs - this is a prebiotic and will make things 100x worse. I imagine you'd have to see a Dr. about it but PEG is not fermentable and is over the counter.

I agree with CassP though - SIBO is often a result of something else (weakened immune system, celiac disease, non-celiac gluten intolerance, even ulcerative colitis and crohn's) and it's definitely worth getting everything checked out.

Good luck!

Lizking531 Rookie

So confusing eh?

Did you become constipated after stopping smoking? If you're eating highly fermentable foods and you're constipated then it compounds the problem because it gives the bacteria even longer to feast away.

I would highly recommend eating foods that aren't highly fermentable and making sure things are moving. There's some debate as to whether people with SIBO should take probiotics - I'm taking 1/2 packet of VSL#3 2 x a day.

Just as an FYI - wheat and milk products (containing lactose) are highly fermentable as well.

If you are constipated and need a laxative then avoid lactulose at all costs - this is a prebiotic and will make things 100x worse. I imagine you'd have to see a Dr. about it but PEG is not fermentable and is over the counter.

I agree with CassP though - SIBO is often a result of something else (weakened immune system, celiac disease, non-celiac gluten intolerance, even ulcerative colitis and crohn's) and it's definitely worth getting everything checked out.

Good luck!

Well, yes & no - a lot of both (not sure if that makes any sense). Overall, I would say more constipated than when I smoked, but that is not without bouts of D here & there. Granted, there's a lot of things at work with cigs & GI stuff.

The fructose stuff does hit home on some accounts, but, as always with this stuff, there's still room for mystery. I read somewhere before to pay attention to your cravings, since many times you will actively crave those things which you should avoid. I definitely have sweet cravings - sometimes those are much worse than any cig craving.

Overall, the concept of things fermenting in my belly does make sense. I have so much gas so often that it's often embarrassing - i.e. the first date with my now-fiance (luckily) - I leaned down to pick up my cat to show her & my leaning was enough internal pressure...well... Sometimes beer can make me swell up like a balloon - like take a sip, belly expands, take a sip belly expands, etc.

Yeah - I've been to the GI specialist, doctors, blood, stool, urine, etc, etc. I have thought about Enterolab or allergy testing, but I'm now so put off by most doctors from the previous run arounds that I don't really care if someone can diagnose anything or not - I'm looking for relief I can live with & work with.

mommyto3 Contributor

You mentioned you often feel like you have a UTI but you don't. I felt like that for probably 4 years, on and off, before I found out I had celiac. I had really bad bladder irritation which would cause me to feel like I had to go all the time. Only difference with a UTI is that you have the burning - I didn't have burning with the irritation which is how I knew it wasn't a UTI.

I just pretty much learned to live with this until I started having all the terrible gut symptoms of Celiac. I visited my doc who was sending me for an ultrasound and she suggested I try gluten free while waiting for the tests. The first week I went gluten free was like a miracle for me. My bladder symptoms completely resolved within a day and I FELT GREAT for the first time in years.

Since going gluten free I have not had that UTI feeling. And the funny thing is that I even had a real UTI but didn't get any symptoms. My doc found it through a routine urine test. Go figure!

Just wanted to let you know that bladder irritation is a pretty common symptom of Celiac.

cassP Contributor

You mentioned you often feel like you have a UTI but you don't. I felt like that for probably 4 years, on and off, before I found out I had celiac. I had really bad bladder irritation which would cause me to feel like I had to go all the time. Only difference with a UTI is that you have the burning - I didn't have burning with the irritation which is how I knew it wasn't a UTI.

I just pretty much learned to live with this until I started having all the terrible gut symptoms of Celiac. I visited my doc who was sending me for an ultrasound and she suggested I try gluten free while waiting for the tests. The first week I went gluten free was like a miracle for me. My bladder symptoms completely resolved within a day and I FELT GREAT for the first time in years.

Since going gluten free I have not had that UTI feeling. And the funny thing is that I even had a real UTI but didn't get any symptoms. My doc found it through a routine urine test. Go figure!

Just wanted to let you know that bladder irritation is a pretty common symptom of Celiac.

ive had that feeling of getting a UTI when i would go back on gluten in the past... and i wonder if that has anything to do with Interstitial Cystitis... its an inflammatory condition that i have seen linked to other autoimmune diseases.

Lizking531 Rookie

ive had that feeling of getting a UTI when i would go back on gluten in the past... and i wonder if that has anything to do with Interstitial Cystitis... its an inflammatory condition that i have seen linked to other autoimmune diseases.

& what sucks about it all is the friggin feeling of chasing my tail around. The symptoms are the same for so many different things & having one thing trigger something else, etc, etc - I'm not really sure what direction to look.

Does anyone have any experience with Lyme disease?

I don't know much about it, other than ticks. I have had some nasty run-ins with ticks in the past - had one of the worst "flu" feelings after getting bit. I hike/hunt/spend a lot of time outdoors - I sure I will be bit again, it's really only a matter of luck or time. I'm not sure if I've been checked for Lyme, but if so, it's only been in the "normal" run of generic bloodwork from a GP. I wonder if this would be worth looking into more seriously or not...

MelindaLee Contributor

Hehehe - and quarters: if you get back 2 dimes & a nickel, ya got a problem :lol:

I cant' say I've ever noticed, or thought about, cooked bananas. I can't say I've had an itchiness in my mouth that stood out specifically (except maybe bananas), I'll have to pay attention better. Bananas can sometime taste kinda metallic/acidic to me, but I just thought that's how it was.

I've read about fructose malabsorbtion before. I'm may need to do a little more reading.

One other thing I feel I should add is that I quit smoking a few months ago. When all my troubles started intially a couple years ago, it was right after I tried to quit before. I made it a couple months but ended up smoking again because, unfortunately, it made my guts feel better. This go round it's been almost 6 months, but with no desire to smoke again. Although I do have a strong desire to get my guts in check.

Not sure if this is related or not, but my friend has severe asthma due to allergies. She cannot eat zuchinni, cucumbers, etc, especially when her asthma is at it's worst. (pretty much anything that is ripening or being harvested at this time of the year)

Archived

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

  • Get Celiac.com Updates:
    Support Celiac.com:
    Join eNewsletter
    Donate

  • Celiac.com Sponsor (A17):
    Celiac.com Sponsor (A17):





    Celiac.com Sponsors (A17-M):




  • Recent Activity

    1. - knitty kitty replied to Jmartes71's topic in Related Issues & Disorders
      1

      New issue

    2. - knitty kitty replied to GlutenFreeChef's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      6

      Blood Test for Celiac wheat type matters?

    3. - trents replied to Charlie1946's topic in Related Issues & Disorders
      38

      Severe severe mouth pain

    4. - knitty kitty replied to Charlie1946's topic in Related Issues & Disorders
      38

      Severe severe mouth pain

    5. - Caligirl57 replied to Charlie1946's topic in Related Issues & Disorders
      38

      Severe severe mouth pain

  • Celiac.com Sponsor (A19):
  • Member Statistics

    • Total Members
      133,085
    • Most Online (within 30 mins)
      7,748

    kk007
    Newest Member
    kk007
    Joined
  • Celiac.com Sponsor (A20):
  • Celiac.com Sponsor (A22):
  • Forum Statistics

    • Total Topics
      121.5k
    • Total Posts
      1m
  • Celiac.com Sponsor (A21):
  • Upcoming Events

  • Posts

    • knitty kitty
      @Jmartes71, Sorry you've been feeling so poorly.   Are you taking any medication to treat the SIBO?   Are you taking any Benfotiamine?  Benfotiamine will help get control of the SIBO.  Thiamine deficiency has symptoms in common with MS. Have you had your gas appliances checked for gas leaks and exhaust fume leaks?  Carbon Monoxide poisoning can cause the same symptoms as the flu and glutening.  Doctors have to check venous blood (not arterial) for carbon monoxide.  Are other inhabitants sick, or just you?  Do they leave the house and get fresh air which relieves their symptoms?  
    • knitty kitty
      European wheat is often a "soft wheat" variety which contains less gluten than "hard wheat" varieties found in the States.   In European countries, different cooking methods and longer  fermentation (rising or proofing) times allow for further breakdown of gluten peptides. Wheat in the States is a blend of hard and soft wheat.  Gluten content can vary according to where the wheat was grown, growing conditions, when harvested, and local preference, so a blend of both hard and soft wheat is used to make a uniform product.   I moved around quite a bit as a child in a military family.  I had different reactions to gluten in different areas of the country every time we moved.  I believe some wheat breeds and blends are able to provoke a worse immune response than others.   Since European soft wheat doesn't contain as much gluten as American wheat, you may try increasing your intake of your soft wheat products.  A minimum of ten grams of gluten is required to get a sufficient immunological response so that the anti-gluten antibodies leave the intestines and enter the bloodstream where they can be measured by the tTg IgA test.  Your whole wheat bread may only have a gram of gluten per slice, so be prepared...  
    • trents
      From my own experience and that of others who have tried to discontinue PPI use, I think your taper down plan is much too aggressive. It took me months of very incremental tapering to get to the point where I felt I was succeeding and even then I had to rely some days on TUMS to squelch flareups. After about a year I felt I had finally won the battle. Rebound is real. If I were you I would aim at cutting back in weekly increments for two weeks at a time rather than daily increments. So, for instance, if you have been taking 2x20mg per day, the first week cut that down to 2x20mg for six days and 1x20 mg for the other day. Do that for two weeks and then cut down to 2x20mg for five days and 1x20 for two days. On the third week, go 20x2 for four days and 20x1 for 3 days. Give yourself a week to adjust for the reduced dosage rather than reducing it more each week. I hope this makes sense. 
    • knitty kitty
      Talk to your doctor about switching to an antihistamine, and supplementing essential vitamins and minerals.  Dietary changes (low carb/paleo) may be beneficial for you.  Have you talked to a dietician or nutritionist about a nutrient dense gluten free diet?   It's harder to get all the vitamins needed from a gluten free diet.  Gluten containing products are required to be enriched or fortified with vitamins and minerals lost in processing.  Gluten free facsimile processed foods are not required to be enriched nor fortified.  So we have to buy our own vitamin supplements.   Glad to be of help.  Keep us posted on your progress!
    • Caligirl57
      I’m pretty sure they do. I have been on myfortic, tacrolimus since 2021 for my liver transplant and added prednisone after kidney transplant.  I’m going to try to cut back omeprazole to 20 mg a day and then after a week try to stop altogether. Thank you for your help.
×
×
  • 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.