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

Bacterial Overgrowth - Specific Carbohydrate Diet?


lucia

Recommended Posts

lucia Enthusiast

Through a combination of an elimination diet and a food diary, I've concluded that, yes, everything I put into my gut is making me sick. Even when I drink water, I am getting some cramping of my stomach. I think I'm getting the most severe cramps from sweet potatos, bananas, and rice, which are starchy. I think I must have bacterial overgrowth. Does that sound like a valid assessment?

I've read that the Specific Carbohydrate Diet will cure bacterial overgrowth (usually in combination with probiotics). Does that mean if I start eating foods off of this diet that I'll start to feel better? I know that total recovery takes awhile, but will I get some relief right away?

I am going to talk to a doctor about this. I have an appointment (finally) with the Celiac Center at Columbia this Friday. I know that a doctor can test for bacterial overgrowth. In the meantime, I'm in a lot of pain. I'm trying to decide what to do until I can talk to a specialist. Does anyone have any advice?


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



Celiac.com Sponsor (A8-M):



MissyJoy Rookie

I was on a very strict diet for over 2 years to get rid of an intestinal yeast over growth. I went to a nutritionist and her plan had two parts to it. 1 - Starve the yeast and 2 - Kill the yeast.

1. to startve the yeast, I had to avoid all food with simple sugars in them, including fruits, potatoes, corn, all dairy, and all grains, except 1/2 cup of Brown rice a day.

2. To kill the yeast, I took 8 drops of Grapefruit Seed extract in a large glass of water a day. Plus took probiotics without food and at bed time.

Being on this diet and taking those supplements really helped me, but it is an intense diet and can take a while.....

brendab Contributor

I was on a very strict diet for over 2 years to get rid of an intestinal yeast over growth. I went to a nutritionist and her plan had two parts to it. 1 - Starve the yeast and 2 - Kill the yeast.

1. to startve the yeast, I had to avoid all food with simple sugars in them, including fruits, potatoes, corn, all dairy, and all grains, except 1/2 cup of Brown rice a day.

2. To kill the yeast, I took 8 drops of Grapefruit Seed extract in a large glass of water a day. Plus took probiotics without food and at bed time.

Being on this diet and taking those supplements really helped me, but it is an intense diet and can take a while.....

I second this diet!

Look at your tongue.......does it have a white coating to it? That is yeast.

lucia Enthusiast

Look at your tongue.......does it have a white coating to it? That is yeast.

My tongue looks like it is wrapped up in white fur. :(

cassP Contributor

Lucia- how long have u been gluten free? and before that - how MUCH gluten was in your diet? i DID have the issue with even JUST WATER- i remember it at work one day- i was fine, and then i just drank a glass of water- and i felt gurgles in my intestines & thought i was gonna have the "D"- & i even complained about how even JUST WATER was messing me up! it was ridiculous.... but i havent felt that in a few years.

im still having issues tho w/ fructose & sugar & grains... little white tongue... need to go back to NO CARBS- just so hard... soon tho

u WILL feel better- just gonna take a little more time & a strict diet- & i also love the GSE

lucia Enthusiast

I've been gluten free now for 4 and 1/2 long months. At first, my GI symptoms receded entirely unless I accidentally consumed gluten. Then, one by one, I became intolerant to foods, including all dairy, soy, and corn. It's only been recently that I get cramps no matter what I eat or drink.

I had a pretty healthy diet before I stopped eating gluten - lots of whole fruits and veggies, and little sugar and processed foods. I struggled with fibromyalgia in my 20s and was only able to find relief through diet and exercise, so I was motivated to eat healthfully. I still ate a fair amount of gluten though, like most Americans.

GlutenFreeManna Rising Star

It sounds like you may have a problem with intestinal yeast. I originally suspected my problem could be yeast when I did my elimination diet and I eliminated all grains, sugars and carby vegetables as well. I was quite surprised when after a month I could add in potatoes and corn without symptoms, but wheat and dairy gave my bad reactions. Then I did more research on celiac/gluten intolerance and figured out that that was really my problem. You may be the opposite--you may have intestinal yeast and not celiac (unless you have +test results). Or you could have both. Anyway, when I was first looking into yeast/candida I stumbled upon a very long thread on a low-carb website. It is very long, but it was a wealth of information. And you can get a lot out of it even if you just read a few pages. People post their symptoms and what they eat and supplements they take, etc. The thing about yeast (if that's your problem) is it seems there are a NUMBER of different approaches to dealing with it. Some sites say no fruit at all, other say only unsweetened berries and lemon are okay, others say fruit is fine in moderation...Some say you need to do diet AND supplements (anti-fungals) to be effective, others say you can just do diet or just do anti-fungal meds (nystatins) to kill the yeast and probiotics to build good bacteria. It's not very scientific and it seems like there's tons of conflicting advice. So you have to figure out what works for you. Here's the thread in case you are interested in reading it: Open Original Shared Link

I really hope you figure out what's bothering you soon.


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



Celiac.com Sponsor (A8-M):



Kathleen Smith Contributor

Hi Lucia,

I have been going to the Celiac Disease Research Center in Columbia myself! I went there because I am a year and half into Gluten Free diet and my GI symptoms of nausea are horrible. It seems no matter what eat, just by eating i get sick.

Good luck to you!

cassP Contributor

i wonder if some of us just have overburdened & tired Livers and Gallbladders- from years of prior gluten.... cause usually if u get nauseaus like an hour after eating- it could be liver or gallbladder... ??? idk... i did a few Liver Flushes over the years- they are a real real huge pain in the a tho.. plus- i only had 1 flush that was actually worth it- like 400 stones came out... the last one i only got maybe 2 stones... and my (hemorrhoids) cant really take it anymore- so i think im done BUT i fully believe in the power of a good Liver Flush-

if u follow all the rules to a T and it's productive- then it's SO worth it

?

i also think daily exercise helps the digestive tract.

& there's a mind connection too- i think we have some of the same chemicals in our digestive tract that we have in our brain

and lastly- i agree with everyone on here about the SIBO & Yeast.

i also did a Parasite Flush a couple of times

sorry, im rambling now- just trying to help

LindaIone Newbie

I also struggled with yeast like symptoms for years. And I also felt like I was allergic to everything! Fruit, sugar, beans, potatoes, gluten, corn. But now I am starting to understand. All those things are carbs. I'm obviously carb sensitive and I wonder how many other people dealing with gluten have the same problem. No reason a person should be sensitive only to wheat/gluten. Since carbs affect your blood sugar just like sugar itself, it may be best to limit them. There is a very interesting book out now called, "Life without Bread". It suggests that carbs are the source of most of our illness, and that our bodies need to use more good fats for energy in place of the carbs. I have been going low carb for a couple of weeks now, and I'll tell you that I miss them - they are truly addictive. But I have noticed that my white coated tongue is going away. Kind of too soon to know if it will be permanent...Good luck.

vbecton Explorer

This is an interesting post! I'm currently 4 months into the gluten-free diet and have eliminated nearly everything. Everything I eat makes me sick. I'm a whole food eater, no grains at all except the odd 1/2 cup of rice. Nothing processed, blah blah blah. The problem is trying to identify the source of the problem because the diets can all be conflicting. I was following the paleo diet which advised that no amount of fruit in the world could hurt you. Well, meet the apple and pear. Those send me straight to the potty! I'm trying the FODMAP diet (only the whole foods part) at the moment thinking I have some sort of fructose issue, but then I think, what's the point...I'm sick from everything. Frustrating.

I know my latest test showed SIBO. Is that the same thing as yeast? I go back to the GI on Wednesday to see how he wants to treat all this.

frieze Community Regular

This is an interesting post! I'm currently 4 months into the gluten-free diet and have eliminated nearly everything. Everything I eat makes me sick. I'm a whole food eater, no grains at all except the odd 1/2 cup of rice. Nothing processed, blah blah blah. The problem is trying to identify the source of the problem because the diets can all be conflicting. I was following the paleo diet which advised that no amount of fruit in the world could hurt you. Well, meet the apple and pear. Those send me straight to the potty! I'm trying the FODMAP diet (only the whole foods part) at the moment thinking I have some sort of fructose issue, but then I think, what's the point...I'm sick from everything. Frustrating.

I know my latest test showed SIBO. Is that the same thing as yeast? I go back to the GI on Wednesday to see how he wants to treat all this.

No, SIBO is small intestine bacterial overgrowth....or something close, lol.

bacteria an yeast are two different things.

cassP Contributor

This is an interesting post! I'm currently 4 months into the gluten-free diet and have eliminated nearly everything. Everything I eat makes me sick. I'm a whole food eater, no grains at all except the odd 1/2 cup of rice. Nothing processed, blah blah blah. The problem is trying to identify the source of the problem because the diets can all be conflicting. I was following the paleo diet which advised that no amount of fruit in the world could hurt you. Well, meet the apple and pear. Those send me straight to the potty! I'm trying the FODMAP diet (only the whole foods part) at the moment thinking I have some sort of fructose issue, but then I think, what's the point...I'm sick from everything. Frustrating.

I know my latest test showed SIBO. Is that the same thing as yeast? I go back to the GI on Wednesday to see how he wants to treat all this.

i COMPLETELY understand- & my problem with the Paleo OR any other diet out there that is prescribed as a ONE SIZE FITS ALL- is that WE'RE ALL DIFFERENT! i absolutely feel fantastic on nothing but meat & veggies... but a friend of mine did the no carb thing, and she ended up in the ER with kidney problems....

anyways- back to your point about the fruits- im right there with u- i suffered BIG TIME for a couple of months untill i realized i MUST have Fructose Malabsorption- i was eating a pear every night to help with my regularity- i kept suffering- cause my BMs were fantastic- and i thought- surely my body will adjust to the fiber and learn to digest it..... nope- never happened.. now that i learned all about FM- ive been able to see how it works- and after trial & error- know that i cant do pears, prunes, apple juice, dates, excess agave nectar or sweet potatoes or bananas.... etc etc....

its frustrating- cause the fruits really help with my bathroom experiences..... i usually do pineapple, half of a banana.... or 1/2 a mango...

FM can vary from person to person too- so u may have to do a little trial & error for yourself- & remember just because it's healthy doesnt mean u can eat it-if you're body doesnt have all the capability to digest the fructose- then it can overburden your kidney's & pancreas.

good luck :)

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. - suek54 replied to suek54's topic in Dermatitis Herpetiformis
      5

      Awaiting dermatitis herpetiformis confirmation following biopsy

    2. - trents replied to catnapt's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      3

      how much gluten do I need to eat before blood tests?

    3. - catnapt replied to catnapt's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      3

      how much gluten do I need to eat before blood tests?

    4. - trents replied to catnapt's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      3

      how much gluten do I need to eat before blood tests?

    5. - catnapt posted a topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      3

      how much gluten do I need to eat before blood tests?

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

    • Total Members
      133,257
    • Most Online (within 30 mins)
      7,748

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

    • Total Topics
      121.6k
    • Total Posts
      1m
  • Celiac.com Sponsor (A21):
  • Who's Online (See full list)

    • There are no registered users currently online
  • Upcoming Events

  • Posts

    • suek54
      Thank you all for your advice and the dermatitis herpetiformis article. The latter made me realise I had stopped taking my antihistamine, which I will restart today. The Dapsone has cleared the rash entirely but I still get quite a bit itching, absolutely nothing to see though. I know its notoriously hard to clear and its still relatively early days for me.  The iodine issue is very interesting. I do eat quite a bit of salt because I have Addison's disease and sodium retention is an issue. I also have autoimmune hypothyroidism, not sure how a low iodine diet would play into that? Because of my Addison's I am totally steroid dependent, I take steroids 4 x daily and cannot mount any defence against inflammation. I need to increase my meds for that. Now that I know what is wrong I can do just that if Im having a bad day. Life is very sweet, just so damn complicated sometimes! Hey ho, onwards. Thank you again for your advice.  
    • trents
      So, essentially all of the nutrition in the food we eat is absorbed through the villous lining of the small bowel. This is the section of the intestinal track that is damaged by celiac disease. This villous lining is composed of billions of finger-like projections that create a huge amount of surface area for absorbing nutrients. For the celiac person, when gluten is consumed, it triggers an autoimmune reaction in this area which, of course, generates inflammation. The antibodies connected with this inflammation is what the celiac blood tests are designed to detect but this inflammation, over time, wears down the finger-like projections of the villous lining. Of course, when this proceeds for an extended period of time, greatly reduces the absorption efficiency of the villous lining and often results in many and various nutrient deficiency-related health issues. Classic examples would be osteoporosis and iron deficiency. But there are many more. Low D3 levels is a well-known celiac-caused nutritional deficiency. So is low B12. All the B vitamins in fact. Magnesium, zinc, etc.  Celiac disease can also cause liver inflammation. You mention elevated ALP levels. Elevated liver enzymes over a period of 13 years was what led to my celiac diagnosis. Within three months of going gluten free my liver enzymes normalized. I had elevated AST and ALT. The development of sensitivities to other food proteins is very common in the celiac population. Most common cross reactive foods are dairy and oats but eggs, soy and corn are also relatively common offenders. Lactose intolerance is also common in the celiac population because of damage to the SB lining.  Eggs when they are scrambled or fried give me a gut ache. But when I poach them, they do not. The steam and heat of poaching causes a hydrolysis process that alters the protein in the egg. They don't bother me in baked goods either so I assume the same process is at work. I bought a plastic poacher on Amazon to make poaching very easy. All this to say that many of the issues you describe could be caused by celiac disease. 
    • catnapt
      thank you so much for your detailed and extremely helpful reply!! I can say with absolute certainty that the less gluten containing products I've eaten over the past several years, the better I've felt.   I wasn't avoiding gluten, I was avoiding refined grains (and most processed foods) as well as anything that made me feel bad when I ate it. It's the same reason I gave up dairy and eggs- they make me feel ill.  I do have a bit of a sugar addiction lol so a lot of times I wasn't sure if it was the refined grains that I was eating - or the sugar. So from time to time I might have a cookie or something but I've learned how to make wonderful cookies and golden brownies with BEANS!! and no refined sugar - I use date paste instead. Pizza made me so ill- but I thought it was probably the cheese. I gave up pizza and haven't missed it. the one time I tried a slice I felt so bad I knew I'd never touch it again. I stopped eating wheat pasta at least 3 yrs ago- just didn't feel well after eating it. I tried chick pea pasta and a few others and discovered I like the brown rice pasta. I still don't eat a lot of pasta but it's nice for a change when I want something easy. TBH over the years I've wondered sometimes if I might be gluten intolerant but really believed it was not possible for me to have celiac disease. NOW I need to know for sure- because I'm in the middle of a long process of trying to find out why I have a high parathyroid level (NOT the thyroid- but rather the 4 glands that control the calcium balance in your body) I have had a hard time getting my vit D level up, my serum calcium has run on the low side of normal for many years... and now I am losing calcium from my bones and excreting it in my urine (some sort of renal calcium leak) Also have a high ALP since 2014. And now rapidly worsening bone density.  I still do not have a firm diagnosis. Could be secondary HPT (but secondary to what? we need to know) It could be early primary HPT. I am spilling calcium in my urine but is that caused by the high parathyroid hormone or is it the reason my PTH is high>? there are multiple feedback loops for this condition.    so I will keep eating the bread and some wheat germ that does not seem to bother me too much (it hasn't got enough gluten to use just wheat germ)    but I'm curious- if you don't have a strong reaction to a product- like me and wheat germ- does that mean it's ok to eat or is it still causing harm even if you don't have any obvious symptoms? I guess what you are saying about silent celiac makes it likely that you can have no symptoms and still have the harm... but geez! you'd think they'd come up with a way to test for this that didn't require you to consume something that makes you sick! I worry about the complications I've been reading about- different kinds of cancers etc. also wondering- are there degrees of celiac disease?  is there any correlation between symptoms and the amnt of damage to your intestines? I also need a firm diagnosis because I have an identical twin sister ... so if I have celiac, she has it too- or at least the genetic make up for having it. I did have a VERY major stress to my body in 2014-2016 time frame .. lost 50lbs in a short period of time and had severe symptoms from acute protracted withdrawal off an SSRI drug (that I'd been given an unethically high dose of, by a dr who has since lost his license)  Going off the drug was a good thing and in many ways my health improved dramatically- just losing 50lbs was helpful but I also went  off almost a dozen different medications, totally changed my diet and have been doing pretty well except for the past 3-4 yrs when the symptoms related to the parathyroid issue cropped up. It is likely that I had low vit D for some time and that caused me a lot of symptoms. The endo now tells me that low vit D can be caused by celiac disease so I need to know for sure! thank you for all that great and useful information!!! 
    • trents
      Welcome, @catnapt! The most recent guidelines are the daily consumption of a minimum of 10g of gluten (about the amount found in 4-6 slices of wheat bread) for a minimum of two weeks. But if possible stretching that out even more would enhance the chances of getting valid test results. These guidelines are for those who have been eating gluten free for a significant amount of time. It's called the "gluten challenge".  Yes, you can develop celiac disease at any stage of life. There is a genetic component but also a stress trigger that is needed to activate the celiac genes. About 30-40% of the general population possesses the genetic potential to develop celiac disease but only about 1% of the general population actually develop celiac disease. For most with the potential, the triggering stress event doesn't happen. It can be many things but often it is a viral infection. Having said that, it is also the case that many, many people who eventually are diagnosed with celiac disease probably experienced the actual onset years before. Many celiacs are of the "silent" type, meaning that symptoms are largely missing or very minor and get overlooked until damage to the small bowel lining becomes advanced or they develop iron deficiency anemia or some other medical problem associated with celiac disease. Many, many are never diagnosed or are diagnosed later in life because they did not experience classic symptoms. And many physicians are only looking for classic symptoms. We now know that there are over 200 symptoms/medical problems associated with celiac disease but many docs are only looking for things like boating, gas, diarrhea. I certainly understand your concerns about not wanting to damage your body by taking on a gluten challenge. Your other option is to totally commit to gluten free eating and see if your symptoms improve. It can take two years or more for complete healing of the small bowel lining once going gluten free but usually people experience significant improvement well before then. If their is significant improvement in your symptoms when going seriously gluten free, then you likely have your answer. You would either have celiac disease or NCGS (Non Celiac Gluten Sensitivity).
    • catnapt
      after several years of issues with a para-gland issue, my endo has decided it's a good idea for me to be tested for celiac disease. I am 70 yrs old and stunned to learn that you can get celiac this late in life. I have just gradually stopped eating most foods that contain gluten over the past several years- they just make me feel ill- although I attributed it to other things like bread spiking blood sugar- or to the things I ate *with* the bread or crackers etc   I went to a party in Nov and ate a LOT of a vegan roast made with vital wheat gluten- as well as stuffing, rolls and pie crust... and OMG I was so sick! the pain, the bloating, the gas, the nausea... I didn't think it would ever end (but it did) and I was ready to go the ER but it finally subsided.   I mentioned this to my endo and now she wants me to be tested for celiac after 2 weeks of being on gluten foods. She has kind of flip flopped on how much gluten I should eat, telling me that if the symptoms are severe I can stop. I am eating 2-3 thin slices of bread per day (or english muffins) and wow- it does make me feel awful. But not as bad as when I ate that massive amnt of vital wheat gluten. so I will continue on if I have to... but what bothers me is - if it IS celiac, it seems stupid for lack of a better word, to intentionally cause more damage to my body... but I am also worried, on the other hand, that this is not a long enough challenge to make the blood work results valid.   can you give me any insight into this please?   thank you
×
×
  • 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.