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

FODMAP Diet Versus Specific Carb Diet Question


Kathleen Smith

Recommended Posts

Kathleen Smith Contributor

Hi All, I am researching (or trying) both FODMAP and the Specific Carb Diet b/c I am gluten free a year and still having nausea and constipation. I am getting a breath test done next Monday but all other tests are good.

Which diet is better if you are symptomatic or if you have smaill intestineal bacterial overgrowth (SIBO)??

The FODMAP seems to allow corn, potatoes, sweet potatoes and rice and the Specific Carb Diet doest not??? That seems like a huge difference in diet!!!!

So just wondering peoples thoughts who know more than I do.

As always thank you in advance and I hope you are all feeling well!


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



Celiac.com Sponsor (A8-M):



kayo Explorer

Hi Kathleen,

I'm following the FODMAP diet and recovering from SIBO. One more day of antibiotics to go. My understanding is that the FODMAP diet starves the SIBO and prevents it from coming back. I feel good on this diet and will continue on it even though my fructose test came back negative. I don't know how anyone follows the SCD. It seems so restrictive and limiting. I suppose I would do it if I needed to but luckily the FODMAP diet is working.

Here are the best resources I found on FODMAP:

Book - "IBS - Free at Last!" by Patsy Catsos

Yahoo group - Open Original Shared Link

Good luck!

  • 1 year later...
Gutsy Girl Rookie

Kathleen and Kayo,

I was wondering the same thing. I have celiac and SIBO.

I wonder if perhaps one type of bacteria - the main classifications I know about are hydrogen versus methane producing bacteria - tends to have different preferences so that folks who have methane bacteria do better on SCD and folks who have hydrogen bacteria do better on FODMAP, for example? Just wondering. I have absolutely no idea.

But I too am comparing these two diets to start myself, and was noticing how they are almost opposite each other.

Takala Enthusiast

?????? Which diet is better if you are symptomatic of what? "still having" sounds more like there is hidden gluten in the diet.

Both FODMAPS and SCD are restrictive, but FODMAPS wins hands down for the number of ridiculous things that must be eliminated in terms of fruits and vegetables. I did a modified SCD diet in the beginning for a few years, which is easy IF you are getting good results, because it is much more likely to be truly gluten free and not as likely to be cross contaminated. I had a lot of trouble finding a benign form of yogurt, a SCD staple, that wasn't full of lactose, or thickened with starch, and therefore didn't do dairy for a while, then gradually tried adding back in cheese, which worked. From this SCD experience, it was easy for me to see that my actual problem was grain- based. Slowly I added back in other forms of carbohydrates that were not grain, successfully, such as legumes (dried beans, for example, cooked & rinsed so they were not starchy.) As long as they were not cross contaminated, I didn't have a problem. When adding a new food, it should be done one at a time, not all at once. Some of the FODMAPS lists I am seeing for "safe" foods include SPELT, which is WHEAT and NOT GLUTEN FREE.

People spend a lot of time & effort messing around with other diet variations, eliminating a lot of perfectly good foods, when they are instead needing to be strictly gluten free and, if necessary, figure out what other foods on a gluten free diet do not agree with them. The FODMAPS diet lists avoid a lot of artificial sweeteners that bother almost everybody... this is a no brainer. But you are trying to eat for celiac/gluten intolerance.

These tend to be milk and soy, for celiacs. And then one or more of the alternative, gluten-free grain products.

Celiac tends to cause thyroid problems and therefore a side effect may be insulin resistance.... any low or no sugar, low carb, high protein diet will go better with a slow thyroid. Soy is also notorious for not being compatible with thyroid problems.

The part of the intestinal lining that processes milk/dairy is also damaged in celiac, so giving up dairy, at least temporarily, to see what happens is one of the most common ways to find out if that is a problem. Then non lactose dairy, such as gluten-free yogurt or hard, aged cheeses, can be reintroduced and seen if that is a problem, as well. If dairy is a problem, it has to go. If lactose is a problem, it has to go. Just like gluten. No amount of giving up a long list of other fruits and vegetables will "fix" this.

When I do baking now, I am still using a lot of nut meals, (non soy) bean flours, potato flours, seed meals, because I am not very good with a lot of grains. The most exasperating thing I'm encountering is random cross contamination for staple food items. I know I can eat fresh corn, for example, but other forms of corn grains, even "gluten free," seem to be a cc minefield, and I am familiar enough with my symptoms I can tell it is low gluten exposure. I might be an oat reactor, and the latest studies (2011) explain that as there are certain varieties/cultivars of oats that celiac/gluten intolerant people will react to anyway, even if they are certified gluten free. Others are okay. That would explain a lot if a manufacturer was running corn and oats thru the same facility. Oh, and there are a lot of manufacturers using the same lines to run "gluten free," and wheat foods.... NOT GOOD.

Other times, from what I am reading, certain gluten-free grains, like millet, are much more likely to be cross contaminated than others, when samples have been tested. There is another thread going now where a lot of people say they are having a non gluten but a reaction to it, anyway. We're all not meant to eat everything, obviously. But is it the "chicken, or the egg?"

Anytime I get into trouble, I can go back onto my version of a modified SCD diet, and get myself back on track within a day. But it is just to get things sorted out, not permanent.

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 hjayne19's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      15

      Insomnia help

    2. - TheDHhurts posted a topic in Gluten-Free Foods, Products, Shopping & Medications
      0

      need help understanding testing result for Naked Nutrition Creatine please

    3. - cristiana replied to hjayne19's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      15

      Insomnia help

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

    • Total Members
      133,108
    • Most Online (within 30 mins)
      7,748

    Maggie1349
    Newest Member
    Maggie1349
    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
      @cristiana,  I react the same way.  Dairy consumption flushes out my digestive system within an hour, too! As casein is digested, it forms casomorphins that bind to opioid receptors in our bodies.  This is similar to digested gluten peptides being able to attach to opioid receptors in our bodies.   We have opioid receptors throughout our bodies including lots in the digestive tract. Casein raises tTg IgA antibodies just like gluten consumption does, which leads to further intestinal damage and continuing inflammation.  No wonder our bodies react to it by pushing the "emergency evacuation" ejection seat button! The mother of my childhood friend was British and introduced me to drinking tea properly with milk or cream.  I miss it so much.  And chocolate ice cream.  Not worth the after effects, though.  I've found taking Omega Three supplements (flaxseed oil, sunflower seed oil, evening primrose oil) helps shake those dairy cravings.   Green leafy veggies like broccoli, kale, and greens (mustard, turnip, collards) are great sources of calcium.  Avoid spinach as it is high in oxalates that block calcium absorption and may cause kidney stones.  Yes, more leafy greens are needed to reach the same amount of calcium in a glass of milk, but the greens have other benefits, like increased dietary fiber and polyphenols that act as antioxidants, reduce inflammation, and promote health.   Exposure to gluten (and casein in those sensitive to it) can cause an increased immune response and inflammation for months afterwards.  The immune cells that make tTg IgA antibodies which are triggered today are going to live for about two years. During that time, inflammation is heightened.  Those immune cells only replicate when triggered.  If those immune cells don't get triggered again for about two years, they die without leaving any descendents programmed to trigger on gluten and casein.  The immune system forgets gluten and casein need to be attacked.  The Celiac genes turn off.  This is remission.   Some people in remission report being able to consume gluten again without consequence.  Another triggering event can turn the Celiac genes on again.   Celiac genes are turned on by a triggering event (physical or emotional stress).  There's some evidence that thiamine insufficiency contributes to the turning on of autoimmune genes.  There is an increased biological need for thiamine when we are physically or emotionally stressed.  Thiamine cannot be stored for more than twenty-one days and may be depleted in as little as three during physical and emotional stresses. Mitochondria without sufficient thiamine become damaged and don't function properly.  This gets relayed to the genes and autoimmune disease genes turn on.  Thiamine and other B vitamins, minerals, and other nutrients are needed to replace the dysfunctional mitochondria and repair the damage to the body.  
    • TheDHhurts
      Hi, I bought Naked Nutrition Creatine. It lists itself as gluten free but is not certified. (It used to be, but they dropped it in the past year or two apparently.) I wrote the company and asked them what testing results they had for creatine and they sent me the attached, which says the test result for gluten is <0.025MCG. I'm used to seeing test results as ppm, so I'm not sure what <0.025MCG means. Can it be converted to ppm easily? I want to confirm that it is safe to use.
    • cristiana
      When I was still recovering my gastroenterologist suggested I bought lactofree product as I was very bloated.  So I bought some from the supermarket and from memory, I drank a nice big glass of milk - and it went right through me literally within an hour or so, if my memory serves correctly.  I came off dairy completely next and it worked like a charm, but started to reintroduce quite gradually it as I missed it! To this day, if I overdo dairy products, they work like a mild laxative.  I've never wanted to give up milk completely as I like it so much, and my mum had osteoporosis and it's an easy way of getting calcium.  But it doesn't really 'sit' well with me.   You may need to experiment a bit as when I was healing certain dairy products were worse than others - I could cope with one brand of Greek yoghurt, but I got extremely and painfully bloated with another brand of live British yoghurt.  
    • wellthatsfun
      i have been strictly gluten free for 7 months. this includes avoiding anything that may contain gluten and making sure surfaces and appliances are clean. i am 18 years old in australia and my tTG-IgA results were 69U/mL, pretty low compared to most people's, for reference. i feel the exact same as before. sure, i was pretty much asymptomatic/silent. the worst i'd get was occasionally bad stools and pitting of the nails/brittle hair since early childhood - and i was diagnosed with low iron and vitamin d which checks out due to easy bruising and such. but those symptoms have remained. maybe i'm jumping the gun, sure. i know it can take years to fully heal. but being over half a year in, i feel that i should be, y'know, healing. i'm nearly at my wits end and wondering if i should have a piece of bread or something to see how i go - to see if i possibly have refractory? my mental health is declining as i feel myself wanting to bang my head against a damn wall out of frustration every day. cravings haven't gotten better. look, i love the stuff i still can have, like salads and such. OH! i haven't lost any weight, which is mind boggling considering i eat very healthily now! i've always been on the chubbier side which is atypical of coeliac. i just don't know what's going on with me. i try to remain hopeful but i'm just so sad all the time. thanks for reading  
    • trents
      @Charlie1946There is a PM (Personal Message) tool built into the forum website that allows you to send a private message to other forum users. Just hover over their name with your mouse cursor and the menu containing that tool will pop up. This is useful if you want to communicate with an individual without everyone else involved in the thread seeing it.  Are you realizing that in my PPI taper down recommendations in an earlier post above, I was responding not to your posts but to @Caligirl57? If you must use a PPI, I certainly would advise taking the lowest dose that is effective for 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.