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

Problems Digesting Sugar?


jjc

Recommended Posts

jjc Contributor

I have been gluten free for a year and am doing pretty well, but I've noticed in the last couple of months that I have problems whenever I eat anything sweet (even fruit). What kinds of test can my doctor run to determine what kinds of sugar I can eat? I hate the thought of not eating ANY sugar at all. Aren't fruits supposed to be healthy sugar and not give me that much of a problem? I am in college and this is getting hard to deal with.


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



Celiac.com Sponsor (A8-M):



Imanistj Contributor

The sugar in fruit is just as fattening as table sugar. Diabetics have to be aware of the sugar intake they get from fruit as well as other foods. Fruit is loaded with vitamins so taking in sugar from fruit is far better for you than getting it from candy. If you are not diabetic or don't have a problem digesting a specific kind of sugar, a well balanced diet can include both fruit and an occasional sweet dessert. Moderation in all things. Gee, I wish I could follow that advice :huh: I just ate an apple and I still want "something sweet."

YoloGx Rookie

I agree--its a bummer not to be able to eat sugary things in this sugar full world. However such is life for some of us, and in the long run our health benefits are worth it since without sugar we usually are a lot healthier than many others around us.

I too haven't been able to eat sugar, fruit, honey etc. without ill effect for some time. Instead I use gluten-free and lactose free stevia for sweetener.

It has been frustrating not eating sugars at times, esp. not to be able to eat fruit either. I have a bad reaction otherwise (itchy flaky with both whitened and reddened "elephant" skin in my nethers as well as flaky itchy ears) which seems to be from candida or fungal overgrowth.

Many people who have celiac as well as other conditions (esp. if one has had antibiotcs--and who hasn't??) have this problem. The thing is to starve the yeast etc. so no sugars and a low carb diet with very limited ground up flours. Whole grains are better than something ground up since it takes longer whole for it to convert into sugar. It helps too to eat lots of green vegetables and make one's own blended vegetable drinks. It really revives one with a big energy boost much better than sugar ever could.

I have gradually gotten more used to not eating sugars--so now it really isn't so hard like it was. The only fruits I eat regularly are lemons (in lemon aide --with stevia-- as well as a condiment on vegetables etc. since with this condition it also tends to make one adversely susceptible to vinegar too).

Recently I have added olive leaf extract and tea to combat the systemic fungi. It really is helping quite a lot. I now can occasionally have blueberries without ill effect. Besides the olive leaf I take oregano oil capsules, caprylic acid, and eat lots of garlic. Plus I take enterically coated acidophilus to build up my good flora and thus better combat the candida or fungal overgrowth.

Another recent addition has been taking a small amount of bitters (dandelion with gentian root) before my meals. It helps not only with better digestion and detoxifying the liver but also against vaginal discharge and anal itching.

Good luck with this. You are not alone.

Bea

lcarter Contributor

There is such a thing as Fructose Malabsorption [the sugar most frequently found in fruit], which is a digestive disorder of the small intestine in which the fructose carrier in enterocytes is deficient. But, do not confuse FM with Hereditary Fructose Intolerance if you look it up on the internet, cause that's a genetic inborn error that shows up in newborns and concerns a different pathway. FM is sometimes seen along with Celiac and Lactose Intolerance. FM medical tests are similar to the test for lactose intolerance, requiring a hydrogen breath test for a clinical diagnosis. The breath test is simple - you ingest a measured amount of the offending sugar and then breath samples are taken in a laboratory. Sometimes stool tests are done too. In fact, they can check all types of sugars this way and it is simple to do. A big offender in the diet and found everywhere is High Fructose Corn Syrup, which must be removed from your diet. By the way, the symptoms of FM are very similar to the digestive disorder part of Celiac - which could be a possibility for those of us who have continuing problems on a gluten free diet. Hope this helps.

Check out this site:

Open Original Shared Link

YoloGx Rookie
There is such a thing as Fructose Malabsorption [the sugar most frequently found in fruit], which is a digestive disorder of the small intestine in which the fructose carrier in enterocytes is deficient. But, do not confuse FM with Hereditary Fructose Intolerance if you look it up on the internet, cause that's a genetic inborn error that shows up in newborns and concerns a different pathway. FM is sometimes seen along with Celiac and Lactose Intolerance. FM medical tests are similar to the test for lactose intolerance, requiring a hydrogen breath test for a clinical diagnosis. The breath test is simple - you ingest a measured amount of the offending sugar and then breath samples are taken in a laboratory. Sometimes stool tests are done too. In fact, they can check all types of sugars this way and it is simple to do. A big offender in the diet and found everywhere is High Fructose Corn Syrup, which must be removed from your diet. By the way, the symptoms of FM are very similar to the digestive disorder part of Celiac - which could be a possibility for those of us who have continuing problems on a gluten free diet. Hope this helps.

Check out this site:

Open Original Shared Link

That info on fructose malabsorption looks interesting! Thanks.

I may have a doctor check into whether or not I have fructose malabsorption sometime.

Meanwhile any sugar at all bothers me similarly--though I can have a little honey once in a blue moon without quite as much distress. Definitely saved for the holidays!

Bea

jackay Enthusiast

I am wondering, too, if I have fructose problems. I will definitely bring this concern to my doctor at my next appointment. I love fruit and eat a lot of it for the calories. I sure hope that it isn't causing some of my problems along with the glucose. If I have to give up fruit my calorie intake will definitely be less. I have lost so much weight and have absolutely no appetite. I do love fruit so can eat it even when I am not hungry.

I did test positive to dairy so can't get calories from that. Nuts are causing problems, too. It is difficult since I need to avoid all the high calorie foods.

  • 2 weeks later...
jjc Contributor

Thanks for the info about fructose malabsorption! I may look into getting tested for it!


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



Celiac.com Sponsor (A8-M):



Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,547
    • Most Online (within 30 mins)
      7,748

    gizmo1jazz2
    Newest Member
    gizmo1jazz2
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.4k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • Scott Adams
      Your post demonstrates the profound frustration and isolation that so many in the Celiac community feel, and I want to thank you for channeling that experience into advocacy. The medical gaslighting you endured for decades is an unacceptable and, sadly, a common story, and the fact that you now have to "school" your own GI specialist speaks volumes about the critical lack of consistent and updated education. Your idea to make Celiac Disease a reportable condition to public health authorities is a compelling and strategic one. This single action would force the system to formally acknowledge the prevalence and seriousness of the disease, creating a concrete dataset that could drive better research funding, shape medical school curricula, and validate the patient experience in a way that individual stories alone often cannot. It is an uphill battle, but contacting representatives, as you have done with Adam Gray, is exactly how change begins. By framing it as a public health necessity—a matter of patient safety and protection from misdiagnosis and neglect—you are building a powerful case. Your voice and your perseverance, forged through thirty years of struggle, are exactly what this community needs to ensure that no one else has to fight so hard just to be believed and properly cared for.
    • Scott Adams
      I had no idea there is a "Louisville" in Colorado!😉 I thought it was a typo because I always think of the Kentucky city--but good luck!
    • Scott Adams
      Navigating medication safety with Celiac disease can be incredibly stressful, especially when dealing with asthma and severe allergies on top of it. While I don't have personal experience with the HealthA2Z brand of cetirizine, your caution is absolutely warranted. The inactive ingredients in pills, known as excipients, are often where gluten can be hidden, and since the FDA does not require gluten-free labeling for prescription or over-the-counter drugs, the manufacturer's word is essential. The fact that you cannot get a clear answer from Allegiant Health is a significant red flag; a company that is confident its product is gluten-free will typically have a customer service protocol to answer that exact question. In situations like this, the safest course of action is to consider this product "guilty until proven innocent" and avoid it. A better alternative would be to ask your pharmacist or doctor to help you identify a major national brand of cetirizine (like Zyrtec) whose manufacturer has a verified, publicly stated gluten-free policy for that specific medication. It's not worth the risk to your health when reliable, verifiable options are almost certainly available to you. You can search this site for USA prescriptions medications, but will need to know the manufacturer/maker if there is more than one, especially if you use a generic version of the medication: To see the ingredients you will need to click on the correct version of the medication and maker in the results, then scroll down to "Ingredients and Appearance" and click it, and then look at "Inactive Ingredients," as any gluten ingredients would likely appear there, rather than in the Active Ingredients area. https://dailymed.nlm.nih.gov/dailymed/   
    • Scott Adams
      What you're describing is indeed familiar to many in the Celiac community, especially in the early stages of healing. When the intestinal villi are damaged from Celiac disease, they struggle to properly digest and absorb fats, a condition known as bile acid malabsorption. This can cause exactly the kind of cramping and spasms you're seeing, as undigested fats can irritate the sensitive gut lining. It is highly plausible that her reactions to dairy and eggs are linked to their higher fat content rather than the proteins, especially since she tolerates lean chicken breast. The great news is that for many, this does improve with time. As her gut continues to heal on a strict gluten-free diet, her ability to produce the necessary enzymes and bile to break down fats should gradually return, allowing her to slowly tolerate a wider variety of foods. It's a slow process of healing, but your careful approach of focusing on low-fat, nutrient-dense foods like seeds and avocado is providing her system the best possible environment to recover. Many people with celiac disease, especially those who are in the 0-2 year range of their recovery, have additional food intolerance issues which could be temporary. To figure this out you may need to keep a food diary and do an elimination diet over a few months. Some common food intolerance issues are dairy/casein, eggs, corn, oats, and soy. The good news is that after your gut heals (for most people who are 100% gluten-free this will take several months to two years) you may be able to slowly add some these items back into your diet after the damaged villi heal. This article may be helpful: Thank you for sharing your story—it's a valuable insight for other parents navigating similar challenges.
    • Beverage
      I had a very rough month after diagnosis. No exaggeration, lost so much inflammatory weight, I looked like a bag of bones, underneath i had been literally starving to death. I did start feeling noticeably better after a month of very strict control of my kitchen and home. What are you eating for breakfast and lunch? I ignored my doc and ate oats, yes they were gluten free, but some brands are at the higher end of gluten free. Lots of celics can eat Bob's Red Mill gluten-free oats, but not me. I can now eat them, but they have to be grown and processed according to the "purity protocol" methods. I mail order them, Montana Gluten-Free brand. A food and symptoms and activities log can be helpful in tracking down issues. You might be totally aware, but I have to mention about the risk of airborne gluten. As the doc that diagnosed me warned . . Remember eyes, ears, nose, and mouth all lead to your stomach and intestines.  Are you getting any cross contamination? Airborne gluten? Any pets eating gluten (they eat it, lick themselves, you pet them...)? Any house remodeling? We live in an older home, always fixing something. I've gotten glutened from the dust from cutting into plaster walls, possibly also plywood (glues). The suggestions by many here on vitamin supplements also really helped me. I had some lingering allergies and asthma, which are now 99% gone. I was taking Albuterol inhaler every hour just to breathe, but thiamine in form of benfotiamine kicked that down to 1-2 times a day within a few days of starting it. Also, since cutting out inflammatory seed oils (canola, sunflower, grapeseed, etc) and cooking with real olive oil, avocado oil, ghee, and coconut oil, I have noticed even greater improvement overall and haven't used the inhaler in months! It takes time to weed out everything in your life that contains gluten, and it takes awhile to heal and rebuild your health. At first it's mentally exhausting, overwhelming, even obsessive, but it gets better and second nature.
×
×
  • 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.