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.

  • 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
      14

      My only proof

    2. - Jmartes71 replied to Jmartes71's topic in Related Issues & Disorders
      14

      My only proof

    3. - marion wheaton posted a topic in Gluten-Free Foods, Products, Shopping & Medications
      0

      Are Lindt chocolate balls gluten free?

    4. - Dorothy O. commented on Scott Adams's article in Latest Research
      7

      Study Estimates the Costs of Delayed Celiac Disease Diagnosis (+Video)

    5. - JoJo0611 replied to JoJo0611's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      4

      CT with contrast.


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      132,402
    • Most Online (within 30 mins)
      7,748

    alanhlam
    Newest Member
    alanhlam
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.5k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • knitty kitty
      @Jmartes71, I understand your frustration and anger.  I've been in a similar situation where no doctor took me seriously, accused me of making things up, and eventually sent me home to suffer alone.   My doctors did not recognize nutritional deficiencies.  Doctors are trained in medical learning institutions that are funded by pharmaceutical companies.  They are taught which medications cover up which symptoms.  Doctors are required to take twenty  hours of nutritional education in seven years of medical training.  (They can earn nine hours in Nutrition by taking a three day weekend seminar.)  They are taught nutritional deficiencies are passe' and don't happen in our well fed Western society any more.  In Celiac Disease, the autoimmune response and inflammation affects the absorption of ALL the essential vitamins and minerals.  Correcting nutritional deficiencies caused by malabsorption is essential!  I begged my doctor to check my Vitamin D level, which he did only after making sure my insurance would cover it.  When my Vitamin D came back extremely low, my doctor was very surprised, but refused to test for further nutritional deficiencies because he "couldn't make money prescribing vitamins.". I believe it was beyond his knowledge, so he blamed me for making stuff up, and stormed out of the exam room.  I had studied Nutrition before earning a degree in Microbiology.  I switched because I was curious what vitamins from our food were doing in our bodies.  Vitamins are substances that our bodies cannot manufacture, so we must ingest them every day.  Without them, our bodies cannot manufacture life sustaining enzymes and we sicken and die.   At home alone, I could feel myself dying.  It's an unnerving feeling, to say the least, and, so, with nothing left to lose, I relied in my education in nutrition.  My symptoms of Thiamine deficiency were the worst, so I began taking high dose Thiamine.  I had health improvement within an hour.  It was magical.  I continued taking high dose thiamine with a B Complex, magnesium. and other essential nutrients.  The health improvements continued for months.  High doses of thiamine are required to correct a thiamine deficiency because thiamine affects every cell and mitochondria in our bodies.    A twenty percent increase in dietary thiamine causes an eighty percent increase in brain function.  The cerebellum of the brain is most affected.  The cerebellum controls things we don't have to consciously have to think about, like digestion, balance, breathing, blood pressure, heart rate, hormone regulation, and many more.  Thiamine is absorbed from the digestive tract and sent to the most important organs like the brain and the heart.  This leaves the digestive tract depleted of Thiamine and symptoms of Gastrointestinal Beriberi, a thiamine deficiency localized in the digestive system, begin to appear.  Symptoms of Gastrointestinal Beriberi include anxiety, depression, chronic fatigue, headaches, Gerd, acid reflux, gas, slow stomach emptying, gastroparesis, bloating, diarrhea and/or constipation, incontinence, abdominal pain, IBS,  SIBO, POTS, high blood pressure, heart rate changes like tachycardia, difficulty swallowing, Barrett's Esophagus, peripheral neuropathy, and more. Doctors are only taught about thiamine deficiency in alcoholism and look for the classic triad of symptoms (changes in gait, mental function, and nystagmus) but fail to realize that gastrointestinal symptoms can precede these symptoms by months.  All three classic triad of symptoms only appear in fifteen percent of patients, with most patients being diagnosed with thiamine deficiency post mortem.  I had all three but swore I didn't drink, so I was dismissed as "crazy" and sent home to die basically.   Yes, I understand how frustrating no answers from doctors can be.  I took OTC Thiamine Hydrochloride, and later thiamine in the forms TTFD (tetrahydrofurfuryl disulfide) and Benfotiamine to correct my thiamine deficiency.  I also took magnesium, needed by thiamine to make those life sustaining enzymes.  Thiamine interacts with each of the other B vitamins, so the other B vitamins must be supplemented as well.  Thiamine is safe and nontoxic even in high doses.   A doctor can administer high dose thiamine by IV along with the other B vitamins.  Again, Thiamine is safe and nontoxic even in high doses.  Thiamine should be given if only to rule Gastrointestinal Beriberi out as a cause of your symptoms.  If no improvement, no harm is done. Share the following link with your doctors.  Section Three is especially informative.  They need to be expand their knowledge about Thiamine and nutrition in Celiac Disease.  Ask for an Erythrocyte Transketolace Activity test for thiamine deficiency.  This test is more reliable than a blood test. Thiamine, gastrointestinal beriberi and acetylcholine signaling.  https://pmc.ncbi.nlm.nih.gov/articles/PMC12014454/ Best wishes!
    • Jmartes71
      I have been diagnosed with celiac in 1994, in remission not eating wheat and other foods not to consume  my household eats wheat.I have diagnosed sibo, hernia ibs, high blood pressure, menopause, chronic fatigue just to name a few oh yes and Barrett's esophagus which i forgot, I currently have bumps in back of my throat, one Dr stated we all have bumps in the back of our throat.Im in pain.Standford specialist really dismissed me and now im really in limbo and trying to get properly cared for.I found a new gi and new pcp but its still a mess and medical is making it look like im a disability chaser when Im actively not well I look and feel horrible and its adding anxiety and depression more so.Im angery my condition is affecting me and its being down played 
    • marion wheaton
      Wondering if anyone knows whether Lindt chocolate balls are gluten free. The Lindt Canadian website says yes but the Lindt USA website says no. The information is a bit confusing.
    • JoJo0611
      I didn’t know there were different types of CT. I’m not sure which I had. It just said CT scan with contrast. 
    • Scott Adams
×
×
  • 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.