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

Questions About Fructose Malabsorption


Blondie

Recommended Posts

Blondie Apprentice

Alright, seems just about right to post this here.

So without elaborating much on the details, im gonna go fructose-low for a couple of weeks to see if there's any improvement (celiac, lactose intolerant, glutenfree 10 months).

So far im pretty sure what to eat and what to avoid, with the exception of Sunflower seeds.

Does anyone know if these contain fructose? If so, is the fructose level high compared to say... potatos?

(These are listed under ingredients in my glutenfree bread)

Also, I would like to know when to expect some improvement?


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



Celiac.com Sponsor (A8-M):



Blondie Apprentice

Bump (can't see my post anywhere)

Blondie Apprentice

Bump

DElizabethE Apprentice

Hi,

I have been waiting to see if someone would reply because I'm curious myself. I am also doing a low fructose diet (along with gluten free, dairy free, soy and corn free) and have been feeling better. I did a lot of research of different foods on www.nutritiondata.com to find out the sugar/fructose content. It helped a lot. I stay away from sunflower seeds but I just looked it up. A 1 oz serving has 0.8g of sugar and the fructose value was incomplete. I'd say they were ok but I thought I read somewhere that you should stay away from them on a low fructose diet. Probably doesn't help you any. Check out that website though. You can look up any food on it with different amounts.

I just felt bad no one replied to your question. Maybe someone else on a low frustose diet can help us out.

Diane B)

Blondie Apprentice

Well, I don't eat them raw, they're just in the bread i buy, i've been tolerating decent amounts of fructose, my problems started when i started drinking A LOT of juices

  • 4 weeks later...
georgie Enthusiast

I am curious about this myself. I had a massive collapse / pain/ D etc and all I could trace it to was a gluten-free soup mix I had that day. When I read the ingredients it had Fructose listed as third ingredient. As the reaction was so severe - I now wonder if I am making myself slightly ill each day by having small amounts of Fructose. I know I react badly to sorbitol, and have always felt ill after an apple for eg. But fructose is in so many foods that I am having a nightmare trying to understand it all.

boron Rookie
So far im pretty sure what to eat and what to avoid, with the exception of Sunflower seeds.

Does anyone know if these contain fructose? If so, is the fructose level high compared to say... potatos?

(These are listed under ingredients in my glutenfree bread)

Also, I would like to know when to expect some improvement?

If you "only have fructose malabsorption (FM) (and not much more severe hereditary fructose intolerance) then you don't need to avoid all fructose, but only amount which is above your personal tolerance threshold. Beside that, fructose amount is not the most important thing. Sugar (sucrose) has 5og of fructose in 100g, but is well tolerated by most persons with FM, if ingested in moderation. Important info is Fructose:glucose ratio. If glucose content is higher than fructose, the food should be OK, unless if it also contains sorbitol.

Sunflower seeds contain no fructose and you can try them.

You can also check: Open Original Shared Link site with lists of problematic and "to try" foods.


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



Celiac.com Sponsor (A8-M):



AndrewNYC Explorer

I am fast becoming an authority on this subject. Backstory is that I had continuing minor bowel irritation for four years after going gluten, dairy and soy free. Then I finally had a massive collapse with onset of out of control bowel trouble and celiac-like neuro trouble, unrelated to vitamin deficiency. Refractory sprue was ruled out; villi appeared completely healed. I removed fructose and that seems to resolve everything, though dealing with the diet is ridiculously difficult as I am trying to be as fructose free as possible, basically eating only meat and the occassional potato or small serving of veggies. I realize this is very unhealthy but the alternative is not attractive either. I react to all levels of fructose so it is difficult. The one thing to note is that dextrose counteracts fructose. Smarties, Pixie Sticks, and Sweet Tarts (I think) all consist solely of dextrose, so eating these around and with a meal should help; and no, I'm not kidding.

I think all vegetables/plants have SOME fructose content with exception of mushrooms and supposedly green leafy lettuce (not butter lettuce). I would not be surprised if sunflower seeds have trace amounts of fructose and I would not be surprised if you found authority that said they have zero fructose, but I would think that authority is inaccurate just because I think my first sentence is correct.

As far as improvement, my symptoms with fructose last for 12 hours after each meal, then I feel back to baseline. I would just try eating meat for two days first and see how you do.

I noted in the first month that I went gluten free a couple years ago that I seemed to have a neuro reaction to various canned fruits, like I was being glutened by said fruit. I thought that was odd, and it was kind of a vague feeling. I reported it to my doctor at the time and he of course told me there was no gluten in fruit and kind of rolled his eyes. Well, I would have been much better off if I had had more knowledge at the time. There is a Mayo article out there that says for celiac patients who do not show full improvement after gluten free that you have to consider 6 things, one of which is fructose malabsorption.

georgie Enthusiast

I would love to learn more about this. As I said - I have not improved on gluten-free diet 100% and after my severe Fructose reaction - the light globe came on as I have always felt off colour after eating fruit. Its a hard diet intolerance as everyone assumes fruit is healthy for you.And most gluten-free bars seem to have honey ....

Andrew - can the symptoms of Fructose intolerance be similar to GI , and include fatigue, neuropathy , and not always be the severe gut reaction ?

I have been eating fructose light this week and seem to have improved. And now - like with Gluten - I am finding that I am more aware of fructose hidden in foods and my reaction if I eat those foods ( onion for eg)

I have always felt best on an Atkins diet but cannot do that now. I seem to suffer 'withdrawals' that make me ill. Is this a sign that my body needs to eliminate the foods it is craving ?

Do you have links to the Mayo article ? I am curious what the 6 other conditions are...

AndrewNYC Explorer
I would love to learn more about this. As I said - I have not improved on gluten-free diet 100% and after my severe Fructose reaction - the light globe came on as I have always felt off colour after eating fruit. Its a hard diet intolerance as everyone assumes fruit is healthy for you.And most gluten-free bars seem to have honey ....

Andrew - can the symptoms of Fructose intolerance be similar to GI , and include fatigue, neuropathy , and not always be the severe gut reaction ?

I have been eating fructose light this week and seem to have improved. And now - like with Gluten - I am finding that I am more aware of fructose hidden in foods and my reaction if I eat those foods ( onion for eg)

I have always felt best on an Atkins diet but cannot do that now. I seem to suffer 'withdrawals' that make me ill. Is this a sign that my body needs to eliminate the foods it is craving ?

Do you have links to the Mayo article ? I am curious what the 6 other conditions are...

Andrew - can the symptoms of Fructose intolerance be similar to GI , and include fatigue, neuropathy , and not always be the severe gut reaction ?

Yes.

I'll look for the article.

  • 1 year later...
sicl4015 Rookie

Hello,

I just added this to my list of eliminated foods and am hunting for the best way to do a "clean" elimination diet process. (gluten, dairy, soy, eggs, corn, oats, nightshades, dietary yeast)

Any information you can provide, ie the mayo article link, would be much appreciated!

Sue

Andrew - can the symptoms of Fructose intolerance be similar to GI , and include fatigue, neuropathy , and not always be the severe gut reaction ?

Yes.

I'll look for the article.

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 Sarah Grace's topic in Related Issues & Disorders
      25

      Headaches / Migraines and Hypoglycaemia

    2. - trents replied to Sarah Grace's topic in Related Issues & Disorders
      25

      Headaches / Migraines and Hypoglycaemia

    3. - Scott Adams replied to Russ H's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      1

      KAN-101 Treatment for Coeliac Disease

    4. - Scott Adams replied to miguel54b's topic in Related Issues & Disorders
      1

      Body dysmorphia experience

    5. - Scott Adams replied to Colleen H's topic in Related Issues & Disorders
      2

      Heat intolerant... Yikes


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      132,152
    • Most Online (within 30 mins)
      7,748

    denise.milillo
    Newest Member
    denise.milillo
    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
      Excessive dietary tyrosine can cause problems.  Everything in moderation.   Sulfites can also trigger migraines. Sulfites are found in fermented, pickled and aged foods, like cheese.  Sulfites cause a high histamine release.  High histamine levels are found in migraine.  Following a low histamine diet like the low histamine Autoimmune Protocol diet, a Paleo diet, helps immensely.    Sulfites and other migraine trigger foods can cause changes in the gut microbiome.  These bad bacteria can increase the incidence of migraines, increasing histamine and inflammation leading to increased gut permeability (leaky gut), SIBO, and higher systemic inflammation.   A Ketogenic diet can reduce the incidence of migraine.  A Paleo diet like the AIP diet, that restricts carbohydrates (like from starchy vegetables) becomes a ketogenic diet.  This diet also changes the microbiome, eliminating the bad bacteria and SIBO that cause an increase in histamine, inflammation and migraine.  Fewer bad bacteria reduces inflammation, lowers migraine frequency, and improves leaky gut. Since I started following the low histamine ketogenic AIP paleo diet, I rarely get migraine.  Yes, I do eat carbs occasionally now, rice or potato, but still no migraines.  Feed your body right, feed your intestinal bacteria right, you'll feel better.  Good intestinal bacteria actually make your mental health better, too.  I had to decide to change my diet drastically in order to feel better all the time, not just to satisfy my taste buds.  I chose to eat so I would feel better all the time.  I do like dark chocolate (a migraine trigger), but now I can indulge occasionally without a migraine after.   Microbiota alterations are related to migraine food triggers and inflammatory markers in chronic migraine patients with medication overuse headache https://pmc.ncbi.nlm.nih.gov/articles/PMC11546420/  
    • trents
      Then we would need to cut out all meat and fish as they are richer sources of tyrosine than nuts and cheese. Something else about certain tyrosine rich foods must be the actual culprit. 
    • Scott Adams
      I agree that KAN-101 looks promising, and hope the fast track is approved. From our article below: "KAN-101 shows promise as an immune tolerance therapy aiming to retrain the immune system, potentially allowing safe gluten exposure in the future, but more clinical data is needed to confirm long-term effects."  
    • Scott Adams
      Thank you so much for having the courage to share this incredibly vivid and personal experience; it's a powerful reminder of how physical ailments can disrupt our fundamental sense of self. What you're describing sounds less like a purely psychological body dysmorphia and more like a distinct neurological event, likely triggered by the immense physical stress and inflammation that uncontrolled celiac disease can inflict on the entire body, including the nervous system. It makes complete sense that the specific sensory input—the pressure points of your elbows on your knees—created a temporary, distorted body map in your brain, and the fact that it ceased once you adopted a gluten-free diet is a crucial detail. Your intuition to document this is absolutely right; it's not "crazy" but rather a significant anecdotal data point that underscores the mysterious and far-reaching ways gluten can affect individuals. Your theory about sensory triggers from the feet for others is also a thoughtful insight, and sharing this story could indeed be validating for others who have had similar, unexplainable sensory disturbances, helping them feel less alone in their journey.
    • Scott Adams
      The most common nutrient deficiencies associated with celiac disease that may lead to testing for the condition include iron, vitamin D, folate (vitamin B9), vitamin B12, calcium, zinc, and magnesium.  Unfortunately many doctors, including my own doctor at the time, don't do extensive follow up testing for a broad range of nutrient deficiencies, nor recommend that those just diagnosed with celiac disease take a broad spectrum vitamin/mineral supplement, which would greatly benefit most, if not all, newly diagnosed celiacs. Because of this it took me decades to overcome a few long-standing issues I had that were associated with gluten ataxia, for example numbness and tingling in my feet, and muscle knots--especially in my shoulders an neck. Only long term extensive supplementation has helped me to resolve these issues.      
×
×
  • 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.