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.


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,545
    • Most Online (within 30 mins)
      7,748

    Jem68
    Newest Member
    Jem68
    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

    • 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.
    • Jsingh
      Hi,  I care for my seven year old daughter with Celiac. After watching her for months, I have figured out that she has problem with two kinds of fats- animal fat and cooking oils. It basically makes her intestine sore enough that she feels spasms when she is upset. It only happens on days when she has eaten more fat than her usual every day diet. (Her usual diet has chia seeds, flaxseeds, and avocado/ pumpkin seeds for fat and an occasional chicken breast.) I stopped using cooking oils last year, and when I reintroduced eggs and dairy, both of which I had held off for a few months thinking it was an issue of the protein like some Celiac patients habe mentioned to be the case, she has reacted in the same fashion as she does with excess fats. So now I wonder if her reaction to dairy and eggs is not really because of protein but fat.   I don't really have a question, just wondering if anyone finds this familiar and if it gets better with time.  Thank you. 
    • Chanda Richard
      Hello, My name is Chanda and you are not the only one that gose through the same things. I have found that what's easiest for me is finding a few meals each week that last. I have such severe reactions to gluten that it shuts my entire body down. I struggle everyday with i can't eat enough it feels like, when I eat more I lose more weight. Make sure that you look at medication, vitamins and shampoo and conditioner also. They have different things that are less expensive at Walmart. 
    • petitojou
      Thank you so much! I saw some tips around the forum to make a food diary and now that I know that the community also struggles with corn, egg and soy, the puzzle pieces came together! Just yesterday I tried eating eggs and yes, he’s guilty and charged. Those there are my 3 combo nausea troublemakers. I’m going to adjust my diet ☺️ Also thank you for the information about MCAS! I’m from South America and little it’s talked about it in here. It’s honestly such a game changer now for treatment and recovery. I know I’m free from SIBO and Candida since I’ve been tested for it, but I’m still going to make a endoscopy to test for H. Pylori and Eosinophilic esophagitis (EoE). Thank you again!! Have a blessed weekend 🤍
    • knitty kitty
      Yes, I, too, have osteoporosis from years of malabsorption, too.  Thiamine and magnesium are what keep the calcium in place in the bones.  If one is low in magnesium, boron, selenium, zinc, copper, and other trace minerals, ones bone heath can suffer.  We need more than just calcium and Vitamin D for strong bones.  Riboflavin B 2, Folate B 9 and Pyridoxine B 6 also contribute to bone formation and strength.   Have you had your thyroid checked?  The thyroid is important to bone health as well.  The thyroid uses lots of thiamine, so a poorly functioning thyroid will affect bone heath.  
×
×
  • 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.