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Going Fructose Free


ILOVEOMC

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ILOVEOMC Enthusiast

My DD is six and is not Celiac at this point (they did endoscopy and biopsy and blood work was done last May). They want us to try the Fructose -free diet and I am having trouble finding foods for her to eat. Any suggestions? or anyone try this diet before? Now we are doing the Gluten-free diet for my celiac son and this fructose thing for my daughter. AUGGHHHH!!! Any help is appreciated with the fructose thing:)


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ILOVEOMC Enthusiast

Doesn't anyone know something about this? It seems harder than going gluten free because I have not found any message board about fructose free.

CMCM Rising Star
Doesn't anyone know something about this? It seems harder than going gluten free because I have not found any message board about fructose free.

I avoid fructose like the plague, and it's actually not that hard.....but mainly just be aware that it's in an incredible number of sweet things. You just have to read every label, basically. You can't eat a lot of prepared foods. Avoid sodas, they are chock full of it (cokes etc. used to be made with sugar, now they are made with high fructose corn syrup). Make your own homemade cookies. Drink only pure 100% fruit juices, but preferable to juice, just eat whole fruit.

You just have to develop a different way of eating, which is a thousand times better for you anyway. You just have to read labels like crazy. Fructose will be in most sweet things, but it's also in things you might not suspect, like catsup, for example. I don't find it all that hard to stay away from it, to tell you the truth, because I don't want to eat it.

cdford Contributor

Processed foods are going to be your main source for fructose unless you have been using it as a white sugar substitute. If so, try using sucanat with honey instead. It works even better and is almost a one for one substitute for white sugar without the nasty long term issues of white sugar. Breadbeckers is a good source for this. You can also use plain sucanat as a substitute for brown sugar.

jenvan Collaborator

These two sites give tips on avoiding and identifying fructose….

Open Original Shared Link

Open Original Shared Link

  • 4 years later...
Melybean Newbie

I have been lactose intolerant since age 9, gluten intolerant since 22, and now fructose intolerant at age 27, so I know how frustrated you are. I am super sensitive to fructose, and have found that the information out there is not only scarce, but very inconsistent. This book was like my savior when I first started avoiding fructose: http://www.(Company Name Removed - They Spammed This Forum and are Banned)/Fructose-Malabsorption-Survival-Guide-1/dp/0984077707. Also, this website was very accurate: Open Original Shared Link They may help you quite a bit. There are a lot of lists out there of things to avoid, but not much out there of what CAN be eaten, so here are some tips. This is all gluten and fructose free - you can add dairy into this since you didn't say they were lactose intolerant:

My rule of thumb (which makes eating very time consuming due to how much cooking I have to do - I cook lunch and dinners for the week on sunday night and then microwave all week), but anyway, my rule of thumb tends to be, except for fruit and some veggies with fructose, if I can't gather it or hunt it like our ancestors, I generally can't eat it, lol.

I eat: most meats (if it's pre-packaged, check for added sugar, garlic, onion, etc.), veggies that are safe: Broccholi, zuchinni, mushrooms, lettuce (red leaf, green leaf, butter lettuce, spinach, generally anything dark, are all okay), potatoes (you can make a great shepard's pie with all the ingredients listed so far), rice (white or brown - although some say brown has a higher fructose content) - you can get rice pasta at most health food stores - it's really good. (You can make mac and cheese for your son!). For breakfast - eggs or cream of rice (it's yummy if you add milk, margerine, and sweetener**I'll get to that in a second). For desert: Potato chips (plain only) would be popular with your kids, or nuts (all except regular peanuts).

**Now, for the sweetener, what has kept me sane is DEXTROSE. I haven't been able to find it in stores, but it's cheap, and you can order it on amazon. It works/looks/tastes just like sucrose, but is fructose free and synonymous with glucose. It's 80% as sweet as sugar, so you'll use a tad more, but you can add this to cream of rice, coffee, etc (not that your kids would drink coffee). I've also been able to make a pretty tasty mirangue using egg whites and dextrose.

Eating out is a challenge - mostly because they put garlic on EVERYTHING, but sushi seems to be okay and mediterranean is also good - they have rice and grilled meat.

Things that I didn't know have fructose that you should avoid - soy, beans, garlic, onion, some spices, peanuts...

I hope this helps you. I know this is tough, especially for a kid.

  • 1 month later...
flash Newbie

I also have gluten intolerance as well as lactose intolerance and recently i've discovered i have fructose intolerance.

what can I do for bread? is it possible to make my own bread? also how about cereals,are there any I can eat? I think wheat is a no go area for fructose/lactose/gluten intolerant.

Things that I didn't know have fructose that you should avoid - soy, beans, garlic, onion, some spices, peanuts...

ugh I really hope this isnt true because soya milk is one of the few milks i can drink as im lactose intolerant and i've just ordered a soya milk maker :(


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    • trents
      You might consider asking for a referral to a RD (Registered Dietician) to help with food choices and planning a diet. Even apart from any gluten issues, you will likely find there are some foods you need to avoid because of the shorter bowel but you may also find that your system may make adjustments over time and that symptoms may improve.
    • Ello
      I wish Dr’s would have these discussions with their patients. So frustrating but will continue to do research. Absolutely love this website. I will post any updates on my testing and results.  Thank you
    • trents
      Losing 12" of your small bowel is going to present challenges for you in nutritional uptake because you are losing a significant amount of nutritional absorption surface area. You will need to focus on consuming foods that are nutritionally dense and also probably look at some good supplements. If indeed you are having issues with gluten you will need to educate yourself as to how gluten is hidden in the food supply. There's more to it than just avoiding the major sources of gluten like bread and pasta. It is hidden in so many things you would never expect to find it in like canned tomato soup and soy sauce just to name a few. It can be in pills and medications.  Also, your "yellow diarrhea, constipation and bloating" though these are classic signs of a gluten disorder, could also be related to the post surgical shorter length of your small bowel causing incomplete processing/digestion of food.
    • Ello
      Yes this information helps. I will continue to be pro active with this issues I am having. More testing to be done. Thank you so much for your response. 
    • trents
      There are two gluten-related disorders that share many of the same symptoms but differ in nature from each other. One is known as celiac disease or "gluten intolerance". By nature, it is an autoimmune disorder, meaning the ingestion of gluten triggers the body to attack it's own tissues, specifically the lining of the small bowel. This attack causes inflammation and produces antibodies that can be detected in the blood by specific tests like the TTG-IGA test you had. Over time, if gluten is not withheld, this inflammation can cause severe damage to the lining of the small bowel and even result in nutrient deficiency related health issues since the small bowel lining is organ where all the nutrition found in our food is absorbed.  The other is NCGS (Non Celiac Gluten Sensitivity or just "gluten sensitivity") which we know less about and are unsure of the exact mechanism of action. It is not an autoimmune disorder and unlike celiac disease it does not damage the lining of the small bowel, though, like celiac disease, it can cause GI distress and it can also do other kinds of damage to the body. It is thought to be more common than celiac disease. Currently, we cannot test for NCGS. Celiac disease must first be ruled out to arrive at a diagnosis of NCGS. Both disorders require elimination of gluten from the diet.  Either of these disorders can find their onset at any stage of life. We know that celiac disease has a genetic component but the genes are inactive until awakened by some stress event. About 40% of the general population has the genetic potential to develop celiac disease but only about 1% develop active celiac disease. The incidence of NCGS is thought to be considerably higher. I hope this helps.
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