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

Why is enough fat important on gluten-free diet?


Rowan13

Recommended Posts

Rowan13 Explorer

I've heard a few times now that it is important to consume enough fat when on a gluten free diet. Obviously fat is important no matter what but why is it especially important when eating gluten-free?  Does it help the small intestine or something else related?


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



Celiac.com Sponsor (A8-M):



Ennis-TX Grand Master

It helps in several regards, for one there are a lot of vitamins are fat solvable, a higher healthy fat intake can help you in processing these making them more bio available for your body. Another reason is the calorie density of fats, when you have to cut a lot of your carbs out and have issues with weight retention, nutrients, etc. the ease of getting large amount of calories in smaller amounts of consumption makes it easy to turn to. I personally digest fats much better then carbs and practically live off a high fat, protein diet. I find I do not get the bloat, gas, and discomfort that carbs cause and have more energy eating less of them and more fats from nuts, seeds, avocados, etc. Healthy fat sources such as seeds, and nuts can also be full other nutrients that you might be deficient in I will link the a few of the ones I eat and you can look at the nutrient profile for yourself to see

Open Original Shared Link

Open Original Shared Link

Open Original Shared Link

As you can see by example in just these not including avocado, sunflower, chia, flax, cashew, hemp (careful on finding gluten-free hemp), pistachio, etc Most of these sources are full of other nutrients some common deficiency among celiacs such as Magnesium, Folate, Zinc, Iron etc.   I would suggesting building your diet around ones that settle with your stomach and help provide what you are missing. You can always blend or get butter versions for ease of digestion and utilize them in cooking quite easy.

Rowan13 Explorer

Ennis_Tx,

Thank you very much for this information. I'm so sorry I'm only answering now but I just went through a difficult time with food reactions, well you know how it goes. Now I'm able to focus a bit more & can take in and really appreciate this information.  I used to love nuts and seeds but started reacting to many of them but I still could eat pumpkin seeds now and then, and sometimes raw sunflower seeds. I've bought some organic chia seeds and want to try soaking those overnight and try some for breakfast. I'm going to make an effort to try adding bits of different nuts and seeds back in. When I've been really sick I've had days of eating just apples, pears and water. I've just cut out dairy so I see I'm going to need to get fat from somewhere.

I did read about all the nutrients that people with celiac disease are especially lacking in & this helps me understand why the fats are so important, in order to get the nutrients into your system. I don't know if you will see this since it took me so long to get back here but I was wondering which butters you meant. Do you mean things like sunflower seed butter?  Or almond butter? I can't eat almond butter right now but I could see what else is out there. Thanks for the warning about hemp. I like cooking & I've just ordered a food processor so maybe I can experiment with making some things myself.

Thanks so much for taking the time to explain all of this and also for the links. It's really helpful.

Ennis-TX Grand Master

Talk with a dietician and see about building a diet around what foods work best for you, pain is finding the balance that is right for your body and comfortable. If nuts and the harder seeds bother you chia and avocado might be worth looking at. As to the butters any kind of nut or seed butter, some people have issues breaking down the whole seed/nut but find the ground butters sometimes even the fact that is is a roasted version is easier on the stomach. Also make sure your getting enough of your other vitamins/nutrients as it is possible to eat too much fat. Everyone is different so finding what works and is right for you is what is important.

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. - tiffanygosci replied to tiffanygosci's topic in Introduce Yourself / Share Stuff
      1

      Celiac support is hard to find

    2. - trents replied to mamaof7's topic in Parents, Friends and Loved Ones of Celiacs
      1

      Help understand results

    3. - mamaof7 posted a topic in Parents, Friends and Loved Ones of Celiacs
      1

      Help understand results

    4. - Dizzyma replied to Dizzyma's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      3

      Newly diagnosed mam to coeliac 11 year old

    5. - tiffanygosci posted a topic in Introduce Yourself / Share Stuff
      1

      Celiac support is hard to find

  • Celiac.com Sponsor (A19):
  • Member Statistics

    • Total Members
      132,955
    • Most Online (within 30 mins)
      7,748

    JodyBledsoe
    Newest Member
    JodyBledsoe
    Joined
  • Celiac.com Sponsor (A20):
  • Celiac.com Sponsor (A22):
  • Forum Statistics

    • Total Topics
      121.5k
    • Total Posts
      1m
  • Celiac.com Sponsor (A21):
  • Upcoming Events

  • Posts

    • tiffanygosci
      EDIT: I did find a monthly Zoom meeting for Celiacs through the Celiac Disease Foundation, so I'll be able to talk with some other people on January 15. And I also found a Celiac Living podcast on Spotify made by a celiac. I feel a little bit better now and I am still hoping I will find some more personal connections in my area.
    • trents
      Welcome to the celiac.com community, @mamaof7! It means for the one celiac disease antibody test that was ordered, she tested negative. However, other tests should have been ordered, especially for someone so young who would have an immature immune system where there would be a high probability of being IGA deficient.  The one test that was ordered was an IGA-based antibody test. It is not the only IGA antibody test for celiac disease that can be run. The most common one ordered by physicians is the TTG-IGA. Whenever IGA antibody tests are ordered, a "total IGA" test should be included to check for IGA deficiency. In the case of IGA deficiency, all other IGA tests results will be inaccurate. There is another category of celiac disease antibody tests that can be used in the case of IGA deficiency. They are known as IGG tests. I will attach an article that gives an overview of celiac disease antibody tests. All this to say, I would not trust the results of the testing you have had done and I would not rule out your daughter having celiac disease. I would seek further testing at some point but it would require your daughter to have been eating normal amounts of gluten for weeks/months in order for the testing to be valid. It is also possible she does not have celiac disease (aka, "gluten intolerance") but that she has NCGS (Non Celiac Gluten Sensitivity, or just "gluten sensitivity" for short) which is more common. The difference is that celiac disease is an autoimmune disorder that damages the lining of the small bowel whereas NCGS does not autoimmune in nature and does not damage the lining of the small bowel, though the two conditions share many of the same symptoms. We have testing to diagnose celiac disease but there are no tests for NCGS. To arrive at a diagnosis of NCGS, celiac disease must first be ruled out. A gluten free diet is the solution to both maladies.   
    • mamaof7
      For reference, daughter is 18 mths old. Was having painful severe constipation with pale stool and blood also bloating (tight extended belly.) Liver and gallbladder are normal. Ultrasound was normal. Dr ordered celiac blood test. We took her off gluten after blood draw. She is sleeping better, no longer bloated and stools are still off color but not painful.    "GLIADIN (DEAMID) AB, IGA FLU Value  0.84 Reference Range: 0.00-4.99 No further celiac disease serology testing to be performed. INTERPRETIVE INFORMATION: Deamidated Gliadin Peptide (DGP) Ab, IgA A positive deamidated gliadin (DGP) IgA antibody result is associated with celiac disease but is not to be used as an initial screening test due to its low specificity and only occasional positivity in celiac disease patients who are negative for tissue transglutaminase (tTG) IgA antibody."   Anyone know what in the world this means. She isn't scheduled to see GI until late April. 
    • Dizzyma
      Hi Trent and Cristiana, thank you so much for taking the time out to reply to me.  My daughters GP requested bloods, they came back as showing a possibility of celiac disease, she advised me to continue feeding gluten as normal and wait on a hospital appointment. When we got that the doctor was quite annoyed that the gp hadn’t advised to go gluten free immediately as she explained that her numbers were so high that celiac disease was fairly evident. That doctor advised to switch to a gluten-free diet immediately which we did but she also got her bloods taken again that day as it made sense to double check considering she was maintaining a normal diet and they came back with a result of 128. The hospital doctor was so confident of celiac disease that she didn’t bother with any further testing. Cristiana, thank you for the information on the coeliac UK site however I am in the Rrpublic of Ireland so I’ll have to try to link in with supports there. I appreciate your replies I guess I’ll figure things as we go I just feel so bad for her, her skin is so sore around her mouth  and it looks bad at an age when looks are becoming important. Also her anxiety is affecting her sleep so I may have to look into some kind of therapy to help as I don’t think I am enough to help. thanks once again, it’s great to be able to reach out xx   
    • tiffanygosci
      I have been feeling so lonely in this celiac disease journey (which I've only been on for over 4 months). I have one friend who is celiac, and she has been a great help to me. I got diagnosed at the beginning of October 2025, so I got hit with all the major food holidays. I think I navigated them well, but I did make a couple mistakes along the way regarding CC. I have been Googling "celiac support groups" for the last couple days and there is nothing in the Northern Illinois area. I might reach out to my GI and dietician, who are through NW Medicine, to see if there are any groups near me. I cannot join any social media groups because I deleted my FB and IG last year and I have no desire to have them back (although I almost made a FB because I'm desperate to connect with more celiacs). I'm glad I have this forum. I am praying God will lead me to more people to relate to. In my opinion, celiac disease is like the only food- related autoimmune disease and it's so isolating. Thanks for walking alongside of me! I'm glad I know how to help my body but it's still not easy to deal with.
×
×
  • 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.