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

Gluten Free Oats


Roda

Recommended Posts

Roda Rising Star

I was wondering if anyone has problems with some brands of gluten free oats but can tolerate other brands. I am leaning on the fact that I probably can't tolerate oats and that sucks! I know some celiacs can't tolerate them, but also alot do. I figured I would be one who could. Just goes to show you never know. Would trying a different brand make any difference?

I decided to try oats for the first time in 7 1/2 months. I have been feeling great and my ttg was negative two months ago. I bought Bobs Red Mills certified gluten free oats. I made apple spice cookies. I have to admit I was a glutten and ate about 7 cookies. They tasteted soooo good. About a half and hour or so later I felt like my stomach was full. Then I started belching all evening long. I didn't have the burning sensation just sour when I would burp. My intestines were rumbling also. I took a couple of tums and went to bed. I used to eat oats before gluten free and seemed fine with them. I ate them occasionally and never had any problem with the fiber. To me this seems a little more than not being used to the fiber. For example if I eat black beans they cause me to get bloated and gassy and I know the brand is gluten free. It is just me not used to that amout of fiber in the beans. I don't get heartburn or burp with them either. There was alot of cinnamon in the recipe and it is large quanties can give me heartburn. However, I find it a little suspicious that I felt fine all day and after eating the cookies I had this problem. I don't feel too bad this morning just a little burping and rumbling in my tummy. I am probably going to try just eating a bowl of the oatmeal in another couple of days to see if the same thing happens and then I'll know for sure. Thanks


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



Celiac.com Sponsor (A8-M):



hasail Rookie

I have only tried the Bob's Red Mill Oats as you did, and I wasn't impressed, to tell you the truth. Although I can't say that I noticed any adverse reactions, I will say that I did not like the taste of the oats. Admittedly, I haven't had oats since my diagnosis, which was over ten years ago, but I don't remember oats tasting like Bob's Oats. They had a funny taste that I cannot put my finger on........the best way I can describe it, is that they taste very "earthy" at not much like oats.

I might have simply gotten a bad batch, but the taste alone, made me think that I'm not THAT desperate to have oatmeal in the morning!

sixtytwo Apprentice

Oh, man, I tried regular Quaker Oatmeal a while ago and did I ever get sick. I like the BRM oats okay, but they take a long time to cook. I decided maybe just to be oat free to be safe. I am gluten intolerant and can get away with some French fries that have been cooked with other things and low risk stuff like that if I don't do it often, so was surprised at the reaction to the oatmeal. I get neurological problems as a reaction to the oats.

However, if you like cream of wheat, then try cream of buckwheat, it is wonderful in the winter. Buckwheat is actually a berry, so no problem for us that eat gluten-free.

  • 2 weeks later...
buxschot Newbie
I was wondering if anyone has problems with some brands of gluten free oats but can tolerate other brands. I am leaning on the fact that I probably can't tolerate oats and that sucks! I know some celiacs can't tolerate them, but also alot do. I figured I would be one who could. Just goes to show you never know. Would trying a different brand make any difference?

I decided to try oats for the first time in 7 1/2 months. I have been feeling great and my ttg was negative two months ago. I bought Bobs Red Mills certified gluten free oats. I made apple spice cookies. I have to admit I was a glutten and ate about 7 cookies. They tasteted soooo good. About a half and hour or so later I felt like my stomach was full. Then I started belching all evening long. I didn't have the burning sensation just sour when I would burp. My intestines were rumbling also. I took a couple of tums and went to bed. I used to eat oats before gluten free and seemed fine with them. I ate them occasionally and never had any problem with the fiber. To me this seems a little more than not being used to the fiber. For example if I eat black beans they cause me to get bloated and gassy and I know the brand is gluten free. It is just me not used to that amout of fiber in the beans. I don't get heartburn or burp with them either. There was alot of cinnamon in the recipe and it is large quanties can give me heartburn. However, I find it a little suspicious that I felt fine all day and after eating the cookies I had this problem. I don't feel too bad this morning just a little burping and rumbling in my tummy. I am probably going to try just eating a bowl of the oatmeal in another couple of days to see if the same thing happens and then I'll know for sure. Thanks

buxschot Newbie

I get the same reaction when I eat those oats...I tried the Rolled oats and the Steel cut oats...Same reaction to both...I never used to have a problem (pre - celiac) with oats (Quaker)...I keep tryin to eat the Red Mill because I like them...but I just cant stand the misery they bring to my gut..

Roda Rising Star

I have decided I am going to continue to be oat free. I had another reaction to them. I was really hoping I could eat them. Oh well! :(

Archived

This topic is now archived and is closed to further replies.


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      132,202
    • Most Online (within 30 mins)
      7,748

    PatBurnham
    Newest Member
    PatBurnham
    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

    • trents
      NCGS does not cause damage to the small bowel villi so, if indeed you were not skimping on gluten when you had the antibody blood testing done, it is likely you have celiac disease.
    • Scott Adams
      I will assume you did the gluten challenge properly and were eating a lot of gluten daily for 6-8 weeks before your test, but if not, that could be the issue. You can still have celiac disease with negative blood test results, although it's not as common:  Clinical and genetic profile of patients with seronegative coeliac disease: the natural history and response to gluten-free diet: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5606118/  Seronegative Celiac Disease - A Challenging Case: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9441776/  Enteropathies with villous atrophy but negative coeliac serology in adults: current issues: https://pubmed.ncbi.nlm.nih.gov/34764141/  Approximately 10x more people have non-celiac gluten sensitivity than have celiac disease, but there isn’t yet a test for NCGS. If your symptoms go away on a gluten-free diet it would likely signal NCGS.
    • Xravith
      I'm very confused... My blood test came out negative, I checked all antibodies. I suppose my Total IgA levels are normal (132 mg/dl), so the test should be reliable. Still, I'm not relieved as I can't tolerate even a single biscuit. I need to talk to my doctor about whether a duodenal biopsy is necessary. But it is really possible to have intestinal damage despite having a seronegative results? I have really strong symptoms, and I don't want to keep skipping university lectures or being bedridden at home.
    • Scott Adams
      They may want to also eliminate other possible causes for your symptoms/issues and are doing additional tests.  Here is info about blood tests for celiac disease--if positive an endoscopy where biopsies of your intestinal villi are taken to confirm is the typical follow up.    
    • Scott Adams
      In the Europe the new protocol for making a celiac disease diagnosis in children is if their tTg-IgA (tissue transglutaminase IgA) levels are 10 times or above the positive level for celiac disease--and you are above that level. According to the latest research, if the blood test results are at certain high levels that range between 5-10 times the reference range for a positive celiac disease diagnosis, it may not be necessary to confirm the results using an endoscopy/biopsy: Blood Test Alone Can Diagnose Celiac Disease in Most Children and Adults TGA-IgA at or Above Five Times Normal Limit in Kids Indicates Celiac Disease in Nearly All Cases No More Biopsies to Diagnose Celiac Disease in Children! May I ask why you've had so many past tTg-IgA tests done, and many of them seem to have been done 3 times during short time intervals?    
×
×
  • 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.