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

Confused About Reaction To Oats


Raywuwei

Recommended Posts

Raywuwei Explorer

I am extremely happy to say that I have been gluten-free for a little over 4 months and I've reduced my tTG levels from >200 to 22. Twenty-two!! I also got my vitamins and minerals tested and the only thing I was deficient in was vitamin D (I live in Oregon, so no surprise there).

I've been very strict with my diet for the last two months and cut out oats completely (though I ate A LOT of gluten-free oats for the first two months of my diagnosis.) Since my test results looked so spectacular, I thought it would be ok to reintroduce oats a little ahead of schedule. So, I are a large bowl of gluten-free oatmeal for breakfast yesterday at 9:30am.

Result: I have had no pain in my lower left abdominal, which is my #1 sign for having been glutened. I did notice that I became gassy around 6pm last night, and at 10am today I had a very loose bm. This is what worries me, since there was no other chance of cross contamination in my day, and my stools have been very consistent for the last two months.

I don't have health insurance right now, so I am bouncing ideas off of you intelligent folks. Thanks for bearing with me!


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



Celiac.com Sponsor (A8-M):



SMDBill Apprentice

To be honest, I just avoid oats. It strikes a few more foods from the menu, but yours is not the first post I've seen about supposedly gluten-free oats. Could they be grown in a field that also grows wheat in opposite seasons? Something absorbed through the soil? I have no idea, but oats are always discussed cautiously in regards to celiac so I don't risk it. You may be more sensitive to gluten than the allowable amount to still claim gluten-free so it could be there is less than the limit but enough to spur a reaction within you.

Either way, getting diarrhea is still tough on an already challenged intestine so it's probably worth changing brands or eliminating them altogether. Only you can know for sure what is best, but it sounds like you eliminated and then reintroduced, only to find you have a slight reaction to it.

shadowicewolf Proficient

I cant handle oats without getting a stomach ache :(

my3monkees Rookie

When my dd was first diagnosed, a friend warned me to be careful when reintroducing oats. Remember gluten free diets can often be lacking in fiber. Unless you make sure to get enough from fruits and veggies. So a large bowl of oatmeal on an unsuspecting intestines, can make you a tad uncomfortable! LOL As long as your are not having a true reaction, just some bloating and gas. You should be fine, just go for smaller portions at first.

Takala Enthusiast

I avoided them (gluten free oats) for years, because I just didn't feel like finding out, I assumed that I would be okay, since I ate them before going gluten free. Then, one New Year's Eve, years later, I got accidentally oated by eating part of a bag of supposedly "gluten free" chips that used oat fiber, but did not disclose on the label. I reacted. And it was the chips because all I had was chips and club soda for my "big splurge." :rolleyes: This wiped out my planned New Year's day trip up into the mountains. Boy, was I really just ticked about this, and that led to my New Rule, which is, don't eat anything new before a holiday, and don't eat out on the eve of one, either. (the year adjacent to that was my one infamous, really bad New Years Eve restaurant glutening, which also wiped out my New Years day. That was 2 years in a row of missing skiing on a day where the slopes are not that busy in the am because everyone else is hung-over. B) ) The only good thing that came out of that restaurant trip was that on the way home on the back roads, we came across a truck overturned in the ditch with people still in it, and called 911. But the lady was quite, quite drunk and screamed at me for doing that, as if nobody was going to notice that her big pickup truck was sitting there on its side. I sort of assessed them, and figured that they hadn't broken anything and weren't going to bleed to death and thought I'd just watch to make sure the vehicle didn't catch on fire, or something, while waiting. So the fire dept shows up just as these drunk people are taking off with somebody else who stopped, (it was really foggy, that freezing fog) and they abandon the truck, so now the fire dept wants to know where they went because the truck's still sitting there warm, with its lights on, on its side, turned the wrong way for what side of the road it's on, in the fog on the curve in the road. The whole thing looks like a scene out of a Stephen King novel. And now the fire dept wants us to wait for the sheriff dept, so we can tell them what vehicle left the scene with the 2 missing drunks. And then the cops are like, where do you live, did you see what happened, what was the license plate number, what do these people look like who just disappeared. :rolleyes: This trip home was getting really complicated.

Next day, after the night I went thru the mud and the water, climbed that truck side and pried the door open expecting to see bodies, and instead get this pair of loony- tune drunks mad at me when I tell them we're calling the rescue for them :ph34r: , I can't even hardly make it out of bed. I am so sick. Off that gluten free menu. :angry: This was back when I was starting to experiment with eating out, and I have to have a big adventure. :lol:

As I have aged and progressed into this gluten free thing, I become more sensitive, so last year I had to give up things processed in a facility with gluten free oats, because I was having reactions to that, too. Who would have thunk it with the part Irish in me, which has at least been able to keep dairy.

dilettantesteph Collaborator

supposedly "gluten free" chips that used oat fiber, but did not disclose on the label.

I hadn't really thought about oat use not being disclosed on the label. Maybe that could explain some of my reactions to processed foods. I react to oats too. Do you remember what brand that was?

Takala Enthusiast

It was the "Food Should Taste Good" brand. I do not see the flavor that I had on their current website, it was a cinnamon flavor with corn, and it tasted like a graham cracker. They may have changed their formulations, because I see now that some of the flavors contain corn bran, but I remember at the time researching, and it was on this site that someone else mentioned some of the other flavors had the oat bran. At the time I then went back to the store and went down the aisle, reading each bag, trying to find the culprit, as in did that flavor/brand mention this, but I did not have success. I did find another flavor at that time (this was years ago) that did have oat bran, but I can't remember what flavor it was.

So I chalked it up to cross contamination. Live and learn. It would be great if they've gotten rid of it.

FAQ page:

Open Original Shared Link


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



Celiac.com Sponsor (A8-M):



dreacakes Rookie

I can't do oats at all! They make me crazy gassy. Listen to your body, it knows the way. :)

BabsV Enthusiast

My nutritionist told me that she recommends being symptom free for at least 6 months before reintroducing gluten-free oats...and no more than a 1/2 cup serving a day. I'm still dealing with issues so haven't touched them since diagnosis 14 months ago...

Roda Rising Star

I react to pure gluten free oats. I have to check with companies because I react to CC from them too.

Darn210 Enthusiast

My daughter's doc said to wait at least 6 months and then start with something like a quarter of a cup. I am of the opinion that it was too much, too soon. I'd wait a few more months and try them again in a small amount. I will add that you probably shouldn't have them more than once or twice a week in the beginning.

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. - Tazfromoz replied to Ginger38's topic in Related Issues & Disorders
      14

      Shingles - Could It Be Related to Gluten/ Celiac

    2. - hjayne19 posted a topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      0

      Celiac Screening

    3. - yellowstone posted a topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      0

      Cold/flu or gluten poisoning?

    4. - Churro replied to Churro's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      17

      Celiac disease symptoms

    5. - Wheatwacked replied to Churro's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      17

      Celiac disease symptoms

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

    • Total Members
      133,073
    • Most Online (within 30 mins)
      7,748

    amaryliss
    Newest Member
    amaryliss
    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

    • Tazfromoz
      My understanding, and ex I erience is that we coeliacs are likely to suffer more extreme reactions from viruses. Eg we are more likely to be hospitalised with influenza. So, sadly, your shingles may be worse because you are coeliac. So sorry you had to go through this. My mother endured shingles multiple times. She was undiagnosed with coeliac disease until she was 65. Me at 45. I've had the new long lasting vaccine. It knocked me around badly, but worth it to avoid shingles.
    • hjayne19
      Hi all,  Looking for some advice. I started having some symptoms this past summer like night sweats and waking at 4 am and felt quite achy in my joints. I was training heavily for cycling for a few weeks prior to the onset of these symptoms starting. I have had low Ferratin for about 4 years (started at 6) and usually sits around 24 give or take. I was doing some research and questioned either or not I might have celiac disease (since I didn’t have any gastric symptoms really). My family doctor ran blood screening for celiac. And my results came back: Tissue Transglutaminase Ab IgA HI 66.6 U/mL Immunoglobulin IgA 1.73 g/ My doctor then diagnosed me with celiac and I have now been gluten free for 3 months. In this time I no longer get night sweats my joint pain is gone and I’m still having trouble sleeping but could very much be from anxiety. I was since referred to an endoscopy clinic to get a colonoscopy and they said I should be getting a biopsy done to confirm celiac. In this case I have to return to eating gluten for 4-6 weeks before the procedure. Just wanted some advice on this. I seem to be getting different answers from my family physician and from the GI doctor for a diagnosis.    Thanks,  
    • yellowstone
      Cold/flu or gluten poisoning? Hello. I've had another similar episode. I find it very difficult to differentiate between the symptoms of a cold or flu and those caused by gluten poisoning. In fact, I don't know if my current worsening is due to having eaten something that disagreed with me or if the cold I have has caused my body, which is hypersensitive, to produce symptoms similar to those of gluten poisoning.        
    • Churro
      I'm no longer dealing with constipation. I got my liver test last month and it was in normal range. Two years ago I did have a vitamin D deficiency but I'm know taking vitamin D3 pills. Last month I got my vitamin D checked and it was in normal range. I don't believe I've had my choline checked. However, I do drink almond milk eat Greek yogurt on a daily basis. 
    • Wheatwacked
      Non-Celiac Gluten Sensitivity (NCGS) can be associated with low ferritin and iron deficiency. Once Celiac Disease (1% of the population affected) has been ruled out by tests the next step is to check for Non Celiac Gluten Sensitivity (10% of the population affected) by eliminating gluten for a trial period, then re-introduce Gluten Challange. Have you been supplementing Iron? How are your liver enzymes? Low levels of ferritin indicate iron deficiency, while  59% transferrin saturation indicates high iron levels.  Possibly indicating Fatty Liver Disease.  Choline is crucial for liver health, and deficiency is a known trigger for Non-Alcoholic Fatty Liver.  Some experts say that less than 10% eat the the Food and Nutrition Board established Adequate Intake that are based on the prevention of liver damage. Severe constipation and hemorrhoids may be linked to a bile or choline deficiency.  "Ninety-five percent of phospholipids (PLs) in bile is secreted as phosphatidylcholine or lecithin."  Fatty acid composition of phospholipids in bile in man   Deficiency of these bile salts causes the bile to get thick. Some people with Celiac Disease are misdiagnosed with Gall Bladder bile issues.  Removal of the gallbladder provides only temporary relief. Whether or not celiac disease or NCGS are your issues you need to look at your vitamin D blood level.   
×
×
  • 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.