Jump to content
This site uses cookies. Continued use is acceptance of our Terms of Use and Privacy Policy. More Info... ×
  • 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

Can I Eat Regular Oats?


Sage122

Recommended Posts

Sage122 Explorer

Im lactose intolerant and gluten intolerant...maybe celiac. I'm not too exactly sure. I couldn't get tested for celiac cause I had already gone gluten free and felt better. The doctor said to assume I was gluten intolerant or gluten sensitive. My dad just found out he had celiac, but he doesn't have a lot of symptoms. So I COULD have celiac.

When I eat gluten, nothing really serious happens. I just get a stomach ache, and I feel all bloated. If I were to consume a large quantity of gluten (say a slice of bread), I get a couple of hives on my arms, and a couple rashes that go away in like 2 or 3 hours.

My friend has celiac and doesn't have many symptoms. I've seen her eat honey nut Cheerios, and nature valley oats and honey granola bars. She has no problem with it and doesnt feel sick after.

When I eat normal oatmeal, or normal oats, I have no problems

2 questions:

1) is it ok for me to eat normal oats, or do I still have to buy my not as good gluten free pure oat oatmeal?

2) How bad is cross contamination? Like if a product says "processed in a facility with wheat," do you still eat it? Can I still eat it????

I'm 14...


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



Celiac.com Sponsor (A8-M):



tarnalberry Community Regular

1) about 10% of celiacs react to oats. if you are bloated or get a stomach ache after eating gluten free oats, you will need to avoid ALL oats. if you don't, you can safely have GLUTEN FREE oats, but not regular ones as they have (most) all tested out at too high of a level of contamination. your friend is playing with fire and likely doing internal damage that she doesn't feel.

2) I can't entirely answer that question for you, as it depends on your level of sensitivity. I eat many things made in shared facilities, and sometimes shared equipment, without problem. Heck, if there is gluten in the house you live in, everything you eat at home is made in a shared facility. Some people find they can't tolerate this. But being made in a shared facility doesn't guarantee there is contamination.

eatmeat4good Enthusiast

Hi Sage,

Welcome!

Unfortunately all regular oats are contaminated with wheat due to the way they process them, so the only thing safe for Celiacs is Gluten Free Oatmeal. Your friend is getting a lot of gluten eating those products, they are not safe for Celiac/Gluten Intolerance. The rash you get may come and go quickly now, but it could be DH which is Dermatitis Herpetiformis and it is the skin form of Celiac. It is very sensitive to cross contamination. If you are going to assume you have Celiac based on your reactions and the fact that your dad has it, then you would want to be careful of cross contamination also.

Sorry, it's a bummer not to be able to eat regular oatmeal. Some with Celiac cannot eat oats either, even if they are certified gluten free, but it doesn't sound like that is the case for you.

Whether or not you have symptoms, if you are Celiac, then even trace amounts of gluten will be doing damage to your intestines. The bloating and the rash are consistent with Celiac. I hope you do some reading here and keep asking questions anytime! Tell your Celiac friend about us too, it sounds like she might want to do some reading about Celiac before she ends up with more damage and symptoms. I'm not trying to lecture...just concerned and we are willing to answer any questions you guys may have. Hope this helps. :)

Oh! And the question about shared facility where they also process wheat. Some of us react to those products and cannot eat them either.

Sage122 Explorer

I might not have Celiac though. I mean based on the fact that my dad has it, do you think i have it? If im only gluten sensitive (non celiac), does eating oats still cause damage? (regular oats).

Oh and ps, I can handle normal gluten-free oats

squirmingitch Veteran

Sage, without being tested it's hard to say if you are celiac or gluten intolerant. BUT your dad having celiac is a big clue. And just b/c you don't have big reactions doesn't mean you are not celiac --- just like your friend who is celiac & doesn't have big reactions. There are even what are called "silent celiacs" who have no reactions at all. But any celiac who eats gluten even cross contaminated oats is doing damage to their intestines & this is a very serious disease. There are many serious illnesses which can develop from this if one keeps eating gluten. Things like insulin dependent diabetes, lupus, lymphoma (cancer) & the list goes on & on; plus there are neurological things that can & often do happen. Celiac is a genetically inherited disease. Your dad has it. The odds are that you do too considering the reactions you are having at this stage of the game. I remember your posting before & most of what you told us then & about how much better you feel off of gluten. You said your family (parents) weren't really on board with you not eating gluten & that you had to buy your own gluten-free foods. This is very interesting that your dad has now tested positive for celiac. I hope that now the situation at home has changed somewhat.

And I want to add too that celiac, especially in someone your age, can go into "remission" at times which means you could eat gluten a year from now & have absolutely no reaction at all --- but that does not mean that damage is not being done to a celiacs guts & the rest of the body.

There are a couple ways you could go with this if you want to find out if you are or are not celiac.

1) You can do a gluten challenge which means eating gluten for a specified time & get the blood work done & an endoscopy.

2)Or maybe you should talk to your parents about seeing your dad's doc who dx'd him. It might be that doc will consider your reactions to gluten along with your dad's dx & do an endoscopy on you to see if there is visible damage to your villi & dx you based on that.

Honestly, since your reactions are not all that bad yet it might be best for you to do the whole thing --- the gluten challenge, celiac blood panel, & endoscopy. Also, if you have siblings they should be tested.

As eatmeat said --- the rash & hives you get could be the early stages of dh which is the skin manifestation of celiac disease. This could also explain why you do not have such strong reactions b/c most of us with dh tend not to have many GI symptoms & even when we do they are not as severe. BUT that does not mean damage is not being done to our guts b/c it is!

Sage, we would welcome your friend as well as your dad if either should decide to join us here. We are always happy to help.smile.gif

Sage122 Explorer

Sage, without being tested it's hard to say if you are celiac or gluten intolerant. BUT your dad having celiac is a big clue. And just b/c you don't have big reactions doesn't mean you are not celiac --- just like your friend who is celiac & doesn't have big reactions. There are even what are called "silent celiacs" who have no reactions at all. But any celiac who eats gluten even cross contaminated oats is doing damage to their intestines & this is a very serious disease. There are many serious illnesses which can develop from this if one keeps eating gluten. Things like insulin dependent diabetes, lupus, lymphoma (cancer) & the list goes on & on; plus there are neurological things that can & often do happen. Celiac is a genetically inherited disease. Your dad has it. The odds are that you do too considering the reactions you are having at this stage of the game. I remember your posting before & most of what you told us then & about how much better you feel off of gluten. You said your family (parents) weren't really on board with you not eating gluten & that you had to buy your own gluten-free foods. This is very interesting that your dad has now tested positive for celiac. I hope that now the situation at home has changed somewhat.

And I want to add too that celiac, especially in someone your age, can go into "remission" at times which means you could eat gluten a year from now & have absolutely no reaction at all --- but that does not mean that damage is not being done to a celiacs guts & the rest of the body.

There are a couple ways you could go with this if you want to find out if you are or are not celiac.

1) You can do a gluten challenge which means eating gluten for a specified time & get the blood work done & an endoscopy.

2)Or maybe you should talk to your parents about seeing your dad's doc who dx'd him. It might be that doc will consider your reactions to gluten along with your dad's dx & do an endoscopy on you to see if there is visible damage to your villi & dx you based on that.

Honestly, since your reactions are not all that bad yet it might be best for you to do the whole thing --- the gluten challenge, celiac blood panel, & endoscopy. Also, if you have siblings they should be tested.

As eatmeat said --- the rash & hives you get could be the early stages of dh which is the skin manifestation of celiac disease. This could also explain why you do not have such strong reactions b/c most of us with dh tend not to have many GI symptoms & even when we do they are not as severe. BUT that does not mean damage is not being done to our guts b/c it is!

Sage, we would welcome your friend as well as your dad if either should decide to join us here. We are always happy to help.smile.gif

Thanks :)

squirmingitch Veteran

Thanks :)

YVW sweets!


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



Celiac.com Sponsor (A8-M):



justlisa Apprentice

I might not have Celiac though. I mean based on the fact that my dad has it, do you think i have it? If im only gluten sensitive (non celiac), does eating oats still cause damage? (regular oats).

Oh and ps, I can handle normal gluten-free oats

The truth is... "gluten intolerance" or "celiac" is TOTALLY IRRELEVANT. If you have either one, gluten can harm you...in many, many ways. In fact, MANY people do not experience immediate symptoms, BUT they develop some devastating symptoms and/or diseases... And, you MUST UNDERSTAND that some things will not "get better" or "go away" just because you've realized, by the time you have those problems, and go gluten free.

There is mounting evidence and personal experience to be found (start researching) that supports the thinking that the medical community has a very long way to go in testing, in understanding and treating gluten intolerance.

Please don't make the mistake of thinking that the only thing that "could" happen is just "a little discomfort".

Personally, I believe that the medical community will, finally, realize the seriousness of gluten intolerance AND how damaging it truly is... Sadly, it's not going to be soon...and there are a lot of people who are just going to get sicker and sicker...

Please learn! YOU are, ultimately, the one who is in charge of your health... your future.

justlisa Apprentice

I would like to add this:

Because of what is currently known, many people think/believe that you will be doing damage to your intestines. This is absolutely true...for some.

For others...not...

You see, when you are gluten intolerant, your body's immune system kicks into overdrive. The immune system attacks the small intestine...hence, the damage.

But...how to explain the people who do not show this "damage"??? And, yet, they develop rashes, neurological problems, joint pain, thyroid diseases, rheumatoid arthritis, lupus, etc, etc, etc. There are some doctors/researchers who are, even, starting to connect diabetes, high blood pressure, heart palpitations, etc.

My point is... Gluten intolerance is autoimmune (triggers the immune system into hyperdrive and it attacks the body because it can't get rid of the real enemy). As a result, many autoimmune; diseases are triggered.

My opinion...based on a lot of reading...

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      130,351
    • Most Online (within 30 mins)
      7,748

    SHallRN
    Newest Member
    SHallRN
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.3k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • knitty kitty
      @Ginger38, Diabetes and Celiac often go hand in hand.  Having more than one autoimmune disease is common with Celiac.  I'd err on the side of caution and go gluten free.   I did not want to go on insulin, either.  I got my diabetes under control by following the low histamine version of the Autoimmune Protocol Diet (Dr. Sarah Ballantyne).  My diet now does include carbs.   We're supporting you through this difficult time.  
    • knitty kitty
      @Ginger38,  I've been there with horrible symptoms and diarrhea accidents and diabetes and the insulin conundrum!  My doctors were just as frustrating!   I had nutritional deficiencies.  I know your doctors refuse to test for this.  So did mine, saying "I can't make money prescribing vitamins."  Some members say a naturopathic doctor is more open to testing for deficiencies.  Remember not to start supplementing until after testing is done.  Otherwise the supplements will raise your blood levels falsely.   I had studied Nutrition at university, so I decided to supplement essential vitamins and minerals.  A B Complex, extra Thiamine (Benfotiamine) for the diabetes, magnesium and Vitamin D are the supplements I started with.   The B vitamins are water soluble so any excess is excreted easily.  Thiamine even in high doses is safe and nontoxic.  Diabetics lose more thiamine in urine because of weird kidney stuff.   I wanted to get my blood glucose levels under control because gluten free foods made my level spike for long periods, too.  I absolutely did not want to go on insulin.  Once you do, the pancreas stops making it.  Very scary.  Best to help the pancreas function with thiamine in the form Benfotiamine. I began the low histamine version of the Autoimmune Protocol Diet (developed by Dr. Sarah Ballantyne, A Celiac herself).  It's a low carb, very strict diet at first, then expanded.  I considered it similar to feeding a sick baby.  You don't give hard to digest foods to a baby.  You give easily digestible foods.  This allows time for the gastrointestinal tract to calm down and heal.  Symptoms started to calm down quickly.  With the vitamins, I started feeling much better.  My blood glucose levels stabilized.  I did not go on insulin.  I do not take anti-glycemic pharmaceutical drugs like Metformin.  Just diet.  You're making the right decision to live as a Celiac.  Your body is telling you clearly.  You can get through this.  You're strong and you're fighting for yourself and your baby.  Good job!  You have the Tribe behind you!
    • maryannlove
      Though trying to diligently eat gluten free, recent bloodwork was bad so searching for culprits.  Eat lot of (preferably mixed) nuts.  Most allergen labels say may be processed on equpment that also processes wheat, etc.  Finally found ONE kind (unsalted mixed) at BJ's.  Wessley (their store brand) that did not contain that warning.  Says in large letters "A GLUTEN FREE FOOD."  Well, all nuts are a gluten free FOOD!  Have been eating and now wonder if this is intentionally decieving.  So stopped eating until find culprit.  Nuts are so good for protein and fiber (especially if trying to not eat meat).  'Tis so frustrating.  Thanks to above, I'll look into Tierra Farms.   
    • somethinglikeolivia
      Fascinating! This was very helpful, thanks for sharing
    • maryannlove
      Despite being very diligent about eating gluten free, my recent bloodwork was bad.  So been on a mission to find the culprit(s).  During Covid my daughter found "certified gluten free" Yasso mint chocolate chip yogurt bars at Costco.  I was elated and have been eating them since.  When delving into possible culprits I discovered that the boxes with 12 bars at both Costco and BJ's no longer say "certified gluten free."  But the boxes with 4 bars at groceries and Target still say "certified gluten free."  Contacted the manufacturer and was told to go by what the box says.  So guess different machinery is used.  Was also told they were in the process of changing boxes.  Will be interesting to see what that brings.  
×
×
  • Create New...