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

Is Oatmeal Safe


Aunt Poppy

Recommended Posts

Aunt Poppy Rookie

Just need to know if Oatmeal is safe?


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



Celiac.com Sponsor (A8-M):



CarlaB Enthusiast

The short answer is no.

Almost all oats are contaminated by wheat. Some celiacs are sensitive to the protein in the oats. Typically, it's best to be completely oat free until you're healed, then try oats that are gluten-free ... you have to buy special gluten-free oats, you can't just buy regular oats at the grocery.

hez Enthusiast

I would also reccomend talking to your doc before hand as well. I eat the gluten-free oats from the company in Wyoming and have enjoyed them. I only eat these oats. I do not eat anything from the grocery store that contains oats (thinking cereal) because of the cc. You should also do some research as well to figure out what the thoughts are from "experts" regarding the issue.

Hez

Mango04 Enthusiast

If you go to the home page of celiac.com and search for "oats" you'll find extensive information on the subject.

Many studies suggest they are safe. It's worth looking over the info. before deciding for yourself. You can get certified gluten-free oats if you're worried about contamination.

mamaw Community Regular

I agree with the other posters..... one thing I might add is if you are gonna eat oats (only the gluten-free ones) start out very slowly.... A quarter cup to a half cup to begin with. I still only eat this amount at one sitting & I have been eating them since they came out....

I still can't believe I missed oats!!!! Must be part horse,,,,,,,,,,,,nayyyyyyyyy!

mamaw

Gonbad Newbie

I have been gluten free since March 2007. I had my Endscope/biopsy done May 2, 2007. After consultation with my doctor he told me to stay off oats until my next endoscope. His argument goes along with what has been said above. It's a significant cross contamination problem. That being said before I was diagnosed I ate oatmeal almost everyday in my company cafeteria. I now eat pretty much only eggs and bacon. However I have slipped and eaten oatmeal a few times and had no reaction. I have now found some Barbara cerials brown rice crispies, and corn flakes that are gluten free (No Malt!!!!). I have found them to be very good. So I will stay off oats until I get a clean bill on my intestines. At that point I will add them back into my diet and see what happens.

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      132,119
    • Most Online (within 30 mins)
      7,748

    Lisa Holloway
    Newest Member
    Lisa Holloway
    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

    • captaincrab55
      Hi Colleen H,   I suffered with the pins and needles/burning feeling in my legs and feet for at least  6 years until my Nephrologist figured out that I had to go on a low salt diet.  He said my kidneys weren't strong enough to remove the salt.  The simple fix was a diuretic, but that med leaves the uric acid behind, so that wasn't an option.  On the bright side the low salt diet lowered my BP over 20 points and and the pins and needles/burning feeling went away.  Good Luck and hope this helps.  
    • Colleen H
      Yes this is very frustrating for me ... not sure what to think.  Feels like I'm having reactions to a lot of things  Now applesauce?? I don't understand 😞 
    • Colleen H
      I did ... But aren't we going to be vitamin deficienct if we are not eating due to being sick ?? If the food we eat is gluten free and we have other sensitivities , how do we get out of the cycle??  Thank you 
    • Colleen H
      Anyone else get pins and needles. ??? Burning feeling ? Heat makes it so much worse 😔  Winter is here.  I had to lower my thermostat because I couldn't take that hot air feeling 😔  Hopefully it goes away soon     
    • trents
      I assume that you already know that genetic testing for celiac disease cannot be used to confirm a celiac diagnosis. About 40% of the general population has the genetic potential to develop celiac disease but only about 1% actually develop celiac disease. It can be used to rule out celiac disease with a high degree of confidence, however, in the case where the genetic testing is negative for the genes. Until and unless you are actually diagnosed with celiac disease I would not raise this as an issue with family. However, if you are diagnosed with celiac disease through blood antibody testing and/or endoscopy with positive biopsy I would suggest you encourage first degree relatives to also purse testing because there is a significant chance (somewhere betwee 10% and almost 50%, depending on which studies you reference) that they will also have or will develop active celiac disease. Often, there are symptoms are absent or very minor until damage to the small bowel lining or other body systems becomes significant so be prepared that they may blow you off. We call this "silent celiac disease". 
×
×
  • 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.