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

Wading Into The Thicket: Oats!


ThisIsMyUserName

Recommended Posts

ThisIsMyUserName Explorer

So having spent the last months reading thousands and thousands of pages on celiac and gluten and so on, I feel pretty confident in the knowledge (if not quite yet the practice) of what I'm supposed to do (note that I have non-celiac gluten intolerance, not celiac). One sticky wicket remains: oats. I have long eaten oatmeal for breakfast every day (with cinnamons and raisins, no sugar) and find it's a super-healthy way to get going that leaves me full for a long time. I asked my (very knowledgable about celiac and gluten intolerance) if gluten-free oatmeal was ok, and he said yes. I read a bunch of academic papers and all seem to point to oats being safe if a) they're gluten-free, not the standard commercial oats and B) you're not one of the people who specifically react to oats. So all would seem well. On the other hand, though, the general advice seems to be either to not have oats (e.g. in gluten-free for dummies, there's a whole section that basically says "Don't eat oats. Really, don't eat them."), or to limit them to some quantity or not to have them for the first few months or years. I am a generaly big believer in collective wisdom, and I've seen this advice a bunch of times when I searched the boards here, but can't find the underlying studies to support that. So, I'm trying to figure it out. Is it that people used to say no because there weren't gluten-free oats and now there are, or that it's wise to avoid it during healing in case you react, or something else?


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



Celiac.com Sponsor (A8-M):



mamaw Community Regular

In general oats  can be hard for many to digest. Years ago  oats  were off the table for  celiac   . Then  came gluten-free  oats......I was never  an oat  for  breakfast  lover  in my gluten days   but for  some  strange  reason  I  decided  I  missed oats! So  I tried  the gluten-free oats & love  oatmeal cookies.... I now  do well  with  1/2 cup of gluten-free  oats  maybe  twice a  month more than like  I  get  a  weird  tummy  feeling  ,  so I guess  I learned  how  much my  gut  can take.....

A new  person  that   hasn't  had  any healing of the gut  may find  it  feels  like  overload  on their  gut or  worse.... When starting out  we  try to tell people  to be kind  & gentle  to their  fragile  tummies to  let  the body  heal  as  much as possible  without  added  stress... gluten-free foods  in the natural state without  a lot  of  processed gluten-free  either....some  foods  are  just  hard to digest....

cristiana Veteran

I found this from Coeliac UK - we add an 'o' in the UK and I am still not sure why!  It doesn't seem necessary!

 

Open Original Shared Link

 

My own nutritionalist said it was worth waiting 6-12 months after taking up gluten free diet so that when oats are introduced it will be obvious if there are problems.  It will also have given your tummy time to heal a bit, as mamaw says.

psawyer Proficient

Oats can be hard to digest, so I would avoid them completely while your gut is healing. Once that is finished, try pure oats. You need to look for ones that are processed specially to avoid contamination from wheat. Safe oats will be labeled as "pure," "wheat-free," or "gluten-free." In Canada, the last one is not yet allowed by CFIC regulations, but those rules are changing.

 

A minority of people with celiac disease can not tolerate even pure oats, so introduce them carefully and watch for reactions. Do not introduce any other new foods around the same time.

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. - Scott Adams commented on Scott Adams's article in Additional Concerns
      4

      Going Low-Gluten May Harm Good Gut Bacteria, Researchers Warn

    2. - chrisinpa commented on Scott Adams's article in Additional Concerns
      4

      Going Low-Gluten May Harm Good Gut Bacteria, Researchers Warn

    3. - Flash1970 replied to Ginger38's topic in Related Issues & Disorders
      7

      Shingles - Could It Be Related to Gluten/ Celiac

    4. - trents replied to Roses8721's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      10

      GI DX celiac despite neg serology and no biopsy

    5. - Roses8721 replied to Roses8721's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      10

      GI DX celiac despite neg serology and no biopsy


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      132,492
    • Most Online (within 30 mins)
      7,748

    K Zappe
    Newest Member
    K Zappe
    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

    • Flash1970
      You might try Heallix.  It's a silver solution with fulvic acid. I just put the solution on with a cotton ball.  It seemed to stop the nerve pain. Again,  not in your eyes or ears.   Go to heallix.com to read more about it and decide for yourself Also,  I do think nerve and celiac combined have a lot to do with your susceptibility to shingles breaking out. 
    • trents
      Celiac disease requires both genetic potential and a triggering stress event to activate the genes. Otherwise it remains dormant and only a potential problem. So having the genetic potential is not deterministic for celiac disease. Many more people have the genes than actually develop the disease. But if you don't have the genes, the symptoms are likely being caused by something else.
    • Roses8721
      Yes, i pulled raw ancetry data and saw i have 2/3 markers for DQ2.2 but have heard from friends in genetics that this raw data can be wildly innacurate
    • Ginger38
      Thanks, I’m still dealing with the pain and tingling and itching and feeling like bugs or something crawling around on my face and scalp. It’s been a miserable experience. I saw my eye doc last week, the eye itself was okay, so they didn’t do anything. I did take a 7 day course of an antiviral. I’m hoping for a turnaround soon! My life is full of stress but I have been on / off the gluten free diet for the last year , after being talked into going back on gluten to have a biopsy, that looked okay. But I do have positive antibody levels that have been responsive  to a gluten free diet. I can’t help but wonder if the last year has caused all this. 
    • Scott Adams
      I don't think any apps are up to date, which is exactly why this happened to you. Most of the data in such apps is years old, and it doesn't get updated in real time. Ultimately there is no substitution for learning to read labels. The following two lists are very helpful for anyone who is gluten sensitive and needs to avoid gluten when shopping. It's very important to learn to read labels and understand sources of hidden gluten, and to know some general information about product labelling--for example in the USA if wheat is a possible allergen it must be declared on a product's ingredient label like this: Allergens: Wheat.      
×
×
  • 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.