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

Irish Oats


TCA

Recommended Posts

TCA Contributor

I heard that Irish Oats are gluten free. My daughter vomited blood last time we tried oatmeal, so I'm not real keen on trying them.

Anyone know anything about them or tried them?


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



Celiac.com Sponsor (A8-M):



gfp Enthusiast
I heard that Irish Oats are gluten free. My daughter vomited blood last time we tried oatmeal, so I'm not real keen on trying them.

Anyone know anything about them or tried them?

There are 2 seperate issues with oats.... firstly strictly they are gluten free but the protein in oats does affect some celiacs like gluten. Secondly oats are almost always grown in a rotation with wheat so some of the wheat that falls to the ground comes up the next year in the oats crop.

Much as I'd love to be able to eat oats ... things like cookies etc. I think for me the risk is too great.

shai76 Explorer

I'm not sure. I'm allergic to oats so the doctor told me I have to stay away from them all. I never thought Irish oats were ay different than any other oats. If I see anything about it I will let you know. :)

Guest nini

I've read that certain brands of oats, some Irish oats, like McCann's, are grown in dedicated fields (not crop rotated with wheat) and are technically gluten-free... but like others have said, the protein aveenin in oats affects many celiacs just like gluten and therefore some react badly to it. Personally it's not worth the risk for me. But some "experts" are saying that Irish oats are safe for Celiacs. It's your call, you will have to decide it the risk is worth it for you to try. Then if you try it and don't react, then you could make the assumption that it doesn't bother you (although I'm not clear if it would do the same internal damage as gluten and you wouldn't neccesarily be aware of it)... too risky for me though.

Guest Viola
I heard that Irish Oats are gluten free. My daughter vomited blood last time we tried oatmeal, so I'm not real keen on trying them.

Anyone know anything about them or tried them?

If your daughter vomited blood last time on oatmeal, why would you even be interested in them? I'm not trying to be mean, just a little confused. :o

DingoGirl Enthusiast

BTE, I just ate my new oatmeal this morning, ordered from Gluten-Free Oats (not Irish oatmeal, just regular oats)....will see how it goes. So far, slight pain that feels like gas, but my reaction to gluten is always about 12 - 13 hours later. I'll post tomorrow on this, in case anyone cares! :rolleyes:

flagbabyds Collaborator

I always get sick from any oats, and they did a biopsy and saw that it might have been damaging my vili.


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



Celiac.com Sponsor (A8-M):



TCA Contributor

My daughter is breastfed and i'm pumping exclusively due to her medical conditions and her feeding tube. I've started the TED, which means I only eat sweet potatoes, turkey, rice, squash and pears for a while, then add foods one at a time to see what she might be allergic to. My milk production is plummeting with the diet change, and I'm trying to find something to pick it back up again. Someone told me about Irish Oats helping and that they were totally gluten free. I have my doubts and don't want to make bad matters worse. I've also tried Fenugreek before, but it made her fussy. I'm probably not going to try it, just thought I would see if they were actually a viable option or not.

Thanks for the info.

minibabe Contributor

Yesterday I was at the suffolk vendor fair and I sat next to Anne Lee and the women that Just released the new "celiac book" about 1 month ago. I asked her the same question. They satated that McCanns Irish Oats are gluten-free. We are allowed to have them. Even the women from "gluten-free living" (i believe that is the name of the magazine) said so also.

Amanda NY

hez Enthusiast

I read somewhere (for the life of me I can not remember where) that Irish Oats can have cc issues. I eat oatmeal with no problem but I only eat gluten-free oatmeal from gluten free oats company. They do not do a rotation crop and test their oatmeal to insure it is gluten-free (family member is a celiac). However, this is a personal decision that requires much research. The protein in oats is similar to the protein in wheat. So there are a number of celiacs who react to the protein in oats even if it is gluten-free.

Dingo Girl- remember that oats contain alot of fiber. This increase can cause bloating, "d" and gas. Which is why it is recommended to start out very slow with oats.

Hez

tarnalberry Community Regular

McCanns has been tested to have contamination levels above 200ppm, and the company confirms that they cannot guarantee their oats to be gluten-free.

DingoGirl Enthusiast

Well, I ate my bowl of oats (from Gluten-Free Oatmeal) and I can tell you it is worth every penny of the $16 (product and shipping cost - two-pound bag)! I had a full cup, with milk and sugar, and 24 hours later, not a bit of a problem. I felt a tiny bit of gas pains a couple of hours afterwards, and that's it. Didn't get sick in any way and feel great! :rolleyes: I plan on having them two to three days a week and am excited to be able to eat oatmeal again.

Thank God for small things. :)

queenofhearts Explorer

Oatmeal used to be one of my very favorite things. I love it raw with milk & fruit-- learned about that in Denmark as a child-- & hate to give it up! Oatmeal bread, oatmeal cookies, all faves... but I've just been diagnosed & I'm going as straight & narrow as I know how until I get a handle on this thing. So I'm not taking the chance with oats.

Anyway, my question is, have any of you tried the non-oat flakes out there? Somehow I can't see myself eating soy flakes with milk for breakfast... but are there other substitutes that might satisfy my muesli jones?

Thanks,

Leah

ravenwoodglass Mentor
Oatmeal used to be one of my very favorite things. I love it raw with milk & fruit-- learned about that in Denmark as a child-- & hate to give it up! Oatmeal bread, oatmeal cookies, all faves... but I've just been diagnosed & I'm going as straight & narrow as I know how until I get a handle on this thing. So I'm not taking the chance with oats.

Anyway, my question is, have any of you tried the non-oat flakes out there? Somehow I can't see myself eating soy flakes with milk for breakfast... but are there other substitutes that might satisfy my muesli jones?

Thanks,

Leah

You might want to try Buckwheat Groats, they are not wheat despite the name. I don't know if they can be eaten without cooking though.

queenofhearts Explorer
You might want to try Buckwheat Groats, they are not wheat despite the name. I don't know if they can be eaten without cooking though.

Thanks, I'm going to have to revisit buckwheat-- I always thought I disliked the flavor but then in reading up on gluten free grains, discovered that what I hadn't enjoyed was kasha, which is processed differently than the "pure" grain.

Thanks for the suggestion!

Leah

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,979
    • Most Online (within 30 mins)
      7,748

    volivier
    Newest Member
    volivier
    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

    • Wheatwacked
      @Riley., Welcome to the forum.   It was once believed that Celiac Disease was only a childhood disease and it can be outgrown.  That was before 1951, before gluten was discovered to be cause of Celiac Disease, also called Infantilism.  Back then Cileac Disease was thought to be only a gastro intestinal disease, once you  "outgrew" the colicky phase, you were cured. You were so lucky to be diagnosed at 5 years old so your developing years were normal.  Gluten can affect multiple systems.  The nervous system, your intellegence. The muscules, skeleton. It can cause neurological issues like brain fog, anxiety, and peripheral neuropathy.  It can cause joint pain, muscle weakness, and skin rashes. Epilepsy is 1.8 times more prevalent in patients with celiac disease, compared to the general population. Because through malabsorption and food avoidances, it causes vitamin D and numerouus other essential nutrient deficiencies, it allows allergies, infections, poor growth, stuffy sinuses and eustacian tubes. There is even a catagory of celiac disease called "Silent Celiac".  Any symptoms are explained away as this, that or the other thing. Gluten is one of the most addictive substances we consume.  Activating the Opiod receptors in our cells, it can numb us to the damage that it, and other foods are causing.  It has become socially acceptable to eat foods that make us feel sick.  "There's a pill for that".   It is generally accepted that n fact you are weird if you don't. The hardest part is that if you don't eat gluten you will feel great and think why not.  But slowly it will effect you, you'll be diagnosed with real diseases that you don't have. You'll be more susseptable to other autoimmune diseases.  As you read through the posts here, notice how many are finally dianosed, after years of suffering at older ages.  Is it worth it? I think not. Perhaps this book will help:  Here is a list of possible symptoms:   
    • Riley.
      Hi! Im Riley, 18 years old and have been diagnosed for 13 years.. the testing started bc I stopped growing and didn’t gain any weight and was really small and thin for my age.  I got diagnosed when I was 5 and have been living gluten free since, in elementary and middle school it was hard for me and I kept contaminating myself bc I wanted to fit in with my friends so so badly. I ate gluten secretly at school and mostly regretted it 30 minutes later.  I’ve had symptoms like diarrhea, nausea, headaches, stomachaches, threw up a lot and was really emotional.  In 2022 I really started working on myself and tried to stay gluten free and if I did eat gluten I wouldn’t tell anyone and suffer in silence.  Last year in July I begged my mom to let me „cheat“ one day bc I just wanted to fit in… I ate a lot of different stuff, all the stuff I missed out on in my childhood like nuggets, pizza and all that.. I didn’t have symptoms that day and was doing really fine My mom and I wanted to test how far we can go and said we would test it for 12 weeks to get my blood taken after to see if I’m doing good or if symptoms start showing  As a now 18 year old girl who finally gained a normal weight and doesn’t get symptoms I’m to scared to get tested/my blood taken cuz I finally found comfort in food and it got so much easier for me and my family.  A year and 4 months later i still didn’t get any symptoms and have been eating gluten daily.  I’m scared to get tested/my blood taken cuz what if I’m actually not fine and have to go back to eating gluten free. Any tips to get over that fear and „suck it up“ cuz I know I could seriously damage my body… sorry if I seem like a idiot here… just don’t really know what to do :,)
    • Mari
      There is much helpful 'truth' posted on this forum. Truths about Celiac Disease are based on scientific research and people's experience. Celiac disease is inherited. There are 2 main Celiac 'genes' but they are variations of one gene called HLa - DQ What is inherited when a person inherits one or both of the DQ2 or the DQ8 is a predisposition to develop celiac disease after exposure to a environmental trigger. These 2 versions of the DQ gene are useful in diagnosing  celiac disease but there are about 25 other genes that are known to influence celiac disease so this food intolerance is a multigenic autoimmune disease. So with so many genes involved and each person inheriting a different array of these other genes one person's symptoms may be different than another's symptoms.  so many of these other genes.  I don't think that much research on these other genes as yet. So first I wrote something that seem to tie together celiac disease and migraines.  Then you posted that you had migraines and since you went gluten free they only come back when you are glutened. Then Scott showed an article that reported no connection between migraines and celiac disease, Then Trents wrote that it was possible that celiacs had more migraines  and some believed there was a causal effect. You are each telling the truth as you know it or experienced it.   
    • tiffanygosci
      Another annoying thing about trying to figure this Celiac life out is reading all of the labels and considering every choice. I shop at Aldi every week and have been for years. I was just officially diagnosed Celiac a couple weeks ago this October after my endoscopy. I've been encouraged by my local Aldi in that they have a lot of gluten free products and clearly labeled foods. I usually buy Milagro corn tortillas because they are cheap and are certified. However, I bought a package of Aldi's Pueblo Lindo Yellow Corn Tortillas without looking too closely (I was assuming they were fine... assuming never gets us anywhere good lol) it doesn't list any wheat products and doesn't say it was processed in a facility with wheat. It has a label that it's lactose free (hello, what?? When has dairy ever been in a tortilla?) Just, ugh. If they can add that label then why can't they just say something is gluten free or not? I did eat some of the tortillas and didn't notice any symptoms but I'm just not sure if it's safe. So I'll probably have to let my family eat them and stick with Milagro. There is way too much uncertainty with this but I guess you just have to stick with the clearly labeled products? I am still learning!
    • tiffanygosci
      Thank you all for sharing your experiences! And I am very thankful for that Thanksgiving article, Scott! I will look into it more as I plan my little dinner to bring with on the Holiday I'm also glad a lot of research has been done for Celiac. There's still a lot to learn and discover. And everyone has different symptoms. For me, I get a bad headache right away after eating gluten. Reoccurring migraines and visual disturbances were actually what got my PCP to order a Celiac Panel. I'm glad he did! I feel like when the inflammation hits my body it targets my head, gut, and lower back. I'm still figuring things out but that's what I've noticed after eating gluten! I have been eating gluten-free for almost two months now and haven't had such severe symptoms. I ate a couple accidents along the way but I'm doing a lot better
×
×
  • 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.