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

When Do You Introduce Gluten To Baby?


Offthegrid

Recommended Posts

Offthegrid Explorer

This is thinking waaaay ahead, but anyhow. I am dx'd gluten intolerant based on blood test but elected not to have the endoscopy. My brother has it. My aunt has it. I believe my mother (not related to aunt) has it along with other food intolerances but she refuses to be tested.

I am certain my hubby has it, but he had a negative blood test so he refuses to give up gluten even for 2 weeks. So there is a high likelihood that if we have children, they would also be gluten intolerant.

Has anyone just purposely kept their kids off gluten as infants and toddlers? When *would* you do a test of gluten? (By test, I mean giving the kid food with gluten in it and seeing if there is a reaction.)


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



Celiac.com Sponsor (A8-M):



JennyC Enthusiast

Gluten should be introduced between 4-6 months. Some studies suggest that if you introduce gluten too early or too late it will increase the child's likelihood of developing celiac disease. Blood tests are not supposed to be reliable until children are at least 24 months old.

dandelionmom Enthusiast

I've heard between 6 and 9 months. I've also heard that continuing to breastfeed through out the first year (or longer) and especially while introducing gluten can help lessen the incidence of celiac disease.

dionnek Enthusiast

I have a 4 1/2 month old baby that I am strictly breastfeeding right now (I have confirmed celiac and am gluten free), and was planning on waiting until 1 year to introduce gluten (stick with gluten free baby foods for the first year) so as to build up his immunity. I'm confused then why they say you should introduce gluten between 4-6 months (or 6-9)? Since they tell you not to introduce peanuts, etc. until 1 year due to allergies, why introduce gluten before then? Just wondering - I'm a very confused mommy!

Juliet Newbie

I don't know the reason why they say between 4-6 months; from the studies I've read, it's at best a correlation and not causal. They found that fewer kids get full blown Celiac within a certain time frame if they are introduced at this early stage versus later. However, the test has not looked at whether or not these same kids get Celiac Disease later in life.

I introduced my daughter (after my son was diagnosed right when she was born) to gluten during this time. She could not handle it. And later, I gave her small bits, too. She's never been able to digest it well. I also got the gene test done to make sure if I even needed to worry about Celiac Disease with her. She had the gene. So our pediatric g.i. said that if she had the gene and she reacted at all to gluten, she probably will get the disease since our son got sooooo sick at such a young age.

cruelshoes Enthusiast

See this link: Open Original Shared Link

The AAP published a study in the May 18, 2005 issue of the Journal of the American Medical Association. In it, it was reported that children that are prone to celiac disease have a greater risk of developing celiac disease if gluten in introduced prior to 4 months or after 7 months. These children were followed for an average of 4.8 years.

Here are the findings:

The Findings

Fifty-one children (3.3%) developed evidence of celiac disease. Twenty five of these children had biopsy confirmed cases. Major findings included:

Children exposed to wheat, barley, or rye in the first three months of life had a five-fold increased risk of celiac disease autoimmunity compared to those exposed at 4-6 months. Children not exposed until their seventh month or later were also at increased risk, but only slightly.

Among the 41 children who were at the greatest risk according to their genetic markers, those exposed to wheat, barley, or rye in the first three months of life had nearly an eight-fold increased risk of celiac disease autoimmunity compared to those exposed at four to six months.

No protective effect of breastfeeding was observed.

These findings were consistent even when the researchers limited their analysis to only the 25 cases of biopsy-confirmed celiac disease.

FWIW, we introduced gluten to both of our older kids at 6 months. One developed celiac and one did not. I have also read studies that breastfeeding CAN have a protective effect.

Guhlia Rising Star

What about those of us that have strict gluten free households? How would you go about introducing it then?


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



Celiac.com Sponsor (A8-M):



shan Contributor

There are so many different opinions on this! In one hospital, i was told by 2 different drs, to try at 4-6 months and hte other said only after a year. I gave mine a couple of spoons at approx 6 months, he wasn't happy and now at 13 months i hope to be trying it again. They said there is no way you can prevent it from being 'passed on', nor can you prevent it from happening altogether - neither myself nor my hubby has it, nor anyone that we know (except my step grandma :) ) yet my dd has it... whenever you give gluten to your child will not be the cause of him or her getting celiac! Celkiac is not contagious it is genetic - you either are born with it or not!!!!!

shayesmom Rookie
Has anyone just purposely kept their kids off gluten as infants and toddlers? When *would* you do a test of gluten? (By test, I mean giving the kid food with gluten in it and seeing if there is a reaction.)

Personally, if I were to have a second child, I would ignore the studies and not introduce gluten until my child had his/her molars. Why? It's all part of the ptyalin debate I guess...and to me, it makes sense.

"Ptyalin and Infant Food. It has traditionally been common to start infants on solid food from 4+ months onwards - however current research and WHO/UNICEF "Baby Friendly" guidelines recommend only breastmilk until 6 months of age.

For almost 200 years, medical science has understood that the saliva amylase Ptyalin is a critical enzyme involved in the commencement of starch break-down into glucose. Science has also known, but seemingly forgotten, that infants do not produce normal levels of Ptyalin until full dentition (growth of teeth).

With ptalin absent from infant saliva, two predictable physiological reactions can occur after the consumption of farinaceous (starchy) foods:

The indigestible starch "ferments" within the intestines causing numerous digestive disorders. Mucus "thickens" potentially causing ear, nose or throat problems. NOTE: What of Third World and Asian babies historically being fed rice and other starches? For thousands of years mothers in these continents traditionally chewed their baby's food first, before feeding it to their infant - thus unknowingly coating it with their own saliva ptyalin.

Low levels of ptyalin within infant saliva has been documented for almost 200 years my many doctors, including Chavasse, Sonsino, Tilden, Routh, Huxley, Youmans, Dalton, Page, Densmore, Shelton and Fry. More recently this debate is again resurfacing, such as through author Kathy Fray controversially bringing the topic to the forefront.

Instead of problematic starchy foods such as baby rice, baby cereals, baby porridge, mashed potatoes, bread rusks, crackers, biscuits, pasta and noodles; the recommended alternatives are vegetables and fruit, topped up with a little protein."

kazzadazza Newbie

well done for THINKING about what you might feed your baby before it is here . swedish research ( i think there are others too ) indicate that babies are less likely to develop celiac disease if they are recieving "substantial" quantities of breast milk when they are first exposed to gluten . there is no need to rush into introducing foods other that breastmilk into a babies diet - where possible babies should be exclusively breastfed until 6 months of age . i think that the most important thing to remember is that you don't just need to go -"well today is the day you must start eating , heres a great big heaping bowl of food for you " . i really like what was recomended to me by a nurse with my youngest . "just let them have a little taste of what your eating " so you just stick your (clean ) finger in and let them have a tiny taste of it . it doesn't need to be everyday , at first . its just a way of very gradually introducing your childs body to the concept of foods other that milk . it ok for them to taste everything AS LONG AS THEY ARE OVER 6 MONTHS . when i started introducing solids as an actual substantial part of their diet , i went for raw organinc wholefoods , banana with my first , avocado with my second ; but mixed mostly with breastmilk to begin . and other foods very gradually , after that . i really don't think that grains should be introduced before 10 months . my research has indicated to me that these measures reduce the likeliness of any innapropriate immune responses . anyway you have plenty of time to research and decide what is best for you .

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. - trents replied to marion wheaton's topic in Gluten-Free Foods, Products, Shopping & Medications
      2

      Are Lindt chocolate balls gluten free?

    2. - BlessedinBoston replied to marion wheaton's topic in Gluten-Free Foods, Products, Shopping & Medications
      2

      Are Lindt chocolate balls gluten free?

    3. - knitty kitty replied to Jmartes71's topic in Related Issues & Disorders
      14

      My only proof

    4. - Jmartes71 replied to Jmartes71's topic in Related Issues & Disorders
      14

      My only proof

    5. - marion wheaton posted a topic in Gluten-Free Foods, Products, Shopping & Medications
      2

      Are Lindt chocolate balls gluten free?


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      132,409
    • Most Online (within 30 mins)
      7,748

    4over2
    Newest Member
    4over2
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.5k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Who's Online (See full list)

  • Upcoming Events

  • Posts

    • trents
      @BlessedinBoston, it is possible that in Canada the product in question is formulated differently than in the USA or at least processed in in a facility that precludes cross contamination. I assume from your user name that you are in the USA. And it is also possible that the product meets the FDA requirement of not more than 20ppm of gluten but you are a super sensitive celiac for whom that standard is insufficient. 
    • BlessedinBoston
      No,Lindt is not gluten free no matter what they say on their website. I found out the hard way when I was newly diagnosed in 2000. At that time the Lindt truffles were just becoming popular and were only sold in small specialty shops at the mall. You couldn't buy them in any stores like today and I was obsessed with them 😁. Took me a while to get around to checking them and was heartbroken when I saw they were absolutely not gluten free 😔. Felt the same when I realized Twizzlers weren't either. Took me a while to get my diet on order after being diagnosed. I was diagnosed with small bowel non Hodgkins lymphoma at the same time. So it was a very stressful time to say the least. Hope this helps 😁.
    • knitty kitty
      @Jmartes71, I understand your frustration and anger.  I've been in a similar situation where no doctor took me seriously, accused me of making things up, and eventually sent me home to suffer alone.   My doctors did not recognize nutritional deficiencies.  Doctors are trained in medical learning institutions that are funded by pharmaceutical companies.  They are taught which medications cover up which symptoms.  Doctors are required to take twenty  hours of nutritional education in seven years of medical training.  (They can earn nine hours in Nutrition by taking a three day weekend seminar.)  They are taught nutritional deficiencies are passe' and don't happen in our well fed Western society any more.  In Celiac Disease, the autoimmune response and inflammation affects the absorption of ALL the essential vitamins and minerals.  Correcting nutritional deficiencies caused by malabsorption is essential!  I begged my doctor to check my Vitamin D level, which he did only after making sure my insurance would cover it.  When my Vitamin D came back extremely low, my doctor was very surprised, but refused to test for further nutritional deficiencies because he "couldn't make money prescribing vitamins.". I believe it was beyond his knowledge, so he blamed me for making stuff up, and stormed out of the exam room.  I had studied Nutrition before earning a degree in Microbiology.  I switched because I was curious what vitamins from our food were doing in our bodies.  Vitamins are substances that our bodies cannot manufacture, so we must ingest them every day.  Without them, our bodies cannot manufacture life sustaining enzymes and we sicken and die.   At home alone, I could feel myself dying.  It's an unnerving feeling, to say the least, and, so, with nothing left to lose, I relied in my education in nutrition.  My symptoms of Thiamine deficiency were the worst, so I began taking high dose Thiamine.  I had health improvement within an hour.  It was magical.  I continued taking high dose thiamine with a B Complex, magnesium. and other essential nutrients.  The health improvements continued for months.  High doses of thiamine are required to correct a thiamine deficiency because thiamine affects every cell and mitochondria in our bodies.    A twenty percent increase in dietary thiamine causes an eighty percent increase in brain function.  The cerebellum of the brain is most affected.  The cerebellum controls things we don't have to consciously have to think about, like digestion, balance, breathing, blood pressure, heart rate, hormone regulation, and many more.  Thiamine is absorbed from the digestive tract and sent to the most important organs like the brain and the heart.  This leaves the digestive tract depleted of Thiamine and symptoms of Gastrointestinal Beriberi, a thiamine deficiency localized in the digestive system, begin to appear.  Symptoms of Gastrointestinal Beriberi include anxiety, depression, chronic fatigue, headaches, Gerd, acid reflux, gas, slow stomach emptying, gastroparesis, bloating, diarrhea and/or constipation, incontinence, abdominal pain, IBS,  SIBO, POTS, high blood pressure, heart rate changes like tachycardia, difficulty swallowing, Barrett's Esophagus, peripheral neuropathy, and more. Doctors are only taught about thiamine deficiency in alcoholism and look for the classic triad of symptoms (changes in gait, mental function, and nystagmus) but fail to realize that gastrointestinal symptoms can precede these symptoms by months.  All three classic triad of symptoms only appear in fifteen percent of patients, with most patients being diagnosed with thiamine deficiency post mortem.  I had all three but swore I didn't drink, so I was dismissed as "crazy" and sent home to die basically.   Yes, I understand how frustrating no answers from doctors can be.  I took OTC Thiamine Hydrochloride, and later thiamine in the forms TTFD (tetrahydrofurfuryl disulfide) and Benfotiamine to correct my thiamine deficiency.  I also took magnesium, needed by thiamine to make those life sustaining enzymes.  Thiamine interacts with each of the other B vitamins, so the other B vitamins must be supplemented as well.  Thiamine is safe and nontoxic even in high doses.   A doctor can administer high dose thiamine by IV along with the other B vitamins.  Again, Thiamine is safe and nontoxic even in high doses.  Thiamine should be given if only to rule Gastrointestinal Beriberi out as a cause of your symptoms.  If no improvement, no harm is done. Share the following link with your doctors.  Section Three is especially informative.  They need to be expand their knowledge about Thiamine and nutrition in Celiac Disease.  Ask for an Erythrocyte Transketolace Activity test for thiamine deficiency.  This test is more reliable than a blood test. Thiamine, gastrointestinal beriberi and acetylcholine signaling.  https://pmc.ncbi.nlm.nih.gov/articles/PMC12014454/ Best wishes!
    • Jmartes71
      I have been diagnosed with celiac in 1994, in remission not eating wheat and other foods not to consume  my household eats wheat.I have diagnosed sibo, hernia ibs, high blood pressure, menopause, chronic fatigue just to name a few oh yes and Barrett's esophagus which i forgot, I currently have bumps in back of my throat, one Dr stated we all have bumps in the back of our throat.Im in pain.Standford specialist really dismissed me and now im really in limbo and trying to get properly cared for.I found a new gi and new pcp but its still a mess and medical is making it look like im a disability chaser when Im actively not well I look and feel horrible and its adding anxiety and depression more so.Im angery my condition is affecting me and its being down played 
    • marion wheaton
      Wondering if anyone knows whether Lindt chocolate balls are gluten free. The Lindt Canadian website says yes but the Lindt USA website says no. The information is a bit confusing.
×
×
  • 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.