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Exclusive Breastfeeding For 12 Months?


allinyourhead

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allinyourhead Newbie

Hi, sorry if this is not posted in the correct forum. I've been doing a little research on this and I have found conflicting information online. I believe I am gluten intolerant/sensitive...I've spent a HUGE portion of my life trying to figure out what is "wrong" with me...I think I am finally on the right track. : fingers crossed :

Anyway, I recently found out that that my mom had exclusively breastfed me for 12 months ~ my first solid food was Cheerios ~ I stopped breastfeeding at the age of 4 :o

I am curious if there is a link between introducing solids at that age and gluten sensitivity.

Thank you in advance for any information you can provide.


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1desperateladysaved Proficient

Hi, sorry if this is not posted in the correct forum. I've been doing a little research on this and I have found conflicting information online. I believe I am gluten intolerant/sensitive...I've spent a HUGE portion of my life trying to figure out what is "wrong" with me...I think I am finally on the right track. : fingers crossed :

Anyway, I recently found out that that my mom had exclusively breastfed me for 12 months ~ my first solid food was Cheerios ~ I stopped breastfeeding at the age of 4 :o

I am curious if there is a link between introducing solids at that age and gluten sensitivity.

Thank you in advance for any information you can provide.

I have always thought that it was better to wait longer rather than shorter to begin introducing foods to an infant. I tried to wait atleast a year with my children. I believe I would have gotten that idea from a La Leche League book of the 80's.

Sesara Rookie

Most of what I have read suggests that introducing solids while still breastfeeding confers protective benefits against Celiac disease, and that gluten is best introduced between 6-12 months. It does seem that it needs to be triggered by something else - there are a number of viruses suspected to be possible triggers of celiac that young children often get around the time of solids introduction. Certainly, it's not abnormal for a child to take very few solids until well over a year - while I'd guess that my son was 7 or 8 months when he was introduced to his very first wheat productsj, he didn't regularly eat solid food until close to 16 months.

So I certainly wouldn't blame your mother for when she introduced solids to you - it's far more likely that a combination of illness and genetics is responsible.

allinyourhead Newbie

I have always thought that it was better to wait longer rather than shorter to begin introducing foods to an infant. I tried to wait atleast a year with my children. I believe I would have gotten that idea from a La Leche League book of the 80's.

Thank you for the reply=) I think you are right...my mother was heavily involved in nursing mothers and according to her, that's what they were teaching back then.

tarnalberry Community Regular

What everyone has said...

And kudos to your mom for nursing for so long! That's fabulous!

faithforlife Apprentice

Yeah my midwives always encourage nursing and they say some babies dont need solids till as late as 18 months. I just start when they start reaching for it! Plus I believe u get exposed to some degree to allergens through the milk. That's why if doctors discover for example a milk intolerance in the baby they try a milk free diet for Mom.

stacytr Newbie

My kids both nursed till they were 4, and were delayed in eating solid foods. We are currently pursuing a celiac diagnosis for my daughter, but I'd be willing to bet that the reason she's doing so well despite her very high lab #'s is the protective benefits that nursing provides. WTG to your mom!!


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melikamaui Explorer

I also practiced extended nursing for both of my kids. (The first nursed until he was two and a half, the youngest nursed much, much longer) My gastro doc said that he was convinced that my little one was healthier than a "normal celiac" because of it. I delayed introducing solid foods with my little one because he wasn't interested in them until he was about 13 months old. My first started solids at 6 months. Both have celiac disease, but both are very healthy otherwise.

StephanieL Enthusiast

I believe they suggest holding off on gluten now till 12 months minimum. Dr. Fassano is currently researching the time it is best to introduce it but in the small study, the later the better.

  • 1 month later...
seattlejoy Rookie

I believe they suggest holding off on gluten now till 12 months minimum. Dr. Fassano is currently researching the time it is best to introduce it but in the small study, the later the better.

Where can I get information about the small study? I have a 10 month old and am terrified to ignite this disease in her so I haven't introduced gluten. I don't know what to do.

StephanieL Enthusiast

Open Original Shared Link

Here it is. He is currently doing a larger study. We tried to get into it but becaus elf DS's atypical issues we were not able.

Hope this helps!

  • 4 weeks later...
come dance with me Enthusiast

My daughter started solids at 4 months, but nothing containing gluten until 9 months when she started having toast fingers, plain pasta and cereals for breakfast. Up until then she pretty much only had rice cereal, fruit or veges. She was breastfed still in conjunction with food until she was about 3-ish. My nephew is 15 months and is still breastfed, he started having solids at 8 months and has been gluten free. His mum cut out gluten from her diet to see if he would stop screaming so much and it worked, he settled and has been a happier baby. I know research shows that gluten does not pass through breastmilk but we won't take that chance, he was miserable for his first 4 months of life, crying constantly like he was in pain until she cut that out the poor little bub.

StephanieL Enthusiast
I know research shows that gluten does not pass through breastmilk but we won't take that chance, he was miserable for his first 4 months of life, crying constantly like he was in pain until she cut that out the poor little bub.

That's not the case. As with all food/nutrients, some women will and some will not pass through into the breast milk. Also, sometimes the same foods will pass through sometimes and not at others. I am all for nursing as long as possible and altering Mom's diet if something isn't working! I have been pregnant and or nursing for 6 years now and on an elimination diet of one kind or another through most of it!

justlisa Apprentice

There is definitive clinical data which shows that Gliadin (the harmful protein in gluten) is found in the breast milk of lactating mothers who are not on a gluten-restricted diet...

Open Original Shared Link

Please, click on the "study" link in this article...

I just wanted to share this...

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    • 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.
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