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Wheat Bran - Try It - It's Great!


Candy

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w8in4dave Community Regular

I know!! I am one that was posting "stuff" because I read it on the "internet" And by gosh you know!! If it is on the net it is true LOL .. Well not funny when it comes to this stuff .. Right? And yes mommida Sadly "The Dr. Said so" can be the Worst!! :( but not always :) 


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StephanieL Enthusiast

I am so very sorry, I thought it was candy that posted the link........  

 

So sorry Stephanie :) I apologize :)

It's all good :)

w8in4dave Community Regular

It's all good :)

Aweeee thanks!  I do my best editing after I hit Post. Even thos I didn't catch that one ... LOL 

Candy Contributor

Looks like you were never diagnosed with Celiac disease?  Just having the genes does not mean you have Celiac.  That might be why you can eat small amounts of wheat  and get away with it.

 

Even if the bran didn't have the protein Celiacs react to in it, the processing would certainly leave some. 

 I totally understand avoiding wheat as a deadly, brain shrinking,gut ripping substance for us pure intolerants. But I don't think wheat bran is "wheat". It doesn't taste like bread or anything else for that matter. It tastes like sawdust, albeit sweet ,sawdust-probably why most people avoid it.It's the outer dry skin on the wheat-I'm in love with it myself.Wheat bran has some of the B-vitamins Celiacs are lacking(like Thiamine,Riboflavin and Niacin),plus potassium ,protein and iron and the fiber we all need,but with no pain in the gut,at least for me.I'm in love with my new friend wheat bran..... I only eat a few tablespoons a week.I'll have Mom send you all funeral notices if it kills me,ha ha. 

Candy Contributor

I've mixed wheat bran into my cereal and it gave me no "wheat" pain   ,and make me feel fuller longer.

I don't think it has wheat protein,since it's just the outer husk of the wheat and is not absorbed by the intestine.  I think wheat bran is a celiac's best friend  !  What do you think.

For that matter ,you can't make a loaf of bread with wheat bran,you know why? Because the bran has no stretchy ,puffy gluten ,like real wheat has.You can't knead bran,or make it rise..it doesn't puff up and you can't roll it , pull it and shape it into bread.It's just flat and dry like autumn leaves.So if you can't make a puffy loaf of wheat bread out of bran,then bran must not be glutinous like wheat is,therefore I shall eat some wheat bran weekly.

kareng Grand Master

For that matter ,you can't make a loaf of bread with wheat bran,you know why? Because the bran has no stretchy ,puffy gluten ,like real wheat has.You can't knead bran,or make it rise..it doesn't puff up and you can't roll it , pull it and shape it into bread.It's just flat and dry like autumn leaves.So if you can't make a puffy loaf of wheat bread out of bran,then bran must not be glutinous like wheat is,therefore I shall eat some wheat bran weekly.

For people like you, who do not have Celiac disease, its fine. Eat all the wheat parts you like. However, this is a website for people with Celiac disease - Celiac dot com. You can't expect us to get behind people eating wheat bran because 1 poster thinks its OK, even with some reputable links saying it contains gluten. As was explained, the processing likely leaves some accidental gluten in it.

If you are going to assert that it has no gluten, we need more proof than a non- Celiac can eat it.

w8in4dave Community Regular

For that matter ,you can't make a loaf of bread with wheat bran,you know why? Because the bran has no stretchy ,puffy gluten ,like real wheat has.You can't knead bran,or make it rise..it doesn't puff up and you can't roll it , pull it and shape it into bread.It's just flat and dry like autumn leaves.So if you can't make a puffy loaf of wheat bread out of bran,then bran must not be glutinous like wheat is,therefore I shall eat some wheat bran weekly.

Just because you cannot make a loaf of bread with it doesn't mean it does not have Gluten in it. Add some yeast to it I am sure you could make bread with it. Have you ever heard of Bran Muffins? Won't see me eating it. 


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Celtic Queen Explorer

Candy, if you want to put your health at risk by eating wheat bran, that's your perogative.  If you aren't Celiac or gluten intolerant, it won't cause you any problems.  But if you are, it will do some damage to your system eventually. 

 

Personally I can find other ways to get fiber and B vitamins without the risk of cross contamination. 

 

As Kareng mentioned, this is a board for Celiacs and gluten intolerants, so you're not going to get a warm welcome here for suggesting that we eat wheat in any way, shape or form.

Scott Adams Grand Master

Candy was banned for trolling--obviously there is no certified gluten-free wheat bran, and it is dangerous and irresponsible to promote it here to celiacs.

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    • marion wheaton
      Thanks for responding. I researched further and Lindt Lindor chocolate balls do contain barely malt powder which contains gluten. I was surprised at all of the conflicting information I found when I checked online.
    • 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. 
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      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 
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