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Newly Diagnosed, Need Advice!


Annie4439

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Annie4439 Rookie

Hello Everyone. First time submitting, long time reader :) My son has celiac. He was screened several years ago because he has juvenile diabetes. Now I have been diagnosed as well, leading me to conclude we have a genetic link in our family, and his was not just diabetes-related.

Even though I know how to shop, what to buy, etc. I'm still getting sick. I've been on the diet for four weeks. The terrible stomach aches and bloating have gone away, but my hair is falling out, and my bowel movements haven't normalized. I also get really loud stomach growling, but not as much as I used to before going gluten free. I know I'm adhering to the diet. The one thing I haven't done is buy new cookware. My thought is that the gluten in my diet has decreased dramatically. Even if my pans have trace amounts, wouldn't my symptoms clear up anyway?


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Emilushka Contributor

Even if my pans have trace amounts, wouldn't my symptoms clear up anyway?

The way the immune system works, it will react strongly to even a very small amount (trace gluten left on your cookware, for example) with a full-blown reaction. The question is just how sensitive your immune system is. Especially when you're first detoxing it's wise to be a little extra-paranoid and get either new non-stick cookware or use stainless steel (which can be washed fully). Beware wooden spoons or nonstick ladles/spoons/utensils as well - they can hold onto trace amounts of gluten.

So no, if you still have trace amounts of gluten coming in, your body will react with a full response and your symptoms will not clear up.

Annie4439 Rookie

The way the immune system works, it will react strongly to even a very small amount (trace gluten left on your cookware, for example) with a full-blown reaction. The question is just how sensitive your immune system is. Especially when you're first detoxing it's wise to be a little extra-paranoid and get either new non-stick cookware or use stainless steel (which can be washed fully). Beware wooden spoons or nonstick ladles/spoons/utensils as well - they can hold onto trace amounts of gluten.

So no, if you still have trace amounts of gluten coming in, your body will react with a full response and your symptoms will not clear up.

Thanks for your response. I was worried that might be the cause so it looks like I need to do some shopping today.

SaraKat Contributor

I was dx'd in August and my left sided rib pain (my only symptom for the most part) got much better about 2 weeks going gluten-free. I didn't buy any new cookware, my Dr told me it wasn't necessary, but if you think that is the only way you are getting gluten- maybe give it a shot.

Emilushka Contributor

I was dx'd in August and my left sided rib pain (my only symptom for the most part) got much better about 2 weeks going gluten-free. I didn't buy any new cookware, my Dr told me it wasn't necessary, but if you think that is the only way you are getting gluten- maybe give it a shot.

Keep in mind that everybody's sensitivity levels are different, so while cookware might be a problem for one person, it might not for another. Everybody's antibodies are probably slightly different and bind in slightly different ways, so for some, it might take more than a trace amount to trigger an autoimmune response and for others, the cookware might be enough to make you sick.

That's the really frustrating thing, I think: figuring out where you stand on the spectrum of sensitivity. Because there's no way we have of knowing without getting sick accidentally.

Skylark Collaborator

Also, be sure you're not eating oats and go completely off dairy. Some celiacs cross-react to oats or to casein as if they were gluten. Soy intolerances are also not uncommon, though it will just make you sick and not have the autoimmune reacton. You can add foods you eliminate later if you get to feeling better.

T.H. Community Regular

You could be getting more gluten in your gluten free food than you are from your pans, actually. :(

( Open Original Shared Link )

Grains that are naturally gluten free, and other food items that would normally not contain gluten, are quite often contaminated when they are harvested, transported, milled, or processed. So this can affect both the whole grains and flours AND the gluten-free products that they are used in, like cookies, breads, etc... Because 'gluten free' is a range, after all, not zero gluten. Sigh. Frustrating for us, huh?

For many celiacs, these small amounts are not an issue. If, however, you are a bit more sensitive, you may still have damage from gluten because your gluten free products are not gluten free enough for your body. There was a study done on celiacs that weren't healing on a gluten free diet, and when they put them on a more restricted gluten free diet than they had been on, many of them began healing (If you are interested, feel free to email me and I can hunt it down for you).

Something that might help to try first?(and save you money on new cookware) You can go down to basic foods - fruits, veggies, plain meats that aren't sliced in the deli (Big CC risk). Get grains from gluten free facilities, like Lundberg and Bob's Red Mill. While these are both still not 'zero gluten,' they are usually gluten free enough for most people.

Intolerances and food allergies can also affect how you are healing.

Just as an aside - this is what happened to me. I did not heal completely, although things improved on a gluten-free diet. We found food allergies and eliminated them. But I still had problems, had to drop tons of food. And only within the last few months (it's been a year now), have I finally realized that I have been having gluten reactions to many of the 'naturally gluten free' products and other things that simply have too much gluten contamination for me, personally. It was a real surprise, considering that two other celiacs in my family don't have this problem at all. But...now it's slowly getting better, so that's a definite plus! :-)


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SaraKat Contributor

Keep in mind that everybody's sensitivity levels are different, so while cookware might be a problem for one person, it might not for another. Everybody's antibodies are probably slightly different and bind in slightly different ways, so for some, it might take more than a trace amount to trigger an autoimmune response and for others, the cookware might be enough to make you sick.

That's the really frustrating thing, I think: figuring out where you stand on the spectrum of sensitivity. Because there's no way we have of knowing without getting sick accidentally.

I understand, that is why sometimes I wish I had more of a reaction when having gluten. My TTG levels were off the charts high, but I don't have many symptoms- except for the rib pain. I have no GI issues at all. I think when I go back in Dec for my first blood test gluten-free for 3 months maybe I will know how sensitive I am. I was just offering up what my Dr told me- he saw my levels and did my biopsy and told me that changing cookware wasn't necessary. If my levels are still high in Dec, maybe I will go to that degree.

I wish a little light went off when you ingest gluten! That would make things so much easier.

Kelly&Mom Rookie

I actually seemed to get worse on a gluten-free diet at first...... still sorting out other food issues. My daughter did improve but not enough so we went back to the Dr. and she was diagnosed with irritable bowel syndrome which is apparently quite common in people with celiac. Since we've restricted the poor thing's diet even more (my husband said, "you're starving her") she is actually improving and able to eat some things that were triggers like soda and watermelon. Hang in there but check out trigger foods for IBS because maybe one of them is causing issues. If you're drinking milk or eating dairy, we were told to take a lactose enzyme for a while until the villa that digest lactose have repaired themselves. Also, take fish oil-were told it helps with healing. Goodluck!

Dixiebell Contributor

My daughter did improve but not enough so we went back to the Dr. and she was diagnosed with irritable bowel syndrome which is apparently quite common in people with celiac.

I would be inclined to believe that she has an irritable bowel because she has celiac. IBS is a symptom, not a diagnosis. Many people are misdiagnosed with IBS and other things before they found out they are celiac or gluten intolerant.

If you're drinking milk or eating dairy, we were told to take a lactose enzyme for a while until the villa that digest lactose have repaired themselves.

This may work for some, but most have to stop any dairy completely for a while. Also, some are casein intolerant too.

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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. 
    • 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 
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