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I Thought Gluten-Free Eating Would Be Healthier!


Monklady123

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Monklady123 Collaborator

So -- I went browsing through the grocery store again today and made a discovery. I had thought that gluten-free would be healthier since I'll be cooking more from scratch. Well... discovered my VERY favorite junk food, Utz ripple cut potato chips, is gluten-free! woot! And what was my very first thought? Not "oh really, these are not good for me".. but instead it was "oh wow, and since I can't eat bread or my favorite crackers etc. any more I can just eat more potato chips." hmmm.. somehow this may not be a good thing. :rolleyes:


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kayo Explorer

I have eaten my fair share of potato chips and then some! I'm glad to have a crunchy and salty comfort food that can be found anywhere. If you can't find Utz try Lays Wavy. They're what I would call a classic ruffle potato chip. To offset the chips just have a bit more broccoli :D

Fey Rookie

I said my goal was to find as many junk food items as possible that were gluten free. It's the only way to keep me from bawling every time I open the pantry and see Oreos.

I am eating much healthier (cooking from scratch vs hamburger helper or burgers/hot dogs for dinner), but it's also a relief to know there's a wide range of easily found snacks that I can get in a pinch. Cheetos, soda, lay's, LARABAR fruit bars (the banana ones are delish, and it's dairy/soy/gluten free), fruits, certain candy bars, etc.

Monklady123 Collaborator

I have eaten my fair share of potato chips and then some! I'm glad to have a crunchy and salty comfort food that can be found anywhere. If you can't find Utz try Lays Wavy. They're what I would call a classic ruffle potato chip. To offset the chips just have a bit more broccoli :D

Good tip Kayo... every piece of broccoli I have cancels out a bunch of chips. Right? B)

Northern Celiac Newbie

Just because it's gluten free doesn't mean it's good for you. I learned that the hard way

Skylark Collaborator

Learning Snickers is gluten-free was not necessarily a good thing for me. :P

Monklady123 Collaborator

Learning Snickers is gluten-free was not necessarily a good thing for me. :P

Ooooooooooh, Snickers! yummmm.......... :D


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dakota girl Rookie

Ditto @ the Snickers! They are my guilty indulgence! I have a hard time passing up a Frito, too! But, many times I'm on a plate of raw vegies w/Sam's Club gluten-free Ranch Dressing...yummy, in a better way!

ravenwoodglass Mentor

Learning Snickers is gluten-free was not necessarily a good thing for me. :P

Snickers are a wonderful treat!

My DD literally jumped for joy when we discoved they were safe. She even wrote her entrance essay for college on the 'ritual' she did to eat them. That ritual was quite a process and rather fun to watch as she would use a knife and fork. Not only did she get in but she also easily got her own room in senior housing her freshman year so she had her own kitchen.

anabananakins Explorer

My response to being unable to eat takeaway anymore has been to eat baked potatos with heaps of butter every night. It's not healthy but knowing I can still have the delicious taste of melted butter on something has gone a long way to soothing the pain of losing bread, lol. Maybe I could have my melted butter with broccoli instead, hmmmm.

Takala Enthusiast

I said my goal was to find as many junk food items as possible that were gluten free. It's the only way to keep me from bawling every time I open the pantry and see Oreos.

I am eating much healthier (cooking from scratch vs hamburger helper or burgers/hot dogs for dinner), but it's also a relief to know there's a wide range of easily found snacks that I can get in a pinch. Cheetos, soda, lay's, LARABAR fruit bars (the banana ones are delish, and it's dairy/soy/gluten free), fruits, certain candy bars, etc.

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You haven't found the K- Toos yet, I take it ?

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BlackSillyYack Newbie

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You haven't found the K- Toos yet, I take it ?

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I ate healthy and did heavy body building BEFORE I got sick.

I was 245 with low body fat 18 months ago. I am a very sickly 170 today.

for the life of me it seems like this disease just HAPPENED all at once. but where as I used to eat nothing but meat and more meat. now all I eat (if I ever eat) are bad things. I have basil fried rice (without soy sauce) almost every day of the week. I have baked THREE betty crocker cakes in the past week and a half, I have a cabinate full of gluten free cookies, and constantly eat a cup o noodles (thai rice noodle gluten free) every night.

I am glad I dont live any place close to where I did before, because the people I used to go to the gym with would disown me. but, I dont care at this point I am just trying to stay alive.

GFinDC Veteran

Well, I am not perfect in that regard either. I used to eat those Starburst fruit chews things because they are one of the few gluten-free things I could find in a convenience store without any dairy or soy. Basically a bunch of corn syrup, sugar and flavoring chemicals. No more though.

Then I found Corn Nuts by Kraft. Corn, corn oil, salt, at least in the orginal flavor. I still like to grab those sometimes when I find them.

Then just yesterday I decided to finally try some Skittles since I kept reading on here that they are gluten free. Yeesh, nothing but sugar and junk. Way too sweet. So then Yahoo health put out a nice article today on what is bad about food and they spotlight Skittles as crap food. I think they are right there. I'd read before that Skittles have lac in the coating but I don't see that in the ingredients. Lac is what they make shellac from.

Open Original Shared Link

Hey all, if you want to avoid the junk, try going dairy free, soy free and nightshade free too. Most of the gluten-free treats have one or more of those in them.

Larabars, now those are ok.

I did find some Planters brand peanut bars the other day that are gluten-free.

Welcome to our wonderful club BSY!

curlyfries Contributor

I ate healthy and did heavy body building BEFORE I got sick.I was 245 with low body fat 18 months ago. I am a very sickly 170 today. for the life of me it seems like this disease just HAPPENED all at once. but where as I used to eat nothing but meat and more meat. now all I eat (if I ever eat) are bad things. I have basil fried rice (without soy sauce) almost every day of the week. I have baked THREE betty crocker cakes in the past week and a half, I have a cabinate full of gluten free cookies, and constantly eat a cup o noodles (thai rice noodle gluten free) every night.I am glad I dont live any place close to where I did before, because the people I used to go to the gym with would disown me. but, I dont care at this point I am just trying to stay alive.

I am confused why you are no longer eating meat. Do you have other food issues as well? How long have you been gluten-free?

Are you feeling better eating the way you are now?

Perhaps you should start trying to add some healthier foods now......vegetables, beans, almond butter, eggs (trying to think of protein replacement)

I can't have sugar in any form. So...no fruit, grains, snacks. Very boring. I recently went to a new free clinic through my job to deal with some other health issues i had been putting off and did not even think to mention this problem and the possibility of candida, bacterial overgrowth.....whatever. I am so used to living this way :P

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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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