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Gluten-Free Cookie ExchangesGluten-Free Cookie Exchanges


Scott Adams

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Scott Adams Grand Master

Cookie exchanges are fun social occasions but let's resolve to make cookies healthier next year. They don't need to be 7 layer high fat, high sugar indulgences that contribute to many chronic diseases like diabetes, high blood pressure, cardiovascular damage and dementia. Yes, high sugar is now identified as a major contributor to dementia and even has its own classification called Type 3 diabetes.

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deb-rn Contributor

Oh My Gosh!  You're speaking my language.  I just did some exhaustive studying about the damage carbohydrates do to your body!  I was so convinced by the decades of research I found, that we went from gluten free/ dairy free/soy free to low carb/high fat/mod protein... no need to worry about gluten when you aren't eating packaged food anymore!  We are just short of being nightshade free, low egg consumption, few tree nuts and no legumes.  I am a great cook and baker.  I have tons of gluten free flours - made mostly of high starch/high carbohydrates!  My husband with IBS his whole life, who started gluten free because I decided I wasn't tolerating it, has had such amazing results with the low carb diet!  Now he's off B/P meds, prescription NSAIDS & acid reflux meds...his prostate shrunk, IBS all but cured and he's not constantly cold anymore!  He was a cookie monster after each meal too.  He swore a few years ago that if he ever got Diabetes, he'd just take extra insulin to cover the cookies!!  LOL... he's singin' a different tune  NOW!  What a dramatic difference he's had.  He says his cataracts have decreased as well.... they are made up of denatured sugars!!!!( he's a retired Eye Doctor)  The more insulin your body is forced to produce, or you have to add by injection, the more conditions that will pile up over time.  Instead of feeding the insulin, as diabetics are told by well-meaning Diabetic Educators, we ALL need to stop eating those carbs... in any form!  Cholesterol is caused by carbs being converted to fat in the liver... NOT by eating saturated (or other) fat!  And the worst part is... it's been known since the 1800's!!  Scientists just didn't want to believe their own trials...or the basic biochemical reactions that take place in our bodies!   The Atkin's diet was borne of this knowlege... but was used primarily for weight loss, not necessarily overall health.  The idea of a "diet" is that you do it until you lose weight... then go back to your old bad habits... and repeat as necessary!  A lifestyle change is a better way to think of it.  We don't think of what we can't eat, but what we  CAN!  I've been experimenting with new veggies.  I made a beef/bone broth/veg soup that had 10 different veggies in it... amazing flavor.  I am writing up the copious notes I took during my research and will offer it in a little presentation to some dear friends that have multiple health issues... no doubt caused by their high intake of carbs and gluten.  Just last year the government quietly stated that there is no corrolation between fat and heart disease.  It wasn't front page news... due to the egg on their face... and possibly the crow they were eating!  As a retired nurse, I feel totally betrayed knowing the earliest double blind tests showed all this, but they were so stuck on the fact that there are less calories in carbs than in fat, that they threw out the parts of the research that didn't agree with their hypothesis of fat causing heart disease and obesity.  Obesity then leads to so many other diseases.  Heck, there was even evidence in the early 1900's that a low carb diet controlled Epilepsy in children!  I mean really... the side effects of those drugs are horrible.  But who's going to make money if we all just eat real food instead of Frankenfood??  The drug companies fund a lot of studies, because they are enormously expensive to do.  They have no interest in letting us in on the news that changing our diet can eliminate the need for drugs!  I am on a mission to get this information out to everyone I can in an effort to take back our lives!  All this obesity leads to so many different inflammatory responses!  Guess when the spike in Autism happened?  When we were all told fat is bad and the food pyramid told us to eat mostly bread and grains!!!  UGH... Inuits live almost exclusively on meat and fat... no diseases there!  It happens that in the absence of carbs, you don't need much of the micronutrients from plants, and what you need is gotten from meat and the fat!  When missionaries and settlers move into a "wild" area, it's only 2 generations before all the diseases of Western Civilization appear, and it's been studied over and over.  Moreover, when scientists move to those areas to study and live as the natives do... THEIR diseases go into remission and they adapt to the diet!  Do we need more proof?  Doctors get about 4 hrs of education on nutrition, so don't blame them.  We have been so indoctrinated by a few people early in the industrial revolution, that we just don't make the connections.  It's so much healthier and cheaper to use food as medicine... rather than continuing to eat ourselves sick!  Let's get back to basics... broccoli and lettuce don't need ingredient labels... eat more of them!

Debbie

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    • SamAlvi
      Thanks again for the detailed explanation. Just to clarify, I actually did have my initial tests done while I was still consuming gluten. I stopped eating gluten only after those tests were completed, and it has now been about 70 days since I went gluten-free. I understand the limitations around diagnosing NCGS and the importance of antibody testing and biopsy for celiac disease. Unfortunately, where I live, access to comprehensive testing (including total IgA and endoscopy with biopsy) is limited, which makes things more complicated. Your explanation about small-bowel damage, nutrient absorption, and iron-deficiency anemia still aligns closely with my history, and it’s been very helpful in understanding what may be going on. I don't wanna get Endoscopy and I can't start eating Gluten again because it's hurt really with severe diarrhea.  I appreciate you taking the time to share such detailed and informative guidance. Thank you so much for this detailed and thoughtful response. I really appreciate you pointing out the relationship between anemia and antibody patterns, and how the high DGP IgG still supports celiac disease in my case. A gluten challenge isn’t something I feel safe attempting due to how severe my reactions were, so your suggestion about genetic testing makes a lot of sense. I’ll look into whether HLA testing is available where I live and discuss it with my doctor. I also appreciate you mentioning gastrointestinal beriberi and thiamine deficiency. This isn’t something any of my doctors have discussed with me, and given my symptoms and nutritional history, it’s definitely worth raising with them. I’ll also ask about correcting deficiencies more comprehensively, including B vitamins alongside iron. Thanks again for sharing your knowledge and taking the time to help. I’ll update the forum as I make progress.
    • knitty kitty
      Blood tests for thiamine are unreliable.  The nutrients from your food get absorbed into the bloodstream and travel around the body.  So, a steak dinner can falsely raise thiamine blood levels in the following days.  Besides, thiamine is utilized inside cells where stores of thiamine are impossible to measure. A better test to ask for is the Erythrocyte Transketolace Activity test.  But even that test has been questioned as to accuracy.  It is expensive and takes time to do.   Because of the discrepancies with thiamine tests and urgency with correcting thiamine deficiency, the World Health Organization recommends giving thiamine for several weeks and looking for health improvement.  Thiamine is water soluble, safe and nontoxic even in high doses.   Many doctors are not given sufficient education in nutrition and deficiency symptoms, and may not be familiar with how often they occur in Celiac disease.  B12 and Vitamin D can be stored for as long as a year in the liver, so not having deficiencies in these two vitamins is not a good indicator of the status of the other seven water soluble B vitamins.  It is possible to have deficiency symptoms BEFORE there's changes in the blood levels.   Ask your doctor about Benfotiamine, a form of thiamine that is better absorbed than Thiamine Mononitrate.  Thiamine Mononitrate is used in many vitamins because it is shelf-stable, a form of thiamine that won't break down sitting around on a store shelf.  This form is difficult for the body to turn into a usable form.  Only thirty percent is absorbed in the intestine, and less is actually used.   Thiamine interacts with all of the other B vitamins, so they should all be supplemented together.  Magnesium is needed to make life sustaining enzymes with thiamine, so a magnesium supplement should be added if magnesium levels are low.   Thiamine is water soluble, safe and nontoxic even in high doses.  There's no harm in trying.
    • lizzie42
      Neither of them were anemic 6 months after the Celiac diagnosis. His other vitamin levels (d, B12) were never low. My daughters levels were normal after the first 6 months. Is the thiamine test just called thiamine? 
    • knitty kitty
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    • lizzie42
      Thank you! That's helpful. My kids eat very little processed food. Tons of fruit, vegetables, cheese, eggs and occasional red meat. We do a lot of rice and bean bowls, stir fry, etc.  Do you think with all the fruits and vegetables they need a vitamin supplement? I feel like their diet is pretty healthy and balanced with very limited processed food. The only processed food they eat regularly is a bowl of Cheerios here and there.  Could shaking legs be a symptom of just a one-time gluten exposure? I guess there's no way to know for sure if they're getting absolutely zero exposure because they do go to school a couple times a week. We do homeschool but my son does a shared school 2x a week and my daughter does a morning Pre-K 3 x a week.  At home our entire house is strictly gluten free and it is extremely rare for us to eat out. If we eat at someone else's house I usually just bring their food. When we have play dates we bring all the snacks, etc. I try to be really careful since they're still growing. They also, of course, catch kids viruses all the time so I  want to make sure I know whether they're just sick or they've had gluten. It can be pretty confusing when they're pretty young to even be explaining their symptoms! 
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