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Natural Feast Pies


Guest Kathy Ann

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Guest Kathy Ann

I heard about Natural Feast Pies online and there was a brief mention on a post some time back too. For multiple allergies, it seemed like they would be a wonderful blessing. But in my travels to several Wild Oats and Whole Foods in the midwestern states, I wondered why I never found them. I finally talked to a midwestern grocery store chain which has health food sections in most of their stores to accomodate states like mine with few health food stores. They said they actually test sampled Natural Feast Pies and decided not to carry them because the customers thought they tasted terrible. That is SO different than what I heard on this board and the way the product is described online. How could they be THAT bad??

Could those of you who have tried them share your opinions? Thanks so much!


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AmandaD Community Regular

I ordered several different kinds from Natural Feast last Thanksgiving - I have Celiac and didn't know how to cook that well yet.

They were the worst pies I've ever had in my entire life. I've learned how to make my own - 100 percent better.

Do NOT waste your money. They cost a fortune and taste like crap.

Guest nini

we actually did a alternative Thanksgiving feast food demo this past month at three health food stores and demoed those pies, EVERYONE THOUGHT THEY SUCKED... they were just plain nasty... but I spoke with the lady that ordered them and she liked them... she said that a lot of the people that buy them don't buy them because they are gluten free, but because they are vegan and therefore they might be used to weirder tasting foods! LOL!... I personally think they are just nasty.

I made the most delicious gluten-free pumpkin pie for thanksgiving using the gluten free pantrys perfect pie crust mix... it turned out perfect and everyone that tried it loved it...

jkmunchkin Rising Star

I sampled them just recently and didn't like them at all. It wasn't the worst thing I definately didn't like it. I tried the blueberry and apple pies.

Guest Kathy Ann

Boy, do I appreciate all your opinions! I would have been easily fooled by the beautiful website. They sure LOOK delicious. I enjoy making great gluten free pies from scratch. It is just always nice to have the convenience of storebought stuff once in awhile.

Thanks again guys!

Mahee34 Enthusiast

I've had the chocolate mousse which i thought was actually really good....and the apple/cranberry which while it isn't the best thing, i don't think it is horrible. then again i'm 24 and can't cook that much on my own just yet :)

Mike Mac Newbie
I heard about Natural Feast Pies online and there was a brief mention on a post some time back too. For multiple allergies, it seemed like they would be a wonderful blessing. But in my travels to several Wild Oats and Whole Foods in the midwestern states, I wondered why I never found them. I finally talked to a midwestern grocery store chain which has health food sections in most of their stores to accomodate states like mine with few health food stores. They said they actually test sampled Natural Feast Pies and decided not to carry them because the customers thought they tasted terrible. That is SO different than what I heard on this board and the way the product is described online. How could they be THAT bad??

Could those of you who have tried them share your opinions? Thanks so much!

I had the Apple Streussel (sp?) recently and thought it was terrific. This is the second time I have tried the product, but the first time I followed the cooking directions to the letter. What a difference! I thoroughly enjoyed the pie and have recently purchased a blueberry pie, which is on the menu for our Sunday dinner.

My advice is to give it a try, but follow the cooking directions. I think you will be glad you did.

Cheers!


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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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