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Juicing


twe0708

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twe0708 Community Regular

Just wondering if anyone does a lot of juicing. Not sure if "juicing" is the right word for it, but I just purchased a Breville Juicer and was wondering if anyone else makes juice out of fresh vegetables and fruits and what their feedback is on this? I have been reading about fresh juice from vegetables and fruit and how much more our bodies absorb vs eating our vegetables cooked. Just surprised I haven't seen any postings about juicing considering our bodies have trouble absorbing nutrients from our food due to our condition.


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MagpieWrites Rookie

I have a juicer, and as the weather warms up, I'll bring it out more often (I'm one of those people that when it's hot, I usually have to be nagged to eat. Juicing keeps the husband from yelling at me! :P ). But it will never be a daily thing for me, for a few reasons.

One - they are a PAIN to clean. I don't have a dishwasher, so anything that has 8 parts (and at least 4 of those packed with pulp to scrap out and take to the composter) all needing to be scrubbed with tiny brushes to get clean... ah.... no. At least not often.

Second, and really the bigger reason for me - I don't know if its because my system is still healing or what - but a lot of juices just don't agree with me. Yeah, you can get a lot more nutritional bang for your buck, but if I have more than one a day (or two) I regret it pretty quickly. Without getting too graphic, the bathroom becomes a focal point in my day! I'm fine with fruits and veggies in their whole forms - but juiced, they just bash their way through my system too fast.

The last one is cost - my husband and I eat a LOT of fresh fruits and veggies, and try to get as much local and organic that we can. Juicing would require an even LARGER amount, and I just can't justify they cost for a daily thing. It is almost a 4/1 take to juice I've found. You need a lot to fill a couple of glasses, and the food that would make a substantial dinner in its whole form leaves you hungry and needing something more in a few hours if juiced.

I do use it some, and love being able to mix some of my own blends (blackberry pineapple ginger is amazing) but it just isn't something I could commit to on a daily basis.

Mskedi Newbie

I pretty much only use my juicer in the summer. It's good stuff, but it is a bit of a pain to clean, as someone else mentioned.

Wenmin Enthusiast

We use the juicer to juice blackberries that we pick ourselves. The juice is then frozen. Later in the year, we take the juice out to make blackberry dumplings. Haven't yet found a gluten free version of this. Maybe it will be a project of mine this summer......

Wenmin

Korwyn Explorer

We don't juice, but we have a blender in which I make 'green drinks'. Veggies, fruits, and berries all go in there and come out tasting wonderful. :) That is my primary source of fiber and my system is much happier. Plus the glycemic index of a whole food blending is much lower than that of a juicer because the fiber content slows absorption of the fructose.

celiac-mommy Collaborator

We have a Power Juicer and we use it so often, it sits on the counter next to the Vitamix. I try to eat raw for the first 1/2 of the day, so juicing is great for me. 1 tip--juice the darkest greens you can find, like kale, and to take the bitterness away, also juice 1/4 of a fresh pineapple (with core). I commonly make this juice: 3 organic carrots, 1 organic apple, a bunch of kale or 4 big handfulls of baby spinach and 1/4 of a fresh pineapple. If I have other stuff I need to get rid of, I throw that in as well. I aim for about 24oz of juice. The Power Juicer is really easy to take apart and clean. I had a Juiceman juicer before and never used it because it was such a pain to clean!

Another great way I use it is to get the most from our garden. For example, it takes FOREVER to grate up all the extra zucchini we have, and then you're left with a ton of juice that you have to squeeze out if you're going to use it for breads and muffins. So I will juice the zucchini, bag the juice and pulp separately, then I have have perfect pulp to make breads, muffins, and pancakes and I use the juice as liquid for pancakes, quickbreads, stocks etc. I also do this with the tons of tomatoes we have.

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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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