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Recovery period meal ideas?


tygerlily

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tygerlily Newbie

Hi all! I’ve been advised to try a gluten-free diet until my endoscopy procedure in August. I’m less than a week in right now and I have been noticing some improvements, but I think I should cut down on the processed foods. I also think I should cut out dairy for the time being as it’s giving me similar symptoms to being glutened. What are some simple, whole-food meals I can eat while my body is in this recovery period? Does anybody have some staples in their meal-plannings worth sharing, or is there a website I can go to for ideas? 

 

Also, while I’m on the topic of cooking, I share a kitchen with my parents who are not gluten-free. How can I avoid cross-contamination while cooking in the kitchen? I’ve already bought my own dishes and utensils and have my own sponge, but what I’m still worried about are pots and pans and other utensils we still share. Like, are stainless steel things okay to be shared as long as they’re washed? If I wash a clean shared utensil with my sponge to make sure it’s clean enough for me to use, is my sponge now contaminated with gluten? Is it better to just put everything in the dishwasher so I can be sure they’re clean?


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knitty kitty Grand Master

@tygerlily,

Hello!  Glad to hear you're trying a gluten free diet!

I found the Autoimmune Protocol Diet to be very helpful in healing and calming those GI symptoms.

Look for the book The Paleo Approach by Dr. Sarah Ballantyne (Celiac herself) and her cookbooks.

The AIP diet cuts out dairy and processed gluten free facsimile foods, and other foods that can possibly cause GI distress like nuts, seeds, and legumes (beans) and nightshades (potatoes, tomatoes, eggplant and peppers).  That leaves basically meat and veggies.

When first starting the AIP diet, I ate smaller meals more frequently because I got hungry frequently, but got filled up fast.  I made a stew in a crock pot and enjoyed small portions throughout the day.  

Really simple meals.  Fry a ground (grass fed) beef burger or lamb chop or a slice of liver and steam some broccoli and carrots.  A meatloaf or roasted Cornish hen (or chicken) with roasted veggies is easy to pop in the oven.  

Don't share things with scratchable surfaces like nonstick coated pans and silicon or plastic utensils.  

Get rid of the sponges.  Not only do they harbor bacteria, but they can't be thoroughly cleaned and disinfected.  Instead use cloths that can be washed in hot water.  Your parents can have one cloth, but you use two.  If you're not sure if a pan is clean, use one of your cloths to rewash it.  Use your second cloth (designated Gluten Free) to wash it again.  It's easy to embroider initials or a flower in a corner of a cloth so you tell which is which.  Or use a Sharpie.  Or use different coloured cloths for each of the three uses.  Keep the cloths in separate soap dishes while they are in use.

I re-read your first post about your symptoms.  Constipation can be a symptom of Thiamine Vitamin B 1 deficiency and/or magnesium deficiency.  

Celiac Disease affects the absorption of nutrients, so getting checked for vitamin and mineral deficiencies is part of proper follow up care for us.  

The Erythrocyte Transketalase test is a more accurate test for Thiamine deficiency than a blood test.  Vitamin levels in the blood don't accurately measure how much of the nutrient is being stored and used inside the cells.  Blood levels can reflect how much of that vitamin you ate in your diet during the previous day or two.  You can have deficiency symptoms before the deficiency shows as lower levels in the blood.  Have all testing done before starting supplementation.  Talk to your doctor before starting as well.  (Doctors aren't very educated about vitamins, so good luck....)

Be sure to get your Vitamin D level up to 80 nMol/L to 100 nMol/L.  At that level, Vitamin D acts as a hormone and will help your periods become regular.  Thiamine can help with PMDD.

The Effects of Vitamin B1 on Ameliorating the Premenstrual Syndrome Symptoms

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4825494/

And...

Vitamin or mineral supplements for premenstrual syndrome

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6491313/

Keep a food/mood/poo'd journal so you can pinpoint problematic foods quickly.  It's handy to show your doctor, too.

I wish you much success on your journey.  Keep us posted on your progress!

Scott Adams Grand Master

Welcome! We do have an extensive recipe section here:

https://www.celiac.com/celiac-disease/gluten-free-recipes/

and this article might be useful:

 

imdoodah331 Rookie

Hi!  Starting a gfd can be overwhelming!  Advice I took from my doctor was to focus first on what I can eat vs what I can't eat.  A weekly meal plan can be helpful.  You begin with a list of your current favorite meals that you would eat in a typical week:  breakfast,lunch, dinner, snacks.  Then, review that list to identify possible sources of gluten/dairy since you are considering eliminating both, and highlight those.  Then you look for alternative ways to prepare those minus the gluten and dairy or made with safe alternatives.  For example if spaghetti is one of your meals, many store brand sauces are not gluten free and also contain dairy, along with traditional pasta.  Buy gluten-free pasta and read labels for pasta sauce, or consider making some from scratch.  This site has a good reference for store bought foods that are safe.  Try to avoid buying a lot of "new to you foods" just because they are gluten-free/DF.  For example, if you've never eaten Quinoa or Tofu, don't go buy a bunch just because it's gluten free - you may not like them.  Also, try to focus on whole, real foods:  meat, vegetables, fruits, and safe bread/grains that are naturally gluten-free/DF and start building your meals with those.  As for separate cooking spaces, cookware, etc. it seems everyone has different levels of sensitivity to cross-contamination and I don't know how super sensitive people do it when they have to live with others in the family who do not follow  this diet.  Thankfully, I don't seem to be super sensitive and my husband has been willing to eat mostly gluten-free/DF along with me.  His occasional "real bread" or snack cakes don't seem to be a problem for me.  Best wishes on your journey!

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    • 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. 
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    • 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 
    • marion wheaton
      Wondering if anyone knows whether Lindt chocolate balls are gluten free. The Lindt Canadian website says yes but the Lindt USA website says no. The information is a bit confusing.
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