Jump to content
  • Welcome to Celiac.com!

    You have found your celiac tribe! Join us and ask questions in our forum, share your story, and connect with others.




  • Celiac.com Sponsor (A1):



    Celiac.com Sponsor (A1-M):


  • Get Celiac.com Updates:
    Support Our Content
    eNewsletter
    Donate

What To Eat And Not Eat During Recovery


Midoriliem

Recommended Posts

Midoriliem Newbie

What are some things to avoid eating during recovery? I am mostly a vegetarian but I do eat fish...I am afraid I eat too much fiber or fruit.

Here is what I eat now (with lactose pills):

Breakfast: yogurt, milk, brown rice, banana, 14 walnuts, milk powder.

Lunch and snack: Boiled egg, small ripe banana. 1.5 c rice,


Celiac.com Sponsor (A8):
Celiac.com Sponsor (A8):



Celiac.com Sponsor (A8-M):



RiceGuy Collaborator

Well, looking at what you've listed, I'd say you should try to eat more veggies. In fact, the only veggie you mentioned is tomato. Bananas are known to be relatively difficult to digest, compared to many other fruits and veggies, and it looks like you eat a lot of them.

As for the dairy, many do find it very helpful, even imperative, to avoid all dairy, especially while healing. Apparently, it's not so much the lactose, but the casein.

If you want rice milk, you can make your own very easily. A Google search will show you numerous recipes, and it's easy to do.

Beans, nuts, and seeds can be difficult for some to digest, so if you are having trouble digesting properly, it may help to cut back on those.

In general, try to avoid the top allergens, eat whole foods, not processed foods, and take supplements to help your body rejuvenate. The easier it is for the digestive system to break things down, the better off you may be.

If you have specific issues to address, you should probably list those, so that anyone responding will be able to make more informed recommendations. In other words, any aches, pains, sleeping problems, digestive issues, allergies, nutrient deficiencies, etc.

Midoriliem Newbie
Well, looking at what you've listed, I'd say you should try to eat more veggies. In fact, the only veggie you mentioned is tomato. Bananas are known to be relatively difficult to digest, compared to many other fruits and veggies, and it looks like you eat a lot of them.

As for the dairy, many do find it very helpful, even imperative, to avoid all dairy, especially while healing. Apparently, it's not so much the lactose, but the casein.

If you want rice milk, you can make your own very easily. A Google search will show you numerous recipes, and it's easy to do.

Beans, nuts, and seeds can be difficult for some to digest, so if you are having trouble digesting properly, it may help to cut back on those.

In general, try to avoid the top allergens, eat whole foods, not processed foods, and take supplements to help your body rejuvenate. The easier it is for the digestive system to break things down, the better off you may be.

If you have specific issues to address, you should probably list those, so that anyone responding will be able to make more informed recommendations. In other words, any aches, pains, sleeping problems, digestive issues, allergies, nutrient deficiencies, etc.

Sorry, I edited it to add in the squash and peas I've been eating lately. I was always told that bananas are easy to digest (hence their inclusion in the BRAT diet). I pretty much only eat whole foods. I have some trouble with diarrhea, though it is much better than it used to be. As far as I know, I have no food allergies beside the obvious gluten, and all my aches, pains, sleeping problems, nutrient deficiencies, and constant cold have gotten better since I went gluten-free...though they come back when I'm glutened.

The reason I question the excluding casein idea is that when I went home briefly to the US (where I think the labeling laws are better than here) I ate lots of dairy products and my digestion improved.

GFinDC Veteran

I would consider adding some quinoa and lentils. Avoid spice mixtures and stick to single ingredient spices. Frozen plain veggies seem to be a little less likely to have gluten added than canned, in my experience. Definitely check all ingredients though. I like them when the ingredients are 2 things, like "peas, water". Be careful of distilled alcohols, wine, yeast, and beer of course. Nuts are often a problem here in the US with added gluten. Any kind of pre-made salad dressing or sauce is suspicious. Candy, too or really anything pre-made/packaged. I like to add canned salmon to rice/quinoa and lentils, along with some green veggies. Avocadoes are great for guacamole.

Midoriliem Newbie
I would consider adding some quinoa and lentils. Avoid spice mixtures and stick to single ingredient spices. Frozen plain veggies seem to be a little less likely to have gluten added than canned, in my experience. Definitely check all ingredients though. I like them when the ingredients are 2 things, like "peas, water". Be careful of distilled alcohols, wine, yeast, and beer of course. Nuts are often a problem here in the US with added gluten. Any kind of pre-made salad dressing or sauce is suspicious. Candy, too or really anything pre-made/packaged. I like to add canned salmon to rice/quinoa and lentils, along with some green veggies. Avocadoes are great for guacamole.

I actually asked the local health-food store lady about quinoa, just to cover my bases, and she said she would order some...it will be interesting to see what she comes up with and how expensive it is! I have checked all my spices, but they're all single spices, I never use canned anything except canned tomatoes that say "tomatoes, salt"- no citric acid, no nothing. I don't drink, and I got my nuts either from the farmer's market or in a package where the only ingredient was the nuts themselves. No sauces or salad dressings, and only gluten-free candy that I've checked. I use canned tuna but only the kind with salt, water, and fish- no oil or anything. The fish idea sounds good with rice and veggies.

My doctor just tells me to be patient, which is good advice, but I want to make sure that I am not getting hidden gluten in the meantime.

Archived

This topic is now archived and is closed to further replies.


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,939
    • Most Online (within 30 mins)
      7,748

    Michelle C.
    Newest Member
    Michelle C.
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.5k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • Wheatwacked
      Marsh 3b is the Gold Standard of diagnosis for Celiac Disease.  Until recently, regardless of antibody tests, positive or negative, you had to have Marsh 3 damage to be awarded the diagnosis of Celiac. As I understand you,  you were having constant symptoms..  Your symptoms improved on GFD, with occassional flare ups. Did your doctor say you do and you are questioning the diagnosis? Regarding your increasing severity when you get glutened it is "normal".  Gluten acts on the Opiod receptors to numb your body.  Some report withdrawal symptoms on GFD.  I was an alcoholic for 30 years, about 1/2 pint of voda a day. Each time I identified a trigger and dealt with it, a new trigger would pop up.  Even a 30 day rehab stint, with a low fat diet (severe pancreatis) during which I rarely had cravings.  Stopped at a Wendys on the way home and the next day I was drinking again.  20 years later, sick as a dog, bedridden on Thanksgiving, after months of reasearch, I realized that gluten free was my Hail Mary.  Back in 1976 my son was diagnosed at weaning by biopsy with Celiac Disease and his doctor suggested my wife and I should also be gluten free because it is genetic.  At 25 years old I felt no gastro problems and promised if I ever did I would try gluten free.  Well, I forgot that promise until I was 63 and my wife 10 years dead.  Three days of gluten and alcohol free, I could no longer tolerate alcohol. Eleven years gluten and alcohol free, with no regrets. Improvement was quick, but always two steps forward and one back.  Over time I found nineteen symptoms that I had been living with for my entire life, that doctors had said, "We don't know why, but that is normal for some people". Celiac Disease causes multiple vitamin and mineral deficiency.  It is an autoimmune disease, meaning your immune system B and T cells create antibodies against ttg(2) in the small intestine in Celiac Disease, and sometimes ttg(3) in skin in Dermatitis Herpetiformus.  'Why' is poorly understood.  In fact, it wasn't even known that wheat, barley and rye gluten was the cause.  Celiac Disease was also called Infantilism, because it was deadly, and believed to only be a childhood disease. So, as part of your recovery you must deal with those deficiencies.  Especially vitamin D because it contols your immune system.  Virtually all newly diagnosed Celiacs have vitamin D deficiency.  There are about 30 vitamin and minerals that are absorbed in the small intestine.  With Marsh 3 damage you may be eating the amount everyone else does, but you are not absorbing them into your system, so you will display symptoms of their deficiency.   As time passes and you replenish your deficiencies you may notice other symptoms improve, some you did not even know were symptoms. Our western diet has many deficiencies built into it.   That is the reason foods with gluten are fortified.  Gluten free processed food are not required to fortify.  Vitamin D, Iodine, choline.  The B vitamins, especially Thiamine (B1) run deficient quickly.  We only store enough thiamine for 2 weeks so the symptoms of Gastrointestinal BeriBeri can come and go quickly.  Magnesium, zinc, etc. each having its own symptoms affecting multiple systems.  High homocystene, an indicator of vascular inflamation can be cause by deficient Choline, folate, B6 and or B12.  Brain fog symptoms by deficient choline, iodine, thiamine B1. Dietary intake of choline and phosphatidylcholine and risk of type 2 diabetes in men: The Kuopio Ischaemic Heart Disease Risk Factor Study  
    • Rogol72
      I cut out the rice because it was affecting my stomach at the time ... not necessarily dermatitis herpetiformis. It was Tilda Basmati Rice, sometimes wholegrain rice. I was willing to do whatever it took to heal. Too much fiber also disagrees with me as I have UC.
    • trents
      But you didn't answer my question. When you consume gluten, is there an identifiable reaction within a short period of time, say a few hours?
    • Scott Adams
      You can still have celiac disease with negative blood test results, although it's not very common:  Clinical and genetic profile of patients with seronegative coeliac disease: the natural history and response to gluten-free diet: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5606118/  Seronegative Celiac Disease - A Challenging Case: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9441776/  Enteropathies with villous atrophy but negative coeliac serology in adults: current issues: https://pubmed.ncbi.nlm.nih.gov/34764141/   
    • Scott Adams
      I am only wondering why you would need to cut out rice? I've never heard of rice being any issue in those with DH.
×
×
  • Create New...

Important Information

NOTICE: This site places This site places cookies on your device (Cookie settings). on your device. Continued use is acceptance of our Terms of Use, and Privacy Policy.