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 do YOU consider "gluten free"


MOOO

Recommended Posts

MOOO Apprentice

Ok, I'm 6-7 months into this gluten free diet thing and I am still struggling understand what exactly I should and shouldn't eat.  This recovery process has been painfully slow for me so I have been trying to be as careful as I possibly can to speed the recovery process. 

Yesterday we were over at my mother-in-laws for dinner for my husbands birthday and she made me my own separate gluten-free enchiladas while everyone else ate food that was catered by Cafe Rio.  My mother-in-law assured me that every ingredient in the enchiladas were gluten-free.  I was so appreciative that she thought of me, and made me my own separate meal, but I was still nervous to eat these enchiladas.  I think I was mostly nervous because I did not know if her enchilada dish, spatula, and whatever else she used to prepare the dish was contaminated.  Sooo I explained to her that I was so grateful she made them for me but I have just been too sick and I couldn't risk eating any food outside of my own home where it is a gluten-free environment.  My whole family looked at me like I was completely crazy.  Am I being crazy? Am I being too picky and too careful? Do you guys eat food cooked for you by other people who do not have a gluten free kitchen/gluten-free area in kitchen?

Also, Do you eat food from the grocery store that says "gluten-free" or only "certified gluten-free"? What is the difference? (I live in the US).

Thank you!


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



Celiac.com Sponsor (A8-M):



Maggie C Newbie

Hi. Everyone is different. I’m not celiac. But very gluten sensitive. You’re not overreacting. I get scared when i eat at someone else’s home. I have to watch how they cook and ask how they made things. I usually bring my own food if I can. As gluten free food I have to look at the ingredients. I’m very sensitive to “may contain” or shared equipment of wheat products. 

Its a big learning curve in the beginning. I’m now allergic to corn- break out in hives and welts. So I’m not eating any processed foods and looking at every label. 

 

RMJ Mentor

I will eat at my brothers’ houses but we discuss recipes first and I look at the labels of the ingredients.

Food just labeled gluten free does not have to be tested for gluten content.  Food that is certified gluten free has been evaluated and tested by an independent agency, although I don’t think they test every lot.

tessa25 Rising Star

You made the correct decision. I only eat food that's cooked in my house because I am having trouble getting my numbers down as well. When invited to somebody else's house I usually ask them what they're serving and then I make an equivalent for myself at home and bring it. That way I'm eating the same thing as everybody else. My friends love having me over because it doesn't cost them anything to feed me. :-)

I purchased a Nima sensor to test the food that I eat when I try new things. Maybe one of those would help you. It's easy to ensure you don't eat gluten if all of your food is made from scratch. But it's not easy to make everything from scratch necessarily. LOL

Ennis-TX Grand Master
3 hours ago, MOOO said:

Ok, I'm 6-7 months into this gluten free diet thing and I am still struggling understand what exactly I should and shouldn't eat.  This recovery process has been painfully slow for me so I have been trying to be as careful as I possibly can to speed the recovery process. 

Yesterday we were over at my mother-in-laws for dinner for my husbands birthday and she made me my own separate gluten-free enchiladas while everyone else ate food that was catered by Cafe Rio.  My mother-in-law assured me that every ingredient in the enchiladas were gluten-free.  I was so appreciative that she thought of me, and made me my own separate meal, but I was still nervous to eat these enchiladas.  I think I was mostly nervous because I did not know if her enchilada dish, spatula, and whatever else she used to prepare the dish was contaminated.  Sooo I explained to her that I was so grateful she made them for me but I have just been too sick and I couldn't risk eating any food outside of my own home where it is a gluten-free environment.  My whole family looked at me like I was completely crazy.  Am I being crazy? Am I being too picky and too careful? Do you guys eat food cooked for you by other people who do not have a gluten free kitchen/gluten-free area in kitchen?

Also, Do you eat food from the grocery store that says "gluten-free" or only "certified gluten-free"? What is the difference? (I live in the US).

Thank you!

I take it you read the Newbie 101 section?
I would not trust my own mother to cook something in her house and me eat it...not even boiled eggs...should would probably do it in pasta pot anyway.

What we do for family dinners is I ask what they want to fix, I get the gluten free certified ingredients, and we COOK them in MY house with my dedicated cookware together. We just started this after several years of fall out. It worked great this Easter cooking again with my mother, came in made sure she washed her hands good and we both put on gloves (I do chef work and cook for others so I have cases of them) and fixed the Easter lunch together. Had a touching moment talking about how she felt cooking with grandma and that I feel the same way cooking holiday meals with her. Nice bit of bonding and hoping to make it a habit now.

IF eating out or to somewhere I am invited I fix and bring my own meals, only 2 menu items I will eat at a local restraunt here but I know how they cook it (they put the veggies on foil sheets and run it in a conveyor oven roasting them, then to plate so no contact with CC issues same with unseasoned roasted fish). And we have a pup up north of here that is owned by a celiac family I just started checking out, that is safe....I only trust other celiacs honestly.

cyclinglady Grand Master

I would never even let my own mother cook for me!  Why?  She does not deal with the gluten-free diet on a daily basis, not to mention my other food intolerances that have not diminished despite healing.    I do visit my folks and I  supervise all the cooking.  Mom is great though about getting gluten-free goodies for us, stocking up on fruits and veggies, etc. before we arrive.    I also keep a bin of cooking items stashed in the spare bedroom.  I have acquaintances who are gluten free, but they have no idea about cross contamination at all.  So, I never take their food.  I am polite, but I stick to the food that I brought.  

 

MOOO Apprentice

Thank you all for your reply and for the reassurance that I am not being too picky.  

I have another question in regards to CC and gluten free foods, it's a bit hard to explain so bare with me. 

When you go to the grocery store there are some foods you can safely assume are gluten free, right? like baby carrots, bottles water, 100% orange juice.  However, I am struggling to figure out if things like cheese, pure spices, raw nuts, and dried fruit should be considered unsafe unless it specifically says "gluten-free" even if the item is only 1 ingredient.  Do these sorts of things run the risk of being CC'd or do they rarely say gluten-free because it is assumed? Haha I'm struggling here.


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



Celiac.com Sponsor (A8-M):



Ennis-TX Grand Master
5 hours ago, MOOO said:

Thank you all for your reply and for the reassurance that I am not being too picky.  

I have another question in regards to CC and gluten free foods, it's a bit hard to explain so bare with me. 

When you go to the grocery store there are some foods you can safely assume are gluten free, right? like baby carrots, bottles water, 100% orange juice.  However, I am struggling to figure out if things like cheese, pure spices, raw nuts, and dried fruit should be considered unsafe unless it specifically says "gluten-free" even if the item is only 1 ingredient.  Do these sorts of things run the risk of being CC'd or do they rarely say gluten-free because it is assumed? Haha I'm struggling here.

In store nuts I found have warnings about processed in or on equipment with wheat...they are hit and miss....I just buy safe ones from places like mygerbs.com nuts.com etc. -__- gotten sick on things like this before where I just assumed it would be safe. Produce is generally gluten free.....I have gotten sick from the open batch ones in a store but that store had a open air bakery with the dough table and flour less then 3 feet from the open veggies so that was a obvious. I go for sealed packaged ones now and wash them well when I get them home. Juice...I do not do for sugar reasons. Spices, depends on brand. I and many others use spicely Organics as they are certified gluten free, some use mcormicks but I do not really trust them, others swear by them. Cheese....I have latose intolerance which is very common with this disease as the damaged intestines do not often produce enough enzymes to break it down properly. I also have a whey allergy so I eat vegan cheeses and almost allf them are gluten-free certified....anyway generally it is gluten free, unless artisan or deli where it can be CCed by processing/cutting, or flavored with say beer, malt....blue cheese does sometimes have wheat in it.

Archived

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

  • Get Celiac.com Updates:
    Support Celiac.com:
    Join eNewsletter
    Donate

  • Celiac.com Sponsor (A17):
    Celiac.com Sponsor (A17):





    Celiac.com Sponsors (A17-M):




  • Recent Activity

    1. - knitty kitty replied to JudyLou's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      11

      Seeking advice on potential gluten challenge

    2. - JudyLou replied to JudyLou's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      11

      Seeking advice on potential gluten challenge

    3. - knitty kitty replied to JudyLou's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      11

      Seeking advice on potential gluten challenge

    4. - trents replied to Mark Conway's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      5

      Have I got coeliac disease

  • Celiac.com Sponsor (A19):
  • Member Statistics

    • Total Members
      133,154
    • Most Online (within 30 mins)
      7,748

    Kathy N
    Newest Member
    Kathy N
    Joined
  • Celiac.com Sponsor (A20):
  • Celiac.com Sponsor (A22):
  • Forum Statistics

    • Total Topics
      121.5k
    • Total Posts
      1m
  • Celiac.com Sponsor (A21):
  • Who's Online (See full list)

  • Upcoming Events

  • Posts

    • JudyLou
    • knitty kitty
      I have osteopenia and have cracked three vertebrae.  Niacin is connected to osteoporosis! Do talk to your nutritionist and doctor about supplementing with B vitamins.  Blood tests don't reveal the amount of vitamins stored inside cells.  The blood is a transportation system and can reflect vitamins absorbed from food eaten in the previous twenty-four to forty-eight hours.  Those "normal limits" are based on minimum amounts required to prevent disease, not levels for optimal health.   Keep us posted on your progress.   B Vitamins: Functions and Uses in Medicine https://pmc.ncbi.nlm.nih.gov/articles/PMC9662251/ Association of dietary niacin intake with osteoporosis in the postmenopausal women in the US: NHANES 2007–2018 https://pmc.ncbi.nlm.nih.gov/articles/PMC11835798/ Clinical trial: B vitamins improve health in patients with coeliac disease living on a gluten-free diet https://pubmed.ncbi.nlm.nih.gov/19154566/   Nutritional Imbalances in Adult Celiac Patients Following a Gluten-Free Diet https://pmc.ncbi.nlm.nih.gov/articles/PMC8398893/ Nutritional Consequences of Celiac Disease and Gluten-Free Diet https://www.mdpi.com/2036-7422/15/4/61 Simplifying the B Complex: How Vitamins B6 and B9 Modulate One Carbon Metabolism in Cancer and Beyond https://pmc.ncbi.nlm.nih.gov/articles/PMC9609401/
    • JudyLou
      Thank you so much for the clarification! Yes to these questions: Have you consulted dietician?  Have you been checked for nutritional deficiencies?  Osteoporosis? Thyroid? Anemia?  Do you take any supplements, or vitamins? I’m within healthy range for nutritional tests, thyroid and am not anemic. I do have osteopenia. I don’t take any medications, and the dietician was actually a nutritionist (not sure if that is the same thing) recommended by my physician at the time to better understand gluten free eating.    I almost wish the gluten exposure had triggered something, so at least I’d know what’s going on. So confusing!    Many thanks! 
    • knitty kitty
      @JudyLou,  I have dermatitis herpetiformis, too!  And...big drum roll... Niacin improves dermatitis herpetiformis!   Niacin is very important to skin health and intestinal health.   You're correct.  dermatitis herpetiformis usually occurs on extensor muscles, but dermatitis herpetiformis is also pressure sensitive, so blisters can form where clothing puts pressure on the skin. Elastic waist bands, bulky seams on clothing, watch bands, hats.  Rolled up sleeves or my purse hanging on my arm would make me break out on the insides of my elbows.  I have had a blister on my finger where my pen rested as I write.  Foods high in Iodine can cause an outbreak and exacerbate dermatitis herpetiformis. You've been on the gluten free diet for a long time.  Our gluten free diet can be low in vitamins and minerals, especially if processed gluten free foods are consumed.  Those aren't fortified with vitamins like gluten containing products are.  Have you consulted dietician?  Have you been checked for nutritional deficiencies?  Osteoporosis? Thyroid? Anemia?  Do you take any supplements, medicine, or vitamins? Niacin deficiency is connected to anemia.  Anemia can cause false negatives on tTg IgA tests.  A person can be on that borderline where symptoms wax and wane for years, surviving, but not thriving.  We have a higher metabolic need for more nutrients when we're sick or emotionally stressed which can deplete the small amount of vitamins we can store in our bodies and symptoms reappear.   Exposure to gluten (and casein in those sensitive to it) can cause an increased immune response and inflammation for months afterwards. The immune cells that make tTg IgA antibodies which are triggered today are going to live for about two years. During that time, inflammation is heightened.  Those immune cells only replicate when triggered.  If those immune cells don't get triggered again for about two years, they die without leaving any descendents programmed to trigger on gluten and casein.  The immune system forgets gluten and casein need to be attacked.  The Celiac genes turn off.  This is remission.    Some people in remission report being able to consume gluten again without consequence.   However, another triggering event can turn the Celiac genes on again.   Celiac genes are turned on by a triggering event (physical or emotional stress).  There's some evidence that thiamine insufficiency contributes to the turning on of autoimmune genes.  There is an increased biological need for thiamine when we are physically or emotionally stressed.  Thiamine cannot be stored for more than twenty-one days and may be depleted in as little as three during physical and emotional stresses. Mitochondria without sufficient thiamine become damaged and don't function properly.  This gets relayed to the genes and autoimmune disease genes turn on.  Thiamine and other B vitamins, minerals, and other nutrients are needed to replace the dysfunctional mitochondria and repair the damage to the body.   I recommend getting checked for vitamin and mineral deficiencies.  More than just Vitamin D and B12.  A gluten challenge would definitely be a stressor capable of precipitating further vitamin deficiencies and health consequences.   Best wishes!    
    • trents
      And I agree with Wheatwacked. When a physician tells you that you can't have celiac disease because you're not losing weight, you can be certain that doctor is operating on a dated understanding of celiac disease. I assume you are in the UK by the way you spelled "coeliac". So, I'm not sure what your options are when it comes to healthcare, but I might suggest you look for another physician who is more up to date in this area and is willing to work with you to get an accurate diagnosis. If, in fact, you do not have celiac disease but you know that gluten causes you problems, you might have NCGS (Non Celiac Gluten Sensitivity). There is no test available yet for NCGS. Celiac must first be ruled out. Celiac disease is an autoimmune disorder that damages the lining of the small bowel. NCGS we is not autoimmune and we know less about it's true nature. But we do know it is considerably more common than celiac disease.
×
×
  • 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.