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

New To Gluten Intolerance


erintroy25

Recommended Posts

erintroy25 Newbie

Im young...25 yrs old. I still live home with the parents & my mom keeps things in the house that I cant eat, Im always temptated to eat what I cant have and lately Ive been finding myself sneaking those things. Its sooo hard.

My other problem is lunch. Im a semi picky eater and when I first found out that I had this problem I ate grilled chicken & salad for lunch...theres only soo much of that that I can eat. I cant eat cold cuts. What else can I eat? Some one please help me??? Ive lost 15lbs in 3weeks.


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



Celiac.com Sponsor (A8-M):



Marz Enthusiast

I can share what I make myself for lunch? :) Depends on where you spend your day and have lunch - is there somewhere you can keep food in a fridge/warm up in a microwave? If that's the case, you can just take supper leftovers for lunch and that opens up your lunch to anything! Are you dairy free as well?

I felt spare taking a tupperware of food to lunch at work, since we are supplied a (non-gluten-free) lunch at work; now I see several people have started doing the same as me, so I don't feel so weird. ;)

For snacks - fruit, nuts, carrot sticks, Fritos chips, Lays, chocolate in order of healthiness :) Rice crackers/thins with anything spread on them - peanut butter, jam, gluten-free Marmite if you're into that stuff, cream cheese.

You could bring tupperwares of yoghurt with you, makes for a nice snack.

If you can go home and cook, you can make yourself anything really - fry up some bacon, eggs, or zap some veges in the microwave?

How about a tuna salad? I mix it up with some onion, lettuce, cucumber, bit of mayo, cheese, salt/pepper.

srall Contributor

Before this (self) diagnosis, I had perfected my pizza crust, and my spaghetti recipe. (And muffins and cookies...sigh) Haven't quite figured out an edible pizza crust yet (mostly because I'm only 5 months in and my system can't handle a lot of the flours) but I made my spaghetti sauce with rice noodles and it tasted the same!

I'm still sticking to whole foods, but I can make minnestrone to die for, that's really easy...just a couple different kinds of beans, diced tomatoes, veggie broth, garlic, carrots, celery and oregano, cumin and basil...simple and you can make a lot and store it.

Fish and salads I have the most success with as far as feeling good. Personally I think you are going to have to learn how to cook (if you don't already know) and experiment with some new foods and spices. I hate the inconvenience of this diet, but I'm loving the food I can eat.

miles Rookie

If you look in the baking and cooking section of this forum you can find many ideas and recipes.

If you look at peoples profiles many have blogs with even more recipes and ideas. One that is very worth checking out is irishdaveyboy

sandsurfgirl Collaborator

Lunch was a pain for me even before gluten free.

I either have leftover from dinner or I bring a bunch of foods, not a "meal" per se.

Today I had chicken breast, cut up carrots, a banana, an orange, an apple and a bag of almonds. I don't eat a lot of bread but if I do have bread, I often prefer it with some honey rather than a sandwich. Glutino has some very yummy crackers so I will bring some of those. I also like Kettle baked potato chips, labeled gluten free. I'm trying to lose weight so you could have regular not baked if you need to gain.

Costco has ham steaks that have no nitrates etc in them. I fry one up in the morning and bring that for a protein. Or hard boiled eggs.

I buy a bag of nuts and pack servings in those little snack size baggies so I can grab and go. Throw some Ghirardelli chocolate chips in there and you have a nice treat.

Sometimes I bring salad but they are such a pain to make.

I make my own salad dressings. Here are my two faves.

Balsamic vinaigrette= balsamic vinegar half cup, half cup olive oil, tbsp mustard, 2 tbsp honey. Adjust to taste.

Citrus vinaigrette- half cup OJ, 2 or 3 tbsp lemon juice, half cup olive oil, basil if you have it, preferably fresh but dried is okay

Lemon juice, honey, olive oil and salt is good too.

Add minced shallots to any dressings and it really gives a nice flavor.

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

      High TTG-IgG and Normal TTG-IgA

    2. - SamAlvi replied to SamAlvi's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      5

      High TTG-IgG and Normal TTG-IgA

    3. - Jsingh replied to lizzie42's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      1

      Son's legs shaking

    4. - lizzie42 posted a topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      1

      Son's legs shaking

    5. - trents replied to Paulaannefthimiou's topic in Gluten-Free Foods, Products, Shopping & Medications
      1

      Bob red mill gluten free oats

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

    • Total Members
      132,868
    • Most Online (within 30 mins)
      7,748

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

    • Total Topics
      121.5k
    • Total Posts
      1m
  • Celiac.com Sponsor (A21):
  • Upcoming Events

  • Posts

    • trents
      Currently, there are no tests for NCGS. Celiac disease must first be ruled out and we do have testing for celiac disease. There are two primary test modalities for diagnosing celiac disease. One involves checking for antibodies in the blood. For the person with celiac disease, when gluten is ingested, it produces an autoimmune response in the lining of the small bowel which generates specific kinds of antibodies. Some people are IGA deficient and such that the IGA antibody tests done for celiac disease will have skewed results and cannot be trusted. In that case, there are IGG tests that can be ordered though, they aren't quite as specific for celiac disease as the IGA tests. But the possibility of IGA deficiency is why a "total IGA" test should always be ordered along with the TTG-IGA. The other modality is an endoscopy (scoping of the upper GI track) with a biopsy of the small bowel lining. The aforementioned autoimmune response produces inflammation in the small bowel lining which, over time, damages the structure of the lining. The biopsy is sent to a lab and microscopically analyzed for signs of this damage. If the damage is severe enough, it can often be spotted during the scoping itself. The endoscopy/biopsy is used as confirmation when the antibody results are positive, since there is a small chance that elevated antibody test scores can be caused by things other than celiac disease, particularly when the antibody test numbers are not particularly high. If the antibody test numbers are 10x normal or higher, physicians will sometimes declare an official diagnosis of celiac disease without an endoscopy/biopsy, particularly in the U.K. Some practitioners use stool tests to detect celiac disease but this modality is not widely recognized in the medical community as valid. Both celiac testing modalities outlined above require that you have been consuming generous amounts of gluten for weeks/months ahead of time. Many people make the mistake of experimenting with the gluten free diet or even reducing their gluten intake prior to testing. By doing so, they invalidate the testing because antibodies stop being produced, disappear from the blood and the lining of the small bowel begins to heal. So, then they are stuck in no man's land, wondering if they have celiac disease or NCGS. To resume gluten consumption, i.e., to undertake a "gluten challenge" is out of the question because their reaction to gluten is so strong that it would endanger their health. The lining of the small bowel is the place where all of the nutrition in the food we consume is absorbed. This lining is made up of billions of microscopically tiny fingerlike projections that create a tremendous nutrient absorption surface area. The inflammation caused by celiac disease wears down these fingers and greatly reduces the surface area needed for nutrient absorption. Thus, people with celiac disease often develop iron deficiency anemia and a host of other vitamin and mineral deficiencies. It is likely that many more people who have issues with gluten suffer from NCGS than from celiac disease. We actually know much more about the mechanism of celiac disease than we do about NCGS but some experts believe NCGS can transition into celiac disease.
    • SamAlvi
      Thank you for the clarification and for taking the time to explain the terminology so clearly. I really appreciate your insight, especially the distinction between celiac disease and NCGS and how anemia can point more toward celiac. This was very helpful for me.
    • Jsingh
      Hi,  My 7 year daughter has complained of this in the past, which I thought were part of her glutening symptom, but more recently I have come to figure out it's part of her histamine overload symptom. This one symptom was part of her broader profile, which included irritability, extreme hunger, confusion, post-nasal drip. You might want to look up "histamine intolerance". I wish I had known of this at the time of her diagnosis, life would have been much easier.  I hope you are able to figure out. 
    • lizzie42
      My 5yo was diagnosed with celiac last year by being tested after his sister was diagnosed. We are very strict on the gluten-free diet, but unsure what his reactions are as he was diagnosed without many symptoms other than low ferritin.  He had a school party where his teacher made gluten-free gingerbread men. I almost said no because she made it in her kitchen but I thought it would be ok.  Next day and for a few after his behavior is awful. Hitting, rude, disrespectful. Mainly he kept saying his legs were shaking. Is this a gluten exposure symptom that anyone else gets? Also the bad behavior? 
    • trents
      Not necessarily. The "Gluten Free" label means not more than 20ppm of gluten in the product which is often not enough for super sensitive celiacs. You would need to be looking for "Certified Gluten Free" (GFCO endorsed) which means no more than 10ppm of gluten. Having said that, "Gluten Free" doesn't mean that there will necessarily be more gluten than "Certified Gluten" in any given batch run. It just means there could be. 
×
×
  • 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.