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

Should I Only Eat Products Labeled gluten-free?


LoriG

Recommended Posts

LoriG Contributor

Hi all,

I have been gluten-free 4-1/2 months and CF 2-1/2 months. My symptoms before enterolab results were chronic fatigue, insomnia, constipation, irritability, and depression. Since going gluten-free, insomnia and constipation are better, but I am learning the fatigue is the worst. I just drag through life. I also am hypothyroid.

Anyway, I have not purposely eaten any gluten so far. I'm not even sure if I'd know I got glutened or anything because everyday I feel the same crappy way. No energy, blah, and irritable which leads to depression because I have been sick for years.

In thinking about being glutened, I started to think maybe I need to be only eating whole foods or those actually "labeled" gluten free or call the company on everything I eat. Right now I look at the ingredients and if there are no gluten or casein ingredients, I eat it. Do I need to be that careful? For instance, I eat Frito corn chips or Garden of Eatin tortilla chips. Those bags don't say gluten free. One time I ate Xylitol tortilla chips that ARE labeled gluten-free and was nauseous for hours. Not sure what that was about?! <_< Was I glutened that one time or not? The problem is, unlike many of you, I don't know if I've been glutened - there is nothing obvious to me.

I am in such despair with the fatigue not getting better and I've spent thousands going around and around particularly with trying supplements to help this go faster. Just recently, I started l-glutamine to see if that will help at all. I am a mom of 3 kids, missing out on life because I am soooo tired.

Thank you so much for your help!


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



Celiac.com Sponsor (A8-M):



Gemini Experienced
Hi all,

I have been gluten-free 4-1/2 months and CF 2-1/2 months. My symptoms before enterolab results were chronic fatigue, insomnia, constipation, irritability, and depression. Since going gluten-free, insomnia and constipation are better, but I am learning the fatigue is the worst. I just drag through life. I also am hypothyroid.

Anyway, I have not purposely eaten any gluten so far. I'm not even sure if I'd know I got glutened or anything because everyday I feel the same crappy way. No energy, blah, and irritable which leads to depression because I have been sick for years.

In thinking about being glutened, I started to think maybe I need to be only eating whole foods or those actually "labeled" gluten free or call the company on everything I eat. Right now I look at the ingredients and if there are no gluten or casein ingredients, I eat it. Do I need to be that careful? For instance, I eat Frito corn chips or Garden of Eatin tortilla chips. Those bags don't say gluten free. One time I ate Xylitol tortilla chips that ARE labeled gluten-free and was nauseous for hours. Not sure what that was about?! <_< Was I glutened that one time or not? The problem is, unlike many of you, I don't know if I've been glutened - there is nothing obvious to me.

I am in such despair with the fatigue not getting better and I've spent thousands going around and around particularly with trying supplements to help this go faster. Just recently, I started l-glutamine to see if that will help at all. I am a mom of 3 kids, missing out on life because I am soooo tired.

Thank you so much for your help!

Don't get hung up on whether or not a product is labeled gluten-free or not. While that certainly makes things easier, all you need to do to remain gluten-free/CF successfully is learn your ingredients well and check labels on the things you eat. I only have called manufacturers two or three times in 3 years to verify gluten-free status because of questionable ingredients I really wasn't sure of. Some people feel they need to do this all the time but I found I didn't have to and have had wonderful success with the diet. No need in making things difficult and with time, it will become second nature for you.

As far as your fatigue is concerned, make sure you have a really good physician who will do COMPLETE thyroid panels on you and ask how you feel with each dose change. Most doctors do not treat thyroid correctly and their patients walk around with subclinical low thyroid and they will tell you every thing is fine....when it's not. Also, give the diet a little while longer if you are anemic as it may take a bit to recover from that. I suspect your thyroid is the culprit, though, with your fatigue. I have Hashimoto's myself and remember the fatigue until I found a doctor who knew what she was doing with that.

Hope you feel better soon!

kbtoyssni Contributor

I don't eat only products labeled gluten-free. This diet would be super expensive that way! I've learned the safe brands and by reading threads on this site frequently you'll learn if mainstream brands have CC issues. A good example are Quaker rice cakes and Frito Lay products (expect for Stax). It seems that many people have trouble with those two.

LoriG Contributor

Gemini,

Thanks for your reply. Trust me - I have been around and around w/ my thyroid this past 6 years and have educated myself. I know now to test tsh, free t3, free t4. I think because of the gluten, I wasn't able to get my thyroid regulated or something.

I was initially on levoxyl 6 years ago, and then in 2006 went to a natural doctor who tested correctly and that's when I realized my thyroid was bad. At that time, my ft4 was too high, and ft3 too low. Since then I've tried many different combo's of meds and doctors and the fatigue was still terrible. Then I went to enterolab and figured out the gluten issue. Currently, I am on armour at 3 grains, waiting for the next blood draw. My free t3 at last draw was 3.3 - I think the range is 2.3 - 4.3 I told this new doc that I want it to the top of the range to see if that helps with the fatigue. So sick of it all really!! Everyone keeps telling me that 4-1/2 months gluten-free is no time at all especially eliminating the fatigue. I see a ND now and he says malabsorption is my issue. Who knows? I think I may just stop eating everything!!! :o

mamaw Community Regular

hI

I would guess your thyroid is not correct. Remember the thyroid runs the whole body so it can play havoc on everything. I almost died because of doctors not treating my thyroid correctly. I'm still not back to normal & I ended up taking Ra to kill off my thyroid in may 07 & use synthroid now but I don't feel good. I have a doctor who hates armour.. and I don't care for the doctor !!!! I'm still on a roller coaster most days......

Good luck

mamaw

cattriona Newbie

Hi LoriG

You have to be careful with some foods that are labelled 'gluten free'. I find that some things may say that they are gluten-free, but they contain things like soy sauce which most of the time has gluten in it. I guess you also have to be careful where the product comes from, as some countries' standards on what's acceptable as gluten-free aren't the same as in countries like America.

I find that a lot of products that aren't labelled gluten-free don't necessarily contain gluten and are fine to eat.

I hope that everything gets better for you!

hathor Contributor

Things that are naturally gluten-free cannot (yet) be labeled that way in the US. So you unnecessarily restrict yourself if you want a gluten-free label first.

I find that I can figure out the gluten-free status (or reputation for possible CC) most of the time by googling on the name of the product plus the word "gluten." I've only had to contact manufacturers a very few times.


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



Celiac.com Sponsor (A8-M):



LoriG Contributor

Thank you for everyone's reply. I will try the google thing!!

kylesmom1112 Newbie

are your medications gluten-free/CF? just a thought..

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 Ginger38's topic in Related Issues & Disorders
      1

      Shingles - Could It Be Related to Gluten/ Celiac

    2. - Ginger38 posted a topic in Related Issues & Disorders
      1

      Shingles - Could It Be Related to Gluten/ Celiac

    3. - Russ H commented on Scott Adams's article in Latest Research
      5

      Study Estimates the Costs of Delayed Celiac Disease Diagnosis (+Video)

    4. - Russ H posted a topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      0

      Coeliac UK Research Conference 2025

    5. - Rejoicephd replied to Rejoicephd's topic in Related Issues & Disorders
      5

      Basic metabolic panel results - more flags


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      132,376
    • Most Online (within 30 mins)
      7,748

    Citydweller
    Newest Member
    Citydweller
    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

    • trents
      I don't know of a connection. Lots of people who don't have celiac disease/gluten issues get shingles.
    • Ginger38
      I’m 43, just newly diagnosed with a horrible case of shingles last week . They are all over my face , around my eye, ear , all in my scalp. Lymph nodes are a mess. Ear is a mess. My eye is hurting and sensitive. Pain has been a 10/10+ daily. Taking Motrin and Tylenol around the clock. I AM MISERABLE. The pain is unrelenting. I just want to cry.   But Developing shingles has me a bit concerned about my immune system which also has me wondering about celiac and if there’s a connection to celiac / gluten and shingles; particularly since I haven't been 💯 gluten free because of all the confusing test results and doctors advice etc., is there a connection here? I’ve never had shingles and the gluten/ celiac  roller coaster has been ongoing for a while but I’ve had gluten off and on the last year bc of all the confusion  
    • Russ H
      There were some interesting talks, particularly Prof Ludvig Stollid's talk on therapeutics for coeliac disease.    https://www.youtube.com/playlist?list=PLRcl2mPE0WdigRtJPvylUJbkCx263KF_t
    • Rejoicephd
      Thank you @trents for letting me know you experience something similar thanks @knitty kitty for your response and resources.  I will be following up with my doctor about these results and I’ll read the articles you sent. Thanks - I really appreciate you all.
    • knitty kitty
      You're right, doctors usually only test Vitamin D and B12.  Both are really important, but they're not good indicators of deficiencies in the other B vitamins.  Our bodies are able to store Vitamin B12 and Vitamin D in the liver for up to a year or longer.  The other B vitamins can only be stored for much shorter periods of time.  Pyridoxine B 6 can be stored for several months, but the others only a month or two at the longest.  Thiamine stores can be depleted in as little as three days.  There's no correlation between B12 levels and the other B vitamins' levels.  Blood tests can't measure the amount of vitamins stored inside cells where they are used.  There's disagreement as to what optimal vitamin levels are.  The Recommended Daily Allowance is based on the minimum daily amount needed to prevent disease set back in the forties when people ate a totally different diet and gruesome experiments were done on people.  Folate  requirements had to be updated in the nineties after spina bifida increased and synthetic folic acid was mandated to be added to grain products.  Vitamin D requirements have been updated only in the past few years.   Doctors aren't required to take as many hours of nutritional education as in the past.  They're educated in learning institutions funded by pharmaceutical corporations.  Natural substances like vitamins can't be patented, so there's more money to be made prescribing pharmaceuticals than vitamins.   Also, look into the Autoimmune Protocol Diet, developed by Dr. Sarah Ballantyne, a Celiac herself.  Her book The Paleo Approach has been most helpful to me.  You're very welcome.  I'm glad I can help you around some stumbling blocks while on this journey.    Keep me posted on your progress!  Best wishes! P.S.  interesting reading: Thiamine, gastrointestinal beriberi and acetylcholine signaling https://pmc.ncbi.nlm.nih.gov/articles/PMC12014454/
×
×
  • 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.