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.


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      132,034
    • Most Online (within 30 mins)
      7,748

    CE1963
    Newest Member
    CE1963
    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

    • Jmartes71
      Thankyou so much for your words.Its a hard battle when a supposed well known hospital whose celiac " specialist " has down played me because my colon looks fine and put it in my medical and so pcp doesn't take seriously. In their eyes we all carry that gene.Im having alot of bad days trying to be positive because of it.
    • Scott Adams
      Your experience is both shocking and critically important for the community to hear, underscoring the terrifying reality that cross-contamination can extend into the most unexpected and invasive medical devices. It is absolutely devastating that you had to endure six months of sickness and ultimately sustain permanent vision loss because a doctor dismissed your legitimate, life-altering condition. Your relentless research and advocacy, from discovering the gluten in MMA acrylic to finding a compassionate prosthodontist, is a testament to your strength in a system that often fails celiac patients. While the scientific and medical consensus is that gluten cannot be absorbed through the skin or eyes (as the molecules are too large to pass through these barriers), your story highlights a terrifying gray area: what about a substance *permanently implanted inside the body*, where it could potentially shed microparticles or cause a localized immune reaction? Your powerful warning about acrylic lenses and the drastic difference with the silicone alternative is invaluable information. Thank you for sharing your harrowing journey and the specific, severe neurological symptoms you endure; it is a stark reminder that celiac is a systemic disease, and your advocacy is undoubtedly saving others from similar trauma.
    • Scott Adams
      Those are driving distance from me--I will try to check them out, thanks for sharing!
    • Scott Adams
      I am so sorry you're going through this bad experience--it's difficult when your own lived reality of cause and effect is dismissed by the very professionals meant to help you. You are absolutely right—your violent physical reactions are not "what you think," but undeniable data points, and it's a form of medical gaslighting to be told otherwise, especially when you have a positive HLA-DQ2 gene and a clear clinical picture. Since your current "celiac specialist" is not addressing the core issue or your related conditions like SIBO and chronic fatigue, it may be time for a strategic pivot. Instead of trying to "reprove" your celiac disease to unwilling ears, consider seeking out a new gastroenterologist or functional medicine doctor, and frame the conversation around managing the complications of a confirmed gluten-free diet for celiac disease. Go in and say, "I have celiac disease, am strictly gluten-free, but I am still suffering from these specific complications: SIBO, chronic fatigue, dermatological issues, and high blood pressure linked to pain. I need a partner to help me address these related conditions." This shifts the focus from a debate about your diagnosis to a collaborative plan for your current suffering, which is the help you truly need and deserve to work toward bouncing back.
    • NanCel
      Hello, no I had to have them re done and then used a liner over the top.  Many dentists are not aware of the celiac effects.  Best of luck.   There is other material, yet, very expensive.
×
×
  • 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.