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

"gluten-intolerant" Vs. "celiac" - Does It Really Matter?


RiceFiend

Recommended Posts

RiceFiend Newbie

I've been on a gluten-free diet now for almost 3 years and felt the dramatic difference it made in my relationship to eating and virtually living in my bathroom after only the first two weeks.

My doc advised me not to get the small biopsy or even bother with the blood tests because of the profound difference the diet has made. Since I still routinely eat out and share a toaster, etc. (but not MY utensils, margarine tub, peanut butter or jam) with other family members, I occasionally get a severe diarrheal attack that I attribute to likely having been exposed to an intolerable level of gluten somewhere. My symptoms generally hit either to wake me up out of sleep at the wee houirs of the morning or first thing in the morning just to mess with allowing me to plan anything. It's like my system just needs to empty it's entire contents to get rid of some offending crumb sitting on top.

So, if it were only me, I think I might be relatively fine with this. However, I have one small child that has nasty stomache cramping and diarrhea often (5+ times per week) at mealtimes and he has tested negative to the blood IGE testing for celiac. Should we go further in testing him or would it help to go further in testing me for the sake of proving/disproving celiac heritage? How harsh would it be to withhold gluten from his diet for two to three weeks to see if there's a difference (considering his breakfast and lunch staples include lots of wheat products)? There is now a second child in the picture too and I will be watching the introduction of solid food VERY carefully in a few months when it's time for this baby to eat his first foods.

So many questions. There must be more of you here who have issues with your kids and your celiac and whether or not the kids are affected? Advice?

RiceFiend (at least I am now... risotto is now my favourite along with Kinnikin Honey Rice Bran Bread)


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



Celiac.com Sponsor (A8-M):



CarlaB Enthusiast

First of all, you need to spring for your own toaster, sharing is a no-no! :o And, I hope you're careful when you eat out.

You could always do a gene test to see if you have the celiac genes. According to Enterolab, the only genes that are NOT gluten intolerant are the DQ4 found in Asians, so virtually everyone has gluten intolerant genes, but it might be good for you to know if you are dealing with celiac or not.

Some people with gluten intolerance also get severe symptoms and even villi damage (though I've only "met" one on this board without a celiac gene and with villi damage).

Has your child had the full celiac panel? That would be IgA, Ttg, and a few more. I think Ige is an allergy testing ... someone else will know for sure.

tarnalberry Community Regular
...

I occasionally get a severe diarrheal attack that I attribute to likely having been exposed to an intolerable level of gluten somewhere.

...

and he has tested negative to the blood IGE testing for celiac.

...

How harsh would it be to withhold gluten from his diet for two to three weeks to see if there's a difference (considering his breakfast and lunch staples include lots of wheat products)?

You *absolutely* need to avoid gluten. There is no way to be certain that you are NOT damaging your intestines, and a lot of signs that say you are.

Blood testing for celiac wouldn't include IgE tests, so I'm confused. IgE is the standard immune molecule response for standard allergies, which celiac is not. The standard blood testing for celiac includes testing for IgG and IgA antiboides. Do you know what the specific results were? Not to mention the fact that blood tests can be unreliable at times.

It needn't be difficult at all to go gluten free, and breakfast and lunch needn't be complicated, but it may require getting inventive and make some new standards working with your son.

darlindeb25 Collaborator

Personally, I feel there is no difference in how you take care of yourself. If you have celiac disease or are gluten intolerance, the treatment is the same. I also believe that celiac disease is the end result of years of damage for some, I feel that you can have aquired celiac disease.

With your child, the decision is yours. If you feed the child gluten free and his symptoms disappear, then I would believe he needs to live gluten free. If you have him tested for celiac disease and you get a negative answer, yet gluten free greatly improves his health--would you let him eat gluten just because a tests says it doesn't matter.

I wish I had known about celiac disease or gluten intolerance when my kids were young. I would have had them gluten free to see if it helped.

Guest cassidy

I would definitely recommend trying your child on a gluten-free diet. It would make sense that celiac/gi is what is wrong since you obviously have it. It seems like the people who have been off gluten since they were kids have an easier time adjusting to the diet because they don't remember their gluten eating days. Plus, if your child has a problem with gluten and you keep feeding him large amounts of gluten, whether he has celiac or not, there could be long-term health consequences. There are plenty of people who have had complications from eating gluten and tested negative for actual celiac.

As for yourself, I think you would be better off with your own toaster and making sure you stay away from those crumbs. I guess you could do a gene test to see if you actually have celiac if that would make you stay away from crumbs more. It can't be good for your body to have D regardless if it is celiac or gi.

  • 2 weeks later...
RiceFiend Newbie
I would definitely recommend trying your child on a gluten-free diet. It would make sense that celiac/gi is what is wrong since you obviously have it. It seems like the people who have been off gluten since they were kids have an easier time adjusting to the diet because they don't remember their gluten eating days. Plus, if your child has a problem with gluten and you keep feeding him large amounts of gluten, whether he has celiac or not, there could be long-term health consequences. There are plenty of people who have had complications from eating gluten and tested negative for actual celiac.

As for yourself, I think you would be better off with your own toaster and making sure you stay away from those crumbs. I guess you could do a gene test to see if you actually have celiac if that would make you stay away from crumbs more. It can't be good for your body to have D regardless if it is celiac or gi.

Thanks for the suggestions. I'm currently planning on trying the gluten-free diet over the summer with my son since I'll be home this summer with the baby. As you know it's VERY difficult to go gluten-free when the #1 staple in school lunchs is a sandwich or other bread product. I'm still not very fond of the rice breads out there so I don't want to force them on him unless needed. In the summer we'll be able to avoid bread and other gluten-carrying food products for a few weeks by eating exclusively at home. I'm nervous that the results will indicate yet another gluten-free diet for the home. There go my food bills!

RiceFiend

gfp Enthusiast

So far as I have seen there is no consistent definition between celiac disease and gluten intolerance.

Some MD's take one definition and others don't differentiate... indeed the most serious researchers don't seem to differentiate at all.

For every definition you find that says one is A and the other B you'll find another conflicting or unrelated definition...

For instance some people differentiate on genes, if you have one set or another set... wheras others differentiate based on biopsy and others on different antibodies... or you can view it as a continum.

I view all divisions as EXTREMELY unproductive. Many people here say "I don't have celiac disease, I'm gluten intolerant" ... Yeah sure... if it makes them comfortable lying to themselves then I guess its OK but its particularly bad for everyone else they set out to confuse just so they can have the label they want.

We simply don't know enough about the disease to make productive subdivisions and then each one bandied about is simply throwing a whole net full of red herrings to the larger part of the medical community who's knowledge of either is pretty poor to start off with.


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



Celiac.com Sponsor (A8-M):



Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,861
    • Most Online (within 30 mins)
      7,748

    Priscilla Buxton
    Newest Member
    Priscilla Buxton
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.4k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • Rogol72
      Some interesting articles regarding the use of Zinc Carnosine to help heal gastric ulcers, gastritis and intestinal permeability. I would consult a medical professional about it's use. https://www.nature.com/articles/ncpgasthep0778 https://www.rupahealth.com/post/clinical-applications-of-zinc-carnosine---evidence-review https://pmc.ncbi.nlm.nih.gov/articles/PMC7146259/ https://www.fallbrookmedicalcenter.com/zinc-l-carnosine-benefits-dosage-and-safety/
    • Jillian83
      He is. Which makes everything even more difficult. I’m not a believer in “staying for the kids” but I have nowhere to go and it’s not just me, it’s me plus my babies. We live in a beautiful place, lots of land in the country and me and the kids love the place we’ve called home for their entire lives. But Im seeing that he’ll never change, that my kids deserve a happy healthy Momma, and that staying in this as is will be the early death of me. Then I look at the scars covering my entire body…this disease and the chronic stress I’ve been enduring for years that tell me I’m no longer beautiful and no one will ever look at me with interest again. I try self care, try to give myself grace so I can just start loving myself enough to gain strength but the slightest sparkle in my eye and skip in my step attracts his wrath and it all comes crashing ten fold. Life is just absolutely railing me from every single direction leaving me wanting to wave that white flag bc I don’t feel like there’s much hope no matter what happens. 
    • trents
    • Jillian83
      Hi, I was recently diagnosed with Celiac and dermatitis herpetiformis after years of suffering without answers. I lost my mind. I lost my job. I lost so much time. I lost Me. Conventional doctors are opulent come near me and the one who did sat across the room, misdiagnosed me, pumped me full of steroids which collapsed my entire hip for 6 months. So without answers I began my holistic journey. Fast forward a couple of years and still struggling with a mysterious whole body itchy, crawling “skin hell”, perfect teeth now deteriorating, thick hair now thinning rapidly and no more than a day or 2 at most relief….An acquaintance opened up a functional medicine practice. Cash only, I found a way. Within a month tests clearly showing my off the charts gluten allergy/sensitivity as well as the depletion of vital nutrients due to leaky gut and intestinal damage. dermatitis herpetiformis was more than likely what I was experiencing with my skin. I was happy. I thought this is easy, eat healthy Whole Foods, follow the diet restrictions and I finally get to heal and feel confident and like myself again very soon! 😔 Supplements are very pricey but I got them and began my healing. Which leads to the other major issue: not working, stay at home Mom of young kids, entirely financially dependent on my man of 7 plus years. He’s never been supportive of anything I’ve ever done or been thru. He controls everything. I’m not given much money ever at a time and when he does leave money it’s only enough to possibly get gas. His excuse is that I’ll spend it on other things. So my “allowance” is inconsistent and has conditions. He withholds money from me as punishment for anything he wants. Since being diagnosed, he’s gained a new control tactic to use as punishment. He now is in control of when I get to eat. He asked for proof of my diagnosis and diet bc he said I made it up just to be able to eat expensive organic foods. Then after I sent him my file from my doctor he then said she wasn’t a real doctor. 😡. I go days upon days starving, sometimes breaking down and eating things I shouldn’t bc I’m so sick then I pay horribly while he gets annoyed and angry bc I’m not keeping up with all the duties I’m supposed to be doing. His abuse turns full on when I’m down and it’s in these desperate times when I need his support and care the most that I’m punished with silence, being starved, ignored, belittled. He will create more of a mess just bc I’m unable to get up and clean so that when I am better, I’m so overwhelmed with chores to catch up that the stress causes me to go right back into a flare from hell and the cycle repeats. I’m punished for being sick. I’m belittled for starving and asking for healthy clean water. I’m purposely left out of his life. He won’t even tell me he’s going to the grocery or to get dinner bc he doesn’t want me to ask him for anything. I have no one. I have nothing. Im not better. My supplements ran out and I desperately need Vitamin D3 and a methylated B complex at the very minimal just to function….he stares at me blankly…no, a slight smirk, no words. He’s happiest when im miserable and I am miserable.  this is so long and im condensing as much as I can but this situation is so complicated and disgusting. And it’s currently my life. The “IT” girl, the healthy, beautiful, perfect skin, perfect teeth, thick and curly locks for days, creative and talented IT girl….now I won’t even leave this house bc Im ashamed of what this has dont to my body, my skin. Im disgusted. The stress is keeping me from healing and I think he knows that and that’s why he continues to keep me in that state. He doesn’t want me confident or successful. He doesn’t want me healed and healthy bc then how would he put the blame of all his problems on me? This journey has been hell and I’ve been in Hell before. I’ve been killed by an ex, I’ve been raped, robbed, held hostage, abused beyond nightmares but the cruelty I’ve experienced from him bc of this disease is the coldest I’ve ever experienced. I’ve wanted to give up. Starving and in tears, desperate…I found a local food pantry in our small town so I reached out just saying I had Celiac and was on hard times. This woman is blessing me daily with prepared gluten free meals, donations, educational info, people who know this disease and how they manage life and the blessings just keep coming. But it’s overwhelming and I feel like I don’t deserve it at all. He just glared and I know he’s going to sabotage it somehow. I don’t even know what to do anymore. I’m so broken and just want peace and healing. 
    • cristiana
      @Colleen H   I am just curious,  when you were tested for coeliac disease, did the doctors find out if you had any deficiencies? Sometimes muscle pain can be caused by certain deficiencies, for example, magnesium, vitamin D, calcium, and potassium.   Might be worth looking into having some more tests.  Pins and needles can be neuropathy, again caused by deficiencies, such as iron and B12,  which can be reversed if these deficiencies are addressed. In the UK where I live we are usually only tested for iron, B12 and vitamin D deficiencies at diagnosis.   I was very iron anemic and supplementation made a big difference.  B12 was low normal, but in other countries the UK's low normal would be considered a deficiency.  My vitamin D was low normal, and I've been supplementing ever since (when I remember to take it!) My pins and needles definitely started to improve when my known deficiencies were addressed.  My nutritionist also gave me a broad spectrum supplement which really helped, because I suspect I wasn't just deficient in what I mention above but in many other vitamins and minerals.  But a word of warning, don't take iron unless blood tests reveal you actually need it, and if you are taking it your levels must be regularly monitored because too much can make you ill.  (And if you are currently taking iron, that might actually be making your stomach sore - it did mine, so my GP changed my iron supplementation to a gentler form, ferrous gluconate). Lastly, have you been trying to take anything to lessen the pain in your gut?  I get a sore stomach periodically, usually when I've had too much rich food, or when I have had to take an aspirin or certain antibiotics, or after glutening.  When this happens, I take for just a few days a small daily dose of OTC omeprazole.  I also follow a reflux or gastritis diet. There are lots online but the common denominators to these diets is you need to cut out caffeine, alcohol, rich, spicy, acidic food etc and eat small regularly spaced meals.   When I get a sore stomach, I also find it helpful to drink lots of water.  I also find hot water with a few slices of ginger very soothing to sip, or camomile tea.  A wedge pillow at night is good for reflux. Also,  best not to eat a meal 2-3 hours before going to bed. If the stomach pain is getting worse, though, it would be wise to see the doctor again. I hope some of this helps. Cristiana    
×
×
  • 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.