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

Trying To Be 100% gluten-free In A Glutenous World


AsillyYak

Recommended Posts

AsillyYak Newbie

HI, I have been gluten free for 9 months now. I have taken full-ownership of this new life style and try to follow the diet to a "T". But I've been sick at least 20 x since then.

Why do I keep getting sick? My Dr. said I may have trouble b/c my blood tested so high for Celiacs. For example, I was at a community event this weekend that served fresh baked bread (a whole table full). I did NOT eat the bread but was surrounded by bread-eaters who did. I drank 2 cups of tea and chatted with the others. I made sure to wash my hands frequently. Is it possible that I was contaminated from the flour dust? Can it get in my mouth by talking or drinking?

Why am I so sensitive? Will it ever get any easier, or will I always be this sensitive? Do I need to look into other conditions/allergies?


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



Celiac.com Sponsor (A8-M):



glutenfreeinminnesota Contributor

HI, I have been gluten free for 9 months now. I have taken full-ownership of this new life style and try to follow the diet to a "T". But I've been sick at least 20 x since then.

Why do I keep getting sick? My Dr. said I may have trouble b/c my blood tested so high for Celiacs. For example, I was at a community event this weekend that served fresh baked bread (a whole table full). I did NOT eat the bread but was surrounded by bread-eaters who did. I drank 2 cups of tea and chatted with the others. I made sure to wash my hands frequently. Is it possible that I was contaminated from the flour dust? Can it get in my mouth by talking or drinking?

Why am I so sensitive? Will it ever get any easier, or will I always be this sensitive? Do I need to look into other conditions/allergies?

Hey! I have been gluten free for 10 months, so I thought I would let you know what is happening to me!! Pretty similar. I have felt "glutened" quite a few times since starting this whole new life style. I try to be so careful...but somehow it seems to happen occasionally. I have been told to get tested, or do the elimination diet for other intolerances/allergies. I have tried eating dairy free/casein free/nut free/gluten free (of course)...and I still seem to feel the same. No matter what, I KNOW I feel WAY better then prior to going on this diet. I think...maybe...and I don't know for sure...but maybe we are more sensitive in the beginning since we are still healing? Maybe when you were talking with friends and drinking tea...a friend got crumbs in your drink? You never know I guess. I am a professional house cleaner and clean up all kinds of gluteny crumbs and what-not on a daily basis...and I even clean toaster trays :o...it has never made me sick. If I was you I would try to see if there is some other intolerance that affects you? Otherwise...just keep being as careful as you can! Good luck.

Cypressmyst Explorer

I am this sensitive as well. Got glutened from beer breath. <_< I so wish I was kidding but I'm not.

I'll be going out to see Dr. Vikki and Rick Petersen at the Health Now clinic in California come Thanksgiving time and phone consultations on this issue have concluded that it is something that will pass once we get the gut back in order.

Gluten free is only the first step in some cases, the imbalance that it caused in the flora and fauna of the intestinal tract needs to be corrected and other toxins (heavy metals and the like) flushed from the body before true healing can begin.

For example, I have an overgrowth of Candida Yeast that I am currently working on starving out by not eating any sugars. Candida can mirror many gluten symptoms as well so when I eat a lot of sugar I sometimes notice a light headedness and itchyness.

So you may want to look into secondary issues in the gut. Getting off gluten is a big piece of the puzzle but it isn't the only piece.

Once the gut is put back in balance many food intolerances clear up. I am gluten/casein free right now but may be able to eat cheese again in the future. Gluten never again though. BUT I shouldn't be this sensitive for the rest of my life.

I will definitely keep you posted as to my progress.

It is a mad world out there.

Gemini Experienced

HI, I have been gluten free for 9 months now. I have taken full-ownership of this new life style and try to follow the diet to a "T". But I've been sick at least 20 x since then.

Why do I keep getting sick? My Dr. said I may have trouble b/c my blood tested so high for Celiacs. For example, I was at a community event this weekend that served fresh baked bread (a whole table full). I did NOT eat the bread but was surrounded by bread-eaters who did. I drank 2 cups of tea and chatted with the others. I made sure to wash my hands frequently. Is it possible that I was contaminated from the flour dust? Can it get in my mouth by talking or drinking?

Why am I so sensitive? Will it ever get any easier, or will I always be this sensitive? Do I need to look into other conditions/allergies?

Many times when people do not do as well on the gluten-free diet as they should is because of the very high incidence of other food intolerances. It's not always about gluten. I also tested in the ridiculous range as far as my blood work was concerned but I am doing fantastic now, after 5 1/2 years gluten-free. It may take longer than you think to recover but you should be noticing positive changes by now and not getting sick all the time. I rarely got sick at all after going gluten-free but I also knew a lot about food as I had studied nutrition when I was younger.

It would be highly unlikely that you would be CC'd by bread sitting out on a table...even a lot of bread. Once cooked, the crumbs aren't quite as air born like flour dust that is seen in bakeries, unless someone breaks open a roll and the crumbs fly into your food, which you in turn would ingest. I can be around bread and people eating bread, as long as I am not eating next to them, and never have a problem and I am a very, very sensitive Celiac. I do not particularly like the smell of gluten bread but that's not the same as being glutened by some.

I really think you may have other food intolerances and that's why you keep getting sick. I also had to go very dairy light myself as I cannot tolerate drinking milk or eating ice cream. Milk in my tea is fine but no more than that or I get sick. You may want to keep a food diary so you can pinpoint exactly what makes you feel ill OR get tested for other allergies/intolerances. Hang in there because it will get better but sometimes it takes a little longer than you would like.

lucia Enthusiast

I react to corn as strongly as if I was glutened.

T.H. Community Regular

Well, re: the the community event?

Possible gluten issues I can think of off hand.

1. the tea. Since you have been following the diet so carefully, I'm assuming you checked the tea ingredients for barley and such, yes? But if the tea was processed on a machine that also processed teas with barley, that could be a CC source. Or if it's not a gluten free facility, that could also cause contamination with the tea. Did anyone else handle the tea bag but yourself? Perhaps someone touched the tea bag with gluteny hands?

2. It might be uncommon, but someone walking near the tea having a few invisible bits of gluten fall off the hand and into your tea...could happen. Unlikely, but still possible.

3. Was the cup disposable or not? If not disposable, maybe it wasn't washed enough to rid the cup of a previous gluten beverage. Or the dishwasher soap had gluten and wasn't rinsed off enough. Or if it's glass, if it had any cracks or parts where gluten could have absorbed into, it could release into your tea. Same goes for whatever the water was boiled in for the tea (if hot tea). Or if it was iced tea, there could be issues with the water used for the ice being contaminted by gluten hands.

4. You washed your hands a lot, but is there any chance you could have touched your lips just once without washing? Another possibility.

5. Oh, and yes, you can get some in your mouth near people eating it. It's more likely with flour, but if something was crusty so that crumbs would flake into the air a little as people took a bite, it's possible. Or that some of these tiny crumbs might have gotten in your tea.

Honestly, lots and lots of ways you could have gotten gluten.

As to why you are sensitive, I've heard some theories.

1. getting more than one gene might make one more sensitive to gluten (I've read hypothesized in one study, but can't find the link at the moment)

2. If you've had it a long time. I have read many people here who were very sensitive and seemed to have the disease for many, many years before being diagnosed.

3. And...who knows, huh? :-P Probably best to just accept we are and go with it, I sometimes think. I'm very sensitive myself, so I can honestly say I sympathize in the worst way.

>>> Will it ever get any easier, or will I always be this sensitive? Do I need to look into other conditions/allergies?

I think that first, I would go SUPER gluten free. And if that doesn't do it, I'd say yeah, start looking at other conditions or allergies. But I'd avoid the teensiest, tiniest risks of gluten first, to make sure.

After reading on this forum about some sensitive people's reactions to gluten free products, and a few reactions from myself and my daughter, I delved into the research like crazy. A lot of things that are on the 'safe' list for celiacs are, really, not safe for ALL of us.

1. Some of us react to lower levels of gluten. So 'gluten free' products sometimes have too much gluten for us and we have to ditch them and make our own products before we can heal.

2. gluten free grains and flours that are 'naturally gluten free' have been found to be contaminated quite often (In the US, legally, a company can say gluten free if the grains are that way naturally, even if the processing contaminates them, sigh). So you might be getting glutened by the flours that are supposed to make you better. You can google and find home based gluten test kits to order to test some of your products and flours and see how much gluten they have (they test down to 10ppm).

3. Some low percentage of celiacs seem to react to gluten-free oats or quinoa just like they react to wheat, barely, and rye.

4. Many foods that are listed as safe, like meats or fruit, can actually be a gluten contamination risk, especially in delis and supermarkets, where they tend to have sausage, coated meats, or other meats with gluten that are sliced and prepared right next to each other. The fruit can often be cut next to gluten ingredients in the stores, too. Or someone with gluten-y hands may have handled it and you aren't able to wash it all off. Fish is often processed in factories that use marinades or soy sauce with gluten and might contaminate the fish. Basically, if a food is touched by anything other than you and your hand? ALWAYS a tiny chance of contamination. Usually it's a small risk, infinitesimal sometimes, but if you are reacting like mad, you might want to avoid as much as you can and slowly add stuff back in as you see what works.

Also, sometimes, a product may be fine once, and then have a tiny bit more gluten the next time and make you react.

And truly, I speak from my own experience on this one. I'm really, really sensitive to gluten. My father, my daughter, and my brother can all eat gluten-free foods that make me sick as a dog. I've reacted to nuts that were processed in a facility with wheat. I've reacted to an oil that was processed on the same machine as wheat germ oil (spectrum brand oils). I've touched a table and accidentally touched my lips and gotten glutened. I've had many gluten-free flours that kicked my butt.

But if I am super, super careful, I don't react. For me, I've had to avoid almost anything processed, even oils and most flours and grains (many of them have now given me a gluten reaction). I try to only get things from completely gluten free facilities if I have to (and even this I'm looking into. Not sure how much some of them test, and if they get contaminated before the factory gets it, I'm not sure how that will be detected, or not). I buy meat that is pre-sealed and was packaged in facilities that ONLY make that meat and don't add anything - like bison meat. I get my own plate, my own saucepans, my own cutting board. I'm in a gluten free household, but I still need my own stuff or sometimes my kids' gluten-free foods can gluten me. I have started an herb and vegetable garden and fruit trees in my backyard so I know the food is gluten free.

It is, frankly, a heck of a lot of work and a pain in the butt. I have to cook in a very different manner, too. But it does seem to stave off the gluten reaction. However, on top of that...I did have other food issues, yes. I thought for a long time that some foods were bothering me that I have since learned are actually not. The gluten reaction is noticeably different from my reactions to other foods, so being totally gluten free helped me eventually figure out when it was gluten and when it was something else.

Wishing you good luck in figuring this out!

celiacsher Newbie

I react to corn as strongly as if I was glutened.

I react to eggs really bad. BUT I do eat some gluten as it does not bother me too much. My doc said its okay to eat a little and all my biopsys have been okay.


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



Celiac.com Sponsor (A8-M):



celiacsher Newbie

I react to corn as strongly as if I was glutened.

I was diagnosed in 2005 so my body has had years to recover and now I feel great except if i eat eggs

Archived

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

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

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





    Celiac.com Sponsors (A17-M):




  • Recent Activity

    1. - Hmart replied to Hmart's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      2

      Is this celiac?

    2. - trents replied to Hmart's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      2

      Is this celiac?

    3. - klmgarland replied to klmgarland's topic in Dermatitis Herpetiformis
      10

      Help I’m cross contaminating myself,

    4. - DebJ14 replied to Jhona's topic in Introduce Yourself / Share Stuff
      30

      Does anyone here also have Afib

    5. - Hmart posted a topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      2

      Is this celiac?


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,925
    • Most Online (within 30 mins)
      7,748

    Linda Stark
    Newest Member
    Linda Stark
    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

    • Hmart
      I was not taking any medications previous to this. I was a healthy 49 yo with some mild stomach discomfort. I noticed the onset of tinnitus earlier this year and I had Covid at the end of June. My first ‘flare-up’ with these symptoms was in August and I was eating gluten like normal. I had another flare-up in September and then got an upper endo at the end of September that showed possible celiac. My blood test came a week later. While I didn’t stop eating gluten before I had the blood test, I had cut back on food and gluten both. I had a flare-up with this symptoms after one week of gluten free but wasn’t being crazy careful. Then I had another flare-up this week. I think it might have been caused by Trader Joe’s baked tofu which I didn’t realize had wheat. But I don’t know if these flare-ups are caused by gluten or if there’s something else going on. I am food journaling and tracking all symptoms. I have lost 7 pounds in the last 10 days. 
    • trents
      Welcome to the forum, @Hmart! There are other medical conditions besides celiac disease that can cause villous atrophy as well as some medications and for some people, the dairy protein casein. So, your question is a valid one. Especially in view of the fact that your antibody testing was negative, though there are also some seronegative celiacs. So, do you get reactions every time you consume gluten? If you were to purposely consume a slice of bread would you be certain to develop the symptoms you describe?
    • klmgarland
    • DebJ14
      I only went on the multi vitamin AFTER a couple of year of high dose, targeted supplementation resolved most of my deficiencies.  I was on quite a cocktail of vitamins that was changed every 6 months as my deficiencies resolved.  Those that were determined to be genetic are still addressed with specific doses of those vitamins, minerals and amino acids. I have an update on my husband and his A Fib.  He ended up in the hospital in August 2025 when his A Fib would not convert.  He took the maximum dose of Flecainide allowed within a 24 hour period.  It was a nightmare experience!  They took him into the ER immediately.  They put in a line, drew blood, did an EKG and chest Xray all within minutes.  Never saw another human for 6 hours.  Never got any results, but obviously we could see he was still in A fib by watching the monitor.  They have the family sign up for text alerts at the ER desk.  So glad I did.  That is the only way we found out that he was being admitted.  About an hour after that text someone came to take him to his room on an observation floor.  We were there two hours before we saw another human being and believe it or not that was by zoom on the TV in the room.  It was admissions wanting to know his vaccine status and confirming his insurance, which we provided at the ER desk.  They said someone would be in and finally a nurse arrived.  He was told a hospitalist was in charge of his case.  Finally the NP for the hospitalist showed up and my husband literally blew his stack.  He got so angry and yelled at this poor woman, but it was exactly what he needed to convert himself to sinus rhythm while she was there.  They got an EKG machine and confirmed it.  She told him that they wanted to keep him overnight and would do an echo in the morning and they were concerned about a wound on his leg and wanted to do a doppler to make sure he did not have a DVT.  He agreed.  The echo showed everything fine, just as it was at his annual check up in June and there was no DVT.  A cardiologist finally showed up to discharge him and after reviewing his history said the A Fib was due to the Amoxicillan prescribed for his leg wound.  It both triggers A Fib and prevents the Flecainide from working.  His conversion coincided with the last dose of antibiotic getting out of his system.  So, make sure your PCP understands what antibiotics you can or cannot take if susceptible to A Fib.  This cardiologist (not his regular) wanted him on Metoprolol 25 mg and Pradaxa.  My husband told him that his cardiologist axed the idea of a beta blocker because his heart rate is already low.  Sure enough, it dropped to 42 on the Metoprolol and my husband felt horrible.  The pradaxa gave him a full body rash!  He went back to his cardiologist for follow up and his BP was fine and heart rate in the mid 50's.  He also axed the Pradaxa since my husband has low platelets, bruises easily and gets bloody noses just from Fish Oil  He suggested he take Black Cumin Seed Oil for inflammation.  He discovered that by taking the Black Seed oil, he can eat carbs and not go into A Fib, since it does such a good job of reducing inflammation.   Oh and I forgot to say the hospital bill was over $26,000.  Houston Methodist!  
    • Hmart
      The symptoms that led to my diagnosis were stomach pain, diarrhea, nausea, body/nerve tingling and burning and chills. It went away after about four days but led me to a gastro who did an upper endo and found I had marsh 3b. I did the blood test for celiac and it came back negative.  I have gone gluten free. In week 1 I had a flare-up that was similar to my original symptoms. I got more careful/serious. Now at the end of week 2 I had another flare-up. These symptoms seem to get more intense. My questions:  1. How do I know if I have celiac and not something else? 2. Are these symptoms what others experience from gluten?  When I have a flare-up it’s completely debilitating. Can’t sleep, can’t eat, can’t move. Body just shakes. I have lost 10 pounds since going gluten free in the last two weeks.
×
×
  • 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.