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

Confused about my history of symptoms


gjmama

Recommended Posts

gjmama Rookie

Hello, I'm new to this site, and very glad to be here!   I want to provide you a very brief history, and then one question. 

3 yrs ago I had an endoscopy because of symptoms (chronic nausea, bloating, D...). Biopsy came back positive for villi blunting. Dr said Celiac.

So, I went off gluten and lactose for a year and felt great (that was 2014).  After a year of being off gluten and lactose, I began to eat gluten again (but not lactose) and continued to eat gluten freely for an entire year (2015).  Now, here's where it starts getting confusing. I felt great for that year eating gluten! How could that be??

But then this year my symptoms came back. So, I went back off gluten again. I am gluten free now, and if I eat gluten I have the same symptoms (nausea, bloating, D...).

Ok, so that's my history.  I am convinced I have celiac now and never plan to eat gluten again. However, my question is:  How could I have felt fine all last year eating gluten? I understand celiac can by symptom-free. However, I do have symptoms now if I eat gluten. Thanks for your help :) 


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



Celiac.com Sponsor (A8-M):



kareng Grand Master
21 minutes ago, gjmama said:

Hello, I'm new to this site, and very glad to be here!   I want to provide you a very brief history, and then one question. 

3 yrs ago I had an endoscopy because of symptoms (chronic nausea, bloating, D...). Biopsy came back positive for villi blunting. Dr said Celiac.

So, I went off gluten and lactose for a year and felt great (that was 2014).  After a year of being off gluten and lactose, I began to eat gluten again (but not lactose) and continued to eat gluten freely for an entire year (2015).  Now, here's where it starts getting confusing. I felt great for that year eating gluten! How could that be??

But then this year my symptoms came back. So, I went back off gluten again. I am gluten free now, and if I eat gluten I have the same symptoms (nausea, bloating, D...).

Ok, so that's my history.  I am convinced I have celiac now and never plan to eat gluten again. However, my question is:  How could I have felt fine all last year eating gluten? I understand celiac can by symptom-free. However, I do have symptoms now if I eat gluten. Thanks for your help :) 

You healed the damage and then it took a while to get enough damage that you felt it was bad enough to notice

gjmama Rookie

Kareng, thank you! Wow, that's so amazingly simple lol. 

mama.liz07 Apprentice

So, does that mean once someone is gluten free for a year or so (or however long it takes to heal) that person might not have symptoms if they accidentally eat gluten?  

If if that is true, how do you know if you are glutenated....and thus avoid whatever the problem food is in the future?  

kareng Grand Master
5 minutes ago, mama.liz07 said:

So, does that mean once someone is gluten free for a year or so (or however long it takes to heal) that person might not have symptoms if they accidentally eat gluten?  

If if that is true, how do you know if you are glutenated....and thus avoid whatever the problem food is in the future?  

Any food with gluten is to be avoided, even if you don't think you feel any symptoms.  Those are the " problem" foods.

Some  people don't have especially noticeable symptoms from a one time small amount of gluten.  But, if you keep eating gluten,  it will damage you.  

kareng Grand Master

Open Original Shared Link

"Eating any gluten, no matter how small an amount, can damage the small intestine. This is true for anyone with the disease, including people who do not have noticeable symptoms. Antibody levels take a long time (sometimes more than a year) to normalize after a person has stopped eating gluten."

jddh Contributor

It's easy to assume that symptoms=gluten and no symptoms means it's ok! We've all done it. ;) But you must avoid gluten at every meal if you have a confirmed diagnosis.

Instead of waiting for symptoms, read up on labelling laws, ingredient checks, and certification programs. Your body will thank you.


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



Celiac.com Sponsor (A8-M):



cyclinglady Grand Master

Here is my story.  No intestinal issues when I was diagnosed.  Was in for a routine colonoscopy (yep, over 50 years old) when my GI suspeced celiac disease because I was anemic (have two types of anemia actually).  He ordered a celiac disease blood panel and added an endoscopy and the rest is history.  Healed up and then got glutened last summer.  I had severe intestinal issues.  I was not sure I had really been glutened.    Six weeks later, my GI retested my antibodies.  He thought  Sibo but it was just a celiac disease flare-up.  celiac disease symptoms can change.   Took 3 to six months to recover and I still can not confirm what actually glutened me!  

mama.liz07 Apprentice

Thanks everyone.  I do know how serious it is to avoid gluten, that is why I'm concerned.  If you don't feel symptoms when you accidentally ingest gluten, how will you know to avoid it.  For example, if you're eating a brand that is supposedly safe, but really has problems with cross contamination, how would you know?  Seems you could eat a little gluten everyday and not know and then end up with quite a bit of damage before you realize what's going on.  Eek.  

kareng Grand Master
1 hour ago, mama.liz07 said:

Thanks everyone.  I do know how serious it is to avoid gluten, that is why I'm concerned.  If you don't feel symptoms when you accidentally ingest gluten, how will you know to avoid it.  For example, if you're eating a brand that is supposedly safe, but really has problems with cross contamination, how would you know?  Seems you could eat a little gluten everyday and not know and then end up with quite a bit of damage before you realize what's going on.  Eek.  

This myth that something supposedly safe will gluten you is just a bunch of fear mongering.  Like any other food, there are occasional recalls on labelled gluten-free foods, but usually it's not for gluten.

 If you are really worried that companies are somehow slipping gluten in foods that are certified gluten-free or have no reason to have gluten, only eat 1 ingredient foods you can wash off first.  Call or email companies and find out what thier processes are.  Learn about foods and if it even makes sense that gluten could be near a product.    Subscribe to Gluten Free Watchdog and other large Celiac groups so you are aware when something, like Cheerios , has issues with its gluten-free practices.  

mama.liz07 Apprentice

Thanks Kareng!  I'm still new to this.  Funny you mention Cheerios because that was the product I was curious about (wondering if they are really safe).  Gluten Free Watchdog...I'll check it out!  :-)  

Thanks for your help...sorry to commandeer this post.  :unsure:

kareng Grand Master
6 minutes ago, mama.liz07 said:

Thanks Kareng!  I'm still new to this.  Funny you mention Cheerios because that was the product I was curious about (wondering if they are really safe).  Gluten Free Watchdog...I'll check it out!  :-)  

Thanks for your help...sorry to commandeer this post.  :unsure:

Read ingredients, just in case.  Some of the smaller companies seem to miss barley malt.  The bigger companies or completely gluten-free companies ( like Glutinos or Schar) usually will do a good job.  The real problems I have seen are small or local companies.  Like the guy that sells at the farmers market or some start up " healthy" company that seems to think barley gluten-free ( in that case, reading the ingredients will clue you in).  I do buy from a family that sells baked goods at the farmers market because I have talked to them about thier practices.  A couple of family members have a severe gluten intolerance and can't handle any cc.  Talk to restaurants-  some are very good or have almost no gluten in any of the foods.   

You are lucky not to react.  You can eat out occasionally, and not react if there is a problem.  An occasional light glutening  ( I don't mean once a day or even once a week) should heal just fine in a short time.   Your sensitivity may change over time, as immune systems seem to change over time.  

 

gjmama Rookie

Interesting reading all your responses....very helpful.

I share Mama.Liz's question...how would you know if you are being glutened on a regular basis if you don't show any symptoms? I understand about calling companies to check if their "gluten free" product is produced in a facility that also handles wheat.  And talking to restaurants.

But I live in a household with many gluten products used in cooking, baking, etc.  Of course, I'm extremely careful and so is my family.

However, I read somewhere a situation about a girl who was having celiac symptoms and finally figured out her dishwasher wasn't getting her dishes clean enough. They made some changes in their method of dishwashing and the symptoms cleared up. If she hadn't had any symptoms, she wouldn't have known she was being glutened until, perhaps, her intestines had been very damaged. It seems that symptoms, although not pleasant, are a wonderful warning sign. :) My question is: are there other ways to find out if you're being glutened on a regular basis without the typical celiac symptoms you can feel? 

kareng Grand Master
1 minute ago, gjmama said:

Interesting reading all your responses....very helpful.

I share Mama.Liz's question...how would you know if you are being glutened on a regular basis if you don't show any symptoms? I understand about calling companies to check if their "gluten free" product is produced in a facility that also handles wheat.  And talking to restaurants.

But I live in a household with many gluten products used in cooking, baking, etc.  Of course, I'm extremely careful and so is my family.

However, I read somewhere a situation about a girl who was having celiac symptoms and finally figured out her dishwasher wasn't getting her dishes clean enough. They made some changes in their method of dishwashing and the symptoms cleared up. If she hadn't had any symptoms, she wouldn't have known she was being glutened until, perhaps, her intestines had been very damaged. It seems that symptoms, although not pleasant, are a wonderful warning sign. :) My question is: are there other ways to find out if you're being glutened on a regular basis without the typical celiac symptoms you can feel? 

About 6 months after diagnosis, you should get a re- test of your antibodies.  Then every year after.  That would tell you something.

Also, you may want to stop the gluten baking.  That flour goes everywhere and can take a day to settle.

Some people have symptoms they didn't realize we're connected to gluten.  It isn't all " stomach" issues.  Migraines are one big one.  You may find that you do get symptoms.

gjmama Rookie

Thanks, Kareng :)

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,928
    • Most Online (within 30 mins)
      7,748

    Grams H
    Newest Member
    Grams H
    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

    • lehum
      Hi and thank you very much for your detailed response! I am so glad that the protocol worked so well for you and helped you to get your health back on track. I've heard of it helping other people too. One question I have is how did you maintain your weight on this diet? I really rely on nuts and rice to keep me at a steady weight because I tend to lose weight quickly and am having a hard time envisioning how to make it work, especially when not being able to eat things like nuts and avocados. In case you have any input, woud be great to hear it! Friendly greetings.
    • 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!  
×
×
  • 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.