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

Does Gluten Intolerance Mean 100% gluten-free?


jayman6

Recommended Posts

jayman6 Rookie

I have had all the tests for celiac done and they have been negative, except for my biopsy which showed some "minor features consistent with celiac." Many times I eat things like pizza and white bread just fine and have no problems. I'm wondering if just cutting back on gluten might help my symptoms, or if I really have to go 100% gluten free. If I am really gluten intolerant, why am I able to handle things like pizza, white bread, and other products with gluten in them with no problems? Is this a sign that gluten is not my problem? Thank you.


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



Celiac.com Sponsor (A8-M):



BlessedMommy Rising Star

If you have a positive biopsy, it's quite possible that you have celiac.

 

Are there any clues other than the biopsy that your doctor could use? Have you had genetic tests done? When you got your blood tests, did they check your total IGA levels?

 

Have you been checked for any other medical conditions? The intestinal damage is concerning. No symptoms definitely doesn't always mean that you don't have a problem with gluten. I would not rule it out until there's further investigation.

jayman6 Rookie

If you have a positive biopsy, it's quite possible that you have celiac.

 

Are there any clues other than the biopsy that your doctor could use? Have you had genetic tests done? When you got your blood tests, did they check your total IGA levels?

 

Have you been checked for any other medical conditions? The intestinal damage is concerning. No symptoms definitely doesn't always mean that you don't have a problem with gluten. I would not rule it out until there's further investigation.

 

Thanks for the reply. I had 4 different blood tests all checking IGA and IGG and all were negative. The doctor said that the result was not conclusive and that the biopsy was not positive. He used the word "suggestive." I have not had genetic tests done but nobody in my family has celiac. I had an endoscopy and colonoscopy that were both negative for other medical conditions. The doctor thinks that if the gluten free diet doesn't work that I have IBS, but I am wondering if it is even worth trying the gluten diet when I seem to handle gluten just fine. I just randomly get flareups that don't seem to be related to any particular food.

nvsmom Community Regular

Welcome to the board.

 

Symptoms (how you feel) have a very low correlation to the damage being done inside of your body. Consider a flu virus, one person may get a fever for a week, coughes, migraines and aches, and then another person with the same virus may be just a bit fatigued for a day and sneeze a few times - same virus but different symptoms. The same thing goes for celiac disease: some of us react violently every time, others (like me) do not react as violently but have symptoms grow in severity over repeated exposures, and yet others have no symptoms at all and never had or the symptoms they do have are not GI related (like my cousin who was diagnosed based on ADD).

 
If you have celiac disease, you can not have any gluten. Ever. You will be damage=ing yourself and setting yourself back a few weeks every time a crumb gets into your system. Even if you feel fine, there is damage and systemic inflammation going on that can not be felt or seen.
 
As for your biopsy, did the doctors offer any other possibilities that caused the damage besides celiac disease (or early celiac disease)? It is not rare to have positive biopsy and negative tests or vice versa. It happens.  Unless the doctor has said otherwise, a positive is a positive and you'll have to eat gluten-free to ensure your health does not deteriorate.
 
Best wishes.
nvsmom Community Regular

Ooops. We posted at the same time.

 

These are the celiac tests that can be done:

  • tTG IgA and tTG IgG
  • DGP IgA and DGP IgG
  • EMA IgA
  • AGA IgA and AGA IgG (older and less reliable tests)
  • total serum IgA (a control test only)

Do you you know which of those tests were done?

BlessedMommy Rising Star

Keep in mind, that celiac may run in your family, the people who have it might be just undiagnosed. That's why it may be worth running the genetic test to evaluate your risk if the other tests are inconclusive.

jayman6 Rookie

Ooops. We posted at the same time.

 

These are the celiac tests that can be done:

  • tTG IgA and tTG IgG
  • DGP IgA and DGP IgG
  • EMA IgA
  • AGA IgA and AGA IgG (older and less reliable tests)
  • total serum IgA (a control test only)

Do you you know which of those tests were done?

 

Online, it shows my test results and all it says is that these tests were done (all were negative): 

 

GLIADIN IGA AB (DEAMIDATED)

GLIADIN IGG AB (DEAMIDATED)

TISSUE TRANSGLUTAMINASE IGA AB

IGA

 

I'm not sure if this is helpful to you?


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



Celiac.com Sponsor (A8-M):



nvsmom Community Regular

Online, it shows my test results and all it says is that these tests were done: 

 

GLIADIN IGA AB (DEAMIDATED)

GLIADIN IGG AB (DEAMIDATED)

TISSUE TRANSGLUTAMINASE IGA AB

IGA

 

I'm not sure if this is helpful to you?

 

Those are the best tests to be run. I was concerned that the doctor had just run total serum IgG and IgA - some have done that.

 

If a test is going to catch celiac disease, those are the ones.  You appear to be one of the few seronegative celiacs. :(

 

Perhaps try keeping a food and symptom journal to help you keep track of how the gluten-free diet is affecting you. Sometimes it helps with seeing the patterns. Many celiac disease symptoms are slow to leave and can take months. Keeping track of how you feel helps when things can be slow to change - most people need 3-6+ months to really start feeling good and to stop having setbacks.  Give it time before you judge the diet's effectiveness.

KMMO320 Contributor

I have had all the tests for celiac done and they have been negative, except for my biopsy which showed some "minor features consistent with celiac." Many times I eat things like pizza and white bread just fine and have no problems. I'm wondering if just cutting back on gluten might help my symptoms, or if I really have to go 100% gluten free. If I am really gluten intolerant, why am I able to handle things like pizza, white bread, and other products with gluten in them with no problems? Is this a sign that gluten is not my problem? Thank you.

I have been gluten free for almost 2 years. A while ago, I decided to have a regular gluten filled muffin. I was fine. I was fine all night. I was fine the next day. Sweet. So 2 days later, I had another muffin. Again i was fine. 2 days later, I had another one. I WAS NOT FINE. OMG WAS I SICK!  I had been hoping that somehow I was cured, or that I had grown out of having Celiac Disease. but that third time eating gluten, I was sick. My symptoms don't last long. Many people get violently ill. I don't, but I know my body and I knew I wasn't well. Luckily, I am able to take some tylonal, a hot shower and sleep it off. But even that minor thing is hard for me and my family when I have stuff to do. I can't always be going to bed because I wanted to eat gluten. So I just stay away. 

My biopsy came back negative, so I don't know if I actually have celiac disease or intolerance but my Dr was willing to make the celiac disease diagnosis, so I treat myself like I have it. 

jayman6 Rookie

Thank you to all of those who posted. I started a gluten free diet again and am just wondering a few things. I've read online that even the smallest amount of gluten can be problematic, but if I'm wondering if that is true for everyone or just people with extreme sensitivity to gluten. Given that my blood test were negative and my biopsy was inconclusive, if I ingest a small amount of trace gluten in something is that really going to set me back? I ask because in order to evaluate my diet I need to know whether eating out at a restaurant where my food might come into contact with something harmful could really throw the entire gluten free diet off so that even if I go 2 months without eating gluten I could still be having problems resulting from the trace gluten. I'm not sure if I am making sense, but if anyone can give insight into this, I would appreciate it.

Questore Rookie

Thank you to all of those who posted. I started a gluten free diet again and am just wondering a few things. I've read online that even the smallest amount of gluten can be problematic, but if I'm wondering if that is true for everyone or just people with extreme sensitivity to gluten. Given that my blood test were negative and my biopsy was inconclusive, if I ingest a small amount of trace gluten in something is that really going to set me back? I ask because in order to evaluate my diet I need to know whether eating out at a restaurant where my food might come into contact with something harmful could really throw the entire gluten free diet off so that even if I go 2 months without eating gluten I could still be having problems resulting from the trace gluten. I'm not sure if I am making sense, but if anyone can give insight into this, I would appreciate it.

 

Some people can get a mere crumb of gluten filled food, and suffer agonies, while others don't feel anything, but have the same damage.  Gluten is a protein that many humans cannot digest, and they affect the interior of the upper GI just as if the lining was burned.  All the miniscule fingers that stick up from the intestines (villi) are burned off...often very patchily, so that even a biopsy can miss it.

 

Only 30% of the people who have a blood test actually are diagnosed for Celiac, but if you continue to have problems, you need to have your genes tested, and have gluten sensitivity testing done, which can be quite as bad as having Celiac in it's effect on the rest of your body, and the uptake of nutrients.  And there are other foods you can have immune responses to, also, so you can't just through up your hands, and bear it. 

 

Please, keep investigating...it's your health, not the Doctor's.  Start a food and reaction diary...it is amazing what it points out that you would never suspect.  And see a Nutritionist/Naturopath if the Doctors can't find an obvious answer.  Your food is supposed to have the nutrition in it your body needs, but it sometimes has irritants that you don't need.  And please...skip all processed food...it's filled with chemicals that no one knows is safe!

FruitEnthusiast Enthusiast

I'm non-Celic Gluten Intolerant according to the blood test, but still I have been trying to recover for two years, and many others have the same experience. It's taken away my ability to live any kind of normal life - I'm just too sick to participate in much of anything. I would hate to see that happen to you. You feel ok now, but repeated exposure can do damage as was mentioned. I hope you'll take this seriously so you don't end up really sick like a lot of us have. Protect your good health while you have it. Once you lose it, it's a long road back.

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,979
    • Most Online (within 30 mins)
      7,748

    volivier
    Newest Member
    volivier
    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

    • knitty kitty
      @tiffanygosci, Hello.  I apologize for your thread being hijacked.   I recognize your symptoms as being similar to what I experienced, the migraines, food and chemical sensitivities, hives, nausea, the numbness and tingling, joint pain, tummy problems, sleep problems, emotional lability, and the mom brain.  My cycle returned early after I had my son, and I became pregnant again with all my symptoms worsening.  Unfortunately, I lost that baby.  In hindsight, I recognized that I was suffering so much from Thiamine deficiency and other nutritional deficiencies that I was not able to carry it.   Celiac Disease affects the absorption of nutrients from our food.  There's eight B vitamins that must be replenished every day.  Thiamine Vitamin B1 becomes depleted first because it cannot be stored very long, less than two weeks.  Other B vitamins can be stored for two months or so.  But Thiamine can get low enough to produce symptoms in as little as three days.  As the thiamine level gets lower, symptoms worsen.  Early symptoms like fatigue and anxiety are often attributed to life situations, and so frequently go unrecognized by medical professionals who "have a pill for that".   I used to get severe migraines and vomiting after gluten consumption.  Thiamine and the other B vitamins are needed to turn carbohydrates, fats and proteins into fuel for our bodies.  With a large influx of carbohydrates from gluten containing foods, the demand for Thiamine increases greatly.  Available thiamine can be depleted quickly, resulting in suddenly worsening symptoms.  Emotional stress or trauma, physical activity (athletes and laborers) and physiological stresses like pregnancy or injury (even surgery or infection) increase the need for Thiamine and can precipitate a thiamine insufficiency. Pregnancy requires more thiamine, not just for the mother, but for the child as well.  The mother's Thiamine stores are often depleted trying to meet the higher demand of a growing fetus.  Thiamine insufficiency can affect babies in utero and after birth (autism, ADHD).  Having babies close together doesn't allow time for the mother to replenish thiamine stores sufficiently.   Thiamine insufficiency can cause migraines, pins and needles (paresthesia), and gastrointestinal Beriberi (gas, bloating, diarrhea or constipation, back pain).   Thiamine deficiency can cause blurry vision, difficulty focusing, and affect the eyes in other ways.  Thiamine deficiency can damage the optic nerves.  I have permanent vision problems.  High histamine levels can make your brain feel like it's on fire or swelling inside your cranium.  High histamine levels can affect behavior and mood.  Histamine is released by Mast Cells as part of the immune system response to gluten.  Mast Cells need Thiamine to regulate histamine release.  Mast Cells without sufficient thiamine release histamine at the slightest provocation.  This shows up as sensitivities to foods, smelly chemicals, plants, and dust mites.  Thiamine and the other B vitamins are needed to lower histamine levels.  Vitamin D is needed to calm the immune system and to regulate our hormones.  Menstrual irregularities can be caused by low Vitamin D.   Celiac Disease is a disease if Malabsorption of Nutrients.  We must take great care to eat a nutritionally dense diet.  Our bodies cannot make vitamins.  We must get them from what we eat.  Supplementation with essential vitamins and minerals is warranted while we are healing and to ensure we don't become deficient over time.  Our bodies will not function properly without essential vitamins and minerals.  Doctors have swept their importance under the rug in favor of a pill that covers the symptoms but doesn't resolve the underlying issue of malnutrition. Do talk to your doctor and dietician about checking for nutritional deficiencies.  Most blood tests for the eight B vitamins do not reflect how much is available or stored inside cells.  Blood tests reflect how much is circulating in the blood stream, the transportation system.  Blood levels can be "normal" while a deficiency exists inside cells where the vitamins are actually used.  The best way to see if you're low in B vitamins is to take a B Complex, and additional Thiamine and look for improvement.   Most vitamin supplements contain Thiamine Mononitrate, which is not easily absorbed nor utilized by the body.  Only thirty percent of thiamine mononitrate listed on the label is absorbed, less is actually utilized.  This is because thiamine mononitrate is shelf stable, it won't breakdown sitting on a shelf in the grocery store.  It's so hard to breakdown, our bodies don't absorb it and can't turn it into a form the body can use.  Take Thiamine in the form Benfotiamine or TTFD (tetrahydrofurfuryl disulfide) which the body can utilize much better.  (Ask for an Erythrocyte Transketolace Activity test for Thiamine level.  Though not accurate, this test does better picking up on a thiamine deficiency than a blood test.) Are you keeping your babies on a gluten free diet?  This can prevent genetically susceptible children from developing Celiac Disease.  
    • trents
      @Riley, on this forum we sometimes get reports from people with similar experiences as you. That is, their celiac disease seems to go into remission. Typically, that doesn't last. At age 18 you are at your physical-biological peek in life where your body is stronger than it will ever be and it is able to fight well against many threats and abuses. As Wheatwacked pointed out, absence of symptoms is not always a reliable indicator that no damage is being done to the body. I was one of those "silent" celiacs with no symptoms, or at least very minor symptoms, whose body was being slowly damaged for many years before the damage became pronounced enough to warrant investigation, leading to a diagnosis. By that time I had suffered significant bone demineralization and now I suffer with back and neck problems. Please, if you choose to continue consuming gluten, which I do not recommend, at least get tested regularly so that you won't get caught in the silent celiac trap down the road like I did. You really do not outgrow celiac disease. It is baked into the genes. Once the genes get triggered, as far as we know, they are turned on for good. Social rejection is something most celiacs struggle with. Being compliant with the gluten free diet places restrictions on what we can eat and where we can eat. Our friends usually try to work with us at first but then it gets to be a drag and we begin to get left out. We often lose some friends in the process but we also find out who really are our true friends. I think the hardest hits come at those times when friends spontaneously say, "Hey, let's go get some burgers and fries" and you know you can't safely do that. One way to cope in these situations is to have some ready made gluten-free meals packed in the fridge that you can take with you on the spot and still join them but eat safely. Most "real" friends will get used to this and so will you. Perhaps this little video will be helpful to you.  
    • Wheatwacked
      @Riley., Welcome to the forum.   It was once believed that Celiac Disease was only a childhood disease and it can be outgrown.  That was before 1951, before gluten was discovered to be cause of Celiac Disease, also called Infantilism.  Back then Cileac Disease was thought to be only a gastro intestinal disease, once you  "outgrew" the colicky phase, you were cured. You were so lucky to be diagnosed at 5 years old so your developing years were normal.  Gluten can affect multiple systems.  The nervous system, your intellegence. The muscules, skeleton. It can cause neurological issues like brain fog, anxiety, and peripheral neuropathy.  It can cause joint pain, muscle weakness, and skin rashes. Epilepsy is 1.8 times more prevalent in patients with celiac disease, compared to the general population. Because through malabsorption and food avoidances, it causes vitamin D and numerouus other essential nutrient deficiencies, it allows allergies, infections, poor growth, stuffy sinuses and eustacian tubes. There is even a catagory of celiac disease called "Silent Celiac".  Any symptoms are explained away as this, that or the other thing. Gluten is one of the most addictive substances we consume.  Activating the Opiod receptors in our cells, it can numb us to the damage that it, and other foods are causing.  It has become socially acceptable to eat foods that make us feel sick.  "There's a pill for that".   It is generally accepted that n fact you are weird if you don't. The hardest part is that if you don't eat gluten you will feel great and think why not.  But slowly it will effect you, you'll be diagnosed with real diseases that you don't have. You'll be more susseptable to other autoimmune diseases.  As you read through the posts here, notice how many are finally dianosed, after years of suffering at older ages.  Is it worth it? I think not. Perhaps this book will help:  Here is a list of possible symptoms:   
    • Riley.
      Hi! Im Riley, 18 years old and have been diagnosed for 13 years.. the testing started bc I stopped growing and didn’t gain any weight and was really small and thin for my age.  I got diagnosed when I was 5 and have been living gluten free since, in elementary and middle school it was hard for me and I kept contaminating myself bc I wanted to fit in with my friends so so badly. I ate gluten secretly at school and mostly regretted it 30 minutes later.  I’ve had symptoms like diarrhea, nausea, headaches, stomachaches, threw up a lot and was really emotional.  In 2022 I really started working on myself and tried to stay gluten free and if I did eat gluten I wouldn’t tell anyone and suffer in silence.  Last year in July I begged my mom to let me „cheat“ one day bc I just wanted to fit in… I ate a lot of different stuff, all the stuff I missed out on in my childhood like nuggets, pizza and all that.. I didn’t have symptoms that day and was doing really fine My mom and I wanted to test how far we can go and said we would test it for 12 weeks to get my blood taken after to see if I’m doing good or if symptoms start showing  As a now 18 year old girl who finally gained a normal weight and doesn’t get symptoms I’m to scared to get tested/my blood taken cuz I finally found comfort in food and it got so much easier for me and my family.  A year and 4 months later i still didn’t get any symptoms and have been eating gluten daily.  I’m scared to get tested/my blood taken cuz what if I’m actually not fine and have to go back to eating gluten free. Any tips to get over that fear and „suck it up“ cuz I know I could seriously damage my body… sorry if I seem like a idiot here… just don’t really know what to do :,)
    • Mari
      There is much helpful 'truth' posted on this forum. Truths about Celiac Disease are based on scientific research and people's experience. Celiac disease is inherited. There are 2 main Celiac 'genes' but they are variations of one gene called HLa - DQ What is inherited when a person inherits one or both of the DQ2 or the DQ8 is a predisposition to develop celiac disease after exposure to a environmental trigger. These 2 versions of the DQ gene are useful in diagnosing  celiac disease but there are about 25 other genes that are known to influence celiac disease so this food intolerance is a multigenic autoimmune disease. So with so many genes involved and each person inheriting a different array of these other genes one person's symptoms may be different than another's symptoms.  so many of these other genes.  I don't think that much research on these other genes as yet. So first I wrote something that seem to tie together celiac disease and migraines.  Then you posted that you had migraines and since you went gluten free they only come back when you are glutened. Then Scott showed an article that reported no connection between migraines and celiac disease, Then Trents wrote that it was possible that celiacs had more migraines  and some believed there was a causal effect. You are each telling the truth as you know it or experienced it.   
×
×
  • 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.