Jump to content
This site uses cookies. Continued use is acceptance of our Terms of Use and Privacy Policy. More Info... ×
  • 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 Celiac.com!
    eNewsletter
    Donate

Have I Always Had Celiac Diseass


whattodo

Recommended Posts

whattodo Enthusiast

Well it has been 9 months since my stomach first started hurting. Before that I have had 2 spells with the same stomach pain with years between them. I must say that the first one happened about 6 years ago.

I have always been a keen bodybuilder although i did not do much weight training. I had always been slim until i started eating enough food to build muscle. I would have to take protein aswell to help as i could never eat loads.

I have however been slightly tired in the evenings but always put this down to going to the gym 5 times a week.

9 months ago i went throught a very stressful time and depression. I didnt eat alot through this and did loose a little weight.

My question is, how long have i had celiac disease (although still not 100% diagnosed, im just certain). What i dont understand is that if it is the same pain as i have had before and it went away with still eating gluten then why is this time lasting longer. The only thing i have done different this time is i have had a biopsy and they have seem that my duodenum has flattened. Could this have been happening before and just got better.

Confused....

Jay

Link to comment
Share on other sites

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



Celiac.com Sponsor (A8-M):



debmidge Rising Star

Jay: You pose an interesting question that many really can't answer. In my husband's case, he was ill for about 27 years (see his capsule below)..when he was given the blood test for the antibodies the result indicated "strongly positive." I asked the gastro then if my husband just came down with celiac and if not, how long has he had it? The doctor replied that the "strongly positive" shows that my husband has had celiac for a long time, possibly all those 27 years (which we are sure he has).

Now the blood test will have a negative result if you get it after you go gluten free. I don't suggest you do this unless you really want to know this answer.

Some people have said on the board that they did eat gluten and had no immediate reaction...while this could be true in that the stomach/intestines didn't revolt, if you have celiac your body will know it and react to it, whether it chooses to alert you about it or not. I worked with a man who had celiac who cheated and it didn't catch up with him for a few weeks each time he cheated. I used to scold him when I saw him eating a wheat roll with butter in the kitchenette.

Did your biopsy show flattened villi at any point?

D.

Link to comment
Share on other sites
whattodo Enthusiast
Jay: You pose an interesting question that many really can't answer. In my husband's case, he was ill for about 27 years (see his capsule below)..when he was given the blood test for the antibodies the result indicated "strongly positive." I asked the gastro then if my husband just came down with celiac and if not, how long has he had it? The doctor replied that the "strongly positive" shows that my husband has had celiac for a long time, possibly all those 27 years (which we are sure he has).

Now the blood test will have a negative result if you get it after you go gluten free. I don't suggest you do this unless you really want to know this answer.

Some people have said on the board that they did eat gluten and had no immediate reaction...while this could be true in that the stomach/intestines didn't revolt, if you have celiac your body will know it and react to it, whether it chooses to alert you about it or not. I worked with a man who had celiac who cheated and it didn't catch up with him for a few weeks each time he cheated. I used to scold him when I saw him eating a wheat roll with butter in the kitchenette.

Did your biopsy show flattened villi at any point?

D.

I have had a biopsy and that came back negative, i had a spell of not eating gluten for about a 2 weeks then a week of eating gluten before the biopsy. They said my duodenum was inflamed and the folds had reduced alot. I have had a blood test but awaiting for the results. Pretty sure that will come back negative as not been eating gluten for the test.

Link to comment
Share on other sites
CMCM Rising Star

Jay....Here are some little factoids I've picked up about this....

* You can have a celiac gene and possibly celiac disease will never actually be triggered. This happened with my grandmother, who died at 99. Her worst physical problem was arthritis.

* It seems that active celiac disease is usually triggered by something....perhaps an emotional event, a trauma, something physical such as surgery...things like that. The triggering event often occurs later in life. With my mom, who has 2 celiac genes, it occurred after surgery when she was in her early 40's.

* More and more doctors are thinking of GLUTEN SENSITIVITY as a broad spectrum which can range from the worst reaction (celiac disease) on one end to zero observable symptoms on the other. Doctors increasingly realize that more people than they ever thought are gluten sensitive. When my mom was diagnosed 40 years ago, they thought 1 in 10,000 might have celiac disease. That figure has been revised down to 1 in 133, and some think a more accurate figure would be 1 in 80 or so. It's not that more people have it, necessarily, but that diagnosis is getting better and more mainstream, despite the fact that humongous numbers of doctors have NO IDEA about it. And now there are suggestions that some degree of gluten sensitivity may affect over 80% of us. Most people have no idea, and simply get vague diagnoses such as IBS.

* A person can be gluten sensitive and be horrendously ill from eating gluten, yet not have celiac disease. Gluten sensitivity in general is far less understood than celiac disease, which only affects about 3% of the gluten sensitive folks out there. The 80% who may be gluten sensitive are up the creek in terms of a diagnosis since doctors focus mostly on celiac disease and known very little about diagnosing "mere" gluten sensitivity...plus, there isn't really a "gold standard" test for gluten sensitivity. So the whole idea of illness caused by gluten is ignored,dismissed, pretty much universally misunderstood. You might be told "it's all in your head."

* The cure for celiac disease AND gluten sensitivity is the same: eliminate gluten from the diet. After a period of time gluten free, many other sensitivities which you have developed may eventually go away.

* A curious thing about reactions to gluten: some people get very sick, immediately. Others get sick a day or two later. Some people never have troublesome reactions....these are dubbed "silent celiacs", and these unfortunate people may never find out they have celiac disease until they get diagnosed with something terrible such as cancer of the stomach. There is a higher rate of some cancers among celiacs, specifically, among untreated celiacs (untreated meaning they continue to eat gluten). When my mom was diagnosed 40 years ago, doctors told her she might get stomach or intestinal cancer as a result of her years eating gluten. The good news is that never happened....she is currently 85 and quite healthy....she has avoided all gluten for 40 years, though!

* Gluten sensitivity can worsen over time. Oddly enough, your body can initially develop a kind of tolerance to gluten--the body does its best to deal with the poison invader gluten, and sometimes your body does better with gluten than at other times. This may explain why sometimes a person will get sick from eating gluten, and other times seem to eat it with no problem. This creates problems diagnosing or even suspecting problems with gluten. For many years, this was true for me. I didn't directly suspect gluten and for most of my life I thought all my problems were related to dairy.

* Eventually, the body's ability to tolerate gluten breaks down and a person will get very sick, or increasingly sick. This happened with me....it got worse over about 30 years, and eventually this created a gazillion other intolerances....at one point I thought there was NOTHING I could eat, I was upset continuously. If you take this increasing problem and mix it with a traumatic or big physical event, then IF you have the predisposing gene the whole thing might actually morph into full blown celiac disease. If you don't have the gene, you might just be just sick sick sick. Either way, you have to eliminate gluten to heal and feel better. Gluten sensitivity (as opposed to celiac disease) is nothing to be dismissed! It's serious, it can make you feel horrible, it can damage your organs, it can cause other sensitivities and reactions.

Hope this helps.

Well it has been 9 months since my stomach first started hurting. Before that I have had 2 spells with the same stomach pain with years between them. I must say that the first one happened about 6 years ago.

I have always been a keen bodybuilder although i did not do much weight training. I had always been slim until i started eating enough food to build muscle. I would have to take protein aswell to help as i could never eat loads.

I have however been slightly tired in the evenings but always put this down to going to the gym 5 times a week.

9 months ago i went throught a very stressful time and depression. I didnt eat alot through this and did loose a little weight.

My question is, how long have i had celiac disease (although still not 100% diagnosed, im just certain). What i dont understand is that if it is the same pain as i have had before and it went away with still eating gluten then why is this time lasting longer. The only thing i have done different this time is i have had a biopsy and they have seem that my duodenum has flattened. Could this have been happening before and just got better.

Confused....

Jay

Link to comment
Share on other sites
Murph Newbie

It is an interesting question.

I was 1st diagnosed as an infant in the 60s and unfortunately the prevailing wisdom at the time was that it goes away and gluten could be reintroduced into the diet at age 5.

And I did seem fine. Bright (skipped a grade), somewhat athletic (could dunk @6'1") tho never strong (I blame celiac now). Celiac wasn't supposed to be a problem until I was "old". Well, I guess I got old at 35 and went thru some pretty hellish times before ending up fully gluten-free. Swore it was a matter of months before I'd deteriorate to requiring institutional care.

But even w/out the worst period I know I would've been better off my whole life if gluten-free from the start.

So basically, I have no idea why I was relatively healthy for so long in spite of celiac issues as a toddler. Makes no sense at all.

Link to comment
Share on other sites
darlindeb25 Collaborator

CMCM--your definition was great. Actually even helped me understand a little more and I have been gluten free for 7 yrs.

I was not diagnosed as a baby, yet my mom said I always spit up on everything, I always got sick in the car, always had a touchy tummy. When I was pregnant with my 2nd son, who is 31 now, I was sick every other night. Was always much worse when pregnant. By my 4th son, I was so sick, I couldn't see someone else in a rocking chair. My 5th and last child, whom I got pregnant for because I was not absorbing my birth control pills :unsure: (a symptom no one picked up on then)--I was ill all the time, I lost 40# while pregnant. I think my stress point was when my sister lost her first baby at birth, I was pregnant with my 4th son. Then when she got pregnant again, Troy was born 6 weeks early and in Pedatric ICU, I found out I was pregnant with Holly and I felt so bad that I was not happy about being pregnant again and yet my sister was having so much trouble.

Stress in your life is a huge factor. Even now, after being gluten-free for 7 yrs, stress always hits my tummy first.

Yesterday, I had a neurologist tell me that because I do not have an official and I felt free to diagnose myself, then I certainly am not celiac. So, I simply told him, "Fine, if it makes you feel better to call me gluten intolerant, then so be it, either way, I CAN'T HAVE GLUTEN!"

You will find a lot of people in this forum and other forums who have a story similiar to yours. I find that very sad. I think research is a must just to find ways to diagnose celiac disease before it's villi damage.

Link to comment
Share on other sites

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. - BluegrassCeliac replied to lasthope2024's topic in Food Intolerance & Leaky Gut
      7

      This forum might be the last hope I have in my life. Please I beg you

    2. - Scott Adams replied to Nacina's topic in Related Issues & Disorders
      1

      14 year old with Celiac & EOE still suffering...

    3. - Nacina posted a topic in Related Issues & Disorders
      1

      14 year old with Celiac & EOE still suffering...

    4. - trents replied to Fluka66's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      5

      Waiting for urgent referral.

    5. - Fluka66 replied to Fluka66's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      5

      Waiting for urgent referral.


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      121,067
    • Most Online (within 30 mins)
      7,748

    myneckmybackmyceliac
    Newest Member
    myneckmybackmyceliac
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      120.3k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • BluegrassCeliac
      Hi,   Not saying Thiamine (B1) couldn't be an issue as well, but Mg was definitely the cause of my problems. It's the only thing that worked. I supplemented with B vitamins, but that didn't change anything, in fact they made me sick. Mg stopped all my muscle pain (HCTZ) within a few months and fixed all the intestinal problems HCTZ caused as well. Mom has an allergy to some sulfa drugs (IgG Celiac too), but I don't think I've ever taken them. Mg boosted my energy as well. It solved a lot of problems. I take 1000mg MgO a day with no problems. I boost absorption with Vitamin D. Some people can't take MgO,  like mom, she takes Mg Glycinate. It's one of those things that someone has try and find the right form for themselves. Everyone's different. Mg deficiency can cause anxiety and is a treatment for it. A pharmacist gave me a list of drugs years ago that cause Mg deficiency: PPIs, H2 bockers, HCTZ, some beta blockers (metoprolol which I've taken -- horrible side effects), some anti-anxiety meds too were on it. I posted because I saw he was an IgG celiac. He's the first one I've seen in 20 years, other than my family. We're rare. All the celiacs I've met are IgA. Finding healthcare is a nightmare. Just trying to help. B  
    • Scott Adams
      It sounds like you've been through a lot with your son's health journey, and it's understandable that you're seeking answers and solutions. Given the complexity of his symptoms and medical history, it might be beneficial to explore a few avenues: Encourage your son to keep a detailed journal of his symptoms, including when they occur, their severity, any triggers or patterns, and how they impact his daily life. This information can be valuable during medical consultations and may help identify correlations or trends. Consider seeking opinions from specialized medical centers or academic hospitals that have multidisciplinary teams specializing in gastrointestinal disorders, especially those related to Celiac disease and Eosinophilic Esophagitis (EOE). These centers often have experts who deal with complex cases and can offer a comprehensive evaluation. Since you've already explored alternative medicine with a nutrition response doctor and a gut detox diet, you may want to consider consulting a functional medicine practitioner. They take a holistic approach to health, looking at underlying causes and imbalances that may contribute to symptoms. Given his low vitamin D levels and other nutritional markers, a thorough nutritional assessment by a registered dietitian or nutritionist specializing in gastrointestinal health could provide insights into any deficiencies or dietary adjustments that might help alleviate symptoms. In addition to routine tests, consider asking about more specialized tests that may not be part of standard screenings. These could include comprehensive stool analyses, food intolerance testing, allergy panels, or advanced imaging studies to assess gut health.
    • Nacina
      Hello, I am a 45 year old mom, who was diagnosed at 29 with Celiac. My now 14 year old son was diagnosed just before his 4th birthday. Needless to say, we are old pros with the diet. He was experiencing some issues, overall health took a major plummet a year ago, and through a bit of work, was diagnosed with EOE. Tried diet alone, but his follow up endoscopy didn't show the improvements his DR. wanted to see, so I tried the medication. (Steroid). He became extremely backed up, and they had him taking Miralax daily. His health plummeted. He is a straight A honor's 8th grader who plays club soccer very competitively. His health continued to decline and at 13 had a colonoscopy and another upper gi. (He was still compacted even with the prep). I finally pulled him off all meds and mira lax, after reading much negative literature online, and put him on a gut detox diet and took him to a nutrition response dr. Finally things have improved. However...over a year later and he is having relapse stomach pain, debilitating stomach pain. Missing a day of school a week, to three this week. This is where we downward spiral with him. He says it doesn't feel the same as when he has gotten backed up before. He is eating prunes, taking his supplements, drinking water...all of the things. Yet, he is feeling horrible. Pain is abdomen, headache, lethargy, diarrhea . He is on a strict gluten dairy, egg free diet. He has adapted well in regards to diet. But I feel like we are missing something here. He is too active, too outgoing to be feeling sick all of the time. His Bilirubin is constantly high. His white blood count always runs slightly low. His vitamin D was very low last time he ran tests, (last month) when he was sick for a week. His celiac markers show negative, so it isn't that. His last endoscopy showed no Eosinaphils in his esophagus.  I have taken him to multiple Ped. Gastro specialists. They run tests, and we get zero answers. I meticulously go through labs, hoping to make some sense and maybe catch something. Any thoughts or ideas would greatly be appreciated. 
    • trents
      But if you have been off of wheat for a period of weeks/months leading up to the testing it will likely turn out to be negative for celiac disease, even if you actually have celiac disease. Given your symptoms when consuming gluten, we certainly understand your reluctance to undergo  the "gluten challenge" before testing but you need to understand that the testing may be a waste of time if you don't. What are you going to do if it is negative for celiac disease? Are you going to go back to merrily eating wheat/barley/rye products while living in pain and destroying your health? You will be in a conundrum. Do I or do I not? And you will likely have a difficult time being consistent with your diet. Celiac disease causes inflammation to the small bowel villous lining when gluten containing grains are consumed. This inflammation produces certain antibodies that can be detected in the blood after they reach a certain level, which takes weeks or months after the onset of the disease. If gluten is stopped or drastically reduced, the inflammation begins to decrease and so do the antibodies. Before long, their low levels are not detectable by testing and the antibody blood tests done for diagnosing celiac disease will be negative. Over time, this inflammation wears down the billions of microscopic, finger-like projections that make up the lining and form the nutrient absorbing layer of the small bowel where all the nutrition in our food is absorbed. As the villi bet worn down, vitamin and mineral deficiencies typically develop because absorption is compromised. An endoscopy with biopsy of the small bowel lining to microscopically examine this damage is usually the second stage of celiac disease diagnosis. However, when people cut out gluten or cut back on it significantly ahead of time before the biopsy is done, the villous lining has already experienced some healing and the microscopic examination may be negative or inconclusive. I'm not trying to tell you what to do I just want you to understand what the consequences of going gluten free ahead of testing are as far as test results go so that you will either not waste your time in having the tests done or will be prepared for negative test results and the impact that will have on your dietary decisions. And, who are these "consultants" you keep talking about and what are their qualifications? You are in the unenviable position that many who joint this forum have found themselves in. Namely, having begun a gluten free diet before getting a proper diagnosis but unwilling to enter into the gluten challenge for valid testing because of the severity of the symptoms it would cause them.
    • Fluka66
      Thank you very much for your reply. I hadn't heard of celiac disease but began to notice a pattern of pain. I've been on the floor more than once with agonising pain but this was always put down to another abdominal problem consequently I've been on a roundabout of backwards and forwards with another consultant for many years. I originally questioned this diagnosis but was assured it was the reason for my pain. Many years later the consultant gave up and I had a new GP. I started to cut out certain food types ,reading packets then really started to cut out wheat and went lactose free. After a month I reintroduced these in one meal and ended screaming in agony the tearing and bloating pain. With this info and a swollen lymph node in my neck I went back to the GP.  I have a referral now . I have also found out that acidic food is causing the terrible pain . My thoughts are this is irritating any ulcers. I'm hoping that after a decade the outlook isn't all bad. My blood test came back with a high marker but I didn't catch what it was. My GP and I have agreed that I won't go back on wheat just for the test due to the pain , my swollen lymph node and blood test results.  Trying to remain calm for the referral and perhaps needed to be more forceful all those years ago but I'm not assertive and consultants can be overwhelming. Many thanks for your reply . Wishing you all the best.
×
×
  • Create New...