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

Endoscopy


alexbecka

Recommended Posts

alexbecka Newbie

I have just had blood tests to test if I have Celiac, and I have been doing my research. Should they come back and I need to have an endoscopy should i have eaten gluten and wheat so I am all blown up and uncomfortable for it to have the best effect and pick up whether I am celiac or not?

I have been monitoring my intake over past few days and have realised after eliminating gluten and wheat, barley etc, my stomach has not blown up and I haven't had the discomfort I have had after eating products with gluten or emulcifiers etc present.

Just wondering if I need to intake some glutenous products prior to having endoscopy or if I can stay off it and feel normal once again and it be able to do the same job???

Assistance and advice would be greatly appreciated.


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



Celiac.com Sponsor (A8-M):



Simon Newbie

Hi, I am not a doctor but can advise on what my wife was told to do after her bloods came back high. The consultant would not do the scope unless she had been having a normal gluten diet for at least 2 weeks before the examination. Her bloods were very high so its possible others may be advised to eat gluten for longer. What she did do however was have gluten but reduce the total volume taken.

She had been advised to have more fibre before the test as her condition was simply put down to IBS so she cut out the bread but carried on eating the pasta, cakes etc. This did reduce the amount of bloating a little.

She was also very lucky as the consultant kindly got her scoped within a few weeks of the bloods comming back. hope that helps a little, any questions drop us a line and I can always get Angela to give you some fist hand answers.

Simon

I have just had blood tests to test if I have Celiac, and I have been doing my research. Should they come back and I need to have an endoscopy should i have eaten gluten and wheat so I am all blown up and uncomfortable for it to have the best effect and pick up whether I am celiac or not?

I have been monitoring my intake over past few days and have realised after eliminating gluten and wheat, barley etc, my stomach has not blown up and I haven't had the discomfort I have had after eating products with gluten or emulcifiers etc present.

Just wondering if I need to intake some glutenous products prior to having endoscopy or if I can stay off it and feel normal once again and it be able to do the same job???

Assistance and advice would be greatly appreciated.

eKatherine Apprentice
Hi, I am not a doctor but can advise on what my wife was told to do after her bloods came back high. The consultant would not do the scope unless she had been having a normal gluten diet for at least 2 weeks before the examination. Her bloods were very high so its possible others may be advised to eat gluten for longer. What she did do however was have gluten but reduce the total volume taken.

She had been advised to have more fibre before the test as her condition was simply put down to IBS so she cut out the bread but carried on eating the pasta, cakes etc. This did reduce the amount of bloating a little.

She was also very lucky as the consultant kindly got her scoped within a few weeks of the bloods comming back.

Two weeks is not long enough to be eating gluten to get a positive biopsy if you've been off gluten for a while. Even if a person has been eating gluten continuously, their biopsy may appear negative. If a person's blood tests are positive, they have the disease, and shouldn't need a biopsy.

The biopsy is only positive if you are in the end stages of the disease. Would a cardiologist induce a heart attack before accepting a diagnosis of heart disease?

BostonCeliac Apprentice

Hi -- I'm in the same boat as you basically, just got back positive blood results and am waiting to meet with my Gastro DR & get an endoscopy. Of course the wait is painful because I want to STOP eating gluten, but my DR told me to keep eating it as normal until AFTER the endoscoopy...

Wish I didn't have to - but I've been cutting down a little on the amount I intake until then.

Good luck!

Guest nini

I wish that these Dr.s would stop recommending the outdated methodology of the biopsy to dx Celiac...as ekatherine stated, the biopsy ONLY catches damage in the final stages of the disease and it doesn't make sense to wait until there is damage before implementing preventative measures. If the blood work is positive you absolutely have it. You can only get false negatives, but never ever false positives from blood work, and the biopsy only can confirm the dx, it can never ever ever rule it out, and according to several Celiac experts, AND MY DR. the biopsy is no longer the Gold Standard as the blood tests are becoming more sensitive AND they are recognizing that positive dietary response is THE MOST valid diagnostic tool.

We are NOT at the mercy of these Dr.s, We do NOT have to have their permission to be on the gluten-free diet, and if your blood work is positive, you absolutely have this, so why wait to get better? I like the analogy of a Dr. waiting for a heart attack to dx heart disease. That is what these GI's are doing when they are demanding that there be confirmed damage from a biopsy before they will dx. Celiac.

My opinion is to forego the biopsy and get on to the business of being healthy. My Dr. did not put me through a biopsy, he said that since my bloodwork was so positive, it was not neccessary. He wanted me to go on the diet immedieately and I haven't looked back... I do not think back and wish I'd had the biopsy, why risk an invasive procedure just to satisfy a Dr.s morbid curiousity? Or is it cos they don't make any profit when the patient doesn't do the biopsy and just starts the diet because they want to get on with feeling better sooner? It's your call.

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,556
    • Most Online (within 30 mins)
      7,748

    Rachel Wilson
    Newest Member
    Rachel Wilson
    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

    • Scott Adams
      Your post demonstrates the profound frustration and isolation that so many in the Celiac community feel, and I want to thank you for channeling that experience into advocacy. The medical gaslighting you endured for decades is an unacceptable and, sadly, a common story, and the fact that you now have to "school" your own GI specialist speaks volumes about the critical lack of consistent and updated education. Your idea to make Celiac Disease a reportable condition to public health authorities is a compelling and strategic one. This single action would force the system to formally acknowledge the prevalence and seriousness of the disease, creating a concrete dataset that could drive better research funding, shape medical school curricula, and validate the patient experience in a way that individual stories alone often cannot. It is an uphill battle, but contacting representatives, as you have done with Adam Gray, is exactly how change begins. By framing it as a public health necessity—a matter of patient safety and protection from misdiagnosis and neglect—you are building a powerful case. Your voice and your perseverance, forged through thirty years of struggle, are exactly what this community needs to ensure that no one else has to fight so hard just to be believed and properly cared for.
    • Scott Adams
      I had no idea there is a "Louisville" in Colorado!😉 I thought it was a typo because I always think of the Kentucky city--but good luck!
    • Scott Adams
      Navigating medication safety with Celiac disease can be incredibly stressful, especially when dealing with asthma and severe allergies on top of it. While I don't have personal experience with the HealthA2Z brand of cetirizine, your caution is absolutely warranted. The inactive ingredients in pills, known as excipients, are often where gluten can be hidden, and since the FDA does not require gluten-free labeling for prescription or over-the-counter drugs, the manufacturer's word is essential. The fact that you cannot get a clear answer from Allegiant Health is a significant red flag; a company that is confident its product is gluten-free will typically have a customer service protocol to answer that exact question. In situations like this, the safest course of action is to consider this product "guilty until proven innocent" and avoid it. A better alternative would be to ask your pharmacist or doctor to help you identify a major national brand of cetirizine (like Zyrtec) whose manufacturer has a verified, publicly stated gluten-free policy for that specific medication. It's not worth the risk to your health when reliable, verifiable options are almost certainly available to you. You can search this site for USA prescriptions medications, but will need to know the manufacturer/maker if there is more than one, especially if you use a generic version of the medication: To see the ingredients you will need to click on the correct version of the medication and maker in the results, then scroll down to "Ingredients and Appearance" and click it, and then look at "Inactive Ingredients," as any gluten ingredients would likely appear there, rather than in the Active Ingredients area. https://dailymed.nlm.nih.gov/dailymed/   
    • Scott Adams
      What you're describing is indeed familiar to many in the Celiac community, especially in the early stages of healing. When the intestinal villi are damaged from Celiac disease, they struggle to properly digest and absorb fats, a condition known as bile acid malabsorption. This can cause exactly the kind of cramping and spasms you're seeing, as undigested fats can irritate the sensitive gut lining. It is highly plausible that her reactions to dairy and eggs are linked to their higher fat content rather than the proteins, especially since she tolerates lean chicken breast. The great news is that for many, this does improve with time. As her gut continues to heal on a strict gluten-free diet, her ability to produce the necessary enzymes and bile to break down fats should gradually return, allowing her to slowly tolerate a wider variety of foods. It's a slow process of healing, but your careful approach of focusing on low-fat, nutrient-dense foods like seeds and avocado is providing her system the best possible environment to recover. Many people with celiac disease, especially those who are in the 0-2 year range of their recovery, have additional food intolerance issues which could be temporary. To figure this out you may need to keep a food diary and do an elimination diet over a few months. Some common food intolerance issues are dairy/casein, eggs, corn, oats, and soy. The good news is that after your gut heals (for most people who are 100% gluten-free this will take several months to two years) you may be able to slowly add some these items back into your diet after the damaged villi heal. This article may be helpful: Thank you for sharing your story—it's a valuable insight for other parents navigating similar challenges.
    • Beverage
      I had a very rough month after diagnosis. No exaggeration, lost so much inflammatory weight, I looked like a bag of bones, underneath i had been literally starving to death. I did start feeling noticeably better after a month of very strict control of my kitchen and home. What are you eating for breakfast and lunch? I ignored my doc and ate oats, yes they were gluten free, but some brands are at the higher end of gluten free. Lots of celics can eat Bob's Red Mill gluten-free oats, but not me. I can now eat them, but they have to be grown and processed according to the "purity protocol" methods. I mail order them, Montana Gluten-Free brand. A food and symptoms and activities log can be helpful in tracking down issues. You might be totally aware, but I have to mention about the risk of airborne gluten. As the doc that diagnosed me warned . . Remember eyes, ears, nose, and mouth all lead to your stomach and intestines.  Are you getting any cross contamination? Airborne gluten? Any pets eating gluten (they eat it, lick themselves, you pet them...)? Any house remodeling? We live in an older home, always fixing something. I've gotten glutened from the dust from cutting into plaster walls, possibly also plywood (glues). The suggestions by many here on vitamin supplements also really helped me. I had some lingering allergies and asthma, which are now 99% gone. I was taking Albuterol inhaler every hour just to breathe, but thiamine in form of benfotiamine kicked that down to 1-2 times a day within a few days of starting it. Also, since cutting out inflammatory seed oils (canola, sunflower, grapeseed, etc) and cooking with real olive oil, avocado oil, ghee, and coconut oil, I have noticed even greater improvement overall and haven't used the inhaler in months! It takes time to weed out everything in your life that contains gluten, and it takes awhile to heal and rebuild your health. At first it's mentally exhausting, overwhelming, even obsessive, but it gets better and second nature.
×
×
  • 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.