Jump to content
  • 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):

What To Do While Waiting For Endoscopy


aliciahere

Recommended Posts

aliciahere Apprentice

So now that I'm diagnosed celiac by bloodwork, I am waiting for the endoscopy. The Dr. indicated that it could be "months and months" until mine is scheduled. Do I clear out my kitchen now, only to have it glutenated when I have to gluten challenge prior to the endoscopy? I'm thinking no, but I would love to get other opinions and to see what other people did. 


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



Celiac.com Sponsor (A8-M):



cyclinglady Grand Master

My endoscopy was 7 weeks after my blood test results were given (my choice....best for my schedule). I kept eating gluten, but my main symptom was anemia so it wasn't hard to do. I didn't have horrible GI symptoms. I ate all my old gluten-containing favorites in excess. That was not good. By the time I had my endoscopy, I did develop some intestinal symptoms mostly from the huge amount I consumed -- I was a glutton for gluten! Hard to say what would be best for you.

Let's see how others respond.

bartfull Rising Star

If it were me I would continue to eat gluten because for a lot if not most people, once you go gluten-free and then challenge, the symptoms are much worse. What I would do is slowly clean out the kitchen but eat all of my favorite things for one meal a day. I might have an english muffin one day, a doughnut the next, maybe make and freeze a lasagna so I could have individual servings. You don't have to eat a LOT for a challenge, just the equivalent of two slices of bread a day. So as you're cleaning the kitchen, keep your "treats" away from the clean part.

 

This will also give you a chance to replace the toaster, wooden spoons, cutting board, etc. a little at a time. Just don't break them out until it's done. And of course you can use up the mayo and other condiments instead of throwing them away.

kareng Grand Master

Sound like you have time to crochet a Bed spread for a King size bed!

Sorry....just wanted to answer the title like that. :)

If you are going to get an endo, keep eating gluten. You might actually talk with the GI group and see if it is really going to be " months and months".

aliciahere Apprentice

hehehe, Kareng, that's funny - love it!

 

I'm in Alberta and wait times for anything "not immediate life threatening" can take months and months, so I'm not surprised, but I will try to get in touch with them to see if it's true.

 

I guess I also am worried about the possible increase in damage and impact to my health (either scenario). I do have some gastro issues, but nothing that I couldn't deal with for a while. It's the mood issues, depression, ability to focus, that I'm concerned about having for months and months.

 

 

Scenario 1: I reduce my gluten intake, but don't eliminate it like I was on before the gluten challenge (I was 80% Paleo). I will still have antibodies active in my system, still have some damage to my intestines, still have some lingering health issues, though not as many as now. I bump up my intake two weeks before, slightly increasing the antibodies, and increasing the damage to my intestines, and impacting my health, though it probably won't hit me as hard because my system is still used to having gluten.

 

Scenario 2: I eliminate gluten as much as humanly possible. This will reduce the antibodies as much as possible, intestines start to heal a bit, most health issues will reduce. Re-introduce gluten two weeks before challenge. Get hit hard by sudden increase. Damage to intestines, antibodies will rise, though only slightly.

 

Scenario 3: Eliminate gluten now, and don't reintroduce prior to endoscopy. Damage may be gone by then, or greatly reduced. They would still get a type of baseline as to what my intestines look like...

 

Scenario 4: Skip the endoscopy, and just eliminate gluten. While this does appeal to me, I do believe that having a baseline record of what my intestines looked like would be valuable in case of issues in the future.

 

 

I can't figure out which scenario would cause the most damage to my health  :(

 

 

 

Uggggg.......perhaps I should have posted this in a separate thread..... lol

ravenwoodglass Mentor

Does your doctor consider you diagnosed? If so I personally would go with option 3 or 4. 

You say you were pretty much gluten free before you challenged to get tested. How did your body react to that challenge? Have you continued to eat gluten after you got the blood work taken? If your symptoms are not too bad you could continue to eat gluten. Keeping in mind that symptoms may get worse or new ones may appear. If your symptoms do happen to become severe do let your doctor know as some will tell you to stop the challenge at that point.

I don't know if they have cancelation lists there but if they do you could ask to be put on one to try and move up your appointment for the endo a bit. 

Best wishes no matter what you decide to do. 

aliciahere Apprentice

Thank you raven, I really appreciate it.

 

My body didn't really like the challenge. Even before, with being mostly gluten free I was starting to become anemic (though controllable through supplements). I hated being on the challenge. I became gassy, bloated, had trouble focusing, easily distracted, mood swings. I got asthma at night during my period (I'm not asthmatic). It was getting worse by the end of six weeks. I was so happy to be diagnosed I almost cried. I've been booked in for a mammogram and ultrasound (at 34), as I have unusual tenderness in one breast (I believe it to be cysts). This developed within the last two weeks of the challenge (I believe it to be related). 

 

I believe that my Dr. does consider me to be diagnosed, but I'm gonna bring it up with him when I see him next week to review other bloodwork (thyroid, hormones/vitamins). He has asked me to go off gluten, then go on it for the two weeks before the endoscopy.


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



Celiac.com Sponsor (A8-M):



nvsmom Community Regular

hehehe, Kareng, that's funny - love it!

 

I'm in Alberta and wait times for anything "not immediate life threatening" can take months and months, so I'm not surprised, but I will try to get in touch with them to see if it's true.

 

I guess I also am worried about the possible increase in damage and impact to my health (either scenario). I do have some gastro issues, but nothing that I couldn't deal with for a while. It's the mood issues, depression, ability to focus, that I'm concerned about having for months and months.

 

 

Scenario 1: I reduce my gluten intake, but don't eliminate it like I was on before the gluten challenge (I was 80% Paleo). I will still have antibodies active in my system, still have some damage to my intestines, still have some lingering health issues, though not as many as now. I bump up my intake two weeks before, slightly increasing the antibodies, and increasing the damage to my intestines, and impacting my health, though it probably won't hit me as hard because my system is still used to having gluten.

 

Scenario 2: I eliminate gluten as much as humanly possible. This will reduce the antibodies as much as possible, intestines start to heal a bit, most health issues will reduce. Re-introduce gluten two weeks before challenge. Get hit hard by sudden increase. Damage to intestines, antibodies will rise, though only slightly.

 

Scenario 3: Eliminate gluten now, and don't reintroduce prior to endoscopy. Damage may be gone by then, or greatly reduced. They would still get a type of baseline as to what my intestines look like...

 

Scenario 4: Skip the endoscopy, and just eliminate gluten. While this does appeal to me, I do believe that having a baseline record of what my intestines looked like would be valuable in case of issues in the future.

 

 

I can't figure out which scenario would cause the most damage to my health  :(

 

 

 

Uggggg.......perhaps I should have posted this in a separate thread..... lol

 

 

I'm in Alberta too, and I chose Scenario 4.  My tTG IgA and EMA IgA were both quite high, I had many symptoms for years, had celiac disease in the family on both sides, and had just bee diagnosed with thyroiditis.  I knew that the wait to see the Gastro was about a year (this was 3 years ago) so I skipped it.  My thinking was that I was 99% sure I had celiac disease so I didn't need it.  I figured that if I continued to have problems in a year or so, then they could scope me then.  At least at that point we could be sure any damage that was there was not caused by gluten because I planned on going gluten-free immediately.  

 

My GI symptoms improved in the first few months so I never did have the endoscopy... actually, I still have never seen a GI specialist.  I didn't really need one though so I'm fine with that.

 

If you do go gluten-free and then do the endoscopy, many guidelines recommend 1-2 slices of bread for 2-4 weeks prior to the procedure.  Two weeks is the minimum according to most doctors.  If you only do 2 weeks, it would be best to eat gluten heavy - two slice, or even three slices, of bread per day.

 

Best wishes in whatever you decide to do.  :)

nvsmom Community Regular

Oops, I forgot to add that I also chose to skip the endoscopy because they can miss celiacs (up to 20% of celiacs) and I didn't want a false negative biopsy to muddy up my determination to eat gluten-free.  I didn't want to risk the false negative result.

Archived

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

  • Celiac.com Sponsor (A19):
  • Member Statistics

    • Total Members
      134,077
    • Most Online (within 30 mins)
      10,442

    terrificterry
    Newest Member
    terrificterry
    Joined
  • Celiac.com Sponsor (A20):
  • Celiac.com Sponsor (A22):
  • Forum Statistics

    • Total Topics
      121.7k
    • Total Posts
      1m
  • Celiac.com Sponsor (A21):
  • Who's Online (See full list)

  • Upcoming Events

  • Posts

    • Aretaeus Cappadocia
      Sigh. I posted this yesterday based on the Safeway website. I went back again today to their website to double check. On the page where they are selling Vanilla Bean flavor, it has a distinct Certified Gluten Free label. Other flavors on the Safeway website didn't have the gluten-free statement. Today I went into the store. None of the flavors I looked at, including Vanilla Bean, have a Gluten Free statement. Is it safe? Who knows. The ingredients are either safe or nearly safe (some have "natural flavor"). There are warnings about "contains milk and soy" but not about wheat - this implies they are safe, but again, who knows. On the other hand, every flavor I checked of their Slow Churn line of ice creams has wheat as an ingredient. 100% not safe.
    • knitty kitty
      Do keep in mind that many of the newly diagnosed have lactose intolerance.  This is because the villi lining the intestinal tract are damaged, and can no longer make the enzyme lactAse which breaks down the milk sugar lactOse.  When the villi grow back (six months to two years), they can again produce the enzyme lactAse, and lactose intolerance is resolved.  However, some people (both those with and without Celiac Disease) are genetically programmed to stop producing lactase as they age.   Do be aware that many processed foods, including ice cream, use Microbial Transglutaminase, a food additive commonly called "meat glue," used to enhance texture and flavor.  This microbial transglutaminase has the same immunogenicity as tissue transglutaminase which the body produces in response to gluten in people with Celiac Disease.  Tissue Transglutaminase (tTg IgA) is measured to diagnose Celiac Disease in blood tests.  Microbial Transglutaminase acts the same as Tissue Transglutaminase, causing increased intestinal permeability and inflammation.   New findings show that microbial transglutaminase may be able to trigger Celiac Disease and other autoimmune and neurodegenerative diseases.   Microbial Transglutaminase is not required to be listed on ingredients labels as it's considered a processing aid, not an ingredient in the U.S.  Microbial Transglutaminase has been GRAS for many years, but that GRAS standing is being questioned more and more as the immunogenicity of microbial transglutaminase is being discovered. Interesting Reading:  Microbial Transglutaminase Is a Very Frequently Used Food Additive and Is a Potential Inducer of Autoimmune/Neurodegenerative Diseases https://pmc.ncbi.nlm.nih.gov/articles/PMC8537092/
    • Aretaeus Cappadocia
      There is a 10 year old post in this forum on Edy's and Dreyer's ice cream. The information is somewhat outdated and the thread is closed to further comment, so here is a new one. Edy's And Dreyer's Grand Vanilla Bean Ice Cream - 1.5 Quart is labeled "Gluten Free". This is a different answer than years gone by. I don't know the answer for any other flavor at this moment. On 1 May, 2026, Edy's website says: "As a general rule, the gluten in Edy's and Dreyer's® frozen dessert products is present only in the added bakery products, such as cookies, cake or brownies. We always label the eight major food allergens on our package by their common name. We recommend to always check the label for the most current information before purchasing and/or consuming a product. The exception to this rule is our Slow Churned French Silk frozen dairy dessert, which contains gluten in the natural flavors." https://www.icecream.com/us/en/brands/edys-and-dreyers/faq It seems that Edy's and Dreyer's are more celiac-friendly than they were 10 years ago. Once I found enough information to make today's buying decision, I stopped researching.
    • Aretaeus Cappadocia
      probably not your situation @Mimiof2, but allow me to add one more to @trents list of celiac-mimics: "olmesartan-induced sprue-like enteropathy"  
    • knitty kitty
      My dad had an Abdominal Aortic Aneurysm.  Fortunately, it was discovered during an exam.  The doctor could feel my dad's heart beating in his stomach/abdomen.  The aneurysm burst when the doctor first touched it in surgery.  Since he was already hooked up to the bypass machine, my dad survived ten more years.  Close call! Triple A's can press on the nerves in the spinal cord causing leg pain.  I'm wondering if bowing the head might have increased the pressure on an aneurysm and then the nerves.   https://gulfcoastsurgeons.com/understanding-abdominal-aortic-aneurysm-symptoms-and-causes/ Abdominal Aortic Aneurysm Presenting as a Claudication https://pmc.ncbi.nlm.nih.gov/articles/PMC4040638/
×
×
  • Create New...