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

To Scope, Or Not To Scope?


glutenfreemamax2

Recommended Posts

glutenfreemamax2 Enthusiast

My labs are "negitive" I have my follow up next Thursday with my PCP. He told me when he ordered the labs that he was going to send me to the GI. I went to my son's GI this morning with him, and the appointment turned into my gluten intolerance(son is cleared, fine, and thriving!) She said that they are probably going to want to do a scope. Why am i so freaked by this? I'm petrified, and have so much anxiety about it, it's unreal. Do they HAVE to do the scope, or can I just do the gluten challenge and go that route? I guess i'm not understanding all the different testings. My labs were negitive like I said. I think i have been glutened lately, because my stomach is singing a different tune (there is a LOT of cc in my house) I'm so scared of the scope. Any sugestions or help would be much appreciated!


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



Celiac.com Sponsor (A8-M):



vegan lisa Rookie

If you are afraid of the scope, it's really not so terrible. The "conscious sedation" they use really will make you so relaxed that you won't care a bit about the scope. Most people don't remember the scope at all, and the nurse told me at mine that many people don't remember being at the hospital at all.

One advantage of the scope is that they can look around and see if something else is going on. They can see other problems that might seem like celiac/gluten intolerance and will then find the correct treatment for you. Or you could get a definitive diagnosis of celiac, which has a specific treatment too! All good news, in my opinion.

One disadvantage is that you could be like me, and get a negative biopsy (and no other issues found) and be left on your own. I'm trying the gluten-free diet, but it's hard to get compliance from family when they think it's "just intolerance, so we don't need to go overboard here...". I don't feel like my situation is ideal, but I don't regret doing the scope at all.

Good luck.

Lisa

cassP Contributor

dont be afraid- it should be a breeze. my colonoscopy was EASY (the prep & gas pain after sucked- but you dont get those with the Endo)

anyways- if you're not eating enough gluten tho- the endo could be a complete waste of your time and money-

also the doctor should take 6 biopsies from different areas of the S.I... if he doesnt- that would also be a complete waste... something to think about

glutenfreemamax2 Enthusiast

dont be afraid- it should be a breeze. my colonoscopy was EASY (the prep & gas pain after sucked- but you dont get those with the Endo)

anyways- if you're not eating enough gluten tho- the endo could be a complete waste of your time and money-

also the doctor should take 6 biopsies from different areas of the S.I... if he doesnt- that would also be a complete waste... something to think about

I'm not eating any gluten. I got some I think on Sunday, and I've had a rash, bloating, c (able to go today, but only a little) increased mucus production, foggy brain, and some joint pain. If that is only a little,or cc, I would HATE to see what would happen to me if I ate gluten like I used to. I know that the scope is not accurate if I don't eat gluten. I really don't want to eat it because of how bad it makes me feel.

We don't have any Celiac Dr's in my area, or Dr's who know much. I fell like I'm banging my head agenst the wall. I'm so afraid of being dismissed as a hypochondriac, and them not taking me seriously. Uggghh. Talk about frustrating. I just want them to recognize that it's something, and not nothing. Just please tell me i'm not crazy, and make my husband understand. When we left today, he said "So if it's just an intolerence, then you don't have to worry about cc and things like that right?:" I can't help but get mad at him.

cassP Contributor

you're NOT crazy... and i understand that feeling and wanting to be validated.

if you feel comfortable posting your blood results up here- we could make more sense out of them maybe.. if u look at my results below in my signature- you can see how they look "negative"... but im a positive.

the biggest thing to know is that you're response to the diet is the biggest indicator. and even if you didnt have Celiac- Celiac is ONLY the Autoimmune response in the Small Intestine, and often also in the Skin.... HOWEVER... gluten & Wheat Germ Agglutin can cause ALL KINDS of damage & inflammation thruout the body- it has been linked to Crohns, Ulcers, Barret's Esophagus, Cancers, and Neurological Disorders.... so please understand that "JUST GLUTEN INTOLERANCE" can be just as big a deal as an official Celiac Dx. and even a little cc can be a big deal too.

cyberprof Enthusiast

My labs are "negitive" I have my follow up next Thursday with my PCP. He told me when he ordered the labs that he was going to send me to the GI. I went to my son's GI this morning with him, and the appointment turned into my gluten intolerance(son is cleared, fine, and thriving!) She said that they are probably going to want to do a scope. Why am i so freaked by this? I'm petrified, and have so much anxiety about it, it's unreal. Do they HAVE to do the scope, or can I just do the gluten challenge and go that route? I guess i'm not understanding all the different testings. My labs were negitive like I said. I think i have been glutened lately, because my stomach is singing a different tune (there is a LOT of cc in my house) I'm so scared of the scope. Any sugestions or help would be much appreciated!

The scope would be useless for you...you've been gluten free. Unless you want to do a gluten challenge - 2 or 3 months with multiple servings of wheat/gluten daily and then do the scope.

You could have gene testing or try enterolab. Or try a gluten challenge and use those results to prove to your doc and your family that gluten makes you sick.

glutenfreemamax2 Enthusiast

The scope would be useless for you...you've been gluten free. Unless you want to do a gluten challenge - 2 or 3 months with multiple servings of wheat/gluten daily and then do the scope.

You could have gene testing or try enterolab. Or try a gluten challenge and use those results to prove to your doc and your family that gluten makes you sick.

CC is a big thing in my house, because my husband cooks most nights. He thinks i'm just OCD about it, and taking it way past extream. This past weekend, I had made 2 different mac and cheeses. One for the kids and him, and one for me. He took the serving spoon out of theirs, and rested it in my pot. He's like oh that little bit shouldn't hurt you. It's only a little. Well today, I'm feeling it. I can't 100% blame it on him, but I don't know what else to do to make him realize that this is harmful to my system. We have our first joint counseling session tomorrow.

Is there a way that I can wash a few pots and spoons to uncontaminate them? I will make my own area if necessary and tell him not to cook for me. That's really mean sounding, but I don't know how to say it nicely :(

Any books that I can read, or information out there I can print to make him more aware of the gluten intolerance? He thinks, like i said, that I'm just being OCD about it. :eyeroll:

I'm kind of looking forward to what the GI says. Uggghhh


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



Celiac.com Sponsor (A8-M):



Dixiebell Contributor

Hopefully he will become more understanding with time.

My husband and I had a few heated arguements over the gluten issue. He is actually not criticing the way I want things done now. It took several months for him to come around. Our son is a scout and I think my husband being around other children with other allergies etc. has shown him that our son isn't odd because he is gluten-free. He has also met other people who are gluten-free.

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      132,398
    • Most Online (within 30 mins)
      7,748

    Megannnnn
    Newest Member
    Megannnnn
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.5k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Who's Online (See full list)

    • There are no registered users currently online
  • Upcoming Events

  • Posts

    • Scott Adams
    • Scott Adams
      I had the same thing happen to me at around your age, and to this day it's the most painful experience I've ever had. For me it was the right side of my head, above my ear, running from my nerves in my neck. For years before my outbreak I felt a tingling sensation shooting along the exact nerves that ended up exactly where the shingles blisters appeared. I highly recommend the two shot shingles vaccine as soon as your turn 50--I did this because I started to get the same tingling sensations in the same area, and after the vaccines I've never felt that again.  As you likely know, shingles is caused by chicken pox, which was once though of as one of those harmless childhood viruses that everyone should catch in the wild--little did they know that it can stay in your nervous system for your entire life, and cause major issues as you age.
    • trents
    • Clear2me
      Thanks for the info. I recently moved to CA from Wyoming and in that western region the Costco and Sam's /Walmart Brands have many nuts and more products that are labeled gluten free. I was told it's because those products are packaged and processed  in different  plants. Some plants can be labeled  gluten free because the plant does not also package gluten products and they know that for example the trucks, containers equipment are not used to handle wheat, barely or Rye. The Walmart butter in the western region says gluten free but not here. Most of The Kirkland and Members Mark brands in CA say they are from Vietnam. That's not the case in Wyoming and Colorado. I've spoken to customer service at the stores here in California. They were not helpful. I check labels every time I go to the store. The stores where I am are a Sh*tshow. The Magalopoly grocery chain Vons/Safeway/Albertsons, etc. are the same. Fishers and Planters brands no longer say gluten free. It could be regional. There are nuts with sugar coatings and fruit and nut mixes at the big chains that are labeled gluten free but I don't want the fruit or sugar.  It's so difficult I am considering moving again. I thought it would be easier to find safe food in a more populated area. It's actually worse.  I was undiagnosed for most of my life but not because I didn't try to figure it out. So I have had all the complications possible. I don't have any spare organs left.  No a little gluten will hurt you. The autoimmune process continues to destroy your organs though you may not feel it. If you are getting a little all the time and as much as we try we probably all are and so the damage is happening. Now the FDA has pretty much abandoned celiacs. There are no requirements for labeling for common allergens on medications. All the generic drugs made outside the US are not regulated for common allergens and the FDA is taking the last gluten free porcine Thyroid med, NP Thyroid, off the market in 2026. I was being glutened by a generic levothyroxin. The insurance wouldn't pay for the gluten free brand any longer because the FDA took them all off their approved formulary. So now I am paying $147 out of pocket for NP Thyroid but shortly I will have no safe choice. Other people with allergies should be aware that these foreign generic pharmaceutical producers are using ground shellfish shell as pill coatings and anti-desicants. The FDA knows this but  now just waits for consumers to complain or die. The take over of Wholefoods by Amazon destroyed a very reliable source of good high quality food for people with allergies and for people who wanted good reliably organic food. Bezos thought  he could make a fortune off people who were paying alot for organic and allergen free food by substituting cheap brands from Thailand. He didn't understand who the customers were who were willing to pay more for that food and why. I went from spending hundreds to nothing because Bezo removed every single trusted brand that I was buying. Now they are closing Whole foods stores across the country. In CA, Mill Valley store (closed July 2025) and the National Blvd. store in West Los Angeles (closed October 2025). The Cupertino store will close.  In recent years I have learned to be careful and trust no one. I have been deleberately glutened in a restaurant that was my favorite (a new employee). The Chef owner was not in the kitchen that night. I've had  a metal scouring pad cut up over my food.The chain offered gluten free dishes but it only takes one crazy who thinks you're a problem as a food fadist. Good thing I always look. Good thing they didn't do that to food going to a child with a busy mom.  I give big tips and apologize for having to ask in restaurants but mental illness seem to be rampant. I've learn the hard way.          I don't buy any processed food that doesn't say gluten free.  I am a life long Catholic. I worked for the Church while at college. I don't go to Church anymore because the men at the top decided Jesus is gluten. The special hosts are gluten less not gluten free. No I can't drink wine after people with gluten in their mouth and a variety of deadly germs. I have been abandoned and excluded by my Church/Family.  Having nearly died several times, safe food is paramount. If your immune system collapses as mine did, you get sepsis. It can kill you very quickly. I spent 5 days unconscious and had to have my appendix and gall bladder removed because they were necrotic. I was 25. They didn't figure out I had celiac till I was 53. No one will take the time to tell you what can happen when your immune system gets overwhelmed from its constant fighting the gluten and just stops. It is miserable that our food is processed so carelessly. Our food in many aspects is not safe. And the merging of all the grocery chains has made it far worse. Its a disaster. Krogers also recently purchased Vitacost where I was getting the products I could no longer get at Whole Foods. Kroger is eliminating those products from Vitacost just a Bezos did from WF. I am looking for reliable and certified sources for nuts. I have lived the worst consequences of the disease and being exposed unknowingly and maliciously. Once I was diagnosed I learned way more than anyone should have to about the food industry.  I don't do gray areas. And now I dont eat out except very rarely.  I have not eaten fast food for 30 years before the celiac diagnosis. Gluten aside..... It's not food and it's not safe.  No one has got our backs. Sharing safe food sources is one thing we can do to try to be safe.        
    • Mmoc
      Thank you kindly for your response. I have since gotten the other type of bloods done and am awaiting results. 
×
×
  • 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.