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

Bingeing Before Biopsy


lucky28

Recommended Posts

lucky28 Explorer

I'm down to my last 12 days before my biopsy. (blood work came back positive ttg and DQ2 positive (2.5 variant) last month. I have had years of "IBS-D" which has gotten much worse in the last year and a half. I also have been consistently Vit. D deficient for the last few years as well as other sx that might be too long to list. Well I had the bright idea to go on a gluten binge -clearing the cabinets. (I plan on going gluten-free the day of my biopsy) Up until the last year or so I was always a motivated, upbeat person, this has slowly, insidiously been changing, but boy oh boy has it really changed in the last few weeks! I have been so extremely exhausted I feel like I can barely function! I'm trying to continue eating gluten until my biopsy because I would prefer to have an "official" diagnosis that I could in turn use to persuade some of my immediate family to also get tested (son, brother and sister), but I don't know if I can. Does anyone know what the least amount of gluten I can eat and have it not affect the biopsy?


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



Celiac.com Sponsor (A8-M):



ravenwoodglass Mentor

3 to 4 slices of bread a day is thought to be enough. You will still have a risk of a false negative on the biopsy so glad to hear you are planning on doing the diet. That really is the best test there is.

Fairy Dancer Contributor

I am having blood tests for gluten next week and am in a similar position. I want to rule out celiac disease (because I have a brother with it) although I personally am beginning to suspect a mild to moderate wheat allergy. For the blood tests though I am supposed to keep eating gluten. However I feel so bad after eating wheat and I get such a painful stomach I really don't want to consume it at all at the moment.

If I talk to people about a possible wheat allergy though they seem to expect me to burst out in hives or go into shock, but I know from past experience with allergies they do not always manifest that way. I have an allergy to duck feathers (diagnosed with proper medical testing many years ago) but had been sleeping with a duck feather duvet and pillows at the time without realising that I was reacting to them. I merely woke up every morning feeling like I had been hit by a ten ton truck in my sleep...which is pretty much how I feel these days when I eat a lot of wheat along with other symptoms such as acid reflux, dizziness, vertigo, stomach pain and diarrhoea. Also a constantly stuffy nose and sore itchy eyes so I am wondering about other allergies as well lol.

I have heard that 4 pieces of bread is the amount the recommend although I struggle to eat that much bread normally as I don't really like the stuff all that much. I am a potato, meat, veg, fruit and nuts person but I started eating more wholegrain pasta and bread over the years because it is supposed to be healthy for you...

Thing is is that I don't think that so called healthy wholegrain stuff is really agreeing with me as the more of it I eat the worse I feel!

violentlyserene Rookie

I'm down to my last 12 days before my biopsy. (blood work came back positive ttg and DQ2 positive (2.5 variant) last month. I have had years of "IBS-D" which has gotten much worse in the last year and a half. I also have been consistently Vit. D deficient for the last few years as well as other sx that might be too long to list. Well I had the bright idea to go on a gluten binge -clearing the cabinets. (I plan on going gluten-free the day of my biopsy) Up until the last year or so I was always a motivated, upbeat person, this has slowly, insidiously been changing, but boy oh boy has it really changed in the last few weeks! I have been so extremely exhausted I feel like I can barely function! I'm trying to continue eating gluten until my biopsy because I would prefer to have an "official" diagnosis that I could in turn use to persuade some of my immediate family to also get tested (son, brother and sister), but I don't know if I can. Does anyone know what the least amount of gluten I can eat and have it not affect the biopsy?

I'm in a similar situation. Sliced bread isn't something I eat generally so I've been making a point to find the gluteny things I like and have what seems like an equivalent amount of those instead of bread. Ikea meatballs and maybe Ihop biscuits and gravy are the last things on my list. There's stuff I make at home of course but I'm satisfied with just being able to use different ingredients for those. At least it means I can justify the breadmaker I've wanted for a while! Eventually I'd like a kitchenaid too.

love2travel Mentor

When I had my gluten challenge admittedly I enjoyed it thoroughly because I had no obvious glutening symtoms. So, I actually drew up a list of what to have for the last time and it included about 90 things! Some were:

- Steak and Ale Pie (with puff pastry crust)

- Chicken and Dumplings

- Chicken and Leek Pie

- phyllo pastry

- croissant

- doughnut

- lots of pizza

- ciabatta and other breads

- buns including cinnamon buns

- scones

- biscuits

- English muffin

- lots of homemade pasta

- Beef Wellington

- Triscuit crackers

- flatbreads

- profiteroles

- homemade things containing durum, semolina, kamut

- Beef and Barley Soup

- barley risotto

And the list goes on but I did have a lot of stuff in addition to bread.

I was told I must eat the equivalent of four pieces of bread a day for at least three months.

Archived

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

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

    • Total Members
      133,858
    • Most Online (within 30 mins)
      7,748

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

    • Total Topics
      121.6k
    • Total Posts
      1m
  • Celiac.com Sponsor (A21):
  • Upcoming Events

  • Posts

    • Flash1970
      I never had bad stomach issues before I was diagnosed.  What I did have was anemia  and hashimoto's thyroid disease. The celiac was suspected because I had to keep taking higher and higher doses of synthroid just to try to get out of hypothyroidism and also the unresolved anemia.  Once I had the blood tests,  celiac was confirmed. 
    • Mari
      It is rather amazing to me that I was able to follow, in a general way, your reasoning in this scientific  thesis. It is very good work on your part taking different research papers and tying the information together if not for a cure for celiac disease, the ability to decrease the symptoms of celiac disease and other autoimmune conditions. Now if you can get this into the scientific conversation about autoimmune  problems. I hope so. On a more practical level please give me the name of the thiamine that you recommend. I forgot to copy it the last time you shared it.    Thanks
    • Mari
      Hi Kelly, We have had at keast 2 discussions abour people with Celiacs moving into assisted living. . No easy solutens to the problems  Celiacs face  when they cannot eat the food served so they need to prepare their own meals or order gluten-free meals.  You seem to be coping quite well. It is not clear to me whether you are suffering because you miss the companionship of shared meals or are a little outraged by the unfairness of your situation/ It is unfair but if you managed to force the  facility to provide a gluten-free kitchen they would go bankrupt.  Just too expensive. Many of the residents would become outraged at not eating the gluten foods they love to eat. .I think you have adapted very wellIf this place does provide some foods that are gluten-free but cross contaminated you may be able to use an antigluten enzyme that you could take with meals. The one advertised here, GliadinX works well for me. Bring your own bread and pastries from your freezer. I sympathize. You could still follow through with the suggestions Scott and Trents made.
    • Rory Bokser
      Hi everyone,   I've been struggling with identifying food triggers beyond gluten — things like dairy, soy, corn, and various FODMAPs. Elimination diets are incredibly helpful but the tracking part is a real pain.   I recently came across an app called Tract (tract.health) that's specifically designed for gut health tracking with IBD, IBS, celiac, and elimination diets. It lets you log meals, symptoms, bowel movements, and stress all in one place, and uses AI to help identify patterns between what you eat and how you feel.   For those of us dealing with multiple food intolerances on top of celiac, something like this could be really useful — especially when you're doing a low-FODMAP or specific carbohydrate diet and need to see correlations over weeks of data.   Has anyone here tried it or something similar? Would love to hear what tools others are using to track food intolerances beyond just gluten.
    • HectorConvector
      I take B12 and Vitamin D (1000 I.U) as well. I can't take 500mg twice a day, only once due to cost reasons. I'm getting more than the minimum rda of Niacin in my diet but not supplementing 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.