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 Our Content
    eNewsletter
    Donate

How Strict Does A Gluten Free Diet Need To Be?


Courtney101

Recommended Posts

Courtney101 Rookie

Since my blood tests for celiac were negative, the doctor told me I do not have celiac disease but may just have a wheat or gluten intolerance. She said that I should try cutting back on wheat a bit and see if that helps my symptoms.

My question is, will just "cutting back" be enough to give an improvement, or do I need to cut it out totally. My Doc says some people can tolerate small amounts, so it shouldn't be necessary to cut it out all together - she only recommends that to people who test positive to celiac.

For those of you who are gluten intolerant but not celiacs, have you found a difference from just cutting back a bit?


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



Celiac.com Sponsor (A8-M):



Dixiebell Contributor

No, cutting back will not be enough. If you are still ingesting gluten, and if it is causing your problems, you will continue to have problems. If you have a wheat or gluten intolerance you should be just as strict as if you were diagnosed celiac. Those tests have a high false negative rate.

What you could do is eat gluten free for three months and then try gluten foods again and see if you have any reactions.

Coinkey Apprentice

When I was figuring out my own gluten intolerance I found that cutting out obvious gluten was enough to see improvements in my symptoms but they didn't clear completely. Once I got some advice from here and other bits and pieces on the internet- I completely stopped all gluten for a month and saw a lot of improvement. Last month I started to see how much I could have without a reaction. I found that I could have a single kitkat mini bite with a slight cramp and nothing else. So the next week I tried two of them (they are about half a cm cubed once you eat the chocolate off it). That caused the usual problems. So, I don't have to worry too much about cross contamination but it's not worth it to eat obvious sources in any amount. So as Dixiebell suggested go completely gluten free for a few months then reintroduce in small amounts to find your threshold.

burdee Enthusiast

When I was figuring out my own gluten intolerance I found that cutting out obvious gluten was enough to see improvements in my symptoms but they didn't clear completely. Once I got some advice from here and other bits and pieces on the internet- I completely stopped all gluten for a month and saw a lot of improvement. Last month I started to see how much I could have without a reaction. I found that I could have a single kitkat mini bite with a slight cramp and nothing else. So the next week I tried two of them (they are about half a cm cubed once you eat the chocolate off it). That caused the usual problems. So, I don't have to worry too much about cross contamination but it's not worth it to eat obvious sources in any amount. So as Dixiebell suggested go completely gluten free for a few months then reintroduce in small amounts to find your threshold.

Just because you don't react with obvious symptoms to small amounts of gluten does NOT mean you 'got away with' eating that. You could develop any number of autoimmune conditions which are related to gluten intolerance (like RA, MS, thyroid problems, sjogren's, lupus, etc., etc.). Of course your doc won't tell you those are related to gluten consumption, but you will get symptoms of those conditions if you continue to eat less than your 'threshhold' amounts of gluten. If you obviously react to gluten at large amounts, you will still react to smaller amounts, but you may not recognize your symptoms as gluten related.

Courtney101 Rookie

Just because you don't react with obvious symptoms to small amounts of gluten does NOT mean you 'got away with' eating that. You could develop any number of autoimmune conditions which are related to gluten intolerance (like RA, MS, thyroid problems, sjogren's, lupus, etc., etc.). Of course your doc won't tell you those are related to gluten consumption, but you will get symptoms of those conditions if you continue to eat less than your 'threshhold' amounts of gluten. If you obviously react to gluten at large amounts, you will still react to smaller amounts, but you may not recognize your symptoms as gluten related.

thanks for the replies everyone :)

I was under the impression that if you have celiac disease, gluten damages the villi of the intestine, but if you are non-celiac gluten intolerant, you don't actually get the physical damage to your intestines, it just makes you feel unwell. Likewise, if you are celiac, then eating even small amounts of gluten WILL cause damage (and can lead to other autoimmune diseases like you mentioned), but if you don't have celiac disease, you don't have an autoimmune disorder only a food intolerance, so how can eating gluten lead to the other illnesses?

Sorry if that makes no sense, it's hard to explain what I mean. Am I wrong?

I'm so confused ><

Dixiebell Contributor

Lots of people have all the symptoms of celiac but test negative for it. The tests are not 100%. They have a high false negative rate. These people eat gluten-free and their symptoms resolve.

Gluten can also damage other organs (brain, skin, bladder, liver, nerves, etc.) not just the intestine.

Kay DH Apprentice

My celiac panel blood tests were negative in 2008 (minor GI problems) and this January. I had the endoscopy and 1 biopsy in May, and it was negative. The tests were flawed for various reasons, but I was still left with not knowing what I have. I do have the HLA-DQ8 gene, like about 12% of the population. It would be good for you to go completely gluten-free to see what effects that has on you. I am more sensitive to gluten now than when I ate the offending complex molecule. I am also healthier overall. If you have celiac or gluten sensitivity, then the best test is how you feel after going gluten-free.

I got the flu a year ago, and a couple of weeks later started the GI, joint, mood, lethargy, and muscle ache symptoms. I went gluten-free, actually gluten-lite a few weeks later because I read that can help joint inflammation. Amazingly, my GI problems resolved in a few days, the brain fog in a week, and the joint problem subsided after a couple of months. It wasn't until I went completely gluten-free in January that my joint, GI, and rashes began to disappear. I sometimes wonder if doctors had ever tested the rashes I had for a few decades for DH, and I went gluten-free, if my thyroid and other problems might not have happened. :)


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



Celiac.com Sponsor (A8-M):



bincongo Contributor

thanks for the replies everyone :)

I was under the impression that if you have celiac disease, gluten damages the villi of the intestine, but if you are non-celiac gluten intolerant, you don't actually get the physical damage to your intestines, it just makes you feel unwell. Likewise, if you are celiac, then eating even small amounts of gluten WILL cause damage (and can lead to other autoimmune diseases like you mentioned), but if you don't have celiac disease, you don't have an autoimmune disorder only a food intolerance, so how can eating gluten lead to the other illnesses?

Sorry if that makes no sense, it's hard to explain what I mean. Am I wrong?

I'm so confused ><

_____________________________

I believe you are correct. The blood tests for antibodies though can be incorrect. If you wanted to know if you had a gene for Celiac than you would also know if you could ever have a chance of developing it. I would recommend gene testing if anyone in your family has Celiac or other autoimmune diseases. I know gene testing isn't fool proof either but it is still pretty good. I know many people on this site say just go gluten free and be done with it. Well for me being completely gluten free is major change in someones life and I wouldn't do it unless I had too. I have too because I am a diagnosed Celiac but if I were just gluten intolerant I would eat based on my symptoms. But that is just my opinion and not shared by all.

anabananakins Explorer

Since my blood tests for celiac were negative, the doctor told me I do not have celiac disease but may just have a wheat or gluten intolerance. She said that I should try cutting back on wheat a bit and see if that helps my symptoms.

My question is, will just "cutting back" be enough to give an improvement, or do I need to cut it out totally. My Doc says some people can tolerate small amounts, so it shouldn't be necessary to cut it out all together - she only recommends that to people who test positive to celiac.

For those of you who are gluten intolerant but not celiacs, have you found a difference from just cutting back a bit?

I'm gluten intolerant; tested negative for celiac and don't have the genes. Seriously, try going entirely gluten free. I probably wouldn't have but for the encouragement to do so that I got here to do it thoroughly and properly, and omg did it change my life! So many random, bizarre symptoms totally resolved. I will eat like I have celiac disease for the rest of my life, no question. I could never go back to feeling like that and getting glutened is awful now. Plus, I think psychologically it's easier being all or nothing about it.

The first time I got glutened was via frying oil. It was maybe 3 weeks into being gluten free. My fries were cooked in the same oil as a breaded product. I knew this in advance but thought I'd be fine as I don't have celiac disease and I made sure not to eat any random crumbs, just the fries. Ha! I was so sick.

I have a friend with celiac disease and I'm actually a lot more sensitive than she is. About the damage it does - I really don't know. But I do know that I get bad neuro symptoms if I eat gluten (mostly balance related) and they've resolved on a gluten free diet. That fits with research findings. Whether I test positive or not, I'm not going to risk doing more neuro damage because that scares me way more than any short term satisfaction I'd get from eating something gluten-y.

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      129,539
    • Most Online (within 30 mins)
      7,748

    Nattific
    Newest Member
    Nattific
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.2k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • Morgan Tiernan
      Hi all! Ive been away for a while navigating this new illness and also studying at university. But im back with so more updates and info, thank you all for your help and support.    Update: I suffered with an infection of my dermatitis herpetiformis a month or so ago. This resulted in a trip to a&e with an extremely swollen face, and a 2 week dose of doxycycline. Of course the infection went down but my dermatitis herpetiformis still remains to pop up every now and again. However, I’m coming up to almost a year being gluten free and I can honestly say the outbreaks are less often and more mild. But I’ve been eating extremely strict on a gluten-free diet (not much eating out and very cross contamination aware), so fingers crossed this continues.  As I am UK based, I have finally got through to dermatology and rheumatology in the NHS (no more private appointments which is great!) She was amazing and agreed on what sounds like dermatitis herpetiformis. However, she has also diagnosed me with chronic urticaria (hives) which will explain the swelling of my face, eyes, lips, and even sometimes tongue! So might be an allergy on the case, or perhaps another autoimmune condition due to the undiagnosed coeliac until this year. A skin biopsy has now been arrange for next month which is positive (there’s talks of me eating gluten for a day to activate the rash also, scary but they will have medication on site!)  Currently, I’m feeling more positive about my diagnosis and am so thankful to my hospital for the ongoing support I wasn’t able to get from my GP.  Things are looking up!
    • Morgan Tiernan
      Hi there! This is something I’ve often wondered too! I’m still going through the process of getting an official dermatitis herpetiformis diagnosis, however I’ve been battling for 3 years and the dermatologists are pretty certain it’s dermatitis herpetiformis/celiac disease with it’s classic appearance and symptoms (it’s nasty stuff!) About 2 years ago before dermatitis herpetiformis was on the cards, I suffered with a terrible episode of seb dermatitis, it was absolutely everywhere and was probs left undiagnosed for months before I could get in with a dermatologist! I used ketaconazole and it seemed to do the trick. However, knowing what we do now, the dermatitis herpetiformis was definitely aggravating/causing this and I found that it was the use of too many steroid creams (they thought I had eczema) and heavy moisturisers bothering my dermatitis herpetiformis.  Since being gluten free for a year, I haven’t really suffered with an episode of the seb dermatitis for a while. Just trying to navigate the dermatitis herpetiformis outbreaks now.  But definitely feel there could be a correlation! 
    • smilebehappy
      Hi, just went to the Tierra Farm site and while no wheat or gluten is listed there was this: Ingredients Dry Roasted Organic Pumpkin Seeds, Sea Salt. *Processed in a facility that handles tree nuts, soy, sesame and milk.  So many of us have other allergies and sensitivities, always check and recheck. These may not be appropriate for all. I have been fine with nuts.com certified gluten free in the past but have not ordered anything in a while so things can change. Hopefully they will continue to be ok.  
    • leahsch
      I have had very mild rosacea on my cheeks for years. I also am celiac abd have recently been diagnosed with rosacea in one eye. I have been prescribed eye drops during the day and a gel at night. 
    • JD-New to Celiac
      Although diagnosed with celiac and dermatitis herpetiformis, I was curious about the celiac genetics and had that testing done on my own. Unfortunately, the lab does not explain the results and any doctor I have asked said I would need to see someone specializing in genetics. I was hoping someone out there might help me understand. Here is what came back and although I understand the HLA DQ2 and HLA DQ8, I wasn't sure what the variants mean and why they repeat twice. Someone said it was a double marker meaning both of my parents gave me copies. I also read having this combination makes my celiac potentially much worse. HLA DQ2 - Positive | HLA DQ8 - Negative HLA Variants Detected: HLA DQA1*05 and again HLA DQA1*05 HLA DQB1*0201 and again HLA DQB1*0201
×
×
  • Create New...