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

How Long Did You Take To Be Symptom Free On Gluten Free?


Fred123

Recommended Posts

Fred123 Newbie

I suffered badly for 2 months prior to a blood test I had which came back equivocal for Coeliac. Unfortunately the TtG was just above normal but the Gliadin IgG was negative. However I was so keen to resolve my illness which consisted of the usual symptoms of bloating, flatulence, diarrhoea and cramps along with a few other peculiar ones like bad breath (really bad no just morning breath trust me), tongue ulcers, itchy skin and a peculiarly horrible 'hungry feeling' a lot of the time. That I quit gluten then and there and believed to notice a difference.

After 3 months I 'settled' down to just the typical symptoms of digestive problems (bloating, flatulence, diarrhoea) as well as bad breath and have as of now, 4 Months down the line from stopping gluten, remained at this point. No longer with stomach cramps, itchy skin and all those other peculiarities apart from bad breath which has remained. However what I have I feel is still significant to effect my way of life. I'm not sure if this is significant enough of an improvement to warrant the belief that I have Coeliac, surely things must have alleviated by now.

I guess my long winded question is the one that is the title, how long should it take for someone who has Coeliac to no longer experience symptoms so significant? I know it varies but just from your experience would be helpful to settle my mind as I am anxious I will not be getting better any time soon.

 

Any help or comments would really be appreciated and I'd be happy to give any more info.


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



Celiac.com Sponsor (A8-M):



cyclinglady Grand Master

It took me about seven weeks to resolve digestive issues that only developed between my blood test and biopsy.  But, I already knew about my food allergies and intolerances.   Everyone is different -- it takes lots of time to heal.

 

Have you identified other possible intolerances?  Typically, because of intestinal damage, you temporarily can't digest milk (lactose).  

GFinDC Veteran

Hi Fred,

 

Time to resolve symptoms and heal is extremely variable.  Up to 16 months is not unusual I believe.  That doesn't mean you won't improve over that time, but it may be a bit bumpy road too.  Symptoms may come and go.  Feeling good for a few days a month and getting sick again.  Eventually you should get to where the number of days in a month feeling good is more than the number of days feeling poorly.  Or you could just suddenly turn a corner and start feeling well all the time.  It varies an awful lot between different people.

 

Take a look at the tips below and try following them for a while.  It may be one or more of them will help you.  Patience with your body is very helpful when starting the gluten-free diet.  A simple diet is helpful also, as there are fewer variables to consider.

 

Open Original Shared Link

 

Some starting the gluten-free diet tips for the first 6 months:

Get tested before starting the gluten-free diet.
Get your vitamin/mineral levels tested also.
Don't eat in restaurants
Eat only whole foods not processed foods.
Eat only food you cook yourself, think simple foods, not gourmet meals.
Take probiotics.
Take gluten-free vitamins.
Take digestive enzymes.
Avoid dairy.
Avoid sugars and starchy foods.
Avoid alcohol.

Helpful threads:

FAQ Celiac com
https://www.celiac.com/gluten-free/forum-7/announcement-3-frequently-asked-questions-about-celiac-disease/

Newbie Info 101
https://www.celiac.com/forums/topic/91878-newbie-info-101/

nvsmom Community Regular

I feel mostly better at 14 months gluten-free. I tend to get the occassional set back for no apparent reason but it only lasts a short time rather than the old downward spiral of a few months.

 

I still get headaches for while on most days, and GI issues after some meals. BM's are still not great.

 

Bloating, gas, stomach pain after most meals, deep fatigue, arthralgias, hair loss, muscle cramps and migraines are all greatly improved.

 

As the others said, it can take a long time to get well. Sadly some symptoms are permanent and never improve if irrepairable damage was done. All you can do is wait and see what the gluten-free diet can do for you.

 

Best wishes.

Chrisz1000 Newbie

There are too many variables to put a definitive timeline on it. As others have said its wildly variable from person to person. It depends on age, how long you have been suffering from the symptoms, or maybe how long you have had silent symptoms.

 

Recovery depends on not just going gluten-free, but also in taking digestive enzymes, pro-biotics, having a rich and balanced diet without any processed foods and WITH excercise. Mental health has a role to play and support from loved ones contributes to recovery and well being.

 

Your ability to not accidentally eat gluten is a big contributor to recovery too... in the first months I was accidentally glutenating myself on average every 9 days - I would have recovered quicker had I not had accidents.Now I can go nearly 2 months between mistakes. I hope to have this up to 6 months at a time.

 

One thing for sure is to stick with it, paricularly if you have seen immediate benefits in the first weeks - that is a sign that gluten free must stay with you for life. 6 months should be the point where you revisit your symptoms... until then, chill out and concentrate on eating gluten free and staying healthy!

  • 4 weeks later...
defeatwheat Rookie

I had some improvement almost immediately but other things took some time. Lots of ups and downs. It depends how bad off you were to start and how quickly you can adapt to the new diet. It's hard to look back for me - but it will get better for you. It takes some time to recover and heal. It took some time for my body to get back to itself. Its probably in the months for some symptoms to get better. (So if you are following the diet and still not there yet, that is normal) For me I am still not where I want to be but compared to where I was - almost hospitalized- I'm doing great. Hang in there! The first year is probably the hardest. Good luck!

dilettantesteph Collaborator

I felt an immediate huge improvement just eliminating cereal and bread.  As time went on, I kept reacting to things and I kept learning about which additional things I needed to eliminate from my diet.  I learned that I was sensitive to much lower levels of contamination than typical and I learned a lot more about what to eliminate.  After about a year I was able to be symptom free.  At 6 years now, it is still a challenge to find enough food to be able to be symptom free.  Previously safe food changes sometimes and becomes unsafe and the only way to find out is by eliminating things one at a time until I find the right one.  What a pain.  It is worth all the effort though.  I'm doing much better.  


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



Celiac.com Sponsor (A8-M):



  • 4 weeks later...
huppa76 Newbie

I'm not a diagnosed with Celiac but believe I am gluten sensitive.

 

I felt a difference in a matter of days in regards to headaches, muscle tension & stiffness in my back, stomach rumbling, flatulence, loose stool (love saying that). I gave up eating wheat in an attempt to lose weight, it didnt occur to me that it was causing so much many of 'small' health related problems. I gave it up on sunday night and on thursday I realised "why the h*ll do I feel so good and so awake???" lol

Joint pain lasted longer and got a bit worse actually before it got better. It was gone after about a month or so.

 

Since it takes such a short time to feel better I am conviced I'm only sensitive to it, rather than Celiac. 

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,664
    • Most Online (within 30 mins)
      7,748

    Lkscot0uky
    Newest Member
    Lkscot0uky
    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

    • Inkie
      Thank you for the information ill will definitely bring it into practice .
    • Scott Adams
      While plain, pure tea leaves (black, green, or white) are naturally gluten-free, the issue often lies not with the tea itself but with other ingredients or processing. Many flavored teas use barley malt or other gluten-containing grains as a flavoring agent, which would be clearly listed on the ingredient label. Cross-contamination is another possibility, either in the facility where the tea is processed or, surprisingly, from the tea bag material itself—some tea bags are sealed with a wheat-based glue. Furthermore, it's important to consider that your reaction could be to other substances in tea, such as high levels of tannins, which can be hard on the stomach, or to natural histamines or other compounds that can cause a non-celiac immune response. The best way to investigate is to carefully read labels for hidden ingredients, try switching to a certified gluten-free tea brand that uses whole leaf or pyramid-style bags, and see if the reaction persists.
    • Scott Adams
      This is a challenging and confusing situation. The combination of a positive EMA—which is a highly specific marker rarely yielding false positives—alongside strongly elevated TTG on two separate occasions, years apart, is profoundly suggestive of celiac disease, even in the absence of biopsy damage. This pattern strongly aligns with what is known as "potential celiac disease," where the immune system is clearly activated, but intestinal damage has not yet become visible under the microscope. Your concern about the long-term risk of continued gluten consumption is valid, especially given your family's experience with the consequences of delayed diagnosis. Since your daughter is now at an age where her buy-in is essential for a gluten-free lifestyle, obtaining a definitive answer is crucial for her long-term adherence and health. Given that she is asymptomatic yet serologically positive, a third biopsy now, after a proper 12-week challenge, offers the best chance to capture any microscopic damage that may have developed, providing the concrete evidence needed to justify the dietary change. This isn't about wanting her to have celiac; it's about wanting to prevent the insidious damage that can occur while waiting for symptoms to appear, and ultimately giving her the unambiguous "why" she needs to accept and commit to the necessary treatment. This article might be helpful. It breaks down each type of test, and what a positive results means in terms of the probability that you might have celiac disease. One test that always needs to be done is the IgA Levels/Deficiency Test (often called "Total IGA") because some people are naturally IGA deficient, and if this is the case, then certain blood tests for celiac disease might be false-negative, and other types of tests need to be done to make an accurate diagnosis. The article includes the "Mayo Clinic Protocol," which is the best overall protocol for results to be ~98% accurate.    
    • Scott Adams
      Welcome to the community! Generally, for a gluten challenge before celiac disease blood tests, Tylenol (acetaminophen) is considered safe and should not interfere with your antibody results. The medications you typically need to avoid are those like ibuprofen (Advil, Motrin) or naproxen (Aleve) that can cause intestinal irritation, which could potentially complicate the interpretation of an endoscopy if you were to have one. However, it is absolutely crucial that you confirm this with either your gastroenterologist or your surgeon before your procedure. They know the specifics of your case and can give you the definitive green light, ensuring your surgery is comfortable and your celiac testing remains accurate. Best of luck with your surgery tomorrow
    • Xravith
      Thank you for the advice. I’ve actually never checked for nutritional deficiencies, but for as long as I can remember, I’ve always taken vitamin and mineral supplements — otherwise my symptoms get worse. This week I stopped eating gluten to confirm whether my symptoms are really caused by it. Starting next week, I’ll reintroduce gluten — it’s sad to go back to how I was before — but at least I’ll be able to take the necessary tests properly. I think the diagnostic process will be long, but at least I’m happy that I finally decided to address this doubt I’ve had for years.
×
×
  • 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.