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 Long Until gluten-free Diet Helps My Symptoms?


abbycat1

Recommended Posts

abbycat1 Newbie

I finally had my endoscopy done six days ago, along with Prometheus bloodwork. I started gluten-free diet that day. I've had diarrhea (which is my worst symptom) twice since then, including today. I am staying gluten-free at least until I see the doc for results in a month, but I am wondering how long it takes to see some improvement. The diet is harder than I thought but I am really trying to be very careful and am determined to stick to it. How long did it take you to feel better after going gluten-free?


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



Celiac.com Sponsor (A8-M):



BabsV Enthusiast

Everyone is going to have a different answer...depends on symptoms, extent of damage, how quickly your body recovers, how strictly you follow the diet, any accidental glutenings, etc.

I am almost 5 months into the diet and while I am definitely improving I am certainly not 100%. Words of wisdom that were passed from these forums (thank you IrishHeart and others!) to me early on: take a probiotic, keep a food diary and skip the gluten-free replacement foods - go natural and simple at the beginning. I was having lots of problems with all sorts of foods - reacting to loads of things even though they were gluten free. My body's response mechanism was in overdrive and it wasn't until I went on a very simple diet of rice, potatoes, fish, and cooked vegetables (plus bananas - I always did ok with bananas) that I really saw some improvements. I've since been able to start adding other foods back into my diet, today I tried a small piece of cheddar cheese and was able to tolerate it! Big news since this is the first dairy I've had in months.

It is a matter of small steps versus leaps forward for many from what I've read. You have to have patience and give it time. The doctor who diagnosed me said that I should give it 3 months before expecting ANY change (possibly) and 6-12 months on the diet until I started to feel like my old self.

Good luck!

addis001 Apprentice

This was an amazing question.. Since I'm already trying to fit gluten free foods into my lifestyle already. You would think it would work overnight. But after two days of doing the gluten free foods, all I have is diarrhea and stomach cramps..

But even though I still need to see a GI. I feel like a proactive approach is helping me to cope better.

Metoo Enthusiast

It takes some people 6 months or more.

The first week I still had a lot of stomach pain (my main symptom) until someone on here said that some people have to stop eating oats even if they are labeled gluten free. Which I was eating everyday. As soon as I stopped the oats, my stomach pain stopped. It took me until 3-4 weeks before I felt like a new person. After that I have accidental glutenings that then take me 2-3 weeks to heal from. (which are miserable since I react worse now).

pricklypear1971 Community Regular

Are you eating milk products? Lots of Celiacs have issues digesting it, either temporarily as they heal or permanently.

Give it a whirl.

abbycat1 Newbie

Yes, I do eat cheese, maybe that is aggravating my system. I'll skip that and see how it goes. Thanks, everyone for your responses!

abbycat1 Newbie

Just wanted to post an update in case it will help any newcomers like myself; it has been one week since I've experienced an episode and it is so wonderful to NOT have to worry about rushing to the bathroom! I went off dairy since my last post and started taking a probiotic and both of those combined with the gluten free seems to have done the trick. I am thrilled! I am still getting used to the diet but there is so much information available here and on the internet that I am learning fast. Thanks to everyone here for their support. I won't get my blood and biopsy results until Feb 2 but at this point the results don't matter to me; I am staying gluten free and NORMAL forever! YAY!


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



Celiac.com Sponsor (A8-M):



Bubba's Mom Enthusiast

I'm so glad you're doing better. I think we kind of expect we're going to feel fantastic right away once going gluten-free and when we don't we get frustrated?

Stay with a mostly whole foods diet (meat, veggies, fruits, eggs, and dairy only if you tolerate it.)

If you eat gluten-free versions of processed foods it isn't good for healing.

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,071
    • Most Online (within 30 mins)
      7,748

    witeferet
    Newest Member
    witeferet
    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

    • trents
      Maybe celiac but maybe NCGS that was misdiagnosed as IBS morphing gradually into celiac. Is NCGS a new category to you? It shares many of the same GI symptoms with celiac disease but does not damage the small bowel lining like celiac.
    • knitty kitty
      Thiamine has antifungal properties.  The body uses thiamine to keep bacteria and yeasts from overgrowth in the digestive system.   Fluconazole use can cause thiamine deficiency.   Supplementing with thiamine in the form Benfotiamine would be beneficial as Benfotiamine promotes intestinal healing.   Thiamine and the other B vitamins tend to be low in Celiac due to malabsorption.  Talk to your doctor about supplementing vitamins and minerals.
    • Scott Adams
      Welcome @Natalia Revelo, your experience is profoundly difficult and, sadly, not entirely unique within the celiac community. It's the frustrating reality of "silent" or ongoing damage that isn't captured by the MARSH score alone, which only measures active villous atrophy. Your normal biopsy suggests your diet is preventing the classic autoimmune attack, but it doesn't mean your gut has fully healed or that other issues aren't at play. The inflammation from your newly discovered milk and egg allergies is a huge clue; this constant allergic response can create a low-grade inflammatory environment that severely hampers nutrient absorption, effectively creating a "leaky gut" scenario independent of celiac damage. This is likely why your iron stores deplete so rapidly—your body is both unable to absorb it efficiently and may be losing it through inflammation. While the functional medicine path is expensive, it's clearly providing answers and relief that traditional gastroenterology, focused solely on the gluten-free diet and biopsy results, is missing. To move forward, continue the gut-healing protocols your functional doctor recommends (perhaps exploring alternative options to glutamine that won't irritate your cystitis), maintain your strict avoidance of all allergens and irritants, and know that true healing is a multi-faceted process. You might seek a second opinion from a different gastroenterologist who is more knowledgeable about non-responsive celiac disease and the complex interplay of food allergies and micronutrient absorption, but your current path, while costly, seems to be leading you toward the steady health you need.
    • knitty kitty
      Have you had a DNA test to look for Celiac disease genes?  If she doesn't have any celiac specific genes, look for another explanation.  If she does have Celiac genes, assume they are turned on and active Celiac disease is progressing.  All first degree relatives (mother, father, siblings, children) should be genetically tested as well.   Sometimes blood tests are ambiguous or false negatives if one has anemia, diabetes or thiamine deficiency.  Certain medications like antihistamines and steroids can suppress the immune system and result in false negatives or ambiguous results on antibody tests.  
    • Heatherisle
      That was just the visual report, so need to wait for confirmation or otherwise from the results. They did take a biopsy from the upper end of the duodenum(D1). D2 looked unremarkable on the camera. Just wish we didn’t have to wait so long for the results as she’s naturally a very anxious person. But thanks so much for taking the time to answer me
×
×
  • Create New...