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
      129,874
    • Most Online (within 30 mins)
      7,748

    Kelly Bates
    Newest Member
    Kelly Bates
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.3k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • knitty kitty
      Being low in B12, Folate B9, ferritin, zinc and copper sounds consistent with anemia which can often occur with Celiac.  What did your doctor recommend? What about your Vitamin D?  It helps regulate the immune system.  
    • ehb
      @knitty kitty thank you I am exploring these options, I really appreciate all the suggestions and info. I am only slightly below the normal range for folate, zinc and copper. And in the low end of the normal range for B12, ferritin, and vitamin A. I’m good for carotene magnesium and iron, but I’ve been taking 400 mg magnesium daily 
    • Alibu
      I just had my endoscopy the other day and the doctor took 12 samples because he said if we're going to find something we're going to find it today LOL. But when he got down there, he said everything looked good. So I have it in my head again that it's going to be negative because everyone I've heard of who had a positive biopsy had their endoscopies where the doctor was like yep, I can see the damage. My tissues all look great apparently. So if they come back negative, I'm not sure where to go from here. Could it still be a non-celiac gluten sensitivity even with my blood work? I thought NCGS didn't show up on blood tests. Is it possible that the biopsy still comes back positive even if everything looked healthy on endoscope? I had it done at a big hospital in the state, so I would think they'd have the kind of equipment where they'd be able to see it well. I even have pictures in my report and they don't seem to have the damage that others have seen.
    • trents
      That's just it. When they are doing an EGD, even with biopsy, if they aren't thinking about celiac disease they may miss it. They should take several samples from both the duodenum and the duodenum bulb. Damage can be patchy and easily missed if sampling isn't through. And patch damage may explain lack of dramatic symptoms. Let me assure you that we frequently have posters on this forum who were silent celiacs for years and were diagnosed incidentally with celiac disease when their docs were checking for other things. They developed other medical problems such as anemia or vitamin and mineral deficiencies, neurological deficits, Hashimodo's thyroid, osteoporois, etc. - non GI symptoms - but their docs recognized those problems as often connected to celiac disease and had them checked for celiac disease, both blood antibody testing and biopsy, and found damage. A couple of years ago the Mayo Clinic did a large study involving over 300 people. They started with those officially diagnosed with celiac disease and also tested their first degree relatives. They found that almost 50% of  the first degree relatives tested positive for celiac disease and many or most were totally caught by surprise because they were largely asymptomatic. Their diagnosis was confirmed by biopsy. I really don't have anything more to say. You have some decisions to make.
    • knitty kitty
      Blood tests are affected by what you've had to eat in the previous day or two and any vitamin supplements you've taken in the past month or two.   If you have been taking vitamins before the time of the blood test, the vitamins supplements could mask a deficiency.  So get the tests before supplementing, or allow eight to twelve weeks for the supplements to wear off.    The thing with blood tests is that they measure what is in the blood, not what is stored inside organs and tissues where vitamins are actually utilized, and may miss subclinical deficiencies.  In times of shortages, the brain can order cells to release their stored vitamins into the blood stream in order to keep important organs like the brain and heart functioning.   Overall, getting blood tests for deficiencies is a good idea if it's available to you.  Ask for an Erythrocyte Transketolace test for Thiamine deficiency.  If you're deficient in any of the B vitamins, take a B Complex with all the B's in it.  The eight B vitamins work with one another like an orchestra.  Supplementing just one can throw the others off.  
×
×
  • Create New...