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

Please Help!


mandm1

Recommended Posts

mandm1 Rookie

I am fairly new here, so please bare with me.

I've been diagnosed with microscopic colitis 2 years ago and my current

biopsy showed that I have an inflammation in my small intestine. My GI

doctor informed me that that inflamation is almost always associated

with Celiac Disease. My ville, however, was normal. After the biopsy, I

was put on gluten-free diet (very strict-I checked every source that might

potentially contain gluten). My blood results (CeliaPlus) came back

today and it showed HLA DQ2 being positive and everything else being

negative. I've been on gluten-free diet for over 3 months and see no

improvements whatsoever. I am so confused and frustrated. I just want

to feel better and finally know what's wrong.

Is HLA DQ2 a good indicator of celiac disease?

Any help would be appreciated.


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



Celiac.com Sponsor (A8-M):



CarlaB Enthusiast

HLA DQ2 is a gene that predisposes you to celiac disease. It's carried by approximately 30% of the population, yet only 1% of the population has celiac. It is not diagnostic of celiac disease.

With negative tests and no dietary response you may not have celiac. You can have false negatives on testing however, so it's the lack of dietary response that concerns me.

Are you still eating dairy?

What are your symptoms?

mandm1 Rookie

I am experiencing diarrhea, stomach ache (including bloating) and weight loss (although my weight has been stable for over 2 months).

Before I went on gluten-free diet, I tried dairy free diet for about 1 month and saw no improvements. How long does it take for your ville to show damage? As I stated earlier, my ville looked normal during biopsy.

I also have concerns with this blood test, as I was tested while being on gluten-free diet!

I appreciate your help

CarlaB Enthusiast

The blood test could be negative from you being gluten-free, but what concerns me is that you've seen no improvement at all. With negative tests and no improvement on the diet, it seems that you may need to keep looking.

Have you been tested for Crohn's?

Are you sure you're 100% gluten-free? Is there any risk of cc?

If you do have celiac, cutting out the dairy could be the key to healing. Since you weren't gluten-free when you were dairy-free, it might not have helped then, but may make a difference now.

The fact that you have stopped losing weight is one improvement.

Hopefully, others will chime in here. Are your only symptoms diarrhea, bloating and weight loss? Or do you have other seemingly unrelated symptoms?

ravenwoodglass Mentor

I agree with cutting out the dairy also for at least a couple of months. Also try to minimize your chances of CC, be very careful at home and if possible avoid restaurants and processed foods for a bit. Make sure you have checked every med you take, script or OTC. If you are taking generic drugs don't assume because the name brand is safe the generic will be too.

Have you been scoped? A colonoscopy would rule out Chrons and a bunch of other stuff if you have not had that done.

It does take a long time for some of us to heal and the fact that you are no longer losing weight is, I agree a good sign.

I hope you get some relief soon.

Nantzie Collaborator

I would also suggest making sure you're 100% gluten-free; avoiding second-hand gluten (cross contamination) like the plague, no shared cooking tools, new cutting board, make sure your haircare products, makeup, lotions are gluten-free, etc.

So many times we hear about people getting a diagnosis and being told by their doctor "don't eat gluten". Which is not even close to an accurate way to describe what the gluten-free diet really is.

This is a good place to come to learn how to do the gluten-free diet. Plus, as you've already seen, there are a lot of people who have experience with other health issues that may provide answers for you as well.

Welcome to the board. Make yourself at home.

Nancy

mandm1 Rookie

Thank you for your input!

Ive had colonoscopy and it confirmed that I have Lymphocytic Colitis.

I am having a very tough tough with adjusting to gluten-free diet, so eliminating other things will be a big challenge for me. Would lacoste breath test show if I have dairy allergy?

I try to be extremely careful with eating gluten-free and avoiding cc. However, I like to eat out once a week (its only been a local restaurant with gluten-free menu and Outback).

I am also somewhat puzzled as to why my Dr. gave me Celiac Panel blood test while I am on gluten-free diet. After reading up on celiac disease, I am under assumption that blood test will not be accurate if your are on gluten-free diet.


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



Celiac.com Sponsor (A8-M):



corinne Apprentice

I have collagenous colitis, but I do not have celiac disease. My villi are normal, but there is inflammation. Collagenous and lymphocytic colitis are both types of microscopic colitis. There is a strong correlation between microscopic colitis and celiac disease. Many people with microscopic colitis have a first degree relative with celiac disease and carry the celiac genes. Sometimes those with celiac disease can also develop microscopic colitis.

Often, those with microscopic colitis will improve with a gluten free diet even though they test negative for celiac disease. Similarly they may not be able digest dairy even when a test for lactose intolerance is negative. It may also be worthwhile to try the specific carbohydrate diet (no grains at all, among other things).

Although changes in diet often help or even completely eliminate symptoms of microscopic colitis, they may not be enough. Peptobismol, imodium or lomotil or other antidiarheals are the first line of treatment. If these don't work asacol or failing this steroids (entocort etc.) can bring relief. I would try diet first. I eat a very simple diet - chicken, fish, well-cooked easy to digest veggies ie carrots+green beans, bananas, avocados and I am mostly symptom free. I take imodium or lomotil for the occasional flare.

If you have questions, feel free to PM me. There are also some boards for microscopic colitis.

Archived

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

  • Get Celiac.com Updates:
    Support Celiac.com:
    Join eNewsletter
    Donate

  • Celiac.com Sponsor (A17):
    Celiac.com Sponsor (A17):





    Celiac.com Sponsors (A17-M):




  • Recent Activity

    1. - hjayne19 replied to hjayne19's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      11

      Insomnia help

    2. - xxnonamexx replied to xxnonamexx's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      43

      My journey is it gluten or fiber?

    3. - knitty kitty replied to Charlie1946's topic in Related Issues & Disorders
      45

      Severe severe mouth pain

    4. - Lkg5 replied to Charlie1946's topic in Related Issues & Disorders
      45

      Severe severe mouth pain

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

    • Total Members
      133,099
    • Most Online (within 30 mins)
      7,748

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

    • Total Topics
      121.5k
    • Total Posts
      1m
  • Celiac.com Sponsor (A21):
  • Upcoming Events

  • Posts

    • hjayne19
      Hi @knitty kitty  Just revisiting this to get some help. I found after understanding the extent of my anxiety, my sleep got a little better. Flash forward to a few weeks later I have had a few bad sleeps in a row and I feel desperate for a good nights sleep. I understand worrying about it won’t help but one thing I had tied things too was dairy. Initially when I went gluten free I felt great for the first few weeks then started having some stomach pain. So thought maybe I was lactose intolerant. I started eating lactose free Greek yogurt and that did help take the cramping away I guess. Over the last few months I haven’t eaten it every single day and I went a few weeks without it. The last few nights I did have a small amount with breakfast and noticed that was the only new thing I’ve really added to my diet. I had seen a few other posts about this. Is it possible to still react to lactose free? Would this potentially be a dairy allergy? Or something else. 
    • xxnonamexx
      I have taken the vitamins for a week. Haven't noticed any major changes but I will give it more time to see.
    • knitty kitty
      @Charlie1946,  Sorry I sidetracked your thread a bit.  Apologies. Proton pump inhibitors, like Omeprazole, change the pH in our gastrointestinal systems which allows opportunistic microbes to move in and take over.  Have you been checked for SIBO?  There's a significant link between length of Omeprazole use and SIBO.  I had SIBO, thrush (Candida) and lichen planus and other problems while I was on Omeprazole.  I had to stop taking it.  It was a horrible time, so I understand how painful and frustrating it is.   You change your microbiome (the bacteria and microbes living inside you) by changing what you eat.  They eat what you eat.  Change the menu and you get different customers.   I changed my diet.  I cut out dairy because I was reacting to the casein and lactose.  I cut out all processed foods and most carbohydrates. I ate meat and veggies mostly, some fruit like apples and mandarin oranges.  By cutting out all the excess carbohydrates, lactose, and empty carbs in processed gluten-free foods, the opportunistic microbes get starved out.  SIBO bacteria send chemical messages to our brains demanding more carbs, so be prepared for carb cravings, but don't let the microbiome control you!   The skin and digestive system is continuous.  The health of our outside skin reflects the health of our gastrointestinal system.  Essential B vitamins, like Thiamine B 1 and especially Niacin B 3, are needed to repair intestinal damage and keep bad bacteria in check.  Niacin helps improve not only the intestinal tract, but also the skin.  Sebaceous Hyperplasia is linked to being low in Niacin B 3.  Lichen Planus is treated with Niacinamide, a form of Niacin B 3.   Vitamins are chemical compounds that our bodies cannot make.  We must get them from our food.  If our food isn't digested well (low stomach acid from Omeprazole causes poor digestion), then vitamins aren't released well.  Plus there's a layer of SIBO bacteria absorbing our vitamins first between the food we've eaten and our inflamed and damaged villi that may have difficulty absorbing the vitamins.  So, taking vitamin supplements is a way to boost absorption of essential nutrients that will allow the body to fight off the microbes, repair and heal.   Doctors are taught in medical learning institutions funded by pharmaceutical companies.  The importance of nutrition is downplayed and called old fashioned.  Doctors are taught we have plenty to eat, so no one gets nutritional deficiency diseases anymore.  But we do, as people with Celiac disease, with impaired absorption.  Nutritional needs need to be addressed first with us.  Vitamins cannot be patented because they are natural substances.  But pharmaceutical drugs can be.  There's more money to be made selling pharmaceutical drugs than vitamins.   Makes me wonder how much illness could be prevented if people were screened for Celiac disease much earlier in life, instead of after they've been ill and medicated for years.   Talk to your doctor and dietician about supplementing essential vitamins and minerals.   Interesting Reading: The Duration of Proton Pump Inhibitor Therapy and the Risk of Small Intestinal Bacterial Overgrowth: A Systematic Review and Meta-Analysis https://pmc.ncbi.nlm.nih.gov/articles/PMC12250812/#:~:text=The long-term use of,overgrowth dynamics is less clear. Lichenoid drug eruption with proton pump inhibitors https://pmc.ncbi.nlm.nih.gov/articles/PMC27275/ Nicotinamide: A Multifaceted Molecule in Skin Health and Beyond https://pmc.ncbi.nlm.nih.gov/articles/PMC11857428/
    • Lkg5
      My sebaceous hyperplasia and thrush disappeared when I stopped all dairy.
    • Charlie1946
      @knitty kitty Thank you so much for all that information! I will be sure to check it out and ask my doctor.  I am just at a loss, I am on my 2nd round of miracle mouthwash and I brush and scrape my tongue and (sorry this is gross) it's still coated in the middle 
×
×
  • 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.