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

Refractory Celiac Disease


Pagosapig

Recommended Posts

Pagosapig Newbie

So I have been gluten free for a little over 8 months now and I am very strict to not cheat and minimize any chances of cross contamination. When I first started the gluten free diet I saw some improvements, but then these stopped and even regressed. I have continued to lose weight and my gut has not been a happy camper. My GI has said that I most likely have refractory celiac disease and expects to do a combination steroids and constant work with my dietician.

The point of this being, has anyone had a similar experience and is there anything else I should know or expect?


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



Celiac.com Sponsor (A8-M):



cyclinglady Grand Master

Your GI based this new diagnosis on a second biopsy? Were you tested for SIBO at the time of your biopsies?

Depending on the damage first found (I had a Marsh stage IIIB), it can take up to three years for complete healing. First, you must consider age (kids tend to heal faster) and then you must master the gluten free diet. That in itself, has a steep learning curve. Cross contamination is a huge issue. Do you ever eat out? Are you eating whole foods or buying a lot of processed foods? Are you eating enough fats and protein?

Many of us on the forum have discovered that we have temporary or permanent food allergies or intolerances due to villi damage (e.g. milk). Are you keeping a food journal that could help identify intolerances? I found that Xanthan gum found in bread gives me comparable gluten effects (starting with a pinching stomach). The weird thing is that is does not bother my husband who can not eat gluten either.

We are all different. It takes a bit of detective work and patience to heal from celiac disease.

Welcome to the forum and check out our newbie thread under the coping section!

dilettantesteph Collaborator

Here is a study that you can show your GI: http://www.biomedcentral.com/1471-230X/13/40

 

"Here we describe the effects of a 3-6 month diet of whole, unprocessed foods, termed the Gluten Contamination Elimination Diet (GCED), on NRCD. We aim to demonstrate that this diet reclassifies the majority of patients thought to have RCD type 1 (RCD1)."

 

 

 

.

kareng Grand Master

http://www.cureceliacdisease.org/archives/faq/what-is-refractory-sprue

 

 

This doesn't say much, but it links to all the things your doc should rule out before calling it "refractory". And that list assumes that you have been re-biopsied and still have damage.   Can't find the one that says it needs to be 1-2 years with a still positive biopsy.  But, just because you are having some GI issues, doesn't mean you have refractory Celiac.  

GottaSki Mentor

I had continued celiac disease damage for three years post complete gluten removal. My annual endoscopic biopsies actually got worse the first year...no change second and third endo...finally has minor improvement at my fourth annual endo.

I do not have refractory celiac disease. I do have other issues that were preventing healing.

If your doctor diagnosed refractory at eight months, I would get another opinion. The steroids used to treat refractory celiac disease can cause other problems so should not be taken unless all other possible causes of no or slow healing have been ruled out.

Are all your celiac antibodies in normal/negative range?

Pagosapig Newbie

Thank you all for the input. I thought it seemed early for that diagnosis, I am now waiting for a second endoscopy to see what the change is in my villi. I'll be the first to admit that I'm still getting a hang of getting enough nutrients and minerals on my limited diet. But I did test negative for SIBO and my antibody levels seem to be where they should be. As far as cc I don't eat out and I keep my cooking to specific pans that are specifically gluten free. I will be asking my dietician to help me test for other food intolerances (I know dairy is one for sure!). Is there anything else I should ask about when I go in next?

GottaSki Mentor

Thank you all for the input. I thought it seemed early for that diagnosis, I am now waiting for a second endoscopy to see what the change is in my villi. I'll be the first to admit that I'm still getting a hang of getting enough nutrients and minerals on my limited diet. But I did test negative for SIBO and my antibody levels seem to be where they should be. As far as cc I don't eat out and I keep my cooking to specific pans that are specifically gluten free. I will be asking my dietician to help me test for other food intolerances (I know dairy is one for sure!). Is there anything else I should ask about when I go in next?

 

The test for SIBO is not very accurate...forget the percentages...you can google them.  With or without SIBO, probiotics are a very good idea for the healing digestive system -- as long as you can tolerate them.  Digestive enzymes can also help during healing.


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



Celiac.com Sponsor (A8-M):



cap6 Enthusiast

Eight months is not that long and depending on your age I wouldn't consider that long enough for a complete gut healing.  Children heal quickly.  The older you are and the sicker you were, the longer the healing process.  Two years is not uncommon.  Before you can consider refractory you need to consider everything - age, how sick where you, is your home total g.f or is it shared, (as mentioned above) do you eat out or eat any processed foods.  Consider that added ingredients in processed foods can contribute to making you feel sick and cause glutened type reactions. 

  • 4 weeks later...
motheroftwins2010 Rookie

My first doctor started throwing around the refractory diagnosis possibility very early too because I actually got much worse on the gluten-free diet (I have been dairy free for many years before I even knew what celiac was), but I switched hospitals to U of Chicago and we finally figured out that I have fructose intolerance (malabsorbtion in the proper term I believe). I have had to cut out ALL fruit, the fructans group, and sweeteners. I pretty much only eat meat, potatoes, rice and corn very occasionally, and the non-fructan veggies. That has drastically helped my circumstances.Try a low fodmap diet with the slow reintroduction it may help. I also second getting checked for SIBO or just treating it if your doctor thinks that's ok. I tried treating the SIBO it wasn't my problem but it helped me know that was not a concern at the time.

  • 5 years later...
Jpate Rookie
On 8/14/2014 at 5:02 PM, Pagosapig said:

So I have been gluten free for a little over 8 months now and I am very strict to not cheat and minimize any chances of cross contamination. When I first started the gluten free diet I saw some improvements, but then these stopped and even regressed. I have continued to lose weight and my gut has not been a happy camper. My GI has said that I most likely have refractory celiac disease and expects to do a combination steroids and constant work with my dietician.

The point of this being, has anyone had a similar experience and is there anything else I should know or expect?

Hi my name is John and I have had RCD2 for the last 6 years. I am and have been on steroids and immunosuppressents. I have lost 6 kilos in weight within the last 2 years. Now I am waiting to go into hospital for a stem cell transplant. If it happens great otherwise I will just get on with life. 

squirmingitch Veteran

Hi John, you replied to a post from 5 years ago. That person hasn't been here for years.

Oh my goodness John!!! RCD2 for 6 years???!!!!! Oh you poor thing! So you say they are going to do a stem cell transplant on you? When? Please keep in touch with us & let us know how it's going. Meanwhile, hug those doggys & eat that fresh produce from your garden.

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      126,787
    • Most Online (within 30 mins)
      7,748

    Sportsmama73
    Newest Member
    Sportsmama73
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      120.9k
    • Total Posts
      69.7k

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • Debado
      Anybody ever heard of getting a migrane from gluten and coconut oil ONLY at night?   If I consume gluten or coconut oil, even in the morning,  I will get a migrane. But not until half way thru the night. I don't get this. Why at night? Why not right after I eat?
    • trents
      Early on,  DQ2 and DQ8 were the primary genes that have been connected to the potential to develop celiac genes but more recent genetic research suggests there may be more.
    • Brandy969
      What markers /genes are these DNA test? 
    • ABP2025
      After I get the endoscopy done, I’ll try to be in gluten-free diet even if I test negative for celiac disease or NCGS to avoid any complications. It does suck because I love wheat breads and Indian breads like rotis and naans, lol. I guess I have to jump to gluten-free options for those. Again, thanks for all your help.
    • knitty kitty
      @Jack Common, You could do a DNA test to see if you have any of the known genes for Celiac Disease.  If you don't have any genes for celiac disease, look to another source for your health problems.  If you do have celiac disease genes and have improvement on the gluten free diet, you probably have active Celiac.  Further testing would be beneficial. Keep in mind that different gluten containing breads have different amounts of gluten.  Think thick chewy pizza crust and artisan breads, and whole wheat breads for the gluten challenge.  Cookies and pastries do not contain as much gluten.   Since your blood tests were inconclusive, continuing with the gluten challenge may be needed to provoke a stronger autoimmune reaction sufficient for antibodies to get into the blood stream.      
×
×
  • Create New...