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

Refractory Celiac Disease


beachbel

Recommended Posts

beachbel Apprentice

Hi! I am looking for anyone who has refractory celiac disease or knows a doctor who might specialize in refractory disease. I have been gluten free for almost two years and my gluten tests are going up, not down. My biopsies continue to show celiac sprue, though not as bad as in the beginning. The doctor has me on a steroid to suppress my immune system. I don't have cancer as far as they can tell, thank goodness. I have had a dietician and the person who runs the local support group look through everything I eat, makeup, soaps etc to make sure I am not getting gluten. My doctor said there are just a lot of unknowns now. I am just wondering if there is anyone else out there with a similar experience and any advice. Thanks!


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



Celiac.com Sponsor (A8-M):



Lisa Mentor

Hi beachbel,

I certainly am not well versed as I would like BUT... (don't you hate it when people say that! :( )

If you continue to show levels of active antibodies, it indicates that your body is reacting to gluten from somewhere, according to what I understand.

If your antibodies were negative you you still had no healing of your villi, I would suspect Refractory Sprue, after a reasonable period of time. A person diagnosed with Refractory Sprue does not respond (as in healing of the villi) to the gluten free diet., but would test negative for antibodies.

With a fine tooth comb, I would revisit everything you come into contact with, ingested or not. If you need help with product information, please feel free to ask.

ShayFL Enthusiast

Do you frequently kiss a gluten eater who has not brushed their teeth before kissing you? Do you work with art materials/craft products that might contain gluten? Did y6ou replace old scratched Teflon pans, toasters, cutting boards and wooden spoons in your kitchen? Do you use a "mixed" kitchen where someone else uses flour products? Do you work somewhere where they bake gluten or cook gluten items?

If you have eliminated ANY possibility of CC.....then Im just thinking out loud here, but what I wonder about Refractory Celiac is if something else in the human diet doesnt mimic gliadin and therefore cause the autoimmune reaction, the antibodies and the subsequent intestinal damage.

Do you still have the symptoms?

I think if it were me, I would try a "grain free" diet for 3 months and see a. how I feel and b. retest blood to see if the antibodies are going down. My reasoning would be that if anything can mimic "gluten/gliadin" then it would be in another grain.

It is just a thought........

beachbel Apprentice
Hi beachbel,

I certainly am not well versed as I would like BUT... (don't you hate it when people say that! :( )

If you continue to show levels of active antibodies, it indicates that your body is reacting to gluten from somewhere, according to what I understand.

If your antibodies were negative you you still had no healing of your villi, I would suspect Refractory Sprue, after a reasonable period of time. A person diagnosed with Refractory Sprue does not respond (as in healing of the villi) to the gluten free diet., but would test negative for antibodies.

With a fine tooth comb, I would revisit everything you come into contact with, ingested or not. If you need help with product information, please feel free to ask.

beachbel Apprentice

Thanks very much. I did not realize that refractory sprue should test negative for antibodies, nor does my doctor. I will go through everything again and see if I can find a gluten source. I am wondering if the problem would be that I do share a kitchen with gluten eaters (my family). I keep separate dishes, wash them separately, keep separate appliances, and wash my hands after handling their food. Is this a bad idea?

ShayFL Enthusiast

Do you share their pots and pans? Their wooden spoons? Their cutting boards?

Is any form of wheat flour EVER used in the kitchen? That fine powder gets everywhere and you cannot clean it up. It can settle on dishes, dish towels, cups, strainers for dishes, countertops....it is an ultra fine powder and you can even breath it through your nose or mouth and some can make it's way into your esophagus and be swallowed. Flour is the devil for Celiacs.

Do any of the gluten eaters share your peanut butter, butter, spreads, etc? Where they might be making a sandwich with your peanut butter and double dip the knife leaving bread crumbs in your peanut butter? This is just one example, there are other ways this can happen in a shared kitchen.

beachbel Apprentice
Do you share their pots and pans? Their wooden spoons? Their cutting boards?

Is any form of wheat flour EVER used in the kitchen? That fine powder gets everywhere and you cannot clean it up. It can settle on dishes, dish towels, cups, strainers for dishes, countertops....it is an ultra fine powder and you can even breath it through your nose or mouth and some can make it's way into your esophagus and be swallowed. Flour is the devil for Celiacs.

Do any of the gluten eaters share your peanut butter, butter, spreads, etc? Where they might be making a sandwich with your peanut butter and double dip the knife leaving bread crumbs in your peanut butter? This is just one example, there are other ways this can happen in a shared kitchen.

I keep separate pots, pans, spoons, cutting boards, spreads, peanut butter etc. We do sometimes make cookies, but I am not in the kitchen while they are made or until everything is wiped down and all gluten-free dishes are in a cupboard, but maybe I will rethink using flour. Any other ideas? Thanks!


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



Celiac.com Sponsor (A8-M):



cruelshoes Enthusiast

I have difficulty telling from your original post which bloodwork you have had done as a followup, or what your levels were. It is important to note that simply retesting the TtG is not adequate. Please see below:

Open Original Shared Link

Follow Up Test #1:

tTG-IgA: This test result should be negative

The numerical value of the test doesn

lovegrov Collaborator

Dr. Cynthia Rudert in the Atlanta, Ga., area.

richard

frec Contributor

Hi beachbel--I've been gluten free for six years. I had never been retested before but, given my current health problems, my new gastro thought it was a good idea. My tTG, IgA was 23--positive for celiac antibodies. My endoscopy showed flattened villi. I was quite surprised. I haven't had digestive problems lately. I have muscle and joint problems.

I live by myself so the odds on cross contamination at home are minimal. I've been re-reading all my labels. I called a few more companies and re-checked websites. I stopped a supplement because the company could not tell me where the natural flavors came from. I eat three products that say "packaged in a facility that also processes wheat"; I decided I should give them up.

When I asked this forum for ideas last month someone mentioned drywall contains gluten. Have you remodeled recently? Someone else told me the powder in latex gloves can have gluten.

I don't know if this is any help. Good luck, and be sure to post if you find some obscure new gluten product! I will too.

dilettantesteph Collaborator

People baking in your house might do it. When I threw out the flour after I found out I was sick I was really careful, but still got sick for 3 weeks. Somehow I got some. You may be sensitive enough to need a gluten free household.

beachbel Apprentice
I have difficulty telling from your original post which bloodwork you have had done as a followup, or what your levels were. It is important to note that simply retesting the TtG is not adequate. Please see below:

Open Original Shared Link

It is possbile to have TtG results that are positive, but not be consuming gluten. There are conditions other than celiac that cause elevated TtG readings. Perhaps your doctor should consider some of these conditions in addition to evaluating you for refractory sprue (which is , thankfully, very rare).

Additionally, there are other conditions besides celiac that can cause villi damage.

[url=https://www.celiac.com/articles/50/1/Main-Causes-of-Flattened-Villi/Page1.html]https://www.celiac.com/articles/50/1/Main-C...illi/Page1.html[/ur

Refractory sprue is nothing to screw around with, so definitely discuss anything you read on this forum with your doctor. I hope you figure out what the culprit is and get to the bottom things.

Thanks so much for the info and links. I am still trying to understand the blood tests and which ones matter. My Tissue Transglutaminase AB, IgA was 22 (reference range above 20 is high), My IGA was 225 (reference range 68 - 378), My IgG was detected, My IgG Titer was<1:40 (reference range greater than 1:160 is significant positive).

Which one indicates I am still getting gluten? Which test is the TtG? I really don't understand what each test means.

I appreciate the list of other things it could be - I will show my doctor.

beachbel Apprentice

Oh I should also mention that I do have hypothyroidism and have been on med for it for about a month now. Any help in understanding my blood test results would be very appreciated.

Thanks.

ShayFL Enthusiast

What thyroid med are you on? Did you call to find out if it is gluten-free? Armour and Synthroid are gluten-free. Generics might not be.

Post your labs. Let us look. Thyroid is my bag. :)

nikki-uk Enthusiast

Just wondered if you have read this also

https://www.celiac.com/articles/1125/1/Celi...ries/Page1.html

Good luck :)

cruelshoes Enthusiast
Thanks so much for the info and links. I am still trying to understand the blood tests and which ones matter. My Tissue Transglutaminase AB, IgA was 22 (reference range above 20 is high), My IGA was 225 (reference range 68 - 378), My IgG was detected, My IgG Titer was<1:40 (reference range greater than 1:160 is significant positive).

Which one indicates I am still getting gluten? Which test is the TtG? I really don't understand what each test means.

I appreciate the list of other things it could be - I will show my doctor.

The test that will show you if you are still consuming gluten is the antiGliadin IgA. The result should be as close to 0 as possible. I don't see that test in the list you posted. Your TtG IgA is definitely positive, but as I posted above, that can be related to other things. Definitely follow up with your doctor. Are you still experiencing symptoms, or have those mostly resolved themselves?

If it were me, I would not allow any cooking with wheat flour at all in my kitchen. There is simply too much risk in that. I have read that flour particles can stay airborn for upwards of 2 hours, before settling on surfaces in your kitchen. From there, it is only a hop skip and jump into your GI tract.

I hope you find your answers soon. Your doctor is wise to be following up on things.

beachbel Apprentice

Shayfl asked for my labs, here they are:

My Tissue Transglutaminase AB, IgA was 22 (reference range above 20 is high), My IGA was 225 (reference range 68 - 378), My IgG was detected, My IgG Titer was<1:40 (reference range greater than 1:160 is significant positive).

Yes, I am still having symptoms, mostly pain, but it is now much improved on Entocort (a steroid) my GI put me on. I spent a week in the hospital just recently because I couldn't tolerate any food except gatorade for over a month. I also have gastroparesis so it is hard for the GI to determine what symptoms are coming from celiac and which from GP. I just had another biopsy this week and do not know the results yet, but my GI said it looks like I still have active celiac disease. My biopsy in September showed slight Celiac sprue but it looked like it was responding to the steroid treatment.

So is the IGA test I had done, different from the IgA test that will show if I am still getting exposed to gluten? I want to make sure I have the proper IgA test done.

I appreciate everyone's ideas, it has given me a lot to talk to the dr about.

ShayFL Enthusiast

I though you had thyroid labs for me to look at. :) Cuz you mentioned being hypothyroid. Are your meds gluten-free? Did you check?

Are you Diabetic? GP is associated with Diabetes. And Diabetes is associated with Celiac. This is a common triad.

Lisa Mentor

We are not doctors and we cannot diagnose anyone on the Internet. In fact, that would be very unwise and potentially dangerous.

You have received some really good directions to look into and good information to present to your doctor. Good luck and please keep us informed. ;)

beachbel Apprentice

Sorry, I didn't mean to lead anyone to believe I am looking for a diagnosis. I am just trying to understand if the proper blood tests have been run as there has been confusion on that even with my doctor. I appreciate all the ideas everyone has given, as my doctor has even been looking for ideas too. I have had two dieticians look through everything I eat and do looking for the culprit gluten and nothing has been found. Again, thanks everyone for the ideas and info.

Lisa Mentor
Sorry, I didn't mean to lead anyone to believe I am looking for a diagnosis.

No, no...we are glad to help point you in any direction that might be helpful. :D

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,858
    • Most Online (within 30 mins)
      7,748

    Janet1234
    Newest Member
    Janet1234
    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

    • Rogol72
      Some interesting articles regarding the use of Zinc Carnosine to help heal gastric ulcers, gastritis and intestinal permeability. I would consult a medical professional about it's use. https://www.nature.com/articles/ncpgasthep0778 https://www.rupahealth.com/post/clinical-applications-of-zinc-carnosine---evidence-review https://pmc.ncbi.nlm.nih.gov/articles/PMC7146259/ https://www.fallbrookmedicalcenter.com/zinc-l-carnosine-benefits-dosage-and-safety/
    • Jillian83
      He is. Which makes everything even more difficult. I’m not a believer in “staying for the kids” but I have nowhere to go and it’s not just me, it’s me plus my babies. We live in a beautiful place, lots of land in the country and me and the kids love the place we’ve called home for their entire lives. But Im seeing that he’ll never change, that my kids deserve a happy healthy Momma, and that staying in this as is will be the early death of me. Then I look at the scars covering my entire body…this disease and the chronic stress I’ve been enduring for years that tell me I’m no longer beautiful and no one will ever look at me with interest again. I try self care, try to give myself grace so I can just start loving myself enough to gain strength but the slightest sparkle in my eye and skip in my step attracts his wrath and it all comes crashing ten fold. Life is just absolutely railing me from every single direction leaving me wanting to wave that white flag bc I don’t feel like there’s much hope no matter what happens. 
    • trents
    • Jillian83
      Hi, I was recently diagnosed with Celiac and dermatitis herpetiformis after years of suffering without answers. I lost my mind. I lost my job. I lost so much time. I lost Me. Conventional doctors are opulent come near me and the one who did sat across the room, misdiagnosed me, pumped me full of steroids which collapsed my entire hip for 6 months. So without answers I began my holistic journey. Fast forward a couple of years and still struggling with a mysterious whole body itchy, crawling “skin hell”, perfect teeth now deteriorating, thick hair now thinning rapidly and no more than a day or 2 at most relief….An acquaintance opened up a functional medicine practice. Cash only, I found a way. Within a month tests clearly showing my off the charts gluten allergy/sensitivity as well as the depletion of vital nutrients due to leaky gut and intestinal damage. dermatitis herpetiformis was more than likely what I was experiencing with my skin. I was happy. I thought this is easy, eat healthy Whole Foods, follow the diet restrictions and I finally get to heal and feel confident and like myself again very soon! 😔 Supplements are very pricey but I got them and began my healing. Which leads to the other major issue: not working, stay at home Mom of young kids, entirely financially dependent on my man of 7 plus years. He’s never been supportive of anything I’ve ever done or been thru. He controls everything. I’m not given much money ever at a time and when he does leave money it’s only enough to possibly get gas. His excuse is that I’ll spend it on other things. So my “allowance” is inconsistent and has conditions. He withholds money from me as punishment for anything he wants. Since being diagnosed, he’s gained a new control tactic to use as punishment. He now is in control of when I get to eat. He asked for proof of my diagnosis and diet bc he said I made it up just to be able to eat expensive organic foods. Then after I sent him my file from my doctor he then said she wasn’t a real doctor. 😡. I go days upon days starving, sometimes breaking down and eating things I shouldn’t bc I’m so sick then I pay horribly while he gets annoyed and angry bc I’m not keeping up with all the duties I’m supposed to be doing. His abuse turns full on when I’m down and it’s in these desperate times when I need his support and care the most that I’m punished with silence, being starved, ignored, belittled. He will create more of a mess just bc I’m unable to get up and clean so that when I am better, I’m so overwhelmed with chores to catch up that the stress causes me to go right back into a flare from hell and the cycle repeats. I’m punished for being sick. I’m belittled for starving and asking for healthy clean water. I’m purposely left out of his life. He won’t even tell me he’s going to the grocery or to get dinner bc he doesn’t want me to ask him for anything. I have no one. I have nothing. Im not better. My supplements ran out and I desperately need Vitamin D3 and a methylated B complex at the very minimal just to function….he stares at me blankly…no, a slight smirk, no words. He’s happiest when im miserable and I am miserable.  this is so long and im condensing as much as I can but this situation is so complicated and disgusting. And it’s currently my life. The “IT” girl, the healthy, beautiful, perfect skin, perfect teeth, thick and curly locks for days, creative and talented IT girl….now I won’t even leave this house bc Im ashamed of what this has dont to my body, my skin. Im disgusted. The stress is keeping me from healing and I think he knows that and that’s why he continues to keep me in that state. He doesn’t want me confident or successful. He doesn’t want me healed and healthy bc then how would he put the blame of all his problems on me? This journey has been hell and I’ve been in Hell before. I’ve been killed by an ex, I’ve been raped, robbed, held hostage, abused beyond nightmares but the cruelty I’ve experienced from him bc of this disease is the coldest I’ve ever experienced. I’ve wanted to give up. Starving and in tears, desperate…I found a local food pantry in our small town so I reached out just saying I had Celiac and was on hard times. This woman is blessing me daily with prepared gluten free meals, donations, educational info, people who know this disease and how they manage life and the blessings just keep coming. But it’s overwhelming and I feel like I don’t deserve it at all. He just glared and I know he’s going to sabotage it somehow. I don’t even know what to do anymore. I’m so broken and just want peace and healing. 
    • cristiana
      @Colleen H   I am just curious,  when you were tested for coeliac disease, did the doctors find out if you had any deficiencies? Sometimes muscle pain can be caused by certain deficiencies, for example, magnesium, vitamin D, calcium, and potassium.   Might be worth looking into having some more tests.  Pins and needles can be neuropathy, again caused by deficiencies, such as iron and B12,  which can be reversed if these deficiencies are addressed. In the UK where I live we are usually only tested for iron, B12 and vitamin D deficiencies at diagnosis.   I was very iron anemic and supplementation made a big difference.  B12 was low normal, but in other countries the UK's low normal would be considered a deficiency.  My vitamin D was low normal, and I've been supplementing ever since (when I remember to take it!) My pins and needles definitely started to improve when my known deficiencies were addressed.  My nutritionist also gave me a broad spectrum supplement which really helped, because I suspect I wasn't just deficient in what I mention above but in many other vitamins and minerals.  But a word of warning, don't take iron unless blood tests reveal you actually need it, and if you are taking it your levels must be regularly monitored because too much can make you ill.  (And if you are currently taking iron, that might actually be making your stomach sore - it did mine, so my GP changed my iron supplementation to a gentler form, ferrous gluconate). Lastly, have you been trying to take anything to lessen the pain in your gut?  I get a sore stomach periodically, usually when I've had too much rich food, or when I have had to take an aspirin or certain antibiotics, or after glutening.  When this happens, I take for just a few days a small daily dose of OTC omeprazole.  I also follow a reflux or gastritis diet. There are lots online but the common denominators to these diets is you need to cut out caffeine, alcohol, rich, spicy, acidic food etc and eat small regularly spaced meals.   When I get a sore stomach, I also find it helpful to drink lots of water.  I also find hot water with a few slices of ginger very soothing to sip, or camomile tea.  A wedge pillow at night is good for reflux. Also,  best not to eat a meal 2-3 hours before going to bed. If the stomach pain is getting worse, though, it would be wise to see the doctor again. I hope some of this helps. Cristiana    
×
×
  • 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.