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 Sprue


debmidge

Recommended Posts

debmidge Rising Star

Hi All

Is there a Refractory Sprue patient in the house? Please tell us how they diagnosed this and what must be done for it and what the prognosis is. There is a need to know because I am suspicious that my husband may be at this juncture.

Thank you.

Debmidge

4/2/04


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



Celiac.com Sponsor (A8-M):



Guest perfect

Hi Debmidge,

There are a few people who posted on the old board who do have Refractory Sprue. This is a tough question because I have yet to read anything about the damage from Celiac Disease healing completely. Until there are autopsies done on people with Celiac Disease to see the results of the damage, healing, and anything else, I think we are all in the dark about this subject.

Josephine Newbie

Thomas, I'm not sure I understand your posting. In most cases, if someone with Celiac follows a completely gluten-free diet, their small intestine does heal. It is possible to determine if healing has taken place while the person is still alive.

I was diagnosed with Celiac just before I turned 41 years old. I had symptoms of the illness from early childhood. One year after going gluten-free, I had blood work that showed no antibodies to gluten. I also had a small bowel follow-through (x-ray) that showed complete healing of my small intestine. The gastroenterologist said that, if he hadn't told the x-ray people I had Celiac, they wouldn't have been able to tell. I'm supposed to see him once a year for follow-up (unless I have a problem and need to see him sooner).

Debmidge, how long has your husband been following a gluten-free diet? Has he had follow-up testing (blood work and either endoscopy or small bowel x-ray)? That's how refractory or resistant sprue is diagnosed. If enough time has passed since going gluten-free, the blood work would show if your husband is unknowingly ingesting gluten. An endoscopy or small bowel x-ray would show if healing is complete.

Regards,

Josephine

Guest perfect

Hi Josephine,

Thanks for the information! :) I

Josephine Newbie

Hi, Thomas!

You're most welcome!

I didn't know about the small bowel follow-through until the gastroenterologist ordered it for me last fall. I, too, had assumed the only way to check would be by doing another endoscopy.

Regards,

Josephine

gf4life Enthusiast

Josephine,

How do they check for celiac disease damage with the small bowel follow thru? Just curious, since I had this done, and my son just had it done last week. Do they have to look for something specific when doing it? I was under the impression that it does not give a good enough view of the villi. That has to be done with an endoscopy & biopsy, and looked at under the microscope.

Even then they can't always see the damage unless they look at the cellular level for excess intraepithelial lymphocytes. Which by the way, most labs don't do unless specifically told by the doctor to do it and they can't say 100% that you don't have celiac disease unless they do look at the cellular level if the villi are not visibly damaged.

Thomas,

I agree that research needs to be done on a much wider scale for them to find out exactly what happens in the intestines of people with celiac disease. There is no way to check every inch of the intestinal tract, except during an autopsy. But it would have to be done by researchers looking for specific damage, or else a regular autopsy would just overlook it. They do have that new pill camera that will take thousands of pictures as it travels through your intestines, and they say it can help with diagnosing celiac disease. But I would think it would only be able to see severe cases of damage that is visible and not the early stages.

God bless,

Mariann

debmidge Rising Star

Hi All

Thanks for your replies. I wanted to have more knowledge of refractory sprue and wanted to hear from people who have been diagnosed with this. My husand is faithful on his diet, I make sure that everything he eats is gluten-free. It's been 6 mos gluten-free and we were expecting that he'd at least would feel better by now and at least gaining more weight back.

So, anyone here get to the refractory spruce stage, please let me know some info like how long were you undiagnosed before going gluten free? What were you experiencing to bring you to the R.S. diagnosis (I realize that an endoscopy would diagnose it, but what symptoms were you still getting that made your doctor do the endoscopy?). What treatment are they giving you for the refractory sprue (R.S.)? How long were you gluten free before you realized that you would be having this RS problem?


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



Celiac.com Sponsor (A8-M):



debmidge Rising Star

I wanted to add that my purpose in knowing this is because my husb went gluten-free before endoscopy. I want him to get endoscopy and I want to let him know that if he has R.S. an endoscopy can pick it up. I realize he needs an endoscopy but he's a stubborn man (it's a good thing HE's never gotten pregnant - he wouldn't want to go thru delivery!). He's doctor procedure phobic. I want him to hear from people with R.S. to know that even if he's got that, there's still hope and a good reason why he should get an endoscopy.

thanks

debmidge

Josephine Newbie

Mariann,

I was diagnosed with Celiac in September 2002 by blood work and biopsy. In September 2003, the small bowel follow-through showed total healing and my blood work showed no antibodies to gluten. The gastroenterologist said that damage would have shown on the x-ray. He diagnoses and treats a lot of people with Celiac and he seems to know what he's talking about.

In the case of a person with minimal damage to their small intestines, perhaps he would not rely on an x-ray for a follow-up; I don't know. This wasn't the case with me and I didn't ask him about other possible scenarios. In my case, by the time I was tested, there was no doubt that I had Celiac.

I'm reminded of my mother, who was diagnosed with Type 1 diabetes at the age of 57. She was exhausted and sick for a year before the diagnosis. She was checked specifically for diabetes 2-3 months prior to diagnosis and the test results were "normal". By the time she was diagnosed, she was "this close" to going into a coma. It seems as if there are medical conditions that, unless and until they are full-blown, doctors are not always able to test for and identify. There is still so much for the scientists to learn.

How is your family doing? Why did you & your son have the small bowel follow-through? Are you still seeking a definitive diagnosis for yourself and your children? I hope you aren't having additional health problems.

Take care,

Josephine

Guest gillian502

I have had two small bowel follow through X-Rays, and asked a lot of questions both times I was there. The info I was given was this: The X-Ray will tell if your celiac disease was so advanced that the lower part of the intestine, closest to the colon, and the upper part of the intestine nearer to the stomach, have appeared to have "reversed." In other words, the upper looks more like the lower part and vise versa. That much is obvious on the X-Ray. However, how well your villi are doing and how much they've regenerated can only be seen through biopsy to the small intestine. That's what two different technicians told me. They could be wrong, though, of course, but they both emphasized when they saw me getting too happy about my good results that the X-Ray ONLY shows a certain amount of information, and many, many things can hide from a small bowel X-Ray. To know more, I would need a CT Scan and another biopsy.

As for Refractory Sprue, I am awaiting information now from a doctor because I too may have RS. My antibodies are still very positive after 7 months gluten-free, and I have stomach and abdominal pain and swelling. The dr. suggested a colonoscopy and another endoscopy because of this. If I don't respond soon to the diet, steroids are next. I am praying I don't have RS, because unfortunately the prognosis is not very good. There are exceptions to every rule, though! My understanding is RS is diagnosed if the patient has no improvement on a gluten-free diet, and needs steroids and other treatments to help them along.

gf4life Enthusiast

Gillian, I hope you do not have RS.

Same goes for your husband, Debmidge.

Josephine, the reason I ask about the small bowel x-ray is that I had it done (when they were looking for anything wrong with me, other than celiac disease!) and it was apparently normal. But they weren't lloking for celiac disease. My son just had it done, because the Ped. GI wanted to make sure this intestines were alright structurally, since my son shows a lot of signs of something else going on with him, other than celiac disease. Neither time will the techs discuss anything with me during the procedure about our particular cases. Only the doctor is allowed to discuss it. They would only tell me what they were going to do, and how it was done, not what theywere looking for. And they won't tell me if they found anything abnormal. So I have to wait for my son's follow-up next week. The doctor wants to check him for Inflammatory Bowel Disease also, but we'll see. My insurance wouldn't pay for the IBD first step blood tests through Prometheus, so I don't know what the next step would be. I do not want to have to put my 7 year old through a colonoscopy.

We are all on the diet and dairy free as well. We all had positive results from Enterolab, so I don't know what will happen, other than we are all feeling better on the diet. Maybe the doctor will just be able to look at the improvement and leave it at that...

God bless,

Mariann

debmidge Rising Star

Hi All

I have my doubts about the X Rays and this is why....during my husband's 2003 celiac disease diagnosis, his Gastro told him that his blood work results indicate that he's more than likely has had celiac disease the entire 28 years or so he's been ill. Over the past 28 years he has had numerous GI Barium X-ray series that he can glow in the dark. If they didn't pick celiac disease up on the x ray then when he was so very ill in the beginning & throughout the illness, I doubt an x ray now would show anything. His last x ray series was 1994 so unless they've improved the quality of the medium, I have my doubts.

Gillian, please keep me informed about your potential R.S. diagnosis and what's being done for you. SteveW in another post has just informed us that he may have Crohn's disease in addition to celiac disease, so that's another complication we should consider. Doctors have to realize that celiacs are not immune from other digestive disorders.

In general, I think it's a good idea to discuss this topic (refractory sprue) as it's relevant to us in that we need to have our hard-headed friends/relatives tested for celiac disease. and we need to talk about the aspects of advanced celiac disease. The threat of R.S. could be what gets them (hard headed friends/relatives) to a doctor sooner.

Debmidge

Josephine Newbie

Mariann,

You must be so worried about your son! I am glad to hear that you are all feeling better on the diet and I hope that, if your son does have an additional health concern, it will be fixed easily.

Take care,

Josephine

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,945
    • Most Online (within 30 mins)
      7,748

    Miyasato
    Newest Member
    Miyasato
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.5k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • Jacki Espo
      This happened to me as well. What’s weirder is that within a couple hours of taking paxlovid it subsided. I thought maybe I got glutened but after reading your post not so sure. 
    • Mari
      Hi Tiffany. Thank you for writing your dituation and  circumstancesin such detail and so well writte, too. I particularly noticed what you wrote about brain for and feeling like your brain is swelling and I know from my own experiences that's how it feel and your brain really does swell and you get migraines.    Way back when I was in my 20s I read a book by 2 MD allergist and they described their patient who came in complaining that her brain, inside her cranium, was swelling  and it happened when she smelled a certain chemical she used in her home. She kept coming back and insisting her brain actually swelled in her head. The Drs couldn't explain this problem so they, with her permission, performed an operation where they made a small opening through her cranium, exposed her to the chemical then watched as she brain did swell into the opening. The DRs were amazed but then were able to advise her to avoid chemicals that made her brain swell. I remember that because I occasionally had brain fog then but it was not a serious problem. I also realized that I was becoming more sensitive to chemicals I used in my work in medical laboratories. By my mid forties the brain fog and chemicals forced me to leave my  profession and move to a rural area with little pollution. I did not have migraines. I was told a little later that I had a more porous blood brain barrier than other people. Chemicals in the air would go up into my sinused and leak through the blood brain barrier into my brain. We have 2 arteries  in our neck that carry blood with the nutrients and oxygen into the brain. To remove the fluids and used blood from the brain there are only capillaries and no large veins to carry it away so all those fluids ooze out much more slowly than they came in and since the small capillaries can't take care of extra fluid it results in swelling in the face, especially around the eyes. My blood flow into my brain is different from most other people as I have an arterial ischema, adefectiveartery on one side.   I have to go forward about 20 or more years when I learned that I had glaucoma, an eye problem that causes blindness and more years until I learned I had celiac disease.  The eye Dr described my glaucoma as a very slow loss of vision that I wouldn't  notice until had noticeable loss of sight.  I could have my eye pressure checked regularly or it would be best to have the cataracts removed from both eyes. I kept putting off the surgery then just overnight lost most of the vision in my left eye. I thought at the I had been exposed to some chemical and found out a little later the person who livedbehind me was using some chemicals to build kayaks in a shed behind my house. I did not realize the signifance  of this until I started having appointments with a Dr. in a new building. New buildings give me brain fog, loss of balance and other problems I know about this time I experienced visual disturbances very similar to those experienced by people with migraines. I looked further online and read that people with glaucoma can suffer rapid loss of sight if they have silent migraines (no headache). The remedy for migraines is to identify and avoid the triggers. I already know most of my triggers - aromatic chemicals, some cleaning materials, gasoline and exhaust and mold toxins. I am very careful about using cleaning agents using mostly borax and baking powder. Anything that has any fragrance or smell I avoid. There is one brand of dishwashing detergent that I can use and several brands of  scouring powder. I hope you find some of this helpful and useful. I have not seen any evidence that Celiac Disease is involved with migraines or glaucoma. Please come back if you have questions or if what I wrote doesn't make senseto you. We sometimes haveto learn by experience and finding out why we have some problems. Take care.       The report did not mention migraines. 
    • Mari
      Hi Jmartes71 That is so much like my story! You probably know where Laytonville is and that's where I was living just before my 60th birthday when the new Dr. suggested I could have Celiacs. I didn't go on a gluten challange diet before having the Celiac panel blood test drawn. The results came back as equivical as one antibody level was very high but another, tissue transaminasewas normal. Itdid show I was  allergic to cows milk and I think hot peppers. I immediately went gluten free but did not go in for an endoscopy. I found an online lab online that would do the test to show if I had a main celiac gene (enterolab.com). The report came back that I had inherited a main celiac gene, DQ8, from one parent and a D!6 from the other parent. That combination is knows to sym[tons of celiac worse than just inheriting one main celiac gene. With my version of celiac disease I was mostly constipated but after going gluten-free I would have diarrhea the few times I was glutened either by cross contamination or eating some food containing gluten. I have stayed gluten-free for almost 20 years now and knew within a few days that it was right for me although my recovery has been slow.   When I go to see a  medical provide and tell them I have celiacs they don't believe me. The same when I tell them that I carry a main celiac gene, the DQ8. It is only when I tell them that I get diarrhea after eating gluten that they realize that I might have celiac disease. Then they will order th Vitamin B12 and D3 that I need to monitor as my B12 levels can go down very fast if I'm not taking enough of it. Medical providers haven't been much help in my recovery. They are not well trained in this problem. I really hope this helps ypu. Take care.      
    • knitty kitty
    • DebJ14
×
×
  • 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.