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

Celiac Without Weight Loss?


NancyL

Recommended Posts

NancyL Explorer

I believe that I "may" have Celiac Disease (won't know until all of the Doctor reports are in)... at the very least there is something that keeps mimicking an appendicitis that keeps happening in my lower stomach/intestines. Since the doc has finished all of her testing and we're just awaiting biopsy results I've decided to do a gluten-free diet to see if it helps at all. I'm tired of relentless E.R. trips with intense stomach pain BUT I have gained weight, not lost it. I have bloating, painful lower quadrants and have had diarrhea every day for over a year and a half (sorry I realize that's tmi but pertinent to my question :unsure: . Yikes The pain comes and goes. When it's "here" it lasts for about 4 or 5 days, gradually increasing up to it's peak and then gradually lessening.

They tested my gall bladder (hida scan, ultra scan, the works), done a ct on my appendix and drawn blood. This last week, I did a colonoscopy and all they found was a small polyp but did a biopsy on it and my intestinal wall (those are the results I'm waiting for). I'm assuming they'll find nothing wrong. I've tried an IBS diet (which is what my gastro doc keeps thinking is wrong but this is extreme for IBS and the IBS diet didn't help). The last test that they "may" do is the endoscopy camera that you swallow that checks (I think) your small intestine.

I had one gastrointestinal specialist say that I have a "depressed intestine" and wanted to put me on the anti-depressant drug of Paxil. What.Ever... I didn't buy that one and switched docs.

My question for you all that have suffered from gluten intolerance, gluten allergy and Celiac's is.... can you have one of these ailments and NOT lose weight but rather gain it?

btw, I don't know if it is important for the question or not, but I'm a mom, am 42 and overweight by about 50 lbs (most of the weight has been gained in the past 2 years and my youngest son is 4 (so not pregnancies fault).


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



Celiac.com Sponsor (A8-M):



GFinDC Veteran

Yes, you can gain weight with celiac instead of losing it. I have read that it may be because the body goes into starvation mode and packs away every calorie. The reason being that with celiac your intestine is damaged and you can't absorb vitamins normally.

Roda Rising Star

Did they do an upper scope as well at the same time? A biopsy from the colon during a colonoscopy will not diagnose celiac. They need to do an EGD and biopsy the small intestine. And yes I didn't loose weight either. I was overweight when I was diagnoed.

starrytrekchic Apprentice

I also gained weight after I started showing symptoms (I'd always been a normal weight). It took years worth of damage--I went 11 years without being diagnosed--for me to start losing weight unexpectedly. My weight's been steady since going gluten free and the symptoms of those 11 years all disappeared, so it was celiac all along--it just initially made me gain instead of lose.

NancyL Explorer

Did they do an upper scope as well at the same time? A biopsy from the colon during a colonoscopy will not diagnose celiac. They need to do an EGD and biopsy the small intestine.

Well drat. Thank you for letting me know that. The surgical nurse told me that the biopsy would be testing for things like cancer, colitis and celiac. No they didn't do an upper scope at the same time. When I woke up (I have to have general anesthesia for colonoscopy because in the past I fought them unknowingly) my Doctor said to keep my prep instructions as the next step would be using a camera (that I swallow?) to check out my small intestine. I've had an EGD before but it was due to having a hiatal hernia and I don't believe they were looking at anything but my esophagus at the time (and it was a different doctor).

I didn't mention this earlier but having looked around the site at other posts, I realize that I have many other symptoms such as very frequent headaches, limb pain/achiness and the "brain fog" that someone described. I'm also tired all of the time. I've started taking a zumba class in the hopes of regaining some of my former energy.

Marlie Apprentice

An endoscopy requires that they take samples(6 or so) of the small intestine. Not all damage can be seen which is why a biopsy is required.

NancyL Explorer

An endoscopy requires that they take samples(6 or so) of the small intestine. Not all damage can be seen which is why a biopsy is required.

Thanks so much for that info. I'll call my doc on Monday. I'd called her on Friday and her nurse said go ahead and try the gluten-free diet but maybe I should put it off until they do a small intestine biopsy (I'm only entering Day 3 of gluten-free). I don't want to skew the results.


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



Celiac.com Sponsor (A8-M):



ravenwoodglass Mentor

Have they done a celiac panel yet? That would be a good first step if they haven't done one already. Keep in mind that even on gluten you could still have a false negative on both blood and biopsy. I also was the heaviest I had ever been in my life before diagnosis and others have also gained weight as they got sicker so that doesn't rule it out although some doctors will say it does. When you are done with all testing do give the diet a good strict try.

NancyL Explorer

Have they done a celiac panel yet? That would be a good first step if they haven't done one already. Keep in mind that even on gluten you could still have a false negative on both blood and biopsy. I also was the heaviest I had ever been in my life before diagnosis and others have also gained weight as they got sicker so that doesn't rule it out although some doctors will say it does. When you are done with all testing do give the diet a good strict try.

I'm not positive that the celiac panel was included in my blood work. Another great question for my doc on Monday. Her nurse is going to love me (not, lol).

I'm reading a lot about false negatives, does that mean that only the biopsy of the small intestine is the only conclusive and reliable way to diagnose Celiac's? Or can that give a false negative as well?

ravenwoodglass Mentor

I'm not positive that the celiac panel was included in my blood work. Another great question for my doc on Monday. Her nurse is going to love me (not, lol).

I'm reading a lot about false negatives, does that mean that only the biopsy of the small intestine is the only conclusive and reliable way to diagnose Celiac's? Or can that give a false negative as well?

The biopsy can also give a false negative. When your done with testing the best way to know if you need the diet is to do the diet.

MsCurious Enthusiast

moved to new topic - sorry

sarbee Newbie

I feel your pain I am 50 lbs overweight also and they keep telling me it cannot be because I would be losing. I have the brain fog elevated liver counts, also diagnosed with IBS, diet does not work. I have my scope tomorrow and I never thought i would say this but I am hoping that it comes back saying I have celiacs. I am so tired of feeling crappy.

I have also been to the Er 8 times in the last 3 years with serve abdominal pains and they took my gallbladder and thought it was my appendix. It was not. I just want to feel better and I cannot lose weight no matter what i do. I feel that I am wasting so much money on wieght watchers because the weight will not come off.

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,956
    • Most Online (within 30 mins)
      7,748

    ramonaja
    Newest Member
    ramonaja
    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.