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

Am I Going Gluten-Free For Nothing?


jnish83

Recommended Posts

jnish83 Newbie

hello friends, I am so confused and frustrated now, as I have been for a year or more...

my current ailments: abdominal pain, gas, diarrhea, yellowish stool, vomiting bile/frothy mucous each morning, severe fatigue, nausea, sometimes feeling like Im going to have diarrhea but in fact am constipated, worsening sypmtoms with my menstrual, trouble waking in the wee hours of the morning in sweats

past ailments: migraines, severe allergies, easily catchs colds, treated for slight anemia twice, depression, anxiety, stress

what the docs have figured out (or not figured out) thus far:

neg stool samples for the usual suspects

seen in Emergency a few years back and had normal abd xrays

the only blood tests that came back slightly abnormal:

Gliadin IGA 5

Gliadin IGG 16

TT IGG: 1.07

TT IGA: 0.43

BIOPSY: "unremarkable villi structure with some inflammation seen"

So, last year in Sept 09, I started suffering with severe abdominal pains after eating even a bite of food. I had abnormal stools, mostly diarrhea. Once they got my weak positive blood tests, I waited a month later for my biopsy. During this month of waiting, I was barely able to eat any food, gluten or non. I had been warned not to change my diet before my biopsy so I was eating some gluten, when I was able to force anything down. My biopsy results finally came back, and they told me it was a negative for celiacs. THEY TOLD ME I HAD IBS AND GO HOME AND TAKE PRILOSEC.

My symptoms slowly abided, as did my weight, I dropped 40 lbs within 2 months because of the severity of my abdominal pain. After a while, I started eating as usual and was fine, until this July 2010, my symptoms returned. I went to my doctor and was put on several different acid reducing medications and IBS medications. My symptoms have continued to worsen, abd pain and diarrhea being the worse symptoms.

A few weeks ago, I go to my doctor yet again, and she checks last years biopsy results again and says "well they did note inflammation so maybe you should try to go gluten-free."

My first thought, "ARE YOU SERIOUS? Here you were warning me last year that celiacs causes destruction of the intestine and your GI doc tells me im negative, but here we are a year later saying um maybe you are still?" Doing some checking on my own, I have found according to many websites that IBS does NOT cause inflammation of the intestine...?

So I have been gluten free for 1 week now. I have to say that my abdominal pain and vomiting had subsided yet I am still having yellow runny stools... I will continue on my gluten-free diet until I figure something else out- possibly forever. But missing out on all the regular food has left me wondering:

"DO I REALLY HAVE CELIACS OR AM I GOING ON A LIFETIME DIET FOR NOTHING?"

oh and another interesting note: my lil (half) brother suffered many abdominal problems as a child, they tested him for celiacs but yet again, by the time they got him in for the test he had not been eating at all and the biopsy was negative. they wrote his symptoms off as a milk-protein allergy and he continued to suffer throughout childhood but now is semi-fine as a young adult, oh and I am very short and brother has problems keeping on weight

can anyone tell me what they think of this quasi-diagnosis??


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



Celiac.com Sponsor (A8-M):



mushroom Proficient

Any GI worth his/her salt should, upon negative test results, recommend that the patient try the gluten free diet anyway because there is a 20% false negative rate on the testing. Doctors like their scientific evidence but we as patients sometimes have to live in the fuzzy zone because it's what makes us feel better.

I would definitely give the gluten free (and lactose free) diet a good three month trial and see how you feel at the end of it. If no improvement whatever, then further exploration is called for. However, any improvement will show that you are reacting to what you eat. You just have to find out which things you are reacting to, because it may well be only gluten and possibly lactose, but could also well be other things as well.

By the way, IBS is a diagnosis of exclusion. If they can't come up with anything else, that's the label they stick on you :P

sb2178 Enthusiast

Yeah, you need longer than a week. And you've already seen some improvement.

I also had weakly positive tests with a negative biopsy, but the diet made an enormous difference in quality of life.

Takala Enthusiast

Well, you could always wait for the autopsy....

Remember that one of the symptoms of celiac and gluten intolerance is brain fog or fuzz on the part of the sufferer, lack of wanting to change diet but this myth that the medical profession can somehow produce a medication to relieve the symptoms, and denial on the part of the medical profession that they keep misdiagnosing the majority of people they see with gluten intolerance and/or celiac.....

you won't miss out on the so called "regular" food once you figure out how sick it made you, and you learn to find, prepare, and eat the better stuff we have.

aedixon Newbie

Wow. I'm glad I found this thread. I feel a tiny bit better.

I have been gluten free (mostly, I think) for about a month now. I've dropped 10 pounds and feel pretty good for the most part.

y work folks love to have food around and go out to eat a lot, so maybe I've just taken too many chances in the name of being a team-player. I recently ate at Chuy's - some corn tortilla-based thingies and beans, rice, guacamole. Actually I've been subsisting on a lot of corn tortillas at home too. I've eaten off some gluten free menus, too, that I'm just not certain about. (Like Carraba's.)

When I was first sort of diagnosed with celiac, I immediately began to eat only sandwiches and Udis muffins, plain rice and veggies with just butter, and fruit, yogurt, coffee and usual beverages. I just didn't have a lot of food in the house at that point and I was overwhelmed with not knowing what I could eat. My digestive system was amazing for about that first week, but it's not been as good since then. Not as bad as before, but not as good as at first. So...

Do you think I'm having a corn or milk issue now?

Maybe I just should not eat anything outside of the house for awhile.

Have any thoughts on how exercise plays into how you feel??

I'll keep on keeping on. Maybe a few more months of stricter eating habits will show more improvement.

Thanks for your comments!

Archived

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

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

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





    Celiac.com Sponsors (A17-M):




  • Recent Activity

    1. - Scott Adams replied to Jhona's topic in Introduce Yourself / Share Stuff
      35

      Does anyone here also have Afib

    2. - Jacki Espo replied to CDFAMILY's topic in Related Issues & Disorders
      5

      Covid caused reoccurrence of DH without eating gluten

    3. - Mari replied to tiffanygosci's topic in Coping with Celiac Disease
      1

      New Celiac Mama in My 30s

    4. - Mari replied to Jmartes71's topic in Coping with Celiac Disease
      2

      My only proof


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,953
    • 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

    • Scott Adams
      If black seed oil is working for his Afib, stick to it, but if not, I can say that ablation therapy is no big deal--my mother was out of the procedure in about 1 hour and went home that evening, and had zero negative effects from the treatment. PS - I would recommend that your husband get an Apple watch to monitor his Afib--there is an app and it will take readings 24/7 and give reports on how much of the time he's in it. Actual data like this should be what should guide his treatment.
    • 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
×
×
  • 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.