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

Vomiting, Unable To Process Foods


loca

Recommended Posts

loca Newbie

Hello :) I've been sick since November 2002. Up to that point, I was a somewhat healthy 18 year old girl, active in school and work and whatnot. Anyway, I have always had an intolerance to wheat gluten, and was ok avoiding it until then. In November 2002, however, one of my younger brothers died and since that day, nothing has been staying in me, really. It started out with cereal and milk. I would end up throwing them up. After that, it was basically everything else, but especially processed foods, sugars (except for honey & pure maple syrup) and anything with animal fats in them. I have been to many doctors hundreds of times in the past year plus, with no help. I lost about 20 lbs. in the two weeks following his death. Most doctors brushed it off as grief and told me to see a counselor. I do, and as much as my brother's death saddens me, I've moved on. I've lost a sister, many friends and I've gotten used to death. Other doctors checked for so many other things: lupus (which was the diagnosis based on the ANA levels and some symptoms for quite a while, until my ANA levels were normal again), pancreatitis, gosh I don't even remember most of it!!!

Anyway, my doctor called me a couple days ago after she read an article in some magazine about Celiac and she wanted me to come in to test me again. I really am sick of the tests and my arm looks like a junkie's arm from so many needle pokes. Before I waste the time (and money!!) to go in and be tested, I wanted to come here and see if my symptoms were like anyone else's or if this is just another hope-its-finally-a-diagnosis.

My main symptoms are:

- Vomiting and diarrhea after eating almost anything but fruits, vegetables and unprocessed foods

- Extreme bloating

- My belly looks fat after I eat some things... I go from a size 3 to a size 10 in a matter of minutes, just with my belly, nothing else.

- I don't gain weight no matter what I do

- I'm always tired, to the point where I sleep 12-18 hours a day (and still sleepy after that!)

- Headaches and trouble concentrating

- Feeling stupid because I can never think straight (and I used to be a straight A+ college student). I feel as if I'm in a different world sometimes.

- Trouble driving because I can't always focus correctly

And during the past year, my blood tests have shown (mostly at different times; I've not had a blood test show the same results twice this whole time):

- Extremely low levels of white cells

- Low hemacrit

- Low red cells

- High RDW (whatever that is)

- Low platelet count

- Extremely low Neutrophils and Lymphocytes (whatever they are too)

- High & low ANA levels

- Anemia

Sorry for the long post, but if any of you have the same symptoms or know that these are symptoms for Celiac, please let me know. I don't want more tests, but I don't want to be sick anymore either!

- Bella. :wub:


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



Celiac.com Sponsor (A8-M):



Guest aramgard

Bella, Are you eating any foods with gluten in them? If so, your symptoms do sound like Celiac. The blood tests are not difficult so, if there is a possibility of your getting better why not try the blood tests. You also may have developed a problem with dairy products, because of damage to your intestine. So if you test positive for Celiac, you should also eliminate dairy from your diet for at least a couple of months. Your symptoms sound a lot like many of us Celiac's, but don't despair. We all get used to the diet and compensate with other foods that we can eat, which are much healthier anyway.

gf4life Enthusiast

Bella, You said you have always had an intolerance to wheat gluten. Were you diagnosed with Celiac before? And have you also been avoiding rye and barley glutens? There are many forms of hidden gluten out there, so maybe you have been having gluten all along and did not know it. The stress of losing your brother could have triggered the disease to go into a more active form. It often take a very stressful event to trigger the disease and from that point on the symptoms are much worse until you can get 100% gluten free. I would highly recommend that you get the blood tests done. Your symptoms are consistent with Celiac Disease.

God bless.

Mariann

loca Newbie

I don't know all what foods have gluten in them... I eat mostly a vegan diet now because I can't have animal products but I was never diagnosed when I was little with Celiac. My mom just noticed that whenever she fed me bread or cereal with wheat gluten in it, I would cry and not be able to digest it right, sometimes it would come back up, sometimes it would hurt my stomach. She figured it was that because my nanny had the same problem with one of her kids. So I haven't been eating wheat gluten, but I wasn't even aware that there was other types of gluten! And does everything that has gluten in it have to be mentioned on the label? Because I have problems with other foods that don't say anything about gluten on the label. :\

Can it be diagnosed with just a blood test? My doctor said she wanted to do some test on my intestine as well as the blood work. If it's just blood work though I guess it's not that bad. :)

Thanks a lot and God Bless :)

- Bella :wub:

Aimee Newbie

Mine was diagnosed by a blood test, and then the doctor said that they wanted to biopsy my small intestine to absolutely confirm things and assess the damage done.

It sounds like it quite possibly could be Celiac from what you've described. I also read somewhere that a traumatic emotional experience could spark it as well, which could explain why it showed up immediately following your brothers death. Mine showed up immediately after a surgery, to the day almost.

I'd let the doc run the tests, esp since you've been so sick and miserable for so long. If they come back positive, I'd also opt for a biopsy to see whats going on and confirm things.

I hope you find some answers soon, it sounds like its difficult to function and you shouldn't have to live your life like that.

=)

gf4life Enthusiast

Bella,

They start with the blood test, and then do a small intestinal biopsy. It is not as bad as it sounds. You are asleep for it, and they put a small tube down your throat, into your stomach and look at the upper part of your small intestine. They take a few small tissue samples. It usually doesn't hurt at all, some people have a little bit of a sore throat afterwards. I've had this done twice, and not had any problems with it. the hardest part for me is not being able to eat or drink for the morning of the test. I always end up with a headache.

As for the foods that do contain gluten, no most do not say gluten on the labels. You have to learn what to avoid. There are some nice lists of what to avoid and what is safe, but if you are not completely off gluten right now, then please do not start yet. You need to be on gluten for the testing. Get your doctor to schedule the testing as soon as possible and get it done. Then you can go completely gluten free.

God bless,

Mariann

Archived

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

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

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





    Celiac.com Sponsors (A17-M):




  • Recent Activity

    1. - Scott Adams replied to HAUS's topic in Gluten-Free Foods, Products, Shopping & Medications
      7

      Sainsbury's Free From White Sliced Bread - Now Egg Free - Completely Ruined It

    2. - Scott Adams replied to deanna1ynne's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      13

      Inconclusive results

    3. - deanna1ynne replied to deanna1ynne's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      13

      Inconclusive results

    4. - cristiana replied to HAUS's topic in Gluten-Free Foods, Products, Shopping & Medications
      7

      Sainsbury's Free From White Sliced Bread - Now Egg Free - Completely Ruined It


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      132,436
    • Most Online (within 30 mins)
      7,748

    Vivien Armstrong
    Newest Member
    Vivien Armstrong
    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
      In the U.S., most regular wheat breads are required to be enriched with certain B-vitamins and iron, but gluten-free breads are not required to be. Since many gluten-free products are not enriched, we usually encourage people with celiac disease to consider a multivitamin.  In the early 1900s, refined white flour replaced whole grains, and people began developing serious vitamin-deficiency diseases: Beriberi → caused by a lack of thiamin (vitamin B1) Pellagra → caused by a lack of niacin (vitamin B3) Anemia → linked to low iron and lack of folate By the 1930s–40s, these problems were common in the U.S., especially in poorer regions. Public-health officials responded by requiring wheat flour and the breads made from it to be “enriched” with thiamin, riboflavin, niacin, and iron. Folic acid was added later (1998) to prevent neural-tube birth defects. Why gluten-free bread isn’t required to be enriched? The U.S. enrichment standards were written specifically for wheat flour. Gluten-free breads use rice, tapioca, corn, sorghum, etc.—so they fall outside that rule—but they probably should be for the same reason wheat products are.
    • Scott Adams
      Keep in mind that there are drawbacks to a formal diagnosis, for example more expensive life and private health insurance, as well as possibly needing to disclose it on job applications. Normally I am in favor of the formal diagnosis process, but if you've already figured out that you can't tolerate gluten and will likely stay gluten-free anyway, I wanted to at least mention the possible negative sides of having a formal diagnosis. While I understand wanting a formal diagnosis, it sounds like she will likely remain gluten-free either way, even if she should test negative for celiac disease (Approximately 10x more people have non-celiac gluten sensitivity than have celiac disease, but there isn’t yet a test for NCGS. If her symptoms go away on a gluten-free diet, it would likely signal NCGS).        
    • JoJo0611
    • deanna1ynne
      Thank you all so much for your advice and thoughts. We ended up having another scope and more bloodwork last week. All serological markers continue to increase, and the doc who did the scope said there villous atrophy visible on the scope — but we just got the biopsy pathology report back, and all it says is, “Duodenal mucosa with patchy increased intraepithelial lymphocytes, preserved villous architecture, and patchy foveolar metaplasia,” which we are told is still inconclusive…  We will have her go gluten free again anyway, but how soon would you all test again, if at all? How valuable is an official dx in a situation like this?
    • cristiana
      Thanks for this Russ, and good to see that it is fortified. I spend too much time looking for M&S gluten-free Iced Spiced Buns to have ever noticed this! That's interesting, Scott.  Have manufacturers ever said why that should be the case?  
×
×
  • 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.