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

Hey Everyone.. New Here.


beachymama

Recommended Posts

beachymama Newbie

Hi everyone!

I'm new here. :) I apologize if this ends up being muddled wall-of-text, I just have so much to say!

I am a 33 year old female, struck with "tummy troubles" sometime around when I started high school. I managed to get through most days by simply not eating until I was safely home and near my bathroom. My parents took me to a gastro, who did (I believe, this was a long time ago) an upper GI only. I had no lower GI or colonoscopy. The gastro prescribed something called Levbid, which I ceased taking shortly thereafter because it didn't help.

From my teen years until now, I just managed to do the above -- I didn't eat. I didn't eat while I was at school, I didn't eat when I worked a full time job, I didn't eat when I had to leave the house. Yet, somehow I'm 5'6" and 230 lbs.

I did have my gallbladder out in 2008. They had done an ultrasound which showed no problems at all with the gallbladder. They removed it anyway and found it was completely full of gallstones which hadn't shown up at all on the images. When I tell people I had my gallbladder out, they assume my urgent bathroom habits are a side effect of that. Having my gallbladder out did nothing but ease the excruciating pain I was getting. I just chalked everything up to miserable untreatable IBS.

I never knew much about celiac until my BFF said my symptoms sounded a lot like it. I always assumed celiac was something like a nut allergy or something - consume gluten and you end up in the ER with anaphalaxis. Not so much, it seems. I looked at the symptoms of celiac, and I have MANY even beyond the bathroom issues -- iron deficient anemia, ADHD, tooth problems (this could be a whole other ranting post in itself about my tooth issues), nosebleeds, migraines, easy bruising, insomnia, it goes on and on.

I went to my regular doctor back in March in hopes of having a celiac panel done while I was having my normal yearly cholesterol and other fun tests done. I received a letter in the mail saying that my results were "within normal limits" and I decided to see a gastro for further testing.

I will spare you the nightmare which has become the gastro, and suffice to say I will be switching doctors as soon as I get the results of my latest genetic testing (which the lab screwed up TWICE) My father, who has ulcerative colitis, sees a wonderful doctor I should have seen to begin with.

So, it seems that the "comprehensive celiac panel" only consisted of these two results:

IgA, Serum --- 146 --- 88-410

tTG IgA AUTOAb --- 4 --- <20

Shouldn't there have been more to it?

I don't know what I'm hoping for.. I just want answers. I'm tired of being sick, I'm tired of not being able to do the stuff I want to do.

Thanks for any advice/insight/anything. :)


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



Celiac.com Sponsor (A8-M):



beachbirdie Contributor

Hi everyone!

I'm new here. :) I apologize if this ends up being muddled wall-of-text, I just have so much to say!

So, it seems that the "comprehensive celiac panel" only consisted of these two results:

IgA, Serum --- 146 --- 88-410

tTG IgA AUTOAb --- 4 --- <20

Shouldn't there have been more to it?

I don't know what I'm hoping for.. I just want answers. I'm tired of being sick, I'm tired of not being able to do the stuff I want to do.

Thanks for any advice/insight/anything. :)

Hi beachymama, welcome to the forum!

Don't apologize for a long explanatory post, it's perfectly fine!

As for testing, you are correct. They did not do a very complete job of testing. In addition to what they tested, they should have done:

Deamidated gliadin peptides, both IgA and IgG version

anti-EMA (anti-endomysial antibodies)

Some people only test positive on ONE of the types, and if they don't test all, they might miss a diagnosis.

You certainly have a lot of symptoms that COULD be celiac related, hopefully your new doc will help sort things out.

Be sure you get paper copies of all your labwork as the results come in, and share them if you are comfortable sharing. Doctors so often will say "normal" when you aren't really in a good place lab-wise. There are quite a few experienced people here who can give educated insight on your tests.

You've come to a great place for support and information. Folks here are very friendly and very helpful!

MitziG Enthusiast

Well, the panel is typical, as in it only included one actual celiac test. Though they at least tested total IGA which is important, cuz if that is low, it negates the other test anyway.

You still need:

Ttg IGG

Deamidated Gluten Peptides

Endomysial Antibodies

Do not be surprised if those are negative too though. Celiac is notorious for false negatives. And then of course, gluten intolerance, which is far more common than celiac, can not be tested for at all.

The gallbladder is a big red flag for celiac- google the connection.

Weight gain is as well, but most drs do not know this and will completely dismiss the possibility of celiac in an overweight person.

For now, keep eating gluten until all testing, including biopsy is done. Then go on a strict gluten-free diet and find out for yourself if gluten is your problem!

beachymama Newbie

Thank you for the warm welcome and information!

I'm very excited about seeing my new doctor. My dad talked to him on Tuesday (he had an appointment scheduled for his own stuff) and the doc was appalled at the way I was being jerked around by my current doctor. He sent home some helpful handouts for me and said I should call to set up an appointment immediately before my current doc does "any more damage" ! I was just tickled that he not only knew what celiac was, but is apparently a pretty big deal around these parts with research and stuff.

I'm still waiting on my genetic test to come back. They said it will take about 10 days to get the results and I'm so not patient.

If the genetic stuff comes back as a screaming positive, does this mean I should have my children tested as well? I have 3 - ages 12, 8 & 6. My 12 year old had awful GERD as a baby, the 8 year old is ADHD like me, and the 6 year old went through several years of unexplained high fevers which they finally just diagnosed as periodic fever syndrome (PFAPA) because that's what they dub it when every test in the book comes back negative. It blows my mind that perhaps my ADHD child could just be having a gluten reaction and could possibly get off his stimulant meds. None of them show any kind of tummy symptoms like I have, but my BFF is celiac and hers manifested as terrible migraines - so I'm guessing anything is possible.

ETA: My paternal grandfather died from lymphoma, which is another reason the new doctor is all "get in here now" with me. I never even realized celiac could cause cancer. :unsure:

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,991
    • Most Online (within 30 mins)
      7,748

    ZENken
    Newest Member
    ZENken
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.5k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Who's Online (See full list)

    • There are no registered users currently online
  • Upcoming Events

  • Posts

    • Wheatwacked
      Testing can't alone be trusted.  Else why would it take so many years of testing and retesting and misdiagnosis to finally be told, yes you have Celiac Disease. As to what to eat, I like pre 1950 style food.  Before the advent of TV dinners.  Fresh food is better for you, and cooking from scratch is cheaper.  Watch Rachel Ray's 30 Minute Meals for how to cook.  Keep in mind that she is not gluten free, but her techniques are awesome.  Just use something else instead of wheat, barley, rye. Dr Fuhrman is a ex cardiologist.  His book Eat to Live and Dr Davis' book Wheatbelly were instrumental in my survival.
    • Scott Adams
      If you have DH you will likely also want to avoid iodine, which is common in seafoods and dairy products, as it can exacerbate symptoms in some people. This article may also be helpful as it offers various ways to relieve the itch--thanks for the tip about Dupixent, and I've added it to the article:  
    • Scott Adams
      I just want to clarify that what I posted is a category of research summaries we've done over the years, and nearly each one shows that there is definitely a connection to celiac disease and migraine headaches. The latest study said: "the study did indicate some potential causal associations between celiac disease and migraine with or without aura, as well as between migraine without aura and ulcerative colitis...this study did not find evidence of a shared genetic basis..." Anyway, there is definitely a connection, and you can go through more of the articles here if you're interested: https://www.celiac.com/celiac-disease/celiac-disease-amp-related-diseases-and-disorders/migraine-headaches-and-celiac-disease/
    • SusanJ
      Two months ago, I started taking Dupixent for dermatitis herpetiformis and it has completely cleared it up. I can't believe it! I have had a terrible painful, intensely itchy rash for over a year despite going fully gluten-free. See if your doctor will prescribe Dupixent. It can be expensive but I am getting it free. When the dermatitis herpetiformis was bad I could not do anything. I just lay in bed covered in ice packs to ease the pain/itching and using way too Clobetasol. Dapsone is also very good for dermatitis herpetiformis (and it is generic). It helped me and the results were immediate but it gave me severe anemia so the Dupixent is better for me. Not sure if it works for everyone. I cannot help with the cause of your stress but from experience I am sure the severe stress is making the celiac and dermatitis herpetiformis worse. Very difficult for you with having children to care for and you being so sick. Would this man be willing to see a family therapist with you? He may be angry at you or imagine that your illness is a psychosomatic excuse not to take care of him. A therapist might help even if he won't go with you. Also do you have any family that you could move in with (with the kids) for a short time to get away? A break may be good for you both.
    • knitty kitty
      @tiffanygosci, Thiamine deficiency is a thing in pregnancy for "normal" people, so it's exponentially more important for those with celiac disease and malabsorption issues. I studied nutrition before earning a degree in Microbiology because I was curious what the vitamins were doing inside the body.  See my blog.  Click on my name to go to my page, scroll to drop down menu "activities" and select blog.   So glad you're motivated to see the dietician!  We're always happy to help with questions.  Keep us posted on your progress! 
×
×
  • 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.