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90 Percent Sure, Going To Gi Monday

addis001

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addis001 Apprentice
addis001
Posted

My history-

Hyperthyroidism 2000-2004

(went through a period of not caring to take my PTU, not having insurance during 2003-2004)

Suddenly in 2005, some of my symptoms were gone and blood tests were normall..

Pain and gall stones found in 2006.

Gallbladder removed in 2008. (insurance finally kicked in)

Hyperthyroidism again in 2nd trimester of pregnancy up until birth March 2010

Symptoms since gallbladder removal-- Some nausea still, even before gallbladder Lactose (milk) intolerance

Since giving birth-- nausea, Tired, fatigue, bouts of diarrhea, weird pain under right rib area near abdomen, bloating

Symptoms since 4 months ago-- All above apply still, but bone pain, muscle weakness, depression type of not wanting to do anything, not hungry some days, some days I'm starving, weightloss , irregular periods

Been feeling better ever since I started taking my prenatals to try and get pregnant again. Fatigue disappeared, and depression lifted. I feel like getting out of bed and meeting the world again..

Family history-- Celiac Disease- Grandmother, Aunt, Cousin

As i look at all the facts staring at me, it seems like I'm armed and ready to go to the GI with all my symptoms.. But in my heart I know I have it no matter what this doctor wants to test me for.. All i want to do is cry.. If it isn't celiac, and my husband thinks I'm a hypochondriac, because he doesn't believe anything until its on paper.. Even though I pushed for the doctor to test my thyroid, and i pushed for the doctor to look at my gall bladder.. i found my diagnosis each time... And now I'm scared that this time I'm right.. I know there are probably a million things worse than being allergic to gluten, but right now I can't think of one thing. Maybe because its late, and I'm an emotional wreck anyway, but its just hard to take in.

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Meggielynn13 Rookie
Meggielynn13
Posted

Reading this makes me feel like I'm reading a list of my own symptoms plus I might have hypothyroidism( minus the pregnancy ones as I have never been pregnant, I'm only 23 :) ) I too had my gallbladder out and had more problems after than I did before. Others have told me that having undiagnosed celiac or gluten sensitivity could have taken my gallbladder. Sounds like what happened to you too. I'm the opposite of you that I want the answers on paper so I know that I'm not being a hypochondriac. My boyfriend knows that I'm not and really does think I'm sick.

Hopefully you get the answers you need. And you do not sound like you are not sick. And reading this makes me feel better about my own situation cause I feel like I'm not the only one going through this. Let everyone know your answers when you get them back. Its great to read that people got the answers that they wanted. I hope to be in that place someday :)

addis001 Apprentice
addis001
Posted
  • Author

Everyone I talk to that had no gallbladder, has had the worse problems battling stomach virus's too.

I had mine removed due to stones. Why was yours removed if you don't mind me asking?

***Update*** Had to go to the ER today.. I've had two days of constant diarrhea, which made me dehydrated.. They gave me an IV and (Zofloft?spelling?) For nausea and the cramping... I really really can't wait until i see the GI now.. It seems all I am is getting worse as time passes...

Meggielynn13 Rookie
Meggielynn13
Posted

I had the stomach virus two days before I had my gallbladder removed and a week after. I normally don't get it so I was wondering why I got it twice in about two weeks. I had my gallbladder removed due to pain in my side constantly and having tons of GI problems that the GI told me was due to IBS. I kept pressuring them to do a hida test cause there were no stones on the ultrasound and I'm glad they did it. It had a 12 to 14 ejection rate. At my age it should have been 90. But having it out I can barely eat anything without having issues 30 to an hour later. Hopefully they test you for celiac. If they don't I'd pressure them to. I did and they're testing me in two weeks. Going gluten free anyways cause of the 20-30% false negative. Let us know how everything works out. Being on here and reading/talking to people has helped me a lot so I don't have to talk about it constantly with family and friends who are sick of hearing it.

researchmomma Contributor
researchmomma
Posted

Everyone I talk to that had no gallbladder, has had the worse problems battling stomach virus's too.

I had mine removed due to stones. Why was yours removed if you don't mind me asking?

***Update*** Had to go to the ER today.. I've had two days of constant diarrhea, which made me dehydrated.. They gave me an IV and (Zofloft?spelling?) For nausea and the cramping... I really really can't wait until i see the GI now.. It seems all I am is getting worse as time passes...

Zofran is what they gave you for nausea and vomiting. I had IVs full of it during my pregnancies. It is fab.

addis001 Apprentice
addis001
Posted
  • Author

YES Zofran!! It saved my life... Its like a miracle drug...

After seeing the GI, he wants to do colonosopy (spelling). he thinks its Crohns, IBS, or ulcer.. At least we're doing something..

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    • trents
      Blood tests low iGA 4 years later digestive issues

      By trents · Posted

      Welcome to the forum, @Mmoc! Please include the reference ranges for the IGA and the TTG tests in your next post if you have access to them. We cannot comment much otherwise as different labs use different reference ranges for these tests and also different units of measurement. There are no universal standards as of yet so the raw test numbers are not always helpful. Having said that, if your IGA (what we usually call "total IGA") is low, the TTG-IGA score will be skewed and cannot be trusted. Other kinds of tests for celiac disease would need to be run, particularly those in the IGG family of tests. Perhaps this will be helpful:  
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      Hi there any advice welcomed. I have had 4 years of symptoms ranging from immune related anaphylactic symptom sudden onset food allergy to peppers/paprika/chilli/capsicum family derivatives. all these allergies fizzled out and following a food challenge test in hospital I reintroduced them a few months ago. Since then my digestive system is a mess. i have since noticed that 4 years ago when testing for iga allergies my iga level was .62 and my ttg was less than .1 (due to symptoms I was probably eating very plainly at that time). should I insist on being retested for celiac? I’ve since read two indicators for celiac include: sensitive to spicy foods when in flare up tooth enamel weakness and symmetrical discolouration patches on teeth which I have had since childhood on my two front teeth     thanks
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      Headaches / Migraines and Hypoglycaemia

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      This article does not address migraines at all.  Yes, red wine and sulfites are often mentioned in connection with migraine triggers. With me, any kind of alcoholic beverage in very modest amounts will reliably produce a migraine. Nitrous oxide generators, which are vaso dialators, also will give me migraines reliably. So, I think most of my migraines are tied to fluctuations vascular tension and blood flow to the brain. That's why the sumatriptan works so well. It is a vaso constrictor. 
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      Then we would need to cut out all meat and fish as they are richer sources of tyrosine than nuts and cheese. Something else about certain tyrosine rich foods must be the actual culprit. 
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