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Tomorrow Is The Day
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tomorrow is the day I find out my Endo and blood results and finally get a Dx, possibly.

I am nervous. There is part of me that is hoping it IS celiac disease because its not the worst thing in the world to manage and it would just explain everything, and part of me is praying to God it is NOT because all I want to do right now is enjoy the things I have been enjoying all my life. lol

I really don't know what else it could be.

I have been gluten-free for 2.5 weeks now and for the most part, I feel pretty good. So I kind of feel like ok..this HAS to be what it is!

Today at work (I waitress) I had some grilled chicken, mashed potatoes covered in a creamy blue cheese sauce. NOW..I have heard 2 things about Blue Cheese..I have heard that it is NO NO because of the way it is made (on bread) and I have heard that it is perfectly fine to eat...so I had this meal Saturday night and felt ok, so I had it again today...MISTAKE!!

I can't say if it WAS the Blue Cheese or if something was CC but I came home with a whopper of a migraine. I had to go straight to bed. I just woke up a little while ago and feel totally drained. My stomach is ok..its just my head. So much pressure. This happened last week after I ate half a donut.

I cant wait for tomorrow. I just want to KNOW!

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Well, I hope you get a clear result. If it is positive you are all set, stay gluten-free. If it is negative, you otter stay gluten-free anyhow since the false results are not always right. You can always do a gluten challenge after a month or two and see what happens. But since you are feeling better without gluten it is best to avoid it IMHO.

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tomorrow is the day I find out my Endo and blood results and finally get a Dx, possibly.

I am nervous. There is part of me that is hoping it IS celiac disease because its not the worst thing in the world to manage and it would just explain everything, and part of me is praying to God it is NOT because all I want to do right now is enjoy the things I have been enjoying all my life. lol

I really don't know what else it could be.

I have been gluten-free for 2.5 weeks now and for the most part, I feel pretty good. So I kind of feel like ok..this HAS to be what it is!

Today at work (I waitress) I had some grilled chicken, mashed potatoes covered in a creamy blue cheese sauce. NOW..I have heard 2 things about Blue Cheese..I have heard that it is NO NO because of the way it is made (on bread) and I have heard that it is perfectly fine to eat...so I had this meal Saturday night and felt ok, so I had it again today...MISTAKE!!

I can't say if it WAS the Blue Cheese or if something was CC but I came home with a whopper of a migraine. I had to go straight to bed. I just woke up a little while ago and feel totally drained. My stomach is ok..its just my head. So much pressure. This happened last week after I ate half a donut.

I cant wait for tomorrow. I just want to KNOW!

I hope you will get to the root of your health problems and get better. I know just that hopeful/dreading feeling of waiting for results. I was glad mine came by e-mail. I was able to hold my breath and then look!

If you have gluten intolerance you will be happy, not because you have one, but because now you can find out what to do. If you don't gluten intolerance then you need to search out another explanation.

My genetic test was positive and my blood antibody test (IGG) was negative. My MD and Chiropractor said the antibody test was a false negative. They trusted the genetic test. Also, by then I was reacting forcefully to gluten.

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Since you are feeling a bit better gluten-free stay that way for a bit and then challenge if you feel the need after a couple of months no matter what the results.

As was mentioned false negatives are unfortunately all too common.

If you had that grilled chicken at work there is a good chance it was CC'd unless they use a clean pan to cook it in and took the other precautions that need to be taken for us.

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Well..blood and.endo are.negative. Aside from some serious ulcers, she said she saw nothing wrong in there. She said there is zero.evidence to support celiac disease or intolerance, even though all my symptoms point to it. She is redoing bloodwork today and in 3 mos, but otherwise, thats it. Im pretty aggravated.with my body right.now. I just dont know what to do.

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Well..blood and.endo are.negative. Aside from some serious ulcers, she said she saw nothing wrong in there. She said there is zero.evidence to support celiac disease or intolerance, even though all my symptoms point to it. She is redoing bloodwork today and in 3 mos, but otherwise, thats it. Im pretty aggravated.with my body right.now. I just dont know what to do.

Well.. you can always go on being undiagnosed. I'm undiagnosed but I'm pretty sure I have celiac. No one can stop you from living gluten-free if it's the only way you're feeling better.

I myself decided to stop going after an official diagnoses once I found out my thyroid "might" have started being effected. I don't want risk any permanent damage to it and a gluten challenge for a 30% accurate testing system is not worth it to me. I don't feel a need to prove it to others any more because all my symptoms are starting to go away.

Don't worry, no matter what it's not the end of the world :-)

You can also ask for your test results and show them to the members here. THey're pretty good at reading them.

Did the doc check for vitamin levels in your blood?

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Thanks. Well whats happening is that I always trusted dr's opinions and this dr is saying she does.not reccomend going gluten-free if there.is no evidence and therefore do NOT go gluten-free. so part.of me is like...so, this is all in my head? For almost 3 weeks I have been gluten-free.and have had only 2.migraines..coincidentally on the same.days.I knowingly.ate.gluten.and all my bowel movements.have been normal ish..after.17 years of loose bms. (ps, forgive my typing, on phone lol)

I have more.energy, less foggy head, etc..

She.says.its my.ulcers.that I have been messing up my sromach...I said ok but what about my head.stuff? She said she had.no answers...so had me give blood.for.a.genetic test. I just.dont know what to do. I was so upset, I came home.and ate pieces of cornbread. Sigh. Maybe i am just.intolerant.and that would be.great I guess.

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Oh...my b12 and iron were great..but vitamin D was.very very low. She.prescribed.some high.dose for me

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Stay on the diet if it is helping and it sounds like it is. Do get actual copies of the endo and blood results and post. Some doctors don't like to diagnose unless villi are totally destroyed and ignore the stages that come before total destruction. Ulcers can be the result of celiac also.

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Even my doctor thought whether I go gluten-free or not was up to me. Doctors are not always right and not always wrong when it comes to celiac disease. Being gluten-free will not harm you in any way even if you're not intolerant, but if you happen to have celiac and don't feel any symptoms the damage will still be done.

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Thanks everyone. I just really thought Id get an answer :( ah well, i should be happy.

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Thanks. Well whats happening is that I always trusted dr's opinions and this dr is saying she does.not reccomend going gluten-free if there.is no evidence and therefore do NOT go gluten-free. so part.of me is like...so, this is all in my head? For almost 3 weeks I have been gluten-free.and have had only 2.migraines..coincidentally on the same.days.I knowingly.ate.gluten.and all my bowel movements.have been normal ish..after.17 years of loose bms. (ps, forgive my typing, on phone lol)

I have more.energy, less foggy head, etc..

She.says.its my.ulcers.that I have been messing up my sromach...I said ok but what about my head.stuff? She said she had.no answers...so had me give blood.for.a.genetic test. I just.dont know what to do. I was so upset, I came home.and ate pieces of cornbread. Sigh. Maybe i am just.intolerant.and that would be.great I guess.

Ugh.

Well, false negatives ARE common. Don't take a negative test as a recommendation to continue eating gluten!

I hate to see you say "maybe I am just intolerant". Non-celiac gluten intolerance is a very real condition and should not be discounted. The symptoms/reactions can be as bad as a person who is celiac, the only difference is that the intestines do not sustain damage. The misery gluten causes is the same as for celiac!

The medical field IS beginning to accept this. Unfortunately it is not yet widespread, but many of the pioneers in the field are writing about it. Dr. Scot Lewey is one (and has many articles on celiac.com), here is a light, easy to read article about his own experience with gluten sensitivity.

So, whether you are "intolerant" or "celiac" is not as important as whether you are healing on a gluten-free diet. If that is the case, then that looks like a good path for you.

I am very glad your doc is working with you and going ahead with the genetics and is also willing to re-test. Most would have quit on you at this point. Of course, you probably don't want to be eating gluten for 3 more months. :blink:

I am shocked she would tell you NOT to go gluten free.

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I think she thought shed save me money, she kept saying how expensive being gluten-free was.

I didnt mean to discount intolerance, I apologize. And believe me, i.feel so miserable most days, I get it. Feeling lousy.now after.eating all that cornbread lol...sigh...but seriously, thanks all for being here. I am going.to keep plugging away. i am thankful at least to find out about my ulcers. She showed me pictures. Not pretty! Kind of scary.to see, actually.

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Also, my primary dr did a blood test..I dont think it was a full panel..and it showed signs of celiac disease, which is why I got sent to the Gastro in the first place.

My Gastro today said that all the blood work she herself took, showed NO signs of celiac disease at all..which contradicted what my Primary took..which led her to believe that there was a mixup in blood work. My Primary's bloodwork showed low IGA levels and the Gastros did not. She thinks one of the 2 tests may be wrong. So I had to retake them today, in addition to genetic testing, which my ins may or may not cover but I had them do it anyway since I was there, I may regret that later :(

I should have though to ask for copies or my tests, but I was shocked. I thought for sure I would have everything explained away today. years and years and years of feeling like this. But yes, like everyone says, I dont need permission to eat or not eat anything. I will just pick myself up and carry on and see how I feel gluten-free and then likely challenge myself at some point.

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The corn bread probably has wheat flour in it if it was a mix? Ah well, something to watch out for later.

Quite a few people do end up without a formal diagnosis. The testing process just isn't really perfected yet. We still don't have the Star Trek tricorder available. May never for that matter.

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For 3 weeks you have been gluten-free & you re-did the blood work for celiac. I hate to say it but there's every chance it will be neg also b/c you were gluten-free for 3 weeks.sad.gif

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The corn bread probably has wheat flour in it if it was a mix? Ah well, something to watch out for later.

Quite a few people do end up without a formal diagnosis. The testing process just isn't really perfected yet. We still don't have the Star Trek tricorder available. May never for that matter.

Oh yeah, it was full gluten cornbread. I was so upset when I came home, I said oh well the Dr says I am not Celiac OR intolerant and to start eating gluten again so fine!!! I felt a little bad but not terrible...so tonight I also ate full gluten chinese food and NOW I feel full blown awful. Going to bed soon.

After I calmed down, my husband said if I feel better not eating it then that says something. He has epilepsy but hasnt had a seizure in years..does that mean he should stop taking his meds because MAYBE he will never have one again? NO. You do what keeps you feeling good.

bleh.

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For 3 weeks you have been gluten-free & you re-did the blood work for celiac. I hate to say it but there's every chance it will be neg also b/c you were gluten-free for 3 weeks.sad.gif

Thats what I asked my dr too...and she said oh no, it will be fine.

Whatever. I decided I am done. I will just do what I know works from now on.

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We always say you don't need anyone's permission to eat gluten-free. And if eating gluten-free makes you feel better then by all means DO SO! Live happy & long.smile.gif

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Another thing...

I have a few ulcers, which I am happy she found. She prescibed me prilosec and I immediatley started feeling better.

Today at the follow up, she says I was negative for H. Pylori, which causes most ulcers..so that must mean that I take too much advil for my migraines. She said 3 times a day every day is too much! I said, I never said I took it every day. I take whatever is handy, be it Advil, Motrin or more often, Tylonal. but yes, I take SOMETHING for my headaches, but not every day, let alone 3 times a day. maybe a few times a month..

She said well then, thats it..you take too much advil and thats why you have ulcers.

I would go to a new dr but really, my Insurance is not great as it is and my copays and deductibles are piling up so fast right now, and Im tired.

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She's a real doozie isn't she? I wonder where she got her med degree? The mail order university of Tim Buck Too? You might be safer & healthier staying away from her!

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We still don't have the Star Trek tricorder available. May never for that matter.

:lol: :lol: :lol:

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    • First, do you have celiac disease?  I assume you do.  Have you recently had a celiac antibodies follow-up blood test panel to see if gluten has been actually getting into your diet by accident or through cross contamination?  If you haven't had the test, you should ask your doctor for one.  You could also also ask for a follow-up endoscopy to see if you intestines have truly healed.  This will rule out if gluten is really the problem.    If gluten is not the problem, then your doctor needs to check you for other issues, like SIBO. There is a test to check for SIBO.  Has this been done?   Once a celiac, always a celiac.  There is no cure for celiac disease except to remain on a gluten free diet for life.    
    • I am so confused right now.... 6 years ago I went on gluten free diet... after being on it for the first yr I was 100%better up until 5 months ago in got the "flu" the doctors told me to cut out dairy sonic did and my diarrhea  became better but not completely gone would not have it every day tho. I went to the gi doctor and they said to cut out fructose and dairy and keep gluten out... yesterday I went to the dietitian to see what I can eat and she gave me the list for fructose... she said it should have been on a antibiotic for sibo.... eventually I will be able to add dairy back and maybe gluten.... I said how can I add gluten back when this was my first problem... she goes well through fructose goes hand in hand with it... I said with gluten I vomit and am sick for weeks.... fructose isn't that bad I vomit sometimes but I'm not sick for weeks.... I'm just confused on really what is going on and was wondering if you or someone you know had sibo from gluten and or fructose and how Is this all related?
    • I see no one has responded to your query.  Unfortunately I have yet to try making a pie crust.  It was something I never mastered before going gluten free.  Have you looked on Pinterest?  You might find something there.
    • I honestly feel like both doctors think it's all in my head even though there is proof.  Yeah there was a point when I felt crazy.  That was when I was being shuffled from dr to dr being given individual diagnoses of my problems.  None of those diagnoses ever made me get better.  Seriously I was diagnosed with heart palpitations, neurocardiogenic syncope, I was given a butt load of steroids because a dr felt like I was producing too much adrenaline, freaking had a few tell me I was depressed, and the good ol IBS.  It seemed most wanted to push pills.  It's all just ridiculous!
    • I can't believe your doctors!!! You have a daughter who is dx'd already! Yet the ped doesn't want to test your other kids unless you have a dx????!!! Are you kidding me???!!! That's absurd!!! They have a first degree relative who has been dx'd with celiac already. There is no need to wait to see what you turn out to be!! And then, and then, and then....don't even get me started on your doctor!!! Does he have brain damage? Oh this is insane & ridiculous!  I have never heard of a disease that doctors are so unwilling to consider or test for OR to diagnose as this one! Usually they are hot to trot to make a dx but say the word celiac & they shake in their boots. Grrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrr!!!!!!!!!!!!!!!!!!
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