Celiac Disease Tests Diagnosis
Celiac Disease
Tests Diagnosis
Does She Have
Celiac Disease
Or Not?My daughter was tested for
Celiac
Disease recently. The first test came back as
'results may support a
Diagnosis of
Celiac disease, but are not specific.' So They
tested again and it came back negative. My daughter STILL is having
major stomach problems which she has had since about age 2 or
younger and gets nauseated and remains on miralax treatments and
they give her no explanation other than maybe she is lactose
intolerent. What do i do? There is OBVIOUSLY something wrong here!
I myself have a major allergy to gluten. I am tired as is she of
being in pain. She seems to even have mood swings associated with
this issue. I too have mood swings associated with my allergy.
Where can i go to get down to this problem and do you think a 3rd
test should be given? Is it possible that this
Disease is that hard to diagnose or is there
something else we should be looking at? Please help. =[
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Celiac
Disease Do Not Know Paternal Side Donor
Insemination?Okay, after a long and painful few months I was
finally given a
Diagnosis of
Celiac disease. For those of you who do not know
Celiac is a hereditary condition. It can also do
damage with giving the victim no symptoms of having the condition.
Therefore, all first and second degree relatives are required to
get tested. There is only one problem. I was born through the
anonymous form of Donor insemination/artifical insemination.
Therefore, my biological father and I have no knowledge of each
other. I do not know which saide of the family the
Disease came from. The test to check for the
'celiac gene' is nearly $500. If it is coming from ym paternal
side, then I do not want to have to put my entire family through
the procress of bloodwork, and endoscopies. If their anyway to find
out from the donor bank if my 'father' had
Celiac
disease. Or better yet, (anyone who is able to do this, I will
create a bunch of black questions for you to answer and
automatically vote you best to give the points.) Is there any
possible way to use this condition as a way to contact the
biological father. I am under 18, that makes it more difficult. I
am desperate to find him, please do not just send me to the donor
sibling registry. I want to know who my father is so desperately.
my mother's test results came back negative for
Celiac disease.
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Diagnosis Please - Celiac's Disease?I find the more wheat I eat,
the more I have these symptoms: Cloudy urine Headaches Muscle
tension Nausea Irregularity Soar throat Mucus build-up in
throat/nose Sore glands in neck Depressed mood Heartburn I've been
tested at a naturopath for food sensitivities. Wheat and every
other grain he tested were absolutely out, but I've never been to
see about Celiac's. If it is Celiac's, why is it important to stay
clear of gluten other than feeling well?
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Celiac
Disease Results?I recently requested all my
sons records from the hospital and came across test results that he
had 10 months ago for
Celiac serology and it looks
to me like it came back positive, but the doctor at the time
reported to me that he did not have it. If there is anyone that can
interpret these results and let me know if he does or does not have
Celiac Disease I would truly
appreciate it. He was 19 months old at the time of the test....he
is now 29 months. Positive AGA IgG 10.3 U/ml Negative AGA IgA - 1.7
U/ml Negative TTG IgA 0.1 U/ml Negative EMA IgA no numbers Summary
Interpretation says Results may support a
Diagnosis of
Celiac disease, but
are not specific. THANKS!!! Thanks for that helpful info Anama.
Here are the reference ranges. Positive AGA IgG 10.3 U/ml <10.0
U/ml Negative AGA IgA - 1.7 U/ml <5.0 U/ml Negative TTG IgA 0.1
U/ml <4.0 U/ml Negative EMA IgA no numbers Negative Thanks
again!
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Dr. Says I May Have
Celiac
Disease But I'm Allergic To Corn... What Would I
Be Able To Eat?!?After years of stomach problems, I am finally
looking into their cause. So far we have found I am allergic to
corn and peanuts, but this is not the final diagnosis. My doctors
have been recently talking about the possibility of it being
Coeliac
Disease or another condition that I think
was Eosinophilic Esophagitis, but not positive on that. Anyway, if
after all my
Tests and procedures have been done
and it turns out I do have Coeliac disease, then what would I be
able to eat, seeing as I am allergic to corn (a common
alternative)?
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Is E, Nodosome Connected To
Celiac Disease?I have
had chronic Erythema nodosome for 30 years but it hasn't bothered
me much during the past 2 years. 3 years ago I was diagnosed as
having
Celiac disease. For the past half a year
the symptoms of
Celiac Disease
have been extreme. (I'm a roll a day girl) Now the E. nodosome has
returned with a vengence. I have never experienced the typical dime
to quarter size patch of inflammation I read about on the internet
-rather it's usually an area about 6 inches across, is flaming red,
tight and feels quite deep - deep enough to tighten the muscles
making it very painful to even lift my feet. They are presenting on
the fronts of my legs, which is most commonly what happens. My
question is - are the 2 symptoms related? I have recently seen
associations cited for Chrone's disease. My Dr. is reluctant to
rescope as he feels I have a working
Diagnosis and
we should go with those test results for another 4 years. Between
the 2 problems, I'm not having much fun at all. Please help if you
can, suggesting treatment that might alleviate this. I was
prescribed Lugol's solution, but have to admint I never actually
used it because of the staining properties - I had just spent
thousands on dental work - and the skull and crossbones on the jar.
I was afraid of it. I am taking an international flight in a month
and want to know if support stockings are recommended as well.
Although this is a condition of the fatty tissue, it feels like
vericose veins (ropey) and I would like some assurance that there
is no connection to thrombosis. Thanks.
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Celiac
Disease Is Tearing My Family Apart?This is
going to sound totally ridiculous (it is even to me) but it really
is an issue. I am a 20-year old student who still lives with his
family. My dad and I have recently discovered we have
Celiac Disease or some form of
gluten intolerance. The problem is we went gluten free for awhile
and missed our window for
Diagnosis (we have to be
regularly consuming gluten to be tested, we don't want to do that).
Our GI doc said to play it safe for now and avoid wheat products.
But something is just not right. My dad and I have extremely
unusual reactions when we have wheat products, and we are
ultra-ultra sensitive it seems. We take a risk every time we eat
out even if we go to a place that has a gluten-free menu. The
slightest cross-contamination affects us. If we get a trace of
gluten we not only get swollen, sick, nauseated, and have bowel
problems, we get heavy psychological symptoms. When I eat gluten, I
become crazy but I internalize it. I get tormented with nightmarish
thoughts and I get depressed and suicidal. I have extremely bad
nightmares at night as well. I had to go to counseling a little
before I found out I had
Celiac
Disease because I was so deeply depressed all the
time. Also when I'm on gluten I have a lapse in judgment and don't
always choose my words wisely when I talk to people. I scare people
away because I get weird. When I'm off gluten, I attract a lot of
people around me, and it's easy to make new friends. My dad on the
other hand becomes violent when he is on gluten. My dad is normally
a very nice, subtle guy but when he's on gluten he'll become crazy
like me but he'll be more external. He'll be violently overreactive
especially to my 16-year-old brother's arguments. When my brother
fights my parents like normal teenagers do, my dad taunts him and
tries to engage in a physical fight with him. Then he'll pin him to
the ground and sometimes hurt him. He just becomes nuts. The
problem is my dad is not diligent at all. He'll only avoid breads
and that is about it. He doesn't want to embark on the
inconvenience of an organic gluten-free diet. He still eats out
constantly which is dangerous and he is not very diligent and he
always gets a dose of cross-contamination. I know my dad's mother
had a boatload of health problems: bloating, nausea, anger issues,
irrationality, and just overall feeling sick all the time. She died
of bone cancer. My GI doc thinks she had our condition, and the
cancer was caused by it. Now my older brother, 23, who lives 20
miles away from us called my mom and said he thinks he has this
gluten intolerance condition too. He has been suffering from the
bloating, nauseau, irritability symptoms that the rest of us have.
So immediately we forwarded him to our GI doc for a test. We're
still waiting for word on the results. But my question is this. How
can
Celiac Disease be this
ridiculous? Is this a somewhat common impact on households? Can
symptoms really be this damaging even on a family-scale? I'm
getting frustrated over this whole gluten thing and the impact it
is causing. How do I deal with it?
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Possible Case Of
Celiac Disease.?Been suffering
with a range of unexplained symptoms for several years (that also
includes possible dumping syndrome), pre-diabetes with unexplained
hypoglycemia, abdominal cramping, light tan stool that floats,
diarrhea, hair loss, vitamin B12 deficiency and many others (i.e.
rapid weight loss, can eat things like a whole pizza and maintain
the same weight, and ofcourse, suffer the after effects). So far
the only
Diagnosis I have received are gallstone
and IBS (due to unknown gastrointestinal symptoms). I have done
many exams as you may have guessed and been to several doctors,
none of them were able to properly diagnose me. I stumbled upon
this 'celiac disease', which seem to be fairly coherent with what
I'm experiencing (emphasizing the cramping), and I saw that the
only way to diagnose it is either blood test or biopsy, which would
be impossible to tell with the list of exams I have done. Opinions
will be welcomed.
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Do I Really Have
Celiac Disease? I've Been
Diagnosed With It, However, I Have Major Doubts.?Do I really have
Celiacs Disease? Here are my test results. Tissue Transglutaminase
IgA Antibody by EIA: NEGATIVE Immunoglobulin A (IGA): 226 (40 - 350
normal range) Endomysial Antibody IgA (EMA): NEGATIVE I was then
given a colonoscopy/endoscopy. My results are as follows: HISTORY:
Diarrhea. Endoscopic impression: Normal examined duodenum. This was
biopsied. The examination was otherwise normal. Please see EGD
report. GROSS: 1. Duodenum biopsies Five soft tissue bits range
from .3 to .4 cm. DF Microscopic Diagnosis: 1. Duodenum, biopsy:
Surface intraepithelial lymphocytosis with preserved villous
architecture. Please see comment. COMMENT: This patient has similar
finding in the colon, suggesting that this is probably gluten
sensitive enteropathy. HISTORY: Indications: Clinically significant
diarrhea of unexplained origin. Endoscopic impression: Scattered
apthous ulcers in the rectosigmoid colon. Inflammation vs.
preparation artifact. Biopsies taken.... The terminal ileum is
normal. This was biopsied. Please see colonoscopy report. 'talks of
different tissue samples taken from right colon, left colon,
terminal ileum and rectosigmoid' MICROSCOPIC DIAGNOSIS: 1. Terminal
ileum, biopsies: No significant abnormalities. 2-4. Colon, right,
left and rectosigmoid, biopsies: Increased intraepithelial
lymphocytes. Please see comment. COMMENT: The colon biopsies show
some but not all of the changes of lymphocytic colitis. this can be
seen in resolving infectious colitis as well as in patients with
Celiac Disease. I was in the Peace Corps in
Honduras. At the age of 29 I was having some major stomach
problems. I am now 31, and all seems to be normal. (even with
consumption of wheat) I sometimes get bloated, I sometimes have
acid reflux and my stool has floated for about a year now. Please
help. My insurance will not allow me a second opinion. I had
hamburgers for lunch and pizza for dinner last week and nothing
happened.
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Am I A
Celiac Or Not?i was recently tested for
Celiac disease. My blood culture came back
positive but my biopsy negative. I was consuming gluten for the
weeks leading up to my test but i confess i missed a few days..i
have just however realised that i was taking laxatives throughout
my gluten consumption to cope with bloating and constipation as i
have done for months so i thought nothing of taking them leading up
to my biopsy automatically. Is there any way taking laxatives could
have given me a false negative result in the biopsy but positive in
my blood culture. Please help. people have said to me to go gluten
free if it makes me feel better, however if i do not get diagnosed
my gluten free food will cost a fortune..if i get diagnosed i get
my food prescribed for £100 a year. I cant afford to go gluten free
without diagnosis. could any answers be kept quite simple and to
the point please, thankyou in adavnce my symptoms are:- severe
agonising bloating and cramps flatulence and other simptoms of IBS
head aches weak bones and teeth constant tiredness lethargy bouts
of depression short tempered and moody aching and clicking bones
and joints spaced out and unable to concentrate. i only use
laxatives if i get to around 3 to 4 days without movement. Which
can last upto a week and a half. I went off gluten after the test
and felt better im back on gluten and have been for 3 days and my
bowels now will not stop moving. Im in agony and my stool is fatty
and fowl. to
Celiac - i am not asking what celiacs
Disease is because i know what it is. I am asking
could laxatives give a false negative duodenal biopsy reading.
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Unexplained Symptoms And No Diagnosis?My mother is having a
terrible time getting to the bottom of her medical issue. Any good
solid information is welcomed. She states: I have been diagnosed
with Hashimotos Thyroiditis and Low Vitamin D. Although my labs
show that I am in the early stages of the
Disease
and there is no evidence that I have been affected by the
Disease (in the form of hypothyroidism) I have all
the symptoms one could imagine. I have had every lab test I can
think of and an ultrasound that showed goiters on my thyroid.
Biopsy showed no cancer. I have had TSH, Free T4, T3, am still
waiting on results for Free T3. I have had a full range of hormone
test. I cannot think of anything I have not had that might tell me
something, but then, I am not the doctor. I have been tested for
Celiac Disease, Pernicious Anemia, Lupus low
calcium and everything comes out negative, everything. I have
strange symptoms that don’t seem to fit hypothyroidism, exactly,
but could fit low T3 or low Dopamine. They are: poor balance,
tingling in face, lips, and hands. In addition to the typical ones
for hypothyroidism. I also am experiencing rather extreme jolts as
I sleep, as if I am having a seizure and strange sensations in my
legs, mostly left leg. So far, my doctors have no explanation. My
endocrinologist agreed to put me on a very low dose of thyroid
replacement. My neurologist thinks I would be helped with
antidepressants. I have had one MRI to rule out MS and am having
another to rule out further
Diagnosis of MS and
may have a spinal tap to rule out any odd infections of the brain.
I have symptoms of Parkinson’s, or rather, low dopamine. So, my
next Dr. visit is with a Rheumatologist. I have also seen an
alternative Dr. and am awaiting test results. He said it looked
like MS and also thyroid issues. He feels, like me, that we are
just missing one important piece of information. We are both hoping
it is the Free T3. Any suggestions?
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Looking For A
Diagnosis ... Does Anyone Have
Similar Symptoms?Here is a list of symptoms I have. All symptoms
have become present within the last 3 years, except for asthma. I
have had asthma my whole life. I am looking for answers because any
research I have done and doctors I have seen have not been able to
Diagnosis me with the underlying cause. -asthma
-MRSA (several outbreaks, last one was 1 1/2 years ago) -Severe
skin rash on hands and feet (dermatologist refers to as dermatitis)
-eczema -Alopecia -Hives -Urinary Tract Infections -tingling in
hands and feet -moody I just got a call from my doctor, informing
me that the
Tests I took most recently all came
back negative. These
Tests included thyroid,
autoimmune, anemia, and
Celiac disease. All
symptoms started to appear about 3 years ago when I had pneumonia.
At the same time, I had my first outbreak of MRSA (which appeared
in 3 separate places at once) and this is when my hair started to
fall out (Alopecia). I am becoming more and more upset about my
health problems because I cannot find any answers. I do not know
what is the cause for all these issues. I am lost with where to
turn next, so I am asking this to the public to see if anyone else
is in a similar situation or knows what I have. I absolutely
appreciate any answers or stories. Thank You!
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Is
Celiac ALWAYS Hereditary?I'm wondering if
Celiac Disease is always
hereditary. Does someone in my family have to have it for me to be
able to? I know if someone you're closely related to has it you're
more likely to have it. I know that Grave's
Disease runs somewhere on my moms side of the
family, but not the immediate family. For years I've gotten really
sharp stomach pain that everyone tells me is my appendix (it would
have burst by now I think...) or gas (it's not gas!) and I've had
other symptoms as well but what bothers me is the stomach pain. I'm
looking it up trying to figure out the possibilities to get tested
for, so don't scold about self-diagnosis, I want to make sure I'm
thoroughly tested. Any info would be great! I wont bother even
getting tested if it HAS to be hereditary. Thanks! :) I have random
dizzy spells where it feels like my brain flops over, keep running
into doorways, losing my balance, I usually have great reflexes and
coordination but not lately, headaches worse than normal, eating
anything had me either on the couch or in the bathroom going,
'ouuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuch' for hours. I started
GF two days ago and so far feel really great, my stomach is not
hurting and I can still eat really good food. I was still concerned
it was my appendix if no one in my family had it, but Ill keep
going GF and see what happens! Thank you!
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Help? Need
Diagnosis Of Rare Digestive Disorder
Possibly Related To Food Allergy?My girlfriend has been having
stomach and digestion problems her whole life. I'm not sure if
there is any correlation with her chornic migraines, but I have
determined that she is accutley alergic to soy, msg, and letuce. We
though she had
Celiac disease, but she did not
test positive for the glueten spore. Come to find almost all bread
contains soy flour. She has had two endoscapies and also had the
gastrointestinal area checked several times. She was doing good for
a while on a completly soy free and msg diet but recently is always
complaining of her stomache feeling lousy. She's afraid to eat
anything in the fear of feeling sick and I really can't blame her.
Sometimes she says it feels like she's digesting razors going down
her small intestine and feels every inch of it through. Since they
would've caught an ulcer on the endoscapy that's been rulled out. I
though it might be chrons
Disease but thought that
woud've came up too on a test. Could all her sympoms be a hormonal
problem? She has already been fully tested for
Celiac Disease and that was not
it. They did find elevated levels of white blood cells so it seems
as if something is attacking her digestive tracks which is similar
to what happens when she eats soy or lettuce or msg. I don't know
if the eleveated blood cell info might help. Conventional Doctors
can't figure out whats wrong with her. Well, it turns out the
endoscapy last october didn't catch her gastracitus and ulcer. She
was vomitting dried and fresh blood yesterday and the ER found that
she has an ulcer in her stomach caused from gastrocitus.
Essentially her stomach is producing too much stomach acid. Now
it's only to find out why this is happening.
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Celiac Disease
Tests Diagnosis
Date Published: