Here is a good article about the facts of celiac disease. Click on this link to see the article Celiac Disease from the American College of Gastroenterology or read it below:
CELIAC DISEASE
By Conor G. Loftus M.D. and Joseph A. Murray M.D.
Division of Gastroenterology and Hepatology
Mayo Clinic, Rochester, Minnesota, USA.
1. What is Celiac Disease (CD)?
Celiac disease (CD) is a chronic (long-term) digestive disease in which patients have
inflammation or irritation in the small intestine, which causes difficulties with absorbing
nutrients from the diet. Patients with CD often have other family members with the
condition and are therefore susceptible to this disease. Inflammation in the bowel occurs
when a patient with CD begins to eat food that contains gluten. Gluten is the name given
to certain types of proteins found in wheat, barley, rye and related grains. Oats are
currently considered not to be toxic to persons with CD. However, due to the high
possibility of contamination with other gluten containing grains, oats are typically not
recommended for people with celiac disease. When food containing the gluten protein
arrives in the small bowel, the immune system reacts against the gluten, causing an
inflammatory reaction in the wall of the bowel. The small intestine lining is covered by
millions of villi (see diagram), which act to increase the surface area of the intestine
allowing improved absorption of food. The villi or finger like projections of the small
intestine are temporarily damaged by the inflammation in CD, which decreases
absorption of food. When gluten is removed from the diet inflammation is reduced and
the intestine begins to heal. The time when a patient develops symptoms varies from
patient to patient after their first contact with the gluten protein.
2. How common is Celiac Disease?
Approximately 1 out of every 250 people may have CD though only 1 out of 10 people
with celiac disease may be actually diagnosed and are aware that they have this disease.
Some of these patients have mild forms of the disease and may have no symptoms or
only mild symptoms. There may be as many as 1 million people in the United States and
3-5 million in the world with CD.
3. Who does Celiac Disease affect?
CD affects whites more often than non-whites. Infants and children may have celiac
disease, but CD is more commonly diagnosed in adulthood, and people can be diagnosed
even in their seventies or eighties. Females are more likely to have celiac disease than
males.
4. What are the main symptoms of Celiac Disease?
The symptoms or signs of disease will depend on how much and how badly the intestine
is inflamed. Some people have mild inflammation with few symptoms. Even though they
may feel quite well there is still damage occurring to the lining of the bowel. Other
people have more severe inflammation, which causes symptoms that may be severe
enough to lead them to visit their doctor. Occasionally individuals will not have any
symptoms even though their small intestine is severely inflamed.
The most common symptoms are:
1. Abdominal pains
2. Bloating and gas
3. Diarrhea
4. Stools that may float or smell very bad
5. Weight loss
6. Poor growth or weight loss in children
7. Anemia (low blood count)
Other symptoms are:
1. Feeling weak
2. Tiredness
3. Low vitamin levels – especially iron, calcium and folate
4. Bone and joint pains
5. Osteoporosis
6. A skin rash that lasts
Someone with celiac disease may have a variety of the above symptoms and different
people with celiac disease may have completely different symptoms.
5. How is Celiac Disease diagnosed?
It is important to remember that most patients with abdominal pain, bloating or diarrhea
do not have celiac disease. In order to test for celiac disease with blood tests and/or
endoscopy the doctor should suspect celiac disease as the cause for the symptoms. When
the doctor thinks that celiac disease is possible, but not very likely, then blood tests alone
are done. If the blood tests are normal, other tests will not be necessary. Sometimes the
doctor strongly suspects that the symptoms are due to celiac disease, or another similar
illness, and will request an endoscopy and biopsy (sampling of the tissue of the small
intestine). All tests for celiac disease must be done while the patient is on a normal diet
that contains gluten. Patients who are concerned that they may have celiac disease should
probably not restrict their diet prior to seeking medical evaluation because this may cause
false test results but they should seek prompt medical testing.
Blood tests:
Specific antibody blood tests are used to diagnose patients with CD. These blood tests are
also used to test people who may be at risk for having CD but have no symptoms
(relatives of patients with CD). The 2 most used tests are the endomysial antibody and
tissue transglutaminase antibody tests. Other tests such as tests for gliadin antibodies are
not as accurate because they can be abnormal in patients who don’t have celiac disease
and are healthy or in people with other digestive problems. Other tests for allergies will
not detect celiac disease. Tests on saliva or stool for antibodies are not good substitutes
for the blood-based tests.
Endoscopy:
Establishing a firm diagnosis of CD requires taking biopsy samples of the small bowel
using endoscopy. Endoscopy involves insertion of a thin flexible tube through the mouth
into the stomach and small bowel. Samples are taken from the wall of the small bowel
and are examined under a microscope for changes of CD. This test is usually performed
with the aid of sedatives.
6. How is Celiac Disease treated?
Celiac disease is treated by avoiding all foods that contain gluten. Gluten is what causes
inflammation in the small bowel. When this is removed from the diet, the bowel will heal
and return to normal. Medications are not normally required to treat CD except in
occasional patients who do not respond to a gluten free diet.
Gluten-free diet:
The following grains contain Gluten and
are
NOT ALLOWED IN ANY FORM:
Wheat, rye, barley, kamut, einkorn, spelt
and triticale
Frequently overlooked foods that often contain gluten
Breading
Imitation bacon
Broth
Imitation seafood
Coating mixes
Marinades
Communion wafers
Processed meats
Croutons
Sauces
Pastas
Stuffings
Getting used to the gluten-free diet requires some lifestyle changes. The key to
understanding the gluten-free diet is to become a good ingredient label reader. If a food
has questionable ingredients avoid it and find a similar product that you know is gluten-
free. Foods containing the following ingredients are questionable and should not be
consumed unless it is verified that they do not contain or are not derived from prohibited
grains; these products are:
Unidentified:
Modified food starch
Hydrolyzed vegetable protein (HVP)
Hydrolyzed plant protein (HPP)
Malt vinegar
Soy sauce or soy sauce solids
Brown rice syrup
Dextrin
Textured vegetable protein (TVP)
Vegetable gum
Be aware that medications may contain gluten ingredients. Gluten containing fillers may
be in both prescription and over the counter medications. It is essential to ensure that any
medications being taken are gluten free.
ALLOWED
Rice, corn, soy, potato, tapioca, bean,
sorghum, quinoa, millet, buckwheat, tef
and nut flours
7. For how long do you remain on the gluten-free diet?
Once a diagnosis of CD is established, these individuals need to remain on the gluten-
free diet for the rest of their lives. While this may be difficult at first, patients usually
adapt quite well over time.
8. Is there any other way of treating Celiac Disease?
No. There is no other treatment currently available. All patients with CD must remain on
a strict gluten-free diet. Medications are not normally required. Supplemental vitamins,
calcium and magnesium may sometimes be recommended but patients are advised to
check with their physician about these supplements. Rarely steroids or other drugs are
used to suppress the immune system but only in the most severe of cases.
9. What will happen if you don’t adhere to the gluten-free diet?
Patients with CD who do not adhere to the gluten-free diet usually continue to suffer
from symptoms such as abdominal pain, bloating, gas and diarrhea. In addition, these
patients are at higher risk for developing complications of CD such as cancer of the small
bowel and narrowings in the bowel due to inflammation.
10. What are other complications of Celiac Disease?
Other complications of CD that may be avoided by strictly following a gluten-free diet
include tiredness, poor growth, decreased adult height, osteoporosis, bone pain, joint
pain, difficulty having children, narrowing of the intestine, cancer of the esophagus (food
tube) and small bowel, lymphoma (another type of cancer) and neuropathy (unsteady
walking and confusion which may be severe).
11. Where can I find more information on Celiac Disease?
http://www.celiac.org/
http://clinicaltrials.gov/ct/gui/action/FindCondition?ui=D002446&recruiting=true
http://www.naspgn.org
http://www.med.utah.edu/pated/handouts/handout.cfm?id=874
http://www.celiac.com/cgi-bin/webc.cgi/st_main.html?p_catid=21
http://www.celiac.com/cgi-bin/webc.cgi/st_main.html?p_catid=16
http://www.causeyourespecial.com/aboutus.html
http://www.allrecipes.com/directory/586.asp
http://www.celiac.com
What is tef? It is listed under “allowed” first section?
Rob: Teff is a grain that is gluten free. Look at this post I wrote about teff. You can add teff to flour mixes or add it to a hot cereal mix. You can make Teff Polenta.
Kathy
MY SON IS 19. HE WAS DIAGNOSED WITH CELIAC AS AN INFANT. HE HAS BEEN EATING NORMAL FOODS FOR AT LEAST 17-18 YEARS AND HAS NEVER SHOWN ANY SYMPTOMS. HE HAD A BIOPSY DONE TWO MONTHS AGO AND THE RESULTS WERE NEGATIVE. DOES THAT MEAN THAT HE COULD HAVE OUTGROWN THE DISEASE?
NICK
~Nick, According to Dr. Peter Green, who wrote “Celiac Disease, A Hidden Epidemic”:
Generally many people who appear symptom free will find that their symptoms will catch up with them in their 40′s if they have not been following a gluten free diet. At that point if they are not familiar with the many ways that Celiac can manifest they may not make the connection between their symptoms and their diet. They may show nothing more than a headache or depression, or possibly ADHD, or they may have something as simple as dermatitis. Many people think nothing of the fact that they don’t have a bowel movement for 2 or 3 days. That can be a significant symptom. Often times Drs will misdiagnose these symptoms. So even though you think your son is symptom free if you dig a little deeper you will find that his diet is affecting him. If he ignores this it could have long lasting effects on his health that become increasingly difficult to deal with.
According to my doctor, chronic constipation can also be a symptom of coeliacs, but few websites mention it.
I have read several papers and case studies in which neurological symptoms were the only symptoms of otherwise silent coeliacs, particularly ataxia and neuropathy. But just try persuading a neurologist that you can’t stand because there is something wrong with your gut!
This is due to malabsorption of B12 and can be helped by adding a liquid B12 supplement. And yes most drs don’t make the connection unless they are intimately familiar with the disease, which most American Drs are not. As an Acupuncturist I find far too many people who should have been diagnosed with celiac by their Drs but weren’t. I have generally noticed that alternative medical practitioners are far more likely to consider Celiac issues as a source of client’s problems than mainstream Drs.
yes chronic constipation is a symptom of CD
One of the main things that many of these articles miss is the fact that while many celiacs are skinny, a great deal of celiacs are actually over fat. This is due to the body attempting to store fat in compensation of nutritional deficiencies and a lowered metabolism. Especially if the celiac issue is combined with autoimmune thyroid disease. Because this is left out of the documentation many doctors rule out the celiac diagnosis as a possibility when dealing with over fat people with intestinal issues.
I was first diagnosed with autoimmune thyroid disease in my early 20s and didn’t find out about the celiac until I was working on my medical degree (late 30′s early 40′s) and noticed that many of the symptoms of Celiac matched my own symptoms. I did my own testing and started on a gluten free diet. Once I realized the connections between autoimmune conditions and Celiac I realized that was the underlying contributor to my hypothyroidism. Now many in my family have been diagnosed with Celiac with at least 1/2 of them overfat.
CAN IT ALSO BE A MISDIAGNOSIS IN REVERSE-MEANING THAT THE DOCTOR MIGHT HAVE THOUGHT THAT IT WAS CELIAC BUT IT WASN’T?
Yes, Nick, you can have a false positive. If you have questions about your tests results go back to a doctor who knows about celiac disease. Good luck.
MY SON HAS BEEN REJECTED FROM JOINING THE ARMY BECAUSE OF CELIAC DESEASE. SINCE HE HASN’T HAD ANY SYMPTOMS IN 20 YEARS…I THINK IT MIGHT HAVE BEEN A MISDIAGNOSIS. DOES ANYONE KNOW IF A GENETIC TEST WILL ANSWER THE QUESTION FOR SURE?
Nick, There is a DNA test that will tell you if you have the two genes necessary to get celiac disease. But I am wondering, he must have been diagnosed as a very young child. Has he been eating gluten-free all his life since then? If he has been eating gluten he can get the blood test and see if he has the anti-bodies against gluten. The Army doesn’t want to have to deal with his eating restrictions if he really DOES have celiac disease. You need to do a little more research with a physician. Good luck ~ Kathy
HE WAS ONE YEARS OLD WHEN HE WAS DIAGNOSED AND HAS BEEN EATING NORMAL FOOD EVER SINCE AND NEVER HAD A REACTION. I’M JUST LOOKING FOR A TEST (IF THERE IS SUCH A TEST) THAT WILL ANSWER THE QUESTION FOR SURE ONCE AND FOR ALL, DOES HE HAVE THE DISEASE OR NOT!!!
I was diagnosed with Coeliac’s disease at the beginning of 2011. Before that I would eat anything and everything and still can’t seem to stop. I’ve been having very bad stomach pains and lots of other pain in my abdomen area for a long time. I try so hard to eat properly because of the fear the doctor has put into me, but get so dang frustrated. I try to bake bread but seem to mess it up. If I get it right then it goes bad fast. It’s like I can’t seem to maintaina healthy diet and enjoy food. I have no patience for making “everything” that I eat and no will power. I’m 238 pounds and 5’8″ tall and way obese according to the BMI index. Living in remote region in Northern Alaska makes it a bit incovenient to buy gluten-free products without bartering a seal and a whale for shipping. So… I . I dont know how much longer I can keep this up. I constantly tell myself that I’ve been eating this way for 41 years and have been miserable for just about that long that why does it matter if I’m gluten free? It’s an everyday struggle with life and I really have no support groups except what’s on this internet.
I have arthritis, iron deficiency, fatigue and other symptoms simular to celiac diease/add/depression for over ten years. I had a blood test a couple of years ago to test for antibodies relating to gluten/celiac but it came back negative. After reading your blog, I see that you had a blood test that was negative but went back for a second blood test that was positive. So I think I will get back in contact with my doctor and see if I can have another blood test ensuring I eat plently of gluten the days leading up to the blood test. After your blood test did you have to have an biopsy test done to confirm it further?