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Celiac Disease
An autoimmune disease in which gluten — found in wheat, barley and rye — damages the small intestine. Get tested before cutting out gluten; a strict, lifelong gluten-free diet is the only treatment.
Don’t go gluten-free before you are tested. If you think you might have celiac disease, talk with your doctor about testing first. Avoiding gluten before testing can make the results inaccurate (NIDDK (opens in a new tab), MedlinePlus (opens in a new tab)), and celiac blood tests are only accurate while you are still eating gluten (Celiac Disease Foundation (opens in a new tab)).
See a doctor about testing if you have:
- Ongoing diarrhea, especially with weight loss, greasy or fatty stools, belly pain or bloating — U.S. gastroenterology guidelines say people with these signs should be tested (ACG guideline, 2023 (opens in a new tab)).
- Iron-deficiency anemia, or low folate or vitamin B12, which can be signs of celiac disease (Celiac Disease Foundation (opens in a new tab)).
- A child who is not growing or gaining weight as expected, has delayed puberty, is losing weight, or has damaged tooth enamel (NIDDK (opens in a new tab)). Young children with failure to thrive or persistent diarrhea should be checked by a pediatric gastroenterologist (Celiac Disease Foundation (opens in a new tab)).
Family members: parents, brothers, sisters and children of someone with celiac disease have about a 1 in 10 chance of having it too (Celiac Disease Foundation (opens in a new tab)). Guidelines say these first-degree relatives should be tested if they have possible signs, and that testing should be considered even if they have none (ACG guideline, 2023 (opens in a new tab)). People with type 1 diabetes should also ask their doctor about testing (NIDDK (opens in a new tab)).
What is celiac disease?
Celiac disease is a long-term digestive and immune disorder that damages the small intestine. It is triggered by eating gluten, a protein found naturally in wheat, barley and rye (NIDDK (opens in a new tab)). In people with celiac disease, gluten sets off an immune attack on the villi — tiny finger-like projections lining the small intestine that absorb nutrients. When the villi are damaged, the body can’t absorb food properly (Celiac Disease Foundation (opens in a new tab)). It is also called celiac sprue, nontropical sprue or gluten-sensitive enteropathy (NIDDK (opens in a new tab)).
How common is it, and who gets it?
Experts estimate about 2 million people in the United States have celiac disease, and about 1 percent of people worldwide; many of them have not been diagnosed (NIDDK (opens in a new tab)). It can only develop in people with certain genes, and it is more likely if someone in your family has it. It affects children and adults everywhere; in the U.S. it is more common in white Americans, and it is diagnosed more often in females than males. It is also more common in people with Down syndrome, Turner syndrome and Williams syndrome (NIDDK (opens in a new tab)). Celiac disease can start at any age after a person begins eating gluten (Celiac Disease Foundation (opens in a new tab)).
Symptoms in adults and children
Symptoms vary widely and can come and go. Digestive symptoms are more common in children than in adults (NIDDK (opens in a new tab)). Some people have no symptoms at all but still have damage to the intestine and are at risk of long-term complications (Celiac Disease Foundation (opens in a new tab)).
- Digestive symptoms can include bloating, gas, ongoing diarrhea, constipation, loose, greasy, bulky, bad-smelling stools, nausea or vomiting, belly pain, and lactose intolerance caused by the intestinal damage (NIDDK (opens in a new tab)). See our Bowel Problems guide for other causes of these symptoms.
- In children, poor absorption of nutrients during growth can lead to failure to thrive, slowed growth and short height, weight loss, delayed puberty, damage to the enamel of the permanent teeth, and mood changes or irritability (NIDDK (opens in a new tab)).
- Symptoms outside the gut can include tiredness, joint or bone pain, depression or anxiety, headaches, balance problems, seizures or nerve tingling (peripheral neuropathy), infertility or missed periods, repeated miscarriages, and mouth problems such as canker sores, a dry mouth, or a red, smooth, shiny tongue (NIDDK (opens in a new tab)). In older children, recurring mouth sores that look like canker sores can be a clue (Celiac Disease Foundation (opens in a new tab)), and a dentist may be the first to notice enamel defects or canker sores (NIDDK (opens in a new tab)).
- Dermatitis herpetiformis is an itchy, blistering rash, usually on the elbows, knees, buttocks, back or scalp. It affects about 2 to 3 percent of children and 10 to 20 percent of adults with untreated celiac disease, and some people have the rash and no other symptoms (NIDDK (opens in a new tab)).
Related conditions
Some people with celiac disease also have other immune-related disorders, including type 1 diabetes; thyroid diseases such as Hashimoto’s and Graves’ disease; Addison’s disease; selective IgA deficiency; Sjögren’s syndrome; and some autoimmune liver diseases (NIDDK (opens in a new tab)).
Why treatment matters: complications
Without treatment, long-term complications can include osteoporosis or bone softening (osteomalacia), anemia, malnutrition, nervous system problems and reproductive problems. Rare complications include a cancer of the small intestine (adenocarcinoma), non-Hodgkin lymphoma, and liver damage that can lead to cirrhosis or liver failure (NIDDK (opens in a new tab)). People who have no symptoms can still develop complications over time if they are not treated (NIDDK (opens in a new tab)).
How it is diagnosed
- Blood tests look for antibodies that are often high in people with untreated celiac disease (NIDDK (opens in a new tab)). For most children and adults the main test is tissue transglutaminase IgA (tTG-IgA), together with a total IgA level to make sure the result can be trusted (Celiac Disease Foundation (opens in a new tab)). Symptoms alone can’t diagnose celiac disease, because they overlap with conditions such as irritable bowel syndrome and lactose intolerance (NIDDK (opens in a new tab)).
- Intestinal biopsy: during an upper endoscopy, a doctor passes a thin, flexible camera through the mouth and takes small tissue samples from the small intestine to look for damage (NIDDK (opens in a new tab)). The lining of the intestine has no nerve endings, so it isn’t painful, though some people have a sore throat afterward (Celiac Disease Foundation (opens in a new tab)). The 2023 American College of Gastroenterology guideline says a biopsy is needed in most people to confirm the diagnosis, with a no-biopsy approach possible for selected children (ACG guideline, 2023 (opens in a new tab)).
- Skin biopsy may be used when a rash could be dermatitis herpetiformis (NIDDK (opens in a new tab)); a positive skin biopsy confirms both the rash and celiac disease without an endoscopy (Celiac Disease Foundation (opens in a new tab)).
- Genetic tests check for the gene types DQ2 and DQ8. Not having them makes celiac disease very unlikely, but having them does not mean you have it — most people who carry them never develop celiac disease (NIDDK (opens in a new tab)). Genetic testing can help when antibody results are unclear, or to check the risk of family members (Celiac Disease Foundation (opens in a new tab)).
Already gluten-free? Your doctor may suggest a “gluten challenge” — eating gluten again for a period so antibodies can build up before testing. It should only be done under the supervision of a doctor experienced in celiac disease, and never during pregnancy (Celiac Disease Foundation (opens in a new tab)).
Side by side
Six approaches compared
For every condition we look at the same six approaches: what each involves, what it typically costs, and what a patient can realistically expect.
| Approach | What it involves | Estimated cost | What to expect |
|---|---|---|---|
| Conventional medicine (AMA) | Diagnosis with blood tests and an intestinal biopsy, then a strict, lifelong gluten-free diet taught by a registered dietitian, with follow-up blood tests, checks for vitamin and mineral shortfalls and bone density, and vaccine review. | Upper endoscopy with biopsy about $990–$4,483 self-pay in published examples; genetic tests run into the hundreds of dollars. Medicare covers dietitian visits (medical nutrition therapy) only for diabetes or kidney disease. Antibody blood test cost being researched. | Most people improve on the diet, often within days to weeks; the intestine can take months (children) to years (adults) to heal. There is no cure, and no medicine yet replaces the diet. |
| Chiropractic | Being researched — coming soon. | ||
| Acupuncture | Being researched — coming soon. | ||
| Herbal medicine | No herb, pill or enzyme supplement treats celiac disease or makes gluten safe. The useful role is checking supplements for hidden gluten and correcting proven deficiencies with your clinician. | Cost estimate being researched. | “Gluten-digesting” enzyme products have no scientific basis for protecting people with celiac disease, and probiotics are unproven for it. Talk with your doctor or pharmacist first. |
| Massage therapy | Being researched — coming soon. | ||
| MBHA Wellness Coach | Reading labels, avoiding cross-contact at home and when eating out, choosing oats safely, budgeting, balanced nutrition, and coping with a lifelong diet at home, school and work. | Cost estimate being researched. Packaged gluten-free foods cost far more than regular versions in a U.S. price study. | Practical habits that make the gluten-free diet easier to stick to — the key to healing — alongside, never instead of, medical care. |
Approach 1 of 6
Conventional medicine (AMA)
The only treatment for celiac disease is a strict gluten-free diet for life (Celiac Disease Foundation (opens in a new tab)). There is no cure (MedlinePlus (opens in a new tab)), and current care means strict adherence to the diet plus lifelong medical follow-up (ACG guideline, 2023 (opens in a new tab)).
1. A strict, lifelong gluten-free diet
Following a gluten-free diet relieves symptoms and heals the small intestine, and it must be followed for life to keep symptoms and damage from coming back (NIDDK (opens in a new tab)). Many people feel better within days to weeks (NIDDK (opens in a new tab)); children and teens typically respond well, and most children feel much better after two weeks on the diet (Celiac Disease Foundation (opens in a new tab)). Healing of the intestine most often takes 3 to 6 months in children and may take 2 to 3 years in adults (MedlinePlus (opens in a new tab)). Even small amounts of gluten, such as crumbs from a shared cutting board or toaster, can trigger damage (Celiac Disease Foundation (opens in a new tab)). Some problems, such as short height and tooth damage, may not improve if diagnosis came late (NIDDK (opens in a new tab)).
2. A registered dietitian
Your doctor may refer you to a registered dietitian who specializes in celiac disease, to teach you how to check labels for gluten, plan everyday meals and make healthy choices (NIDDK (opens in a new tab)). Guidelines describe an interview with a dietitian experienced in the gluten-free diet as the standard way to check how well the diet is going (ACG guideline, 2023 (opens in a new tab)).
3. Checking nutrients and bones
- At diagnosis, your doctor may test for low levels of certain vitamins and minerals and may recommend or prescribe supplements if you need them (NIDDK (opens in a new tab)). People with celiac disease are often low in nutrients such as iron, calcium, folate, vitamin B12 and vitamin D (Celiac Disease Foundation (opens in a new tab)).
- A bone mineral density test may be ordered to check for osteoporosis (NIDDK (opens in a new tab)).
- The Celiac Disease Foundation’s follow-up checklist also includes reviewing hepatitis B, flu and pneumococcal vaccines (Celiac Disease Foundation (opens in a new tab)), and the ACG guideline suggests pneumococcal vaccination for people with celiac disease (ACG guideline, 2023 (opens in a new tab)).
- Medicines rarely contain gluten, but ask a pharmacist about the ingredients of prescription and over-the-counter medicines and supplements (NIDDK (opens in a new tab)). Don’t stop a prescribed medicine on your own.
4. Follow-up visits
Follow-up may include blood tests for celiac antibodies, which typically return to normal with treatment, and sometimes another biopsy to see whether the intestine has healed (NIDDK (opens in a new tab)). The Celiac Disease Foundation recommends seeing your doctor 3 to 6 months after diagnosis and yearly after that (Celiac Disease Foundation (opens in a new tab)). The dermatitis herpetiformis rash may take 6 months to 2 years on the diet to clear, and a medicine such as dapsone may be prescribed in the meantime (NIDDK (opens in a new tab)).
5. When the diet doesn’t seem to work
In about 20 percent of people, symptoms continue or come back despite a gluten-free diet. The usual cause is small, hidden amounts of gluten; other causes include irritable bowel syndrome, lactose intolerance, microscopic colitis, pancreas problems or bacterial overgrowth (NIDDK (opens in a new tab)). Rarely, the intestine stays damaged even on a strict diet. This is called refractory celiac disease; it can lead to malnutrition or a type of lymphoma and needs specialized care (NIDDK (opens in a new tab), ACG guideline, 2023 (opens in a new tab)).
New medicines
Several drug treatments are being tested in clinical trials, but for now the gluten-free diet remains the only available treatment (Celiac Disease Foundation (opens in a new tab)).
What it costs
- Upper endoscopy with biopsy: prepaid self-pay prices of about $990–$4,483; a typical hospital cash price of about $1,367 may not include anesthesia or the lab fee for examining the biopsy (The Pricer, 2026 (opens in a new tab)). Ask each provider for a written estimate.
- Genetic testing: runs into the hundreds of dollars and may be covered by some insurance plans (Celiac Disease Foundation (opens in a new tab)).
- Dietitian visits: Medicare covers medical nutrition therapy with a registered dietitian only for people with diabetes or kidney disease, or a kidney transplant in the last 36 months (Medicare.gov (opens in a new tab)), so celiac disease alone doesn’t qualify. Check what your plan covers.
- Antibody blood tests: MBHA cost estimate being researched.
Approach 4 of 6
Herbal medicine
No pill lets you eat gluten safely. The gluten-free diet is the only treatment for celiac disease (Celiac Disease Foundation (opens in a new tab)). Products sold as “gluten-digesting” enzymes are dietary supplements, not approved medicines. A 2017 review of 14 of them found their claims to break down harmful gluten had no scientific basis; their own labels said they had not been evaluated by the FDA and were not meant to treat or prevent any disease (Krishnareddy et al., 2017 (opens in a new tab)). A 2015 lab study found that five such supplements left the harmful parts of gluten largely intact (Janssen et al., 2015 (opens in a new tab)). Don’t use them to eat gluten or as a safety net.
Supplements can contain hidden gluten
Herbal and nutritional supplements and vitamins can contain gluten, so ask a pharmacist about the ingredients (NIDDK (opens in a new tab)). Dietary supplements labeled “gluten-free” must meet the same FDA rule as foods (Celiac Disease Foundation (opens in a new tab)). One “gluten-digesting” enzyme product in the 2017 review even declared wheat as an allergen (Krishnareddy et al., 2017 (opens in a new tab)).
Probiotics
The 2023 ACG guideline found too little evidence to recommend for or against probiotics for celiac disease; despite their wide use, a benefit has not been shown (ACG guideline, 2023 (opens in a new tab)). Probiotics are sold as supplements that don’t need FDA approval, and some products have contained microbes not listed on the label (NCCIH (opens in a new tab)).
Correcting deficiencies — with your clinician
Vitamins and minerals do have a role when tests show you are low: your doctor may recommend or prescribe them (NIDDK (opens in a new tab), MedlinePlus (opens in a new tab)). Talk with your doctor before taking any supplement or complementary product (NIDDK (opens in a new tab)). We don’t list doses here.
Approach 6 of 6
MBHA Wellness Coach
Living gluten-free is a big change. An MBHA Wellness Coach can help you turn your doctor’s and dietitian’s advice into everyday habits — a coach supports, but doesn’t replace, your dietitian.
Reading labels
- The FDA rule: foods labeled “gluten-free,” “no gluten,” “free of gluten” or “without gluten” must contain less than 20 parts per million (ppm) of gluten (FDA (opens in a new tab)), an amount too small to cause problems for most people with celiac disease (NIDDK (opens in a new tab)).
- The rule doesn’t cover meat, poultry and some egg products (regulated by the USDA) or most alcoholic drinks (NIDDK (opens in a new tab)). Traditional beers, ales and lagers are not gluten-free (Celiac Disease Foundation (opens in a new tab)).
- Without a gluten-free label, read the ingredients. Gluten hides in malt, colorings, flavorings, starches and thickeners, and in foods like soups, condiments, salad dressing, candy, hot dogs and ice cream (NIDDK (opens in a new tab)). “Wheat-free” doesn’t mean gluten-free, and a missing “contains wheat” warning doesn’t rule out barley or rye (Celiac Disease Foundation (opens in a new tab)).
- If you aren’t sure, don’t eat it — contact the maker (NIDDK (opens in a new tab)).
- Non-food products can carry gluten too: lipstick and lip balm, toothpaste and mouthwash, cosmetics, children’s modeling dough and communion wafers (NIDDK (opens in a new tab)).
Avoiding cross-contact at home
- Cross-contact happens when gluten-free food touches food with gluten — while it is grown, processed, stored, prepared or served (NIDDK (opens in a new tab)).
- Store and prepare your gluten-free food separately from family members’ foods that contain gluten (NIDDK (opens in a new tab)). Crumbs from a shared toaster or cutting board are enough to cause harm (Celiac Disease Foundation (opens in a new tab)).
- Skip bulk bins, which risk cross-contact (Celiac Disease Foundation (opens in a new tab)).
- Home gluten-detection gadgets aren’t recommended for routine use: they can’t tell trivial traces from meaningful exposure (ACG guideline, 2023 (opens in a new tab)).
A word on oats
Most people with celiac disease can eat moderate amounts of oats, but oats are often cross-contaminated with wheat, so choose only oats labeled gluten-free (NIDDK (opens in a new tab)). A small number of people react to oats themselves, so ask your doctor or dietitian before adding them and watch for symptoms (ACG guideline, 2023 (opens in a new tab), Celiac Disease Foundation (opens in a new tab)).
Eating out and social events
- Look for restaurants with gluten-free menus, check menus online or call ahead, tell your server you have celiac disease, and ask how food is prepared (NIDDK (opens in a new tab)).
- The FDA suggests asking what the restaurant means by “gluten-free,” what ingredients are used, and how the dish is prepared (FDA (opens in a new tab)).
- Tell hosts ahead of gatherings, and bring safe food if you’re not sure there will be any (NIDDK (opens in a new tab)).
Budgeting
Packaged gluten-free foods tend to cost more, and restaurants may charge more for gluten-free dishes (NIDDK (opens in a new tab)). In a U.S. price study (prices collected in 2016), gluten-free products cost 183% more than their wheat-based versions overall, with bread and pasta about 229% and 227% more (Lee et al., 2019 (opens in a new tab)). Building meals around naturally gluten-free foods — meat, fish, fruit, vegetables, rice and potatoes — is the most cost-effective and healthy approach (Celiac Disease Foundation (opens in a new tab), NIDDK (opens in a new tab)).
Eating well, not just gluten-free
A gluten-free diet planned without expert help may fall short on fiber, iron and calcium, and some packaged gluten-free foods are higher in fat and sugar (NIDDK (opens in a new tab)). People with celiac disease are also often low in B vitamins such as folate, niacin, riboflavin and B12 (Celiac Disease Foundation (opens in a new tab)). A coach can help you plan varied meals with naturally gluten-free grains such as rice, corn, quinoa, buckwheat and amaranth (NIDDK (opens in a new tab)), and keep track of the checks your dietitian recommends.
The emotional side
A lifelong diet completely free of gluten can be costly and challenging (Celiac Disease Foundation (opens in a new tab)), and depression and anxiety can be part of celiac disease itself (NIDDK (opens in a new tab)). Support groups can help as you adjust (NIDDK (opens in a new tab), MedlinePlus (opens in a new tab)), and specialists recommend referral to a mental health professional when needed for coping with the diet or with problems affording food (Celiac Disease Foundation (opens in a new tab)).
School and work
- In federally funded schools, families can request a Section 504 plan to arrange accommodations for a child with celiac disease; a letter from the child’s doctor helps (Celiac Disease Foundation (opens in a new tab)).
- Classroom materials such as modeling dough and baking projects can expose children to gluten, so gluten-free alternatives and good handwashing matter (Celiac Disease Foundation (opens in a new tab)).
- At work and when traveling, a coach can help you plan safe lunches and snacks and practice explaining your needs — the same steps as for eating out (NIDDK (opens in a new tab)).
Another approach
Celiac disease, gluten sensitivity or wheat allergy?
All three can cause symptoms after eating wheat, but they are different conditions — one more reason to be tested before changing your diet.
- Celiac disease is an autoimmune disease: gluten from wheat, barley and rye triggers immune damage to the small intestine, and the gluten-free diet must be strict and lifelong (NIDDK (opens in a new tab), NIDDK (opens in a new tab)).
- Non-celiac gluten (or wheat) sensitivity can cause similar symptoms, such as belly pain and tiredness, but it does not damage the small intestine the way celiac disease does (NIDDK (opens in a new tab)). It is identified when symptoms improve without gluten after celiac disease and wheat allergy have been ruled out. Researchers are still studying its cause, and parts of wheat other than gluten may play a role (Celiac Disease Foundation (opens in a new tab)).
- Wheat allergy is a food allergy. It can cause hives, a rash, stomach upset or a runny nose, and occasionally anaphylaxis, a life-threatening reaction. It is diagnosed by an allergist with skin-prick or blood tests, is most common in children, and is often outgrown (ACAAI (opens in a new tab)). It does not cause long-term damage to the small intestine (NIDDK (opens in a new tab)). Many people with a wheat allergy can eat other grains, but not everyone, so ask your allergist (ACAAI (opens in a new tab)). See our Allergies guide for the signs of anaphylaxis.
Going gluten-free “just in case” isn’t harmless: researchers have found no evidence that a gluten-free diet improves health or helps weight loss for people without a gluten-related condition, and it can make celiac testing inaccurate (NIDDK (opens in a new tab)).
Still being researched: Chiropractic, Acupuncture, Massage therapy. We add each approach once its costs and results are sourced. Are you a practitioner with experience treating Celiac Disease? Tell us.
Member stories
Living with Celiac Disease? Share your experience
Real experiences help others choose. Tell us what you tried — conventional medicine, chiropractic, acupuncture, herbs, massage or coaching — what it cost and what changed.
Sources
- NIDDK — Definition & facts for celiac disease (opens in a new tab)
- NIDDK — Symptoms & causes of celiac disease (opens in a new tab)
- NIDDK — Diagnosis of celiac disease (opens in a new tab)
- NIDDK — Treatment for celiac disease (opens in a new tab)
- NIDDK — Eating, diet & nutrition for celiac disease (opens in a new tab)
- MedlinePlus — Celiac disease (opens in a new tab)
- FDA — ‘Gluten-free’ means what it says (opens in a new tab)
- Celiac Disease Foundation — What is celiac disease? (opens in a new tab)
- Celiac Disease Foundation — Symptoms of celiac disease (opens in a new tab)
- Celiac Disease Foundation — Celiac disease in children (opens in a new tab)
- Celiac Disease Foundation — Screening (opens in a new tab)
- Celiac Disease Foundation — Diagnosis (opens in a new tab)
- Celiac Disease Foundation — Treatment & follow-up (opens in a new tab)
- Celiac Disease Foundation — Future therapies for celiac disease (opens in a new tab)
- Celiac Disease Foundation — Non-celiac gluten and wheat sensitivity (opens in a new tab)
- Celiac Disease Foundation — Gluten-free foods (opens in a new tab)
- Celiac Disease Foundation — Label reading & the FDA (opens in a new tab)
- Celiac Disease Foundation — School resources (K–12) (opens in a new tab)
- Rubio-Tapia et al. — ACG guidelines update: diagnosis and management of celiac disease, American Journal of Gastroenterology, 2023 (PubMed) (opens in a new tab)
- Guideline Central — Summary of the ACG celiac disease guideline, 2023 (opens in a new tab)
- American College of Allergy, Asthma & Immunology (ACAAI) — Wheat and gluten allergy (opens in a new tab)
- Krishnareddy et al. — Commercially available glutenases: a potential hazard in coeliac disease, 2017 (PubMed) (opens in a new tab)
- Janssen et al. — Ineffective degradation of gluten by currently available digestive enzyme supplements, PLOS ONE, 2015 (PubMed) (opens in a new tab)
- Lee et al. — Persistent economic burden of the gluten free diet, Nutrients, 2019 (PubMed) (opens in a new tab)
- NCCIH — Probiotics: usefulness and safety (opens in a new tab)
- Medicare.gov — Medical nutrition therapy services (opens in a new tab)
- The Pricer — Endoscopy cost without insurance (opens in a new tab)
This page is for education only and is not medical advice. Costs are typical U.S. ranges and estimates; yours will depend on your provider, location and insurance. Talk with your doctor before starting, stopping or combining any treatment. In an emergency, call 911. See our disclaimer.
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