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| What is Celiac disease and am I more likely to have it if I have diabetes? |
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| Written by Jennifer Stallings, RD, LDN, CDE, CPT | |||||
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Celiac disease is genetic. It seems more common in those with family members with other autoimmune disorders such as type 1 diabetes, autoimmune thyroid disease, autoimmune liver disease, rheumatoid arthritis, Addison’s disease, and Sjogren’s syndrome or if the person has an autoimmune disorder themselves. Sometimes the disease is triggered for the first time after surgery, pregnancy, childbirth, viral infection, or severe emotional stress. Symptoms of celiac disease vary from person to person. Symptoms can occur in the digestive system or other parts of the body. Digestive symptoms are more common in infants and young children and may include abdominal bloating and pain, chronic diarrhea, vomiting, constipation, pale, foul-smelling, or fatty stool, irritability, and weight loss. Malabsorption of nutrients can be detrimental to a child’s normal growth and can result in failure to thrive, delayed growth and short stature, delayed puberty, and dental enamel defects. Adults are less likely to have digestive symptoms. They have unexplained iron-deficiency anemia, fatigue, bone or joint pain, arthritis, bone loss or osteoporosis, depression or anxiety, tingling numbness in hands and feet, seizures, missed menstrual periods, infertility or recurrent miscarriage, canker sores inside the mouth, and an itchy skin rash called dermatitis herpetiformis. Some people with the disease may not have any symptoms at all. The final step is a gluten free diet, and if symptoms go away, a diagnosis is confirmed. Treatment is a gluten free diet no matter what the symptoms are. This diet is very cumbersome, and a person should meet with a dietitian for education on label reading and for foods that one should avoid.
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