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Showing results for tags 'recovery time'.
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Hello, I just wanted to see if anyone else had similar symptoms during recovery. After dealing with severe abdominal pain for a couple of months, an endoscopy/biopsy confirmed I had Celiac. For the first few weeks going gluten free, I was generally feeling better. While I still had symptoms, they weren’t usually severe and my appetite was returning. I was finally able to sleep through the night and wasn’t bedridden the majority of the time. Fast forward to yesterday (6 weeks post-diagnosis) and I’ve been sick as a dog. I’m almost back to where I was pre-diagnosis: waves of nausea, heartburn, joint pain (especially in hips), restlessness, fatigue, loss of appetite, brain fog, and water just goes through me so I’m urinating frequently. I’m confused because I’ve been so careful about not eating out, cross contamination, and sticking to the gluten-free diet. I feel miserable! I haven’t been able to get out of bed most of the day. Anyone else get these debilitating episodes?? The only thing I can think of is eating Aussie Bites within the past couple of days. They’re labeled as gluten-free but they have oats and millet, so maybe I’m sensitive to that. And I just read that they were likely stored in a facility containing wheat 🙄. I also was having lactose almost daily until I cut it out a couple days ago after reading that it can irritate the intestines. So I’m wondering first how others have been able to recover from severe flare ups. But also is it normal to just have crazy, seemingly random flare ups throughout your recovery like this? I’m feeling really stressed and demotivated because this illness takes up so much of my time and mental space. I’m a graduate student and this has really interfered with my productivity. If it helps, my TTG was high at diagnosis (above 250) and there was a lot of villi damage. I was also tested for diabetes and got the full panel (CBC, kidney, etc.) at time of diagnosis and all came back negative. Glucose was fine. Had abdominal CT scan, which was also normal, and I’m waiting to hear back on follow up TTG + vitamin lab work results.
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Celiac.com 03/09/2023 - After nearly a year on a gluten-free diet, I now look back at my recovery to evaluate its success—the severe joint pain, muscle weakness, bone pain, fatigue, abdominal bloating, steatorrhea, and weight loss plagued me until my treatment commenced in earnest. Much of the extra-intestinal symptoms resolved within the first few months. However, the intestinal and stomach symptoms have taken much longer, and my weight loss recovery is ongoing. The road to recovery has been long and arduous. Many of us experience an array of residual and persistent symptoms even with the complete removal of gluten from our diets. Intestinal Absorption Traditionally, response to a gluten-free diet has been assessed by blood antibody tests and biopsies. It has long been known that the intestinal villi, seen in biopsy samples, do not always revert back to normal even after a prolonged gluten-free diet (1) . A recent study by Cummins et al. found that area of the villi improved significantly by three months on a gluten-free diet, but improved only slightly more during the six to 24 month period (2) . After two years on a gluten-free diet, the villi area increased to about four times that at diagnosis of CD, but was still only about half of normal. Similarly, Wahab et al. found that at two years of follow-up on a gluten-free diet, 37% of the celiac patients still had varying degrees of villous atrophy (3) . After five years, 12% of the adult patients had villous atrophy, of which half still had total villous atrophy. All children in the study recovered completely and recovered faster than the adults in long term follow-up. Besides intestinal biopsy, assessment of serum IgA class endomysial antibody (EmA) has been evaluated as a predictor of intestinal mucosal recovery4 . However, EmA conversion from positive to negative status was not found to be a reliable predictor of complete mucosal recovery. Intestinal mucosal recovery was incomplete in 47% of patients who had become EmA negative after 12 months on a gluten-free diet, and EmA sensivitivity for total villous atrophy and partial villous atrophy was only 33% and 9%, respectively. Likewise, Cummins et al. found that even after two years on a gluten-free diet, patients who tested positive or negative for anti-endomysial antibodies showed no difference in villous atrophy (2). Another assessment of recovery is disaccharidase activity, which can be deficient secondarily to mucosal injury from celiac disease. Disaccharides are sugars (such as lactose, sucrose, and maltose) which must be split by disaccharidases (enzymes produced by villi in the small intestine) to be absorbed properly as monosaccharides and utilized by the body. Disaccharides such as lactose and sucrose are likely to be malabsorbed in patients with villous atrophy2 . Cummins et al. found that lactase activity increased by more than double after two years on a gluten-free diet, but this was still only about 55% of normal. Similar two-year recovery patterns were seen for activity levels of sucrase (83% of normal) and maltase (79%), yet, because disaccharidase activities improve despite incomplete recovery of the surface lining, they are thought to be the main reason why clinical symptom relief comes early on in treatment. (1) Gastrointestinal Symptoms Fine et al. found that celiac patients initially experienced chronic diarrhea (79%), excessive flatulence (74%), abdominal bloating (68%), nausea (36%), vomiting (19%), and constipation (6%)5 . After one year on a gluten-free diet these gastrointestinal symptoms completely resolved with the exception of chronic diarrhea, although 17% of celiac patients had chronic diarrhea to a lesser extent than before starting the diet. Anemia Celiac patients’ anemia-related symptoms receded and resolved as normalization of hemoglobin levels correlated with intestinal mucosal improvement on a gluten-free diet, even without oral iron supplementation (6) . This finding suggested that iron absorption was inefficient due to villous atrophy, and that oral iron therapy may not be effective during the first six months of treatment. After six months on a gluten-free diet, 78% of adult celiac patients recovered from iron deficiency anemia based on an assessment of their hemoglobin levels, and only 28% were no longer iron deficient based on serum ferritin levels. From 12 to 24 months of treatment, 94% of the patients were no longer anemic; however, only 55% of the patients reversed from iron deficiency (i.e., iron absorption was greater than iron loss) after 24 months of treatment. Bone Osteoporosis and osteopenia are common findings in newly diagnosed and untreated celiac patients. The deficiency of serum vitamin D which results in secondary calcium malabsorption is associated with low bone mineral density at diagnosis. A five year study follow-up with of adult celiac patients on a gluten-free diet found that bone mineral density improves or may normalize over the long-term, but that nearly all of the improvement occurs in the first year (7) . Blood 25(OH) vitamin D, the active form of vitamin D, increased 14% in the first year of a gluten-free diet, and increased another 80% by the fifth year. A slight (7%) but significant increase in blood calcium was seen after the first year with a further slight increase by the fifth year. Villous atrophy changes and the adherence to a gluten-free diet did not correlate with bone mineral density improvement. Patients’ weight gain in the study was associated with an increase in their bone mineral density. In a separate one-year study, bone mineral density and bone metabolism markers significantly improved in 43 percent of CD patients despite incomplete mucosal recovery (8) . These markers improved even in postmenopausal women and patients with low serum vitamin D levels. These studies confirm that recovery can take a long time and can often be incomplete in adults. Cummins et al. studied patients for villous atrophy up to 15 years after diagnosis, while most of the studies followed patients from one to five years after diagnosis. Indeed, more follow-up studies need to be performed to address the length of time it takes to achieve complete recovery in all aspects. To the extent that recovery is still incomplete, future studies need to identify and explain the reasons why.
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Celiac.com 03/14/2017 - Recent studies of adult celiacs have suggested that complete, not just partial, mucosal recovery and healing is possible, but, in many cases, may take longer than is currently understood. Recently Dr. Hugh James Freeman of the Department of Medicine, Gastroenterology, University of British Columbia, Vancouver, BC, Canada, conducted a study to assess healing time in celiac patients. In this study, 182 patients (60 males, 122 females) referred for evaluation of symptoms, including diarrhea and weight loss, were selected only if initial biopsies showed characteristic inflammatory changes with severe architectural disturbance. All patients were treated with a strict gluten-free diet, and diet compliance was regularly monitored. Up to 90% or more of patients showed a complete mucosal response or healing, many within 6 months. However, most patients required up to 2 years for full healing and recovery to take place in the gut. In this evaluation, women in each of 4 different age ranges showed better mucosal response and healing than men, while elderly celiacs had lower rates overall. Such factors should be considered before labeling a patient with "non-responsive" disease. However, celiacs who are diagnosed later, start a gluten-free diet later, and who have inflammatory changes with persistent gut damage may be at increased risk for a later small bowel complication, including lymphoma. The overall good news here is that full mucosal healing can and does occur in most people with celiac disease. Some people may take longer to heal, but the evidence shows that most do eventually heal. Source: International Journal of Celiac Disease, 2017, Vol. 5, No. 1, xx. DOI:10.12691/ijcd-5-1-4
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