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Gluten Free For 3 Months And Still Spend Days In Bed From Pain And Nausea


MissBonnie

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cyberprof Enthusiast

Is it possible for my food to absorb "gluten fumes" from the microwave? I'm just wondering if this might be an issue...

I think so. I'm certainly concerned about it because in the early days gluten-free, I got glutened and I think that was the source.

I cover EVERYTHING in the microwave, even at home where it gets little to no gluten. I use a plastic dome cover over plates. I wrap bacon in paper towels. I even cover things like butter when I'm melting it or soup when I'm heating it up. I put plastic wrap over bowls.

Call me paranoid, but I get sick a lot less often now.

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dilettantesteph Collaborator

I'm a super sensitive celiac. I wasn't able to find a gluten free cereal which I could tolerate. Could you try a diet of produce and meats?

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Kim69 Apprentice

Hi miss Bonnie. Yes I am working full time as an engineer. To begin with I had a lot of time off work - a day off here and there and I worked from home in my pajamas. Now, a year later, I am certainly getting better, but on the weekends I am often in bed by 2pm for a few hrs. And by 2pm at work I am basically useless I am so tired. I managed to stay at work today till 4pm but I commented to my husband that really by 2 or 3 pm Every day i am ready for a nap. I am investigating as many avenues as possible and am further limiting my food in the hope of hitting the right combo of foods.

I am also seeing a therapist (who will be very disappointed that I have stopped eating breakfast cos I feel yuck) who is helping me deal with my issues with food and lack of energy.

It looks like you have a really healthy diet and it's really annoying to think that perhaps you may have other food intolerances. Fructose is a big no no for me - I can eat no apples, pears, onions, asparagus etc and I also can't eat legumes, cauliflower and more - I had a breath test to diagnose and avoiding these foods is reducing the pain so that I have some pain free hours. I still have issues with

gas so I have recently got stricter removing that. I haven't noticed any improvement though.

I hope you start to feel better soon, so that you can get

back to living!

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Coolclimates Collaborator

yes, your problems could be caused by lactose intolerance or other food intolerances. I would get checked for other food allergies to see if there is something else that is making you so sick. Although my blood tests showed I was not allergic to anything, I have pushed to get retested, this time with the skin prick testing. I have not been healing even though I've been on a very strict gluten-free diet, and have heard that the skin tests are better than the blood tests.

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GlutenFreeManna Rising Star

yes, your problems could be caused by lactose intolerance or other food intolerances. I would get checked for other food allergies to see if there is something else that is making you so sick. Although my blood tests showed I was not allergic to anything, I have pushed to get retested, this time with the skin prick testing. I have not been healing even though I've been on a very strict gluten-free diet, and have heard that the skin tests are better than the blood tests.

If you are talking about food allergy testing, my allergist told me the opposite was true--tha thte blood testing was more accurate than the skin pricks. My skin prick tests showed no food allergies but my blood tests picked up a mild wheat allergy. That said, it is also possible to have intolerances that make you very sick and not have it show up as an allergy with allergy testing. I have an anaphylactic reaction to milk. My tonuge tingles and gets puffy and I have difficulty breathing. If I can get Benedryl in me before it get too bad the swelling goes down enoguh I can avoid the emergency room, but it's still really bad. My dr has prescribed an epi-pen for the allergic response. My blood and skin prick tests, however showed no sign of an IgE milk allergy. The dr did admit the tests are not 100% (there is a small chance of false negatives). He said my best test was my own body's reactions and that I should avoid all milk and continue to carry the epi-pen.

Now, I'm guessing you do not have life threathening reactions to something, but intolerances that don't show up on tests could still make you very sick. IMO the best method of finding these intolerances is with an elimination diet. Strip your diet down to 3-4 foods only or cut out all 8 top allergens plus anything you suspect may be a problem for you. If you feel better after two weeks then add one new food per week until you have a reaction or are sure you ar eokay with that food. If you do not feel better after two weeks then rotate to a different set of foods and try again.

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    • trents
      But if you have been off of wheat for a period of weeks/months leading up to the testing it will likely turn out to be negative for celiac disease, even if you actually have celiac disease. Given your symptoms when consuming gluten, we certainly understand your reluctance to undergo  the "gluten challenge" before testing but you need to understand that the testing may be a waste of time if you don't. What are you going to do if it is negative for celiac disease? Are you going to go back to merrily eating wheat/barley/rye products while living in pain and destroying your health? You will be in a conundrum. Do I or do I not? And you will likely have a difficult time being consistent with your diet. Celiac disease causes inflammation to the small bowel villous lining when gluten containing grains are consumed. This inflammation produces certain antibodies that can be detected in the blood after they reach a certain level, which takes weeks or months after the onset of the disease. If gluten is stopped or drastically reduced, the inflammation begins to decrease and so do the antibodies. Before long, their low levels are not detectable by testing and the antibody blood tests done for diagnosing celiac disease will be negative. Over time, this inflammation wears down the billions of microscopic, finger-like projections that make up the lining and form the nutrient absorbing layer of the small bowel where all the nutrition in our food is absorbed. As the villi bet worn down, vitamin and mineral deficiencies typically develop because absorption is compromised. An endoscopy with biopsy of the small bowel lining to microscopically examine this damage is usually the second stage of celiac disease diagnosis. However, when people cut out gluten or cut back on it significantly ahead of time before the biopsy is done, the villous lining has already experienced some healing and the microscopic examination may be negative or inconclusive. I'm not trying to tell you what to do I just want you to understand what the consequences of going gluten free ahead of testing are as far as test results go so that you will either not waste your time in having the tests done or will be prepared for negative test results and the impact that will have on your dietary decisions. And, who are these "consultants" you keep talking about and what are their qualifications? You are in the unenviable position that many who joint this forum have found themselves in. Namely, having begun a gluten free diet before getting a proper diagnosis but unwilling to enter into the gluten challenge for valid testing because of the severity of the symptoms it would cause them.
    • Zackery Brian
      I'm sorry to hear about the challenges you've been facing with your health. Dealing with celiac disease and multiple food sensitivities can indeed be overwhelming. Here are a few thoughts and suggestions based on your experience and the replies you've received: Confirming Diagnosis: It's great that your gastroenterologist confirmed your celiac disease diagnosis through additional tests. Understanding the specifics of your condition can help tailor your approach to managing it more effectively. Food Sensitivity Testing: While blood tests for food sensitivities can provide some insights, they may not always be completely accurate. As mentioned by others, false positives are common, and individual responses to specific foods can vary. Discussing your test results and symptoms with a healthcare professional knowledgeable about celiac disease and food sensitivities can help clarify your situation. Research and Education: Exploring conditions like Mast Cell Activation Syndrome (MCAS) and histamine intolerance could shed further light on your symptoms and provide additional avenues for managing your health. Gathering information from reliable sources and discussing your findings with your healthcare team can help you make informed decisions about your care. Dietary Management: Managing celiac disease and multiple food sensitivities can be challenging, but finding a balance that works for you is crucial. Working with a dietitian who specializes in celiac disease and food intolerances can help you develop a personalized dietary plan that meets your nutritional needs while minimizing symptoms. Stress Management: Chronic pain and health issues can take a toll on mental and emotional well-being. Finding healthy coping strategies to manage stress, such as mindfulness, relaxation techniques, or engaging in activities you enjoy, may help improve your overall quality of life. Remember, you're not alone in your journey, and seeking support from healthcare professionals, support groups, or online communities can provide valuable encouragement and guidance.
    • Fluka66
      Thank you very much for your reply. I hadn't heard of celiac disease but began to notice a pattern of pain. I've been on the floor more than once with agonising pain but this was always put down to another abdominal problem consequently I've been on a roundabout of backwards and forwards with another consultant for many years. I originally questioned this diagnosis but was assured it was the reason for my pain. Many years later the consultant gave up and I had a new GP. I started to cut out certain food types ,reading packets then really started to cut out wheat and went lactose free. After a month I reintroduced these in one meal and ended screaming in agony the tearing and bloating pain. With this info and a swollen lymph node in my neck I went back to the GP.  I have a referral now . I have also found out that acidic food is causing the terrible pain . My thoughts are this is irritating any ulcers. I'm hoping that after a decade the outlook isn't all bad. My blood test came back with a high marker but I didn't catch what it was. My GP and I have agreed that I won't go back on wheat just for the test due to the pain , my swollen lymph node and blood test results.  Trying to remain calm for the referral and perhaps needed to be more forceful all those years ago but I'm not assertive and consultants can be overwhelming. Many thanks for your reply . Wishing you all the best.
    • Moodiefoodie
      Wow! Fascinating info. Thanks so much! I really appreciate the guidance. @Spacepanther Over the years I have had rheumatologists do full lab work ups on me. They told me they had screened me for arthritis, lupus, and Lyme disease (all negative). In addition to joint pain and stiffness I had swelling in both knees that later moved to my elbow as well.  I also experience stiffness and pain in my neck and shoulders when it flares. I vomited fairly often growing up, but there wasn’t a real pattern to it and I didn’t know it wasn’t normal (thought people caught stomach viruses often).  I don’t usually have stomach symptoms immediately after eating gluten that I notice.  The only other joint condition I know of is fibromyalgia. Good luck! Hope you can get it figured out. I only assumed my joint symptoms were due to the celiac’s because it is under control for the most part on a gluten-free diet.  The rheumatologist also mentioned that some inflammatory/autoimmune diseases can be slow-moving and not detectable until they progress.
    • knitty kitty
      @Spacepanther, I found these articles about the connection between Celiac and joint pain. Musculoskeletal Complications of Celiac Disease: A Case-Based Review https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10201087/ And   Intestinal microbiome composition and its relation to joint pain and inflammation https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6814863/ And The gut microbiome-joint connection: implications in osteoarthritis https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6903327/ Sounds like it's time to change the diet to change the microbiome.
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