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hez

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  1. I was very sick for about 5 months before I was diagnosed. After I was dx with celiac disease I started telling people. Their comment was always "You've been sick?". I later realized that because I had two kids I had no choice but to do it (I did not do it well). I think this is true for so many of us. You work through the pain because there is not an alternative. The good news is that there is a cure, make sure you are gluten-free and stay gluten-free.

    I have finally started feeling better and what a difference it makes! Stay gluten-free and your life will get easier and you will feel better.

    In the meantime try to take care of yourself. Make sure you have some quick gluten-free frozen meals for those days you are tired, watch a funny movie and laugh, surround yourself with supportive friends, come to this board for encouragement.

    Hez

  2. For me there seems to be evidence that the celiac disease comes from my Mom's side of the family. My Mom might have celiac disease but does not want the endoscopy so she is just gluten-free. My maternal grandma has "stomach issues" and I suspect it is celiac disease.

    I am not sure on my Dad's side but there are other auto immune diseases there.

    I think it is very possible both of my parents carry the gene.

    Hez

  3. It might be helpful to compare celiac disease with a peanut allergy. Alot of people understand the severity of a peanut allergy, ours is just as serious to our long term health. Another thought is an analogy. Kati had a great one with pizza. Friends wanting her to just eat the cheese. She put liquid soap on the pizza and then wiped it off. Would you want to eat the pizza? They did not want the pizza! We do not want the gluten, not even a crumb. I think it is exciting that they are interested in knowing about celiac disease. Good luck!

    Hez

  4. Let me start by saying that I am not an expert. I have two childeren. One has had blood work which has come back negative (could change later). My second child will be tested in October (need to wait until well child check up). So, I have no experience with endoscopy and children. However, if having a firm diagnosis would give you peace of mind, I would do the procedure. I am not sure I would choose this diet unless I had to nor would I do this to my kids. But this is a personal call that you will have to make. The other upside to having a firm diagnosis would be with your other child and yourself and getting tested. I have heard that there are some children with autism that improve with a gluten-free diet. Again you would need to research that since I have no experience. Take a deep breath and listen to yourself. Trust your instincts! Good Luck, Hez

  5. Kim- I went years with this disease not knowing I had it. I only wish I knew sooner. I would strongly urge your husband to go get the blood test. I am 35 and the doc thinks I have 10 years damage to my small intestine (have no idea how she knows that). I do know that healing is slow coming because of the damage.

    I, like your husband was tired (but I am a stay at home Mom, who isn't exhausted) and would have occasional d. But other than that I felt fine. At least until November. That is when I had the dreaded "d" all the time! I could hardly get through the day, I was so tired. My weight started to come off (I was small already). After a month of feeling bad I went to the doctor. By April I had a firm diagnosis. If I had known sooner I would not have done so much damage to myself.

    Yes, things could possibly get worse for your husband. It did for me. It is only a blood test and the alternative of doing nothing is far worse (if something is wrong). Hope this helps! Hez

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