Celiac Disease (also known as Coeliac Disease) has many different symptoms. Many have the classic "IBS" symptoms which have lead to their diagnoses. For me it was malabsorption of nutrients during my lifetime and a doctor knowledgeable of Celiacs to actually test me for it. For starters there is no prescription that can be given for Celiac, only a gluten free diet can lead to recovery and even this can take time (up to a year depending on the damage done). This doesn't mean your cured, it just means you will be absorbing nutrients again and probably feeling better then you have in a long time, you must stay on a gluten free diet. It's been a challenge but by no means is this "disease" something to fear. I'm actually grateful to be diagnosed with celiac's as now I can look forward to other things in life, I only wish it could have been caught sooner. The anemia was making me tired all the time no matter how much I fought it. the years of malabsorption of calcium, Vit D, C make bones easily broken over time, lack of folic acid and Vit B's had given way to neuropathy and pain. It was actually a Neurologist who had a sister with Celiacs who originally diagnosed me (referral) and finally sent me on the right path to recovering from all this ( I was passing out/fainting 3-4 times a week).
I am posting this here because not only do I read about people going through some of the same aches and pains as I had (nerves, "phantom pains", stomach pains, fatigue, headaches, etc) but most IBS sufferers should be tested for this they say, from what I hear they have not. Some of the numbers I have seen for Celiac's disease are that 1 in 150 people may very well have Celiac's or a simple gluten intolerance (wheat, barley, rye and usually oats due to cross contamination).
ask for a test for Celiac's from your doctor and if they don't know what it is, find a doctor that does. I hate to see more people suffer longer then they have to here-I think we have enough on our plates as it is
