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What Supplements Help?


Ally2005

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Ally2005 Apprentice

Hi, I was just diagnosed 6 days ago and have been eating gluten-free since then. The damage to the intestinal lining was severe. So far, there is no change in my symtoms. I was wondering if there was any thing else I could do/take to help heal my digestive tract. and speed recovery.

Aly


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cdford Contributor

There are several good discussions on supplements. Usually a good multi vitamin is a start. From there, you probably need to supplement based on your own personal needs. Those of us with neurological problems steer toward the B vitamins. Those with anemia steer toward the iron. The ones of us with muscular or bone concerns add calcium and magnesium. There are a lot of options...just verify with the manufacturer that the supplement is gluten-free. Your doctor may want to suggest specific things for your unique situation. He may also be able to assess whether you can take the oral supplements or require injections of certain ones.

KaitiUSA Enthusiast

A multi vitamin is a good thing to have...I would recommend a liquid vitamin because of the way it is absorbed by your body. I would also recommend probiotics .Probiotic bacteria favorably alter the intestinal microflora balance, inhibit the growth of harmful bacteria, promote good digestion, boost immune function, and increase resistance to infection. I also would highly recommend Enzymes which are great for digestion. Sublingual B12 vitamins are great too because you put them under your tongue and they go into your blood stream that way so you know your body is absorbing it. There are many discussions on here about supplements so you might want to take a look at them and then you can get an idea on what people take.

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    • trents
      Not necessarily. The "Gluten Free" label means not more than 20ppm of gluten in the product which is often not enough for super sensitive celiacs. You would need to be looking for "Certified Gluten Free" (GFCO endorsed) which means no more than 10ppm of gluten. Having said that, "Gluten Free" doesn't mean that there will necessarily be more gluten than "Certified Gluten" in any given batch run. It just means there could be. 
    • trents
      I think it is wise to seek a second opinion from a GI doc and to go on a gluten free diet in the meantime. The GI doc may look at all the evidence, including the biopsy report, and conclude you don't need anything else to reach a dx of celiac disease and so, there would be no need for a gluten challenge. But if the GI doc does want to do more testing, you can worry about the gluten challenge at that time. But between now and the time of the appointment, if your symptoms improve on a gluten free diet, that is more evidence. Just keep in mind that if a gluten challenge is called for, the bare minimum challenge length is two weeks of the daily consumption of at least 10g of gluten, which is about the amount found in 4-6 slices of wheat bread. But, I would count on giving it four weeks to be sure.
    • Paulaannefthimiou
      Are Bobresmill gluten free oats ok for sensitive celiacs?
    • jenniber
      thank you both for the insights. i agree, im going to back off on dairy and try sucraid. thanks for the tip about protein powder, i will look for whey protein powder/drinks!   i don’t understand why my doctor refused to order it either. so i’ve decided i’m not going to her again, and i’m going to get a second opinion with a GI recommended to me by someone with celiac. unfortunately my first appointment isn’t until February 17th. do you think i should go gluten free now or wait until after i meet with the new doctor? i’m torn about what i should do, i dont know if she is going to want to repeat the endoscopy, and i know ill have to be eating gluten to have a positive biopsy. i could always do the gluten challenge on the other hand if she does want to repeat the biopsy.    thanks again, i appreciate the support here. i’ve learned a lot from these boards. i dont know anyone in real life with celiac.
    • trents
      Let me suggest an adjustment to your terminology. "Celiac disease" and "gluten intolerance" are the same. The other gluten disorder you refer to is NCGS (Non Celiac Gluten Sensitivity) which is often referred to as being "gluten sensitive". Having said that, the reality is there is still much inconsistency in how people use these terms. Since celiac disease does damage to the small bowel lining it often results in nutritional deficiencies such as anemia. NCGS does not damage the small bowel lining so your history of anemia may suggest you have celiac disease as opposed to NCGS. But either way, a gluten-free diet is in order. NCGS can cause bodily damage in other ways, particularly to neurological systems.
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