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jcski

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jcski Newbie

Hi I was just recently diagnosed with Celiac, I've had two surgeries in the last year Ulnar Nerve Replacement and just two weeks ago gallbladder not for gull stones but because it was inflamed and functioning at 13% which is actually how I found out I had Celiac's. I've been following the Gluten Free Diet now for a month and feel a little better but still a slow recovery. My question is now that I know, how do I find out what Vitamins I'm deficient in do I go back to the Gastro Doctor and than what's the follow up do I get tested again after a certain amount of time? Also now that I've caught the celiac does this mean it will eliminate the other potential issues if I stay on a strict diet? Any help would be greatly appreciated.


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eatmeat4good Enthusiast

Your regular Dr. can test your vitamin levels.

Celiacs are often deficient in the fat soluble vitamins A,E,D,K but there are others like calcium, magnesium, zinc, and iron, and the B vitamins especially B 12 and folic acid.

You can do a follow up blood panel to be sure your antibodies are down. Not everyone does this but some do.

The longer your are gluten free the less risk of long term side effects of gluten, but it is important to watch for autoimmune symptoms since secondary autoimmune disease goes along with Celiac very commonly.

You should have a full thyroid panel done since Hashimoto's and Graves are two conditions closely associated with Celiac disease. Thyroid problems are very common.

Chopper Apprentice

You should have a full thyroid panel done since Hashimoto's and Graves are two conditions closely associated with Celiac disease. Thyroid problems are very common.

I was just diagnosed yesterday with autoimmune hypothyroidism and limited scleroderma. In my online searches it seems these commonly occur in celiacs. My gallbladder was my first symptom as well, followed by gastroparesis and gastritis. I didn't know until yesterday all this could be connected. I think there needs to be even more awareness in this area. I wish you well!

Marilyn R Community Regular

Hi I was just recently diagnosed with Celiac, I've had two surgeries in the last year Ulnar Nerve Replacement and just two weeks ago gallbladder not for gull stones but because it was inflamed and functioning at 13% which is actually how I found out I had Celiac's. I've been following the Gluten Free Diet now for a month and feel a little better but still a slow recovery. My question is now that I know, how do I find out what Vitamins I'm deficient in do I go back to the Gastro Doctor and than what's the follow up do I get tested again after a certain amount of time? Also now that I've caught the celiac does this mean it will eliminate the other potential issues if I stay on a strict diet? Any help would be greatly appreciated.

I finally found a good Multi-Vitamin with Minerals that I can tolerate. It must be gluten-free/Soy Free and Dairy Free because I'm super sensitive. I got them at a health food store: Vita Logic Daily Extra. And I haven't had a problem with Citracal either, which is what my rheumy recommended for Calcium and vitamin D. I tried to handle all of my daily nutrition needs via food intake for the first gluten-free year, but I failed.

(I turned up deficient in Vitamin D even though I live in the sub-tropics and spend quite a bit of time outdoors on a daily basis, and have Osteopenia.

I know a doctor who was shocked that her brother had severe osteoporosis at 40 years who was diagnosed with celiac disease and otherwise asymptomatic.

Now that you know, please know you can live a really long, good and normal life even though you have celiac disease. You are preventing more complications and diseases. My mother lived to 87 years old, and she had it. I think my maternal Grandfather had it and died at the age of 92.

Recovery takes time, and you may discover some new food intolerances. Certain food proteins are similar in structure to gluten, and your autoimmune system may start to attack them. (Common ones are dairy, soy, corn, nightshade family vegetables, egg, legumes.) Since you asked for advice, my top advice is to try not to compensate the lack of gluten for other foods you love best. Try to mix your protein sources up over the course of a few days.

You will start feeling better! Some of the malaise you're feeling can be attributed to withdrawal. I wish you the best ... you've been through so much already, and I know you're going to feel better! :)

And welcome to the forum. You'll learn so much here...

Again, wish you well.

goodnews Apprentice

Hi I was just recently diagnosed with Celiac, I've had two surgeries in the last year Ulnar Nerve Replacement and just two weeks ago gallbladder not for gull stones but because it was inflamed and functioning at 13% which is actually how I found out I had Celiac's. I've been following the Gluten Free Diet now for a month and feel a little better but still a slow recovery. My question is now that I know, how do I find out what Vitamins I'm deficient in do I go back to the Gastro Doctor and than what's the follow up do I get tested again after a certain amount of time? Also now that I've caught the celiac does this mean it will eliminate the other potential issues if I stay on a strict diet? Any help would be greatly appreciated.

I can't help you with your question as I am pretty new to this and don't really know...but I do have a question for you. You mentioned that you found out you had celiac because your gallbladder was inflamed and functioning at 13%. I am just wondering how they determined it was celiac. I am wondering because they were testing me for celiac through a gene test after a biopsy that looked like it, and then they did a the HIDA scan today and said my gallbladder is inflamed and functioning at 23% and said I had to get it taken out. I am just curious how they would know whether it is form celiac or not. Thanks in advance. :)

deezer Apprentice

I can't help you with your question as I am pretty new to this and don't really know...but I do have a question for you. You mentioned that you found out you had celiac because your gallbladder was inflamed and functioning at 13%. I am just wondering how they determined it was celiac. I am wondering because they were testing me for celiac through a gene test after a biopsy that looked like it, and then they did a the HIDA scan today and said my gallbladder is inflamed and functioning at 23% and said I had to get it taken out. I am just curious how they would know whether it is form celiac or not. Thanks in advance. :)

I'm not sure how they would know for sure that Celiac is the cause for Gallbladder problems, but if you have Celiac there is a good chance that it is related due to all of the inflammation in your gut.

deezer Apprentice

Your regular Dr. can test your vitamin levels.

Celiacs are often deficient in the fat soluble vitamins A,E,D,K but there are others like calcium, magnesium, zinc, and iron, and the B vitamins especially B 12 and folic acid.

You can do a follow up blood panel to be sure your antibodies are down. Not everyone does this but some do.

The longer your are gluten free the less risk of long term side effects of gluten, but it is important to watch for autoimmune symptoms since secondary autoimmune disease goes along with Celiac very commonly.

You should have a full thyroid panel done since Hashimoto's and Graves are two conditions closely associated with Celiac disease. Thyroid problems are very common.

What are all of the tests that should be run for follow-up & upon initial diagnosis in addition to the Thyroid Panel?


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jcski Newbie

Thanks everyone, this was so helpful and made me feel so much better and not so alone. To the person who asked about the gallbladder they didn't say it was from celiac but that's how I found out as I researched I did see that a lot of people celiac do have gallbladder problems in fact is seems we have all sorts of problems. First they did a biopsy because they thought it was ulcers when those results came back the test showed signs of celiac than they did the bloodwork and confirmed it. Looking back this makes sense to me since I never really liked pasta or bread because they made me sick I guess for me it was more like, oh that makes sense.

I guess I'm mostly tired and maybe the celiac is compounding the trying to recover from surgery but great news I had my first day where I felt like getting out the bed and didn't sleep all day.

Thanks so much everyone.

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    • trents
      You might consider asking for a referral to a RD (Registered Dietician) to help with food choices and planning a diet. Even apart from any gluten issues, you will likely find there are some foods you need to avoid because of the shorter bowel but you may also find that your system may make adjustments over time and that symptoms may improve.
    • Ello
      I wish Dr’s would have these discussions with their patients. So frustrating but will continue to do research. Absolutely love this website. I will post any updates on my testing and results.  Thank you
    • trents
      Losing 12" of your small bowel is going to present challenges for you in nutritional uptake because you are losing a significant amount of nutritional absorption surface area. You will need to focus on consuming foods that are nutritionally dense and also probably look at some good supplements. If indeed you are having issues with gluten you will need to educate yourself as to how gluten is hidden in the food supply. There's more to it than just avoiding the major sources of gluten like bread and pasta. It is hidden in so many things you would never expect to find it in like canned tomato soup and soy sauce just to name a few. It can be in pills and medications.  Also, your "yellow diarrhea, constipation and bloating" though these are classic signs of a gluten disorder, could also be related to the post surgical shorter length of your small bowel causing incomplete processing/digestion of food.
    • Ello
      Yes this information helps. I will continue to be pro active with this issues I am having. More testing to be done. Thank you so much for your response. 
    • trents
      There are two gluten-related disorders that share many of the same symptoms but differ in nature from each other. One is known as celiac disease or "gluten intolerance". By nature, it is an autoimmune disorder, meaning the ingestion of gluten triggers the body to attack it's own tissues, specifically the lining of the small bowel. This attack causes inflammation and produces antibodies that can be detected in the blood by specific tests like the TTG-IGA test you had. Over time, if gluten is not withheld, this inflammation can cause severe damage to the lining of the small bowel and even result in nutrient deficiency related health issues since the small bowel lining is organ where all the nutrition found in our food is absorbed.  The other is NCGS (Non Celiac Gluten Sensitivity or just "gluten sensitivity") which we know less about and are unsure of the exact mechanism of action. It is not an autoimmune disorder and unlike celiac disease it does not damage the lining of the small bowel, though, like celiac disease, it can cause GI distress and it can also do other kinds of damage to the body. It is thought to be more common than celiac disease. Currently, we cannot test for NCGS. Celiac disease must first be ruled out to arrive at a diagnosis of NCGS. Both disorders require elimination of gluten from the diet.  Either of these disorders can find their onset at any stage of life. We know that celiac disease has a genetic component but the genes are inactive until awakened by some stress event. About 40% of the general population has the genetic potential to develop celiac disease but only about 1% develop active celiac disease. The incidence of NCGS is thought to be considerably higher. I hope this helps.
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