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How To Approach Doctor With Celiac Concern?


Curlyqueen

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Curlyqueen Rookie

I expressed my concern about celiac disease with my new doctor but she didn't seem interested however she agreed to send me to get a tTG blood test. How do you handle doctors who don't understand or are less knowledgeable on celiac disease?

Background: I'm currently waiting on a tTG blood test result from my new primary care physician. I have two primary care physicians because I moved for school. My original primary care doctor is in NYC and my new doctor is in Rhode Island. I have been dealing with Anemia for almost 2 years now. At first it was getting better then it got worst. I can't seem to keep my b12 levels up. its to the point I'm doing weekly injections myself and its still low. I can tell that its low because when I sleep I get tingling in my arms and I'm fatigued. Due to the low b12 I get migraines however, they aren't as bad as they use to be. My doctors can't seem to figure out whats wrong with me. I don't want to insult them but I think its celiac disease or gluten sensitivity. I have a lot of the symptoms( I didn't mention them all here) and they seem to be getting worst. To top it off I have an extreme alcohol intolerance. Maybe its not extreme but I can not drink alcohol and i use to be able to drink alcohol. I had a low tolerance but I could enjoy a beer. Now all it takes are a couple sips and its like i get sick instantly. Its as if it goes straight into my blood. I'm 22 years old and I would like to be able to drink alcohol, have energy, and most importantly I would like to know what is wrong with me. Problem is I don't want to insult my doctors by telling them what I think they should do which is a full celiac blood panel.


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ravenwoodglass Mentor

Don't worry about insulting your doctor, he is working for you. Go in with a list of your symptoms and simply request a full celiac panel along with a total IGA. Make sure you are eating a regular gluten filled diet until all testing for celiac is done and when that is finished do a trial of the gluten-free diet no matter what the results are. False negatives on both blood and biopsy are not uncommon so a dietary trial is always advised even if the testing is negative or inconclusive.

Curlyqueen Rookie

Thanks! I needed that advice and wish I had did that a long time ago. I'm now starting to consider just going gluten free and see if I feel better. I would like to have an official diagnosis but it doesn't seem necessary.

  • 1 month later...
Curlyqueen Rookie

Don't worry about insulting your doctor, he is working for you. Go in with a list of your symptoms and simply request a full celiac panel along with a total IGA. Make sure you are eating a regular gluten filled diet until all testing for celiac is done and when that is finished do a trial of the gluten-free diet no matter what the results are. False negatives on both blood and biopsy are not uncommon so a dietary trial is always advised even if the testing is negative or inconclusive.

It came back negative but within that time I went gluten free and felt a lot better. Now I'm seeing a GI because I'm convinced that I have a digestive issue of some sort if not a gluten sensitivity or intolerance. Is there a difference between intolerance and sensitivity? The genetic testing my GI did also came back negative so I'm thinking possibly gluten sensitivity. The weirdest thing happened, ever since I went gluten free my eczema which had been active for years came back out of no where and in new places. I thought going gluten free would make it go away...hhmm maybe theres an allergy I'm over looking.

Anyway thanks again for your original response it helped!

domesticactivist Collaborator

If you just got rid of gluten and didn't replace it with "gluten-free" substitute stuff it could be that with the reduction of starch in your diet the candida or other bad elements in your gut flora are dying off. Die off is a good thing but can cause eczema to flare up, especially if it happens quickly. My partner's eczema flares every time we add a new probiotic food, or increase amounts too quickly.

It's also possible that you have an allergy to something new in your diet.

Or, it could be that with your immune system no longer reacting to gluten, it's all amped up and needing something to do.

Curlyqueen Rookie

If you just got rid of gluten and didn't replace it with "gluten-free" substitute stuff it could be that with the reduction of starch in your diet the candida or other bad elements in your gut flora are dying off. Die off is a good thing but can cause eczema to flare up, especially if it happens quickly. My partner's eczema flares every time we add a new probiotic food, or increase amounts too quickly.

It's also possible that you have an allergy to something new in your diet.

Or, it could be that with your immune system no longer reacting to gluten, it's all amped up and needing something to do.

Interesting...at first when I went gluten free it was very sudden and I didn't use gluten free substitutes. Now I'm all about Udi's bread( I love it). But you brought to light something I didn't think about. I just thought that this might be a sign that gluten isn't necessarily the enemy but something else. Is this something that I should mention to my doctor? The fact that my eczema flared up after I went gluten free?

Thanks for sharing this is really something new to me. I'm going to try to do some more research on this. I appreciate the feed back.

domesticactivist Collaborator

I do think it's very valuable to write up all the symptoms you've been having, whether they seem related or not. Maybe another person looking at them will have another perspective or see a pattern you have missed. Maybe just writing them out will alert YOU to a pattern! I would bring that information to my doctor.

Oh, and you could say it could be that gluten AND something else are the enemies. I felt like crap when I first went gluten free. We ended up doing the GAPS diet and I majorly improved. But now I'm doing a gluten challenge and any doubts I may have had that gluten was a primary problem for me are definitely settled.


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    • knitty kitty
      You're right, doctors usually only test Vitamin D and B12.  Both are really important, but they're not good indicators of deficiencies in the other B vitamins.  Our bodies are able to store Vitamin B12 and Vitamin D in the liver for up to a year or longer.  The other B vitamins can only be stored for much shorter periods of time.  Pyridoxine B 6 can be stored for several months, but the others only a month or two at the longest.  Thiamine stores can be depleted in as little as three days.  There's no correlation between B12 levels and the other B vitamins' levels.  Blood tests can't measure the amount of vitamins stored inside cells where they are used.  There's disagreement as to what optimal vitamin levels are.  The Recommended Daily Allowance is based on the minimum daily amount needed to prevent disease set back in the forties when people ate a totally different diet and gruesome experiments were done on people.  Folate  requirements had to be updated in the nineties after spina bifida increased and synthetic folic acid was mandated to be added to grain products.  Vitamin D requirements have been updated only in the past few years.   Doctors aren't required to take as many hours of nutritional education as in the past.  They're educated in learning institutions funded by pharmaceutical corporations.  Natural substances like vitamins can't be patented, so there's more money to be made prescribing pharmaceuticals than vitamins.   Also, look into the Autoimmune Protocol Diet, developed by Dr. Sarah Ballantyne, a Celiac herself.  Her book The Paleo Approach has been most helpful to me.  You're very welcome.  I'm glad I can help you around some stumbling blocks while on this journey.    Keep me posted on your progress!  Best wishes! P.S.  interesting reading: Thiamine, gastrointestinal beriberi and acetylcholine signaling https://pmc.ncbi.nlm.nih.gov/articles/PMC12014454/
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