Jump to content
  • Welcome to Celiac.com!

    You have found your celiac tribe! Join us and ask questions in our forum, share your story, and connect with others.




  • Celiac.com Sponsor (A1):



    Celiac.com Sponsor (A1-M):


  • Get Celiac.com Updates:
    Support Our Content
    eNewsletter
    Donate

Clarification From Doctors Visit


jtangema

Recommended Posts

jtangema Apprentice

Hi,

I met with my GI doctor last week. I was diagnosed in February and have been on the gluten-free diet since then. I haven't felt any differently since then. Last weekend I ate something that had wheat in it (didn't know til after i ate it) and didn't get any symptoms afterwards. So I visited my doctor to follow up and make sure I am doing things correctly.

He told me that it isn't worth doing another blood test to see if I am still being contaminated because some people do get better levels with the diet and other people don't see any changes in their numbers even on the diet. He told me that I just have it very mild and that I may never get symptoms from eating gluten. I asked about other food allergies and he didn't seem too concerned about testing for that- he said I could do a fructose and lactose intolerance test, which I will do.

I am just concerned because I didn't get any answers out of him and am very frustrated. I don't know it I need to change something or if this is just the way it will be. Any help would be great!

Thanks

Jennifer


Celiac.com Sponsor (A8):
Celiac.com Sponsor (A8):



Celiac.com Sponsor (A8-M):



CarlaB Enthusiast

How were you diagnosed? Were you feeling bad last Feb. when you started the diet -- what were your symptoms that made them suspect celiac? That info would help me answer you more specifically.

Ursa Major Collaborator

Oh, no, not another clueless doctor! He is utterly wrong about numbers not changing for some people even when on the diet. If that happens, it means that they aren't really gluten-free, so is significant.

There is no such thing as having celiac disease very mild. You either have it, or you don't. Some people get terrible symptoms, and apparently you don't. But that doesn't show the damage that occurs in your intestines. I've heard of people who's villi were completely destroyed, yet their only symptom was anemia!

You may want to eliminate dairy (and I mean ALL of it) and soy, to see if it makes a difference. Those two are the most common ones people with celiac disease have also. Also, both can destroy your villi as well.

If you see an improvement, that means that one of them (or both) are a problem as well. Most people with celiac disease can't tolerate dairy at least for a while, until their villi are completely healed. Some are able to have it again after that.

Also, have you made sure you have eliminated all possible sources of cross-contamination? There is so much doctors don't know, and therefore don't tell you. You need to go through all your personal care products, as many contain gluten. Check your shampoo, conditioner, mousse (if you use any), lotion, lipstick/lip balm, soap, toothpaste etc. for things like 'wheat germ oil', barley extract and oat bran. Replace everything that has one of those with gluten-free brands. Also, watch out for vitamin E, as it is often made from wheat germ oil.

If you still use your old toaster you're likely glutening yourself. The same goes for plastic colanders and wooden cutting boards and cooking spoons, and scratched non-stick cookware.

Okay, now that I set your head spinning, I'll let you digest that. There is more, but this will do for now.

I hope you figure it out. Forget about your doctor, it's better to figure it out yourself, you can do it with help from this site!

chrissy Collaborator

this is exactly why we do follow up tests on our girls----to see how well they are staying gluten free.

AndreaB Contributor

I am one that didn't have symptoms with eating foods, that I knew of. I had allergy testing done and got the results in April and then went through enterolab in May (see sig). Now if I get glutened I have stomach/intestinal distress until it clears my system but it's not bad.

Stay gluten free and I second Ursula. Go soy and dairy free. I would suggest going off of both of them for 4-6 months and then adding back in one, if you desire, after that to see if you have a reaction.

I am gluten, soy and dairy free and have posted in the recipes section some recipes that I have from some cookbooks. It's an adjustment but totally doable. Many on this forum are free of those 3 things. Many more are free from 2 of them.

gfp Enthusiast
Oh, no, not another clueless doctor! He is utterly wrong about numbers not changing for some people even when on the diet. If that happens, it means that they aren't really gluten-free, so is significant.

Yes but I think in this case its possible the advice isn't SO bad... perhaps just confusing....

There is no such thing as having celiac disease very mild. You either have it, or you don't. Some people get terrible symptoms, and apparently you don't. But that doesn't show the damage that occurs in your intestines. I've heard of people who's villi were completely destroyed, yet their only symptom was anemia!

You could also take it that the GI means symptoms wise.... I mean reading jtangema's post and allowing for the normal level of confusion we all mostly had when first diagnosed I think what he meant was pretty much what you just said. That is he was refering to symptoms ... He obviously made it clear that this didn't mean it was OK to cheat so I think the "mild" he's refering to symptoms.

On repeated antibody testing ....

I think this is completely different for adults and kids....

With kids it is necassary because the parents need to know how well the kids are keeping to the diet. In adults I can see why he doesn't want to keep testing... (my GI always wants to test me amd I refuse) ...

The logic here is if you have been accidentally glutened or are just not keeping to the diet.

Someone might not react quickly to a single glutening in terms of antibodies... and antibodies are going to hand around for a long time after.

In my situation, I know from time to time I get glutened through eating out... its a fact of life of eating out IMHO and I do everything to minimise it but you can't eliminate the risk other than not eating out.

So keep testing me randomly and I'll have elevated levels from time to time BUT I do understand why.

However: andthis is a big however...

You may want to eliminate dairy (and I mean ALL of it) and soy, to see if it makes a difference. Those two are the most common ones people with celiac disease have also. Also, both can destroy your villi as well.

If you see an improvement, that means that one of them (or both) are a problem as well. Most people with celiac disease can't tolerate dairy at least for a while, until their villi are completely healed. Some are able to have it again after that.

Also, have you made sure you have eliminated all possible sources of cross-contamination? There is so much doctors don't know, and therefore don't tell you. You need to go through all your personal care products, as many contain gluten. Check your shampoo, conditioner, mousse (if you use any), lotion, lipstick/lip balm, soap, toothpaste etc. for things like 'wheat germ oil', barley extract and oat bran. Replace everything that has one of those with gluten-free brands. Also, watch out for vitamin E, as it is often made from wheat germ oil.

If you still use your old toaster you're likely glutening yourself. The same goes for plastic colanders and wooden cutting boards and cooking spoons, and scratched non-stick cookware.

Okay, now that I set your head spinning, I'll let you digest that. There is more, but this will do for now.

I agree 100% ... as I have repeatedly said..just post diagnosis is when we were all at our lowest both physically and mentally.

My heartfelt advice for ANYONE newly diagnosed is do it 110%....because this will set you into recovery much faster and not keep setting you back while you gain knowledge on other issues like hidden gluten and CC.

I have to say I don't think this GI is half as bad as most because he is actually treating the adult patient as an ADULT... what they are missing out of is what you can only learn by going gluten-free ... which is all the potentiual sources of CC and hidden gluten.

jtangema: Its perfectly normal to be confused at this point. we all were too.

I hope you figure it out. Forget about your doctor, it's better to figure it out yourself, you can do it with help from this site!

I wouldn't say forget this Dr. they seem at least 50% clued up which is 49% higher than most GI's! Honestly I think this is a GI you can work with. The ones I would say forget are the ones who insist on repeated challenges ....I think your confusion is probably not understanding the GI and that doesn't mean your stupid ... diagnosis is often like a bombshell and when we walk away we are often left confused simply because it was too much to take in.

My advice is pretty much as Ursual said....

Firstly eliminate gluten 100% to the point of no possible contamination.... prepare yourself for 2-3 months of cooking everything yourself... because in this tiome your body will repair AND you will learn a heck of a lot ...

When your first diagnosed you have maximum damage so your whole digestive system is functioning at minimal efficiency. Just a single accident can knock you back a week in recovery so its like 3 steps forwards and one back.

If you can then simply take away that risk as much as possible... including pans, toaster ovens and stuff.

This will make it much easier to stay gluten-free ....

Once you reach a point (you yourself will know) then you can start experimentally adding eating outside the house (its a whole new game.. you have to transfer what you know to a waiter and make sure he tells the chef... BUT you need to be very certain to do this efficiently)

Foods like soy and dairy do affect a lot of people especially at first because the intenstines are so damaged that these react as well. My diary tolerance is pretty much linked to how well I have been gluten-free... whne I have an accident my dairy tolerance plumets .. when I'm good for a long time its much better and I get very mild reactions sometimes.

Soy I have always been OK with (so gfar as I can tell) BUT... I choose to limit it...

I don't think my body processes it too well bUT also I don't want to start eating a lot of it and end up with another intolerance! This would seriously limit what I could eat.

Okay, now that I set your head spinning, I'll let you digest that. There is more, but this will do

for now.

Couldn't agree more :D

Archived

This topic is now archived and is closed to further replies.

  • Get Celiac.com Updates:
    Support Celiac.com:
    Join eNewsletter
    Donate

  • Celiac.com Sponsor (A17):
    Celiac.com Sponsor (A17):





    Celiac.com Sponsors (A17-M):




  • Recent Activity

    1. - trents replied to JudyLou's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      1

      Seeking advice on potential gluten challenge

    2. - JudyLou posted a topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      1

      Seeking advice on potential gluten challenge

    3. - marzian commented on Scott Adams's article in Diagnosis, Testing & Treatment
      5

      A Future Beyond the Gluten-Free Diet? Scientists Test a New Cell Therapy for Celiac Disease (+Video)

    4. - Jmartes71 posted a topic in Related Issues & Disorders
      0

      Medications

    5. - Scott Adams replied to GlutenFreeChef's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      11

      Blood Test for Celiac wheat type matters?

  • Celiac.com Sponsor (A19):
  • Member Statistics

    • Total Members
      133,136
    • Most Online (within 30 mins)
      7,748

    GFTom
    Newest Member
    GFTom
    Joined
  • Celiac.com Sponsor (A20):
  • Celiac.com Sponsor (A22):
  • Forum Statistics

    • Total Topics
      121.5k
    • Total Posts
      1m
  • Celiac.com Sponsor (A21):
  • Upcoming Events

  • Posts

    • trents
      Welcome to the celiac.com community, @JudyLou! There are a couple of things you might consider to help you in your decision that would not require you to do a gluten challenge. The first, that is if you have not had this test run already, is to request a "total IGA" test to be run. One of the reasons that celiac blood antibody tests can be negative, apart from not having celiac disease, that is, is because of IGA deficiency. If a person is IGA deficient, they will not respond accurately to the celiac disease blood antibody tests (such as the commonly run TTG-IGA). The total IGA test is designed to check for IGA deficiency. The total IGA test is not a celiac antibody test so I wouldn't think that a gluten challenge is necessary. The second is to have genetic testing done to determine if you have the genetic potential to develop celiac disease. About 30-40% of  the general population have the genetic potential but only about 1% actually develop celiac disease. So, genetic testing cannot be used to diagnose celiac disease but it can be used to rule it out. Those who don't have the genetic potential but still have reaction to gluten would not be diagnosed with celiac disease but with NCGS (Non Celiac Gluten Sensitivity).  Another possibility is that you do have celiac disease but are in remission. We do see this but often it doesn't last.
    • JudyLou
      Hi there, I’m debating whether to consider a gluten challenge and I’m hoping someone here can help with that decision (so far, none of the doctors have been helpful). I have a history of breaking out in a horrible, burning/itchy somewhat blistering rash about every 8 years. This started when I was in my early 30’s and at that point it started at the ankles and went about to my knees. Every time I had the rash it would cover more of my body, so my arms and part of my torso were impacted as well, and it was always symmetrical. First I was told it was an allergic reaction to a bug bite. Next I was told it was eczema (after a biopsy of the lesion - not the skin near the lesion) and given a steroid injection (didn’t help). I took myself off of gluten about 3 weeks before seeing an allergist, just to see if it would help (it didn’t in that time period). He thought the rash looked like dermatitis herpetiformis and told me to eat some bread the night before my blood tests, which I did, and the tests came back negative. I’ve since learned from this forum that I needed to be eating gluten daily for at least a month in order to get an accurate test result. I’m grateful to the allergist as he found that 5 mg of doxepin daily will eliminate the rash within about 10 days (previously it lasted for months whether I was eating gluten or not). I have been gluten free for about 25 years as a precaution and recommendation from my doctor, and the pattern of breaking out every 8 years or so remains the same except once I broke out after just one year (was not glutened as far as I know), and now it’s been over 9 years. What’s confusing to me, is that there have been 3 times in the past 2 years when I’ve accidentally eaten gluten, and I haven’t had any reaction at all. Once someone made pancakes (they said they were gluten-free, they were not) and I ate several. I need to decide whether to do a gluten challenge and get another blood test. If I do, are these tests really accurate? I’m also concerned that I could damage my gut in that process if I do have celiac disease. My brother and cousin both had lymphoma so that’s a concern regarding a challenge as well, though there is a lot of cancer in various forms in my family so there may be no gluten connection there. Sorry for the ramble, I’m just doubting the need to remain gluten free if I don’t have any reaction to eating it and haven’t had a positive test (other than testing positive for one of the genes, though it sounds like that’s pretty common). I’d appreciate any thoughts or advice! 
    • Jmartes71
      Hello, just popped in my head to ask this question about medications and celiac? I have always had refurse reaction to meds since I can remember  of what little meds my body is able to tolerate. I was taking gabapentin 300mg for a week,  in past I believe 150? Any ways it amps me up not able to sleep, though very tired.However I did notice it helped with my bloating sibo belly.I hate that my body is that sensitive and medical doesn't seem to take seriously. Im STILL healing with my skin, eye, and now ms or meningioma ( will know in April  which)and dealing with this limbo nightmare. I did write my name, address ect on the reclamation but im not tech savvy and not sure if went through properly. I called my city representative in Stanislaus County and asked if theres a physical paper i can sign for proclamation for celiac and she had no clue about what I was saying, so I just said I'll go back on website. 
    • Scott Adams
      I'm not saying that some celiacs won't need it, but it should be done under a doctor's supervision because it can cause lots of problems in some people.
    • Jmartes71
      I also noticed I get debilitating migraines when I smell gluten, wheat and its not taken seriously when it affects one in every way.Im still begging to properly be heard.I also noticed tolerance level is down the drain with age and life changes. I have been told by incompetent medical that im not celiac or that sensitive. Diagnosed in 1994 by gi biopsy gluten-free ever since along with other lovely food allergies. Prayers
×
×
  • Create New...

Important Information

NOTICE: This site places This site places cookies on your device (Cookie settings). on your device. Continued use is acceptance of our Terms of Use, and Privacy Policy.