Jump to content
This site uses cookies. Continued use is acceptance of our Terms of Use and Privacy Policy. More Info... ×
  • 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

Which Types Of Doctors Do Celiacs Need?


Beloved

Recommended Posts

Beloved Apprentice

I've been trying my best to live gluten-free since Nov 07. My doctor considers the matter resolved since trying a gluten-free diet, and honestly he hasn't endeavored to learn anything more about celiac or gluten. I've been pretty much on my own.

What I want to know is, are there specific kinds of tests a celiac should get regularly? Is it worth it to spend money on a Dietitian? I would imagine that damage to the gut causes increased risk of colon cancer, so what about that?

Can anyone think of anything? I'd like to run them by my doctor because he's always willing to recommend me to someone if he thinks I need it.


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



Celiac.com Sponsor (A8-M):



thleensd Enthusiast

I was diagnosed last week. The first thing my GI doc did was give me a referral to a dietician (Kaiser- "nutrition services" or something like that). I'm going Friday. I've been doing a ton of reading, though, and that seems to arm me pretty well. I'll do my best to let you know if they offer anything interesting. (PM me if I forget) One of my seemingly unrelated (but definitely related!) symptoms has been extreme energy drops two hours after a meal (like a blood sugar crash--but blood sugar tested ok every time), and I'm going to ask about that.

Other than that, my GI wants to see me in three months, then once a year after that.

Good luck.

I've been trying my best to live gluten-free since Nov 07. My doctor considers the matter resolved since trying a gluten-free diet, and honestly he hasn't endeavored to learn anything more about celiac or gluten. I've been pretty much on my own.

What I want to know is, are there specific kinds of tests a celiac should get regularly? Is it worth it to spend money on a Dietitian? I would imagine that damage to the gut causes increased risk of colon cancer, so what about that?

Can anyone think of anything? I'd like to run them by my doctor because he's always willing to recommend me to someone if he thinks I need it.

Beloved Apprentice

Cool thank you!

You know, I have to wonder if there isn't a specialist for this type of thing. I mean, shouldn't somebody want to focus on it?

lizard00 Enthusiast

A GI would be the best person to follow your care, as there are screenings that should be performed on a celiac that are either done later, or not routinely on a non-celiac.

They should also be more knowledgable than a GP, and if you encounter further problems, you already are established with them and in a better position to find help.

In your situation, it might be best if your doctor could refer you (or maybe your doc has to). I went to my first GI unreferred, and he thought I was crazy and made myself sick. My GP made the appt with the second one, and things were completely different. I'm not sure how much difference it made, the first could have just been arrogant, but it seemed that having my GP behind me validated why I needed to be there.

happygirl Collaborator

See info here on follow up testing and consider discussing with your doctor.

Open Original Shared Link

Open Original Shared Link

mamaw Community Regular

Honestly you can learn more on here & other sites on your own than most dieticians can share with you .Some insurances will not pay for the dietician & it is not worth going. If the dietician has celiac or gluten intolerance then they can help. I've lost faith in most.

small intestine cancer does happen but it is still rare. It is best to not cheat & continue on a strict gluten-free journey.

Usually blood testing is done on a yearly basis to check to make sure where your level is..... not all doctors have this done.

hth mamaw

Beloved Apprentice

What is a GI?


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



Celiac.com Sponsor (A8-M):



lizard00 Enthusiast
What is a GI?

A gastroenterologist, or gastro-intestinal doctor. (Hence the GI)

Crystal Brown Rookie

It really depends on your GI. A large number of GI doctors will diagnose you, recommend the nutritionist and then send you off to fend for yourself.

The thing is, the follow-up is almost as crucial as the diagnosis.

I went to my first Celiac support group meeting, in Napa, CA and there was an exceptional doctor who spoke and shared some key points.

1. You need to know which vitamins you are low in and take supplements in the right dosage.

- She covered all possible types of vitamin deficiencies and their symptoms.

2. You may need guidance in finding out if you have an accompanying problem - like a hypo or hyperthyrodism, microscopic colitis and so on.

3. Any other allergies.. Finding out what these are and treating them accordingly.

4. The possibility of leaky gut or candida.

5. Exercise! <--- I'm still working on that one :P

- A good exercise program is also crucial.. Motivation, even more crucial *lol*

If you'd like, I can provide her name and email. She was VERY informative. I'm looking forward to her opening up her new practice, so she can be my new follow-up doc!

I hope this kind of helps. Oh! And ask your GI and then any possible Nutritionist how familiar they are with follow-up with Celiac Disease. A good way to see if you have a good Nutritionist.. just ask them the following question, What gluten-free foods they would recommend, in order to retain the needed amounts of vitamins normally found in gluten containing foods? A good nutritionist should be able to not only provide a list of those foods, but know them right off the bat. If he/she hands you a bag of nuts and tells you to eat them for calorie intake - RUN!

Good luck =)

Green Eyes Rookie

Since being diagnosed 7 months ago I felt like I was left to fend for myself. My GI doctor refused to monitor me or do periodic testing (which I felt I needed because I don't react to small amounts of gluten). I was sent to a dietitian which didn't have a clue!!! I felt alone and felt like there should be professionials to guide me.

This site provided my knowledge. I have read books, this site routinely, etc. But I still wanted a "professional." I found a new GI doctor and he is absolutely wonderful. Not only does he listen to me but is willing to work with me. He is very knowledgable about celiac and even a speaker at the Celiac Meeting tonite!!! I also found a chiropractor that was knowledgable about celiac. Now I feel like I'm armed to protect my health!!!

I went thru numerous doctors before I found someone to work with me. If you feel you need additional "professional" help, keep looking until you find what you want - it is worth it!!!

Jennifer

Beloved Apprentice

Thank you guys, I'm going to see about getting a reference to a GI from my regular doctor. I'm sure he must know someone, because that's the same kind of person you go to for acid reflux right? (my mom has that)

Beloved Apprentice
If you'd like, I can provide her name and email. She was VERY informative. I'm looking forward to her opening up her new practice, so she can be my new follow-up doc!

Does she have a website you can send me?

thleensd Enthusiast

Went to a nutritionist/dietician today. Eh. After talking to me for about 2 minutes she said I probably knew more about it than her. True. At least she was nice. She told me I could take a multi-vitamin, but I wasn't really missing things from my diet...unless I went carb free. But I'm not.

She did give me two good things. One was a print-out of websites I could go to to buy gluten free foods, and the other was a 58 page book published by Celiac Disease foundation. It has good stuff in it! Easy to read, etc. You can probably get it on their website: www.celiac.org

Seems to me the best solution is read, read, read. Get the newest books you can, though. I have one that is five years old and have found some inconsistencies with the latest research.

That and eat a balanced diet.

Cheers.

  • 2 weeks later...
MammaG Newbie
Honestly you can learn more on here & other sites on your own than most dieticians can share with you .Some insurances will not pay for the dietician & it is not worth going. If the dietician has celiac or gluten intolerance then they can help. I've lost faith in most.

small intestine cancer does happen but it is still rare. It is best to not cheat & continue on a strict gluten-free journey.

Usually blood testing is done on a yearly basis to check to make sure where your level is..... not all doctors have this done.

hth mamaw

Yes we went to a dietitian once our son was diagnosed and she was not helpful. She said she had been gluten-free for 14 years so I thought she would be of great help. But some of the items that she told us were safe we have had reactions to. Between her and another aquaintence I have met it seems that the ones who have had been gluten-free for a while end up giving you old information. Things that are now considered gluten-free but weren't before (like vinegar) and particular products that used to be gluten-free but aren't now. I agree with the comment that this is really a good place to find out about up-to-date information on what is safe to eat. Ingredients can change or the source of natural flavors (a potential hidden source of gluten) has been switched within a companies products so if you have a question check here and check with the manufacturer. Good luck.

MammaG Newbie
It really depends on your GI. A large number of GI doctors will diagnose you, recommend the nutritionist and then send you off to fend for yourself.

The thing is, the follow-up is almost as crucial as the diagnosis.

I went to my first Celiac support group meeting, in Napa, CA and there was an exceptional doctor who spoke and shared some key points.

1. You need to know which vitamins you are low in and take supplements in the right dosage.

- She covered all possible types of vitamin deficiencies and their symptoms.

2. You may need guidance in finding out if you have an accompanying problem - like a hypo or hyperthyrodism, microscopic colitis and so on.

3. Any other allergies.. Finding out what these are and treating them accordingly.

4. The possibility of leaky gut or candida.

5. Exercise! <--- I'm still working on that one :P

- A good exercise program is also crucial.. Motivation, even more crucial *lol*

If you'd like, I can provide her name and email. She was VERY informative. I'm looking forward to her opening up her new practice, so she can be my new follow-up doc!

I hope this kind of helps. Oh! And ask your GI and then any possible Nutritionist how familiar they are with follow-up with Celiac Disease. A good way to see if you have a good Nutritionist.. just ask them the following question, What gluten-free foods they would recommend, in order to retain the needed amounts of vitamins normally found in gluten containing foods? A good nutritionist should be able to not only provide a list of those foods, but know them right off the bat. If he/she hands you a bag of nuts and tells you to eat them for calorie intake - RUN!

Good luck =)

This is exactly the kind of information I am looking for. What deficiencies I need to check for and what other complications I need to be on the lookout for. If you or anyone else could point me in the direction of some specific resources I'd love it. Thank you.

  • 4 weeks later...
Happy Holly Apprentice

Went to a nutritionist/dietician today. Eh. After talking to me for about 2 minutes she said I probably knew more about it than her. True. At least she was nice. She told me I could take a multi-vitamin, but I wasn't really missing things from my diet...unless I went carb free. But I'm not.

I have heard the same thing from many many celiac sprue friends. It is next to impossible to find a dietician that knows much if anything about glutten free diets. I even had one friend go to a dietician who told her to eat a lot of "whole grains." Good grief!!

Before spending the time or money on a dietician call first and ask questions. Find out how much they know about celiac sprue and gluten free diets.

I still have not found a dietician here (I live in Hampton Roads Virginia). It would be so helpful to know what my diet is lacking in. I know I'm probably not eating the most well-balanced diet since I've been gluten and wheat free.

Tara32 Newbie

[

Hi,

I was diagnosed with Celiac in Jan. 2008 after over 10 years of suffering. I went to a dietician too, but she didn't tell me anything new than what I found online on my own. My Doc has me tested one a year to see if my numbers are dropping. That means that my intestines are healing and I am absorbing nutrients. You really should see a specialist if you do not feel like you are getting the answers you want from your doc. If he/she is willing to send you, than take advantage of it. Hope this helps. God Bless!!

nanlou Newbie
I've been trying my best to live gluten-free since Nov 07. My doctor considers the matter resolved since trying a gluten-free diet, and honestly he hasn't endeavored to learn anything more about celiac or gluten. I've been pretty much on my own.

What I want to know is, are there specific kinds of tests a celiac should get regularly? Is it worth it to spend money on a Dietitian? I would imagine that damage to the gut causes increased risk of colon cancer, so what about that?

Can anyone think of anything? I'd like to run them by my doctor because he's always willing to recommend me to someone if he thinks I need it.

  • 1 month later...
lm9 Newbie
It really depends on your GI. A large number of GI doctors will diagnose you, recommend the nutritionist and then send you off to fend for yourself.

The thing is, the follow-up is almost as crucial as the diagnosis.

I went to my first Celiac support group meeting, in Napa, CA and there was an exceptional doctor who spoke and shared some key points.

1. You need to know which vitamins you are low in and take supplements in the right dosage.

- She covered all possible types of vitamin deficiencies and their symptoms.

2. You may need guidance in finding out if you have an accompanying problem - like a hypo or hyperthyrodism, microscopic colitis and so on.

3. Any other allergies.. Finding out what these are and treating them accordingly.

4. The possibility of leaky gut or candida.

5. Exercise! <--- I'm still working on that one :P

- A good exercise program is also crucial.. Motivation, even more crucial *lol*

If you'd like, I can provide her name and email. She was VERY informative. I'm looking forward to her opening up her new practice, so she can be my new follow-up doc!

I hope this kind of helps. Oh! And ask your GI and then any possible Nutritionist how familiar they are with follow-up with Celiac Disease. A good way to see if you have a good Nutritionist.. just ask them the following question, What gluten-free foods they would recommend, in order to retain the needed amounts of vitamins normally found in gluten containing foods? A good nutritionist should be able to not only provide a list of those foods, but know them right off the bat. If he/she hands you a bag of nuts and tells you to eat them for calorie intake - RUN!

Good luck =)

Hi,

Could I get the name and email of this dr. I'd like to ask her a few questions because all this information is extremely informative. I hope she can help me out.

Thank you

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      126,201
    • Most Online (within 30 mins)
      7,748

    Rach 123
    Newest Member
    Rach 123
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      120.9k
    • Total Posts
      69.2k

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • kopiq
      I also have food particles left on toiet paper when i wipe and my stool is light yellow not absorbing fats. I urinate about 15 times a day and have very sticky snot,dry throat.
    • kopiq
      Hi all, I was diagnosed by blood work about 2 months ago and have since went on a strict gluten free diet. I have an endoscopy in January and the GI dr said nothing about staying on gluten for it; hes aware i went no gluten. starting to heal symptoms include: (this is huge) sensation coming back to genitals and when having a bowl movement. everything has been numb for a long time down there including lower belly button area. good size (not abnormal) bowel movements once a day or every two days. small dot size wart just fell off my finger that was there for years. have not broke out with a cold sore this winter (every winter prior for years i would develop a cold sore on my lip) Ongoing issues I don't sweat. not from my hands, or armpits or feet. I do not get butterflys in stomach. my hands have been so dry for years ive been using a crack cream as they crack and bleed very severely in the fall and winter.  (since going gluten free ive not used crack cream but they are still very very dry and chapped/flaky, no sweat or moisture in palms of hands at all. I dont crave food. i have no cravings at all, not for pizza, ice cream , nothing. my cravings are dead. smell of foods kinda make me hungry, but my stomach blocks it. pins needles in feet get weak legs standing up from sitting and dizzy, things almost turn black. i cannot tolerate veggies or vitamins. Iam vitamin D deficient according to my Dr and Ive tried vitamin D pills. they give me a massive migraine for 8 hours and upset my stomach. the heat from the direct sun make me extremely tired to the point of wanting to pass out. again i don't sweat. broccoli gives me a migraine headache as well. mushrooms, bell peppers burn my stomach. fruits burn my stomach, fats (peanut butter, any oil or fat from meats make me sick to my stomach for a couple hours or longer. salt and pepper burns my stomach. all these issues cause pain at my belly button area and expand to the rest of my upper stomach and sides the more i ingest through out the day. I currently eat bland basmati rice, chicken, pork chops (fat trim), boiled russet potatoes no skin for three meals a day. my snacks are gluten free ground buckwheat flour pancakes. (just water, no oil , salt, dairy.) how am i to get vitamins in my system if i cannot tolerate them in my stomach? i mentioned epidermal vitamin patchs but dr said no. why cant i stand the heat from the sun ? why cant i sweat? thanks for any info.                
    • trents
      Because you have significantly reduced your gluten intake over a considerable amount of time, it is likely that you will test negative on the antibody tests. However, if the $112 for the Quest test is not a burden, it wouldn't hurt to try. It tests for total IGA (to ascertain if you are IGA deficient) and tTG-IGA. If total IGA is deficient, it can result in false negatives in other IGA tests. The tTG-IGA is the single most popular test ordered by physicians. The Quest test is not a complete celiac panel by any means (refer to the linked article above) but it might be a good place to start. Personally, I think you know enough to conclude that you need to get serious about avoiding gluten, whether you have celiac disease or NCGS. Human nature being what it is, however, many people seem to need an official diagnosis of celiac disease in order to stay on the bandwagon. Otherwise, they seem to rationalize cheating on the gluten-free diet. And there is this misconception out there that NCGS is inconvenient and uncomfortable but not harmful so it's okay to cheat. The more we learn about gluten-related disorders the more they seem to not fit into our neat little black and white categories. By the way, celiac disease is not a food allergy. It is classified as an autoimmune disorder.
    • More2Learn
      These responses are all extremely helpful, ty.  Really good reminder about omega 6.  I also know I'm low in zinc; I took the zinc test where I drank it on a spoon and couldn't taste it.  To that end, I try to eat a lot of oysters.  I do think it would be a good idea to get the blood test.  Two questions: 1-  Is there any reason you wouldn't recommend that I just buy and take a test like this as a first step? 2- I've been somewhat gluten free since ~Jan 2023 (technically organic, gluten free, soy free, light on dairy).  I eat a lot of meat, vegetables, rice -- a common breakfast for me is three eggs and a sausage link, and I can't remember the last time I had a sandwich or bread.  However, because in my mind I didn't think I had an allergy, and I more was doing gluten free to avoid artificially iron-enriched foods, I do make exceptions.  I'll eat breaded calamari.  When my Dad visits, I split mozzarella sticks with him because he loves them so much.  I'll eat the "gluten sensitive" items at a restaurant and if they asked, "is cross contamination ok?",  I always said yes.  Based on that, since I never probably fully eliminated gluten, but it was significantly reduced... is that good enough to take the blood test?  Because the pain in my side gets SO bad (really sometimes I can't function, and I absolutely thought I was dying), I am hesitant to do the gluten challenge.  Would it make sense to take the test, and if it's negative, then consider doing the challenge and seeing if I can deal with eating the bread every day? Thanks again!
    • Yaya
      For me, with osteoporosis, Celiac and more than 1 heart condition, the slower, safer route is preferable.  I'm on 5 meds per day.  Too much of anything can disturb absorption of this or that. Have a Happy Thanksgiving.  I'm gone for a few days.  
×
×
  • Create New...