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

Celiac Disease Center - U Of Chicago


October3

Recommended Posts

October3 Explorer

I have an appt to take my son to the CDC in Chicago next week. We're traveling in from out of town that morning and I'm making plans to meet up with friends and trying to get a sense of the timeline. FWIW, this is a second opinion type appt. My son has already had an extensive work up which has been pretty inconclusive and I'm just wanting the doc in Chicago to weigh in on whether or not we should go gluten-free at this point, or whether there is anything else that needs to be tested. I'm wondering if they recommend a gluten-free diet do they have you meet with a nutritionist or do any other eduction, or whether I should expect 15 min in the room with the doc and that's it. Can anyone share their experience?

Thanks in advance,


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



Celiac.com Sponsor (A8-M):



Luddie Newbie

I have an appt to take my son to the CDC in Chicago next week. We're traveling in from out of town that morning and I'm making plans to meet up with friends and trying to get a sense of the timeline. FWIW, this is a second opinion type appt. My son has already had an extensive work up which has been pretty inconclusive and I'm just wanting the doc in Chicago to weigh in on whether or not we should go gluten-free at this point, or whether there is anything else that needs to be tested. I'm wondering if they recommend a gluten-free diet do they have you meet with a nutritionist or do any other eduction, or whether I should expect 15 min in the room with the doc and that's it. Can anyone share their experience?

Thanks in advance,

My doc has a nutritionist on staff with him and also does monthly workshops for his patients with her to help us learn about the "new way of eating" that we celiacs must do!

This doc is now my primary care physician, too, as the other one I have been seeing for years never, ever thought about my having celiac disease. I guess in kindness I must say I didn't present a lot of "typical" symptoms (except thyroid disease, which I now understand can be a result of celiac disease). So, my experience has been pretty good with my doc (who also answers emails and urgent cell phone calls promptly). His appointments are supposed to be 15 minutes, but if I ask for an abnormal blood chemistry appointment, he can stretch it to 30. Maybe you'll find that, too. It's not the doctor, it's the rules of the particular practice he's in.

Good luck.

Luddie

October3 Explorer

My doc has a nutritionist on staff with him and also does monthly workshops for his patients with her to help us learn about the "new way of eating" that we celiacs must do!

This doc is now my primary care physician, too, as the other one I have been seeing for years never, ever thought about my having celiac disease. I guess in kindness I must say I didn't present a lot of "typical" symptoms (except thyroid disease, which I now understand can be a result of celiac disease). So, my experience has been pretty good with my doc (who also answers emails and urgent cell phone calls promptly). His appointments are supposed to be 15 minutes, but if I ask for an abnormal blood chemistry appointment, he can stretch it to 30. Maybe you'll find that, too. It's not the doctor, it's the rules of the particular practice he's in.

Good luck.

Luddie

Thanks Luddie. I'm assuming your doc is at the U of Chicago? I have read about their workshops / support groups but since we live 5 hrs away I'm thinking that won't be a big help to us. I was wondering if they do any other education actually in the clinic, such as a meeting with the nutritionist during your visit, or if you have to make a separate appointment with the nutritionist. I had read that the Celiac Disease Center in Maryland has everyone go to the nutritionist when first diagnosed so I didn't know if it was standard practice at a celiac disease-specific clinic like this or not. Its good to hear your doc is so easy to reach. That is one of my main complaints about the doc we have been working with - impossible to ask questions between visits. I was impressed that Dr. Guandalini himself responded (and very thoroughly) to a question I sent to the Celiac Disease Hotline email.

kareng Grand Master

Thanks Luddie. I'm assuming your doc is at the U of Chicago? I have read about their workshops / support groups but since we live 5 hrs away I'm thinking that won't be a big help to us. I was wondering if they do any other education actually in the clinic, such as a meeting with the nutritionist during your visit, or if you have to make a separate appointment with the nutritionist. I had read that the Celiac Disease Center in Maryland has everyone go to the nutritionist when first diagnosed so I didn't know if it was standard practice at a celiac disease-specific clinic like this or not. Its good to hear your doc is so easy to reach. That is one of my main complaints about the doc we have been working with - impossible to ask questions between visits. I was impressed that Dr. Guandalini himself responded (and very thoroughly) to a question I sent to the Celiac Disease Hotline email.

Why don't you ask? Either thru the email or the appointment line. They make appointments but might not realize you can't come back next week for something else. Make sure they have any tests you have already had. Is there any blood work they want done first?

Luddie Newbie

Thanks Luddie. I'm assuming your doc is at the U of Chicago? I have read about their workshops / support groups but since we live 5 hrs away I'm thinking that won't be a big help to us. I was wondering if they do any other education actually in the clinic, such as a meeting with the nutritionist during your visit, or if you have to make a separate appointment with the nutritionist. I had read that the Celiac Disease Center in Maryland has everyone go to the nutritionist when first diagnosed so I didn't know if it was standard practice at a celiac disease-specific clinic like this or not. Its good to hear your doc is so easy to reach. That is one of my main complaints about the doc we have been working with - impossible to ask questions between visits. I was impressed that Dr. Guandalini himself responded (and very thoroughly) to a question I sent to the Celiac Disease Hotline email.

Actually, no, I'm not in Chicago. I'm in Ohio, and my MD is here, too, associated with the University in an Alternative Medicine practice. So, no direct "translation" of care for you there in Chicago. But keep asking questions, as practices do add things from time to time. It must be really frustrating to be dealing with this for a child. It's hard enough to deal with my own condition! Hope you get some good answers and advice.

Luddie

lil'chefy Apprentice

Actually, no, I'm not in Chicago. I'm in Ohio, and my MD is here, too, associated with the University in an Alternative Medicine practice. So, no direct "translation" of care for you there in Chicago. But keep asking questions, as practices do add things from time to time. It must be really frustrating to be dealing with this for a child. It's hard enough to deal with my own condition! Hope you get some good answers and advice.

Luddie

Hey Luddie, where do you live at in ohio? I need a good doc, who is knowledgable about DH/ celiac!

Erin

Luddie Newbie

Hey Luddie, where do you live at in ohio? I need a good doc, who is knowledgable about DH/ celiac!

Erin

Hi Erin,

I live in the Columbus, Ohio area. I'm not sure about the protocol on this forum for giving you information (i.e., my name or doctor's name). Anyone know if it's okay or how to do that privately? Wouldn't want to do anything that's not squeeky clean.

Thanks!

Luddie


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



Celiac.com Sponsor (A8-M):



kareng Grand Master

Hi Erin,

I live in the Columbus, Ohio area. I'm not sure about the protocol on this forum for giving you information (i.e., my name or doctor's name). Anyone know if it's okay or how to do that privately? Wouldn't want to do anything that's not squeeky clean.

Thanks!

Luddie

If you have only good things to say about someone, like a doc, it's OK. You could also PM ( private message) the person. Click on thier picture, then you go to thier profile, then under thier picture there is a " send me a message". .

Doing this from memory, but you can figure it out.

I should add that if you are the doc or work for the doc, do it privately or not at all.

lil'chefy Apprentice

If you have only good things to say about someone, like a doc, it's OK. You could also PM ( private message) the person. Click on thier picture, then you go to thier profile, then under thier picture there is a " send me a message". .

Doing this from memory, but you can figure it out.

I should add that if you are the doc or work for the doc, do it privately or not at all.

Not asking for you to do anything out of line....I live in Dayton OH, and am really having dr. issues. If you r not comfortable, it's cool.

  • 2 weeks later...
October3 Explorer

I thought I would update, just in case someone was doing a search and ran across this thread. I couldn't have been more pleased with the experience at U of Chicago. Every single staff person we encountered, from the security people giving us directions to the doctor himself, was super friendly and helpful. The doctor said several times that I should take as much time as I wanted with him and be sure to ask all my questions. The appt was not rushed at all. He did a thorough exam and also reviewed the records I brought and took a lot of time making notes and asking questions about my son's history. He didn't brush anything off. Very good experience altogether. We don't have any answers yet, but I was pleased that they are moving forward with asking questions because we had kind of hit a wall with the old GI where no further testing was being pursed to explain my son's symptoms. They are reviewing the slides from my son's biopsy to see if anything was missed, which is so nice that they will do that rather than another scope. It was most definitely worth the trouble and cost to travel in order to go there.

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      130,682
    • Most Online (within 30 mins)
      7,748

    PeterC
    Newest Member
    PeterC
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.3k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • Rebeccaj
      Hello , I would like to know what happens to people living or working in a industry or living with people that are non celiac or allergy Pron or anaphylaxis.    what are the symptoms and have you reached neurological symptoms during Airbourne exposure or hours later. persistent just ptsd related or unknown as its usually only high inflammation in the body when consumed with Vegas nerve symptoms of ingested or neuroglial of ingestion of inhalation accidently as my doctor has given me the ok to work but then my boss has let me go for a focal seizure as  Allery or ptsd unsure  any Insite of what someone else has gone through I was diagnosed when I was 27 so gluten free for the rest of my life but my family are not . ?
    • Beverage
      I strongly agree with others about processed gluten free foods, like breads and pasta, being bad for us. Read the labels, full of this starch and that starch, seed oils that are inflammatory, etc. Before you were celiac, you probably wouldn't even touch something with those ingredients. I do much better with whole foods, meat, veggies, a little fruit. I made 90% myself, make extra and freeze it for future meals. Cutting out processed gluten free food and eating mostly real whoke food helped me feel much better. And definitely benfotiamine!
    • knitty kitty
      Please be sure to try Benfotiamine or Thiamine Hydrochloride.  The form Thiamine Mononitrate is not absorbed nor utilized well.  Benfotiamine is much more bioavailable.  Perhaps Thiamine Mononitrate was in your previous B Complex supplements, explaining why they didn't work for you.   All the B vitamins work together.  Thiamine needs the other B vitamins to make enzymes and ATP, so you will need to take them.  Taking them in individual supplements is fine.  I've done the same.  Just remember you need all eight.   Let me know how it's going for you!
    • Zuma888
    • Zuma888
      Thanks! I am currently trying B1 out on its own. I tried many brands of B-complex and they always make me feel nauseous and tired. I think I may have to try taking each B vitamin on its own.
×
×
  • Create New...