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

New Fav Website!


anti-soprano

Recommended Posts

anti-soprano Apprentice

Sorry if this is old news to any of you- but it's new to me, so I decided to share.  This is my new favorite website about Celiac Disease.  Lots of information in a concise and easy to read format from real, live, medical professionals.  Must be nice to be a celiac in chicago with this resource!

 

Open Original Shared Link


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



Celiac.com Sponsor (A8-M):



w8in4dave Community Regular

Ohhh I like it!! It has alot of info in there!! Thanks!! Altho I don't live in Chicago. But it is nice to have some nice sites to send people to when they want to know about Celiac disease. I try and explain but sometimes they still do not get it. 

mamaw Community Regular

yes lots  of info.... But  I think this  site  is  very  helpful getting  info  from others  who  walk the  walk!!!!

Rachel2writer Newbie

Thanks! As someone newly diagnosed, I'm always happy to have more resources.

anti-soprano Apprentice

yes lots  of info.... But  I think this  site  is  very  helpful getting  info  from others  who  walk the  walk!!!!

Agreed, Mamaw!   People in this forum are great and so very helpful.  This site is also wonderful for many other reasons.  I also don't feel alone here ...or crazy.  I know I can post about my frustrations and people will understand.  I know I can post some bizarre thing that my body is doing and someone out there has already been-there-done-that. Invaluable feedback.

 

However, if you want to know medical facts, I would suggest going to my new fav website (as opposed to my longtime fav website): What's the medical difference between gluten intolerance and celiac, how to conduct a gluten challenge (how much and for how long), what are the genetic odds that immediate family members also have celiac, etc.  The info is provided by experts in the field and is up to date.  Just the facts ma'am.

powerofpositivethinking Community Regular

anti-soprano because of your post I visited the Chicago site even though I use it often, and just for fun searched "DGP"  They now have this posted:

 

Open Original Shared Link

 

I got a positive DGP-IgG score but nothing else, and although they kind of dance around the question, it relates the test to celiac instead of gluten intolerance.  I plan on sending this link to family members.

 

Thank you!

anti-soprano Apprentice

anti-soprano because of your post I visited the Chicago site even though I use it often, and just for fun searched "DGP"  They now have this posted:

 

Open Original Shared Link

 

I got a positive DGP-IgG score but nothing else, and although they kind of dance around the question, it relates the test to celiac instead of gluten intolerance.  I plan on sending this link to family members.

 

Thank you!

Woo-Hoo!  Go science!!

So glad I posted this :D  


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



Celiac.com Sponsor (A8-M):



Tbolt47 Newbie

Sorry if this is old news to any of you- but it's new to me, so I decided to share.  This is my new favorite website about Celiac Disease.  Lots of information in a concise and easy to read format from real, live, medical professionals.  Must be nice to be a celiac in chicago with this resource!

 

Open Original Shared Link

I agree, and I think the Univ. of Chicago website is most informative site as well. Here is one I find a close second:

Open Original Shared Link

It is authored by a women who has Celiac and happens to be an MD ,some of her children were diagnosed as well.

w8in4dave Community Regular

I like thepatientceliac also .. but it was having a very slow time coming up!! I might look at it again when the web is not guite so busy!! 

IrishHeart Veteran

KarenG, "GottaSki" Lisa and I are always posting links to the U of C website. :)

We also agree...it has the most comprehensive information in one spot.

 

I also like Tricia Thompson and Shelley Case's sites for nutritional information

and the book Real Life With Celiac Disease by Melinda Dennis

and Daniel Leffler.

Excellent Resource--covering dozens of topics written by over 50 celiac specialists.

 

And "the patient celiac" is extremely informative. Jess knows her stuff. And she graciously shares

her knowledge on various celiac-related sites as well as her own. 

w8in4dave Community Regular

Yes they are all great Irish Heart , but yet I hang in here :) This is a very nice site!! I do refer to this site if and when people have questions, either they don't understand and I cannot explain , Or don't have time to explain, I just hand them a sheet of paper with the website on it. I just really like to see it from all sides from different people and such , different perspectives , different stories. But having a  site like this where you can talk and get more and more information from, trials , and tribulations. Is wonderful!! Makes me feel I am not alone in this world! And seems so much stuff comes together for me when I read some of the stuff some have to say. I visit other sites , read them , think wow that was a good site!! Then I come in here :) 

IrishHeart Veteran

We do kinda grow on ya, don't we? (like mold)

And we are wicked smart. (ahem, and humble)

:D

seriously, though.....I have always found the advice from real live celiac veterans to be the best resource there is,

next to the celiac specialists.

w8in4dave Community Regular

Yes they are all great Irish Heart , but yet I hang in here :) This is a very nice site!! I do refer to this site if and when people have questions, either they don't understand and I cannot explain , Or don't have time to explain, I just hand them a sheet of paper with the website on it. I just really like to see it from all sides from different people and such , different perspectives , different stories. But having a  site like this where you can talk and get more and more information from, trials , and tribulations. Is wonderful!! Makes me feel I am not alone in this world! And seems so much stuff comes together for me when I read some of the stuff some have to say. I visit other sites , read them , think wow that was a good site!! Then I come in here :)

Absolutely!! 

moosemalibu Collaborator

All of the websites that have been mentioned in this thread have been super helpful for me and my family while I am learning about my recent diagnosis. Thanks so much! I have a background in science so it's lovely to read all the scientific statistic based research as well as personal experiences.

eers03 Explorer

It is a great site.  They need a link to this forum, though!  The people on here are amazing.

Archived

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

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

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





    Celiac.com Sponsors (A17-M):




  • Recent Activity

    1. - cristiana replied to KathyR37's topic in Coping with Celiac Disease
      4

      New here

    2. - trents replied to KathyR37's topic in Coping with Celiac Disease
      4

      New here

    3. - Theresa2407 replied to Theresa2407's topic in Gluten-Free Foods, Products, Shopping & Medications
      2

      Probiotics

    4. - KathyR37 replied to KathyR37's topic in Coping with Celiac Disease
      4

      New here


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,818
    • Most Online (within 30 mins)
      7,748

    STy
    Newest Member
    STy
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.4k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • sleuth
      @fatjacksonthecat I have been doing some digging about the topic of nicotine and celiac.  I came across many studies that showed that the nicotine patch helped many with long covid and chronic fatigue syndrome.  I have a son who was diagnosed with celiac and his symptoms are severe when he is glutened.  He shows a lot of neurological inflammation and suffered with fatigue, brain fog, depression, anxiety and insomnia. There have been studies revealing that nicotine smoke actually masking celiac symptoms.  I also read that microdosing with a nictoine patch prevents one from addiction.  We are currently trying this out and so far it has lifted the brain fog and helped with anxiety and mood.  One of the studies I have read showed that it's not so much the dose, but the length of time a person is on the patch that showed improvements.  Many showed significant improvement as early as week 3 and continued through week 12.  We are taking 3 day breaks in between to make sure we don't down regulate the nicotine receptors.   How have things been for you?  Are you still chewing nicotine gum?  Perhaps, try the patch?  And how long did it take to ease up on your symptoms when glutened?
    • cristiana
      Hi @KathyR37 and a very warm welcome here.  I am so very sorry that you are going through all of this. I just wanted to check, have you ever been tested for any other gastrointestinal conditions? Cristiana  
    • trents
      @KathyR37, I would suspect that in addition to gluten intolerance, you have other food intolerances/sensitivities. This is very common in the celiac community. The most common offenders are oats, dairy, soy, corn and eggs with dairy and oats being the big two. Have you considered this? Have you tried keeping a food diary to detect patterns?
    • Theresa2407
      thank you for your advice.   I have always taken them and I use Stonehedge because they are in a glass bottle, but don't have to be refrigerated.  I also like they are 3rd party tested and state gluten free. But you never know if something better has come alone over the years.
    • KathyR37
      Thank you for your response. I have already learned about the info you sent but i appreciate your effort. I am the only one in my family cursed by this disease. I have to cook for them too. I make sure that my utensils are free of gluten and clean after using them for other food. I use non-porous pots and pans and  gloves when cooking for them. One huge problem I have is a gag reflex out of this world and if something doesn't taste good it is not going down. Most commercially made breads and such taste like old cardboard.Pastas are about the same. I did find one flour that I like and use it regularly, but it is so expensive! All gluten free food is way more expensive. I only eat twice a day because I cannot afford to buy all that. We live on a very low income so my food purchases are quite limited.
×
×
  • 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.