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

This Is Silly, I'm Staying gluten-free!


Kimbalou

Recommended Posts

Kimbalou Enthusiast

So, my GI doc told me to "liberlize" my diet and go ahead and eat wheat, gluten, etc. My endoscopy is next Wed. Yesterday I ate what I wanted (a pretzel, scone, starbucks coffe, milk...and paid the price!!) I know for sure that the Celiac diet has helped me this past week, so when I ate what I wanted yesterday, it wasn't worth it! The horrible gas and abdominal pain! So, I'm gluten-free again, and I will take that chance. I'm sure my gut won't heal in 1 week! I'm sure I've had this for years.

It's as if the Dr. said "we know Gluten is poisoning you, but go ahead and eat it so we can make sure your biopsy is positive.". Crazy, if you ask me. so, if my biopsy comes up neagtive, it would be a miracle to be cured in 1 week. My blood tests were highly positive, so I will go by that.

I am getting the endoscopy, but I will eat gluten-free and not suffer...


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



Celiac.com Sponsor (A8-M):



Free-CountryGirl Apprentice

Agreed, stop eating the gluten :)

But I have ask, why do u need an endoscopy is your had positive blood tests?? Isn't that enough??

WheatChef Apprentice

The only good medical advice:

-Doctor, it hurts when I do this.

-Don't do that.

jerseyangel Proficient

The only good medical advice:

-Doctor, it hurts when I do this.

-Don't do that.

:lol: :lol: Ya got that right!

Kimbalou Enthusiast

Agreed, stop eating the gluten :)

But I have ask, why do u need an endoscopy is your had positive blood tests?? Isn't that enough??

The doctors like to get a definite diagnosis, and the only way is with a biopsy. I've decided to do it in case there is something else going on as well.

T.H. Community Regular

The more I hear about doctors telling us to do something that is hurting us, so that they can do a test, the more I sit and think: what ever happened to 'do no harm?'

Just because a test wasn't worked out in a lab, but was rather a gluten elimination followed by a gluten challenge, doesn't mean it doesn't have medical validity. It may mean you do a couple more tests to check for other potential reasons that the gluten caused an issue...but doing those tests wouldn't cause harm, while eating the gluten is.

It doesn't seem like the way of thinking that applies to celiacs is in our best interest, at times.

ravenwoodglass Mentor

The doctors like to get a definite diagnosis, and the only way is with a biopsy. I've decided to do it in case there is something else going on as well.

There can be other things going on but the hard question is...how often are those other things caused by the reaction to gluten? And if they are would they resolve with the diet rather than you having to take meds. For myself gluten was the reason for both an ulcer and severe diverticulosis and both resolved after I had been gluten free for a while without the scripts that I was given for the ulcers. You may want to consider holding off on the endo and having it done a few months after you are on the diet if you are still having issues. I'm not saying don't have the endo, the choice whether to do the test or not is yours alone.


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



Celiac.com Sponsor (A8-M):



Happytobefree Newbie

So, my GI doc told me to "liberlize" my diet and go ahead and eat wheat, gluten, etc. My endoscopy is next Wed. Yesterday I ate what I wanted (a pretzel, scone, starbucks coffe, milk...and paid the price!!) I know for sure that the Celiac diet has helped me this past week, so when I ate what I wanted yesterday, it wasn't worth it! The horrible gas and abdominal pain! So, I'm gluten-free again, and I will take that chance. I'm sure my gut won't heal in 1 week! I'm sure I've had this for years.

It's as if the Dr. said "we know Gluten is poisoning you, but go ahead and eat it so we can make sure your biopsy is positive.". Crazy, if you ask me. so, if my biopsy comes up neagtive, it would be a miracle to be cured in 1 week. My blood tests were highly positive, so I will go by that.

I am getting the endoscopy, but I will eat gluten-free and not suffer...

I went this route also, but you have to intake gluten daily for a minimum of 4 weeks to get visible damage in your stomach and/or intestine. I think my GI thinks I am nuts because all my symptoms couldn't be proven. I had been gluten free for a year and a half before I went to get tested. I was so scared of intake and had forgotten exactly how I felt when I ingested gluten. I got a painful reminder, but I journaled all my experiences so I could inspire myself to live without. I held up for 2 to 3 weeks of the 2 month period my GI requested I ingest gluten. I will not do that again. I know I am so much better off without.

Good luck.

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,803
    • Most Online (within 30 mins)
      7,748

    mcgrawka
    Newest Member
    mcgrawka
    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

    • nanny marley
      Oh yes I can understand the tiredness after going threw all that, must be exhausting especially on the mind I have high aniexty so I can understand that , I wish there more easier ways for people to get help , I had a MRI on my spine some years ago without anything it was really quick and no prep , I understand the need for  them to see better with the bowel ,but you think they would use something a little less traumatic  for ibd sufferers on the bowels by now ,I hope your feeling better today 🙏
    • Colleen H
      The previous post did not come through right. I wonder if tingling burning feet are part of it.. I'm not sure if it's the med reaction that people with gluten intolerance get or the food we ate  It's frustrating because a person who did not want to admit to himself I had this condition wanted me to eat this chicken sandwich and now I'm stuck with a variety of symptoms plus now I'm hungry on top of it..  I'm new to this so I forget that "one bite" of the wrong thing can hurt us.😔. Do we stop eating if someone exposed us to gluten ??  My stomach is rumbling but my joints hurt ...  It's weird because I can feel the anxiety coming on.  I get joint problems ,  I don't know if anyone ever got hot flashes?? I suppose if it affects people head to toes you can get that too.   It's weird...hard to decipher what is what.   Also how long do I have to deal with this attack??  Makes me feel like not getting up out of bed.  I get too many symptoms which  horrible.  Thank you for your response..  
    • Colleen H
      Hello  I was glutened by a person that knew it.  I'm having 
    • wellthatsfun
      as my last post stated, i was diagnosed via endoscopy on the 14th of june. i have been eating amazing home cooked meals, luckily, mainly cooked by my boyfriend who is extremely careful about contamination (and is an incredible cook at that). however, i find myself in a mental rut still. being 18, this is the time in my life where i should be exploring things, going out, having fun. yet every corner i turn i'm tortured by the amazing smell of something i can't have anymore. the wonderful sight of such yummy foods. it's near torture. if my boyfriend and his friend who lives with us buy something i can't have, they'll usually eat it outside of the house or the car or wherever we are - which is greatly appreciated - but even seeing a burger or chips or a sausage roll in their hands guts me almost beyond repair. i just wanna have it again too. i miss it. i feel left out and it makes me very sad all the time. it's not their fault. they are allowed to eat whatever they want to, whatever their intestines will allow. it just stings, bad. and i feel so ungrateful given i basically have a private chef who is doubly the love of my life. but it's just so hard. i know i'll adapt. i haven't given up hope.i just wanted to vent. thank you for reading
    • RDLiberty
      Thank you. I must have misinterpreted a study or something. Thank you for the clarification. Much appreciated. Almost three years into my celiac diagnosis and I'm still learning new things. 
×
×
  • 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.