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

Not Sure What To Do


frustratedandtired

Recommended Posts

frustratedandtired Rookie

Hello all...

First off let me say I am glad to find this site. I have not been diagnosed with celiac and not sure if that is what my problems are from yet. The dr I saw Friday mentioned it and told me to find a primary dr that can accomidate short notice appt's. My ex also called me that evening to say that I needed to get tested for it without me even mentioning it to him. He had seen Elizabeth Hasselbeck on a show telling her story. I have been told nervous stomach, spastic colon, crohns (colonoscopy ruled it out) and IBS. I have always told them that I believe my problem is with my small intestines. I am always in pain. I have lost weight. At this point I eat about 6000 calories a day if not more just to maintain what I managed to put back on. I eat constantly. The headaches and the joint pain now are getting worse. My knuckles on my right hand are twice the size of my left. I'm weak and tired most of the time. The digestive issues .... well i wont go into those. I have had issues for years. When my symptons get extreme then I finally go to the dr. I get so frustrated not getting what I feel is a correct diagnosis I stop going. I feel like I'm wasting my time and my money for nothing. I am willing to try anything at this point. I will definately try the gluten free diet but from what I have read, I need to eat normal till tested. I will call the gastro dr and make a appt. I will let him know I would like to be tested and hopefully he will do so.


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



Celiac.com Sponsor (A8-M):



Wolicki Enthusiast

Hello all...

First off let me say I am glad to find this site. I have not been diagnosed with celiac and not sure if that is what my problems are from yet. The dr I saw Friday mentioned it and told me to find a primary dr that can accomidate short notice appt's. My ex also called me that evening to say that I needed to get tested for it without me even mentioning it to him. He had seen Elizabeth Hasselbeck on a show telling her story. I have been told nervous stomach, spastic colon, crohns (colonoscopy ruled it out) and IBS. I have always told them that I believe my problem is with my small intestines. I am always in pain. I have lost weight. At this point I eat about 6000 calories a day if not more just to maintain what I managed to put back on. I eat constantly. The headaches and the joint pain now are getting worse. My knuckles on my right hand are twice the size of my left. I'm weak and tired most of the time. The digestive issues .... well i wont go into those. I have had issues for years. When my symptons get extreme then I finally go to the dr. I get so frustrated not getting what I feel is a correct diagnosis I stop going. I feel like I'm wasting my time and my money for nothing. I am willing to try anything at this point. I will definately try the gluten free diet but from what I have read, I need to eat normal till tested. I will call the gastro dr and make a appt. I will let him know I would like to be tested and hopefully he will do so.

Well, here's something to think about. There are SO many doctors who have no clue about Celiac. Many of us have gone from doctor to doctor, and suffered for years because no one knew. I was sent to a GI after 10 yrs of suffering and having a positive blood test, only to be told I don't have it because no D.

You can continue to go from doctor to doctor and remain frustrated. OR you can do a trial gluten free diet. Positive dietary result is proof of celiac or gluten intolerance. If you feel better on the gluten free diet, then you have your answer. There is no treatment other than the diet, so what do you have to lose? That's just MHO <_<

Janie

cricuteer Rookie

Well, here's something to think about. There are SO many doctors who have no clue about Celiac. Many of us have gone from doctor to doctor, and suffered for years because no one knew. I was sent to a GI after 10 yrs of suffering and having a positive blood test, only to be told I don't have it because no D.

You can continue to go from doctor to doctor and remain frustrated. OR you can do a trial gluten free diet. Positive dietary result is proof of celiac or gluten intolerance. If you feel better on the gluten free diet, then you have your answer. There is no treatment other than the diet, so what do you have to lose? That's just MHO <_<

Janie

This is also what I am doing! I thought after all I have read with the horror stories of people being misdiagnosed for years and doctors not truly understanding the condition that I needed to just do this on my own. Maybe it's not the right approach for everyone, but I'm a low-income person that can't afford to be tested for everything in the book. The first and only doctor I saw didn't even suggest testing of ANY sort, just said that I had IBS told me to eat more fiber and sent me on my way.

I'm in for the long-haul with my trial. Day 4, not feeling any better at this point but have already started losing weight.

frustratedandtired Rookie

Thank you for your replies.

I have a appt Thursday with a new gastro dr. It is where my daughter recently went because she has had issues lately as well. When i made the appt I let them know I wanted to be tested for Celiac disease. I have been tested for everything else. Given the fact that my youngest daughter is having problems, and that I read somewhere that girls with Turners Syndrome are at higher risk as well and my oldest daughter having Turner's, I feel for me it is best to be tested if possible. I will do the gluten-free diet reguardless of what they say. I am willing to try anything at this point.

This may be TMI...I read where you may see a "few" drops of oil in your stools. I have been telling them for years about this and it is MUCH more than a few drops. It covers all the water in the toilet. Does IBS cause this? I wouldn't think so.

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,661
    • Most Online (within 30 mins)
      7,748

    CarlaP
    Newest Member
    CarlaP
    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

    • Xravith
      Thank you for the advice. I’ve actually never checked for nutritional deficiencies, but for as long as I can remember, I’ve always taken vitamin and mineral supplements — otherwise my symptoms get worse. This week I stopped eating gluten to confirm whether my symptoms are really caused by it. Starting next week, I’ll reintroduce gluten — it’s sad to go back to how I was before — but at least I’ll be able to take the necessary tests properly. I think the diagnostic process will be long, but at least I’m happy that I finally decided to address this doubt I’ve had for years.
    • Julie 911
      I finally got rhe answer and Tylenol is ok. Thanks everyone 
    • dublin555
      Hey Julie! I was in a similar situation before my biopsy and my gastro said Tylenol was fine. Just avoid ibuprofen or anything anti-inflammatory until you're cleared. Hope your surgery goes smoothly!
    • trents
      I don't see how cornstarch could alter the test results. Where did you read that?
    • knitty kitty
      For pain relief I take a combination of Thiamine (Benfotiamine), Pyridoxine B 6, and Cobalamine B12.  The combination of these three vitamins has analgesic effects.  I have back pain and this really works.  The B vitamins are water soluble and easily excreted.   Hope this helps!  Keep us posted on your results!
×
×
  • 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.