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

Newly Diagnosed


Emilydeaconx

Recommended Posts

Emilydeaconx Rookie

Hey

 

For the past 2 weeks i have been feeling very very dizzy, shaking, belly cramps, nausea the lot. So bad that i’ve called the hospital the other night because i couldn’t walk. I was told 2 weeks ago that there’s a definite chance i’m coeliac but i am currently waiting on a letter for an appointment for the biopsy. Due to my symptoms the consultant at the hospital told me to stop eating gluten for a bit as the biopsy could take a while. I have been gluten free for only 1 day and obviously still have dizziness and cramps, does anyone know if these will disappear within a couple days? i have had 2 weeks off work and i can’t really take anymore time off so i’m praying these symptoms will disappear soon!! Please could someone help?? 


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



Celiac.com Sponsor (A8-M):



Ennis-TX Grand Master

Varies from person to person, my symptoms change but vary from vomiting, diarrhea, motor control loss, numbness, constipation, and bunches of small other things that are always changing. The initial pain and vomiting pass in a day or, then the pain and D or C come and go for weeks, the numbness I get can last months slowly lessening.

You issues might depend on the cause, are the symptoms related to the nutrient absorption from damaged intestines? Then you have to supplement and it can take 4-12months or more to heal your gut. IF they are caused by the raised antibodies it can depend on how strict you diet is and how your immune takes to wind down. I have seen members be over it in a week...some still have issues 4months later as it slowly goes down. Your really just going to have to wait it out and see. By the way the medical gluten free diet is very strict....you have to replace scratched pans, cutting boards, pots, colanders, new condiment jars, throw out wooden spoons, etc. Sort of a decon phase cleaning everything out is gluten is a protein smaller then a germ...and bleach does it kill it, its like blood were a CSI tech can still find it. 500F+ will destroy it so the oven self clean cycle can be used to decon some pans, cast iron, etc. Might be useful https://www.celiac.com/forums/topic/91878-newbie-info-101/

But as a heads up, you will be having to eat gluten every day at least 2 weeks before they do that endoscope. Via the gluten challenge. Open Original Shared Link

 

GFinDC Veteran

Hi Emily,

You don't have to eat a lot of gluten each day for the antibody testing to work.   Usually they say a single slice of regular gluten bread is sufficient.  So you could cut down on it like that and your symptoms might not be so bad.  Another thing you could try is avoiding all dairy and soy for a few months.   Celiac affects our ability to digest dairy and that by itself can cause many unpleasant symptoms.  Soy is not good for the gut and may retard healing.   Soy lecithin is not a big problem though.

You can also try taking probiotics and Pepto Bismol.  They may help some.  If you are having lots of gas avoiding sugar and sweets is helpful.

It's helpful not to quit eating gluten before the endoscopy.  Going off gluten for a month or so and then going back on it for testing can be very unpleasant.  Possibly worse symptoms than you have now.

A diet of mostly whole foods is helpful for healing.

pikakegirl Enthusiast

I did not have any help after diagnosis but if i could go back and give myself help i would tell myself that healing takes lots of time so buckle up and learn to be patient. The body is strong and is healing the minute the gluten is eliminated. However the gi is weaker and mine full of candida as well as malabsorption problems like leaky gut. I found my bifida was gone so probiotics are a daily need to breakdown vital food. I finally went on an elimiation diet and it did wonders to calm my bowel habits. I could have avoided major pain if i had known i could not convert folic acid and b6. Also eliminating processed foods also took all the vitamin fortification from my diet. Now from genetic test for MTHFR i do lmethyfolate 3000k daily and d3 from fish source, bluebonnet 2000iu daily. Also b vitamins separetely. B12 in liquid from live wise though blood work was normal pernitious anemia is a problem in Celiacs. B6 as p5p since problems converting. Love life extension, now, live wise and solgar brands for least binders which irritate. All from Amazon since i live in a remote area. My k2 was low also. Demand a vitamin panel from drs and list them for the dr. Malnutrition has many symptoms which i found were a major cause to not feeling better. Last note check the thyroid. I knew i had hasimotos but the healing process put my doseage out of whack sending me to hospital for wild symptoms, just needed close monitoring and adjustment over the healing years. Hope some of this give you ideas, you are your best healer.

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      128,073
    • Most Online (within 30 mins)
      7,748

    David Croft
    Newest Member
    David Croft
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121k
    • Total Posts
      70.6k

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • trents
      @KRipple, thank you for the lab results from your husband's celiac disease blood antibody testing. The lab result you share would seem to be the tTG-IGA (Tissue Transglutaminase IGA) and the test result is in excess of 10x normal. This is significant as there is an increasing tendency for physicians to grant a celiac disease diagnosis on the basis of antibody testing alone when the scores on that particular test exceed 10x normal. This trend started in the UK during the COVID pandemic when there was tremendous pressure on the medical system over there and it has spread to the USA. The tTG-IGA is the centerpiece of celiac disease blood antibody testing. All this to say that some doctors would grant a celiac disease diagnosis on your husband's bloodwork alone and not feel a need to go forward with an endoscopy with biopsy. This is something you and your husband might wish to take up with his physicians. In view of his many health issues it might be wise to avoid any further damage to his small bowel lining by the continuing consumption of gluten and also to allow healing of such to progress. The lining of the small bowel is the place where essentially all of our nutrition is absorbed. This is why celiac disease when it is not addressed with a gluten free diet for many years typically results in additional health problems that are tied to nutritional deficiencies. The millions and millions of tiny finger-like projections that make up the nutrient absorbing surface of the small bowel lining are worn down by the constant inflammation from gluten consumption. In celiac disease, the immune system has been tricked into labeling gluten as an invader. As these finger-like projections are worn down, the efficiency of nutrient absorption becomes more and more compromised.
    • KRipple
      Thank you so much! And sorry for not responding sooner. I've been scouring the hospital records and can find nothing other than the following results (no lab info provided): Component Transglutaminase IgA   Normal Range: 0 - 15.0 U/mL >250.0 U/mL High   We live in Olympia, WA and I will be calling University of Washington Hospital - Roosevelt in Seattle first thing tomorrow. They seem to be the most knowledgeable about complex endocrine issues like APS 2 (and perhaps the dynamics of how APS 2 and Celiacs can affect each other). His diarrhea has not abated even without eating gluten, but that could be a presentation of either Celiac's or Addison's. So complicated. We don't have a date for endoscopy yet. I will let my husband know about resuming gluten.    Again, thank you so much for sharing your knowledge with me!
    • Jmartes71
      Ginger is my best friend, it helps alot with tummy issues..
    • aattana
      Hi Phosphone, did you ever figure out what elevated your DGP?  I am in the same boat. 
    • trents
      Scott makes a good point about the prednisone. It has a general suppressing effect on the immune system. Don't misunderstand me. In view of your husband's several autoimmune afflictions, it would seem to be an appropriate medication therapy but it will likely invalidate endoscopy/biopsy test results for celiac disease.
×
×
  • Create New...