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

Am I Crazy, Sorry For The Long Post....


aliciahere

Recommended Posts

aliciahere Apprentice

K, I know that this is going to be a long post. I just need somewhere to put this online. I know that there are a lot of case studies and histories and everything, but I just need to know that I'm not crazy, and just to get it out of my system.

 

OK, so I'm four weeks into a challenge to try to confirm celiac. For the past two years, I had been eating Paleo (though not religiously, probably close to the 80/20). I did still occasionally have wheat products as they didn't "seem" to bother me. I try to donate blood as often as I can, and one time I came up with low hemoglobin, so they sent me to my Dr. Dr. checked for low iron, came back positive. Sent me on my way with OTC supplements and with blood work to check for low iron (and celiac, IgA) in three months.  I was tested in three months, my Iron came back normal, however my IgA was higher than what he would like to see. It was at a 6.8. Dr. asked if I was eating a low carb/low wheat diet - yeah Paleo. Now he advised me to eat the two slices of bread for a month and check blood work again (though the only thing he is testing for is Iga).

 

If I had to call it, I would have never suspected celiac, as my symptoms are fairly minor, however looking back, everything seems to fit. My history:

 

- Diagnosed with hypothyroidism in my early 20's. Put on Synthroid. Doses increased when I was pregnant. However, when I was starting to go Paleo, they went down a bit (auto-immune).

- Diagnosed with Reynauld's disease last year. I've really had it since I was a teenager, however, last winter was particularly bad and I finally got a diagnosis. The specialist thought that it was type 1, which is not considered auto-immune, however with all of this, I'm now questioning that.

- Increase in gas since starting the gluten challenge. I realized that when I was on Paleo, I had virtually no gas. Now that I'm eating it again, I am gassy (though not in a way that I would suspect something is wrong, I would call it above average gas). I did have this gas all through my 20's, prior to eating paleo.

- Brittle fingernails. They also have ridges and dry splitting cuticles. Have had this since I was a teenager.

- Inter-uterine growth restricted for my oldest , with low birth weight (though it was the opposite with my son, he was large and heavy).

- Low libido. It was getting better on paleo, but now back to nothing.

- Terribly sore and tense neck and shoulder muscles constantly since last summer. I have had several massages, and done exercises, but nothing seems to fix it.

- I used to always get sick prior to changing my diet. Multiple colds per year, and the worst cold symptoms that would last forever. On paleo I got much fewer colds, and with minor symptoms. Now on the challenge, I've gotten a cold :P

- Multiple cold sores prior to changing my diet. Throughout my late teens, it was almost constant. While on paleo, they were much less. Now on the challenge, I have a cold sore (haven't had one in months).

 

 

Family history:

 

- My mom has hypothyroidism and takes synthroid. She also has terrible seasonal allergies. She also has bad knees. She has a typical diet, and is a smoker.

- My mother's father is from Ireland and died of Alzheimer (which has more and more evidence to suggest that it is an auto-immune disease)

 

 

Am I going crazy to STRONGLY suspect that I do have celiac? A big reason I want to confirm the diagnosis so that I can get my family tested. Otherwise I would just start the diet on my own. My plan is to go six weeks and get the bloodwork done, and if it still doesn't fully confirm celiac, then I would request the full range of bloodwork and test again at 12 weeks.


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



Celiac.com Sponsor (A8-M):



cyclinglady Grand Master

Usually for the blood test to be accurrate, you should be consuming gluten for 8 to 12 weeks and just four weeks before an endoscopy/biopsy. Do the research and share it with your doctor. The University of Chicago's celiac website is good for patients and professionals.

Here is the list of celiac disease diagnostic tests:

-tTG IgA and tTG IgG

-DGP IgA and DGP IgG

-EMA IgA

-total serum IgA and IgG (control test)

-AGA IGA and AGA IgG - older and less reliable tests largely replace by the DGP tests

-endoscopic biopsy - make sure at least 6 samples are taken

Welcome to the forum and let us know how it goes!

murphy203 Rookie

What CL said! I started with anemia, too, which led ultimately to a diagnosis of celiac disease. Please do take the anemia seriously -- I didnt, and suffered its symptoms needlessly. A HEAVY dose of iron supplements and a relatively quick diagnosis of the underlying cause have my #s moving in the riht direction. Best wishes in your journey, and is Alzheimers seriously autoimmune? Gah!!

aliciahere Apprentice

Thank you CL and murphy. I will certainly keep up on my iron. My Dr. wanted me to test after a month, so I will, but if it comes back negative, I will absolutely insist on the full blood work at 12 weeks.Yeah, it's not definitive yet, but it's looking more and more like it is an autoimmune (I hope this link works)Open Original Shared Link

aliciahere Apprentice

And I really, really hope it does come back positive after six weeks.... I feel so crummy. I'm wondering if this "cold" that I have is really a cold, or if it's just a gluten reaction, *sigh*

kareng Grand Master

Just a comment - Who is paying for the Celiac blood test?  I doubt insurance will pay for it, have it be negative and then pay for it again in 2 months.  Just something to consider.

aliciahere Apprentice

Oh, I'm in Canada  :wub:


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



Celiac.com Sponsor (A8-M):



  • 4 weeks later...
aliciahere Apprentice

Yay!!! I'm not crazy! :D  I didn't think I would be happy to be diagnosed with something, but it's been confirmed that I'm celiac. My IgA came back after only a six week challenge at 15, so confirmed. I won't have a scope/biopsy for months though. 

 

I think I may need to get a new Dr. though. As I was discussing how worried I was about how  I appear to have three auto-immune diseases (Celiac, Thyroid, Reynaulds), he stated, "Celiac is an allergy, not auto-immune"   :blink: 

RMJ Mentor

Yikes, you definitely need a new doctor!

Archived

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

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

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





    Celiac.com Sponsors (A17-M):




  • Recent Activity

    1. - Rogol72 replied to HAUS's topic in Gluten-Free Foods, Products, Shopping & Medications
      8

      Sainsbury's Free From White Sliced Bread - Now Egg Free - Completely Ruined It

    2. - Scott Adams replied to HAUS's topic in Gluten-Free Foods, Products, Shopping & Medications
      8

      Sainsbury's Free From White Sliced Bread - Now Egg Free - Completely Ruined It

    3. - Scott Adams replied to deanna1ynne's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      13

      Inconclusive results

    4. - deanna1ynne replied to deanna1ynne's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      13

      Inconclusive results


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      132,441
    • Most Online (within 30 mins)
      7,748

    Linda Boxdorfer
    Newest Member
    Linda Boxdorfer
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.5k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Who's Online (See full list)

  • Upcoming Events

  • Posts

    • Rogol72
      @HAUS, I was at an event in the UK a few years back. I remember ringing the restaurant ahead to inquire about the gluten free options. All I wanted was a few gluten free sandwiches, which they provided and they were delicious. The gluten-free bread they used was Warbutons white bread and I remember mentioning it on this site before. No harm in trying it once. It's fortified with Calcium and Iron. https://www.warburtonsglutenfree.com/warbs_products/white-loaf/ The only other gluten-free bread that I've come across that is fortified is Schar with Iodized salt, nothing else.
    • Scott Adams
      In the U.S., most regular wheat breads are required to be enriched with certain B-vitamins and iron, but gluten-free breads are not required to be. Since many gluten-free products are not enriched, we usually encourage people with celiac disease to consider a multivitamin.  In the early 1900s, refined white flour replaced whole grains, and people began developing serious vitamin-deficiency diseases: Beriberi → caused by a lack of thiamin (vitamin B1) Pellagra → caused by a lack of niacin (vitamin B3) Anemia → linked to low iron and lack of folate By the 1930s–40s, these problems were common in the U.S., especially in poorer regions. Public-health officials responded by requiring wheat flour and the breads made from it to be “enriched” with thiamin, riboflavin, niacin, and iron. Folic acid was added later (1998) to prevent neural-tube birth defects. Why gluten-free bread isn’t required to be enriched? The U.S. enrichment standards were written specifically for wheat flour. Gluten-free breads use rice, tapioca, corn, sorghum, etc.—so they fall outside that rule—but they probably should be for the same reason wheat products are.
    • Scott Adams
      Keep in mind that there are drawbacks to a formal diagnosis, for example more expensive life and private health insurance, as well as possibly needing to disclose it on job applications. Normally I am in favor of the formal diagnosis process, but if you've already figured out that you can't tolerate gluten and will likely stay gluten-free anyway, I wanted to at least mention the possible negative sides of having a formal diagnosis. While I understand wanting a formal diagnosis, it sounds like she will likely remain gluten-free either way, even if she should test negative for celiac disease (Approximately 10x more people have non-celiac gluten sensitivity than have celiac disease, but there isn’t yet a test for NCGS. If her symptoms go away on a gluten-free diet, it would likely signal NCGS).        
    • JoJo0611
    • deanna1ynne
      Thank you all so much for your advice and thoughts. We ended up having another scope and more bloodwork last week. All serological markers continue to increase, and the doc who did the scope said there villous atrophy visible on the scope — but we just got the biopsy pathology report back, and all it says is, “Duodenal mucosa with patchy increased intraepithelial lymphocytes, preserved villous architecture, and patchy foveolar metaplasia,” which we are told is still inconclusive…  We will have her go gluten free again anyway, but how soon would you all test again, if at all? How valuable is an official dx in a situation like this?
×
×
  • 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.