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

Hashimoto's And Celiac?


salexander421

Recommended Posts

salexander421 Enthusiast

I know they are both autoimmune disorders so I know someone can obviously have both. I'm wondering if there is any literature that states the percentage of people with Hashimoto's who have Celiac as well? My Mom, her twin sister, and my cousin (mom's twin sister's daughter)all have hashimoto's. My mom and cousin are both on a gluten free diet but are not super strict, especially my mom who cheats pretty frequently. My aunt goes back and forth, one minute she thinks she has a problem with gluten and the next she is eating regular gluten foods. It's a mess! :P My mom and my aunt also both struggle with anemia and my aunt just had a hysterectomy at age 49, she was EXTREMELY anemic before hand. My aunt also gets a rash on her belly. I really suspect celiac here, especially with the issues that me and my girls have dealt with so far. Oh yeah, their brother (my uncle) has type 1 diabetes and overall not really healthy. I'm just looking for statistics here since they seem to respond well to that. Thanks!


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



Celiac.com Sponsor (A8-M):



Roda Rising Star

I don't know the statistics, but my search in 2008 lead me to celiac. I was looking for a connection on hashimoto's disease and low ferritin/anemia. I found lots of articles referencing celiac. It was this research that eventually prompted me to get tested by my endocrinologist for celiac.

BrittLoves2Run Apprentice

I too am wondering about this today. I just had a Celiac blood panel and a Thyroid test done this morning. All the women in my family have underactive thyroid.. and i'm thinking I have Celiac too. I couldn't believe how hesitant my doctor was to test for Celiac!

  • 2 weeks later...
zeeclass6 Explorer

I've had Hashimoto's for 15 years and have been gluten free for 3 weeks now on the advice of a new doctor. All the women in my family have thyroid problems and/or auto-immune problems of some sort.

My 90-year-old mother was first diagnosed with Hashi 5 years ago! Her sister had Hashi and then it flipped and became Graves.

None of us ever suspected a problem with gluten. But my mother dropped a bombshell on me the other day. She said that she remembers HER grandmother (in the 1930s) going to a special store to get gluten-free flour to make bread! But as far as I know, nobody in my family avoids gluten or has been diagnosed with Celiac, not even my mother or her sister.

My Celiac test was negative twice in 10 years. But recently I found out that my IGA is low, so it may be possible that I have some form of Celiac or just gluten sensitivity and not have known it. My clueless doctor didn't understand that maybe I should have further testing (IGG).

I have eaten gluten all my life and never considered that it was a problem, until the past few months. Body aches (feeling like there is glue in my body; very stiff), joint and muscle pain, slow healing of "pulled" muscles, worsening reflux, low B-12, and adhesive capsulitis in my shoulder prompted me to finally say, "Whoa, WHAT is going on????!!!" Suddenly, in the course of about a year, it seemed that something was crippling me for "no reason."

I got a lot of thyroid books out of the library and stumbled upon the Stop The Thyroid Madness (STTM) website (and eventually bought the book....both are EXCELLENT).

I saw a doctor from The Holtorf Group in N. Calif. They are extremely expensive. They ran a lot of tests. I found out that I have Fibrin in my blood and apparently have a problem called Hypercoagulation (thick clotty blood). I have no idea why, or when this started. Also, although my TSH was "perfect at 1.26" other tests (free T3, Reverse T3 and reflexes) showed that indeed I was still hypo and needed, at the very least, some T3.

I am not going back to the Holtorf doctor for several reasons. First, they are extremely expensive and aggressively push their private label supplements at you. Second, they do not really understand how to prescribe T3 and will not prescribe natural thyroid or do saliva cortisol tests. Thirdly, the doctors there are overloaded and do not have the time to even spend 5 minutes on the phone with you if you have questions later. "Just take the supplements." Yeah....$1,0000 in supplements! You read that right, one thousand dollars. I did not buy them. Are they crazy?!!!

Anyway, at the prompting of information from STTM, I got more blood tests and discovered that I am also anemic (low Ferritin, low saturation, high TIBC).

Then I saw the new doctor who said outright to me "You have an auto-immune disease. You should not be eating gluten!" He is the first doctor who ever mentioned this to me. (The expensive Holtorf doctor never mentioned gluten to me). Like I said, I've eating gluten my whole life. I didn't think it was a problem. But I've been gluten-free for 3 weeks now and in general I notice a lot less gas and bloating. And I'm not craving carbs or ANYTHING anymore. In fact, I barely have an appetite (is that bad?? I'm a little worried about that). So I assume that I must be sensitive to gluten....otherwise, why would these symptoms go away from eliminating gluten?

I have not done a challenge test yet. This weekend I plan to eat a few regular crackers and see how my body reacts.

I have an appointment with a Hematologist soon to discuss the coagulation thing and whether any of it is related to Celiac or gluten intolerance. I suspect that I may have some sort of malabsorption problem.

Everything in the body is related. The thyroid regulates a lot of things. Auto-immune diseases can really wreak havoc.

I hope that soon I will find the answers to my problems. Not sure whether I will need to continue staying gluten free or not. Not sure whether I will need Heparin injections for the coagulation problem. And I'm hoping that I can switch from Synthroid to Natural Desicated Thyroid, because I think that taking only Synthroid for 15 years has been a BIG part of my problem, causing these muscle problems, lingering depression, and other issues.

It is very hard to find a doctor who knows the proper tests to run, and even harder to find a doctor who interprets the tests properly and treats properly.

When it comes to thyroid issues, you need to educate yourself. I have found that most Endocrinologists are pompous idiots or slacker doctors who are not up on the latest research (such as Reverse T3, the importance of iron tests, B-12, or gluten/food issues relating to auto-immune problems). Educate yourself. Otherwise you will be at the mercy of sub-par doctors who will keep you sick.

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. - trents replied to Atl222's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      5

      Increased intraepithelial lymphocytes after 10 yrs gluten-free

    2. - cristiana replied to Atl222's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      5

      Increased intraepithelial lymphocytes after 10 yrs gluten-free

    3. 0

      Celiac Friendly Sports Camps - Academy Camps - Virtual Open House

    4. - lizzie42 posted a topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      0

      Low iron and vitamin d

    5. - Scott Adams replied to Atl222's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      5

      Increased intraepithelial lymphocytes after 10 yrs gluten-free

  • Celiac.com Sponsor (A19):
  • Member Statistics

    • Total Members
      133,209
    • Most Online (within 30 mins)
      7,748

    bwt34221
    Newest Member
    bwt34221
    Joined
  • Celiac.com Sponsor (A20):
  • Celiac.com Sponsor (A22):
  • Forum Statistics

    • Total Topics
      121.6k
    • Total Posts
      1m
  • Celiac.com Sponsor (A21):
  • Upcoming Events

  • Posts

    • trents
      Cristiana, that sounds like a great approach and I will be looking forward to the results. I am in the same boat as you. I don't experience overt symptoms with minor, cross contamination level exposures so I sometimes will indulge in those "processed on equipment that also processes wheat . . ." or items that don't specifically claim to be gluten free but do not list gluten containing grains in their ingredient list. But I always wonder if I am still experiencing sub acute inflammatory reactions. I haven't had any celiac antibody blood work done since my diagnosis almost 25 years ago so I don't really have any data to go by.   
    • cristiana
      I've been reflecting on this further. The lowest TTG I've ever managed was 4.5 (normal lab reading under 10).  Since then it has gone up to 10.   I am not happy with that.  I can only explain this by the fact that I am eating out more these days and that's where I'm being 'glutened', but such small amounts that I only occasionally react. I know some of it is also to do with eating products labelled 'may contain gluten' by mistake - which in the UK means it probably does! It stands to reason that as I am a coeliac any trace of gluten will cause a response in the gut.  My villi are healed and look healthy, but those lymphocytes are present because of the occasional trace amounts of gluten sneaking into my diet.   I am going to try not to eat out now until my next blood test in the autumn and read labels properly to avoid the may contain gluten products, and will then report back to see if it has helped!
    • lizzie42
      Hi, I posted before about my son's legs shaking after gluten. I did end up starting him on vit b and happily he actually started sleeping better and longer.  Back to my 4 year old. She had gone back to meltdowns, early wakes, and exhaustion. We tested everything again and her ferritin was lowish again (16) and vit d was low. After a couple weeks on supplements she is cheerful, sleeping better and looks better. The red rimmed eyes and dark circles are much better.   AND her Ttg was a 3!!!!!! So, we are crushing the gluten-free diet which is great. But WHY are her iron and vit d low if she's not getting any gluten????  She's on 30mg of iron per day and also a multivitamin and vit d supplement (per her dr). That helped her feel better quickly. But will she need supplements her whole life?? Or is there some other reason she's not absorbing iron? We eat very healthy with minimal processed food. Beef maybe 1x per week but plenty of other protein including eggs daily.  She also says her tummy hurts every single morning. That was before the iron (do not likely a side effect). Is that common with celiac? 
    • Scott Adams
      Celiac disease is the most likely cause, but here are articles about the other possible causes:    
    • xxnonamexx
      Please read: https://www.fda.gov/news-events/press-announcements/fda-takes-steps-improve-gluten-ingredient-disclosure-foods?fbclid=IwY2xjawPeXhJleHRuA2FlbQIxMABicmlkETFzaDc3NWRaYzlJOFJ4R0Fic3J0YwZhcHBfaWQQMjIyMDM5MTc4ODIwMDg5MgABHrwuSsw8Be7VNGOrKKWFVbrjmf59SGht05nIALwnjQ0DoGkDDK1doRBDzeeX_aem_GZcRcbhisMTyFUp3YMUU9Q
×
×
  • 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.