Jump to content
  • 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):

The signs point to celiac!


HannahR67

Recommended Posts

HannahR67 Newbie

 

I am 22 and have had Type 1 Diabetes for years. I've just had a total thyroidectomy for Thyroid Cancer and was convinced my Thyroid wasn't functioning properly, but never had the correct blood-work to prove it (only TSH). 

My doctor did a blood test for Celiac, but I had already been off gluten for about a week or 2 before the test. I only started eating gluten again 2 days before. I told my doctor this, but she said it was fine. Now here I am months later with a negative blood test and still not eating gluten because it makes me so sick. 

Since my thyroid surgery/hormone replacement and quitting gluten ALL my symptoms are gone. Its hard to tell what was caused by my Thyroid and what was gluten. I already have had Type 1 diabetes since 3rd grade, another autoimmune.

It would be best to have a diagnoses of Celiac so people would take me more seriously with Gluten Free and understand me! Many people think I'm overreacting and that "Gluten sensitivity" isn't real.

I have had stomach issues my whole life. I've been feeling especially awful the past 2 years. Extreme brain fog, anxiety, depression, constipation, diarrhea, joint pain, severe abdominal pain under my left rib, losing hair, bladder pain, extreme dizziness/blurry eyes, migraines....I could go on and on! I lost 20 lbs a few months ago out of nowhere. I have also in the past been tested Iron deficient and vitamin D deficient. 

 

With everything happening I know gluten can't be good for me with how it makes me feel. My question is, can I still be diagnosed at this point of being off gluten for a month+? I don't want to start eating it again, but I do want a proper diagnosis. Would my intestines still show damage at this point? 

My blood test results are confusing. It says IGA was 123 (reference range 65-450 mg/dl) and Tissue Transglutaminase <1.2 (Negative <4). That's all I see for values. Does this make sense and should I trust it?

 

Thank you! Hannah


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



Celiac.com Sponsor (A8-M):



Gemini Experienced

Hannah........Thyroid disease and Type 1 diabetes are the top 2 "other" autoimmune diseases that occur with Celiac.
Apparently, the thyroid and the pancreas are 2 other places that the autoimmune system likes to gravitate to and destroy.  I suspect that genetics plays key role.  But let me tell you something.......I have Celiac and Hashi's thyroid disease.  My brother had Type 1 diabetes very young, like you did.  I strongly suspected he also had Celiac because he had severe gastro problems his whole life, which the docs attributed to his diabetes.   <_< 

Well.....it didn't end well for my brother.  Because his docs kept blowing off a potential Celiac diagnosis, he never had good health.  He struggled to control his diabetes because he probably wasn't absorbing his food and meds well.  It's very easy to develop artery blockages if your blood sugar isn't managed well and he did.  Had a couple of stents put in when he was only 49 years old.  This past summer, at the age of 60, he died of a massive heart attack, in the hospital, because he had been having a problem with diarrhea AGAIN and, couple that with his kidney disease, he could not stay hydrated.  He died and I will always put part of the blame on the AMA because they never took Celiac seriously, even with a diagnosed sister.  This is what happens when the root cause of a problem is not looked for and found.

I would suggest that you have gene testing done because that, at least, will tell you if you have the genetics to trip for Celiac.  It is not a diagnosis but you have the potential to acquire the disease. Unless you start eating gluten again, the antibody testing will not be viable.  Have you considered doing a biopsy to visibly check the small intestine and take samples?  How long have you been gluten free?  It can take a bit for healing to occur so there may be damage that can be detected.

Other than that, LISTEN to your body.  You said all your symptoms went away eating gluten free and I doubt that your thyroid was responsible for all your symptoms.  If you cannot obtain an official diagnosis, do not let that stop you from achieving health.  Do not end up like my brother!  I know you are young but forget about those who throw doubt at you.  Tell them your health is more important and the testing available cannot be done without ingesting gluten, which makes you severely ill.  It's none of anyone's business how you eat.  You are so young and have your whole life ahead of you so do what's best for Hannah!   :)

HannahR67 Newbie
4 minutes ago, Gemini said:

Hannah........Thyroid disease and Type 1 diabetes are the top 2 "other" autoimmune diseases that occur with Celiac.
Apparently, the thyroid and the pancreas are 2 other places that the autoimmune system likes to gravitate to and destroy.  I suspect that genetics plays key role.  But let me tell you something.......I have Celiac and Hashi's thyroid disease.  My brother had Type 1 diabetes very young, like you did.  I strongly suspected he also had Celiac because he had severe gastro problems his whole life, which the docs attributed to his diabetes.   <_< 

Well.....it didn't end well for my brother.  Because his docs kept blowing off a potential Celiac diagnosis, he never had good health.  He struggled to control his diabetes because he probably wasn't absorbing his food and meds well.  It's very easy to develop artery blockages if your blood sugar isn't managed well and he did.  Had a couple of stents put in when he was only 49 years old.  This past summer, at the age of 60, he died of a massive heart attack, in the hospital, because he had been having a problem with diarrhea AGAIN and, couple that with his kidney disease, he could not stay hydrated.  He died and I will always put part of the blame on the AMA because they never took Celiac seriously, even with a diagnosed sister.  This is what happens when the root cause of a problem is not looked for and found.

I would suggest that you have gene testing done because that, at least, will tell you if you have the genetics to trip for Celiac.  It is not a diagnosis but you have the potential to acquire the disease. Unless you start eating gluten again, the antibody testing will not be viable.  Have you considered doing a biopsy to visibly check the small intestine and take samples?  How long have you been gluten free?  It can take a bit for healing to occur so there may be damage that can be detected.

Other than that, LISTEN to your body.  You said all your symptoms went away eating gluten free and I doubt that your thyroid was responsible for all your symptoms.  If you cannot obtain an official diagnosis, do not let that stop you from achieving health.  Do not end up like my brother!  I know you are young but forget about those who throw doubt at you.  Tell them your health is more important and the testing available cannot be done without ingesting gluten, which makes you severely ill.  It's none of anyone's business how you eat.  You are so young and have your whole life ahead of you so do what's best for Hannah!   :)

Thank you for your response! I'm so sorry to hear about your brother. It must be so frustrating. I have definitely noticed my blood sugar control has been a lot better since gluten free! I've taken my insulin control into my own hands instead of waiting for my doctors to help me adjust it. Its taken some research online to start to understand it better.  I really want to get an endoscopy and will start working in that direction. Its hard because I do feel a little bit crazy constantly at the doctors! 

I actually had to demand that they look further into my thyroid. With all my celiac symptoms and thyroid symptoms I had a doctor tell me "this is in your head, your family has mental health issues in their past..... get more sun". Too funny because I was a camp counselor and outside in the sun everyday! And it ended up being CANCER!!! I have found a PCP who listens since then. 

I know I might seem crazy, but I will push to get an endoscopy. Its worth it, with everything going against me right now! Thank you for your encouragement. 

Gemini Experienced
36 minutes ago, HannahR67 said:

Thank you for your response! I'm so sorry to hear about your brother. It must be so frustrating. I have definitely noticed my blood sugar control has been a lot better since gluten free! I've taken my insulin control into my own hands instead of waiting for my doctors to help me adjust it. Its taken some research online to start to understand it better.  I really want to get an endoscopy and will start working in that direction. Its hard because I do feel a little bit crazy constantly at the doctors! 

I actually had to demand that they look further into my thyroid. With all my celiac symptoms and thyroid symptoms I had a doctor tell me "this is in your head, your family has mental health issues in their past..... get more sun". Too funny because I was a camp counselor and outside in the sun everyday! And it ended up being CANCER!!! I have found a PCP who listens since then. 

I know I might seem crazy, but I will push to get an endoscopy. Its worth it, with everything going against me right now! Thank you for your encouragement. 

We have all heard the "this is in your head" BS from docs and I am no exception.  I guess he never read that some mental health issues are firmly connected to Celiac.  It affects the brain as well as the small intestine.

I am SOOOOOOOO glad you pushed back hard with your thyroid.  My God, what would have happened if you hadn't? With the fact that you are controlling your blood sugar better gluten free, that's another red flag so don't doubt it.

Thank you for your words about my brother.  It is very hard and I miss him. It was a death that really should not have happened.  Hindsight is always 20/20......

Good luck with your demands!  I suspect you will not be taking no for an answer. LOL! 

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. - akebog posted a topic in Gluten-Free Restaurants
      0

      Fusilli Pizzeria, Miller Place, NY

    2. - nancydrewandtheceliacclue replied to nancydrewandtheceliacclue's topic in Super Sensitive People
      12

      Celiac flare years after diagnosis

    3. - Aretaeus Cappadocia replied to nancydrewandtheceliacclue's topic in Super Sensitive People
      12

      Celiac flare years after diagnosis

    4. - Aretaeus Cappadocia replied to nancydrewandtheceliacclue's topic in Super Sensitive People
      12

      Celiac flare years after diagnosis

    5. - Peace lily commented on Scott Adams's article in Latest Research
      2

      New Study Reveals How the Immune System Learns Which Foods Are Safe to Eat

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

    • Total Members
      134,062
    • Most Online (within 30 mins)
      10,442

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

    • Total Topics
      121.7k
    • Total Posts
      1m
  • Celiac.com Sponsor (A21):
  • Upcoming Events

  • Posts

    • akebog
      Very good pizzeria with small dining room in back of the restaurant. The owner's daughter has celiac & they have gluten free pizza & a gluten free menu. Some items from the regular menu can be made gluten free also. They have a lunch menu which we ordered from & my chicken with spinach & mozzarella over gluten-free penne was delicious. They also have Tuesday night pasta specials & Thursday night chicken pasta specials. We plan on going back for dinner soon.
    • nancydrewandtheceliacclue
      @Aretaeus Cappadocia and @Russ H thank you both for your helpful advice and information. I haven't seen a GI in years. They never helped me aside from my inital diagnosis. All other help has come from my own research, which is why I came here. I will be even more careful in the future. 
    • Aretaeus Cappadocia
      @nancydrewandtheceliacclue, you are welcome. After looking at this thread again, I would like to suggest that some of the other comments from @Russ H are worth following up on. The bird-bread may or may not be contributing to what you are experiencing, but it seems unlikely to be the whole story. If you have access to decent healthcare, I would write down your experiences and questions in outline form and bring this to your Dr. I suggest writing it down so you don't get distracted from telling the Dr everything you want to say while you have their attention.
    • Aretaeus Cappadocia
      @Russ H, I partly agree and partly disagree with you. After looking at it again, I would say that the slick graphic I posted overestimates the risk. Your math is solid, although I find estimates of gluten in white bread at 10-12% rather than the 8% you use. Somewhat contradicting what I wrote before, I agree with you that it would be difficult to ingest 10 mg from flinging bread.  However, I would still suggest that @nancydrewandtheceliacclue take precautions against exposure in this activity. I'm not an expert, I could easily be wrong, but if someone is experiencing symptoms and has a known exposure route, it's possible that they are susceptible to less than 10 mg / day, or it is possible that there is/are other undetected sources of exposure that together with this one are causing problems. At any rate, I would want to eliminate any exposure until symptoms are under control before I started testing the safety of potentially risky activities. Here is another representation of what 10 mg of bread would look like. https://www.glutenfreewatchdog.org/news/wp-content/uploads/2019/10/10mgGlutenCrumbsJules.jpg Full article that image came from: https://www.glutenfreewatchdog.org/news/what-does-10-mg-of-gluten-look-like/
    • nancydrewandtheceliacclue
      @Aretaeus Cappadocia thank you for your reply and the link, that is very helpful to get a visual of just how small of an amount can cause a reaction. I know I am not consuming gluten or coming into contact with gluten from any other source. I will stop touching/tossing bread outside! My diet has not changed, and I do not have reactions to the things I am currently eating, which are few in number. My auto immune reaction just seems so severe. The abdominal pain is extreme. It takes a lot out of me. I guess I will be this way for the rest of my life if I ever happen to come into contact with gluten? I appreciate the help. 
×
×
  • Create New...