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

Does This Sound Like Celiac?


nomad4life

Recommended Posts

nomad4life Rookie

Hi,

I was diagnosed with Hashimoto's Thyroiditis about a year ago. I have been euthyroid (good labs) for months with almost no relief in symptoms. the lupus / arthritis / hormone panels all came back normal. My GP and Endo both say nothing I can do but 'hang in there' and hope the antibodies eventually die down. I am more focused on finding a fix as my life is on hold. I have an appointment with my GP tomorrow and I plan to ask for a Celiac panel based on a few things I've read online. Given I know nothing about this I thought I'd ask for some input as to whether or not you think Celiac is worth exploring and might be a possibility.

I have had asthma and severe environmental allergies (tress, mold, grass, pollen, all animals, feathers etc) since I was a child ~ 6ish. I have also developed a tree nut allergy and fruit allergy as an adult.

At 16 I had further allergy testing done due to abd pain / cramping and they found I had a casein allergy. For about the next 8 years (4 of which were HORRIBLE) I had a terrible time with my digestive system. Not a lot of diarrhea but a lot of gas / bloating / and severe pain that felt like my intestines were being twisted in knots. It always started pretty soon after eating and lasted 30-120 minutes. I would eventually have a lot of flatulence and then I'd feel better.

My doc at the time told me it was motility issues related to being asthmatic. For the 4 horrible years I cut out all daisy, all oils, and fats as they seemed to make it worse. I actually lived solely on plain bread, plain pasta, plain rice and fruits and vegetables as that seemed to reduce the pain episodes - although I still often felt sick.

For the last ten years - it has been on and off, the gas/bloating is still always there but the cramping / pain only happens rarely. I eat yogurt and put milk in my tea as I seem to get symptoms no matter what I eat so I take a little dairy. I still sometimes have diarrhea for no apparent reason (I'm not sick) but not often enough that I would be concerned. I've also had cankers in my mouth all my life.

I have never mentioned any of this to my GP or Endo as I never thought of it having any connection to my thyroid or thyroid symptoms (terrible memory / brain fog / poor concentration / fatigue / muscle aches and pains) and because I've had this most of my life. My ferritin is 13 and my Vit D is very low - I am on supplements for these.

Is this enough history to warrant a exploration of Celiacs? My sister just had a biopsy for Celiac's although they think she just has IBS (awaiting results) but she had many abd symptoms.


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



Celiac.com Sponsor (A8-M):



mushroom Proficient
Hi,

I was diagnosed with Hashimoto's Thyroiditis about a year ago. I have been euthyroid (good labs) for months with almost no relief in symptoms. the lupus / arthritis / hormone panels all came back normal. My GP and Endo both say nothing I can do but 'hang in there' and hope the antibodies eventually die down. I am more focused on finding a fix as my life is on hold. I have an appointment with my GP tomorrow and I plan to ask for a Celiac panel based on a few things I've read online. Given I know nothing about this I thought I'd ask for some input as to whether or not you think Celiac is worth exploring and might be a possibility.

I have had asthma and severe environmental allergies (tress, mold, grass, pollen, all animals, feathers etc) since I was a child ~ 6ish. I have also developed a tree nut allergy and fruit allergy as an adult.

At 16 I had further allergy testing done due to abd pain / cramping and they found I had a casein allergy. For about the next 8 years (4 of which were HORRIBLE) I had a terrible time with my digestive system. Not a lot of diarrhea but a lot of gas / bloating / and severe pain that felt like my intestines were being twisted in knots. It always started pretty soon after eating and lasted 30-120 minutes. I would eventually have a lot of flatulence and then I'd feel better.

My doc at the time told me it was motility issues related to being asthmatic. For the 4 horrible years I cut out all daisy, all oils, and fats as they seemed to make it worse. I actually lived solely on plain bread, plain pasta, plain rice and fruits and vegetables as that seemed to reduce the pain episodes - although I still often felt sick.

For the last ten years - it has been on and off, the gas/bloating is still always there but the cramping / pain only happens rarely. I eat yogurt and put milk in my tea as I seem to get symptoms no matter what I eat so I take a little dairy. I still sometimes have diarrhea for no apparent reason (I'm not sick) but not often enough that I would be concerned. I've also had cankers in my mouth all my life.

I have never mentioned any of this to my GP or Endo as I never thought of it having any connection to my thyroid or thyroid symptoms (terrible memory / brain fog / poor concentration / fatigue / muscle aches and pains) and because I've had this most of my life. My ferritin is 13 and my Vit D is very low - I am on supplements for these.

Is this enough history to warrant a exploration of Celiacs? My sister just had a biopsy for Celiac's although they think she just has IBS (awaiting results) but she had many abd symptoms.

Welcome to the forum, nomad4life.

Your history is not an entirely straightforward one, but as you have discovered in your research there are several overlaps in your symptoms with celiac disease symptoms., with your Hashimoto's being the first. There are many other autoimmune diseases which are common in celiacs. Celiac digestive symptoms vary a great deal, with some people having no symptoms at all, but bloating/gas is common. And it is true that sometimes the symptoms can wax and wane. The brain fog, fatigue, aches and pains are also common in celiacs, as are the low nutrient levels of ferritin and Vit D amongst others. Often we don't mention a lot of these symptoms to our doctors because we are brushed off with oh, it's just this, or its just that, and not taken seriously.

I would definitely make a list of all your symptoms which match those of celiac disease and discuss with your doctor that you would like to be tested for it. Bear in mind, though, that it is possible to have a negative blood test and still have celiac disease or be gluten intolerant. If you are tested and the test is negative, or if you can't find a doctor willing to test you, I would still give the gluten free diet a trial to see if it makes any difference for you.

Good luck tomorrow.

Ahorsesoul Enthusiast

I hope you try a totally gluten free diet for a few weeks to see if there is any improvement.

nomad4life Rookie

Thanks for the replies. I saw the doctor today and she ordered ttg. The other tests aren't covered so she said to do this one first and if it comes back + then no need to do the others. She was willing to refer me for a biopsy as she said that is the only way to be sure but we decided to see what the ttg result is first. She was more than willing to help me out and said if there was anything else I came across that I thought might be helpful to investigate, she would order it.

Archived

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

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

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





    Celiac.com Sponsors (A17-M):




  • Recent Activity

    1. - AlwaysLearning replied to Colleen H's topic in Coping with Celiac Disease
      3

      Gluten related ??

    2. - Colleen H replied to Colleen H's topic in Coping with Celiac Disease
      3

      Gluten related ??

    3. - Jmartes71 replied to Jmartes71's topic in Coping with Celiac Disease
      4

      My only proof

    4. - AlwaysLearning replied to Jmartes71's topic in Coping with Celiac Disease
      4

      My only proof


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      132,090
    • Most Online (within 30 mins)
      7,748

    Jamie B
    Newest Member
    Jamie B
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.5k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • AlwaysLearning
      Get tested for vitamin deficiencies.  Though neuropathy can be a symptom of celiac, it can also be caused by deficiencies due to poor digestion caused by celiac and could be easier to treat.
    • Colleen H
      Thank you so much for your response  Yes it seems as though things get very painful as time goes on.  I'm not eating gluten as far as I know.  However, I'm not sure of cross contamination.  My system seems to weaken to hidden spices and other possibilities. ???  if cross contamination is possible...I am in a super sensitive mode of celiac disease.. Neuropathy from head to toes
    • Jmartes71
      EXACTLY! I was asked yesterday on my LAST video call with Standford and I stated exactly yes absolutely this is why I need the name! One, get proper care, two, not get worse.Im falling apart, stressed out, in pain and just opened email from Stanford stating I was rude ect.I want that video reviewed by higher ups and see if that women still has a job or not.Im saying this because I've been medically screwed and asking for help because bills don't pay itself. This could be malpratice siit but im not good at finding lawyers
    • AlwaysLearning
      We feel your pain. It took me 20+ years of regularly going to doctors desperate for answers only to be told there was nothing wrong with me … when I was 20 pounds underweight, suffering from severe nutritional deficiencies, and in a great deal of pain. I had to figure it out for myself. If you're in the U.S., not having an official diagnosis does mean you can't claim a tax deduction for the extra expense of gluten-free foods. But it can also be a good thing. Pre-existing conditions might be a reason why a health insurance company might reject your application or charge you more money. No official diagnosis means you don't have a pre-existing condition. I really hope you don't live in the U.S. and don't have these challenges. Do you need an official diagnosis for a specific reason? Else, I wouldn't worry about it. As long as you're diligent in remaining gluten free, your body should be healing as much as possible so there isn't much else you could do anyway. And there are plenty of us out here who never got that official diagnosis because we couldn't eat enough gluten to get tested. Now that the IL-2 test is available, I suppose I could take it, but I don't feel the need. Someone else not believing me really isn't my problem as long as I can stay in control of my own food.
    • AlwaysLearning
      If you're just starting out in being gluten free, I would expect it to take months before you learned enough about hidden sources of gluten before you stopped making major mistakes. Ice cream? Not safe unless they say it is gluten free. Spaghetti sauce? Not safe unless is says gluten-free. Natural ingredients? Who knows what's in there. You pretty much need to cook with whole ingredients yourself to avoid it completely. Most gluten-free products should be safe, but while you're in the hypersensitive phase right after going gluten free, you may notice that when something like a microwave meal seems to not be gluten-free … then you find out that it is produced in a shared facility where it can become contaminated. My reactions were much-more severe after going gluten free. The analogy that I use is that you had a whole army of soldiers waiting for some gluten to attack, and now that you took away their target, when the stragglers from the gluten army accidentally wander onto the battlefield, you still have your entire army going out and attacking them. Expect it to take two years before all of the training facilities that were producing your soldiers have fallen into disrepair and are no longer producing soldiers. But that is two years after you stop accidentally glutening yourself. Every time you do eat gluten, another training facility can be built and more soldiers will be waiting to attack. Good luck figuring things out.   
×
×
  • 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.