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

How Many Of You Suffer From Hyperthroidism?


Ms. Skinny Chic

Recommended Posts

Ms. Skinny Chic Explorer

My doctor recently placed me on Tapazole (Methimazole) for hyperthyroidism. Everyone else seems to gain weight, after going on a gluten free diet. I continued to lose weight, which is scary.

The gluten free diet has improved my health tremendously. Has anyone else struggled with thyroid issues and celiac disease. How long did it take for you to recover from both?


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



Celiac.com Sponsor (A8-M):



Di-gfree Apprentice

Hi, I have celiac and hashimoto's, and I think I'm ok as far as the celiac goes, seeing as I've been gluten-free for about 14 years. I'm having a hard time sorting out the Hashimoto's (or 'recovering')because it's complex with adrenals, low ferritin, low B12, other hormonal craziness, etc., etc., factoring in. And, I'm thin, too, by the way.

How did your hyperthyroidism diagnosis come about? Were you tested for thyroid antibodies?

Keri Newbie

Sometimes Hashimoto's can start out as hyperthyroid and then go hypo. or you might have graves disease, which is hyperthryoid. Both are autoimmune thyroid disorders and occur more frequently in people with Celiac disease. you should be tested for thyroid antibodies.

I just found out I have gluten issues, last week, but was diagnosed with Hashimoto's several years ago. We'll see how a gluten free diet will help my throid issues. I also have low iron which I was thinking was related to celiac disease, but maybe it is thyroid related according to the last post? anyone have any thoughts?

  • 3 weeks later...
Ms. Skinny Chic Explorer
Hi, I have celiac and hashimoto's, and I think I'm ok as far as the celiac goes, seeing as I've been gluten-free for about 14 years. I'm having a hard time sorting out the Hashimoto's (or 'recovering')because it's complex with adrenals, low ferritin, low B12, other hormonal craziness, etc., etc., factoring in. And, I'm thin, too, by the way.

How did your hyperthyroidism diagnosis come about? Were you tested for thyroid antibodies?

I was diagnosed with hyperthyroidism because of thyroid antibodies... I have a history of hyperthyroidism.. The doctors had a hard time sorting it out this time, because my body kept exhibiting hypo and hyper symptoms...

I had a hard time with low b 12 also.. My B 12 levels have improved, since I started taking tapazole for my thyroid.

I have alot of the same issues as you....

Ms. Skinny Chic Explorer
Sometimes Hashimoto's can start out as hyperthyroid and then go hypo. or you might have graves disease, which is hyperthryoid. Both are autoimmune thyroid disorders and occur more frequently in people with Celiac disease. you should be tested for thyroid antibodies.

I just found out I have gluten issues, last week, but was diagnosed with Hashimoto's several years ago. We'll see how a gluten free diet will help my throid issues. I also have low iron which I was thinking was related to celiac disease, but maybe it is thyroid related according to the last post? anyone have any thoughts?

How do you get the diagnosis of hashimoto's???? My thyroid has been bouncing all over the place. Sometimes, I have hyper symptoms and other times hyp symptoms..

Di-gfree Apprentice
I was diagnosed with hyperthyroidism because of thyroid antibodies... I have a history of hyperthyroidism.. The doctors had a hard time sorting it out this time, because my body kept exhibiting hypo and hyper symptoms...

I had a hard time with low b 12 also.. My B 12 levels have improved, since I started taking tapazole for my thyroid.

I have alot of the same issues as you....

Do you remember the name of antibodies? Can you post your thyroid numbers, if you don't mind? There are two thyroid antibodies we're supposed to check - one for Hashimoto's, and one for Graves', I think. I've only had the TPO (Hashimoto's) antibodies tested, myself (should get the other one done, too). With Hashimoto's we can fluctuate between hypo and hyper - not sure if that actually shows up in bloodwork, though.

Are you taking sublingual B12? With celiac, most of us don't absorb B12, digestively, very well, I don't think - I know I do not.

Nancym Enthusiast

I had Graves disease long before my issues with gluten were identified. I was one of the rare ones who actually GAINED weight while being hyperthyroid. Sheesh!


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



Celiac.com Sponsor (A8-M):



Ms. Skinny Chic Explorer
I had Graves disease long before my issues with gluten were identified. I was one of the rare ones who actually GAINED weight while being hyperthyroid. Sheesh!

I don't know what is wrong with my thyroid... My doctor is scratching his head about it , as well.. My T3 levels have dipped even lower, after taking tapazole.. My TSh is currently 0.04..

What is wrong with me???

  • 3 weeks later...
Kit Newbie
I don't know what is wrong with my thyroid... My doctor is scratching his head about it , as well.. My T3 levels have dipped even lower, after taking tapazole.. My TSh is currently 0.04..

What is wrong with me???

Kit Newbie
I don't know what is wrong with my thyroid... My doctor is scratching his head about it , as well.. My T3 levels have dipped even lower, after taking tapazole.. My TSh is currently 0.04..

What is wrong with me???

I hope by now you are feeling better...Is your TSH at .04...or does it say <.04? <.04 means it is less than .04 which is the least your particular lab can detect. That means your TSH is unmeasurable. What are your lab ranges and free T3 and free T4...do you know? Do you have reverse T3 numbers?

Hyperthyroidism is extremely dangerous. Before the introduction of anti-thyroid drugs like Tapazole (methimazole) and PPU, there was only a 50% survival rate.

It is expected that your free T3 should fall on Tapazole...you have too much of it, which is why your metabolism is too fast and your weight is too low. Are you seeing an endocrinologist? In the case of hyperthyroidism, you don't want to monkey around with a GP, this is serious stuff.

I have both Hashimotos and Graves' disease, high antibodies for both (TPO and TSI). After seven years on a gluten-free diet (biopsy diagnosed as of May 1, 2002) my thyroid issues haven't resolved, and I bounce back and forth between hyper and hypo. I'm going to finally have it surgically removed next month, and can't wait to be on an even keel again! I have a wonderful naturopath who will put me on Armour (have been on it when hypo) and am looking forward to getting my life back.

Allow me to suggest another site for thyroid disease research. Mary Shomon publishes books on thyroid disease distributed in mainstream outlets (Borders, Barnes and Noble, etc.) and runs this wonderful site that can help you in educating yourself about thyroid disease: Open Original Shared Link

To the person who mentioned gaining weight when hyper...happens to me too. My appetite gets hotter than my metabolism. It isn't that rare, but can make it hard to suspect hyperthyroidism and get a diagnosis. Conversely, my son, who does not show antibodies for either Hashis or Graves' has low T3, and is doing very well on cytomel. He is 19, and at six foot four, only weighs 135 lbs. This after gaining 15 pounds on Cytomel! So his hypothyroidism caused him to be too skinny due to lack of appetite. It also caused some terrible emotional issues he had to deal with for his entire childhood. He is doing much much better now, thank goodness.

Good luck to you both, and make sure you get the proper treatment. An endocrinologist is absolutely a must for hyperthyroidism...it can kill you.

Kit in St. Louis.

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. - Florence Lillian replied to lmemsm's topic in Gluten-Free Recipes & Cooking Tips
      13

      gluten free cookie recipes

    2. - Russ H replied to Charlie1946's topic in Related Issues & Disorders
      15

      Severe severe mouth pain

    3. - cristiana replied to Charlie1946's topic in Related Issues & Disorders
      15

      Severe severe mouth pain

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

    • Total Members
      132,914
    • Most Online (within 30 mins)
      7,748

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

    • Total Topics
      121.5k
    • Total Posts
      1m
  • Celiac.com Sponsor (A21):
  • Who's Online (See full list)

  • Upcoming Events

  • Posts

    • xxnonamexx
      very interesting thanks for the info  
    • Florence Lillian
      More cookie recipes ...thanks so much for the heads-up Scott.  One can never have too many.  Cheers, Florence.
    • Russ H
      Hi Charlie, You sound like you have been having a rough time of it. Coeliac disease can cause a multitude of skin, mouth and throat problems. Mouth ulcers and enamel defects are well known but other oral conditions are also more common in people with coeliac disease: burning tongue, inflamed and swollen tongue, difficulty swallowing, redness and crusting in the mouth corners, and dry mouth to name but some. The link below is for paediatric dentistry but it applies to adults too.  Have you had follow up for you coeliac disease to check that your anti-tTG2 antibodies levels have come down? Are you certain that you not being exposed to significant amounts of gluten? Are you taking a PPI for your Barrett's oesophagus? Signs of changes to the tongue can be caused by nutritional deficiencies, particularly iron, B12 and B9 (folate) deficiency. I would make sure to take a good quality multivitamin every day and make sure to take it with vitamin C containing food - orange juice, broccoli, cabbage etc.  Sebaceous hyperplasia is common in older men and I can't find a link to coeliac disease.   Russ.   Oral Manifestations in Pediatric Patients with Coeliac Disease – A Review Article
    • cristiana
      Hi @Charlie1946 You are very welcome.   I agree wholeheartedly with @knitty kitty:  "I wish doctors would check for nutritional deficiencies and gastrointestinal issues before prescribing antidepressants." I had a type of tingling/sometimes pain in my cheek about 2 years after my diagnosis.  I noticed it after standing in cold wind, affecting  me after the event - for example, the evening after standing outside, I would feel either tingling or stabbing pain in my cheek.   I found using a neck roll seemed to help, reducing caffeine, making sure I was well-hydrated, taking B12 and C vitamins and magnesium.  Then when the lockdowns came and I was using a facemask I realised that this pain was almost entirely eliminated by keeping the wind off my face.  I think looking back I was suffering from a type of nerve pain/damage.  At the time read that coeliacs can suffer from nerve damage caused by nutritional deficiencies and inflammation, and there was hope that as bodywide healing took place, following the adoption of a strict gluten free diet and addressing nutritional deficiencies, recovery was possible.   During this time, I used to spend a lot of time outdoors with my then young children, who would be playing in the park, and I'd be sheltering my face with an upturned coat collar, trying to stay our of the cold wind!  It was during this time a number of people with a condition called Trigeminal Neuralgia came up to me and introduced themselves, which looking back was nothing short of miraculous as I live in a pretty sparsely populated rural community and it is quite a rare condition.   I met a number of non-coeliacs who had suffered with this issue  and all bar one found relief in taking medication like amitriptyline which are type of tricyclic anti-depressant.   They were not depressed, here their doctors had prescribed the drugs as pain killers to address nerve pain, hence I mention here.  Nerve pain caused by shingles is often treated with this type of medication in the UK too, so it is definitely worth bearing in mind if standard pain killers like aspirin aren't working. PS  How to make a neck roll with a towel: https://www.painreliefwellness.com.au/2017/10/18/cervical-neck-roll/#:~:text=1.,Very simple. 
    • Scott Adams
      We just added a ton of new recipes here: https://www.celiac.com/celiac-disease/gluten-free-recipes/gluten-free-dessert-recipes-pastries-cakes-cookies-etc/gluten-free-cookie-recipes/
×
×
  • 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.