Jump to content
This site uses cookies. Continued use is acceptance of our Terms of Use and Privacy Policy. More Info... ×
  • 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 Celiac.com!
    eNewsletter
    Donate

Is There Any Reason Celiacs Would Need More Iodine Than Other People Do?


The Fluffy Assassin

Recommended Posts

The Fluffy Assassin Enthusiast

In case you missed any of my thrilling story, here it is in a nutshell: All summer, I've been feeling very strange. I posted various interesting and elaborate and incorrect rationalizations of what might be going wrong. Eventually, I hit on the very, very obvious: that if you give up salting your food (like I did decades ago) and then start cooking nearly all your own food (like I did two years ago) and then switch to whole foods (like I did early this year) and then give up soy including gluten-free tamari (like I did in July) you're likely to trigger a pretty major electrolyte imbalance. I did take multivitamins which included 100% of the RDA of iodine, but as of a few weeks ago I had the brilliant idea to stop taking them on the grounds that maybe I was getting too much of some micronutrient, and wound up in the emergency room. They told me I was hypothyroid and to see a primary care physician within the week. I cut out all the goitrogens from my diet (broccoli, kale, millet, etc.), restarted my multivitamins (since replaced with kelp extract), started salting my food, and ate a lot of avocado and coconut, said to be good for hypothyroidism. And when within the week I went to a doctor, the labs said... thyroid normal. (TSH had been 7.310; now is 2.944.) (Some nutshell, huh?:))

However, I woke this morning feeling very cold; I've always been cold-natured. I wonder if I may have always been subclinical hypothyroid. I was taking the multivitamins half in the morning and half in the evening, which maybe helped. The kelp extract tablets aren't scored and would be difficult to cut in half as they're round. They contain 150% of the RDA for iodine. I'm wondering if there's any chance that celiacs just need more darn iodine. I believe that I read that iodine is taken in in the duodenum, the part of the intestine that is damaged by celiac disease, but I've been gluten free for nearly two years and would think I would have largely healed.

My pattern all summer has been (more or less) two good days, two bad days. After getting my iodine up, it became two good days, one bad day (and I was glutened for the first time in ages before the bad day). Now it's two good days, one fair day. So maybe iodine deficiency just takes a while to resolve, and I need to be more patient. But it would be lovely to have some answers. The clinic just pretty much washed their hands of me; you're normal, bye-bye. (Granted, I literally told the doctor when he asked what he could do for me that he could tell me I'm fine and everything is normal, but I'm pretty sure I made clear that I was kidding.)

So what are thoughts?

Edit: On further thought (with googling) I find that there is a reason autistic people would need more iodine, though nobody seems to say definitively that persons with Asperger's (like me) would. So there's a thought. Ravenwoodglass has mentioned that iodine can trigger dh outbreaks in sufferers; this kind of indicates that celiac wouldn't be the root of my apparent iodine uptake problem. Again, what are thoughts?

Link to comment
Share on other sites

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



Celiac.com Sponsor (A8-M):



Ahorsesoul Enthusiast

This is interesting. I'll have to see how much iodine I get daily. I never use salt unless I eat french fries (once or twice a year). I'm on thyroid meds but maybe some iodine will help. I'll let you know how it works.

Link to comment
Share on other sites
The Fluffy Assassin Enthusiast
This is interesting. I'll have to see how much iodine I get daily. I never use salt unless I eat french fries (once or twice a year). I'm on thyroid meds but maybe some iodine will help. I'll let you know how it works.

Be careful with it. I'm having my usual second and third thoughts. Since I've been losing weight ever since going gluten-free, one would think that if anything I'd be hyperthyroid. It's possible that the iodine in the multivitamins was just enough to make me hyperthyroid, that quitting them made me temporarily hypo and that restarting them made my TSH normal in time for the second blood draw. By now, I would be hyper again, and by that logic, the kelp would make me even more hyper. I'm certainly amped up a bit.

Then again, in general, I still feel just like I did when I went to the emergency room only less so. So I guess it's likelier that I'm again hypo (or still subclinical hypo). It's probable that all the weight loss was just due to eating healthier. (Prior to going gluten-free, I was a buffet hound.)

See? Second and third thoughts. One of the health food stores I visited had liquid kelp extract, which would presumably let you start with smaller doses. The tablets were either 150% or more of the RDA; it irritates me when vitamin/mineral/etc. manufacturers don't offer tablets with just 100% or less of the RDA. It seems to me that if I want to take more, I can just take two.

Link to comment
Share on other sites
missy'smom Collaborator

Fluffy, I'm sorry that you're still struggling to find answers. I would find a new doc.. I don't know the first thing about iodine but what you're going through in general sounds somewhat familiar. The nurses in the office where I got tests for a UTI said to each other "she has diabetes" but a word was never said to me. They called me up and told be that I was neg, for UTI that was it, and the doctor never followed up. Then again, I was in the hospital overnight for obeservation and the nurses thought I was asleep but were talking to each other saying " she has diabetes or hypoglycemia or both, what're they going to do with her" "they'll have to put her on a pump"-because I have such a fear of needles. But again, not a word was said to me. When I finally followed up with a new Doc. I demanded testing. I guess I share those stories to show that the medical profession drops the ball and things can fall through the cracks. I always suspected it in part because, I thought I was just too darn sensitive to what kinds of foods I could eat and when and feel good. It seems to me that something is going on if you are so sensitive. Keep searching for answers and use those tests to your advantage. I hope you can find someone in the medical profession to be your ally! so that you aren't stuck in this continual circle of self diagnosis and experimenting.

Link to comment
Share on other sites

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      121,173
    • Most Online (within 30 mins)
      7,748

    Art34
    Newest Member
    Art34
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      120.3k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • MMH13
      Thank you so much, everyone. For the moment my doctor just has me taking iron but hopefully we can reconnect soon. I'm going to look into genetic testing, too. Great advice all around and I appreciate it--and you can bet I'm going off the PPIs!
    • Eldene
      I walk fast for fitness, 4 to 6 km per day. I am also 74 years old. Apart from the Celiac challenge, my lifestyle is healthy. I had a sciatiac nerve pinching under my one foot, with inflamation in my whole shin. It was almost cured, when the other shin started paining and burning. I do stretches, use a natural cooling gel and rest my feet. Can Celiac cause muscle pains/inflamation, or is it just over-excercising?
    • LovintheGFlife
      I recently started shopping at a nearby Trader Joe's store. I was surprised at the number and variety of (healthy) gluten-free options sold there. I must admit their low prices are also quite tempting. However, I am curious as to the labeling on all their packages. While none of their products are certified as gluten-free, many are identified as 'GLUTEN FREE' on the packaging. Are these items safe for celiacs? Has anyone tried Trader Joe's products and have there been any adverse reactions?
    • Beverley Ann Johnson
      HI, my doctor suggested one week of consuming gluten before blood tests.  I have been gluten free for 3 years.  Has anyone been through this and will I get exact results after one week of consuming gluten?  I don't even know if I can do this, if I get sick I am not sure if I can continue, any suggestions??  Thanks in advance.  
    • Denise I
      I did reach out to them on April 4th and left a message. I will try calling again. Thank you!
×
×
  • Create New...