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

Can We Talk About Iodine?


Blaze422

Recommended Posts

Blaze422 Rookie

As my rashes are slowly going away ( diet and dapsone ) one of the reasons I am pretty sure I have DH is that itching increases with salty foods.

I understand that gluten will cause antibody production and the longer I stay off gluten, then less reactive ..(ie..less antinbodiy prduction) will result from accidental ingestion of gluten.

Does iodine cause a "relapse" in the healing process... Or is it only temporary increase in itchiness?


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



Celiac.com Sponsor (A8-M):



pricklypear1971 Community Regular

For me, it made the rash flare. It didn't increase gluten antibodies, but it made the rash angry...

Iodine was like water on a grease fire.

Not all salt is iodized. If you are interested in testing iodine I'd try something direct - like a bite of seaweed. Or, a bit of iodized salt in a dish.

Or, research the salty foods that make you itch and find out if they're iodized. Probably the best, first choice.

squirmingitch Veteran

Same here as Prickly only my problem with iodine lasted longer than Prickly's experience. I had to go low iodine for literally well over a year. I would keep testing it along the way & had to keep backing off of it. But since Sept., have been eating it to my heart's content & have no problems. I have not yet added back seafood or iodized salt but everything else is back on the table.

 

And I am very happy to say that 2 years & 1 month strict gluten-free; I have not itched in 4 or 5 days now & all my places are healing rapidly & no new ones have appeared. YAY! 

GF Lover Rising Star

Same here as Prickly only my problem with iodine lasted longer than Prickly's experience. I had to go low iodine for literally well over a year. I would keep testing it along the way & had to keep backing off of it. But since Sept., have been eating it to my heart's content & have no problems. I have not yet added back seafood or iodized salt but everything else is back on the table.

 

And I am very happy to say that 2 years & 1 month strict gluten-free; I have not itched in 4 or 5 days now & all my places are healing rapidly & no new ones have appeared. YAY! 

 

:o WOW.  Squirmy, that is wonderful to hear  :D  My first smile of the Day  :lol:

 

Colleen

pricklypear1971 Community Regular

Same here as Prickly only my problem with iodine lasted longer than Prickly's experience. I had to go low iodine for literally well over a year. I would keep testing it along the way & had to keep backing off of it. But since Sept., have been eating it to my heart's content & have no problems. I have not yet added back seafood or iodized salt but everything else is back on the table.

And I am very happy to say that 2 years & 1 month strict gluten-free; I have not itched in 4 or 5 days now & all my places are healing rapidly & no new ones have appeared. YAY!

Excellent news!

squirmingitch Veteran

Thanks to both of you! Guess who is smiling also? :P Hubs has good news too in that he hasn't had any itchies in about 10 days --- all his skin is all healed up & you can't even tell he ever had anything. He's a happy camper!!!!

 

Not to steal your thread Blaze......just letting you & everyone know that perseverance DOES pay off & there is an end to this for all of us. It may take a lot longer for some but there IS an end.

 

And last but not least....... either hubs or I or both could have flares yet but one day there has to be a point where there are no flares. For now we are just enjoying the present & it's present to us. :lol:

Blaze422 Rookie

Congrats for sure!

Squirmy....when you say you would test iodine...can you explain what you mean...what you did?

Also, do you season with non-iodized salt...my understanding is it taste essentially the same.


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



Celiac.com Sponsor (A8-M):



squirmingitch Veteran

When I say I tested iodine, I would eat high iodine foods --- cheese is my Achilles heel & so I would eat cheese a couple times a day for a few days & maybe have some yogurt too. Each time I tried; I would get a flare up in a couple days so I would go off the iodine rich foods again. I finally got to a point where I did not test it for 4 or 5 months b/c I was tired of the disappointment. And then in Sept. I began testing again & all was good so I added more iodine like milk, egg yolks, butter, etc... & I have had no problems. I find zero taste difference between iodized table salt & non iodized table salt & yes, that's what I season with.

 

BTW, when I got iodine caused flares, if I quit the iodine foods, the flare would back off in 3 days time. But we are all different so your timeline may be shorter or longer. My hubs took 10 days to come down from iodine induced flares & he tried it twice & refused to try it again for close to a year.

pricklypear1971 Community Regular

I'd have a typical two week flare. Meaning it flared up and went down within two weeks.

Seaweed, asparagus and potatoes got me.

Geez, the seaweed....

Blaze422 Rookie

Ok...not to over analyze it...but why stop now?..

Are you both saying the flare up would result in both increasing itchiness and ALSO spreading/increased reddening of the rash?

I realize everyone is different, but I'm wondering if iodine will cause a relapse of the healing/ a new area of rash,/ a darker hue to the rash....or merely a temporary worsening of the itch.

Thanks for your patience!

squirmingitch Veteran

No problem Blaze! Ask any questions you want. I realized after I posted that I may not have made everything as clear as I could have. Okay, for me & also for my hubs this is how the iodine would affect us:

We would get many new blisters or lesions. We knew it was iodine b/c there were so many MORE suddenly popping up rather than "the usual".

Places that had been healing would backslide & reflare resulting in increased reddening, raised & itching & some would re new blistering

Places that were almost healed up would get red, raised & increased itching or renewed itching

 

I'm suspecting you're also wondering or asking why at some point the iodine doesn't have the maddening flare effect anymore. I can't really answer that. Maybe Prickly can. I can only surmise that the antibodies in our skin become less powerful as individuals & that's when the iodine does not have the same effect on the rash along with a lessening of the sheer # of antibodies????? Oh yes, I did have a time or 2 where I missed that carrageenan (seaweed) was in something & that was the very devil to pay!!!!!!! 

And if you're asking why would we go back to iodine rich foods...... we all NEED iodine as I'm sure you know so we try to go back on it asap PLUS we ALL need our calcium which comes mainly from dairy so we don't want to deprive our bodies any longer than we have to. Why didn't I take calcium supplements (non dairy ones that is)? I tried but my gut just couldn't handle them. For years & years before I discovered I had celiac I tried every single calcium supplement on the market & could not tolerate any of them. Indigestion big time, gerd, you name it. Now it all makes sense b/c it was the villi not able to handle the lactose. But when I went gluten-free then I knew to get non diary supplements. Still my gut was not in any shape to process such a hard mineral???? We celiacs have some weird stuff go on with foods, supplements so I didn't question it too deeply --- I just know I don't do well with calcium supplements of any kind. Same thing for me & B supplements --- they don't like me. I can EAT calcium rich foods now & have no problem & EAT high B foods & have no problem. I just think of it like this --- my body likes to get my vitamins & minerals from the foods I eat & personally, I think that's the best way for all of us to get what we need. I realize sometimes we have to supplement (if we can) but when we don't have to & can get it from food then we should.

 

I tried calcium supplements for so many years prior to celiac discovery b/c I am/was a prime candidate for osteoporosis. Petite, thin, smoker, going into early menopause, Caucasian. Now I'm post menopause & celiac so add those in & I really need my calcium!!!

pricklypear1971 Community Regular

I had been clear almost 2 months, then went iodine crazy at thanksgiving the first year (about 5 months gluten-free, 2 months LI). New breakout. Not as bad, but bad enough to not eat leftovers and go LI for a week. Again.

Iodine makes the gluten antibodies angry - makes the rash flare. I don't know the scientific interaction. Gluten antibodies cause dh, iodine can make dh flare.

Not everyone reacts to iodine. But if you do, watch it! Yes, it can turn healed skin into blisters, it can make a small rash big.

Iodine deficiency used to be an issue in this country (hence iodine fortified salt). Deficiency causes goiter, etc. your thyroid needs a certain level of iodine to maintain function. I have Hashimotos so low iodine long term/permanently wasn't a good idea.

Blaze422 Rookie

Good stuff...thanks.

I'm thinking almond milk is safe and a good source for calcium.

squirmingitch Veteran

If you're going to avoid iodine then read the ingredients. Almond Breeze has carrageenan (seaweed) which is one of the biggies that usually gets those of us who need to steer clear of iodine. You'll find many of those nut milks contain carrageenan.

 

Open Original Shared Link

Blaze422 Rookie

Silk pure almond milk..no carrageenan

pricklypear1971 Community Regular

You should probably read the thyca.org low iodine guidelines. The guidelines are for people undergoing thyroid radiation therapy, who must follow a two week low iodine diet. The guidelines are pretty good.

Open Original Shared Link

The silk milk contains sea salt - which will have varying degrees of iodine. You may call to ensure it isn't iodized sea salt.

Your iodine tolerance will vary from ours. I probably could have drank it. Squirmy probably wouldn't have :). I just dropped milk and milk subs since the only thing I wanted it for was half n half...for my coffee....which I just dropped for two weeks and hated the world.

Oh, and egg yolks. If you buy egg whites read the labels carefully. There were only two brands I found that weren't full of crap (iodine, or couldn't verify gluten-free) - one was Trader Joe's and the other I don't remember.

FYI I first added back organic half n half (no carageenan), then a whole egg every other day. I turn white at the sight of egg whites, still.

squirmingitch Veteran

Terrific! :)

Blaze422 Rookie

Now you understand why I drink..Or at least why I drank..LOL

If you try to avoid dairy, it has carrageenan.

You try to avoid carrageenan and it has iodine.

You try to avoid iodine and it is high is salycylates.

I am getting better and am trying not to drive my wife nuts.

Fanatical about avoiding gluten in food, lotions, shampoos etc

Trying to be LI but it my understanding that 50 micrograms of iodine or less a day is ok and so if my eggs whites have trace iodine, I eat it... The sea salt in almond milk might be a problem..

My low SAL strategy is to try to be smart and avoid high sal items like my wine and coffee but not to be neurotic at this point.

No dairy. No alcohol.

Probiotics, MSM,food grade Diamatacious earh

Moisturize with coconut oil.

dapsone for 1 more month

You guys are great...thanks again!

ItchyAbby Enthusiast

Hi Blaze - My favorite dairy sub has been coconut milk. I get the Arroy-D brand as it has nothing in it beside 100% coconut milk. No thickeners/gums/salt/preservatives. And it is thick and creamy and tastes so good in tea that I may never go back to dairy milk. (Ok, I probably will, but I will still love coconut milk)

 

I think it is normal to be a bit fanatical and neurotic in the beginning. You are learning a whole new food language! I also think the rash just makes us angsty - but maybe that's just me. When my rash flares, so does my anxiety. When the rash calms down, so does my anxiety. And so it goes, up and down, up and down, for a while. But it DOES get better, I promise. I am 7 months and some change in and am seeing and feeling much improvement.

 

Just try to keep it simple. Eat whole foods as it is nearly impossible to avoid iodine in packaged foods. (Bonus! No labels to read!). Use kosher salt for seasoning. Eat some of that coconut oil, too - it makes not being able to have butter bearable. Keep a food journal to help you target things that might be aggravating. Find a few good comfort dishes that you can make regularly (My two current favorites: shepherd's pie with sweet potatoes on top, and roasted chicken legs with crispy skin with a big salad and roasted sweet potatoes. I could eat either of these for days and be content. Sweet potatoes got me through this! Heh.). Like Prickly, I cannot stand the idea of egg whites - so, I just gave up on eggs for a while. I decided to have one whole egg today, just to test. We'll see how that goes. As you can see, there is a bit of trial and error. You will get better at it and become more aware of your body than you ever wanted to be! :lol:

pricklypear1971 Community Regular

Low sal and low iodine and gluten free made me a very irritable girl.

I DREAMED of shrimp. You could have tortured me with shrimp. First time I aye two and didn't itch I was high as a kite.

I am extremely thankful now that when I break out the rash is minuscule (it may cover some geography but the lesions are so tiny you'd think they're goosebumps) I don't have to do LI. I just lay off huge doses.....

I don't do low sal now. I was only good at that for a few weeks. Made me angry.... I did stay away from food colorings and added msg's....highly "fake" foods - even if gluten-free for a loooong time.

I still won't touch riceworx chips with a ten foot pole....

Oh - if you can - try Junior Mints!!! gluten-free, milk free and egg free??? Anyway I ate them like crack (til I became intolerant of fake mint flavoring, oops)...but they got me through some bad times.

I can't explain the mint thing - I can have fresh mint and some organic extracts and Bob's products but Junior Mints and Andes mints create a bathroom experience I won't repeat.

Blaze422 Rookie

Itchy...I know there's an area for recipes but I have to share this with you. For New Years my wife made black eyed peas ( not sure the specifics) but I put it over a bed of sweet potato/apple mash.

You take an equal amount of pealed sweet potatoes and apples and after dicing them, add a little water and simmer medium heat ,covered for 20 minutes. Stir frequently. Lower temp and simmer another 20 minutes. Add ginger and cinnamon and then mash with potato masher.

awesome!

mendylou Rookie

I can identify with all of you.  Ihave been gluten-free and as free of iodine as I can be for over 3 years.  I have had DH breakouts this entire time but they are not as severe as they used to be.  One thing I really miss eating is shrimp. I have not had any in over 3 yrs.  One of the first foods I want to eat once my skin clears is shrimp. I may pay the price at that time but I have to try it and see what happens.

squirmingitch Veteran

Pardon my last post. I meant Terrific as a response to Blaze's saying he was going with Silk Almond milk -- no carrageenan.

 

Abby! Good for you!

 

Mendylou, I really feel for you @ 3yrs. ((((HUGS))))

 

Okay. Blaze, now I know you must be a southerner!!!!!! Blackeyed peas for New Years --- you just gotta be from the south or your wife is. I'm in Fl. but mom was from Bama.

I did low iodine, gluten-free, & low sal for 9 long months. It's a total b%$@#! No other way to put it. Let's see if I can remember my allowed foods for 9 interminable months:

Celery (still haven't wanted to get near the stuff since I don't HAVE to eat it now), deeply peeled potatoes, sweet potatoes, iceberg lettuce, chicken, beef, pork, egg whites, rice, saffron, cashew butter, instant decaf coffee, leeks, apples, green beans till they came out my ears, snow peas, sugar snap peas, cauliflower, zuchinni, yellow squash, white acre peas, black eyed peas, field peas, lemon, cashews, bananas. The end. That's it. That's all. Breakfast, lunch & dinner, 7 days a week, for nine months. Then we said screw the low sal thing & absolutely nothing happened that made our rash worse for eating sals. We were the same as if we had been low sal. But OH!!!!! we could eat SOOOOOOO many more things! It was as if an entire world opened up for us!!!!!! Food, glorious FOOD!!!!!

 

Blaze, is the Dapsone working for you? How much are you taking per day? And have you noticed a difference? Tell us please what is going on with your rash at this point & how that differs from when you first came on this board?

 

Another day of no itching for both hubs & I. I'm running my hands over my skin & it feels so soft & smooth & I haven't felt it like this for what seems like forever. Only my lower legs still have rough patches which are rapidly healing. After having itching somewhere on my body continually since 2010; to not itch is a bit odd feeling but it is exhilarating!!!!!!!! 

pricklypear1971 Community Regular

Pardon my last post. I meant Terrific as a response to Blaze's saying he was going with Silk Almond milk -- no carrageenan.

Abby! Good for you!

Mendylou, I really feel for you @ 3yrs. ((((HUGS))))

Okay. Blaze, now I know you must be a southerner!!!!!! Blackeyed peas for New Years --- you just gotta be from the south or your wife is. I'm in Fl. but mom was from Bama.

I did low iodine, gluten-free, & low sal for 9 long months. It's a total b%$@#! No other way to put it. Let's see if I can remember my allowed foods for 9 interminable months:

Celery (still haven't wanted to get near the stuff since I don't HAVE to eat it now), deeply peeled potatoes, sweet potatoes, iceberg lettuce, chicken, beef, pork, egg whites, rice, saffron, cashew butter, instant decaf coffee, leeks, apples, green beans till they came out my ears, snow peas, sugar snap peas, cauliflower, zuchinni, yellow squash, white acre peas, black eyed peas, field peas, lemon, cashews, bananas. The end. That's it. That's all. Breakfast, lunch & dinner, 7 days a week, for nine months. Then we said screw the low sal thing & absolutely nothing happened that made our rash worse for eating sals. We were the same as if we had been low sal. But OH!!!!! we could eat SOOOOOOO many more things! It was as if an entire world opened up for us!!!!!! Food, glorious FOOD!!!!!

Blaze, is the Dapsone working for you? How much are you taking per day? And have you noticed a difference? Tell us please what is going on with your rash at this point & how that differs from when you first came on this board?

Another day of no itching for both hubs & I. I'm running my hands over my skin & it feels so soft & smooth & I haven't felt it like this for what seems like forever. Only my lower legs still have rough patches which are rapidly healing. After having itching somewhere on my body continually since 2010; to not itch is a bit odd feeling but it is exhilarating!!!!!!!!

Clear, painless skin is exhilarating. It's amazing how it just disappears.

squirmingitch Veteran

Amen! :D

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 marion wheaton's topic in Gluten-Free Foods, Products, Shopping & Medications
      2

      Are Lindt chocolate balls gluten free?

    2. - BlessedinBoston replied to marion wheaton's topic in Gluten-Free Foods, Products, Shopping & Medications
      2

      Are Lindt chocolate balls gluten free?

    3. - knitty kitty replied to Jmartes71's topic in Related Issues & Disorders
      14

      My only proof

    4. - Jmartes71 replied to Jmartes71's topic in Related Issues & Disorders
      14

      My only proof

    5. - marion wheaton posted a topic in Gluten-Free Foods, Products, Shopping & Medications
      2

      Are Lindt chocolate balls gluten free?


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      132,407
    • Most Online (within 30 mins)
      7,748

    H2HPizzaWagon
    Newest Member
    H2HPizzaWagon
    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

    • trents
      @BlessedinBoston, it is possible that in Canada the product in question is formulated differently than in the USA or at least processed in in a facility that precludes cross contamination. I assume from your user name that you are in the USA. And it is also possible that the product meets the FDA requirement of not more than 20ppm of gluten but you are a super sensitive celiac for whom that standard is insufficient. 
    • BlessedinBoston
      No,Lindt is not gluten free no matter what they say on their website. I found out the hard way when I was newly diagnosed in 2000. At that time the Lindt truffles were just becoming popular and were only sold in small specialty shops at the mall. You couldn't buy them in any stores like today and I was obsessed with them 😁. Took me a while to get around to checking them and was heartbroken when I saw they were absolutely not gluten free 😔. Felt the same when I realized Twizzlers weren't either. Took me a while to get my diet on order after being diagnosed. I was diagnosed with small bowel non Hodgkins lymphoma at the same time. So it was a very stressful time to say the least. Hope this helps 😁.
    • knitty kitty
      @Jmartes71, I understand your frustration and anger.  I've been in a similar situation where no doctor took me seriously, accused me of making things up, and eventually sent me home to suffer alone.   My doctors did not recognize nutritional deficiencies.  Doctors are trained in medical learning institutions that are funded by pharmaceutical companies.  They are taught which medications cover up which symptoms.  Doctors are required to take twenty  hours of nutritional education in seven years of medical training.  (They can earn nine hours in Nutrition by taking a three day weekend seminar.)  They are taught nutritional deficiencies are passe' and don't happen in our well fed Western society any more.  In Celiac Disease, the autoimmune response and inflammation affects the absorption of ALL the essential vitamins and minerals.  Correcting nutritional deficiencies caused by malabsorption is essential!  I begged my doctor to check my Vitamin D level, which he did only after making sure my insurance would cover it.  When my Vitamin D came back extremely low, my doctor was very surprised, but refused to test for further nutritional deficiencies because he "couldn't make money prescribing vitamins.". I believe it was beyond his knowledge, so he blamed me for making stuff up, and stormed out of the exam room.  I had studied Nutrition before earning a degree in Microbiology.  I switched because I was curious what vitamins from our food were doing in our bodies.  Vitamins are substances that our bodies cannot manufacture, so we must ingest them every day.  Without them, our bodies cannot manufacture life sustaining enzymes and we sicken and die.   At home alone, I could feel myself dying.  It's an unnerving feeling, to say the least, and, so, with nothing left to lose, I relied in my education in nutrition.  My symptoms of Thiamine deficiency were the worst, so I began taking high dose Thiamine.  I had health improvement within an hour.  It was magical.  I continued taking high dose thiamine with a B Complex, magnesium. and other essential nutrients.  The health improvements continued for months.  High doses of thiamine are required to correct a thiamine deficiency because thiamine affects every cell and mitochondria in our bodies.    A twenty percent increase in dietary thiamine causes an eighty percent increase in brain function.  The cerebellum of the brain is most affected.  The cerebellum controls things we don't have to consciously have to think about, like digestion, balance, breathing, blood pressure, heart rate, hormone regulation, and many more.  Thiamine is absorbed from the digestive tract and sent to the most important organs like the brain and the heart.  This leaves the digestive tract depleted of Thiamine and symptoms of Gastrointestinal Beriberi, a thiamine deficiency localized in the digestive system, begin to appear.  Symptoms of Gastrointestinal Beriberi include anxiety, depression, chronic fatigue, headaches, Gerd, acid reflux, gas, slow stomach emptying, gastroparesis, bloating, diarrhea and/or constipation, incontinence, abdominal pain, IBS,  SIBO, POTS, high blood pressure, heart rate changes like tachycardia, difficulty swallowing, Barrett's Esophagus, peripheral neuropathy, and more. Doctors are only taught about thiamine deficiency in alcoholism and look for the classic triad of symptoms (changes in gait, mental function, and nystagmus) but fail to realize that gastrointestinal symptoms can precede these symptoms by months.  All three classic triad of symptoms only appear in fifteen percent of patients, with most patients being diagnosed with thiamine deficiency post mortem.  I had all three but swore I didn't drink, so I was dismissed as "crazy" and sent home to die basically.   Yes, I understand how frustrating no answers from doctors can be.  I took OTC Thiamine Hydrochloride, and later thiamine in the forms TTFD (tetrahydrofurfuryl disulfide) and Benfotiamine to correct my thiamine deficiency.  I also took magnesium, needed by thiamine to make those life sustaining enzymes.  Thiamine interacts with each of the other B vitamins, so the other B vitamins must be supplemented as well.  Thiamine is safe and nontoxic even in high doses.   A doctor can administer high dose thiamine by IV along with the other B vitamins.  Again, Thiamine is safe and nontoxic even in high doses.  Thiamine should be given if only to rule Gastrointestinal Beriberi out as a cause of your symptoms.  If no improvement, no harm is done. Share the following link with your doctors.  Section Three is especially informative.  They need to be expand their knowledge about Thiamine and nutrition in Celiac Disease.  Ask for an Erythrocyte Transketolace Activity test for thiamine deficiency.  This test is more reliable than a blood test. Thiamine, gastrointestinal beriberi and acetylcholine signaling.  https://pmc.ncbi.nlm.nih.gov/articles/PMC12014454/ Best wishes!
    • Jmartes71
      I have been diagnosed with celiac in 1994, in remission not eating wheat and other foods not to consume  my household eats wheat.I have diagnosed sibo, hernia ibs, high blood pressure, menopause, chronic fatigue just to name a few oh yes and Barrett's esophagus which i forgot, I currently have bumps in back of my throat, one Dr stated we all have bumps in the back of our throat.Im in pain.Standford specialist really dismissed me and now im really in limbo and trying to get properly cared for.I found a new gi and new pcp but its still a mess and medical is making it look like im a disability chaser when Im actively not well I look and feel horrible and its adding anxiety and depression more so.Im angery my condition is affecting me and its being down played 
    • marion wheaton
      Wondering if anyone knows whether Lindt chocolate balls are gluten free. The Lindt Canadian website says yes but the Lindt USA website says no. The information is a bit confusing.
×
×
  • 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.