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

Hashimoto's Thyroiditis


kimis

Recommended Posts

kimis Collaborator

My Dr. called yesterday to say my thyroid gland is enlarged and my bloodwork confirms Hashimoto's. He also said something that I had never heard before. His almost exact words were....Somewhere in your younger years you got a virus that got in to your thyroid gland. WTF did you say? I started the pills today and I see him in 7 weeks. I have to say I am a bit nervous taking levothyroxine due to all I have read on those thyroid sites, but I must give it a chance so I can decide for myself. I have had a strange feeling in my head, neck and chest all morning.....oh I hate starting new meds!!!!!! My imagination is sooooo much worse than any side effect!


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



Celiac.com Sponsor (A8-M):



Mother of Jibril Enthusiast

I've read that there lots of possible triggers for Hashimoto's... viruses, bacteria, puberty, pregnancy, trauma, food intolerances, etc... The strangest might be microchimerism; apparently, fetal cells have been found in the thyroids of people with Graves disease and Hashimoto's. That could explain why these disorders are 10X more common in women and why your body starts seeing your thyroid as "foreign." However, in my case... I definitely had symptoms of hypothyroidism LONG before I became pregnant.

I've been taking levothyroxine (100mcg/day) for about four months now. My labs (TSH, free T4, free T3) are all back to normal and I feel better than I have in years! I've made some other good changes too... vitamin D, no more gluten, no more corn... but levothyroxine is working for me. I know a lot of people swear by Armour. I'm sure for some people it works better than anything else. IMO, the most important thing is how you personally feel on the medication (whichever one you take).

ShayFL Enthusiast

Give the Synthroid a go. But if it doesnt work for you after a reasonable amount of time, dont be afraid to ask for Armour.

I do great on straight Armour, but my Sister uses a combo of Synthroid and Armour and feels amazing.

Thyroid is tricky and there is no one drug that works perfectly for everyone. There are many options both natural and synthetic. It can take awhile to get it right. So be patient.

And welcome to the club!

kimis Collaborator

WOW...a new club! Now I'm in two clubs, and 8 months ago I wasn't in any clubs at all. I know that many of you have more than celiac to deal with, and I know there is probably a connection between celiac and the other things. This forum has helped me countless times on issues beyond celiac, and everyone has been so comforting and helpful and especially sympathetic.

Back to the levothyroxine...did any of you feel kinda anxious taking it the first few days? I panic over things easily, and I can't tell if I am doing this to myself or what. I read about the side effects before, and I was afraid I might feel racy or have trouble falling asleep. The whole heart palpitation thing scares me the most. So, basically I am asking what your experiences were when you first started this or a similar drug, and how they changed over time. I know everyone is different, but it makes me feel so much better knowing....you know? Thanks again!

MaryJones2 Enthusiast

Thyroid medication dosage is notoriously hard to nail and it takes a while for your body to get used to thyroid medication. If you've only been on it a few days you might want to give it a week or two and if you are still having problems you might need to switch medications or adjust your dose. It often takes a few months for everything to plane out.

ShayFL Enthusiast

I had palps, severe anxiety and racing thoughts on Synthroid. It was so bad one night I called 911. I thought I was having a heart attack. The paramedics were so nice to me. But that drug didnt agree with me At ALL!! And I was on a very low dose. I took it for a month and then got off it.

Armour agreed with me straight off. But me and my Doc. started low 15 mg (1/4 grain) and upped it by 15 mg every 2 weeks when symptoms would return. I would feel better then after a few weeks get the hypo symptoms again. When I got to 120 mg (2 grains) the raises got longer apart. I would go about 2 months then between raises. Got to 195 mg (3 1/4 grains) but then I really started hammering my Ferritin to get it up to snuff and I got a little hyper recently. So have dropped down to 3 grains and feel very good today. Just hyperish for about a week. Then I caught on and realized that the increased Ferritin was making my thyroid conversion from T4 to T3 more efficient and I didnt need as much medication. I expect I will need to reduce again as I get my Ferritin to "optimal" levels.

It is a balancing act and it can change after you think you have the right amount. For instance some women need an extra 15 mg the week before their period as thyroid is reduced then. Some also need an extra 15 mg or so in the winter months. Cold affects your thyroid and conversion of hormones. Menopause will change your requirements for thyroid.

Some Docs wont change your dosage as long as you are in the "normal" range. Countless millions suffer because of this. Best to find a really good Holistic Doc. who specializes in thyroid/hormonal issues. Trust me. Worth it even if you have to pay out of pocket.

If your Ferritin is too low, it might be very hard to get to a good level of thyroid hormone.

Did they test your Ferritin?

Also, if you adrenals are deficient, you will get "hyper" feelings even on a very small amount of thyroid hormone (natural or synthetic). You wont actually be "hyper" but you will feel that way.

Did they test your cortisol levels?

Parathyroid hormone levels PTH?

Live2BWell Enthusiast

I was Dx with Hashimotos a year ago (give or take.) It's been a LONG healing process, and I have come to understand that treating autoimmune thyroid and healing is nothing like treating/healing hypothyroidism even though the medication is the same. It's been a complicated process. Hang in there!

I am on 100mcg of Synthroid and recently dignosed Celiac. I am having to make a total lifestyle change, but my health is slowly improving.

I am learning my triggers, which I still have autoimmune triggers (thyroid) despite medication.

Take care of you!


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



Celiac.com Sponsor (A8-M):



angelschick Apprentice

I also have Hasi, DX about 4 years ago. I am on Armour - synthroid did nothing for me at all. I didn't experience side effects, I didn't experience anything! LOL! I would suggest you poke around these sites -

www.realthyroidhelp.com

www.stopthethyroidmadness.com

It's a long process so try not to expect instant results. Hang in there!

Amy

kimis Collaborator
I was Dx with Hashimotos a year ago (give or take.) It's been a LONG healing process, and I have come to understand that treating autoimmune thyroid and healing is nothing like treating/healing hypothyroidism even though the medication is the same. It's been a complicated process. Hang in there!

I am on 100mcg of Synthroid and recently dignosed Celiac. I am having to make a total lifestyle change, but my health is slowly improving.

I am learning my triggers, which I still have autoimmune triggers (thyroid) despite medication.

Take care of you!

Jessica, What are autoimmune triggers?

Another question I have is...Why is Armor less common than levothyroxines? From the little I have read, it seems like Dr.s don't agree with giving it.

Roda Rising Star
My Dr. called yesterday to say my thyroid gland is enlarged and my bloodwork confirms Hashimoto's. He also said something that I had never heard before. His almost exact words were....Somewhere in your younger years you got a virus that got in to your thyroid gland. WTF did you say? I started the pills today and I see him in 7 weeks. I have to say I am a bit nervous taking levothyroxine due to all I have read on those thyroid sites, but I must give it a chance so I can decide for myself. I have had a strange feeling in my head, neck and chest all morning.....oh I hate starting new meds!!!!!! My imagination is sooooo much worse than any side effect!

I was diagnosed with Hashimoto's in 2000 during my 3rd but 1st suscessful pregnancy. I was already being treated for an underactive tyroid before I got pregnant with my oldest son. Found out about half way thru the pregnancy it was Hashimoto's. I am recently diagnosed with celiac in Oct. this year. I know everyone has different advice so you just need to sort it all out and decide what is best for you. You need to find a good endrcrinologist. Alot of your GP's don't like to treat or change dosage of meds if your levels are in "range". A good endocrinologist will adjust your meds more so on symptoms and they have a lower range that they go by when adjusting meds. I am currently taking 125 mcg of levothyroxine once a day and 5 mcg of cytomel twice a day. This is the first time that I have ever been on a combination of meds. The levothyroxine is T4 and cytomel is T3. My doctor likes this combination better rather than Armour (not sure if spelling is correct) since she thinks it is easier to regulate. I think it works better also.

The only time I have had adverse effects from thyroid medication was after the birth of both of my children. I was on levothyroxine only at the time. During the course of my pregnancy my dosage was adjusted up several times. After delivery I got very nervous, shakey and dropped weight really fast. I didn't need as much so it took awhile to lower the dosage back to where I was not overactive from it. Other than that I have no other problems with it.

Hang in there!

Rhoda

emcmaster Collaborator

I was dx with Hashimoto's 10 years ago, when I was 13, long before I got sick and even longer before I was dx Celiac. My thyroid antibodies were 30x the normal amount, which should have clued my doctors to Celiac when I did start getting sick. But that's a moot point now...

Anyway, I've been on levothyroxine or synthroid for many years, without a problem. I currently take 175 mcg/day. I also have a goiter.

Are you seeing an endocrinologist? I think it's really important to see someone who knows what they are talking about when it comes to thyroid. I've seen family practice docs to treat thyroid before and it has always resulted in my meds being adjusted and my feeling awful because it was too high or low. I currently see Dr. Steven Dofman in Dallas and he is one of the most highly regarded endocrinologists in the country.

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,543
    • Most Online (within 30 mins)
      7,748

    yfuvhg
    Newest Member
    yfuvhg
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.4k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • Beverage
      I had a very rough month after diagnosis. No exaggeration, lost so much inflammatory weight, I looked like a bag of bones, underneath i had been literally starving to death. I did start feeling noticeably better after a month of very strict control of my kitchen and home. What are you eating for breakfast and lunch? I ignored my doc and ate oats, yes they were gluten free, but some brands are at the higher end of gluten free. Lots of celics can eat Bob's Red Mill gluten-free oats, but not me. I can now eat them, but they have to be grown and processed according to the "purity protocol" methods. I mail order them, Montana Gluten-Free brand. A food and symptoms and activities log can be helpful in tracking down issues. You might be totally aware, but I have to mention about the risk of airborne gluten. As the doc that diagnosed me warned . . Remember eyes, ears, nose, and mouth all lead to your stomach and intestines.  Are you getting any cross contamination? Airborne gluten? Any pets eating gluten (they eat it, lick themselves, you pet them...)? Any house remodeling? We live in an older home, always fixing something. I've gotten glutened from the dust from cutting into plaster walls, possibly also plywood (glues). The suggestions by many here on vitamin supplements also really helped me. I had some lingering allergies and asthma, which are now 99% gone. I was taking Albuterol inhaler every hour just to breathe, but thiamine in form of benfotiamine kicked that down to 1-2 times a day within a few days of starting it. Also, since cutting out inflammatory seed oils (canola, sunflower, grapeseed, etc) and cooking with real olive oil, avocado oil, ghee, and coconut oil, I have noticed even greater improvement overall and haven't used the inhaler in months! It takes time to weed out everything in your life that contains gluten, and it takes awhile to heal and rebuild your health. At first it's mentally exhausting, overwhelming, even obsessive, but it gets better and second nature.
    • Jsingh
      Hi,  I care for my seven year old daughter with Celiac. After watching her for months, I have figured out that she has problem with two kinds of fats- animal fat and cooking oils. It basically makes her intestine sore enough that she feels spasms when she is upset. It only happens on days when she has eaten more fat than her usual every day diet. (Her usual diet has chia seeds, flaxseeds, and avocado/ pumpkin seeds for fat and an occasional chicken breast.) I stopped using cooking oils last year, and when I reintroduced eggs and dairy, both of which I had held off for a few months thinking it was an issue of the protein like some Celiac patients habe mentioned to be the case, she has reacted in the same fashion as she does with excess fats. So now I wonder if her reaction to dairy and eggs is not really because of protein but fat.   I don't really have a question, just wondering if anyone finds this familiar and if it gets better with time.  Thank you. 
    • Chanda Richard
      Hello, My name is Chanda and you are not the only one that gose through the same things. I have found that what's easiest for me is finding a few meals each week that last. I have such severe reactions to gluten that it shuts my entire body down. I struggle everyday with i can't eat enough it feels like, when I eat more I lose more weight. Make sure that you look at medication, vitamins and shampoo and conditioner also. They have different things that are less expensive at Walmart. 
    • petitojou
      Thank you so much! I saw some tips around the forum to make a food diary and now that I know that the community also struggles with corn, egg and soy, the puzzle pieces came together! Just yesterday I tried eating eggs and yes, he’s guilty and charged. Those there are my 3 combo nausea troublemakers. I’m going to adjust my diet ☺️ Also thank you for the information about MCAS! I’m from South America and little it’s talked about it in here. It’s honestly such a game changer now for treatment and recovery. I know I’m free from SIBO and Candida since I’ve been tested for it, but I’m still going to make a endoscopy to test for H. Pylori and Eosinophilic esophagitis (EoE). Thank you again!! Have a blessed weekend 🤍
    • knitty kitty
      Yes, I, too, have osteoporosis from years of malabsorption, too.  Thiamine and magnesium are what keep the calcium in place in the bones.  If one is low in magnesium, boron, selenium, zinc, copper, and other trace minerals, ones bone heath can suffer.  We need more than just calcium and Vitamin D for strong bones.  Riboflavin B 2, Folate B 9 and Pyridoxine B 6 also contribute to bone formation and strength.   Have you had your thyroid checked?  The thyroid is important to bone health as well.  The thyroid uses lots of thiamine, so a poorly functioning thyroid will affect bone heath.  
×
×
  • 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.