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

Need Advice With Thyroid Problems


mygfworld

Recommended Posts

mygfworld Apprentice

I have celiac and now hashimotos. The dr is still doing testing to see bow much it is growing and cancer etc. I've been on Synthroid for over a year now. I still have significant pressure and discomfort on my neck. Is this normal? One possibility is to have the thyroid removed or "killedoff". Has anyone had either done? Any long term problems with having the thyroid removed? Voice problems?

Any advice would be appreciated.


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



Celiac.com Sponsor (A8-M):



georgie Enthusiast

Have you thought of using another type of Thyroid medication like Erfa Thyroid ( from Canada) or adding Cytomel to the Synthroid ?

Synthroid is T4 only.

Cytomel is T3 only

Erfa and other Natural Dessicated Thyroid medications ( Armour, Naturethyroid) are T4,T3,T2,T1

When our thyroid work they make T4,T3,T2,T1

Most old fashioned Drs and Endos say that a T4 is still OK as it 'converts' once you take it.

Modern progressive Drs and Endos say we need both T4 and T3 etc

My Goitre and thyroid nodules completely disppeared on Armour Thyroid. No surgery was necessary. How are your blood tests lately ? What are the levels of your Free T4, Free T3 and Thyroid Antibodies?

Check our Dr T Friedman - Endo - website. Lots of info there. Sounds like the Synthroid you are taking is not doing it all - a very common problem . Easily fixable once you find the right Dr.

oliv Newbie

I was diagnosed with Hashimoto's in 2005 (prior to a diagnosis of celiac sprue in 2009) and was prescribed synthroid alone until 2007, followed by synthroid plus cytomel until last year, when I started natural thyroid. While on synthroid, with or without cytomel, I regularly had goiter pain and swelling that would not resolve. The Dr. could only tell me that my thyroid would become inflamed "because it wants to". Hmmm.

Out of frustration with my continuing symptoms (and ill-informed Dr.), and after reading the very useful information at Stop The Thyroid Madness (Open Original Shared Link), I switched to Nature-throid, with no regrets.

Another complicating factor is that synthroid is no longer guaranteed to be gluten free (www.glutenfreedrugs.com), though the generics, cytomel, and most natural dessicated thyroid preparations are safe.

twe0708 Community Regular

My daughter is 16 and takes 10 mg once a day of methimazole for hyperthyroidism. She's been the on meds for 7 years and now the doctor wants to kill her thyroid off. I am concerned about this because I have read about some horrible side effects, but I also know she can't stay on the medicine for the rest of her life. Anyone else have their thyroid killed off and have any side effects?

kimann79 Apprentice

My daughter is 16 and takes 10 mg once a day of methimazole for hyperthyroidism. She's been the on meds for 7 years and now the doctor wants to kill her thyroid off. I am concerned about this because I have read about some horrible side effects, but I also know she can't stay on the medicine for the rest of her life. Anyone else have their thyroid killed off and have any side effects?

I was diagnosed with Graves disease at fifteen and my thyroid was irradiated. It's been AWFUL. I can't even tell you how many years I spent dealing with the fallout from that and, at thirty, am just beginning to get a handle on it. I'm not sure what the other options are but I would look into them.

In answer to the OP question...I had great luck turning from Synthroid to Cynomel (I am getting ready to switch to desiccated but I needed to deal with a reverse T3 problem.) I second checking out stopthethyroidmadness.com. It's chock full of awesome relevant, up to the minute information. I'll personally never go back on Synthroid.

Skylark Collaborator

I read something in another thread about timed release T3. Does anyone have any info on it?

  • 6 months later...
twe0708 Community Regular

I have celiac and now hashimotos. The dr is still doing testing to see bow much it is growing and cancer etc. I've been on Synthroid for over a year now. I still have significant pressure and discomfort on my neck. Is this normal? One possibility is to have the thyroid removed or "killedoff". Has anyone had either done? Any long term problems with having the thyroid removed? Voice problems?

Any advice would be appreciated.

Did you ever have your thyroid killed off? My daughter's doctor still wants to kill hers off. I guess as a female you can't be on the medicine for over active thyroids while having kids, so he said she needs to have it taken care of soon. Are all of these other medicine options that are being recommended safe to take while having kids?


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



Celiac.com Sponsor (A8-M):



georgie Enthusiast

I found it didn't work as well for me due to malabsorption. If there was a gut flare ( for whatever reason) you ran low on thyroid as well....

I read something in another thread about timed release T3. Does anyone have any info on it?

georgie Enthusiast

Just be really really careful that it is Graves Disease and not Hashimotos Disease. Hashimotos can cycle up and down/ resemble Graves and does not need to be 'killed off'. It just needs a good thyroid medication and treatment plan.

Did you ever have your thyroid killed off? My daughter's doctor still wants to kill hers off. I guess as a female you can't be on the medicine for over active thyroids while having kids, so he said she needs to have it taken care of soon. Are all of these other medicine options that are being recommended safe to take while having kids?

beefree11 Newbie

My daughter had her right lobe removed in 2005 after nodules were found. There was no cancer. Her blood tests revealed Hashimoto's and thyroiditis, so she was placed on T4 only-Synthroid.

Her doses were changed constantly with each new blood test. Until 2009, when her new doctor placed her on Cytomel too. She has been doing very well. He also found that she is gluten intolerant, allergic to wheat, casein/cow milk, soy, corn/maize and eggs. She still has her left lobe. She is also on a very small amount of Iodoral iodine, and feels pretty good in comparison to when she was on the T4 only regimen.

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,546
    • Most Online (within 30 mins)
      7,748

    KimberlyAnne76
    Newest Member
    KimberlyAnne76
    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

    • Scott Adams
      Your post demonstrates the profound frustration and isolation that so many in the Celiac community feel, and I want to thank you for channeling that experience into advocacy. The medical gaslighting you endured for decades is an unacceptable and, sadly, a common story, and the fact that you now have to "school" your own GI specialist speaks volumes about the critical lack of consistent and updated education. Your idea to make Celiac Disease a reportable condition to public health authorities is a compelling and strategic one. This single action would force the system to formally acknowledge the prevalence and seriousness of the disease, creating a concrete dataset that could drive better research funding, shape medical school curricula, and validate the patient experience in a way that individual stories alone often cannot. It is an uphill battle, but contacting representatives, as you have done with Adam Gray, is exactly how change begins. By framing it as a public health necessity—a matter of patient safety and protection from misdiagnosis and neglect—you are building a powerful case. Your voice and your perseverance, forged through thirty years of struggle, are exactly what this community needs to ensure that no one else has to fight so hard just to be believed and properly cared for.
    • Scott Adams
      I had no idea there is a "Louisville" in Colorado!😉 I thought it was a typo because I always think of the Kentucky city--but good luck!
    • Scott Adams
      Navigating medication safety with Celiac disease can be incredibly stressful, especially when dealing with asthma and severe allergies on top of it. While I don't have personal experience with the HealthA2Z brand of cetirizine, your caution is absolutely warranted. The inactive ingredients in pills, known as excipients, are often where gluten can be hidden, and since the FDA does not require gluten-free labeling for prescription or over-the-counter drugs, the manufacturer's word is essential. The fact that you cannot get a clear answer from Allegiant Health is a significant red flag; a company that is confident its product is gluten-free will typically have a customer service protocol to answer that exact question. In situations like this, the safest course of action is to consider this product "guilty until proven innocent" and avoid it. A better alternative would be to ask your pharmacist or doctor to help you identify a major national brand of cetirizine (like Zyrtec) whose manufacturer has a verified, publicly stated gluten-free policy for that specific medication. It's not worth the risk to your health when reliable, verifiable options are almost certainly available to you. You can search this site for USA prescriptions medications, but will need to know the manufacturer/maker if there is more than one, especially if you use a generic version of the medication: To see the ingredients you will need to click on the correct version of the medication and maker in the results, then scroll down to "Ingredients and Appearance" and click it, and then look at "Inactive Ingredients," as any gluten ingredients would likely appear there, rather than in the Active Ingredients area. https://dailymed.nlm.nih.gov/dailymed/   
    • Scott Adams
      What you're describing is indeed familiar to many in the Celiac community, especially in the early stages of healing. When the intestinal villi are damaged from Celiac disease, they struggle to properly digest and absorb fats, a condition known as bile acid malabsorption. This can cause exactly the kind of cramping and spasms you're seeing, as undigested fats can irritate the sensitive gut lining. It is highly plausible that her reactions to dairy and eggs are linked to their higher fat content rather than the proteins, especially since she tolerates lean chicken breast. The great news is that for many, this does improve with time. As her gut continues to heal on a strict gluten-free diet, her ability to produce the necessary enzymes and bile to break down fats should gradually return, allowing her to slowly tolerate a wider variety of foods. It's a slow process of healing, but your careful approach of focusing on low-fat, nutrient-dense foods like seeds and avocado is providing her system the best possible environment to recover. Many people with celiac disease, especially those who are in the 0-2 year range of their recovery, have additional food intolerance issues which could be temporary. To figure this out you may need to keep a food diary and do an elimination diet over a few months. Some common food intolerance issues are dairy/casein, eggs, corn, oats, and soy. The good news is that after your gut heals (for most people who are 100% gluten-free this will take several months to two years) you may be able to slowly add some these items back into your diet after the damaged villi heal. This article may be helpful: Thank you for sharing your story—it's a valuable insight for other parents navigating similar challenges.
    • 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.
×
×
  • 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.