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 Our Content
    eNewsletter
    Donate

Update:post Doctors Test


Booghead

Recommended Posts

Booghead Contributor

Yesterday we went to my follow up with my Family Doctor. He said all my test results including TSH (which I previously posted)show hyperthyroidism not hypothyroidism. He suspects graves. They took more blood to run all three tests again just to be triple sure. I always feel nervous when they take blood, because I worry that it will come back normal and I will be back at square one. But that's just silly I suppose.

My heart rate was fairly elevated at the appointment, he says its probably from the hyperthyroid. He doesn't want any strange heart problems popping up so he put me on a blood pressure medicine, which he says can help cover up the symptoms of the hyperthyroid (like a band-aid he said). He also ordered a Radioactive Iodine Uptake test for next week. I will go in and get injected, come back 4 hours later for a scan and then the next day as well. Anyone ever had this test done? I want to know what to expect.

He says I will probably have either an overactive node or a completely overactive thyroid. He made is sound like either way I will need to have something removed (either a whole thyroid or just the node). What do you guys think about this?

Thanks for the input and the support. I really appreciate having you guys as a back board to bounce ideas off of.


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



Celiac.com Sponsor (A8-M):



kareng Grand Master

I had that when I was 14-15. I had the radioactive test & doctors threatening to remove my thyroid. I don't remember the iodine test being a big deal. That was 35 years ago. I'm surprised they don't have any better tests now. It was determined I had a thyroid infection. They gave me thyroid medicines and monitored it every month. In about a year, it was healed. You need to see an endocrinologist. Your parents may have to suck it up and take you in to the University Hospital in SLC.

hspichke Apprentice

I had the radioactive iodine scan done a few months ago. After I had my son (hes 10 months now) I developed hyperthyroidism, the Dr told me that it should have gone back to normal shortly after but it hadn't so he thought I had Graves and sent me for the test. It was normal. They just had me take a pill come back and pointed this machine at my knee for 2 min then had me lay under an xray machine for 10 min on each side. Didn't feel a thing but it was very boring!

However, like I said my test was normal so he said that was odd and sent me home and wanted me to get my TSH levels checked in 12 wks and I am now waiting for results!

Booghead Contributor

We are seeing an endocrinologist before the radioactive iodine test. If she says it isn't necessary then we won't do it.

I forgot to tell everyone that my doctor highly recommended a endocrinologist, and he gave us a referral. She works at MckayDee Hospital. He isn't going to do all these crazy things himself. I don't even know if it is legal for a family doctor to remove some ones thyroid. :P He just wanted to do the test to see if it was the whole thyroid or just a small section of it. He says the antibody tests are only done when hashimotos is suspected, and that there aren't any for graves.

Skylark Collaborator

There is an antibody test called TSI for Graves' disease. I'm awfully glad you're getting referred.

kareng Grand Master

He isn't going to do all these crazy things himself. I don't even know if it is legal for a family doctor to remove some ones thyroid.

Sounds like a horror movie plot! :P

GFinDC Veteran

When I had first my thyroid tested several years ago I went to my GP. He had me get an MRI with contrast. Then he referred me to a thyroid specialist. I went to the thyroid specialist and he said I should not have gotten the MRI with contrast. The specialist said the right thing to do is get an ultrasound first. The ultrasound is much cheaper, less risky, and faster, plus no contrast solution needed.

He also said the ultrasound gives just as good information about the thyroid as the MRI in most cases. The thyroid specialist stood behind my back and "plapated" my thyroid with his fingers. Basically felt the thyroid on both sides of my neck and front for bumps etc. I had/have a thyroid cyst so he did a fine needle aspiration (FNA).

He found I had a benign thyroid nodule. He told me that is not a problem, as most people develop benign thyroid nodules at some point in life. But to keep having it checked every year. That was years ago. I have another nodule now but still not a problem. My endocrinologist has me get an ultrasound on it every so often to monitor it.


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



Celiac.com Sponsor (A8-M):



Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      130,025
    • Most Online (within 30 mins)
      7,748

    kdking61
    Newest Member
    kdking61
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.3k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • KimMS
      Thanks for sharing that site! Do you know if that site has any information about manufacturing/possible cross contact on it? I can't find it. When I have called manufacturers, most of them say they can't guarantee no cross contact in manufacturing (except Lannett, Mylan and possible Amneal, which aren't available near me).
    • Diana Swales
      After years of living with Celiac Disease, learning through every bump and breakthrough, and guiding others through the gluten-free maze — I've officially qualified as a **Nutrition Coach** with Precision Nutrition. Now I’m ready to take this journey deeper… but I need your help. To complete my final certification hours, I’m offering **a limited number of FREE spots** (yes, completely free!) to work with me over the next few weeks. I’m looking for **5 people** who: Are newly diagnosed with Celiac Disease or gluten-intolerant Feel overwhelmed, confused, or frustrated with food Want support from someone who truly understands Are ready to build confidence and calm in their daily eating We’ll work together on what matters to *you*: Your food choices Your mindset Your kitchen habits Your ability to speak up for your needs This isn’t just about avoiding gluten — it’s about reclaiming ease, joy, and nourishment. If you're interested, comment below or DM me the word **"Ready"** and I’ll send you the info to get started. Let’s make food feel safe again. With care, **Diana**
    • Dora77
      Hi everyone, I have celiac disease and I’m asymptomatic, which makes things more stressful because I don’t know when I’ve been glutened. That’s why I try to be really careful with cross-contamination. For almost a year, I’ve been having yellow/orange floating stools consistently. I’m not sure if it’s related to gluten exposure or something else going on. I’ve been trying to identify any possible mistakes in my routine. Today, I made myself some gluten-free bread with cheese. Normally, I’m very careful: I use one hand to handle the cheese packaging (which could be contaminated, since it’s from the supermarket and was probably sitting on a checkout belt that had flour residue), and the other hand to touch my gluten-free bread and plate. But today I accidentally touched the bread with the same hand I used to grab the cheese pack from the fridge. The fridge handle might also have traces of gluten since I live in a shared household where gluten is used. I’m worried this mistake could have contaminated my bread. There were no visible crumbs or flour, but I know even trace amounts can be a problem. Has anyone had similar experiences or symptoms from this level of contact? Could this kind of exposure be enough to trigger symptoms or cause intestinal damage? Thanks for reading.
    • Mswena
      So eight days in a row of gluten on top of gluten on top of gluten, I just had to resort to the EpiPen. I wish I could post a picture because you wouldn’t believe how enormous my gut is! It makes my head look like a pinhead.Ahhhgggsahhhhh!!!! I have discovered that I have to read the ingredients when I use a product up that I’ve been able to use without getting a reaction, because they can change the ingredients and bam my toothpaste now has gluten!!! my doctor told me gluten free means it has 20 ppm which someone with a severe a celiac as I’ve got that thing there kills me. I try to find certified gluten-free in everything. I can’t eat any oats unless it’s Bob’s red mill certified gluten-free. Good luck everybody this autoimmune disease is wicked wicked
    • Mswena
      I have been using a little bit of Lubriderm when I wash my hands because it’s the lotion offered at a place I frequent once a week. Assuming it was gluten-free I bought a bottle. I couldn’t figure out why I was getting gluten EVERY night. I use a little of the lotion in the morning on my neck, with no reaction, but at night, I use it on my arms and legs and face and get gluten gut pretty bad. After eight nights of having to have diphenhydramine injections for severe gluten, I googled “is Lubriderm gluten-free” and it led me to this forum. I am going to go back to olive oil as I have been gut sick sooooooo bad with a huge gut and pain eight days in a row now. Sick of feeling sick.
×
×
  • Create New...