I posted a few days ago regarding feeling hyperthyroid again even though I've been on
methimazole since the beginning of August. My labs are as follows:
10/5/05
TSHPituitary and tsh
Tsh .46 (.4-4.5
normalNormal saline flush range for our lab)
FT4 1.04
8/23/05
TSHPituitary and tsh
Tsh 0.19
FT4 1.3
8/2/05
TSHPituitary and tsh
Tsh 0.19
FT4 1.21
My endo said that sometimes when the thyroid is stabilizing you can have
littleLittle noses decongestant
Little tummys blips where you are hyper again. He is going to recheck labs again in 2 weeks, plus a fasting glucose. Should I also ask for a FT3 test? He said that if I continue to have symptoms, pounding heart (although I'm on 50 mg of atenolol), jello-like legs, shakiness and etc. despite normal labs, then we'll have to dig deeper to see what could be causing it. I was also wondering if an I-123 uptake scan shows nodules or not? Or can only an ultrasound do that? My four hour uptake scan was 24.7%. I guess I just wish I knew whether or not my symptoms were still due to Graves since my labs are normal. I really hate feeling this way!!!
I came off atd's after two years, and requested a TSI antibodies test be ran to ensure that I was in remission. The two years of being on atd's taught me a lot about the lack of knowledge in the Medical community about Graves and how it affects us, and how we end up being sick unnecessarily. If you've been on too high a dosage of atd's for more than 6-8 weeks, after starting Methimazole/Tapazole, then hypo will be imminent. Breathlessness, weight gain, lethargy, constipation, depression, carpal tunnel were all hypo symptoms for me, and once I learned that, things ran a lot smoother. Usually by the 6-8 week mark of starting atd's, they should be reduced, gradually. I was taken off them after 5-6 months cold turkey, along with my bp meds, and that's not good. Don't let that one happen cuz it was no fun at all. If left on a large dose as I was, (my dr only focused on TSH) it just made my antibodies run amuck and did nothing for my health other than allow him to get the TSH up at the risk of my feeling like death warmed over.
I am now hypo, which I suspected long before the hyperT/Graves kicked in. I would imagine that all the testing that was done in previous years before, if I had copies of labs from all dr's who just couldn't figure out what was wrong, I'd guess only TSH was tested, which to me is just a diagnostic tool. I've been told I'm normal for my TSH to fall anywhere in the range of .50-5.50 and that just does NOT work anymore. Find out where you feel best at and work to keep that level.
Just remember, FreeT3 and FreeT4 in the mid to upper 1/3 range, and make notes on specific symptoms and you'll find where you feel best at while on atd's and once you gain remission. And if they are not reduced and you are not kept with stable blood levels, that is when RAI is suggested because unfortunately, you'll be told you're not repsonding to treatment. Taking the atd's every 8 hours in even doses works good too, although most scripts say X-amt of pills a day, not in split dosages.
DooDaa