Just a quick update from my January checkup…

6 March 2017

Where has the time gone? Long story short, making progress with 2 of 3 measures now testing within the normal range:

  • T3 is at 139.1 ng/dL (range is 80-204)
  • Free T4 is at 1.34 ng/dL(range is 0.8 – 1.8)

I’m still showing that I’m considerably hyperthyroidic from a numbers perspective with a TSH still measuring a very low 0.016 ulU/mL (range is 0.35 – 4.5). The big issue with this number is that we have no way of knowing what my reading was prior to being diagnosed as having Graves’ so all we are doing is managing around a low number in trying to get me to be in range without really knowing if my ‘normal’ range could already be a low number.

Overall, still doing well and we’ll see if numbers will further improve at my next check up in April.

A little late with how my last check-up went…

08 October 2016

So I had another follow-up visit with my endocrinologist last month and things look to be settling down a bit on the reduced dose of methimazole (5 mg daily). Free T4 measured at the upper bound of ‘normal’ at 1.8 ng/dL, however, TSH is still way below at 0.01 mlU/L. That compares to 3.9 and 0.02, respectively, back in July.

Not sure how much these numbers truly mean to me as I’m feeling pretty normal despite all these swings. Metabolically, I can feel the effects of the methimazole as it was causing me to put on extra weight when I was at 10 mg a day. At the lower dose, I’ve been holding steady at my pre-Grave’s weight, although it would have been great if I could have kept half my losses at the peak of my episode. All in all, I suppose my body knows what my norm is and I’m fine with that.

Next appointment is at the beginning of the new year.

Ciao for now!

Up and down

2016-07-13

Just got my latest labs and my counts are showing that I’m hyper once again. TSH is back to 0.02 and Free T4 is 3.9. As a result, my doc is putting me back on 10 mg of methimazole daily. I’m going to try and see if he will agree to 5 mg a day instead as the 10 mg got me to being hypo. Since I being off the prescription, I did manage to drop 10 lb. over the last 6 wks and I have noticed that my hands have been feeling warmer as they normally have been before the methimazole. If I have to stay at 10 mg, I think I have to start a new exercise regimen and do something aerobic on a more regular basis to keep the weight in check.

This is pretty disheartening and a setback for trying to reach remission. But despite all of this, I’m still feeling rather normal and it hasn’t really slowed me down from doing my normal routine, knock on wood. I’ll have another follow-up in 6 wks time but for now, I’m just going to enjoy a long vacation starting this weekend (Alaskan cruise, Vancouver and then Seattle).

Cheers!