Back from the endo.
I think I got some of the numbers wrong because it was just crazy busy there and I had a resident on top of that too.
The endo said my sono was great and my bp was great too 128/70, so the new med is really working well.
She said my labs were great too. She said my Tg was less than 0.2 so that is undetectable. (I hope I have that number right) and then she said that my tsh is .05. This is where I cant remember. It could have been .5. But she said that I am still too hyper and since all my testing has been coming out good, she has to balance out the high synthroid dose with the heart palpatations and worse the osteoporosis, since the high dose ruins your bones, which in my case it probably is doing due to the dexa scan and already getting one reclast infusion. She said she wants to get the tsh down to 0 too??
So she is lowering my synthroid to 150. I have to get a blood test in 6 weeks. She said dont throw out your old synthroid yet, because we might have to sub the higher dose a day or two a week etc. Its a balancing act she has to work n but she said she will work on it etc.
I did ask her if she had any other patients with columnar cell variant. and she said she had a few, but they only have really small, small tumors. She said, yours by far is the biggest one I have (12.5 plus the other 4 cm one.) I joked and said, well I guess its good to be remembered for something.
She commented - Oh I knew you were going to do really well?? Hmm, the rad onc. never even said anything like that to me, not once ever. Of course the surgeon never said anything all that much, especially since he almost killed me.
Dh said, she said, well its been almost 4 yeas. I honestly didnt hear her say that, but its really only almost 3 etc.
So we shall see how this all works out, but I am praising God for the good news. With everything else that is not going well with our family, I sure could use that good news, its like a ray of sunshine
Dh said, lets go out to dinner to celebrate.
to celebrate along with me.
