Hi Kathleen: Thank you for answering my inquiry.
This is the first time I have talked to anyone about
this. What have I been doing the last 2 years? I
have just been taking tapazole-waiting and worrying.
I didn’t experience the problems with the med that
you did. I have made some changes in my life which
enables me to spend some time now on researching GD.
Tapazole keeps me in my normal ranges, but when I
reduce I get the hyper. I have had no problems othe
than the mild stare/hair loss/dry hair/eye puffiness.
I am definetly going to have my doctor check my live
next time since apparently from what I’ve been read-
ing it may be an issue??!!** My plans are to stay on
tapazole forever or until thyroid burns itself out.
The other alternatives are not appealing to me.Tell
me more about your situation if you’d like. I’m
definetely interested. You made a good point re:
the people w/out problems are probably not writing!!
I figure I better learn everything I can now to
better prepare myself if things should get worse.
I wish I could say I wasn’t freaked out, but this
damn thing is really putting a cramp in my style!
HaHaHa!!! Actually, I think there is a lesson
to be learned in this for me.
Regards, Lucy
Anonymous
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