[jillie74]

in reply to: Memory Loss #1069979

Wow! I appreciate the advice! He said he normally only tests the liver enzymes once a year. He seemed surprised to even hear that liver damage is a side effect of the drug. I am definately going to get some referrals for another Endo in the Pittsburgh area. I welcome any suggestions!

THanks!

[jillie74]

in reply to: Memory Loss #1069977

Thanks! My endo did seem surprised by it. In fact, he told me that a lot of the symptoms I said I was having since starting the PTU he was unfamiliar with. That made me wonder how he can possibly prescribe drugs if he can’t assure patients of what is normal and what is not. He did bloodwork Tuesday and I INSITED he do a liver enzyme, as well. (I had hepatitis from mono about 15 years ago). He did it, but shrugged it off. He called today and said my enzyme count was at 99!!!! (It was 32 in May!!!) Now, he sounds like he is confused… like this is a new thing. Argh. Really frustrating!!!

But thanks for your updates! IT makes me feel less senile!!

Jill ” title=”Very Happy” />

[jillie74]

in reply to: confusing? recently diagnosed..anyone?? #1071400

Thanks! My Endo. is practically non-existant. In fact, I found out I had Graves because he left me a voicemail saying "Your tests came back positive for Graves Disease. We’re calling in a prescription. Thanks." Needless to say, I am trying to get a good referral for a different doctor in the Pittsburgh area.

And yes, the PTU tastes awful. But, I guess it’s better than a pounding heart, shaking hands, and hot sweats….

THanks!!!!

[jillie74]

in reply to: confusing? recently diagnosed..anyone?? #1071398

I was diagnosed just a few weeks ago and was prescribed PTU. I only started the medication today, but have now seen an article from the FDA posted just June 3. Is it better to be on an alternative medication or are both options the same risk for side effects?

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