1st blood test results are: TSH .075, T3 145, Free T4 1.91
3 endo’s, $450 wasted , was rushed out of their office(s) in record 10 mins to be told I am HYPERthyroid, MY ONLY option I-131 RAI. Each endo reluctantly said that for 18-20 months they try, put me on Methimazole 10MG 1X day & Metoprolol 25MG 2x day, I asked what are the prolong side effects of the RAI treatment or the medication. They pulled the ignore and dismiss card on me mighty quick, yet again NO ANSWERS!!!
Refuse to destroy glands, easy for endo, more trouble for patient in the future.
Took Methimazole for 2 weeks with beta blocker felt worse than before. Stopped Methimazole due to extreme itching, hair loss that would not dissipate. 2nd of my blood test results from hospital clinic:
TSH <.01 Free T3 5.74 Free T4 2.0 Antithryoid Antibodies:
Thyroglobulin <60 111 Thyroid Peroxidase <60 91
Have new appt for new endo @ hospital enodcrine teaching clinic for mid Oct 2007, I’m on beta blockers 2X day, could I end up in thyroid storm b4 this appt or will beta blocker tide me over till then?
ATD meds, could I ruin my liver, kidneys, whether med is PTU or Methimazole (are there any other meds like this other than these 2?) RAI, can it be done in hospital? Very tired of RAI treated patients telling me they REGRET being FORCED into treatment. Spoke to numerous patients who say they prefer being HYPER than HYPO any day because their endo’s can’t get their dosages of Synthroid straighten out’. No guarantee I could have residual side effects, risk of cancer, Synthroid dosage given wrong after RAI to even affect my liver, kidney, bone marrow problems, etc…all this damn risk?