Thanks so much for sharing your stories here. I was diagnosed with Graves’ a month ago, and thank God I did my homework before going to the endocrinologist. I had my first appointment today and he automatically recommended RAI. When I told him I wasn’t going to do that, he warned me that ATDs produce side effects in 10% of patients. 10%!!! Thank you sir, I’ll bet on being on of the 90% who turns out fine. I’m looking for another doctor now.
