4osty
Explorer
I’m asking on behalf of a friend who has Graves’ disease and is thinking about starting Reta. Her main worry is how Reta might affect her condition. Besides talking it over with her endocrinologist, is there anything else she ought to think about?
Has anyone here with Graves’ disease used Reta? How did it go for you? Any personal experiences you can share would give her a starting point — thanks in advance.
Has anyone here with Graves’ disease used Reta? How did it go for you? Any personal experiences you can share would give her a starting point — thanks in advance.