Two weeks after my long awaited endo appointment, i was just starting to calm down until todays post when i received a copy of his letter to my GP (who had actually suggested a trial of T3).
During my appointment, the endo refused point blank to even discuss T3 as "it has no place in the treatment" levo is good enough. He told me my levels will always fluctuate and that basically, the best thing that could happen was for the antibodies to hurry up and destroy my thyroid completely so that I could get to the maximum dose of levo........and presumably no longer be a burden.
I have another blood test in 2 weeks and at that point he quotes that "further titration of Thyroxine will be required". He goes on to say that if there is too much instability, he will look at a course of block and replace. Is this usual for hypo.......I've had this treatment years ago when i was hyper.