My endo wrote to my GP to recommend I start on T3 but my GP won't prescribe it. He said that their prescription advisors (I think that's how he referred to them) say not to prescribe it as there's not enough evidence to support it's use. He said the endo's letters normally says words to this effect but my letter said that there is evidence starting to emerge that it does help. So they need to go back to their prescription advisors to see if they need to change their policy. Which he said he would do.
Has anyone else come across this? Just wondering how likely a policy change is!
My only other option is a private prescription which I can't afford so I'm stalled for now and fed up about after feeling like I was finally making some progress.