Hi All,
I recently moved to Lancashire from London and my new GP has told me they won't prescribe me any more Liothyronine. (I was on a T4/T3 combo - I have Hashimotos) I know this has happened to many of you and I think it's just awful. I have sent an email to my local MP but no reply yet.
My brain is like scrambled egg, I'm exhausted, I have a clonking headache and my bones ache - I'm not sure which way to turn.
I do have some 2 types of Cynomel from overseas but neither of them seem to help!!! I thought the UK Liothyronine was meant to be weaker than the overseas ones but perhaps that isn't the case.
Challenging my doctor seems overwhelming and I just don't feel I have the strength to go that route - getting it in the first place was difficult enough!!!
I'm wondering whether seeing a private doctor to get a private prescription might be a solution. Does anyone have any recommendations or idea of costs of getting Liothyronine or NDT on a private prescription?
Thanks for your help.