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.
Written by
BBLYTH
To view profiles and participate in discussions please or .
A uk script can be filled in the EU, many people have got from France at much reduced cost, I get mine from Germany but took trip first to establish relationship with pharmacy get 200 20mcg sent to me for around £60 . Well worth trip as over here £230 for 28!!! Good luck
Is your UK script for 'liothyronine' or specifically for Thybon Henning? i.e. do we need a different script to order from a German pharmacy? (I thought we had to get a special script on a 'named patient' basis).
No, your GP can just write out script for Liothyronine 20mcg X 100 and you can contact a pharmacy in Munich (that's where we went) explain situation they speak very good English and they will mail meds to you. I paid with debit card.
Thank you SlowDragon. Very helpful. 😊 The NHS only gave me T3 because I pushed them to - the endo had to recommend it for my GP to prescribe it. 😩 But I was doing fairly well on it!
Okay. That can't happen in the U.S. An endo has to write a prescription here, which I think is better because too many GP's know absolutely nothing about the endocrine system, therefore don't really even know how much T3 is proper to prescribe. The best "doctors" to have are those who have actually experienced being hyper or hypothyroid themselves, or had someone in their family who has, thereby forcing them to actually use their medical degree(s) to actually learn something and enable them to help others in the same fashion; something Jesus Christ and all other religious leader(s) I have come to study and know call for in (all) their doctrines. But, then, the world calls for materialism and money and possessions, inordinately, and, too many times, these things hypnotize humans and carry the day as humanity suffers on, on this desecrated land mass we call earth. Peace be upon you.
Content on HealthUnlocked does not replace the relationship between you and doctors or other healthcare professionals nor the advice you receive from them.
Never delay seeking advice or dialling emergency services because of something that you have read on HealthUnlocked.