In 1990 I was diagnosed with Graves Disease. I had a sub total thyroidectomy which rendered me hypothyroid and since then I have needed 100mcg of levothyroxine. No problems whatsoever.
My consultant was Sir Richard Bayliss who told me it's a tablet a day, a Drs vist and a blood test and collect a prescription for 365 tablets once a year. Worked perfectly fine for at least 10 years.
And then they introduced 28/56 day prescribing. It is a massive irritation and I cannot begin to explain the amount of time wated over cocked up prescriptions not dealt with, not sent to the pharmacy, etc. Even when it works with an auto arrangement between pharmacy and dr it still takes 25 minutes of my time five times a year. Time I don't have.
When I challenged it my GP said they had a responsibility to monitor me but if they don't see me for 12 months they arent monitoring me are they. I did suggest that indicated I should have a blood test everybtwo months as that was the only way to monitor the condition. I got a dirty look and a harrumph.
What is mildly entertaining is that since December 2016 my prescriptiin has said next review due Oct 2016. I haven't had a blood request form given since.
I am thrilled that my GP has the time to waste writing endless unnecessary prescriptions. Regrettably I don't have time to waste.
It's barking and I wouod like to suggest that if GPs have so much time to waste and pfaff their complaints about patients wasting time fall on thin ice and indicate zero respect for my time. Shocking.