Bad management and poor care.
Early May I saw my neurologist who said he would prescribe more medication
but to wait ten days before seeing my GP for the prescription so he could get a letter to him.
Ten days later I went in to my GP who wanted to know why I had come, I told him and he still did not know why.
He eventually found a letter in my notes which told him what drug to prescribe which he did.
I took three doses, one per day with terrible side effects, so stopped it and contacted the Parkinsons nurse who had a word with the neurologist.
Last week she rang me to tell me the GP had in fact prescribed the wrong drug and that there would be a new prescription this week.
I rang the surgery to see if the drug was there (after waiting a week)
No one knows anything about it. More than a month has now gone by and I still am no wiser as to what is happening.
I really do give up. The whole thing is a total shambles.