does anybody else find that their letters from the neurologist are incorrect? We received a copy of the letter from the neurologist to the GP giving him the details of her new prescription and regime. It is not what we discussed at the appointment. This is the second time this has happened.
my mums dose has now been reduced at the time she needs it the most! Very frustrating as they will now have to wait for another letter to be sent to GP and may run out of meds by then!
just wondering if anyone else has suffered this?