Yesterday I was seen by my current Neuro, the 4th visit in less than a year. He spent 45 minutes and answered all the questions that my wife and I offered. He recognized that we live in a remote area and provided his email address to enhance our ability to communicate. I feel so fortunate.
He also seemed content with my request to take the least meds that are effective instead of pushing pills. However, the most significant statement that he made was that the non-motor symptoms are frequently the most debilitating aspects of PD. Reassuring to know I'm not fantasizing or going crazy.