I agree. I have learned that just a visit to the neurologist for my spouse is not going to be enough. Researching and finding ways to make his life a better life is my extra way of showing that their is hope. I know he loves me and understands me alot better than when physicians and ancillary staff that speak to him. I guess you can say I decipher what was said and what it means! Hugs to everyone fealing with this condition we call "Parkinsons ".