Can I just say how COOL it is to meet people such as you who stay so educated and informed on this kind of information. It is inspiring to know you are out there empowering and learning what you need to know for YOU. We hope to be the same way when the time calls.

In the meantime you are right, there is no need for us to worry about this stuff yet, but since my husbands diagnosis a few weeks ago I seem to need to learn all I can about the disease and treatments. I think it may be a coping mechanism. It's lessening as the days go by and I come into acceptance about this new reality. I imagine by the time we meet our Movement Disorder specialist in AUgust I'll have no questions LOL!