I take the medication for myself so I can transact, not for anyone else. But I am aware that it is empowering for people to see what I do and, for the most part, people in the Parkinson's community are just really happy that Parkinson's is getting mentioned, and not in a pitying way.

I got sick of turning on the TV and seeing my face.

A lot of times, when you have a disability, one of the things you deal with is other people's projections of what your experience is and their fear about it, and not seeing the experience you're having. There's nothing horrifying about it to me. It is what I deal with. It is my reality and my life, but it's not horrible.

Pay attention to what's happening around you. Read the book before you see the movie. Remember, though you, alone, are responsible for your own happiness, its still okay to feel responsible for someone else's. Live and to learn.

If you asked my kids to describe me, they'd go through a whole list of words before even thinking about Parkinson's. And honestly, I don't think about it that much either. I talk about it because it's there, but it's not my totality.

I don't keep up with it all. But Taylor Swift writes songs about everybody she goes out with, right? What a way to build a career.

The secret to a good marriage, as far as I am concerned, is a joke I make: Keep the fights clean and the sex dirty.