Well, in my view it is, and medication is only one part of that. For me, the other very important part is multidisciplinary care. Physiotherapists, social workers, nurses, occupational therapists, speech language pathologists--these people may provide more useful input to people with Parkinson's than we do, or at least different input, that's extremely valuable, and the funding for that is simply non-existent.
On November 16th, 2010. See this statement in context.