That is a good question. Actually, we broke it down into four different main sections. The first one is on communication. The whole section is on communication and how those in the health care system, whether it be physicians, physiotherapists, or nurses, should be communicating with individuals with Parkinson's, trying to give information that patients want to hear--but not too much information that they don't want to hear--and trying to make sure that when they do communicate things, they actually give the instructions, writing them down.
Those may be more basic recommendations, but still they're very important recommendations to give better care for individuals with Parkinson's. As I said, we have a whole section on communication.