I simply wondered about the guidelines that will soon be published.
In particular, will we go into the point that Mr. Sherwood wanted to raise our awareness about, specifically that doctors are more interested in issues related to the collateral, subjective and emotional effects of the illness, in order to get a better handle on everything?
In her testimony, Ms. Squire said that, once the doctor told her that she had Parkinson's, he closed her file and put it away, leaving her to take in this news. That was 16 years ago and, maybe the way of giving the diagnosis has improved, but Mr. Sherwood seemed to say that there was still a lot of work to do in this area. Do the guidelines you've developed address this as well?