I noticed that in the submission they were talking about medical certificates and the engagement of medical doctors and/or nurse practitioners for making some judgments. From my experience in looking at PTSD and having some experiences with it in some previous life iterations, people's responses to it are very varied. It becomes a very subjective response to it.
How much engagement do we have in terms of sudden infant death syndrome, PTSD and the variance of that? How are those judgments made? The policy framework seems sort of clinical. How much of that is dictated, or do we have medical health professionals coming in and saying a person is suffering from PTSD and therefore needs to be engaged for a more lengthy period of time? Do we have some flexibility on that, or how are those determinations made?