It's really attempting to be responsive to the needs of the patient and the family around them, as long as you can manage things like other complications and pain management with it.
My second question is sort of around that. It's making sure that we have the words right on health care providers, palliative health care providers, and supporting palliative caregivers. There is no term “palliative health care provider”. We have health care providers who are providing palliation. We have caregivers who are providing palliation.
I'm assuming that we would want to make sure that we've identified the training and the educational needs of both health care providers and caregivers. Even for volunteers there would be palliative care training, right?