Jump to: Page Content, Site Navigation, Site Search,
You are seeing this message because your web browser does not support basic web standards. Find out more about why this message is appearing and what you can do to make your experience on this site better.
BMJ 2003;327:222-223 (26 July), doi:10.1136/bmj.327.7408.222-b
| The first 150 words of the full text of this article appear below. |
EDITORAs care givers of children who are dying, we were disappointed that the experience of dying children and their families was not broached by Ellershaw and Ward or Clarke.1 2 Do we in society continue to find it impossible to think about death in childhood? To imagine that children with life threatening illness and their families can experience a good death? What could possibly be experienced as good during this dying journey?
Paediatric palliative and hospice care continues to lack a significant
voice in medical debates, literature, and research, as well as in the design
and delivery of services. Why, for example, is there currently only one active
free standing children's hospice in North America? Yet a significant number of
children die of a life threatening illness or injury each year. In a
population of 250 000 (50 000 children) five children are likely to die each
year from
Laura Beaune, palliative care coordinator
laura.beaune@sickkids.ca
Christine Newman, palliative care physician
Hospital for Sick Children, Toronto, ON, Canada M5G 1X8