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NATIONAL NORMS FOR VOLUNTEERS |
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In 2001, the Secretariat on Palliative and End-of-Life Care was created under the umbrella of Health Canada and the guidance of Minister Sharon Carstairs. The Secretariat’s overall goal is to create a Canadian Strategy for palliative and end-of-life care. This responds to a clear mandate of the 2000 Senate Report Quality End-of-Life Care: The Right of Every Canadian. The Secretariat formed five Working Groups, one being the Best Practices and Quality Working Group and this opened a window to pursue Volunteer Component needs for developing national best practices. Consequently, a subcommittee to this Working Group was formed, the Task Group on Best Practices and Quality in the Volunteer Component, with membership from across the country. The Task Group has begun to develop a framework to guide the process of developing national best practices for volunteer services in palliative care. The goal is to create a companion document to the CHPCA Model specifically for the Volunteer Component. This document can then be adapted for other clinical and psychosocial care components. The process to create the best practices will be participatory and consensus based. All hospice palliative care programs in Canada will be receiving an information package from the Task Group in the coming months. This package will include an outline of the guiding framework and details on how to become involved in the process. The contents of the guiding framework will include:
After receiving the mailing hospice palliative care programs will be asked to assist with the creation of the draft companion document. The Task Group will be using surveys to obtain responses from volunteers and the paid staff that support them. A National Symposium on Best Practices and Quality in the Volunteer Component is being planned for the Spring of 2004. Please find below summary reports on the work of the Task Group. Task
Group Meeting – Précis Minutes – March 2003
Task
Group Meeting – Minutes – June 2003
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