(Nov 17, 2021) Today the Pan-Canadian Palliative Care Research Collaborative announced the receipt of $2.5 million from Health Canada to support a network of researchers, clinicians, and community in advancing palliative care for patients and caregivers. View press release here.
The CSPCP is proud to work with the PCPCRC as a part of the network and are excited to be a part of cross-collaborative and impactful research that supports the needs of Canadians.
The funding will support 14 projects across the country that focus on impacting patient and caregiver experiences through new models and tools, new medications and therapies for symptom management, and the impacts of COVID-19 on care, grief, and bereavement.
(June 2021) We are pleased to share this report from the End-of-Life Care Unit at Health Canada.
English: Read more
French: Read more
The report features many new practices and innovative tools that can improve the future of home and community-based palliative care – for example, making virtual care more accessible, increasing the availability of palliative symptom management kits, and giving family caregivers adequate support to provide palliative care for loved ones at home. It is hoped that sharing some of these new practices and tools may inspire readers to use and adapt them as required, or develop and share their own innovations. By sharing knowledge and experience, together we can come out of the pandemic stronger than before.
Thank you to Dr. Stephen Singh for participating in the discussions on behalf of the CSPCP.
(April 20, 2021) If passed as presented, the proposed 2021 federal budget includes:
Better Palliative Care
To provide Canadians, including those who live in long-term care and their families, with better palliative and end-of-life care, including culturally sensitive care:
- Budget 2021 proposes to provide $29.8 million over six years, starting in 2021-22, to Health Canada to advance the government’s palliative care strategy and lay a better foundation for coordinated action on long-term and supportive care needs, improving access to quality palliative care. Initiatives could include: raising awareness of the importance of palliative care; providing public education on grief; improving palliative care skills and supports for health care providers, families, caregivers, and communities; enhancing data collection and research; and improving access to culturally sensitive palliative and end-of-life care.
The first federal Annual Report on Medical Assistance in Dying in Canada (2019) was released on July 24, 2020.
If you have questions about the report, please contact the End-of-Life Care Unit in Health Canada: firstname.lastname@example.org
This report was issued in May 2019.
To view English click here
To view French click here