World Hospice and Palliative Care Day is Saturday October 12th.

“We believe that it takes a society to create better treatments, better care, and better support for people living in Canada. Part of making further advancements is offering recommendations to federal and provincial governments that can make supports for people with cancer more accessible, like palliative care.” Source: CCS

The Canadian Cancer Society’s (CCS) report analyzing palliative care across Canada will direct advocacy and support initiatives in the coming years. This report highlights 4 key findings about palliative care:

1. Canada still lacks the capacity to consistently deliver palliative care in communities, particularly in hospice.

2. There are significant social barriers to talking about death and dying, and confusion about the benefits of palliative care.

3. All provinces and territories noted that more could be done to improve cultural safety in palliative care, including grief and bereavement supports.

4. Access to palliative care would be enhanced with additional training of healthcare professionals in more healthcare settings.

To ensure that palliative care reaches those who require it, there needs to be a shift in the awareness and understanding of services for everyone, including providers, caregivers, and patients. There also needs to be an increased understanding of the landscape of palliative care services across Canada. The palliative care needs of a population cannot be met by palliative care specialists alone.

Source: 4 key findings about palliative care. CCS

To read more, visit: https://cancer.ca/en/about-us/stories/2024/4-key-findings-about-palliative-care 

#BustingTheMyths about Hospice Palliative Care

It’s Hospice Palliative Care Week in Canada. 

The campaign (May 5th – 11th) this year focuses on #BustingTheMyths about Hospice Palliative Care

This year, the Canadian Hospice Palliative Care Association (CHPCA) designed a “Busting the Myths” campaign as a response to the need to educate Canadians including caregivers, physicians and all healthcare providers, citizens and political leaders around common myths about hospice palliative care.

The #BustingTheMyths campaign aims to empower Canadians through education by identifying and clarifying misperceptions about Hospice Palliative Care in Canada.

Working together to educate one another is a vital step in the pursuit of excellent Hospice PalliativeCare.

Source: CHPCA Canadian Hospice Palliative Care Association

April 2nd is National Carers Day

About National Carers Day

In April 2010, the Parliament of Canada unanimously adopted a motion declaring the first Tuesday in April “The Invisible Work Day.” This day was designated to recognize the importance of the “invisible” unpaid work carried out by parents and caregivers on behalf of their children and aging family members, as well as the volunteer work done in the community.  Recognizing that caregivers come from all walks of life and take on many roles, the first Tuesday in April is a special day where we can recognize all caring Canadians.

#NationalCarersDay

Source: https://www.carerscanada.ca/national-carers-day/

Innovative Undergraduate and Graduate Social Work Programs at Wilfrid Laurier University

Honoured to be teaching with the Lyle S. Hallman Faculty of Social Work at Wilfrid Laurier University again this year. Excited to be teaching "Social Work Practice with Groups" to the Undergraduate Bachelor of Social Work Program, and "Advanced Practice with Families" to the Graduate Master of Social Work Program. 

For more information about the innovative B.S.W Program or the M.S.W. Program, please visit:  
https://www.wlu.ca/academics/faculties/faculty-of-social-work/index.html

Why we need better #end-of-life #policies in #seniors’ residences. #LTC

“How we die is regularly in the headlines as we await government legislation to be tabled in response to the 2015 Supreme Court of Canada decision legalizing physician-assisted dying. Palliative care gets less attention, but it is what most of us will want at the end of life: drugs to relieve agitation, pain, agonal breathing and other symptoms. Nurses can provide soothing medications, but only after doctors have issued prescriptions, often with increasing dosages. But as the Crosbie family discovered, doctors are few and far between in long-term care facilities, especially on weekends. Their experience is a cautionary tale.”

Toward Evidence-Based End of Life Care. ~NEJM

"The disquieting patterns of end-of-life care in the United States have been well documented. In the last month of life, one in two Medicare beneficiaries visits an emergency department, one in three is admitted to an intensive care unit, and one in five has inpatient surgery. But one of the most sobering facts is that no current policy or practice designed to improve care for millions of dying Americans is backed by a fraction of the evidence that the Food and Drug Administration would require to approve even a relatively innocuous drug".