In an enlightening discussion, Bronwyn Gray shares insights into her short film Worth More, which addresses the complex and sensitive issue of Medical Assistance in Dying (MAiD). Her hope is that the film will spark meaningful conversations and inspire action against MAiD across Canada.
Bill C-62's delay on extending MAiD access to those with mental illness until 2027 prompts a critical reflection on societal support. Keith Dow urges focusing on the root causes of suffering and ensuring comprehensive support systems, emphasizing that expanding MAiD criteria may sidestep essential, underlying questions.
"I don't want to be a burden." Dr. Quentin Genuis challenges society's misconception equating worth with independence. True dignity lies in embracing interdependence, affirming each person, especially the suffering or disabled, as a gift, not a burden.
Within Canada's medical assistance in dying (MAiD) legislation, questions of competence loom large. Dr. Ephraim Radner draws upon personal experiences and theological reflections to bring to light the ethical dilemmas surrounding the legislation. What constitutes competence in the face of existential decisions like life and death? Is it age, experience, or something deeper?
Julia Beazley, Director of Public Policy for the Evangelical Fellowship of Canada grapples with Canada's expansion of medical assistance in dying ("MAiD"). In this article she encourages us to consider policy, foster belonging, challenges ableism and amplify the voices of those with disabilities.
Deina Warren, discusses Canada's MAiD framework. Reflecting on a recent court case involving an Alberta father and his autistic daughter, she emphasizes the need for life-affirming care and advocates for improved quality of life.
In the aftermath of Tracy Latimer's tragic death, Chantal Huinick grappled with profound questions of existence and justice. She unveils the enduring impact of Tracy's legacy on her life and work.
Crossing the threshold of being disabled myself has been such a privilege and a joy because it has transformed the way I can connect with people. Even if our diagnoses are wildly different, and our bodily experiences seem to have little in common, there’s still a deep understanding of what it is to live in a way that doesn’t always fit the systems of our world.
Today, we are pleased to welcome Matthew Piamonte to the site for a guest post on Canada's Medical Assistance in Dying Bill C-14. Matthew is finishing his residency training in family medicine [Read More]
Many who have not had the experience of illness or disability struggle to understand or validate the quality of life, skills and value of people who live with illness or disability.