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Association of Substance Use Pattern and Family Factors With Use-Related Problems According to Arabic Drug Abuse Screening Test-10: A Cross-Sectional Study.

Authors: Murad HAS, Bakarman M
Journal: Substance use : research and treatment
mental health psychology open access

Abstract

The arrival of Voluntary Assisted Dying (VAD) has led to significant changes to end-of-life choices in many global jurisdictions. Variously referred to as voluntary euthanasia, Medical Assistance in Dying (MAiD), and Physician Assisted Suicide (PAS), VAD is a legal and clinical practice that, in the context of advanced illness with a short prognosis, permits a person to voluntarily receive support to end their suffering by dying at the time of their choosing through use of a chemical substance. VAD is increasingly available as an end-of-life choice with many global jurisdictions legalising and implementing this support. VAD’s arrival has influenced the systems that provide care at the end of life in ways which can be seen as both a stimulus and an opportunity to consider how community members support themselves and each other as dying approaches. Contemporary dying is not a solitary activity; it impacts people and happens within communities. As we prepare for dying, those around us support, console, grieve, make meaning, and are ultimately left behind. The experience of dying, and the planning that usually occurs in preparation for it, takes place within socio-cultural contexts and is shaped, interpreted and responded to by prevailing systems of meaning. Additionally, death and dying involves interpersonal and community resources which become more important as dying comes closer and our dependence on others increases. While the critical nature of formal and clinical care may be undeniable, these types of care constitute only a small part of necessary responses to end-of-life needs. Communities have a significant role in support when dying approaches. VAD’s arrival is largely due to an increasing societal expectation that it should be an available end-of-life choice. While access to VAD is desired by many, the capacities and resources community members need to safely navigate these new end-of-life choices has received less focus. Accessing VAD requires new skills and resources with knowledge of available choices being only one key component. Increasing community knowledge of available end-of-life choices is a challenge and may be an easier task than enhancing the skills and resources necessary to navigate complex health processes. Even sufficient knowledge of VAD processes and availability have been elusive post implementation. There is evidence that Australians have a relatively poor understanding of VAD processes. A recent study conducted 18 months after VAD became available in Queensland, Australia demonstrated that one third of respondents were unaware that VAD was a legal option. Even fewer (26%) reported knowing how to access it. These gaps reflect the challenge in ensuring communities’ knowledge and capacity to access end-of-life choices. There is a need to proactively support community awareness of all end-of-life choices, particularly in response to major health policy changes, such as the introduction of VAD.