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Improving Online Therapy Practices Through Insights from MAiD Regulation Research

Improving Online Therapy Practices Through Insights from MAiD Regulation Research

Online therapy practitioners can gain valuable insights from the recent study, "‘My Advocacy is Not About Me, My Advocacy is About Canadians’: A Qualitative Study of how Caregivers and Patients Influence Regulation of Medical Assistance in Dying in Canada." This research highlights how caregivers and patients actively shape regulations and improve practices within the MAiD system in Canada. These insights can be leveraged to enhance online therapy services.

Understanding Regulatory Roles of Caregivers and Patients

The study, conducted by researchers at Queensland University of Technology and Dalhousie University, explores how caregivers and patients in Canada influence the regulation of Medical Assistance in Dying (MAiD). They are not merely passive recipients of care but active regulatory actors who contribute to law reform and the practical operation of MAiD.

Key Findings and Their Implications for Online Therapy

The research identifies several ways caregivers and patients engage in regulatory actions:

Applying These Insights to Online Therapy

Online therapy practitioners can adopt similar approaches to improve their services:

The Role of Practitioners in Regulatory Actions

Just as caregivers and patients in the MAiD system have significantly influenced law reform and practice, online therapy practitioners can play a crucial role in shaping the future of mental health services. By actively participating in regulatory actions, practitioners can help ensure that online therapy remains accessible, effective, and responsive to clients' needs.

Conclusion

The study on MAiD regulation underscores the importance of involving caregivers and patients in regulatory processes. Online therapy practitioners can draw from these findings to enhance their practices, advocate for better mental health policies, and ensure that their services are client-centered and continuously improving.

To read the original research paper, please follow this link: ‘My Advocacy is Not About Me, My Advocacy is About Canadians’: A Qualitative Study of how Caregivers and Patients Influence Regulation of Medical Assistance in Dying in Canada.


Citation: Jeanneret, R., Eliana, D., & White, B. P. (2024). ‘My Advocacy is Not About Me, My Advocacy is About Canadians’: A Qualitative Study of how Caregivers and Patients Influence Regulation of Medical Assistance in Dying in Canada. *Medical Law Review*. https://doi.org/10.1093/medlaw/fwae012
Marnee Brick, President, TinyEYE Therapy Services

Author's Note: Marnee Brick, TinyEYE President, and her team collaborate to create our blogs. They share their insights and expertise in the field of Speech-Language Pathology, Online Therapy Services and Academic Research.

Connect with Marnee on LinkedIn to stay updated on the latest in Speech-Language Pathology and Online Therapy Services.

Apply Today

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Apply Today

If you are looking for a rewarding career
in online therapy apply today!

APPLY NOW

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Does your school need
Online Therapy Services

SIGN UP