Toolkit

#Introduction

This playbook provides an introduction to Adverse Childhood Experiences (ACES), Resilience, and Collective Impact, along with a series of tools to guide your organizations in developing a collective impact plan for addressing ACES and building resilience in your community.  

 

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This toolkit is designed specically to support and guide mainstream organizations on their journeys towards creating safer environments for Indigenous People. Gathering knowledge through our own journey is ongoing and we will continue to update this guidance as we learn new lessons.

This toolkit is designed to support Indigenous organizations with the planning and implementation of community level COVID-19 vaccination clinics, with assistance from mainstream organizations such as local public health units, primary care agencies, and/or hospital settings.

This toolkit was created to provide guidance on communication/engagement strategies and culturally safe practices/policies for vaccine implementation for Indigenous people in Ontario. It covers 6 areas of focus:

Funding Agency: Social Sciences and Humanities Research Council of Canada Insight Development Grant

Principal Investigator: Dr. Julia Gruson-Wood, Postdoctoral Fellow, Department of Family Relations & Applied Nutrition, University of Guelph

Funding Agency: Social Sciences and Humanities Research Council of Canada Insight Development Grant

Principal Investigator: Dr. Julia Gruson-Wood, Postdoctoral Fellow, Department of Family Relations & Applied Nutrition, University of Guelph

Funding Agency: Social Sciences and Humanities Research Council of Canada Insight Development Grant

Principal Investigator: Dr. Julia Gruson-Wood, Postdoctoral Fellow, Department of Family Relations & Applied Nutrition, University of Guelph

The Alliance and our partners at the Canadian Institute for Health Information (CIHI) have developed an interactive Data Quality Assessment Tool for Community Health Centres who have agreed to share their EMR data with CIHI. With this tool, participating CHCs can review the completeness and accuracy of their  organization’s clinical and sociodemographic data for primary health care clients.

The Clinician Change Virtual Care Toolkit shares information and resources of virtual care in practice to support clinicians with the tools they need to provide safe, high quality virtual care.

This toolkit contains: