Equity-Mobilizing Partnerships in Community (EMPaCT)
Learning from Diversity: An Innovation in Inclusive Engagement
If we want an inclusive health system that is socially just and fair for all, we need to hear from people who have diverse lived experiences and apply a health equity lens to everything.
EMPaCT is an innovation that addresses both.
Monthly, EMPaCT collaborates with project implementers in the healthcare system (EMPaCT Impact Partners) to help them identify tangible ways to advance health equity within their work.
Equity-Mobilizing Partnerships in Community (EMPaCT) is a patient engagement model co-designed to:
- Centre the voices of diverse community members
- Build capacity for inclusive and impactful partnerships
Diverse members of community co-created EMPaCT to:
- Highlight community needs and priorities – based on their lived experiences
- Meet monthly to consult with Impact Partners to identify key areas for action on health equity within their work
We are an expert advisory group independent of any specific project. Impact Partners who engage EMPaCT contribute to its financial sustainability.
Who consults with EMPaCT?
EMPaCT works with project implementers (EMPaCT Impact Partners) seeking to learn from people with diverse lived experiences, enhance the inclusivity of their work and reduce health inequities.
Impact Partners include:
- health system decision-makers
- policy-influencers including health/social service administrators
- research teams
What do consultations result in?
Consultations help Impact Partners understand:
- how different communities might be impacted by a project
- what unintended outcomes may occur as a result of the project
- how equity in health can be better addressed for the communities involved
EMPaCT also conducts Health Equity Assessments (HEAs). Unlike most HEAs which are conducted by scientists, academics and policy administrators, EMPaCT HEA evaluations and recommendations are based on the diversity of lived experiences that members of EMPaCT bring to the process as a collective analytical lens.
To our understanding, we are the first community-based group of people with diverse lived experiences to offer and conduct HEAs.
For more, view this video: EMPaCT: Partnering for Change
Impact Partners complete an Intake Form and consultation slide template and return them to EMPaCT prior to the Scoping meeting.
As a key part of the process, Impact Partners receive coaching to prepare them for an effective engagement with EMPaCT.
Step 1: Scoping Meeting: The Scoping meeting refines the scope of the consultation to focus on what value EMPaCT can bring to the Impact Partner’s project.
The Impact Partner revises both the Intake Form and consultation slides as needed and returns them to EMPaCT prior to the Preparatory Meeting.
Step 2: Preparatory Meeting: The Preparatory meeting focuses on the key questions for discussion and the communication skills needed so that the consultation results in authentic dialogue for co-learning.
The refined consultation slides form the foundation of the consultation.
Step 3: EMPaCT Community Consultation: During the consultation, Impact Partners engage members of EMPaCT to learn:
- how different communities might be impacted by the project
- what unintended outcomes may occur from the Impact Partner’s project
- how equity in health can be better addressed for the communities involved
Step 4: Written Report: Impact Partners receive a written report containing recommendations from the consultation process validated by all members of EMPaCT.
Step 5: Feedback from Impact Partner: Impact Partners provide feedback on how they modified their project based on the findings of the report. They also provide feedback on the process of engagement. The process creates transparency in the patient engagement and community consultation process.
Digital library: Members of EMPaCT co-create digital tools and use them to share key concepts. You can access these tools here: EMPaCT Digital Library
Impact Partner consultation reports: These are confidential reports issued to Impact Partners that summarise their engagement with EMPaCT. These reports include key findings from the consultation and actionable recommendations for project-implementers.
Webinars and presentations: Members of EMPaCT are frequently invited to present on issues related to patient engagement and diversity, equity and inclusion. You can view these resources here: EMPaCT Digital Library
Academic co-authored publications:
Building equitable patient partnerships during COVID19: Challenges and key considerations. https://www.longwoods.com/content/26582/healthcare-policy/building-equitable-patient-partnerships-during-the-covid-19-pandemic-challenges-and-key-considerati?platform=hootsuite&utm_campaign=HSCampaign . Sayani, A., Maybee A., Manthorne J., Parsons. J., Bloch. G., Hwang, S. W, Nicholson, E., & Lofters, A. (2021). Healthcare Policy 17 (1).
Equity-Mobilizing Partnerships in Community – EMPaCT: Co-designing patient engagement to promote health equity. https://www.longwoods.com/content/26768/healthcare-quarterly/equity-mobilizing-partnerships-in-community-empact-co-designing-patient-engagement-to-promote-hea . Sayani, A., Maybee A., Manthorne J., Parsons. J., Bloch. G., Hwang, S. W, Nicholson, E., & Lofters, A. and the members of Equity-Mobilizing Partnerships in Community (2022). Healthcare Quarterly 24 (Special issue).
Community engagement toolkit
To request a specific knowledge translation product please email Dr. Ambreen Sayani at ambreen.sayani@Wchospital.ca.
You can learn more about the members of EMPaCT below:
My name is Fatah and I am a young person who identifies as Muslim, Black, and ethnically Somali. I was raised in Scarborough and still reside in the east-end of the GTA. I have experience living amongst immigrant and racialized communities and have grown up seeing economic disparities and disparities in access to health.
I advocate for mental health care, health equity, issues impacting youth, and upward social mobility for the communities I come from and live alongside.
I am a white 30-something woman with Scottish and English roots who calls Toronto home. My parents moved to Canada the year before I was born, and my siblings and I grew up in Montreal and Toronto. I am motivated by loved ones’ experiences navigating the healthcare system for complex and chronic health conditions and mental health concerns.
I advocate for a healthcare system that centres the needs of everyone and promotes health and wellbeing.
I’m a young woman with a strong desire to support those in need. Throughout my adolescence and into my adulthood, I frequently visited hospitals. I have had type 2 diabetes since I was a young child. Although my family is from El Salvador and Nicaragua, I was born in the beautiful city of Toronto, Ontario. As a society’s crown ward, I was involved in the child welfare system and am now making the transition to independence. I discovered that I required a lot of assistance in figuring out where to seek care for my physical and mental health.
I am employed by the community and justice services sector. I want to raise awareness of issues like how underpaid and understaffed hospital employees are. We must make sure that healthcare professionals are treated fairly and with respect.
My life experiences allow me to bring the perspective of a newcomer to Toronto and challenges shared by many inexperienced with navigating Canadian systems. I also bring experience as a caregiver to elder loved ones, supporting them through home care and various other health care services. Guyanese born, I’m also able to share my experience living, learning and working in Toronto as a Black male and will continue to advocate for equity and social justice in all discussions.
I am an organizer and advocate working with underserved communities, specifically refugees and refugee claimants. I connect with families all across the GTA and work primarily in the Thorncliffe Park and Flemingdon Park area.
I advocate for residents and agency employees. I coordinate a resident-lead group called Engaged Communities that focuses on youth development, mobilizing and amplifying community voices, particularly youth and newcomer voices. I am also a caregiver for my mom who has an autoimmune brain condition. This has inspired me to advocate for caregivers too.
In the eighties, I came to Canada alone as a visa student with no English. Then I became an immigrant after working as a live in nanny/ domestic housekeeping job under the immigration caregiver program. And finally rooted as a Canadian citizen with no regrets.
The life journey in Canada is bitter and sweet! New bonds friendships, churches and communities cares, unexpected adopted parents…discrimination, inequity, injustice…poverty, homeless, hunger…has paved latter part of my life as an anti-poverty activist, fighting to have policy/ systemic changes to make peoples lives better!
I grew up in Quebec with a Dutch mother, and an English Canadian father who died when I was 12. I have two birth sons, a chosen son who came to us as a 16 year old refugee from Sudan and four grandchildren. I took care of my mother who died a few years ago of dementia in the Netherlands.
I advocate for changing health systems and information to centre on the person and for inclusive patient/public engagement so that our health system can serve all people fairly.
I was raised by a single mother who had recently immigrated to Canada from Ghana. As a first-generation child, I have seen the difficulties of transitioning into Canadian culture/workforce and the struggles of raising a family on a single income. I am a black woman and a member of the invisible disability community.
I am a proud advocate of providing equitable health services especially for lower socioeconomic communities. I hope to continue to provide awareness on racism, feminism, sexual assault, systemic inequalities, mental health and well being.
I am a woman and a senior who lives with schizoaffective disorder. I became ill in my teens and spent years trying to find help in the siloed and disjointed mental health system in Ontario. I now spend my days promoting understanding and support for those with psychotic illnesses.
A veteran of the mental health system in Ontario, I advocate better and more timely mental health services in addition to the right to literacy for all.
I am a woman from a minority religion. I came to Canada from a country where women and children are the most vulnerable population. I am a human rights especially women and children’s rights defender. I advocate for women empowerment, gender equity & gender equality.
I want to make sure that everyone has access to high-quality services in an equitable manner without any decimation and abuse.
I am a middle-aged, indigenous woman. My reserve is the Crees of Waskaganish First Nations. I was a part of the Sixties Scoop when indigenous people were taken away from their families and raised in non-indigenous homes. I worked at Anishnawbe Health as an outreach worker.
I advocate for eliminating racism and discrimination towards all races and cultures. I am a promoter of showing love and kindness towards all people. I believe in equality for all people because we are all unique in our own ways, and we all have something special to offer the world.
I am a black woman of mixed heritage and culture. I am a single parent to a transgender daughter who lives on the spectrum and caregiver to her and my 91 year old mother who suffers from many ailments.
I advocate for social responsibility and I want to make sure that the healthcare system in Ontario and Canada works for everyone.
I am woman, person of colour and from a religious minority. I moved to Canada in 2014 with two young kids and aging parents. I am often sandwiched between caring for both of these generations as their health, social and emotional needs are different yet intertwined.
I advocate for fairness and equity – all of us need access to the right resources, tools and opportunities so that we can thrive and live a healthy life.
I am a black female, mother, spouse, life-long learner, servant leader, immigrant, and Canadian. I have lived in Toronto Canada most of my life and enjoy telling new Canadians about their roots that made this country. Grade 6 was my life-defining year. It’s the year I noticed a child’s physical response to learning, the year I found and read little Anne Frank’s diary and wept alone in the back corners of the library, overwhelmed at the extent of evil and injustice in this world. I decide there and then that one has the choice to be a destroyer or a healer. I chose the latter, and have lived a life of service, love, joy, peace, and advocacy.
I was born on July 18, 1992 in Toronto. I have Filipino, Polish and Canadian-Indigenous heritage. I am a quadriplegic due to a Spinal Cord Injury (SCI) and Acquired Brain Injury (ABI) suffered in a motor vehicle accident. I spent a year recovering in three different hospitals after my accident.
I advocate for people living with disabilities because I experience the issues with accessibility, discrimination, social support, transportation, employment and more.