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How do we know when we’ve achieved cultural safety? When both sides leave feeling content. This is one answer shared as we met with Indigenous patient partners during a recent project to develop resources about culturally safe patient engagement.
We’re thrilled to introduce you to someone new who will be supporting patient engagement across BC. We sat down with her to ask about what drew them to work in patient engagement, and their hopes for the health care system.
We’ve just released a new resource called Diversity, Equity & Inclusion: Elevating the Voices of All British Columbians! Thank you to the patient and health care partners who contributed to developing this guide.
We’re thrilled to introduce you to someone new(ish!) who will be supporting patient engagement across BC. Leslie Chan is the Project Coordinator on the BC Patient Safety & Quality Council’s Patient & Public Engagement team and will be supporting PVN’s work closely.
Formed in 2020, the Patient Voices Network’s Diversity, Equity, and Inclusion (DEI) Working Group started off by exploring guiding definitions for DEI work and how these definitions could support future work. This article is a follow up to September’s update on our DEI Working Group.
It’s key that changes made to our health care system are inclusive of patients – and that’s what the Patients as Partners Initiative strives to accomplish. The initiative included a few PVN patient partners in this important work.
Our Diversity, Equity and Inclusion Working Group was formed in 2020 to explore how to reduce barriers to joining PVN. It also aims to explore how a welcoming environment – one that supports emotional safety and builds trust – can be promoted across the network. The group consists of…
What makes patient engagement successful? How do we know if it’s ‘good’ or ‘working well’? Despite the growing momentum and practice of patient engagement in quality improvement, system redesign, and other health system projects, there remains no widely agreed upon way to determine how well, or if these efforts are…
The BC Centre for Palliative Care (BCCPC) defines advance care planning as a process of thinking about and sharing your values, beliefs and wishes for future health and personal care with the people you trust. It helps individuals get the care that is right for them, even if they are…
2020 was a year of learning to do things in new ways: grocery shopping in a mask, socializing six feet apart, working from home and seeing your doctor through a computer screen. For many British Columbians, 2020 was the first time they encountered virtual care by connecting with a care…
Seeking the patient perspective doesn’t have to be complicated; it simply entails a commitment to ask and listen. Patient advisors not only bring a valuable perspective but also share original ideas and unique skills. Including the patient and family perspective changes the conversation and aligns the team’s focus towards common goals.
Health Quality BC administers the Patient Voices Network. Using evidence-informed strategies, the Council shifts culture, improves clinical practice and advances person- and family-centred care to support high-quality care for every person in our province.