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Because your voice matters.

Patient and Family Advisors, Access to Service Project – Victoria Hospice Society

Posted

Closed

Commitment: One-time

Open to Vancouver Island Region, Patient partners across BC

Posted

Victoria Hospice Society is seeking to engage people with lived experience with a life-limiting condition – either personally or through supporting a loved one. The purpose of this engagement is to gather meaningful patient, family and caregiver insights to:

– Ensure that Hospice’s new referral pathways reflect real-world needs and experiences
– Identify barriers and opportunities that may not be visible to internal teams
– Validate proposed changes before implementation to ensure usability and clarity
– Inform the development of clear, compassionate communication materials grounded in patient and family perspectives
– Provide strategic input for decision-makers regarding how to advance a person-centred approach to care and services with Victoria Hospice more generally

We will hold 1-3 focus groups from January-March 2026, approximately 60-90 minutes long each. Options will be provided for either in-person participation (at the Victoria Hospice Society, Royal Jubilee Hospital campus) or online (via Microsoft Teams), depending on participant availability and preference.

Level of Engagement

This opportunity is at the level of Consult on the IAP2 Spectrum of Public Participation.

Eligibility

  • Willing & comfortable to share health care experiences in a group setting
  • Specific health care experiences [details below]
  • An interest in improving health care services
  • Lived experience with a life-limiting condition, either personally or supporting a loved one
Patient Partners ARE NOT required to be PVN members to participate in this engagement opportunity.

Health Care Partner Contact Information

Sarah Gustin Consultant, Corporate Services | Victoria Hospice Society (778) 235-0846 sarah.gustin@victoriahospice.org

From Our Community

Layton Engwer

Patient Partner, Sooke

Layton Engwer

PVN helped empower me to make meaningful contributions to Primary Care (PC) locally and provincially.  It also facilitated creation of PC Patient Voices which is focused on PC and provides education support and building on shared experiences.