Blog

Answer a quick survey to tell us what you like and don't like on our site, and share your suggestions on how we can improve it. Your feedback will be very helpful!

As we continue into the new year, we’re excited to announce some changes within our Patient & Public Engagement team.

2020 marks an exciting milestone for the Patient Voices Network: 10 years since the network began! Read on to learn more about how we’ll be celebrating all year long.

We’re thrilled to announce that the new patient partner representatives have been selected! See who they are and learn more about how they were selected.

Cancer treatment involves decisions and effects that often overwhelm and scare patients. To help in these delicate moments, the UBC School of Population and Public Health created a peer navigation program to match prostate cancer survivors as peer supporters for patients undergoing treatment. In this blog post, Dr. Arminée Kazanjian tells us more about the TrueNTH Prostate Cancer Peer Navigation Program:

2019 is coming to a close, and we’re amazed by how quickly the year went by! As the holidays approach, it’s time for our annual reflection on our evolution over the past year and the meaningful role our patient and health care partners have had in improving BC’s health…

As a palliative patient, Sally Rosevear’s husband passed away at home without comfort measures, emotional support or assistance with personal care, despite her efforts to get him the best treatment possible. She decided to share their story to improve health care and help prevent other patients from experiencing what she and her husband went through.

The BC Patient Safety & Quality Council revealed the winners of its 2020 Quality Awards, and we’re thrilled to have our patient partners Betty Murray and Wendy Alston as the winner and runner-up of the Leadership in Advancing the Patient Voice category! We’re also happy to see amazing projects that contributed to improving the quality of care. Learn more about them in this post!

You probably remember signing our Volunteer Agreement (VA) when you joined PVN, right? The VA is an essential tool to outline the responsibilities and supports available for volunteers, ensuring that they’re aware of the expectations when participating in engagements. After feedback, we decided to update the VA to make it even more helpful for everyone in our Network. Here we explain the changes and how they impact your participation as a patient partner.

After our post with 10 Ways to Implement Person- and Family-Centred Care in Your Health Care Practice, patient partners asked us for ways that they, too, can approach patient- and family-centred care. So we put together a helpful list for patients and families. We hope you like it!