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Because your voice matters.

2019 Newsletters

Check out the newsletters we sent in 2019:

December 20: Thank You for Making 2019 a Great Year!

December 18: Our Patient Partner Won a Leadership in Advancing the Patient Voice Quality Award!

December 4: Registration is Now Open for Quality Forum 2020! | Changes to Our Volunteer Agreement

November 7: New “What Matters to You?” Results are Out! | We’re in the New SPORcast Episode

October 28: #ConquerSilence on Canadian Patient Safety Week | Join Our Oversight & Advisory Committee

October 10: October is Patient- and Family-Centred Care Month!

September 26: Canada’s First Patient-Led Podcast is Playing!

September 9: Join the Fight Against Sepsis

September 4: Our Patient Engagement Learning Series is Back! Primary Care in BC

August 8: Share Your Work at Quality Forum 2020!

July 11: Check Out This New Resource: A Guide to Patient Engagement

June 26: How to Craft Outstanding Quality Awards Nominations

June 20: Applying Cultural Safety & Humility in Patient Engagement

June 5: Who Will You Nominate for a Quality Award?

May 23: Meaningful Stories about Asking What Matters

May 9: International Webinar, Patient Engagement in Research, Self-Care Tips & More!

April 23: It’s Patient Experience Week at PVN

April 5: “What Matters to You?” Day Celebrations | More Quality Forum Videos

March 21: Patient Partner Compensation: Initial Survey Results

March 7: Watch Quality Forum 2019 Sessions Online

February 22: Watch Quality Forum 2019 Presentations Live Online! | e-Health Conference Scholarship

February 7: Help Us Name Our New Networking Program! Designing Health Care Solutions with Empathy

January 24: It’s Here! Introducing our Patient Engagement Learning Series | Resource Round-up

January 10: Help Us Learn More about Patient Partner Compensation | PVN Patient Partner Helps Design Educational Videos

From Our Community

Christine Wallsworth

Patient Partner, Vancouver

Christine Wallsworth

Patient and family partners should not be a check box on research proposals! They need to be involved right from the start. I know patient and family partners are doing their part by providing their knowledge to researchers from their lived experience.  It’s a win-win for us to work together through PVN to make sure our input drives improvements.