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A Clarion Call for Africa to Embrace Patient Inclusion and Patient Engagement in Healthcare Research
By Oluwafemi Ajayi, Gail Sickle Initiative The word patient is generic and cuts across different health challenges around the globe. […]
What social determinants of health actually do within the scope of a person’s life
By Alex Haagaard A society is a group of people living together in a way that is organized by certain […]
Confidence in Building – We Got This!
By Joletta Belton People often ask me how I got involved with health research and education. It’s not a simple […]
Co-creating through Social Media Crowdsourcing
Developing an infographic with and for patient partners about conference abstracts by Dr. Dawn Richards
A square peg in a round hole: Patient and public author affiliations in academic journals
by: Dawn P. Richards (patient partner and Five02 Labs Inc, Toronto, Ontario, Canada) and Jim Elliott (independent advocate for patients in research, Wales, UK)
Engaging Patient Partners as Peer Reviewers of Grant Applications: Tips for Everyone Involved
By: Dawn Richards, Deb Baranec, Eileen Davidson, Trudy Flynn
Case Study: Expanding and supporting the patient partner community in research
By: Laurie Proulx, Nadine Lalonde, Anna Samson, Linda Roy, Julie McKenna
IMHA’s Patient Engagement Research Ambassadors’ Journey to Developing “A How-to-Guide to Patient Engagement in Research”
by: Dawn P Richards, Christine Thomas, and Gillian Newman
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