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Patient Engagement Research Ambassadors’ 2024 Community Patient Engagement Report: How we co-created it and some highlights
Click Here for Report By Deb Baranec, Beth Ciavaglia, Anna Samson, Dawn Richards The Institute of Musculoskeletal Health and Arthritis’s […]
PxP Africa Attendee Chat Summary
The inaugural PxP Africa meeting was led by Joab Wako and Kwanele Asante, who are also members of the steering […]
Fact vs. Fiction: Helping you sift through online information
Written by Trinity Lowthian and Dawn Richards With all the information that’s available on social media or generally on the […]
A Resource for Patient Partners in Research about Letters of Support
Written by Deb Baranec, Jim Kempster, and Dawn Richards Graphic Created by Tianna Magel What is a Letter of Support […]
An accessibility checklist for virtual conference – by and for patients
Checklist Developed by: Oluwafemi Ajayi, Rebecca Esparza, Rae Martens, and Shyamsundar Muthuramalingan Illustration by: Candace Ramjohn Blog by: Rebecca Esparza and […]
How to Read a Scientific Paper
Co-Created by Dawn Richards and Jim Kempster with input from CIHR-IMHA PERA members Graphics created by Tianna Magel Scientific […]
Providing input on a research team’s draft manuscript: Why this is important and some guidance
A Blog and Checklist for Patient Partners/People with lived experience By Anna Samson, Chantale Thurston, Don Wood, Trinity Lowthian, Dawn […]
Asking patient partners/people with lived experience to provide input on a draft manuscript: Things to consider and some guidance
A Blog and Checklist for Research Teams By Anna Samson, Chantale Thurston, Don Wood, Trinity Lowthian, Dawn Richards and Perri […]
Illustrating Patient Experiences
Interview with Candace Ramjohn, By Melody Choi Candace Ramjohn, a self-identified “visual alchemist,” sees visual media not just as a […]
Attending In-person Research Conferences When Your Patient or Family Partners Have a Chronic Illness
By Rae Martens (ferprogram.ca) As I write this, I am currently flat on my back on the couch with my […]
Patient Engagement in Research Workshop: An initiative for Researcher education
Written by Trudy Flynn, Patient Partner and Tianna Magel, Project and Research Analyst at CIHR-IMHA Edited by Hetty Mulhall A […]
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. […]
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