PxP
@PxPHub
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👉For Patients, By Patients 👈 The PxP initiative brings together resources for the patient engagement community in health research.
Canada
Joined June 2023
📢Sign up now for #PxP25! .September 9-12, depending where you are based in the world. Our conference is virtual and free to attend. #PPI #ConsumerInvolvement #ForPatientsByPatients
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Need to write a Letter of Support but don’t know where to get started?. We’ve created this resource for you if you’re a patient partner and you’ve been asked to write a Letter of Support for a researcher or research team. Link:
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PxP Steering Committee Member Simon Stones shares a quote on the importance of patient partner leadership and why they should be at the forefront of initiatives like PxP. Learn more about PxP 2025 here: #PxP25 #PatientEngagement
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RT @breastlessAfrik: African Patient Dialogue🌍🌍🌍. New Paradigm: From research participants, to research partners . @JoabWako and I thrilled….
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📢Introducing PxP Africa!. Led by @JoabWako and @breastlessAfrik PxP Africa will spotlight the critical role of patient partners—especially African patients—as active contributors in research, not just research participants. Learn more and register:
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RT @KT_trainee: For Patients, By Patients. Register now for this free, virtual conference for anyone with an interest in health research. S….
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RT @TO_dpr: 📢Patient Partners! Been asked to write a Letter of Support (LOS) and not entirely sure what that is? We co-created a resource w….
pxphub.org
Written by Deb Baranec, Jim Kempster, and Dawn Richards Graphic Created by Tianna Magel What is a Letter of Support […]
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Tips for in-person conferences are also available here:
pxphub.org
By Rae Martens (ferprogram.ca) As I write this, I am currently flat on my back on the couch with my […]
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At PxP, the concept of accessibility has been critical since the start of the planning discussions by the PxP Steering Committee members for both PxP 2023 and 2024. It is also a key part of planning for the 2025 PxP conference.
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Accessibility should be an important part of engaging patient partners in any research project or initiative, and especially in a conference designed by and for patient partners.
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Members of the #PxP24 steering committee put together this accessibility checklist for virtual conferences:.👉@SickleGail @rebeccaesparza.
pxphub.org
Checklist Developed by: Oluwafemi Ajayi, Rebecca Esparza, Rae Martens, and Shyamsundar Muthuramalingan Illustration by: Candace Ramjohn Blog by: Rebecca Esparza and […]
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Want some tips and guidance for “How to Read a Scientific Paper”? . Check out our latest resource: #PxP #PatientPartners #Research #HowtoReadaScienticPaper
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RT @womenofteal: Patients, Advocates, Caregivers -.Check out this blog post on How to Read a Scientific Paper by @PxPHub . Excellent ! .htt….
pxphub.org
Co-Created by Dawn Richards and Jim Kempster with input from CIHR-IMHA PERA members Graphics created by Tianna Magel Scientific […]
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RT @breastlessAfrik: I AM an access activist 🇿🇦💊💉🩺. And I thrive on *global knowledge gathering and sharing*. Honoured to be a member of th….
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RT @breastlessAfrik: Setting a new #globalhealth #research paradigm . I AM honoured to be part of the #PxP25 Conference Steering Committee🌏….
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A big thank you to the #PxP25 Steering Committee for co-creating this year’s conference which will take place September 9-12 (exact dates and times depending where you are based in the world). Learn more 👉 #PatientEngagement
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📢 Save the date! PxP (For Patients, By Patients) is coming back September 9-12, 2025! 🎉. A free, virtual event focused on #PatientEngagement — created by patients, for patients. 💌Stay in the loop: sign up for the PxP newsletter (link in bio). #PxP25 #ForPatientsByPatients
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