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      Patient engagement in Canada: a scoping review of the ‘how' and ‘what' of patient engagement in health research
      • A Former User

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      Agree

      Patient engagement in Canada: a scoping review of the ‘how' and ‘what' of patient engagement in health research

      When I tweeted it (from PAN) we got 110 clicks on the link - that must be a record!

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      Suggestions on Patient Engagement Frameworks & Pt. Engagement 2.0
      • A Former User

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      Thank you Annette. You are a great resource. Frank Gavin and others members of the PPAWG would probably welcome seeing this material. It should be considered as material for discussion at our March meeting. This was a topic that generated a lot of interest at the PiR course.

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      Basic Tips on Effective Communication from Patient Voices
      • A Former User

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      Completed survey - I'll look forward to seeing how this project evolves!

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      Terrific Australian resource for co-design. Download this toolkit today!
      • A Former User

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      Thanks for this Carolyn- I am looking forward to reviewing this very comprehensive document. I would like to have a better understanding of how to use co-design in a variety of health care settings or other consumer situations

      Jeanne

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      Assessing Participant-Centered Outcomes to Improve Clinical Research
      • A Former User

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      YW & happy new year 🙂

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      Virtual library on resources for caretakers in QC / Bibliothèque virtuelle sur les ressources pour aidants naturels au Québec
      • A Former User

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      I am involved in caregiver projects with The Change Foundation in Ontario. Thanks!

      Je participe à des projets de proches aidants avec The Change Foundation en Ontario. Merci!

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      St. Mike's Hospital New Course on Pt/Family Engagement in Research
      • A Former User

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      I took this online course last year and found it very interesting. The presentations were well done and stimulating and unlike most online forums,there was lots of exchanges of information between participants - it made me think about how much this area has evolved and how it is current evolving as people's perceptions change about the value of patient engagement

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      "We struggled for meaningful engagement opportunities"
      • A Former User

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      I agree. I realize that there is a genuine interest on the part of HCPs with some being responsible for starting support groups such as Type 1 Diabetes Think Tank and doing so very successfully. Working with patients directly over time has resulted in sincere empathy for patients and a real desire to make a positive difference for those living with challenges in their daily lives. I believe research dollars are much more likely to result in better outcomes when research addresses patient's voiced challenges. I think that those researchers who have access to blogs or or support groups are in a better position to identify and seek to research patient's articulated needs. It seems like a good research topic to develop strategies that yield genuine patient engagement.

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      Patient & Family Partners in Research - are these truly the issues and experiences?
      • A Former User

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      Denyse, I'm again re-reading this thread. I love your approach and think it is great advice for newcomers to being partners in research:

      "The key is listening, observing and asking questions that bring the discussions back to the question - is this putting the "patient-first" and if so, how? What are the benefits? How does this help, not help? Does it create any barriers, obstacles or leave gaps?"

      I found during my first experience on the Research Management Committee evaluating grant proposals that asking questions from the patient perspective was a powerful way of re-focusing the group. It also meant I didn't feel the need to be expert.

      Keep us posted on your progress. Also, check out the course on PiR under Opportunities. It is a good one that involves lots of discussion online. Cheers! Alies

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      What questions should providers ask caregivers about themselves?
      • A Former User

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      Denyse, I realize that I am too terse in my explanations. Will try and do better. The goal is to find 1-3 questions we can suggest providers ask caregivers to prompt a conversation to uncover caregiver needs.

      I did receive some good feedback from members both online and off line. In the end I summarized the 3 questions that providers should consider asking caregivers:

      • How are you coping today?
      • What is the one thing that you find difficult about having the additional role of providing support and care for your (parent, spouse, child, ...)?
      • How has the rest of your life been affected by your role as caregiver? Work, friends, family, health...

      The idea is to make it simple for providers to start a conversation with caregivers about how they are doing so as to identify what kind of help the caregiver needs for themselves. This is in addition to any help the caregiver needs to actually take care of their patient.

      Hope that helps and any further thoughts you have are most welcome. Alies

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      IMP: Review of Pan-Canadian Health Organizations due by Nov 24, 2017
      • A Former User

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      Hi Amy,

      I am sorry I missed you for breakfast. I went to the 21st floor for breakfast hoping to see you. I realized later that maybe this was just for presenters. I could not find Kirk Kelly on the list of presenters for Friday so perhaps this was a pay to participate session.

      Hopefully we will meet up during this conference.

      Lorraine

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      Training Patient and Family Storytellers and Patient and Family Faculty
      • A Former User

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      Bingo Amy!

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      Two-way street? A critical look at patient and family engagement
      • A Former User

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      I loved this talk - Jennifer is terrific. I'm moderating a panel at the Brain Partners Conference in Toronto where Jennifer will speak on this again. Looking forward to what a room full of researchers will think! No one has any answers so I think the call will be for researching a 'science of engagement'.

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      Consultations with members of the public
      • A Former User

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      A good set of questions. Thank you Lorraine.

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      Making Patients and Doctors Happier — The Potential of Patient-Reported Outcomes
      • A Former User

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      Statistics paint a powerful message. We have a lot of work to do to change these metrics.

      Lorraine

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      Helen Bevan Slide Show-Where social movements meet co-design: participation in healthcare innovation and improvement
      • A Former User

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      Congrats Annette and RIGHT ON.

      Denyse 🙂

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      Pharma and the Universal Patient Language.
      • A Former User

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      thx for this Annette.

      Bristol Meyers Squibb is providing REWARDS to patients for their trust in the BRAND via CONTESTS ... as unpalatable as this might seem it is not a new concept tho sometimes a hard pill to swallow in Canada. Tongue out An additional article outlining how PATIENT SATISFACTION is the next competitive battleground for health care is a reality we all have to deal with it seems see: http://www.miramedgs.com/ealerts/673-patient-satisfaction-is-the-next-competitive-battleground

      warm regards,

      anita l-l

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      Article to share on Patient Engagement in Research
      • A Former User

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      Thanks Amy, I am a co-author on the study, so pleased to see you post it.

      (Maybe not co-author but collaborator or patient partner - not positive)

      Annette

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      For review and comment - Making Stories Matter presentation
      • A Former User

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      I think it sounds like a great plan 🙂

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      Rémunération pour les patients partenaires: combien et pour quoi?
      • A Former User

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      Désoler si le texte n’apparait pas au complet, car je ne suis pas habitué avec le format du site, mais si vous copiez le texte Word du site et que vous ouvrez votre Word et coller alors le texte apparaitra au complet.

      Bonne journée

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