Patient and public involvement
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10 easy ways you can connect with patients online

10 easy ways you can connect with patients online | Patient and public involvement | Scoop.it
We like this one: Ask patients questions.

Via ET Russell
Emily Goodall's insight:

Very good tips for using social media, not just for health care professionals but science communicators in general. Those in academia take note, think outside the University walls and connect with the public - they most likely fund your research!

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Ask for evidence · Sense about Science

Ask for evidence · Sense about Science | Patient and public involvement | Scoop.it
Sense about Science ? Equipping people to make sense of science and evidence
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Patient Powered Improvement – the new PPI | Public Involvement ...

Patient Powered Improvement – the new PPI | Public Involvement ... | Patient and public involvement | Scoop.it
The old PPI is dead; long live the new PPI. It is time we started talking about PPI in new terms because we have a new NHS structure in England. Involvement.
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Health and Sport Committee takes evidence on new medicines review - Parliament & Government | the ALLIANCE

Health and Sport Committee takes evidence on new medicines review - Parliament & Government | the ALLIANCE | Patient and public involvement | Scoop.it
The authors of the Scottish Government’s newly published review of access to new medicines highlighted the importance of transparency and public and patient involvement in the decision-making process when they appeared before the Scottish...
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Sheffield Motor Neurone Disorders Research Advisory Group

Sheffield Motor Neurone Disorders Research Advisory Group | Patient and public involvement | Scoop.it
Emily Goodall's insight:

The only patient and public invovlement group in the UK available for Motor Neurone Disease (MND) research. Based in Sheffield, members are made up of MND patients, carers and family members affected by the disease who inform the research taking place at the Sheffield Institute for Translation Neuroscience (SITraN).

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Emily Goodall's curator insight, May 18, 2013 9:47 AM

The only patient and public invovlement group in the UK available for Motor Neurone Disease (MND) research. Based in Sheffield, members are made up of MND patients, carers and family members affected by the disease who inform the research taking place at the Sheffield Institute for Translation Neuroscience (SITraN).

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Patient and Public Involvement in Research – Passing the town hall ...

Patient and Public Involvement in Research – Passing the town hall ... | Patient and public involvement | Scoop.it
Patient and Public Involvement in Research – Passing the town hall meeting test. Posted on 03/04/2013 by adamgordon1978. Dr Adam Gordon is Consultant and Honorary Associate Professor in Medicine of Older People at Nottingham ...
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PatientsLikeMe and CISCRP Team up with Sanofi to Spotlight Medical Heroes ... - MarketWatch (press release)

PatientsLikeMe and CISCRP Team up with Sanofi to Spotlight Medical Heroes ...
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Clinical support for patient self-management is rhetoric rather than reality - HealthCanal.com

Clinical support for patient self-management is rhetoric rather than reality - HealthCanal.com | Patient and public involvement | Scoop.it
Clinical support for patient self-management is rhetoric rather than reality HealthCanal.com All staff, including clinical, management and administrative staff, at 44 practices were trained in a new self-management approach, designed by the...
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