Annette Dancer and Claire Mitchell give us their perspectives on the benefits of working together in stroke research
Category Archives: Patient & Public Involvement
Here's what patients and carers have told us will make the 2018 Cochrane Colloquium, Cochrane For All, accessible, inclusive and interesting.
Member of the JLA Priority Setting Partnership on hyperacusis explain how they are working to ensure research into this hearing problem is directed by those affected by it
Announcing our #cochraneforall tweetchats - another opportunity to tell us what we could do to increase the involvement of patients and carers in next year's Cochrane conference.
Richard Morley and Sarah Chapman acknowledge the sensitivities around 'patient' and alternative terms, as work gets under way to make the Cochrane conference 2018 a 'Patients Included' event
Steven Williams blogs about the recently launched 'My Signals', in which health and social care staff and service users describe research that is important for them.
Announcing our plans to make the Cochrane Colloquium, our global conference, to be held in Edinburgh in 2018, a Patients Included event.
For our series Dementia in the Spotlight, Wendy Mitchell, who has young onset dementia, writes about taking part in dementia research and being valued again
Five Cochrane trainee doctors to share their experiences of talking with patients about sex.
Read about Cochrane’s new citizen science platform and their fast, furious and successful their recent 48 hour citation screening challenge!
Allied Health Professional and qualitative researcher Fran Toye looks at how qualitative research can allow hidden voices to emerge and improve patient care
Here are the top ten priorities in cavernoma research, established by a James Lind Alliance Priority Setting Partnership