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  • ALPHA – a young people’s research advisory group
  • Involving young people in the design and delivery of health research
  • Welcome to INVOLVE
  • YPAG: The Young Persons’ Advisory Group
  • Putting the horse before the cart: an agenda for public engagement
  • ‘If you build it they will come’
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  • Involving children and young people in research: not the usual suspects
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  • Involving ‘seldom heard’ groups in HIV research
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  • Learning to listen at Parkinson’s UK
  • Welcome to the Autumn 2014 Newsletter
  • Welcome to the Autumn 2014 Newsletter
  • What I wish I’d known before going into public involvement research
  • The NIHR-wide learning and development group – a member’s view
  • Planting the public involvement seed early in researchers’ careers
  • Building Research Partnerships
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  • Learning and development for public involvement: a personal reflection
  • The National Institute for Health Research (NIHR) strategic review of public involvement in research
  • Plain English summaries in National Institute for Health Research (NIHR) funded research
  • Parents advising researchers: Experiences from the ‘Beating Anxiety Together’ study
  • The changing face of public involvement in research teams
  • Inspiring involvement in research
  • Welcome to the Spring 2014 Newsletter
  • Around the table: Maryrose Tarpey
  • Around the table: Maryrose Tarpey
  • Around the table: Patricia Wilson
  • Around the table: Kati Turner
  • Around the table: Sophie Staniszewska
  • Around the table: Diana Rose
  • Around the table: Andrew Gibson
  • Around the table: Jonathan Boote
  • Criteria for inclusion
  • Around the table: Rosemary Barber
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  • You’ve done the research – now what?
  • Merging worlds – the importance of support roles for patient and public involvement (PPI)
  • SCIE: Talking and walking co-production
  • Optimising adult mental health service configurations across health and social care
  • Webinars: an insider’s view
  • Exploring the impact of public involvement in research: examples
  • Public involvement/ participation/ engagement in research
  • The lived experience of co-producing research
  • Launch of the Public Involvement Impact Assessment Framework
  • Clinical Research Ambassador Group
  • The Tourettes Listening Project
  • EQUIP: Building the skills of service users and carers to become involved in research
  • STOP Diabetes study
  • PPI in research – passing the town hall meeting test
  • Budgeting for involvement
  • Beyond the usual suspects, towards inclusive user involvement
  • Involving patients and the public in the work of the Medical Research Council Clinical Trials Unit
  • Public involvement in clinical trials
  • Public involvement and the REF ‘impact’ agenda: squaring the circle?
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  • What’s the evidence for? A critical reflection on the evidence base for public involvement in research
  • Patient involvement in setting research priorities in the Netherlands
  • University of Western Australia Consumer and Community Participation Program
  • The Center for Evidence-based Policy at Oregon Health & Science University: Working to engage US patients and stakeholders in health research
  • Patient and health consumer involvement at ZonMw
  • BPSU PPI Guidance for Researchers
  • The road towards PPI in research in Denmark
  • Newsletter Spring 2013 invoDIRECT
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  • All Trials Registered, All Results Reported
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  • Involving women with gestational diabetes
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  • INVOLVE 2012 Conference – Facts and figures
  • Putting research on everyone's agenda
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  • Welcome to the INVOLVE Autumn 2012 Newsletter
  • Becoming ‘them’ and remaining ‘us’ … or the road to ruin?
  • Community Researchers
  • Is there another ‘P’ to consider in relation to longitudinal birth cohort studies?
  • Involving people with communication disability in participatory research: the Friendship and Aphasia project
  • Resource for researchers templates
  • Developing training and support for public involvement in research
  • The Past Caring Project: a carer-led narrative research project about carer bereavement
  • International Collaboration on Participatory Health Research
  • The VIPER Project: involving young disabled people in research
  • Putting our strategy into practice
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  • Developing training and support case studies
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  • Issues to think about before you start – support
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  • Support for peer interviewers
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  • Involving patients and the public in talking about medical research
  • Consumers take the initiative in patient and public involvement (PPI) training
  • Top ten research priorities relating after stroke
  • The patient inside and ‘outside’ the committee
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  • Bringing our strategy to life
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  • Improving musculoskeletal research in North Bristol through public participation
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